ALS Directory of Information

ALS Society Page ALS and Lou Gehrigs Disease Articles

Advocacy Advocacy

ALS Research ALS Research

Awareness Awareness

Caregivers Caregivers

Charity Events Charity Events

Drug Trials Drug Trials

Fundraising Fundraising

General General

Healthcare Professionals Healthcare Professionals

Press Releases Press Releases

Researchers Researchers

Volunteer Volunteer

Recent ALS Information, Research Updates, and Related Articles:

1. Study Links Neurodegeneration in Head Trauma and ALS

Nearly four years since researchers identified the mystery component of toxic protein aggregates in ALS and frontotemporal lobar degeneration (FTLD)-affected motor neurons as TAR DNA-binding protein ( ◊
"Study Links Neurodegeneration in Head Trauma and ALS"

2. New Genes, Proteins and Biomarkers

Buried deep within thick skulls and boney spines, the neurons of the central nervous system are, perhaps, the most protected cells of the body. This is good news for healthy neurons, but bad news for ◊
"New Genes, Proteins and Biomarkers"

3. A clinical study of Ceftriaxone in ALS

A clinical study of Ceftriaxone in ALS. ◊
"A clinical study of Ceftriaxone in ALS"

4. The Ladies’ Auxiliary of the C.I.B.P.A. Hosts Fundraising Fashion Show

Just in time for fall, the Ladies’ Auxiliary of the Canadian Italian Business & Professional Association (C.I.B.P.A.) will be hosting “Moda in Motion 2010 Fashion Show.” ◊
"The Ladies’ Auxiliary of the C.I.B.P.A. Hosts Fundraising Fashion Show"

5. ALS Vaccine To Target Misfolded SOD1

Mutations in the gene encoding superoxide dismutase cause approximately 20 per cent of familial ALS cases, according to a paper recently published in Human Molecular Genetics. ◊
"ALS Vaccine To Target Misfolded SOD1"

6. Cast Your Vote to Support the ALS Community in the Greater Toronto Area

Two Torontonians, Shana Valo, 26, and Alix Duck, 27, are on a mission to support families living with ALS and have entered the Pepsi Refresh Everything Project to make this possible. ◊
"Cast Your Vote to Support the ALS Community in the Greater Toronto Area"

7. Is BMAA a neurotoxin relevant to ALS?

Cyanobacteria, also known as the blue-green algae that smother ponds, lakes and seas around the world, produce several toxins. Among them is beta-methylamino-L-alanine (BMAA), an amino acid that some ◊
"Is BMAA a neurotoxin relevant to ALS?"

8. Neurodegenerative Disease Research Accelerates

While scientists worldwide strive to understand neurodegeneration and find ways to slow or stop it, variations in how they perform experiments and interpret their findings can slow the global effort t ◊
"Neurodegenerative Disease Research Accelerates"

9. Optineurin Mutations in ALS

Although most ALS cases are sporadic, 10 per cent are familial, meaning they result from a hereditary gene defect. ◊
"Optineurin Mutations in ALS"

10. ALS BC Advocacy Committee Receives Exceptional Advocacy Award

The ALS Society of British Columbia & Yukon’s advocacy committee under the leadership of Chairperson John Pendray, received the ALS Society of Canada’s Brett Yerex Exceptional Advocacy Award (group) i ◊
"ALS BC Advocacy Committee Receives Exceptional Advocacy Award"

11. Krieger Receives Honourary Life Member Award

Vancouver, BC resident Dr. Charles Krieger received the ALS Society of Canada’s Honourary Life Member Award in recognition of his long time involvement and contribution to Canada’s ALS community durin ◊
"Krieger Receives Honourary Life Member Award"

12. Williams Receives Exceptional Advocacy Award

Edmonton, AB resident David Williams received the ALS Society of Canada’s Brett Yerex Exceptional Advocacy Award (Individual) in recognition of his volunteer contribution to the ALS community of Canad ◊
"Williams Receives Exceptional Advocacy Award"

13. Mahoney Receives Myra Rosenfeld Volunteer Award

Ellen Mahoney of Victoria, BC, received the ALS Society of Canada Myra Rosenfeld Volunteer Award in recognition of her volunteer contribution to the ALS community of Canada during an awards ceremony o ◊
"Mahoney Receives Myra Rosenfeld Volunteer Award"

14. Georgetown WALK For ALS Receives Exceptional Fundraising Award

The organizing committee of the Georgetown, Ontario WALK for ALS has received the 2009 Exceptional Fundraising Award from the ALS Society of Canada during an awards ceremony on May 1, 2010 in Toronto ◊
"Georgetown WALK For ALS Receives Exceptional Fundraising Award"

15. Dr. Jim McEwen Receives William Fraser Leadership Award

Vancouver, BC resident Jim McEwen, PhD, received the ALS Society of Canada’s William Fraser Leadership Development Award recognizing his outstanding leadership skills in the ALS community on May 1, 20 ◊
"Dr. Jim McEwen Receives William Fraser Leadership Award"

16. John and Madonna Kavanagh Receive Honourary Life Member Award

Long Pond, Newfoundland residents John and Madonna Kavanagh received the ALS Society of Canada’s Honourary Life Member Award in recognition of their tireless dedication and volunteer contributions to ◊
"John and Madonna Kavanagh Receive Honourary Life Member Award"

17. Njilas Receives Leader of Tomorrow Award

Guelph, ON resident Kinga Njilas received the ALS Society of Canada’s Leader of Tomorrow Award in recognition of her outstanding efforts to raise awareness and funds for ALS on May 1, 2010 in Toronto. ◊
"Njilas Receives Leader of Tomorrow Award"

18. Peoples Drug Mart Receives Exceptional Public Awareness Award

Ian Maxwell, President and CEO of Peoples Drug Mart located in Victoria, BC, received ALS Society of Canada’s Exceptional Public Awareness Award, which recognizes their efforts to raise awareness of A ◊
"Peoples Drug Mart Receives Exceptional Public Awareness Award"

19. Provincial Respiratory Outreach Program Receives Exceptional Support Servic

Simon Cox, executive director of The Provincial Respiratory Outreach Program (PROP) in British Columbia, received the 2009 ALS Society of Canada’s Marcel Bertrand Exceptional Support Services Program ◊
"Provincial Respiratory Outreach Program Receives Exceptional Support Servic"

20. Smailes Receives WALK for ALS Volunteer Award

Kamloops, BC resident Clayton Smailes (posthumously) was recognized for his efforts to raise awareness of ALS by the ALS Society of Canada, who presented the Mary Pollock WALK For ALS Volunteer Award ◊
"Smailes Receives WALK for ALS Volunteer Award"

21. Vincent and Allana Damphousse Receive Honourary Life Member Award

Baie-D’Urfé, QC residents Vincent and Allana Damphousse received the Honourary Life Member Award in recognition of their volunteer contributions to Canada’s ALS community during an awards ceremony on ◊
"Vincent and Allana Damphousse Receive Honourary Life Member Award"

22. Vincent et Allana Damphousse Faits Membres Honoraires

Vincent et Allana Damphousse, de Baie-D’Urfé, au Québec, ont tous les deux reçu le titre de membre honoraire de la Société canadienne de la SLA en reconnaissance de leur engagement bénévole, lors du g ◊
"Vincent et Allana Damphousse Faits Membres Honoraires"

23. June is ALS Awarness Month

June is ALS awareness month in Canada. In each province, public awareness and fundraising campaigns will be carried out throughout the month. ◊
"June is ALS Awarness Month"

24. Message from Leona Aglukkaq, Minister of Health re: ALS Awarness Month

As Minister of Health, I am proud to recognize June as Amyotrophic Lateral Sclerosis (ALS) Awareness Month in Canada. ◊
"Message from Leona Aglukkaq, Minister of Health re: ALS Awarness Month"

25. ALSUntangled investigates stem cell transplants in Mexico and Germany

Although stem cell transplants might eventually represent an effective treatment for ALS, many challenges need to be overcome, such as how to deliver the cells into motor areas throughout the nervous ◊
"ALSUntangled investigates stem cell transplants in Mexico and Germany"

26. Guidelines for preclinical animal research

We know more about the biology underlying ALS than ever before, but little of this knowledge has been translated into effective treatments for patients. ◊
"Guidelines for preclinical animal research"

27. Clive Svendsen Received Sheila Essey Award for ALS Research

The American Academy of Neurology has announced that Clive Svendsen, PhD, a scientist at the Cedars-Sinai Regenerative Medicine Institute in Los Angeles, CA, received the 2010 Sheila Essey Award for A ◊
"Clive Svendsen Received Sheila Essey Award for ALS Research"

28. New Mutation Associated with Familial ALS

Researchers from Imperial College London have discovered a new genetic mutation associated with ALS. ◊
"New Mutation Associated with Familial ALS"

29. Lithium trial failure raises hope for future success

Treating ALS patients with lithium and riluzole is no better than treating them with riluzole alone, according to a report published April 6 in Lancet Neurology. ◊
"Lithium trial failure raises hope for future success"

30. Respiratory Therapy Federation Raises Funds For ALS

TORONTO, May 10, 2010 - The Conestoga Respiratory Therapy Federation (C.T.R.F.) assisted the ALS Society of Canada in our efforts to find a cure by raising ◊
"Respiratory Therapy Federation Raises Funds For ALS"

31. Phase 1 clinical trial of ISIS-SOD1Rx initiated

On March 5, 2010, Isis Pharmaceuticals Inc. announced that it initiated a Phase 1 study of ISIS-SOD1Rx, an antisense drug designed to inhibit the production of a mutant enzyme implicated in the approx ◊
"Phase 1 clinical trial of ISIS-SOD1Rx initiated"

32. Abnormal SOD1 folding is unique to familial ALS, researchers say

Mutations in the gene encoding superoxide dismutase 1 (SOD1) cause up to 20 per cent of inherited ALS cases (familial ALS). They’ve even been observed in a small fraction of sporadic cases. It has bee ◊
"Abnormal SOD1 folding is unique to familial ALS, researchers say"

33. Swimming-based exercise preserves motor neuron function

Whether exercise predisposes to or protects against amyotrophic lateral sclerosis is a topic of ongoing debate. ◊
"Swimming-based exercise preserves motor neuron function"

34. Stage 3 ceftriaxone trial begins

A stage 3 trial has begun studying the efficacy of ceftriaxone, to see if it prolongs survival and/or slows decline in function in patients living with ALS. ◊
"Stage 3 ceftriaxone trial begins"

35. Synapse formation can be triggered artificially

The formation of synapses – the junctions through which neurotransmitters relay chemical signals allowing neurons to communicate information – typically requires contact between presynaptic and postsy ◊
"Synapse formation can be triggered artificially"

36. Phase 3 talampanel trial begins

Talampanel, a drug currently not approved in Canada or the United States, is undergoing an international Phase 3 trial involving 500 patients with ALS in centres across Europe, Canada and the US. In a ◊
"Phase 3 talampanel trial begins"

37. Genetic contributors to motor neuron diseases

The recent discovery of a number of genes known to cause motor neuron diseases such as ALS has provided new insights into the mechanisms underlying motor neuron degeneration, according to a recent art ◊
"Genetic contributors to motor neuron diseases"

38. Defining survival as an outcome measure for clinical trials in ALS

Clinical trials in ALS often use patient survival as an outcome measure to examine whether a treatment prolongs life. But variables affecting survival rates – such as emergency tracheostomy – are dif ◊
"Defining survival as an outcome measure for clinical trials in ALS"

39. Encouraging trial results for KNS-760704

At the 20th Internal Symposium on ALS/MND, researchers presented the results of a Phase 2 clinical trial testing the safety and tolerability of a drug called KNS-760704 for use by ALS patients. KNS-7 ◊
"Encouraging trial results for KNS-760704 "

40. Molecule discovered that might help ALS Patients

University of Texas researchers identified a molecule that reduces symptoms and prolongs life in mice with a type of ALS, according to a study in the Dec. 11, 2009, issue of Science. Lead author Eric ◊
"Molecule discovered that might help ALS Patients"

41. Misfolded SOD1 not a feature of sporadic ALS

Abnormal folding of superoxide dismutase 1 (SOD1) – a protein known to gain harmful properties from heritable gene mutations in familial ALS – does not appear to cause cases of familial ALS without SO ◊
"Misfolded SOD1 not a feature of sporadic ALS"

42. TDP-43 mutations cause motor deficits in zebrafish

Mutations in the TAR DNA-binding protein (TDP-43) gene cause motor neuron defects in zebrafish and lead to impaired swimming, researchers from Université de Montreal report. Interestingly, insufficie ◊
"TDP-43 mutations cause motor deficits in zebrafish"

43. Evidence for ALS as a disorder of RNA metabolism

Defects in RNA binding might represent a disease mechanism common to all cases of ALS, a leading Canadian researcher reports. ◊
"Evidence for ALS as a disorder of RNA metabolism"

44. Formaldehyde exposure linked to ALS risk

Formaldehyde exposure is associated with an increased risk for ALS, according to a longitudinal study conducted by Mark Weisskopf, PhD, ScD, and colleagues from the Harvard School of Public Health, ◊
"Formaldehyde exposure linked to ALS risk"

45. Cognitive and behavioural dysfunction in ALS

Amyotrophic lateral sclerosis – a disease once thought to only rob patients of their ability to move – is now recognized as having cognitive and behavioural effects in one out of two patients. This o ◊
"Cognitive and behavioural dysfunction in ALS"

46. ALS patients with SOD1 mutations are less likely to have cognitive deficits

Patients with familial ALS (FALS) caused by mutations in the SOD1 gene are less likely to exhibit cognitive changes than those without SOD1 mutations, according to a report published in The Journal of ◊
"ALS patients with SOD1 mutations are less likely to have cognitive deficits"

47. Invitation to Submit a Letter Of Intent

Invitation to Submit a Letter Of Intent(LOI) - National Population Health Study of Neurological Conditions // Invitation a presenter une lettre d'intention -Étude nationale de la santé des population ◊
"Invitation to Submit a Letter Of Intent"

48. NRP Priority Announcement

NRP Priority Announcement ◊
"NRP Priority Announcement"

49. Gene variant implicates faulty cellular secretion in ALS

A variation in the chromogranin gene may confer susceptibility to ALS and accelerate disease onset, researchers from Laval University report. ◊
"Gene variant implicates faulty cellular secretion in ALS"

50. Live imaging of the inflammatory response to ischemic brain injury

A new technology has revealed that inflammatory cells in the olfactory bulb of the brain may act as sensors and modulators of inflammation following brain injury, scientists report. ◊
"Live imaging of the inflammatory response to ischemic brain injury "

51. FUS pathology in frontemporal lobar degeneration

Abnormalities in Fused in Sarcoma (FUS), a protein implicated in ALS, might also be to blame for a subgroup of frontotemporal lobar degeneration (FTLD) cases, scientists report. ◊
"FUS pathology in frontemporal lobar degeneration"

