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  1. Jim 'Catfish' Hunter ALS Foundation donates $100k toward research & equipment
  2. Motor neurone disease victim fights to the end
  3. ALS Functional Rating Scale
  4. Living with ALS
  5. Is Something in Your Mouth Harming You?
  7. Scientists Regenerate Wing In Chick Embryo
  8. neck brace
  9. Fund-Raising on Borrowed Time
  10. Needing Reassurance
  11. Where have they all gone
  12. Diaphragm pacer update
  13. Can Rilutek make symptoms worse???
  14. Watson carries on fight
  15. should we add a obituaries sticky here ?
  16. PatientsLikeMe Community,
  17. Advocacy Update: Medicare Rx Drug Benefit Open Enrollment
  18. Stuart remains alive because of a gift not available in any mall
  19. Dying professor ponders all but death, Terry Hoy,
  20. Does anyone here have a portex trache?
  21. Hitachi-led group develops communication device for paralyzed
  22. Stephen - Founder of ALS TDF and Inspiration for PatientsLikeMe
  23. Experts discuss ALS research
  24. Esther's myspace page now online
  25. Media Alert: Genetic Links to ALS to Be Unveiled in New Research
  26. Cognitive impairment appears to be common in patients with amyotrophic lateral sclero
  27. In Remembrance
  28. A boost for ALS research at UMAfter the death of their father from ALS, two sons have
  29. NASA Technology
  30. NsGene’s proprietary neurotrophic factor, NsG33, will be evaluated by Genzyme for the
  31. Stem Cells Are at Top of Senate Agenda
  32. First International Gene Screen for Typical ALS Is on Track; Packard Center Researc
  33. temp
  34. TGen may have found Lou Gehrig's trigger
  35. ALS Research News (A monthly summary of significant articles about ALS research)
  36. Basu: Fighting for life, finding financial ruin
  37. Stricken by ALS, fitness mogul hunts for genes
  38. Marijuana-like Drugs Help Treatment of Nervous System Diseases
  39. ALS and Stem Cell Research
  40. Als Newsmagazine Needs Your Help
  41. Research From Around the World
  42. FDA Withholds OK of Involuntary Emotional Expression Drug
  43. Study gives hope to Lou Gehrig's patients
  44. Lou Gehrig's disease hurts his body; technology helps his brain
  45. Stem Cells Are Where It's At
  46. ALS slows but doesn’t diminish Helen Wade
  47. Schillings continue fight against ALS
  48. Carol Nockold, 51, maker of "Real Good Food"
  49. Dying nurse forced to wait for vital help
  50. The artist and his doctor
  51. The New Brick by Brick Newsletter is out
  52. House Votes on Lifespan Respite Care Bill Tomorrow
  53. Professor Hal Rothman
  54. Friends of Edward
  55. Full-time carers for mum
  56. Naked Folk,, photography/fundraiser
  57. The world's strongest man
  58. Doctor's ALS fraud case goes to jurors
  59. Military service may be linked to Lou Gehrig's disease,
  60. 'So much' is powerful look at ALS
  61. Trophos Successfully Completes Phase Ib ALS Clinical Trials for TRO19622, a Novel Com
  62. Ironman Hawaii on TV Saturday
  63. Polo match to help fight Lou Gehrig's Disease Sunday
  64. abigail alliance for access to developmental drugs
  65. United States Senate have passed the Lifespan Respite Care Act
  66. New regulations could cost Lyme disease patients
  67. Procedure detects nerve disease
  68. Photos tribute honors senior's father's illness
  69. you could be the 500 pals
  70. Stem Cell Innovations and ALS Association announce collaboration
  71. ALS lab still in the hunt
  72. Human Stem Cells Delay Start of Lou Gehrig's Disease in Rates
  73. Worrying Again
  74. March and Roll with Us to Capitol Hill
  75. Indestructible Newsletter #5
  76. Stephen Hawking says disease means no 'boring' committees
  77. FDA Proposes Rules Overhaul to Expand Availability of Experimental Drugs
  78. Robotics, laser and wireless technologies make driving safer for wheelchair users
