PDA

View Full Version : ALS


Pages : 1 [2] 3 4 5



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