52. TDP-43 mutations cause ALS and FTLD-like disease in mice

Mice expressing a gene mutation known to cause amyotrophic lateral sclerosis and frontotemporal lobar degeneration exhibit behavioral and pathological features resembling the human diseases, researche ◊
"TDP-43 mutations cause ALS and FTLD-like disease in mice"

53. Exercise and ALS

Exercising involves motor neuron activation, which is accompanied by such consequences as oxidative stress, free radical production and glutamate stimulation. These exercise-induced effects are strict ◊
"Exercise and ALS "

54. New guidelines from the American Academy of Neurology

New guidelines from the American Academy of Neurology identify the most effective treatments for amyotrophic lateral sclerosis (ALS) ◊
"New guidelines from the American Academy of Neurology "

55. ALS Canada on Parliament Hill Oct. 7, 2009 with Prime Minister Harper

ALS Canada goes to Parliament Hill on Wednesday, October 7th, 2009 and meets with Prime Minister Harper ◊
"ALS Canada on Parliament Hill Oct. 7, 2009 with Prime Minister Harper"

56. ALS Society of Canada provides critical funding for new ALS scientists

The ALS Society of Canada is thrilled to announce the creation of the Ronald Peter Griggs Memorial Postdoctoral Fellowship in ALS Research. The Griggs Fellowship will be awarded to three post-doctora ◊
"ALS Society of Canada provides critical funding for new ALS scientists"

57. Toronto Artist Paints Cards to Raise Awareness for ALS

TORONTO, August 6, 2009- Four of Elizabeth Berry’s paintings will be featured on the ALS Society of Canada’s new cards to promote awareness of the fatal neurodegenerative disease also known as Lou Geh ◊
"Toronto Artist Paints Cards to Raise Awareness for ALS"

58. ALS Society of Canada Funds Neuromuscular Disease Research in Partnership

TORONTO, July 9, 2009- The ALS Society of Canada is pleased to announce the four recipients of the 2009 Neuromuscular Research Partnership (NRP) grants. Recipients will receive funding for their proje ◊
"ALS Society of Canada Funds Neuromuscular Disease Research in Partnership"

59. Bernice Ramsay Clinical Fellowship

The Bernice Ramsay Clinical Research Fellowship supports specialized training in clinical care and research skills related to ALS. This fellowship is funded by the ALS Society of Canada and has a dura ◊
"Bernice Ramsay Clinical Fellowship"

60. ALS PSA Wins 2009 Applied Arts Design & Advertising Award

TORONTO, June 25, 2009- The ALS Society of Canada’s television public service announcement, “Head and Shoulders”, has won the 2009 Applied Arts Design & Advertising Award for best single television co ◊
"ALS PSA Wins 2009 Applied Arts Design & Advertising Award"

61. ALS Canada Applauds Government of Canada’s Research Investment

TORONTO, June 5, 2009 – Canadians with neurological conditions, caregivers and representatives from Neurological Health Charities Canada celebrate the announcement of $15 million in research funding, ◊
"ALS Canada Applauds Government of Canada’s Research Investment"

62. Online Auction Funds Research for ALS

TORONTO, June 10, 2009 - The ALS Society of Canada is holding an online auction this month at www.auctionforals.ca. All proceeds go towards funding research and support services for those living with ◊
"Online Auction Funds Research for ALS"

63. June Brings ALS Awareness

TORONTO, June 1, 2009 – June is ALS Awareness Month in Canada. Various activities will be held across Canada in recognition of ALS Awareness Month. Public awareness and fundraising campaigns, includin ◊
"June Brings ALS Awareness"

64. TORONTO SCHOOL SUPPORTS A FRIEND IN THE FIGHT AGAINST ALS

Kids today get a bad rap. They are criticized for watching too much TV, playing too many video games and generally, just not caring. But Hodgson Senior Public School in Toronto is one example of kid ◊
"TORONTO SCHOOL SUPPORTS A FRIEND IN THE FIGHT AGAINST ALS"

65. Denise A. Figlewicz, PhD - Vice President Research

Denise Figlewicz, PhD, was promoted to Vice President Research at the ALS Society of Canada on May 11, 2009. ◊
"Denise A. Figlewicz, PhD - Vice President Research"

66. ALS Society of Canada provides critical funding for new ALS scientists

The Amyotrophic Lateral Sclerosis Society of Canada is thrilled to announce the creation of the Ronald Peter Griggs Memorial Postdoctoral Fellowship in ALS Research. The Griggs Fellowship will be awa ◊
"ALS Society of Canada provides critical funding for new ALS scientists"

67. April E-News

April E-News ◊
"April E-News"

68. A Blockbuster Approach to Funding ALS Research

Two seemingly disparate strands – a runaway blockbuster and a clinical trial of a promising new therapeutic approach to a fatal neuromuscular disease – are being woven together in a new initiative by ◊
"A Blockbuster Approach to Funding ALS Research"

69. Mutations in a New Gene Identified as a Cause of Familial ALS

Two separate teams of ALS researchers have revealed that mutations of the fused in sarcoma/translated in liposarcoma (FUS/TLS) gene are implicated in the development of inherited or familial ALS (FALS ◊
"Mutations in a New Gene Identified as a Cause of Familial ALS"

70. Betty's Run for ALS is Online

The ALS Society of Alberta is pleased to announce the launch of a new Betty’s Run web site, www.bettysrun.ca which will make it easier for Albertans to make a difference in the lives of people living ◊
"Betty's Run for ALS is Online"

71. Consultation on Neurological Conditions in Canada

In Canada, there is a lack of information about the extent and impact of neurological conditions (brain and nervous system diseases, disorders, conditions and injuries). This makes it difficult to pla ◊
"Consultation on Neurological Conditions in Canada"

72. 2009 Neuromuscular Research Partnership - Call for Proposals

The ALS Society of Canada is pleased to announce the 9th Neuromuscular Research Partnership call for proposals. This Partnership is a collaboration between the ALS Society of Canada, Muscular Dystrop ◊
"2009 Neuromuscular Research Partnership - Call for Proposals"

73. Passing of Sidney Valo, QC.

It is with regret that the ALS Society of Canada announces the passing in December, 2008, of Sidney Valo, QC. Sid Valo was a founding partner of Pallett Valo in Mississauga, Peel Region’s top law firm ◊
"Passing of Sidney Valo, QC."

74. Top Team Fundraiser prize for the 2008 WALK for ALS

Wilma Turner from British Columbia who participated in the West Koootenay Walk on June 1, 2008 is the winner of the Top Team Fundraiser prize for the 2008 WALK for ALS. Each person who was a member o ◊
"Top Team Fundraiser prize for the 2008 WALK for ALS"

75. New PSA: Head and Shoulders

Toronto, Ontario (November 10, 2008) – The ALS Society of Canada has launched a new public service advertising campaign created by Lowe Roche, Toronto to raise awareness about Amyotrophic Lateral Scle ◊
"New PSA: Head and Shoulders"

76. First Bernice Ramsay Discovery Grants Awarded

The ALS Society of Canada has awarded the 2008 Bernice Ramsay Discovery Grants in ALS Research to Avi Chakrabartty, PhD, and Alex Parker, PhD. Their projects are titled “Composition of ALS pathologica ◊
"First Bernice Ramsay Discovery Grants Awarded"

77. Fellowship continues to keep Tim E. Noël's spirit alive

Tim E. Noël’s philosophy of life was simple: “Today is a gift. That's why they call it the present. And you should never let the thieves of yesterday or tomorrow rob you of that gift.” Diagnosed with ◊
"Fellowship continues to keep Tim E. Noël's spirit alive"

78. ALS Society of Canada welcomes $15-million funding promise

The ALS Society of Canada welcomes the Conservative Party of Canada’s October 9th announcement that they will work with major Canadian health charities and commit $15 million for a four-year study of ◊
"ALS Society of Canada welcomes $15-million funding promise"

79. We're Back!! ELIZABETH’S CONCERT OF HOPE - THE MOBILITY TOUR -

In 1999, following her diagnosis of ALS, a rapidly progressive fatal neuromuscular disease, Elizabeth Grandbois (Founder) committed the time she had left to raising awareness and funds to support thos ◊
"We're Back!! ELIZABETH’S CONCERT OF HOPE - THE MOBILITY TOUR -"

80. Milton Safenowitz Fellowship awarded to University of Toronto researcher

Teresa Sanelli, PhD, is the 2008 recipient of The ALS Association’s Milton Safenowitz Post-doctoral Fellowship for ALS Research, the only fellowship of its kind in the United States. A researcher of t ◊
"Milton Safenowitz Fellowship awarded to University of Toronto researcher"

81. Lessons learned in ALS research

A number of therapies have shown promise in pre-clinical models of motor neuron disease. Many of these treatment approaches, however, failed in human studies. American researchers Veena Lanka and Meri ◊
"Lessons learned in ALS research"

82. Management of ALS

French researchers Philippe Corcia and Vincent Meininger, published a study in Drugs 2008:68(8):1037 earlier this year entitled Management of Amyotrophic Lateral Sclerosis. Even though ALS remains fat ◊
"Management of ALS"

83. ALS Canada Supports Lithium Trial

Toronto, August 28, 2008: The ALS Society of Canada is supporting two parallel and extremely important missions to help people with ALS. The first is supporting the funding of a national clinical tri ◊
"ALS Canada Supports Lithium Trial"

84. Brothers Biking Across Canada in Memory of Father

The Teeter brothers – Michael, Aaron and Adam – lost their father Steve Teeter, to ALS in 1994 at the age of 37. Teeter was diagnosed in 1991 and would have been 52 this past July. Hoping to raise fun ◊
"Brothers Biking Across Canada in Memory of Father"

85. Globe and Mail Supplements

ALS Canada includes three Globe and Mail Supplements on May 14, 21 and 28, 2008. ◊
"Globe and Mail Supplements"

86. Larry, Joanne and living with ALS

Larry and Joanne were married in the summer of 1998, just beginning their life together. It was only six months later that they received the news that would forever change their lives. ◊
"Larry, Joanne and living with ALS"

87. Living with ALS

Those touched by ALS share their stories. ◊
"Living with ALS"

88. Ex-CFLer facing game of his life

Tony Proudfoot, UNB grad from class of '71 to talk about the ultimate life lesson ◊
"Ex-CFLer facing game of his life"

89. The Government of Canada honours Thérèse Casgrain Volunteer Award recipient

OTTAWA, ONTARIO, April 30, 2008 — The Honourable Monte Solberg, Minister of Human Resources and Social Development, today honoured Ms. Elizabeth Grandbois and Dr. Kwang Yang. ◊
"The Government of Canada honours Thérèse Casgrain Volunteer Award recipient"

90. Researchers identify a gene responsible for Lou Gehrig's disease

Montreal, March 31, 2008 – A team of Canadian and French researchers has identified a novel gene responsible for a significant fraction of ALS (sporadic amyotrophic lateral sclerosis) cases. ◊
"Researchers identify a gene responsible for Lou Gehrig's disease"

91. No idol chatter: Zack Werner on his father's battle with ALS

Zack Werner is best known as a judge on the popular Canadian Idol TV show, where each season he dishes out brutal yet honest advice to young singing hopefuls. ◊
"No idol chatter: Zack Werner on his father's battle with ALS"

92. Richardsons receive Exceptional Fundraising Award

TORONTO, May 12, 2008 – North Vancouver residents Lisa and Dave Richardson received the Exceptional Fundraising Award (Individual) from the ALS Society of Canada. ◊
"Richardsons receive Exceptional Fundraising Award"

93. LeBlanc family receives the Mary Pollock WALK for ALS Volunteer Award

TORONTO, May 9, 2008 – Red Deer residents Vince, Beth and Greg LeBlanc have been recognized for their work with the Red Deer Walk Committee. ◊
"LeBlanc family receives the Mary Pollock WALK for ALS Volunteer Award "

94. Thompson receives Honorary Life Member Award

TORONTO, May 9, 2008 – Newmarket’s Doretta Thompson receives the ALS Society of Canada Honorary Life Member Award in recognition of her volunteer contributions to Canada’s ALS community ◊
"Thompson receives Honorary Life Member Award"

95. Martin receives William Fraser Leadership Award

TORONTO, May 12, 2008 – Edmonton resident Cathy Martin has received the William Fraser Leadership Development Award from the ALS Society of Canada during an awards ceremony on May 3rd in Toronto. ◊
"Martin receives William Fraser Leadership Award"

96. Proudfoot receives Public Awareness Award

TORONTO, May 9, 2008 – Former Montréal Alouettes defensive back and sports broadcaster Tony Proudfoot has been recognized by the ALS Society of Canada for his efforts to create awareness of ALS. ◊
"Proudfoot receives Public Awareness Award"

97. McConkey receives Honorary Life Member Award

TORONTO, May 9, 2008 – Burlington resident Sean McConkey has been recognized for the Honorary Life Member Award for his continued volunteer contributions to Canada’s ALS community ◊
"McConkey receives Honorary Life Member Award"

98. Merner receives Exceptional Public Awareness

TORONTO, May 12, 2008 – Richmond, BC resident Lyle Merner (posthumously) was recognized for his efforts to raise awareness of ALS. ◊
"Merner receives Exceptional Public Awareness"

99. Stotts and Huras receive Exceptional Fundraising Award

TORONTO, May 12, 2008 – Calgary residents Gerry Stotts and Dan Huras received the Exceptional Fundraising Award (Group) from the ALS Society of Canada during an awards ceremony on May 3rd in Toronto. ◊
"Stotts and Huras receive Exceptional Fundraising Award"

100. Rasmussen receives Exceptional Support Services Award

TORONTO, May 12, 2008 – Winnipeg resident and health-care provider Diana Rasmussen received the first-ever Marcel Bertrand Exceptional Support Services Award from the ALS Society of Canada ◊
"Rasmussen receives Exceptional Support Services Award"

101. Butters and Golf Pros receive Exceptional Fundraising Award

TORONTO, May 12, 2008 – Vancouver, BC resident Brian Butters, executive director, Professional Golf Association of BC and 56 participating golf pros have received the Exceptional Fundraising Award (Gr ◊
"Butters and Golf Pros receive Exceptional Fundraising Award"

102. June brings ALS Awareness

TORONTO, June 1, 2008 – June is ALS Awareness Month in Canada. Various activities will be held across Canada in recognition of ALS Awareness Month. Public awareness and fundraising campaigns, includ ◊
"June brings ALS Awareness"

103. Founding Law Partner Valo battles ALS

Sid Valo had a surprise for everybody when he not only showed up at Pallett Valo’s 11th annual Beat The February Blues party on February 7, but stayed for much of the night. ◊
"Founding Law Partner Valo battles ALS"