  79. Rockers take stage for ALS support group
  80. The Wheelchair & Scooter Market is Expected to Grow to $5.3 billion by 2012
  81. Als Clinical Trials: State Of The Pipeline
  82. Living with ALS
  83. General presses war against ALS
  84. ALS can't quite stop ex-dancer
  85. Going down swinging
  86. Inconsiderate Morons Who Make Life Hell For People In Wheelchairs Are As Bad As Drink
  87. The Fight Of His Life T
  88. Hawking to promote Israeli ALS research
  89. Music Inspired By ALS Research
  90. ALS TDF Results Well Received at the Yokohama ALS/MND Conference
  91. Get Going
  92. Oklahoma researcher receives MDA grant
  93. Ardsley students win MIT grant to develop wheelchair invention
  94. Man with ALS says he has learned from struggle
  95. UCI receives $500,000 for ALS program
  96. Chat Online With Augie Nieto On Jan. 9
  97. Friends grant Christmas wish
  98. Doubt on Gulf War chemical claim
  99. President Bush Signs the Lifespan Respite Care Act of 2006
  100. Robotics, Lasers And Wireless Technologies Make Driving Safer For Wheelchair Users
  101. Because they love her
  102. Giving your website 'wheelchair access' can prevent litigation and increase market ex
  103. Law professor battles ALS
  104. Sergio De Luca juggles array of therapies to slow ALS
  105. Family finds hope in tough times
  106. Beating the odds and making music
  107. The gift of hope
  108. Welcome to the ALS/MND Registry
  109. Ex-Raiders fullback is battling Lou Gehrig's disease
  110. Austin woman to walk to Boston for ALS awareness
  111. Fourth Graders Learn More about ALS
  112. Happy New Year To Everyone
  113. For his birthday, a sweet ride
  114. AEROSMITH Donates Autographed Guitar For Charity
  115. stem cell research
  116. Swimmers plunge into Long Island Sound for a cause
  117. Boost in mystery muscle creates endurance mice
  118. Pot may be both good and bad, researchers say
  119. hello mark,,,sully
  120. Julia Adams takes note of living, not dying
  121. Community huddles up for Coach Kelly
  122. Smoke clears for several shows at Shank
  123. Stem cell scientist Hynek Wichterle tackles Lou Gehrig’s disease in a privately-funde
  124. Rewiring Lost Connections
  125. Ex-DAVID LEE ROTH/CACOPHONY Guitarist JASON BECKER Needs Your Help Again
  126. We must immediately put pressure on Congress to enact the Stem Cell Research Enhancem
  127. Young Caregivers: Parents
  128. BobbyB! You are Kick-***!
  129. Captain of Your Own Care
  130. ALS mentioned on Ghost Whisper (the series)
  131. Todd Kelly may face federal charges
  132. Coast to coast bike ride is in honor of Willamette student who died of ALS
  133. Response by readers touches former coach
  134. Helen Hayes Hospital, upstate resort put wheelchair users on skis
  135. Facing certain death,
  136. Lost to Lou Gehrig's disease
  137. ALS patients become prisoners in their bodies
  138. Raising awareness,Fred Siwak
  139. A new type of stem cell discovered
  140. Augie Nieto Chat Reminder
  141. Als/mnd Chatroom
  142. Immediate Action Needed
  143. Pasta dinner to raise funds for retired officer's medical treatments
  144. One Problem Congress Could Fix
  145. Dunkin' Donuts drive-thru accused of disability discrimination
  146. Democrats' Stem-Cell Measure Passes, Isn't Veto-Proof (Update1)
  147. National Vote Underway for All-Time Greatest Heroes
  148. Power Wheelchairs Available
  149. Ride For 3 Reasons
  150. Fighting for life
  151. Faith and friends sustain Ken and Phyllis Swigart as they deal with a debilitating di
  152. Weston | A Family Copes With Illness
  153. Final dance’ partners
  154. HELP what should i ask my neuro
  155. Moping is not an option; enjoying every moment is
  156. Lou Gehrig's Disease victim to keep swinging away
  157. Statement of The ALS Association: The Prescription Drug User Fee Act
  158. 'I can't ever give up'