104. Fundraising for ALS is a family affair

Kaitlynn Roberts' first funeral made a tremendous impact on her at age 14. It was two years ago and her cousin Peter Kostiuk had become the 12th relative known to die from Amyotrophic Lateral Scle ◊
"Fundraising for ALS is a family affair"

105. Women of Light, Strength, and Faith

Jean Stilwell, mezzo-soprano opera singer and ALS Society of Canada’s national spokesperson, has just embarked on a new project, playing the role of Carmen in Cantores Celestes’ spring concert entitle ◊
"Women of Light, Strength, and Faith"

106. Study Reports That Lithium Delays Progression of ALS

Italian researchers recently published a ground-breaking study that indicated that the drug lithium delayed ALS progression in a small group of patients ◊
"Study Reports That Lithium Delays Progression of ALS"

107. Research News Special Report

Hundreds of ALS researchers and clinicians came to Toronto to attend the 18th International Symposium on ALS/MND, December 13, 2007, at the Westin Harbour Castle. The annual symposium was organized by ◊
"Research News Special Report"

108. ALS Research Comes of Age: ALS Journal Appoints New Editorial Team

The ALS Journal, the official publication of the World Federation of Neurology (WFN) Research Group on ALS/MND, is undergoing a mini-makeover, reflecting exciting change in the pace of ALS research. ◊
"ALS Research Comes of Age: ALS Journal Appoints New Editorial Team"

109. Tanguay Lab Continues Innovative Research

Tanguay was recently awarded a one-year, $40,000 grant for his project “Over expression of small mitochondrial chaperones in a mouse model of ALS”. The award is jointly funded by the ALS Society of C ◊
"Tanguay Lab Continues Innovative Research"

110. Proudfoot Savours Every Moment

Former Alouette lives life to the fullest as he wages courageous ALS battle and comes to grips with his fate ◊
"Proudfoot Savours Every Moment"

111. Brothers Biking Across Canada in Memory of Father

While most people use their summers for barbeques and beach days, the Teeter family will be pedalling their bicycles across Canada for ALS. ◊
"Brothers Biking Across Canada in Memory of Father"

112. Former Alouette lives life to the fullest as he wages courageous ALS battle

On May 7, 2007, my life changed forever. That was the day Dr. Angela Genge of the Montreal Neurological Institute informed my wife Vicki and me that I had Amyotrophic Lateral Sclerosis. ◊
"Former Alouette lives life to the fullest as he wages courageous ALS battle"

113. End of Year Tax Benefits

Support an important cause and see your money spent on research, not on taxes. ◊
"End of Year Tax Benefits"

114. Researchers Converge on Toronto for the 18th International Symposium on ALS

Toronto, November 14, 2007: Hundreds of ALS researchers and clinicians will be coming to Toronto for the 18th International Symposium on ALS/MND taking place December 1 – 3 at the Harbour Castle Westi ◊
"Researchers Converge on Toronto for the 18th International Symposium on ALS"

115. Neuromuscular Research Partnership 2007 Recipients

A list of NRP funding recipients and projects for 2007. ◊
"Neuromuscular Research Partnership 2007 Recipients"

116. Top scientists gathering in Toronto to hear latest research into ALS/MND

TORONTO, November 22, 2007: Hundreds of scientists and clinicians are on their way to Toronto, Canada for this year’s international research meeting on amyotrophic lateral sclerosis/motor neurone dise ◊
"Top scientists gathering in Toronto to hear latest research into ALS/MND"

117. Tax Savings through the Donation of BCE Shares

BCE, Bell Canada Enterprises is a public company that is pending privatization. This means that shareholders will need to sell their shares. BCE stock is one of the most widely held in the country and ◊
"Tax Savings through the Donation of BCE Shares"

118. Ask the ALS Experts

People with ALS, caregivers and clinical staff can hear presentations and ask questions of renowned international ALS researchers at a free Ask the Experts session at Westin Harbour Castle, Toronto, o ◊
"Ask the ALS Experts"

119. Doctoral Award Recipients Chosen for Passion and Innovation

Attracting bright, young investigators to ALS research isn’t an easy task, but through the funding of generous research awards, promising scientists are joining the fight against this devastating dise ◊
"Doctoral Award Recipients Chosen for Passion and Innovation"

120. Research Could Lead to Understanding of Motor Neuron Degeneration

In an effort to leverage funds and increase the ALS profile among young researchers, the Tim E. No?l Fellowship in ALS Research was created in 2006 using money from the Tim No?l Endowment Fund. Sher ◊
"Research Could Lead to Understanding of Motor Neuron Degeneration"

121. Hike The Trail To Help Us Prevail!

September 20, 2007: TORONTO, ON – The ALS Society of Canada and ALS Society of Ontario are hosting the 3rd Annual HIKE 4 ALS at The Kortright Centre for Conservation in Vaughan. The Hike will take pl ◊
"Hike The Trail To Help Us Prevail!"

122. ALS Advocate Inducted Into Terry Fox Hall of Fame

Elizabeth Grandbois, an ALS advocate living with the disease, will be inducted into the Terry Fox Hall of Fame in recognition of her efforts to increase public awareness and improve quality of life fo ◊
"ALS Advocate Inducted Into Terry Fox Hall of Fame"

123. TheStar.com - Health - Gehrig's discovery sparks hope

ALS is a progressive neurodegenerative disease, with no known cure. It was first mentioned in 1869 by French neurologist Jean-Martin Charcot. It kills motor neurons in the brain and spinal cord needed ◊
"TheStar.com - Health - Gehrig's discovery sparks hope"

124. Bernice Ramsay ALS-MND Symposium Awards

The ALS Society of Canada has established the Bernice Ramsay ALS-MND Symposium Awards to defray the travel and registration costs for ALS scientists, researchers and clinical professionals who attend ◊
"Bernice Ramsay ALS-MND Symposium Awards"

125. ALS Society of Canada elects new Chair of the Board

Effective April 28, 2007, Benjamin S. Wendland was elected to the position of Chair of the Board for the ALS Society of Canada. ◊
"ALS Society of Canada elects new Chair of the Board"

126. Annual Report Wins Award

The ALS Society of Canada received a Gold Hermes Creative Award for its 2005 Annual Report. Recipients of the Gold Award are those, “judged to exceed the high standards of the industry norm.” ◊
"Annual Report Wins Award"

127. A Symposium on Amyotrophic Lateral Sclerosis

TORONTO, June 7, 2007: David S. Cameron, President & CEO of the ALS Society of Canada, says, “The purpose of the Symposium on ALS is to provide a unique learning experience for health-care professiona ◊
"A Symposium on Amyotrophic Lateral Sclerosis"

128. Researchers develop first antibody that detects only known cause of ALS

Researchers at the University of Toronto's Faculty of Medicine have developed the first antibody that detects the only known cause of amyotrophic lateral sclerosis (ALS), also called Lou Gehrig’s dis ◊
"Researchers develop first antibody that detects only known cause of ALS"

129. Zack Werner Named National Chair and Spokesperson for WALK for ALS

TORONTO, June 1, 2007: He’s gained the public’s attention by traveling across Canada in search of the next great Canadian singer, now popular Canadian Idol judge and successful Canadian music executiv ◊
"Zack Werner Named National Chair and Spokesperson for WALK for ALS"

130. Easing The Pain For Children

TORONTO, June 1, 2007: Guilt. Abandonment. Sorrow. Confusion. Isolation. These are just some of the feelings a child whose parent has ALS may experience on a regular basis. Now there is hope. Jane Mc ◊
"Easing The Pain For Children"

131. Awareness Blooms In June

TORONTO, June 1, 2007: June is ALS awareness month in Canada. Throughout each province, public awareness and fundraising campaigns will be carried out with the WALK for ALS, the sale of cornflower la ◊
"Awareness Blooms In June"

132. Protein’s Role Emerging in ALS and Cognitive Change

[Quick Summary: The protein discovered to be a potential common link in ALS and frontotemporal dementia is thought to interact with the genetic message instructing how to assemble components within mo ◊
"Protein’s Role Emerging in ALS and Cognitive Change"

133. Easing The Pain For Children

TORONTO, May 11, 2007: Guilt. Abandonment. Sorrow. Confusion. Isolation. These are just some of the feelings a child whose parent has ALS may experience on a regular basis. Now there is hope. Jane Mc ◊
"Easing The Pain For Children"

134. ALS Society of Canada elects new Chair of the Board

Effective April 28, 2007, Benjamin S. Wendland was elected to the position of Chair of the Board for the ALS Society of Canada Wendland’s previous experience in human resources and management will ◊
"ALS Society of Canada elects new Chair of the Board"

135. Judge dies after 20 years with ALS

Superior Court judge, justice Sam Filer died at Sunnybrook Health Sciences Centre from complications related to ALS after a house fire on Wednesday, March 28. He was 71 years old and had been living w ◊
"Judge dies after 20 years with ALS"

136. Jewish News - Article About Zack Werner's Walk for ALS Involvement

He's national spokesperson and honorary chair of ALS Walks for Canada. "I started last summer," Werner said in an interview February 25, during a visit to Winnipeg. ◊
"Jewish News - Article About Zack Werner's Walk for ALS Involvement"

137. Job Posting - Clinical Fellowship in Amyotrophic Lateral Sclerosis

The Montreal Neurological Institute and Hospital, and the Department of Neurology and Neurosurgery at McGill University are seeking highly qualified candidates for the Fondation Andre Delambre Fellows ◊
"Job Posting - Clinical Fellowship in Amyotrophic Lateral Sclerosis"

138. Judge dies after 20 years with ALS

Superior Court Judge, justice Sam Filer died at Sunnybrook Health Sciences Centre from complications related to ALS after a house fire on Wednesday, March 28. ◊
"Judge dies after 20 years with ALS"

139. Native Winnipeger Zack Werner on tour with Canadian Idol

Toronto, February 22, 2007: National Chair and Spokesperson for the WALK for ALS, Winnipeg native Zack Werner while in his hometown on Sunday, February 25 will meet with ALS board members and Walk vol ◊
"Native Winnipeger Zack Werner on tour with Canadian Idol"

140. The 2nd International Frontotemporal Dementia in ALS Research Conference

Sunday June 10 - 13, 2007 Best Western Lamplighter Inn London, Ontario Canada ◊
"The 2nd International Frontotemporal Dementia in ALS Research Conference"

141. Compassionate Care Benefit Evaluation Study Seeking Family Caregivers

If you have provided (or are providing) care for a family member at end-of life and are either a: ◊
"Compassionate Care Benefit Evaluation Study Seeking Family Caregivers"

142. ALS Society wins 2006 Mercury Award

Toronto, February 8, 2007: The ALS Society of Canada has won a Silver Mercury Award for our publication Research News in the 20th Annual International MERCURY 2006/07 Awards competition. ◊
"ALS Society wins 2006 Mercury Award"

143. ALS Society receives grant through CyberAlert PR Grants Program

January 19, 2007: The ALS Society of Canada is the recipient of one of 24 grants valued at $2,700 in U.S. funds from the CyberAlert PR Grants Program. The grant entitles the ALS Society one free year ◊
"ALS Society receives grant through CyberAlert PR Grants Program"

144. A call for participation in ALS research

For more then two decades, Dr. Guy Rouleau and his lab at the University of Montreal have put a continuous effort into the identification of genes causing ALS. ◊
"A call for participation in ALS research"

145. The 2nd International Frontotemporal Dementia in ALS Research Conference

The 2nd International Frontotemporal Dementia in ALS Research Conference is scheduled for: Sunday June 10 - 13, 2007 Best Western Lamplighter Inn London, Ontario Canada ◊
"The 2nd International Frontotemporal Dementia in ALS Research Conference"

146. Operating Grant: Neuromuscular Research

The Institute of Genetics, the Institute of Musculoskeletal Health and Arthritis and the Institute of Neurosciences, Mental Health and Addiction and CIHR in partnership with the ALS Society of Canada ◊
"Operating Grant: Neuromuscular Research"

147. Taking steps for those who can’t - Toronto – September 25, 2006

Toronto – September 25, 2006 On Saturday, September 30, GTA residents will take to the streets and pathways to raise funds for ALS. ◊
"Taking steps for those who can’t - Toronto – September 25, 2006"

148. Walking for those who can’t

Scarborough - September 28: Scarborough residents Rachael Henfrey, eight, her 10-year-old sister Rebecca, aunt Chita Lontoc and other family members are participating in the North York WALK for ALS on ◊
"Walking for those who can’t"

149. Interview with Denise Figlewicz, Director of Research

Dr. Denise Figlewicz, PhD, will lead the development and implementation of a national research strategy, represent ALS Canada among scientific communities and act as advisor to government and industry ◊
"Interview with Denise Figlewicz, Director of Research"

150. Penn researchers find Lou Gehrig's, FTD disease protein

(Philadelphia, PA) -- Researchers at the University of Pennsylvania School of Medicine have discovered the major disease protein for two neurodegenerative disorders: a type of frontotemporal dementia ◊
"Penn researchers find Lou Gehrig's, FTD disease protein"

151. Walking for those who can’t

Scarborough residents Rachael Henfrey, eight, her 10-year-old sister Rebecca, aunt Chita Lontoc and other family members are participating in the North York WALK for ALS on Saturday September 30th at ◊
"Walking for those who can’t"

152. Marcher pour ce qui ne peuvent pas

Le résident de High Park à Toronto Luc Ouellette s’engage au MARCHE pour la SLA de Toronto à Etobicoke avec sa mère. La mère Bibiane Ouellette, une Montréalaise de 62 ans, a été diagnostiquée avec la ◊
"Marcher pour ce qui ne peuvent pas"

153. Taking steps for those who can’t

On Saturday, September 30, GTA residents will take to the streets and pathways to raise funds for ALS. ◊
"Taking steps for those who can’t"

154. The Concert Master Steps Down

Elizabeth Grandbois's benefit shows have put ALS in the spotlight, but now the disease is slowing her stride. ◊
"The Concert Master Steps Down"

155. Denise A. Figlewicz, PhD - Director of Research

Denise Figlewicz, PhD, joined the ALS Society of Canada on September 5, 2006 as Director of Research. The position of Director of Research is a newly created position for ALS Canada. ◊
"Denise A. Figlewicz, PhD - Director of Research"

156. National Health Charity Hires Director of Research

Denise Figlewicz, PhD, will join the ALS Society of Canada on September 5, 2006 as Director of Research. This is a newly created position for ALS Canada. Dr. Figlewicz has been involved in the ALS res ◊
"National Health Charity Hires Director of Research"

157. Example of leveraging of funds and increasing the profile of ALS research

The first-ever Tim E. Noël Fellowships in ALS Research have been awarded to Edor Kabashi, Joe V. Chakkalakal and François Gros-Louis. “The awards are a wonderful example of leveraging of funds an ◊
"Example of leveraging of funds and increasing the profile of ALS research"

158. Zack Werner Named National Chair and Spokesperson for WALK for ALS

He’s gained the public’s attention by travelling across Canada in search of the next great Canadian singer, now popular Canadian Idol judge and successful Canadian music executive, Zack Werner, is pac ◊
"Zack Werner Named National Chair and Spokesperson for WALK for ALS"

159. Government extends definition of “Family Member”

On Wednesday, June 14th the Conservative Government announced changes to the Compassionate Care Benefit which have broadened the definition of “family” to include other family members, friends and nei ◊
"Government extends definition of “Family Member”"

160. Elizabeth's Hope will air on August 24 & 30, 2006

A poignant, inspirational story of an Ontario woman's personal and public crusade against one of the most heinous diseases known to man, the medical world's forgotten killer....ALS. There is no cure ◊
"Elizabeth's Hope will air on August 24 & 30, 2006"

161. The ALS Society of Canada 2006 Research Forum

The ALS Society of Canada’s Research Forum, with the theme of “Inspiration,” took place March 24 - 26 at the Bank of Montreal Institute for Learning in Toronto. The forum addressed the issues of re ◊
"The ALS Society of Canada 2006 Research Forum"

162. Stem-Cell Therapy Restores Movement in Paralyzed Mice

Researchers at Johns Hopkins University recently reported preliminary evidence that cells derived from embryonic stem cells can restore movement in an animal model of amyotrophic lateral sclerosis (AL ◊
"Stem-Cell Therapy Restores Movement in Paralyzed Mice"

163. “Cat” Walks the Waterfront for ALS – On Her Hands

(Halifax – June 3, 2006) --- Halifax gymnast CATHERINE KENNEDY, endorsed by the ALS Society of Nova Scotia, will tumble and walk along the Halifax Waterfront, on her hands, from Chebucto Landing to S ◊
"“Cat” Walks the Waterfront for ALS – On Her Hands"

164. Tilson speech recognized June as ALS month

David Tilson, MP for Dufferin-Caledon, made a statement in the House of Commons last Thursday which gave recognition to the month of June as ALS month. ◊
"Tilson speech recognized June as ALS month "

165. The International Symposium on ALS/MND

The International Symposium on ALS/MND is a unique annual event which brings together leading international researchers and Health and Social Care Professionals to present and debate key innovations i ◊
"The International Symposium on ALS/MND"

166. Awareness Blooms In June

TORONTO, June 1, 2006 —June is ALS awareness month in Canada. Throughout each province, public awareness and fundraising campaigns will be carried out with the WALK for ALS, the sale of cornflower lap ◊
"Awareness Blooms In June"

167. Awareness Blooms in June

June is ALS awareness month in Canada. Throughout each province, public awareness and fundraising campaigns will be carried out with the WALK for ALS, the sale of cornflower lapel pins and golf tourna ◊
"Awareness Blooms in June"

168. David Tilson to Reintroduce Bill to Designate June as ALS Month

David Tilson to Reintroduce Bill to Designate June as ALS Month ◊
"David Tilson to Reintroduce Bill to Designate June as ALS Month"

169. A call for participation in ALS research

For more then two decades, Dr. Guy Rouleau and his lab at the University of Montreal have put a continuous effort into the identification of genes causing ALS. The success of this research is largely ◊
"A call for participation in ALS research"

170. BBDO Canada Receives Public Awareness Award

BBDO Canada has received the Exceptional Public Awareness Program Award (group) from the ALS Society of Canada. BBDO Canada created a Public Service Announcement (PSA) campaign to educate and increase ◊
"BBDO Canada Receives Public Awareness Award"

171. Gibson Receives Advocacy Award

Dr. Gillian Gibson has received the Brett Yerex Exceptional Advocacy Award from the ALS Society of Canada. Gibson was instrumental in the creation of the ALS Clinic at G.F. Strong Hospital in Vancouve ◊
"Gibson Receives Advocacy Award"

172. Pica Receives Fundraising Award

Pierangela Pica has received the Excellence in Fundraising Program Award from the ALS Society of Canada. Pica was recognized for her work at ALS B.C.—Victoria Chapter during an awards ceremony in Toro ◊
"Pica Receives Fundraising Award"

173. Hlady Receives Walk for ALS Award

Andrea Hlady has received the Mary Pollock Walk for ALS Award from the ALS Society of Canada. Hlady was recognized for her work at ALS B.C.—Victoria Chapter during an awards ceremony in Toronto, on Sa ◊
"Hlady Receives Walk for ALS Award"

174. Bertrand Receives Volunteer Award

Marcel Bertrand has received the Myra Rosenfeld Volunteer Award from the ALS Society of Canada. The award was presented to Bertrand at a ceremony held in Toronto on Saturday, May 6. ◊
"Bertrand Receives Volunteer Award"

175. Gardner Receives Leadership Award

Michael Gardner has received the William Fraser Leadership Development Award from the ALS Society of Canada. Gardner was recognized for his work at ALS B.C. during an awards ceremony on Saturday, May ◊
"Gardner Receives Leadership Award"

176. Phillips Receives Public Awareness Award

Bob Phillips has received the Exceptional Public Awareness Award (individual) from the ALS Society of Canada. The award was presented to Phillips at a ceremony held in Toronto, Saturday, May 6. ◊
"Phillips Receives Public Awareness Award"

177. ALS: Strategies for Quality Living - Friday, June 2, 2006

Care for people with ALS requires a team of health care professionals and caregivers who effectively deal with various aspects of care. ◊
"ALS: Strategies for Quality Living - Friday, June 2, 2006 "

178. Bono Pro Bono

The ALS Society of Canada has secured the rights for six months to use the U2 song "Walk On" free-of-charge for our public service announcements (PSAs) to promote the WALK for ALS fundraiser. ◊
"Bono Pro Bono"

179. Baseball is Back at Jarry Park - All-star Game to Benefit ALS

Join former Montreal Expos Warren Cromartie, Andre Dawson, Steve Rogers, Dennis Martinez and Jim Fanning as well as celebrities from Montreal’s entertainment, business and professional sports communit ◊
"Baseball is Back at Jarry Park - All-star Game to Benefit ALS"

180. Media invitation - Baseball is back at Jarry Park !...

MONTREAL, March 28 /CNW Telbec/ - The Montreal entertainment, business and professional sports communities, including ex-players from the Montreal Expos, have teamed up for a Celebrity Softball Game i ◊
"Media invitation - Baseball is back at Jarry Park !... "

181. Elizabeth's Concert of Hope begins a National Tour

As the curtain falls in Hamilton it marks the beginning of the final leg of the journey….a National Tour. Elizabeth and the tour team will take Elizabeth's Concert of Hope on the road. In partnership ◊
"Elizabeth's Concert of Hope begins a National Tour"

182. Time to pass the torch

Elizabeth Grandbois is holding her final Concert of Hope at the Dofasco Centre for the Arts. After six concerts, Grandbois has raised more than $1.8 million for ALS. ◊
"Time to pass the torch"

183. ER - Thursday February 2, 2006 on CTV

Emmy-winner James Woods guest stars as a doctor and former medical school faculty member with ALS. The progression of his disease is followed in flashbacks, as we see how he impacts each of the ER doc ◊
"ER - Thursday February 2, 2006 on CTV"

184. Grandbois pleased with lineup; Glass Tiger, Carol Welsman join Elizabeth's

Elizabeth Grandbois' giddiness bursts through the telephone line as a reporter barely finishes asking a question regarding how she feels about next month's Elizabeth's Concert of Hope -- the finale ◊
"Grandbois pleased with lineup; Glass Tiger, Carol Welsman join Elizabeth's"

185. Tim E. Noël Fellowship in ALS Research

We are pleased to announce the creation of the first-ever fellowship in ALS research by the ALS Society of Canada. The funds that have accumulated within the Tim E. Noël Endowment Fund have reached ◊
"Tim E. Noël Fellowship in ALS Research"

186. OBITUARY Andre Delambre, CA 1944 - 2006 Right-hand man to Celine Dion

OBITUARY Andre Delambre, CA 1944-2006 Right-hand man to Celine Dion and Rene Angelil for the past 24 years, Andre Delambre (Executive Vice-President, Finance and Administration, for Les Productions Fe ◊
"OBITUARY Andre Delambre, CA 1944 - 2006 Right-hand man to Celine Dion"

187. Researchers Uncover New Toxic Mechanism in ALS

Exactly how ALS — Lou Gehrig’s disease — damages motor neurons is one of medical science’s lingering mysteries. At least six mishaps within cells appear to contribute to the death of the nerves that e ◊
"Researchers Uncover New Toxic Mechanism in ALS"

188. New research findings

In the December 20th online issue of Nature Neuroscience, ALS Canada board member and researcher Dr. Jean-Pierre Julien and his colleagues report that mutant SOD1 molecules - those that bring about a ◊
"New research findings"

189. Seventh Neuromuscular Research Partnership Competition

A short description... ◊
"Seventh Neuromuscular Research Partnership Competition"

190. SEED Grant Program

The SEED Grant Program has been funded again for 2006! Please watch for additional information in January on how to apply for a Service and Education Enhancement and Development (SEED) Grant. ◊
"SEED Grant Program "

191. Clinical Research on Familial ALS

Investigators at the ALS Center at Emory University are investigating the possibility of designing a clinical trial for persons at risk for familial (inherited) ALS. Since this is a rare disease, th ◊
"Clinical Research on Familial ALS"

192. ALS Release A Guide to ALS Care for the Primary Care Physician

TORONTO, December 6, 2005: The ALS Society of Canada is pleased to introduce - A Guide to ALS Care for the Primary Care Physician. The purpose of the newly published bilingual electronic guide, avai ◊
"ALS Release A Guide to ALS Care for the Primary Care Physician"

193. New research findings

In an upcoming issue of Nature Neuroscience, ALS Canada board member and researcher Dr. Jean-Pierre Julien and his colleagues report that mutant SOD1 molecules - those that bring about a familial form ◊
"New research findings"

194. Release of Clinical Care Guide for General Practitioners

The ALS Society of Canada is pleased to introduce - A Guide to ALS Care for the Primary Care Physician. The purpose of the newly published electronic guide, available on CD-ROM and as a PDF document ◊
"Release of Clinical Care Guide for General Practitioners"

195. BBDO receives a silver award at the 2005 Canadian Marketing Awards

BBDO Canada has received a Silver Award at the 2005 Canadian Marketing Awards on November 25, 2005 in Toronto. The agency received the award for the work it has done on the ALS Society of Canada’s “W ◊
"BBDO receives a silver award at the 2005 Canadian Marketing Awards"

196. Veteran actor James Woods will guest star on 'ER'

NEW YORK — James Woods is going to check into NBC's "ER," which airs in Canada on CTV. He will guest star as Dr. Nate Lennox, a patient who is suffering from Lou Gehrig's disease. His character i ◊
"Veteran actor James Woods will guest star on 'ER'"

197. ALS Canada Launches a $75,000 Post-doctoral Fellowship in ALS Research

ALS Canada’s board of directors approved the creation of a post-doctoral fellowship in ALS research valued at $75,000 annually and renewable for up to three years at its November meeting. The interest ◊
"ALS Canada Launches a $75,000 Post-doctoral Fellowship in ALS Research"

198. Mutant Protein May Act Outside Cells in ALS Findings

Canadian scientist Jean-Pierre Julien presented new evidence that a mutant protein associated with some inherited forms of ALS may be secreted outside cells and act in a toxic manner, providing insigh ◊
"Mutant Protein May Act Outside Cells in ALS Findings"

199. ALS Patient Morrie Schwartz Interview - November 22 - on ABC News

Helping to raise awareness about ALS on a national level, we are pleased to share that on Tuesday November 22, Ted Koppel’s final broadcast for ABC News: Nightline will feature a rebroadcast of his in ◊
"ALS Patient Morrie Schwartz Interview - November 22 - on ABC News"

200. Hike the Trail to Help Us Prevail - Toronto, October 13, 2005

TORONTO, OCTOBER 13, 2005: Lace up your hiking boots and join ALS Societies across Canada as they hike the trail in support of research and client services for those living with this devastating dise ◊
"Hike the Trail to Help Us Prevail - Toronto, October 13, 2005"

201. London institutions receive $5.5 million for medical training and research

University of Western Ontario alumni Donald Rix donated $2 million to the university's medical school. The funds will go toward the clinical skills learning building named after him at the UWO Schuli ◊
"London institutions receive $5.5 million for medical training and research"

202. A Special ALS Performance

A SPECIAL ALS PERFORMANCE of Last of the Red Hot Lover's, a brilliant Neil Simon comedy takes place at the Village Theatre in Hudson, Quebec Thursday, May 15. ◊
"A Special ALS Performance"

203. First Annual ALS Conference in Hamilton, Ontario

Working together for ALS patients and their families ◊
"First Annual ALS Conference in Hamilton, Ontario"

204. Facing Lou Gehrig's disease with steely determination

Dan Gentilcore, the honorary chairman for the Jim Hughes Golf Classic in support of Amyotrophic Lateral Sclerosis, and Bob Hetts, tournament organizer, hand over $25,000 to the ALS Society of Canada. ◊
"Facing Lou Gehrig's disease with steely determination"

205. BBDO's Knipe Dies at 38

NEW YORK Andy Knipe, a creative director at BBDO since 1992, has died after a five-year battle with ALS, the agency confirmed. He was 38. ◊
"BBDO's Knipe Dies at 38 "

206. ' I am a walrus. '

How does a man facing a death sentence voice the humour that can be a part of human tragedy, especially when he is the victim in the unfolding drama? ◊
"' I am a walrus. '"

207. Results of the sixth NRP competition

To leverage our dollars, or grow the value of our ALS dollar, we work in partnership with our colleague organization Muscular Dystrophy Canada (MDC) and with the Canadian Institutes of Health Research ◊
"Results of the sixth NRP competition"

208. June is ALS Awareness Month!

June is ALS Awareness Month! ◊
"June is ALS Awareness Month!"