  159. Roto-Rooter Offers Chance To Win 'Pimped Out John'
  160. The Future of Food
  161. Tdf Is Now Tdi
  162. Augie Nieto On NBC
  163. Richland will be site of region’s first ALS clinic
  164. Geron says stem cells nurture damaged spine
  165. Spanish judge orders euthanasia death inquiry
  166. Michael J Fox for Cures from ESCR will attend Bush's State of the Union Address!!!!
  167. O.C. entrepreneur gives $18 million to ALS research
  168. Former Hagerstown man writes book on wife's ALS struggle
  169. Governor's Proclamation
  170. Our Five-Year Plan? Let Human Cells EXcellerate Therapy
  171. Please! pass this on to promote Project A.L.S. awareness to ALS
  172. Indestructible To Receive Its World Premiere At The 17th Annual Cinequest Film Festiv
  173. The artist and his doctor
  174. Nelsons coping with another twist of fate
  175. Non-Invasive Mask Ventilation
  176. Participation needed in study
  177. Stem Cell Promise
  178. Teachers plan benefit concert for counselor
  179. Mike will be taking the plunge for MND sufferers
  180. "We Belong" (D. E. Lowen/D. Navarro)
  181. Nietos go another round against ALS
  182. DynaVox Technologies today announced the release
  183. goodsearch, charity, donate $$
  184. Cannabinoid Agonist Significantly Increases ALS Life Span, Study Says
  185. The choice: Anger and grief ... or living to the limits
  186. A mother's long goodbye
  187. A question or two
  188. Italian Researchers Find ALS Genes
  189. Marathon to raise funds, awareness for ALS
  190. Finder: Dozier, Duranko tackling ALS
  191. I wish Bill Gates would get ALS ,,not
  192. Facing Illness
  193. UW's Erickson making a new game plan: this time, for life
  194. Marked rise in MS in the US debated by scientists
  195. Quebec researchers develop ALS vaccine
  196. Living the Moment with ALS
  197. Karen's Corner – Stephen Pallotta and the power of prayer
  198. Connecting for a Cure
  199. LORI BANKER-HORNER, L.P.N. • Amyotrophic Lateral Sclerosis (ALS) Association - Wiscon
  200. Couple faces lung transplant, Lou Gehrig's disease
  201. Proctor Black Woods Blizzard tour underway
  202. New member with some questions
  203. Stachybotrys Mold
  204. Passing out smiles
  205. How much of Ordot's environmental problem comes from U.S. government?
  206. Rockin' for Research
  207. Her faith keeps her going
  208. Spanish scientists - To develop a thought-controlled robotic wheelchair
  209. could viagra help with als?
  210. PatientsLikeMe Secures $5 Million Series A Financing
  211. CytRx to Proceed with Arimoclomol Maximum Dose Study
  212. Tickets on sale for ALS Vegas Night
  213. registration is now available for the 2007 National ALS Advocacy Day
  214. Bidet seats - good or bad?
  215. A decade after Dolly, what will the cloners create next?JAMES MORGAN February 08 2007
  216. The ALS Association Recognizes Its Jim “Catfish” Hunter Chapter as Chapter of the Yea
  217. Blais’ army continues waging heroic battle
  218. getting organized and getting things done, effective activists
  219. Nick Huber cherishes his wife and job, but at 27 is fighting for each new day
  220. Dedication
  221. A life without fear
  222. Muonone
  223. An Invitation to Join The ALS Advocacy Community
  224. this is a test.
  225. Myostatin - The Next Generation's Steroids
  226. Hyperintensity of the Precentral Gyral Subcortical White Matter and Hypointensity of
  227. Betrayed by his body, LV historian keeps fading
  228. Every Day Is Precious
  229. Pagliarini starts as governor's deputy chief of staff
  230. Not ready to give up
  231. Ailing Man Accuses Wife Of Assaulting Him In Bed
  232. Here's a reference to a study gone bad.
  233. Reminder: ALS TDI will host a conference call Tuesday, February 13th beginning at 7 P
  234. Research Supports Medicinal Marijuana
  235. We are pleased to share with you that the President’s Fiscal Year 2008 Budget include
  236. Human Stem Cell Transplants Repair Rat Spinal Cords
  237. What Do you Think Poll ?
  238. Prior Lake principal reveals ALS diagnosis
  239. the `ALS Registry Act'.
  240. What's happening
  241. Remove roadblocks to stem-cell research in Iowa
  242. Letter for you to send to Your congress person to ask for veto override
  243. Huang Wins Muscular Dystrophy Association Grant
  244. Viruses get the silent treatment, any disease is a target
  245. Polishing the soul, cleaning the spirit: Mike Wagner shines despite Lou Gehrig's dise
  246. How ALS/Lou Gehrig's Disease Changed My Life
  247. My boss that's my wife
  248. Research Update – from the ALS Association's National Office
  249. Neurological "Volume Knob"
  250. PatientsLikeMe Public ALS Registry
  251. ALS Spotlight Award goes to staff writer