209. Grade Six Student Raises Money For ALS

Alex Dawson, a grade six student at Rolph Road Public School, completed a school project about ALS and helped to raise funds and awareness for this devastating disease. ◊
"Grade Six Student Raises Money For ALS"

210. Cahill's battle with ALS comes to an end

Jim Cahill's well-publicized battle with ALS reached an end Thursday. A well-known athlete and outdoorsman who was diagnosed with the incurable disease in August of 2002 died peacefully. ◊
"Cahill's battle with ALS comes to an end"

211. The Score Raises Funds for ALS

Monday, May 2nd, marked the 66th anniversary of the end of Lou Gehrig’s consecutive games streak. To the Point with host Greg Sansone on The Score television network, devoted one hour to the subject o ◊
"The Score Raises Funds for ALS"

212. BBDO Canada received a film Bronze Lion for Hugging PSA

Ten Canadian agencies were among those honored at the 52nd Cannes International Advertising Festival... also known as the Olympics of advertising. The international festival held in Canada. ◊
"BBDO Canada received a film Bronze Lion for Hugging PSA"

213. ALS Awareness and Tim Hortons

Prince County Tim Hortons outlets and the host committee of the International Softball Federation 2005 Junior Men's World Softball Championship have teamed up to raise money to promote awareness and ◊
"ALS Awareness and Tim Hortons"

214. ichannel Special Presentation of Elizabeth's Hope

ichannel's special presentation of the documentary "Elizabeth's Hope," features an additional interview with Elizabeth Grandbois. The interview is conducted by Christopher Heard. ◊
"ichannel Special Presentation of Elizabeth's Hope"

215. Lane Smith, 69; dies of amyotrophic lateral sclerosis

Lane Smith, the actor who portrayed President Nixon in the 1989 docudrama "The Final Days" and apoplectic Daily Planet editor Perry White in the 1990s television series "Lois and Clark: The New Advent ◊
"Lane Smith, 69; dies of amyotrophic lateral sclerosis"

216. ALS Society of Canada in partnership with the Institute of Neurosciences

Institute of Neurosciences, Mental Health and Addiction In partnership with Amyotrophic Lateral Sclerosis Society of Canada (ALS Canada) ◊
"ALS Society of Canada in partnership with the Institute of Neurosciences"

217. Canon Canada Cheque Presentation in Toronto

A short description... ◊
"Canon Canada Cheque Presentation in Toronto"

218. Hike The Trail To Help Us Prevail

Toronto – May 4, 2005: For the 3,000 Canadians who suffer from the devastating effects of ALS, taking even small steps requires a big effort. The ALS Society of Canada has decided to match those effor ◊
"Hike The Trail To Help Us Prevail"

219. Elizabeth's Hope

"Elizabeth's Hope" is the inspiring story of an Ontario woman's personal and public crusade against ALS. The one-hour documentary captures the passion of Elizabeth Grandbois ◊
"Elizabeth's Hope"

220. Jason Wilson receives Brain Star award

In recognition of his article entitled “Quantitative measurement of neurodegeneration in an ALS-PDC model using MR microscopy”, University of British Columbia PhD fellow Jason Wilson has been awarded ◊
"Jason Wilson receives Brain Star award"

221. Tilson Recognizes ALS Month in House

PARLIAMENT HILL – David Tilson, MP for Dufferin-Caledon made a statement in the House of Commons today which gave recognition to the month of June as ALS month. After introducing a private members bi ◊
"Tilson Recognizes ALS Month in House"

222. Manuel pour les personnes qui vivent avec la SLA

La troisième édition du Manuel pour les personnes qui vivent avec la SLA est un excellent outil de référence remplis de conseils pratiques. Cet ouvrage donnera aux lecteurs des suggestions pour la pri ◊
"Manuel pour les personnes qui vivent avec la SLA"

223. June is ALS Awareness Month

Toronto, Ontario – May 24, 2005: June is ALS Awareness Month in Canada. Amyotrophic Lateral Sclerosis, more commonly known as Lou Gehrig's disease, is a rapidly progressive and fatal neuromuscular di ◊
"June is ALS Awareness Month"

224. McDonald's and Canon Sponsor Walk for ALS 2005

Get ready to walk through the streets in support of the local people living with ALS. Families, friends, volunteers and donors are getting geared up for the annual WALK for ALS. ◊
"McDonald's and Canon Sponsor Walk for ALS 2005"

225. ALS Society of Canada Elects New President

Effective April 30 2005, Sean G. McConkey was elected to the position of president for ALS Society of Canada. McConkey’s extensive experience in human resources and management will serve ALS Cana ◊
"ALS Society of Canada Elects New President"

226. Tilson Introduces Bill To Designate June As ALS Month

PARLIAMENT HILL – David Tilson, MP for Dufferin-Caledon introduced his first Private Members Bill that if enacted would designate the month of June as Amyotrophic Lateral Sclerosis (also known as ALS ◊
"Tilson Introduces Bill To Designate June As ALS Month"

227. Second Annual ALS Client Services Day in Ottawa

Reminder for the 2nd Annual ALS Client Services Day in Ottawa, June 15th at the Sheraton Ottawa Hotel, hosted by the ALS Society of Canada. ◊
"Second Annual ALS Client Services Day in Ottawa"

228. Home care for ALS patients deserves support

We join the chorus of applause for the Citizen's sensitive, far-reaching series on palliative care. We especially appreciated the "portrait" of Phil Budakowski and his family's courageous journey wi ◊
"Home care for ALS patients deserves support"

229. First International Research Workshop on Frontotemporal Dementia (FTD)

The first international research workshop to address frontotemporal dementia in ALS will be held from May 15 - 17, 2005 at the Best Western Lamplighter Inn in London, Ontario. More than 80 90 researc ◊
"First International Research Workshop on Frontotemporal Dementia (FTD)"

230. Hike The Trail To Help Us Prevail

Toronto – May 4, 2005: For the more than 2,000 Canadians who suffer from the debilitating effects of ALS, taking even small steps requires a big effort. The ALS Society of Canada has decided to mat ◊
"Hike The Trail To Help Us Prevail"

231. On a mission to find a cure

There comes a chilling moment, staring as we are at a microscopic cross section of a human spinal cord, when Janice Robertson steps away from her telescope and offers a layperson an up-close image of ◊
"On a mission to find a cure"

232. Playing in Famous Players Cinemas across Canada

What would you do while you still could? Our 30-second ‘hugging spot’ will be shown in Famous Players Cinemas across the country. The 30-second PSA has two versions, French and English. ◊
"Playing in Famous Players Cinemas across Canada"

233. Strong Earns U.S. Research Prize

Dr. Michael Strong, a neurologist and researcher at Western, the Robarts Research Institute and Lawson Health Research Institute, is being honoured by the American Academy of Neurology for his outstan ◊
"Strong Earns U.S. Research Prize"

234. Involving the Canadian public in CIHR peer review committees

The Canadian Institutes of Health Research have committed to enhancing public and stakeholder engagement in health research in Canada. To this end, CIHR is seeking applications from members of the pub ◊
"Involving the Canadian public in CIHR peer review committees"

235. Michael Fitz-James started first newspaper for Canadian lawyers

D. Michael Fitz-James, the founding editor of The Lawyers Weekly, died at 54 on March 27, 2005 of amyotrophic lateral sclerosis (ALS). The Lawyers Weekly is known as the first newspaper for the legal ◊
"Michael Fitz-James started first newspaper for Canadian lawyers"

236. Mc Donald’s and Canon Sponsor Walk For ALS 2005

TORONTO: Get ready to walk through the streets in support of local people living with ALS. Families, friends, volunteers and donors are gearing up for the annual WALK for ALS. Returning donors, McDona ◊
"Mc Donald’s and Canon Sponsor Walk For ALS 2005"

237. BBDO Canada received a bronze award at the 2005 Marketing Awards

The ALS Society of Canada is pleased to announce that its advertising agency -- BBDO Canada received a bronze award at the 2005 Marketing Awards for the PSA campaign 'What would you do, while you sti ◊
"BBDO Canada received a bronze award at the 2005 Marketing Awards"

238. ALS clinic lands a star: One of the world's top experts leaves Toronto

VANCOUVER - As of today, Vancouver's G.F. Strong Rehabilitation Hospital will be home to Canada's largest clinic for patients with amyotrophic lateral sclerosis -- Lou Gehrig's disease -- and it wi ◊
"ALS clinic lands a star: One of the world's top experts leaves Toronto"

239. ALS Society Ad Campaign Asks: "What would you do, while you still could?"

The ALS Society of Canada has launched a new public service advertising campaign created by BBDO Canada to raise awareness about ALS and the ALS Society's efforts to support research towards a cure f ◊
"ALS Society Ad Campaign Asks: "What would you do, while you still could?""

240. Symposium - ALS Strategies for Quality of Life and Quality Care

David S. Cameron, National Executive Director of the ALS Society of Canada, says “The purpose of ALS Strategies for Quality of Life and Quality Care symposium is to provide a unique learning experienc ◊
"Symposium - ALS Strategies for Quality of Life and Quality Care"

241. Hike For ALS Announced

Hike 4 ALS is a new national fundraising program targeting outdoor enthusiasts interested in hiking in ontario and canada. ◊
"Hike For ALS Announced"

242. The means to fight

Michael Halls, whose historic $5-million gift boosted the fight against ALS, loses his long personal battle with the disease. ◊
"The means to fight"

243. First International Research Workshop on Frontotemporal Dementia in ALS

The first international research workshop to address frontotemporal dementia in ALS will be held from May 15 - 17, 2005 at the Best Western Lamplighter Inn in London, Ontario. Workshop organizer D ◊
"First International Research Workshop on Frontotemporal Dementia in ALS"

244. New Research Grant for Dr. Jean-Pierre Julien

Dr. Jean-Pierre Julien, an ALS Society of Canada board member and a prominent ALS researcher at Laval University Research Centre in Quebec has been awarded a research grant from the the ALS Associatio ◊
"New Research Grant for Dr. Jean-Pierre Julien "

245. Manual for People Living With A L S

Toronto, January 28, 2005: The third edition of the Manual for People Living with ALS Manual is an excellent educational resource and tool. It will help readers to organize personal health information ◊
"Manual for People Living With A L S"

246. In Memoriam – Rick Wilkinson

It is with deep regret that we announce that Rick Wilkinson from Duncan, BC, died of ALS on February 1st. Wilkinson was diagnosed with ALS in 2003. Wilkinson was active in the ALS Society of B.C.’ ◊
"In Memoriam – Rick Wilkinson"

247. ALS Society returns feeling in P S A's

If you lost feeling in your limbs, what would you yearn to do? That’s the idea behind the ALS Society of Canada’s new multimedia campaign that aims to raise awareness of both the disease and the organ ◊
"ALS Society returns feeling in P S A's"

248. Details Discovered on How Human Stem Cells become Nerve Cells

[QUICK SUMMARY: In the first report showing that human embryonic stem cells can be made to form motor neurons in the lab, investigators find a precise sequence of molecular signals that guide cells in ◊
"Details Discovered on How Human Stem Cells become Nerve Cells"

249. Brummitt-Feasby ALS House Housing with Care and Support for ALS Patients

January 14th, 2005 marked the official opening of North America’s first residence for people living with ALS, also known as Lou Gehrig’s disease. In attendance will be ALS Manitoba executive director ◊
"Brummitt-Feasby ALS House Housing with Care and Support for ALS Patients"

250. Volunteers Prepare for Walk for ALS

Walks to raise funds for ALS will take place in June and September of 2005. This year the activity—which is the ALS Society of Canada’s most important signature event—has been rebranded with a new na ◊
"Volunteers Prepare for Walk for ALS"

251. Epidemiology Studies Explore Potential Risk Factors for ALS

[QUICK SUMMARY: The risk for ALS in men is increased by 50 percent by military service according to one study; another study fails to find that physical activity increases ALS incidence in the general ◊
"Epidemiology Studies Explore Potential Risk Factors for ALS"

252. Novartis Drug Does Not Slow ALS Progression

Novartis has been conducting a Phase 2 trial with its drug TCH 346 and has advised that the drug has shown no impact on the rate of progression or survival of ALS. For more information click on www.a ◊
"Novartis Drug Does Not Slow ALS Progression"

253. Elizabeth's Concert of Hope - February 12, 2005

The fifth annual Elizabeth’s Concert of Hope will be held on Saturday, February 12th, 2005 at the Dofasco Centre for the Arts in Hamilton. Proceeds from the concert will be used to fight ALS, a progr ◊
"Elizabeth's Concert of Hope - February 12, 2005"

254. Screening Effort Identifies Ceftriaxone as Potential ALS Therapeutic

A consortium of researchers has found that Ceftriaxone, a drug that alters glutamate, has been found to prolong survival in animal models of ALS. ◊
"Screening Effort Identifies Ceftriaxone as Potential ALS Therapeutic"

255. ALS hospice now open to full-time residents Province to pay $375,000 a year

Kevin Rollason Kevin Rollason More than three years after North America's first ALS hospice opened its doors, the provincial funding is now in place to let dying residents live there full-time. H ◊
"ALS hospice now open to full-time residents Province to pay $375,000 a year"

256. Brummitt-Feasby ALS House

January 14th, 2005 marks the official opening of North America’s first residence for people living with ALS, also known as Lou Gehrig’s disease. The house has three long-term beds, one respite bed, a ◊
"Brummitt-Feasby ALS House"

257. Neuromuscular Research Partnership (NRP) - Request for Applications

The ALS Society of Canada, Muscular Dystrophy Canada and the Canadian Institutes of Health Research are pleased to announce the Neuromuscular Research Partnership Competition for a sixth year. ◊
"Neuromuscular Research Partnership (NRP) - Request for Applications"

258. Giving hope to ALS sufferers

Elizabeth Grandbois plans to unleash her irresistible charm on the federal government as soon as her fifth annual Concert of Hope is over in February. Seven years ago, Grandbois was diagnosed with ◊
"Giving hope to ALS sufferers"

259. Two Studentships Granted

David S. Cameron, national executive director of the ALS Society of Canada is pleased to announce that the ALS Society has created a new program to fund young researchers as they embark on their caree ◊
"Two Studentships Granted"

260. Stem Cell Treatments in China

Many in the ALS community are looking for more information about the stem cell treatments being provided in China . At this time, there is not sufficient information about Dr. Huang Hangyun’s work in ◊
"Stem Cell Treatments in China"

261. Medical Student Honored for ALS Research

Kevin Harris, BSc, a third-year medical student at the University of British Columbia in Vancouver has been selected to receive the 2004 Milton Shy Award. ◊
"Medical Student Honored for ALS Research"

262. Schilling Had Extra Inspiration

The late Jeff Julian must be smiling today. His pal, Curt Schilling, kept a promise. Schilling is the ace of the world champion Boston Red Sox pitching staff. How strange does that sound — world c ◊
"Schilling Had Extra Inspiration"

263. ALS Society of Canada holds its First Research Forum

Toronto, October 12, 2004: The ALS Society is hosting its first research forum October 15 & 16, 2004 at the Bank of Montreal Institute for Learning, 3550 Pharmacy Ave. in Scarborough. The purpos ◊
"ALS Society of Canada holds its First Research Forum "

264. ALS Hope, Washington U. form neurological research center

The Chris Hobler/James Maritz Foundation has committed $1 million (US funds) to partner with Washington University to establish the Hope Center for Neurological Disorders. The center is expected to ac ◊
"ALS Hope, Washington U. form neurological research center"

265. Over 350 walk to D'Feet ALS

CLYDE RIVER -- More than 350 people from all walks of life gathered Saturday at Raceway Park in Oyster Bed Bridge to take part in the first event of its kind in P.E.I., aimed at raising funds and awar ◊
"Over 350 walk to D'Feet ALS"

266. Steps In The Right Direction

THIS ISN'T THE WEEKEND it's the walk-end. A lot of feet are stepping out this weekend to help out local charities and causes in various fundraising events across the city on the heels of last weeken ◊
"Steps In The Right Direction"

267. Elizabeth’s Concert of Hope founder honoured by Governor General

Elizabeth Grandbois’ head shakes in disbelief. Her right hand covers part of her face as she attempts to hide it. She’s trying to conceal the embarrassment from winning a prestigious Governor Genera ◊
"Elizabeth’s Concert of Hope founder honoured by Governor General"

268. CBC Radio Documentary Wins at Prestigious Prix Italia

CBC Radio’s OUTFRONT has won the prestigious Prix Italia in the Cultural Documentary category. Lisa Hébert and Carol Spendlove received the honour for their piece Voice Box & Flute. ◊
"CBC Radio Documentary Wins at Prestigious Prix Italia"

269. In Memorium – Dan Maloney

Dan Maloney passed away on Friday, September 10 and a service will be held in Victoria BC on Monday, September 20 Dan Maloney was diagnosed with ALS in May 1999. He joined the Victoria Chapter, AL ◊
"In Memorium – Dan Maloney"

270. Neighbour inspiration for woman at ALS walk

Thinking of her neighbour will help put a bounce in Darlene Harper's step during the first-ever fundraising walk for ALS on Prince Edward Island. Harper said she is inspired by Stan MacNevin, who ◊
"Neighbour inspiration for woman at ALS walk"

271. Annual Tim Noel Golf Outing

2004 marked the 5th successful year of the annual Tim Noel Golf Outing. ◊
"Annual Tim Noel Golf Outing "

272. ALS Canada awarded the 2007 International Symposium

In late November/early December 2007, the ALS Society of Canada will play host to the 18th International Symposium of ALS/MND in Toronto. ◊
"ALS Canada awarded the 2007 International Symposium "

273. 2004-2005 Research Funding Announced

2004-2005 Research Funding Announced ◊
"2004-2005 Research Funding Announced"

274. Charity Golf Tournament raises - $25,590

On July 8, 2004 Aon Reed Stenhouse held their 8th annual golf Tournament... ◊
"Charity Golf Tournament raises - $25,590"

275. Being housebound is not a barrier to voting - Here is what to do

BEING HOUSEBOUND IS NOT A BARRIER TO VOTING – HERE IS WHAT TO DO Voting is an important aspect of supporting our democratic tradition. This is true for all Canadians, including those living with ◊
"Being housebound is not a barrier to voting - Here is what to do"

276. Canadian Wins Milton Shy Award for ALS Essay

A Canadian medical student has been honoured with the prestigious G. Milton Shy Award for his medical essay about people living with ALS. ◊
"Canadian Wins Milton Shy Award for ALS Essay"

277. Regenerative Medicine and Nanomedicine RFA / Appel de demande au thème Méde

This information is forwarded from the CIHR. The ALS Society is a potential partner in this project and we encourage all ALS researchers to take a close look at this RFA. ◊
"Regenerative Medicine and Nanomedicine RFA / Appel de demande au thème Méde"

278. SPRING WALK RESULTS

Spring is the official opening of the Walk to D’Feet ALS season in Canada and without fail the Spring Walks have got us pointed in a very positive direction. May led off with walks in Brantford and ◊
"SPRING WALK RESULTS"

279. OBIT

Duncan McKinnon and Jerry Gladman each made a difference. ◊
"OBIT"

280. William Weir carries Olympic Torch

William Weir, living with ALS, was one of a select group of Canadians who carried the Olympic torch through the streets of Montreal on June 20, Father's Day ◊
"William Weir carries Olympic Torch"

281. 500 Canadians in the March of Faces

Pamela McFarlin from Barrie Ontario is our 500th Person with ALS to take part in the ALS March of Faces project. ◊
"500 Canadians in the March of Faces"

282. Director of Communications assumes new role with ALS Ontario

It is with mixed feelings that I advise you of the departure of Susan Graham Walker, Director of Communications, Advocacy and Research Administration. Susan has accepted the offer from the ALS Society ◊
"Director of Communications assumes new role with ALS Ontario"

283. $225,000.00 raised at the 8th annual Betty’s Run for ALS

Betty's Run in Calgary Alberta raised $225,000 for ALS services and research. ◊
"$225,000.00 raised at the 8th annual Betty’s Run for ALS"

284. ALS Society On-line - Relaunched!

We are pleased to announce the re-launch of www.als.ca. ◊
"ALS Society On-line - Relaunched!"

285. Go Flames Go!

ALS makes one of the busiest web sites with Angie Rea, of the ALS Climb to Kilimanjaro, pictured at the top of the mountain in her Flames jersey and puck. What great awareness on the eve of JUNE ALS ◊
"Go Flames Go!"

286. Jerry Gladman Wins Award

Toronto Sun journalist, Jerry Gladman, who lives with ALS has been awarded the Sun Media 2003 Edward Dunlop award for journalistic excellence for his feature series, Living and Dying with ALS. ◊
"Jerry Gladman Wins Award"

287. ALS Society of Quebec appoints new Executive Director

A short description... ◊
"ALS Society of Quebec appoints new Executive Director"

288. Mountain climbers raise $260,000 to help fight ALS

When Paul Lambe and his Investors Group colleagues reached the peak of Africa's Mount Kilimanjaro, they had 30 minutes to take pictures before severe illness kicked in. The 39-year old Brampton fi ◊
"Mountain climbers raise $260,000 to help fight ALS"

289. HBO Spotlights the Quest of Three Sisters in the Search for a Cure for ALS

"Three Sisters: Searching for a Cure," an HBO special that airs on May 19, 2004 documents the Estess sisters and their battle against time and the devastation of Lou Gehrig’s disease. This is the stor ◊
"HBO Spotlights the Quest of Three Sisters in the Search for a Cure for ALS"

290. Monthly Giving Family

The ALS Society Monthly Giving Program is growing with the enthusiastic support of people like Barb Hopkins and her family. ◊
"Monthly Giving Family"

291. COPING & HOPE WITH ALS

How do you cope with ALS day-to-day? The ALS Society of Canada is looking for your story of how you manage. We then want to share these stories with others through our web site and newsletters. If ◊
"COPING & HOPE WITH ALS"

292. Betty's Run Raises over $1 million for ALS

Dedication and determination have paid off. A group of people in Alberta have been proving this theory. Betty’s Run for ALS has now raised over $1 million for ALS services and research. It is now ◊
"Betty's Run Raises over $1 million for ALS"

293. Calgary ALS Symposium

A conference for all those affected by ALS. ◊
"Calgary ALS Symposium"

294. International meetings set for Philadelphia

The Annual Meeting of the International Alliance of ALS/MND Associations from November 28-30 brings together ALS/MND Associations from around the world to share initiatives and develop strategies for ◊
"International meetings set for Philadelphia"

295. HIV/AIDS drug being lab tested

The ALS Therapy Development Foundation has announced testing of an HIV/AIDS medication called Nelfinavir. Nelfinavir is one of eight different compounds in line for testing in the ALS/TDF labs in Bos ◊
"HIV/AIDS drug being lab tested"

296. ALS4 gene found

Scientists have discovered the precise location of the fourth known gene for familial ALS. ◊
"ALS4 gene found"

297. A Plea for Progress - Senate Hearing on Bill C-6

Nigel Van Loan, caregiver and member of the ALS Society of Canada Board (and President of ALS Ontario) appeared before the Senate Social Affairs, Science and Technology Committee in March This com ◊
"A Plea for Progress - Senate Hearing on Bill C-6"

298. Investor's Group team climbs for ALS

If you’re going to dream, dream big. A Canadian team took this thought to heart last month. On February 27th a team of 13 Investor Group representatives along with Sharon Babineau, an ALS Society o ◊
"Investor's Group team climbs for ALS"

299. Elizabeth's Concert of Hope reaches the $1million mark

Imagination came to life this February. The fourth annual Elizabeth’s Concert of Hope held February 7th, at DuMaurier Ltd. Centre, in Hamilton raised over $300,000. This has put the total dollar amo ◊
"Elizabeth's Concert of Hope reaches the $1million mark"

300. Advocacy Award honours Brett Yerex

Brett J. Yerex has been honoured posthumously by the ALS Society of Canada. To acknowledge Brett’s advocacy efforts on behalf of people with ALS, the society’s advocacy award will now be named the Br ◊
"Advocacy Award honours Brett Yerex"

301. Ontario Executive Director accepts new appointment

Karen Ormerod, Executive Director of the ALS Society of Ontario for the past five years, has accepted the position of President and Chief Executive Officer of the Osteoporosis Society of Canada effect ◊
"Ontario Executive Director accepts new appointment"

302. Ottawa Regional ALS Conference

The ALS Society of Ontario, Champlain Region and the Rehabilitation Centre, Ottawa are pleased to announce their first one-day interactive conference for people affected by ALS: families, friends, vol ◊
"Ottawa Regional ALS Conference"

303. Climb Celebration for James Lister

A gathering organized by Larry Mallon to honour James Lister, one of Larry's inspirations for Climbing Kilimanjaro. ◊
"Climb Celebration for James Lister"

304. ALS Volunteer Awards for 2003

The ALS Society of Canada is pleased to announce those receiving awards for 2003. ◊
"ALS Volunteer Awards for 2003"

305. William Weir to Carry Olympic Torch

William Weir, diagnosed with ALS in 2000, was the first place winner at the Olympics Team Samsung Torchbearer Search. ◊
"William Weir to Carry Olympic Torch "

306. A Journey of Personal Discovery and Human Spirit

Toronto native, Dennis Flaherty, recounts the 14-month effort by a dedicated team to raise funds for ALS and the challenge of climbing Mt. Kilimanjaro for the campaign. Twelve Canadians left for Tanza ◊
"A Journey of Personal Discovery and Human Spirit"

307. Oxidative Stress Not the Whole Story

Dr.Heather Durham's research, funded in part by the ALS Society is searching for new ways to augment defensive mechanisms to assist cells in defending themselves against multiple disease-causing stre ◊
"Oxidative Stress Not the Whole Story"

308. Catch a Wave

New technology is allowing locked-in patients to communicate — using their brainwaves. Relax. Take a moment. Keep your eyes open and focus on a single spot. ◊
"Catch a Wave "

309. ALS May Hit Gulf War Vets Twice as Often

Veterans who were deployed to the Gulf War may be developing a higher rate of ALS. New research into the occurrence of ALS in American veterans deployed to the Persian Gulf during the 1991 Gulf War re ◊
"ALS May Hit Gulf War Vets Twice as Often"

310. HAART Offers New Insights

When ALS clinician and researcher Dr. John Turnbull gave his patient, Elizabeth Grandbois, HAART, she showed significant improvement. Now a clinical trial is underway to determine if and how the drug ◊
"HAART Offers New Insights"

311. A Fundamental Discovery About the Basis for ALS

Scientists have made a fundamental discovery that could reveal a common underlying mechanism of ALS and other forms of Motor Neuron Disease (MND). The findings, from researchers in the United Kingdom ◊
"A Fundamental Discovery About the Basis for ALS "

312. Scientists Announce Two New Genetic Sites Linked to Familial ALS

Genetic sites on chromosomes 16 and 20 appear to have links to ALS. Genetic screening of four families with familial ALS (fALS) revealed a common suspect region on chromosome 16, and a link to chromos ◊
"Scientists Announce Two New Genetic Sites Linked to Familial ALS "

313. Gene Therapy Prolongs Mouse Life

A new scientific breakthrough offers hope for an effective therapy for ALS. The gene for a nerve-nourishing protein was packaged in a viral vector and successfully delivered to the nervous systems of ◊
"Gene Therapy Prolongs Mouse Life"

314. Stem Cell Therapy

New Hopes and Realities. Stems cells are an important part of the future of ALS research, say scientists. But both their advantages and challenges must be kept in perspective. ◊
"Stem Cell Therapy"

315. New Horizons in Canada and Beyond ...

Good Neighbours,Bad Neighbours: Non-neuronal play an active role in ALS. A new study led by researchers at University of California demonstrates for the first time in mouse models that the cells surro ◊
"New Horizons in Canada and Beyond ... "

316. Understanding SOD-1

Several mutations in SOD-1 have been identified in patients. But how do these mutations result in toxic proteins, and what can knowing the mutation-type tell us about the behaviour of disease? Dr. Eli ◊
"Understanding SOD-1"

317. A Fresh Perspective on ALS

Peripherin is a key protein found in the neurofilament aggregates that clog motor neurons in ALS. By searching for toxic mutations in peripherin, Dr. Janice Robertson hopes to discover the mechanisms ◊
"A Fresh Perspective on ALS "

318. What Tissue Repair Reveals About ALS

When healthy tissues become damaged, they have surprising powers of regeneration. But do ALS-affected tissues always behave in the same way? Dr. Tessa Gordon says that when they don’t, it can provide ◊
"What Tissue Repair Reveals About ALS "

319. New Frontiers in ALS Research

Dr. Michael Strong is a leading ALS clinician and researcher. With help from the NRP, he is discovering the role of neurofilament aggregates in ALS pathways. ◊
"New Frontiers in ALS Research "

320. Fishing for Therapies

Dr. Greg Ross is investigating the molecular pathways that lead to cell death in order to discover drugs that can block those pathways—and keep motor neurons alive. ◊
"Fishing for Therapies "

321. ALS Research, With a Little Help from Some Mice

Animal models help researchers investigate the causes of ALS. By mutating his way through the entire mouse genome, Dr. John Roder is developing new animal models for ALS research and contributing to n ◊
"ALS Research, With a Little Help from Some Mice "

322. Calcineurin's Orchestral Manoeuvres in Muscle

Dr. Robin Michel was the first to demonstrate calcineurin’s crucial role in the growth of adult muscle. With the hope that his research in muscle signalling may lead to new therapies. Already, Mich ◊
"Calcineurin's Orchestral Manoeuvres in Muscle "

323. Pathways to Cell Survival

The regulatory pathways that lead to the death of motor neurons in ALS could be the result of an imbalance of key enzymes. Dr. Charles Krieger is investigating how these enzymes contribute to cell dea ◊
"Pathways to Cell Survival "

324. Food Therapy?

Could a phytochemical found naturally in food help delay the onset of ALS? Dr. Bernhard Juurlink is using ALS mouse models to find out. ◊
"Food Therapy?"

325. ALS From All Angles

Why do motor neurons die in ALS? Dr. Heather Durham and her team seek to understand the unique vulnerabilities of motor neurons in order to help them live. ◊
"ALS From All Angles"

326. A Mouse Model for Juvenile ALS

As research on ALS progresses, the implications for a potential treatment become more promising. Dr. Jean-Pierre Julien’s mouse model for juvenile ALS may bring another level to our understanding of h ◊
"A Mouse Model for Juvenile ALS "

327. Jim Hughes Golf Classic

2004 marks the Fourth Annual Friends of Jim Hughes Golf Classic and our second one without Jim who lost his battle with Lou Genrig's disease on January 12, 2003. ◊
"Jim Hughes Golf Classic"

328. Provincial Contributions to the ALS Research Fund in 2003

The Provincial ALS Societies contribute to the ALS Research Fund, mainly through the WALK TO D'FEET ALS. ◊
"Provincial Contributions to the ALS Research Fund in 2003"

329. ALS Represented At Senate Hearings

Nigel van Loan, caregiver, Board Member of the ALS Society of Canada and President of the ALS Society of Ontario, addressed the Senate Committee holding ◊
"ALS Represented At Senate Hearings"

330. Elizabeth's Concert Of Hope

The fourth annual Elizabeth's Concert of Hope raised more than $300,000., mostly from sponsors. This most successful and popular event has now contributed more than $1.2 million to ALS research and ◊
"Elizabeth's Concert Of Hope"

331. Successful Trial of a Treatment

The results of the first clinical trial on three people from Quebec affected by Duchenne Muscular Dystrophy raise the possibility of a treatment for this debilitating ◊
"Successful Trial of a Treatment"

332. A Réussite D’un Traitement

Ottawa (le 18 février 2004) Les résultats des premiers essais cliniques, effectués sur trois patients de la région de Québec atteints de la dystrophie musculaire de Duchenne, ouvrent la voie à un pr ◊
"A Réussite D’un Traitement"

333. Successful trial of a treatment for Duchenne MD Research

The results of the first clinical trial on three people from Quebec affected by Duchenne Muscular Dystrophy raise the possibility of a treatment for this debilitating disease. ◊
"Successful trial of a treatment for Duchenne MD Research "

334. On The Line - ALS Episode

Wendy Crewson, the Hamilton-born actor who plays Dr. Anne Packard on the hit U.S. TV series 24, joins singer-songwriter Murray McLauchlan next Thursday on On the Line, a live call-in show on CTS ◊
"On The Line - ALS Episode"

335. A Report

The following article comes from the ALSA website. We thank them for allowing us to share it with you. The International Symposium on ALS/MND draws researchers and clinicians together from around the ◊
"A Report"

336. Advocacy Award Named

The Executive Committee of the Board of the ALS Society of Canada is pleased to announce that the Society’s advocacy award will be named in honour of Brett J. Yerex. Brett Yerex, who died in early ◊
"Advocacy Award Named"

337. New Research Collaboration With ALSA

The ALS Society of Canada is pleased to announce the expansion of its research program and first collaboration with its partner organization the ALS Association (ALSA) in the US. The two groups will ◊
"New Research Collaboration With ALSA"

338. 2004 Neuromuscular Research Partnership

Please forward to anyone you believe would be interested. The ALS Society of Canada, Muscular Dystrophy Canada and the Canadian Institutes of Health Research are pleased to announce the ◊
"2004 Neuromuscular Research Partnership"

339. New Year Message

If you wish to receive the PRINT version of the latest ALS Society of Canada newsletter, COAST TO COAST, please forward your mailing address in an e-mail to COAST@als.ca The on-line version can ◊
"New Year Message"

340. ALSa-initiated Research To Test Promising

Reprinted with permission from ALSA. [QUICK SUMMARY: New cultured cell study indicates HDAC inhibitors prevent protein aggregation. Protein aggregates are associated with several neurodegenerative ◊
"ALSa-initiated Research To Test Promising"

341. ALS Society Of Canada - Greetings And

At this time of year the team at the ALS Society of Canada would like to extend warm greetings to all in the ALS network and to say THANK YOU - Thank you to all the CANADIANS LIVING WITH ALS who ◊
"ALS Society Of Canada - Greetings And"

342. Latest Newsletter On Line

The latest edition of the ALS Society of Canada newsletter, COAST TO COAST, is available on line at ◊
"Latest Newsletter On Line"

343. Summary Of International Symposium

The following lengthy summary is provided by the MNA Association. Summaries of the ASK THE EXPERT session and the ALLIED HEALTH PROFESSIONALS session along with audio coverage of sessions by Canadian ◊
"Summary Of International Symposium"

344. Le Projet De Loi C-13 Sur La Procréation

Nouveau cadre pour la recherche sur les cellules souches embryonnaires Dystrophie musculaire Canada, la Société Parkinson Canada et la Société canadienne de la SLA félicitent le gouvernement canadien ◊
"Le Projet De Loi C-13 Sur La Procréation"

345. Assisted Human Reproduction Bill C-13

Regulated Embryonic Stem Cell Research to Proceed Muscular Dystrophy Canada, Parkinson Society Canada and the ALS Society of Canada congratulate the Government of Canada and the members of the House ◊
"Assisted Human Reproduction Bill C-13"

346. ALS Societies Of Ontario And Toronto

The ALS Society of Ontario and the ALS Society of Metropolitan Toronto are pleased to announce that they have amalgamated the two organizations. This will result in improved services for those affecte ◊
"ALS Societies Of Ontario And Toronto"

347. $1.4 Million Preliminary Walk To D'feet

The Canadian Walks to D'Feet ALS for 2003 have raised at least $1.4 million. These preliminary reports suggest another outstanding success. "We expect the numbers will eventually exceed 2002 result ◊
"$1.4 Million Preliminary Walk To D'feet"

348. Canadian Team To Climb Kilimanjaro

Investors Group team set for climb March 2004 Toronto, Ontario – A team of up to fifteen Investors Group representatives from across Canada will make their first acquaintance at the base of Mt. ◊
"Canadian Team To Climb Kilimanjaro"

349. Statement On Three Drug Therapies

A meeting of the Canadian Phase IV Riluzole Study (ALS-601) Steering Committee was recently convened to discuss the use of Riluzole-Nimodipine-Minocycline combination therapy in the treatment of ALS ◊
"Statement On Three Drug Therapies"

350. Appointment Of National Executive Direct

On behalf of the ALS Society of Canada it gives me great pleasure to announce the appointment of Mr. David S. Cameron to the position of National Executive Director. David has been the Executive ◊
"Appointment Of National Executive Direct"

351. December Gala To Benefit The ALS Society

September 4, 2003 - As some of you may have read in the newspapers, our Society has received an unexpected offer of financial support and compassion to our cause. Mr. René Angélil and Mrs. Céline ◊
"December Gala To Benefit The ALS Society"

352. Gala-bénéfice Au Profit De La Société De

4 septembre, 2003 - Comme certains d’entre vous ont pu le lire dans les médias, notre Société vient de recevoir une offre inespérée d’appui financier et de sensibilisation à notre cause. Monsieur ◊
"Gala-bénéfice Au Profit De La Société De"

353. Scientists Announce New Genetic Sites

Three independent groups of researchers have identified families with linkage to chromosome 16, providing strong evidence that another gene associated with familial ALS is close to being identified. ◊
"Scientists Announce New Genetic Sites"

354. ALS Quebec Appoints Director General

Lise Deschesnes, President of the Board of Directors of the ALS Society of Quebec, announced the appointment of Mrs. Marie Josée Godbout as Director General of the Society. Mrs. Godbout has begun her ◊
"ALS Quebec Appoints Director General"

355. 2003-2004 Research Funding Announced

Nearly $4million of neuromuscular research funded has been approved for 2003-2004. The partnership between The ALS Society of Canada and Muscular Dystrophy Canada with the support of the Canadian ◊
"2003-2004 Research Funding Announced"

356. Julien Awarded Canada Research Chair

ALS researcher Dr. Jean-Pierre Julien has been awarded a Canada Research Chair. Dr. Julien, who recently moved his lab from Montreal to the University of Laval in Quebec City, will receive $1.4 ◊
"Julien Awarded Canada Research Chair"

357. Rolling For ALS

Mike Pellatt, ALS BC Board member rolled his way across Vancouver Island with lots of help from his friends He raised lots of awareness and $12,000. Congratulations Mike. ◊
"Rolling For ALS"

358. Stem Cell Research On Muscle Regeneration

Study identifies the cells responsible for regenerating damaged muscle – and the switch that triggers the repair process OTTAWA, ON (June 26, 2003) – A research team from the Ottawa Health Research I ◊
"Stem Cell Research On Muscle Regeneration"

359. First 2003 Walks Hit $100,000 Already

The first four 2003 WALKS TO D'FEET ALS have already reached the $100,000 threshold. Three in Ontario, including Cobourg ($40,000), Niagara Falls ($32,500) and Peterborough ($12,500), and the most re ◊
"First 2003 Walks Hit $100,000 Already"

360. More Research Results

POTENTIAL TREATMENT DEVELOPED FOR MYOTONIC MUSCULAR DYSTROPHY Quebec researchers are first in the world to develop a technique to treat the disease (OTTAWA, May 13, 2003) – A team of researchers ◊
"More Research Results"

361. Fundamental Discovery

Ingenium Pharmaceuticals AG and a coalition of international research organizations announced in the journal Science of Research a fundamental discovery about the genetic and molecular basis for Motor ◊
"Fundamental Discovery"

362. Global Awareness Day Conversation

The International ALS/MND Alliance has organized a Global Awareness Day international conversation linking people in the ALS network worldwide. Co-ordinated by the Motor Neurone Disease Association ◊
"Global Awareness Day Conversation"

363. A Special ALS Performance

A SPECIAL ALS PERFORMANCE of Last of the Red Hot Lover's, a brilliant Neil Simon comedy takes place at the Village Theatre in Hudson, Quebec Thursday, May 15. The show that evening is being dedicate ◊
"A Special ALS Performance"

364. AGM By Teleconference

The ALS Society of Canada held its Annual General Meeting by teleconference on May 3rd, in response to the SARS situation in Toronto. The Board of Directors with representation from all provinces ◊
"AGM By Teleconference"

365. ALS Society Volunteer Awards

The ALS Society of Canada has announced the winners of its annual volunteer awards. MYRA ROSENFELD VOLUNTEER AWARD Ron and Carole Martens of British Columbia have been given the Myra Rosenfeld ◊
"ALS Society Volunteer Awards"

366. Current Status On Thrombopoietin

With permission of the ALS Association we are 'reprint' the following statement on this area of investigation. Susan Graham Walker The ALS Association is actively investigating thrombopoietin (rhTPO) ◊
"Current Status On Thrombopoietin"

367. Un Cocktail De Médicaments Accroît

Montréal, le 1er avril 2003 – Un nouveau cocktail de trois médicaments utilisé pour traiter la sclérose latérale amyotrophique (SLA), appelée aussi maladie de Lou Gehrig, pourrait allonger la ◊
"Un Cocktail De Médicaments Accroît"

368. Drug Combination Increases Life Span

Montreal, April 1 2003 – A new three-drug cocktail used to treat mice with ALS, or Lou Gehrig’s disease, may increase life span and decrease disease progression according to a study conducted at ◊
"Drug Combination Increases Life Span"

369. Research Find Creatine Provides No Help

Copyright 2003 The New York Times Company The New York Times March 25, 2003, Tuesday, Late Edition - Final SECTION: Section F; Page 6; Column 1; Health & Fitness LENGTH: 312 words HEADLINE: ◊
"Research Find Creatine Provides No Help"

370. Outfront Features ALS Story

LISTEN TO CBC ON MARCH 11- OR LATER ON YOUR COMPUTER Sarah Green (Ottawa) along with husband Paul and family will be sharing their story about living with ALS on an upcoming CBC Radio 1 Outfront pr ◊
"Outfront Features ALS Story"

371. ALS Benefit Concert

THE AMADEUS CHOIR Presents a Benefit Concert in support of those living with ALS FEATURING Conductor/Artistic Director LYDIA ADAMS Works by Glick, Raminsh, Ruth Henderson, Faure and Handel ◊
"ALS Benefit Concert"

372. Interim Executive Director Appointed

The Selection Committee, as agreed by the Board of Directors, has completed its initial work, and is pleased to announce the Appointment of Helene Vassos to the position of Interim Executive Director ◊
"Interim Executive Director Appointed"

373. Drug Screening Project Data

This is used with permission from ALSA The ALS Association has received a number of letters appealing for release of the results of the Neurodegeneration Drug Screening Consortium. We recognize and ◊
"Drug Screening Project Data"

374. Use Of Aids Cocktail In People With ALS

Clinical Bulletin from The ALS Association National Office Last week, Canadian media released a story about a woman with ALS who has been treated for the last 18 months with an AIDS cocktail. ◊
"Use Of Aids Cocktail In People With ALS"

375. Participate In End Of Life Care Research

A research team headed by Dr. Donna Wilson at the University of Alberta is conducting a large scale study to identify best practice delivery models or approaches to providing end-of-life care. ◊
"Participate In End Of Life Care Research"

376. Body & Health ALS Episode

Friday Feb 14th - Best of Body & Health with Wendy Crewson and Elizabeth Grandbois. BODY & HEALTH is shown daily on all of the Global affiliates station. ◊
"Body & Health ALS Episode"

377. Latest Coast To Coast Available

The latest issue of the ALS Society of Canada newsletter COAST TO COAST is available web - http://www.als.ca/newsletters.asp ◊
"Latest Coast To Coast Available"

378. Hamilton Spectator - Seizing Life

PUBLICATION: The Hamilton Spectator DATE: 2003.01.29 SECTION: News PAGE: A01 COLUMN: City columnist SOURCE: The Hamilton Spectator BYLINE: ◊
"Hamilton Spectator - Seizing Life"

379. National Executive Director Moving On

Suzanne Lawson, Executive Director of the ALS Society of Canada, has resigned her position to assume the position of Director of Volunteer Resources at The Hospital for Sick Children in Toronto on Mar ◊
"National Executive Director Moving On"

380. BC & NB Unit Partners Lose Key Volunteer

The ALS Society is saddened by the passing of two Canadians – one on the east coast and one on the west - who made a significant and lasting contribution to the mission of the Society as they lived ◊
"BC & NB Unit Partners Lose Key Volunteer"

381. 2003 Neuromuscular Research Competition

The ALS Society of Canada, the Muscular Dystrophy Association of Canada (MDAC) and the Canadian Institutes of Health Research (CIHR) are pleased to announce the ◊
"2003 Neuromuscular Research Competition"

382. Study Shows Mitochondria Likely To Go

A scientist new to The Packard Center for ALS Research has shown that key reactions in mitochondria, the small bodies within cells that supply energy to cells, are disrupted just before cells begin t ◊
"Study Shows Mitochondria Likely To Go"

383. Celebrex Works Well In ALS Mouse Models

A commonly-used drug for arthritis may be of benefit to ALS patients, if first-stage animal studies are any sign. In an article in this month's Annals of Neurology, scientists with Johns Hopkins and ◊
"Celebrex Works Well In ALS Mouse Models"

384. Intravenous Infusions Of Umbilical Cord

The following statement from the American ALS Association has the support of the chair of the ALS Society of Canada Health Professional Advisory Committee. It is shared widely for your information. ◊
"Intravenous Infusions Of Umbilical Cord"

385. Good News About Charitable Giving

The Canadian Centre for Philanthropy has written this response ◊
"Good News About Charitable Giving"

386. Manual For People Living With ALS

The Manual for People Living with ALS is now available in French. Any Unit wishing to order a supply for distribution to French-speaking people wi ◊
"Manual For People Living With ALS"

387. News From The International ALS/mnd

A series of press releases from the UK MND Association give a run down on some of the Symposium highlights: ◊
"News From The International ALS/mnd"

388. Familial ALS Information Being Sought

Dr. Guy Rouleau's molecular neurogenetics laboratory is located at McGill University's Centre for Research in Neuroscience within the Montreal General Hospital. The laboratory was founded 1989 ◊
"Familial ALS Information Being Sought"

389. A Good Time To Plan Charitable Giving

With the busy and much-anticipated holiday season upon us, our attention naturally turns to giving gifts to family, friends and colleagues. This is also the time when a large number of charitable ◊
"A Good Time To Plan Charitable Giving"

390. Supporting The ALS Society When You Shop

This is something to share with your friends! Make your Holiday Shopping EASIER and SUPPORT THE ALS SOCIETY OF CANADA We are participating with two Canadian groups. When you shop on-line through ◊
"Supporting The ALS Society When You Shop"

391. Caring For An Ill Loved One

WNetwork has just posted an article by ALS Society of Canada Board Member on her experience of caring for her husband who died of ALS. Visit the site at ◊
"Caring For An Ill Loved One"

392. ALS Presentation To The Finance Committee

November 6, 2002 The ALS Society of Canada appeared before members of the government Standing Committee on Finance at the pre-budget hearings this week. Caregivers Teresa Riverso and Audrey McKinnon ◊
"ALS Presentation To The Finance Committee"

393. Gemini Humanitarian Award For ALS Work

A BIG night for Wendy Crewson and the ALS Society of Alberta. Go to this site to hear Wendy Crewson's acceptance speech! ◊
"Gemini Humanitarian Award For ALS Work"

394. ALS Society Executive Director Receives

The international Association for Volunteer Administration (AVA) honoured Suzanne Lawson CVA, Executive Director of the ALS Society of Canada with its life-time achievement award at its International ◊
"ALS Society Executive Director Receives"

395. First Study To Probe Early Mental Effect

LONDON, ON/TORONTO, ON (Oct. 24, 2002) – A new study by one of Canada’s leading ALS researchers will be the first of its kind to look at the impact of this devastating neurological disease on memory a ◊
"First Study To Probe Early Mental Effect"

396. Walk To D'feet ALS - Walk Images

This year's ALS Walk to D'Feet ALS images are now available.
Click Here to view the photos. ◊
"Walk To D'feet ALS - Walk Images"

397. Actress Wendy Crewson To Receive Award

(Toronto – October 8, 2002) – Award-winning actress Wendy Crewson will be honoured for her volunteer role with the ALS Society of Alberta by receiving the prestigious Gemini Humanitarian Award at the ◊
"Actress Wendy Crewson To Receive Award"

398. Canon Canada Becomes National Sponsor

LONDON, ON, Sept. 30 /CNW/ - The ALS Society of Canada is proud to announce Canon Canada Inc. has become a national sponsor of the Walk to D'Feet ALS, the new ALS Society of Canada national signature ◊
"Canon Canada Becomes National Sponsor"

399. Coast To Coast - September 2002

The latest issue of the ALS Society of Canada newsletter is available on line - http://www.als.ca/newsletters.asp Spread the news! If you wish to receive a copy by mail, please call Indra Patterson ◊
"Coast To Coast - September 2002"

400. Research Notes

INTERNATIONAL CO-OPERATION IN ALS RESEARCH Funding of a genetic register of ALS patients throughout the world with mutations in Cu/Zn Superoxide Dismutase 1 (SOD1-the first gene to be discovered link ◊
"Research Notes"

401. In Synchrony

Looking at Disability Supports from a Progressive Disability Perspective Working in partnership with three other organizations serving Canadians with progressive disorders, the ALS Society of Canada ◊
"In Synchrony"

402. ALS In The News - August

During the month of August we tracked the following articles in newspapers across the nation. Regina Leader Post & Edmonton Sun – Young country singer Adam Gregory helps make Tanya Sherriff’s last da ◊
"ALS In The News - August"

403. Novartis ALS Trial - Closes July 15th

Recruitment for the Novartis ALS trial (TCH102) will close on July 15th. There are plans for more trials with the compound TCH346, although the results from the 102 trial will be required before goin ◊
"Novartis ALS Trial - Closes July 15th"

404. ALS Society Of Canada - 2001 Annual Report

The ALS Society of Canada 2001 annual report is now available. If you wish to view the annual report please go to the web at the following address: ◊
"ALS Society Of Canada - 2001 Annual Report"

405. Coast To Coast - June 2002

The latest issue of the ALS Society of Canada newsletter - Coast to Coast is available on line - http://www.als.ca/newsletters.asp. If you wish to ◊
"Coast To Coast - June 2002"

406. Neuromuscular Research Partnership

The Neuromuscular Research Partnership Program (NRPP) is a result of an agreement between the Amyotrophic Lateral Sclerosis Society of Canada (ALS Canada), the Muscular Dystrophy Association of Canada ◊
"Neuromuscular Research Partnership"

407. Stemcells: We Know They Can Divide

Stem Cells We Know They Can Divide, But Can They Conquer ALS? By Laurie LaRusso, MS, ELS Note: The ALS Society of Canada shares this article with permission from the ALS Therapy Development ◊
"Stemcells: We Know They Can Divide"

408. ALS Society Applauds Stem Cell Legislation

Ottawa, Ontario – The ALS Society of Canada, Muscular Dystrophy Association of Canada and Parkinson Society Canada are united in their support of the Legislation pertaining to Assisted Human ◊
"ALS Society Applauds Stem Cell Legislation"

409. Trois Organismes De Bienfaisance

Ottawa, Ontario – La Société de la sclérose latérale amyotrophique du Canada, l’Association Canadienne de la Dystrophie Musculaire et la Société Parkinson Canada ont exprimé leur soutien commun au pro ◊
"Trois Organismes De Bienfaisance"

410. Canadian March Of Faces Banners

A new tool for your local fundraising and awareness activities now available through the ALS Society of Canada. A 25th anniversary project of the ALS Society of Canada. Each MARCH OF FACES banner ◊
"Canadian March Of Faces Banners"

411. ALS Spokesperson - Jean Stilwell

The ALS Society of Canada is proud to be a partner in the production of Jean Stilwell's latest CD. Jean is the ALS Society national spokesperson. Hers is an eloquent voice speaking with passion of her ◊
"ALS Spokesperson - Jean Stilwell"

412. ALS On TV - Check Your Local Listings

IN the next month there will be four shows with an ALS focus. HEALTH ON THE LINE - DISCOVERY HEALTH CHANNEL - ALLIANCE ATLANTIS MARCH 13 (Rogers 171 or satellite) 11am Live show hosted by ◊
"ALS On TV - Check Your Local Listings"

413. Stem Cell Research Support

The ALS Society of Canada Supports CIHR-funded Stem Cell Research Guidelines to benefit Canadians Toronto, 5 March,2002 – The Canadian Institutes of Health Research (CIHR) guidelines for research in ◊
"Stem Cell Research Support"

414. Gala Raises $200,000 For ALS

The Second Elizabeth's Concert of Hope held in Hamilton, Ontario on Saturday night raised $200,000 for ALS research and services for those living with ALS. The Hamilton Spectator coverage of the ◊
"Gala Raises $200,000 For ALS"

415. Volunteer Investment Project

Creating Vision, Building Skills Three conferences for ALS Society volunteers and staff Sponsored by the ALS Society of Canada and the ◊
"Volunteer Investment Project"

416. Elizabeth's Concert Of Hope

Elizabeth Grandbois's Concert of Hope is back for the second year running. Last year, in an effort to raise awareness and funding for treatment and research, a group of dedicated volunteers got ◊
"Elizabeth's Concert Of Hope"

417. 2002 Research Competition Announced

The 2002 Neuromuscular Research Partnership (NRP) competition has been announced following the signing of the memorandum of understanding among the ALS Society of Canada, the Muscular Dystrophy ◊
"2002 Research Competition Announced"

418. On Volunteering - A Reflection

As the International Year of the Volunteer comes to a close, Doretta Thompson, Chair of the Public Awareness Committee and member of the Board of Directors of the ALS Society of Canada offers a person ◊
"On Volunteering - A Reflection"

419. Research Gift From Us Scientist

American researcher Dr. Clay Armstrong, recipient of Canada’s prestigious Gairdner Award for 2001has donated the $30,000 prize to the ALS Society of Canada for research. Dr Armstrong, of the ◊
"Research Gift From Us Scientist"

420. It Gives Me Hope

by Sheila Power, ALS Society of Newfoundland, St John’s. One of my earliest memories is sitting next to my Nanny waiting for my parents, brothers and sisters to come home. I remember them coming ◊
"It Gives Me Hope"

421. Desert Storm Vets Have High Rate Of ALS

According to a news release on December 10, 2001 from the Department ofVeterans Affairs, researchers conducting a large epidemiological study supported by both the Department of Veterans Affairs and ◊
"Desert Storm Vets Have High Rate Of ALS"

422. Concert Of Hope Tickets Available

Tickets are on sale for the Second Annual Elizabeth’s Concert of Hope being held February 9th, 2002 at the duMaurier Ltd. Centre, Hamilton, Ontario. Sponsored by Merrill Lynch, host Ian Thomas will ◊
"Concert Of Hope Tickets Available"

423. Symposium Highlights - Scientific Session

The following summary was written by Lucie Bruijn, Science Director and Vice President of ALSA. We thank ALSA for permission to reprint it here. 12th International Symposium on ALS/MND November ◊
"Symposium Highlights - Scientific Session"

424. Symposium Highlights - Clinical Sessions

12th International Symposium on ALS/MND - November 18-20, 2001 Oakland California Highlights and Summary of Clinical Sessions The following summary was written by Mary Lyon, Vice President of ◊
"Symposium Highlights - Clinical Sessions"

425. Caregiving At A Distance

By Marjorie Willison, Halifax, Nova Scotia When my brother Garth was diagnosed with ALS in November of 1999, I never imagined that I would be able to provide much caregiving for him. ◊
"Caregiving At A Distance"

426. Preventing Nerve Cell Death In ALS

ALS attacks the nerve cells that control the voluntary muscles throughout the body. When these muscles fail to receive messages, they eventually lose strength, atrophy and die. Dr. Gregory Ross’ ALS ◊
"Preventing Nerve Cell Death In ALS"

427. Drug Treatment Is The Goal

Making scientific discoveries that will be a target for drug development to combat ALS – that is a research objective for Dr.John Roder. Relevant research from a centre with a strong reputation ◊
"Drug Treatment Is The Goal"

428. Mp Constituency Week

The ALS Society of Canada encourages all Canadians in the ALS network to contact their Member of Parliament during constituency week - November 10-17, 2001. This provides an excellent opportunity ◊
"Mp Constituency Week"

429. Coast To Coast - October 2001

The latest issue of the ALS Society of Canada newsletter is available at www.als.ca. Click on NEWSLETTERS In this issue: A profile of ALS researcher, Dr. Gregory Ross, of Queen's University ◊
"Coast To Coast - October 2001"

430. Video For Caregivers

MAKING HARD DECISIONS THE ESSENCE OF BEING HUMAN TWO NEW VIDEOS addressing the questions surrounding end-of-life issues can now be ordered on-line. In conversation with journalist Judy Maddren ◊
"Video For Caregivers"

431. North America’s First ALS Hospice Opens

WINNIPEG –October 11, 2001 – Canada’s and North America’s first hospice for people living with amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig’s disease, officially opened toda ◊
"North America’s First ALS Hospice Opens"

432. Gene For Juvenile Form Of Familial ALS

Two groups of scientists have identified a gene, that when mutated, is responsible for juvenile ALS, also known as ALS2. This very rare variant of familial ALS starts before age 25 and tends t ◊
"Gene For Juvenile Form Of Familial ALS"

433. Drug Trial Information - An Article

Seminars in Neurology [Sem Neurology 21(2):167-175, 2000. © 2000 Thieme Medical Publishers, Inc.] Thieme Medical Publishers, Inc. is the exclusive copyright holder of this work and therefore direct ◊
"Drug Trial Information - An Article"

434. Drug Trial Information

Thieme Medical Publishers has given the ALS Society of Canada permission to post this article on clinical drug trials. Please adhere to the copyright agreement below. ◊
"Drug Trial Information"

435. Coast To Coast - June 2001

The latest issue of the popular COAST TO COAST newsletter is now available by clicking on NEWSLETTER at the top of the page: In this issue: ALS Society volunteer awards; great fundraising stories ◊
"Coast To Coast - June 2001"

436. Great Kids, Great Stories

When young people decide to make a difference great things happen. Here are three stories that have happened in the last few months. What an inspiration they are for all of us – young and old. ◊
"Great Kids, Great Stories"

437. Walk To D'feet ALS Ready To Move

Eight locations will launch a WALK TO D’FEET ALS in the fall of 2001. The new signature event is co-ordinated by the ALS Society of Canada to raise awareness and funds for local services for those ◊
"Walk To D'feet ALS Ready To Move"

438. Tim E. Noel Dies

It is with sadness that we announce the death of Tim E Noel. Tim Noel, deputy governor of the Bank of Canada died on Wednesday July 11, 2001. Since his diagnosis with ALS in 1999 Tim has ◊
"Tim E. Noel Dies"

439. Research Funding Announced

The Neuromuscular Research Partnership (NRP) has announced $4.83 million of research grants in 2001-2002. This is quadruple the amount granted last year to more than twice the number of researchers. ◊
"Research Funding Announced"

ALS Society Page	ALS and Lou Gehrigs Disease Articles
Advocacy	Advocacy
ALS Research	ALS Research
Awareness	Awareness
Caregivers	Caregivers
Charity Events	Charity Events
Drug Trials	Drug Trials
Fundraising	Fundraising
General	General
Healthcare Professionals	Healthcare Professionals
Press Releases	Press Releases
Researchers	Researchers
Volunteer	Volunteer