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  1. Life with MND pages
  2. Gareth from Southborough
  3. cant use my PS3 anymore
  4. Social Networking Sites
  5. TV Advert - Why not
  6. anyone got amalgam fillings?
  7. Nightmares
  8. Hospice
  9. Hobbies? interests?
  10. Experiences with Vitamins
  11. What did you do before Christmas
  12. MNDA "To Do" List
  13. Off to see neuro tomorrow
  14. Hi......don't mean to sound like a stuck record
  15. constant pain in degraded left hand
  16. Exercise for MND
  17. Am I wrong to feel like this?
  18. Chewy vitamins.
  19. First tumble in work!
  20. This just doesnt happen! but then again.......
  21. In view of
  22. Other Afflictions
  23. Open Letters - Notice of action against Government
  24. MND and the Menopause
  25. Sleep problem - whining noise?
  26. Communications with Bulbur
  27. Would Forum Members find a Research Discussion Area Helpful?
  28. Anaemia and inflammation: effects of MND?
  29. Mentoring Youth
  30. MND Documentary
  31. Anyone use a hand splint
  32. Would you like to take photos/video but can't hold the camera anymore? Check this out
  33. Rapid change
  34. Ventilator Design Fault
  35. Government's unlawful enquiry into disabled living
  36. Protein
  37. Any questions you may have?
  38. People who have been cured?
  39. Juice
  40. Vegan/ Veggie Diet
  41. Recipe suggestions for people with difficulty swallowing, sucking, moving tongue etc
  42. Money raiser.
  43. A question about nerves
  44. Monthly MND News
  45. MND on the big screen
  46. The Anatomy of a Neuron
  47. The un-official guide to fighting MND
  48. MND on the small screen - Model Talker
  49. Unsteady Balance - Old Age or MND Related?
  50. Does anyone else do a Blog or Website?
  51. Northern Region Spring Conference
  52. Turning in Sleep
  53. Going Off Food
  54. Losing the ability to walk
  55. Dx dates
  56. What do you think caused your MND ?
  57. I retired today
  58. Going from ALS / Bulbar to PLS
  59. new soap thing for when your hands no longer work very well.
  60. Manchester MNDA conference
  61. Finally moved
  62. Conference Reading May 15th
  63. Our Agenda for the MNDA AGM
  64. When to expect an 'official' diagnosis?
  65. Wanted - motor neurone disease t shirts - new or used
  66. Tough few weeks
  67. massage and relief from stiffness
  68. Now tell me, what do you think of this?
  69. Furry Tongue!
  70. Are there any viable treatments available in the world?
  71. Forum Members needed for Parliament Neurological Review
  72. Plymouth Support Group
  73. Chronic Fatigue and MND
  74. Sheffield Half marathon / fun run MND support
  75. Rapid progression
  76. Does Cannabis help with living with MND?
  77. Oxfordshire Branch MND Association
  78. Lyme Disease Question
  79. Charity Compassion in Dying: new free information line 0800 999 2434
  80. sleep
  81. Government Defeated in High Court on Social Care
  82. summer get together ?
  83. problem solved :)
  84. Getting a bra off
  85. Neater Eater products
  86. Air travel
  87. Children of PALS
  88. Upleasant comments made by radio station!
  89. Care for carer?
  90. easyjet
  91. twitter
  92. Opening doors
  93. National Audit Office
  94. Chris Broad on This Morning
  95. Prolonging life in the hope of a cure
  96. Your Help Requested: Views on Assisted Dying.
  97. help reading electromyogramme
  98. can anyone help with interpreting an EMG?
  99. Hypnosis
  100. Ticking off the wish list
  101. young carers
  102. 2nd opinion
  103. Trouble Eating
  104. Assisted Dying: Your views wanted to pass direct to Demos (independent) think tank.
  105. Dr Red Blueberry punch
  106. Clos-o-mat toilet in London
  107. Is being slightly over weight better?
  108. Passive Range Of Motion Exercises
  109. Tracheoscopy - why not and where's the debate?
  110. My TV Appearance
  111. My symptoms
  112. Can anyone help with the confusion
  113. Where do we turn now and who is willing to help?
  114. electric toothbrush
  115. Fishing with the stars
  116. Cynthia: How to get a good nights sleep?
  117. New nightmare.........the remote!
  118. MND user as all disabled folk robbed of basic human rights
  119. Robin Turvey
  120. AGM & Conference at Stansted?
  121. Cough assist
  122. Problems/triubles come in three four and fives?
  123. distress alert button
  124. Can Exercise help?
  125. wheelchair accessible holidays uk
  126. Help advice with asking for as taking Oxygen
  127. Loss of hands and fingers
  128. Bravery and Motor Neurone Disease
  129. Understanding MND.
  130. Kindle
  131. SPORK- (spoon, fork and knife in one)
  132. Muscle spasms
  133. feeding difficulties
  134. Mouth problem
  135. Newcastle Chronicle: Anyone in the North East interested in sharing their story?
  136. Difficult Question: Sex after MND?
  137. I need a scrubber!!
  138. laughing fits
  139. MND Break through BBC news
  140. Painful Journey of Motor Neurone Disease
  141. Slow service from NHS and Social Services
  142. Uncurable Motor Neurone Disease (for all sufferers)
  143. MNDA AGM, Election of Executives - Forum Debate
  144. Publicise MND in UK TV soaps
  145. Lonely Heartfelt Tears (for Debbie)
  146. Total immediate paralysis, any one heard of this with MND?
  147. Getting MND in the media
  148. Dealing with losing some dignity
  149. Hair loss
  150. What is a Plasma Exchange?
  151. new peg
  152. pancriatitas
  153. Got my stick at last hooray
  154. Ventilator queries
  155. a curry, a beer and a dog named Alfie
  156. Cold feet
  157. pain with mnd
  158. Wacky races
  159. Just when you think things are good.........
  160. Parenting with MND
  161. Letter sent to local press re Housing folk with MND
  162. Fund raising Poetry for Motor Neurone Disease
  163. new hoist
  164. Christmas Ball
  165. For all MND sufferes worried about dying, have hope
  166. AGM Minutes
  167. To bio- or not to bio-bidet...
  168. MND on TV tonight (12/09/11) Channel 4 7:55pm-8:00pm
  169. MNDA local branch meetings
  170. Fund raising and awareness
  171. Excessive yawning
  172. Good News on the Housing Front
  173. Personal Independence Payment (PIP)
  174. Double vision and increasingly poor eyesigjt
  175. MND Kids club
  176. Had OT out today, here's what we agreed on
  177. Kindle switch
  178. Donating
  179. South Wales MND Nurse Leaving
  180. Stu Millheiser A True Angel On Earth
  181. Wheel Chair Users Gadgets to control
  182. Family help Cardiff Uni find motor neurone disease gene
  183. 1st Anniversary
  184. How is everyone?
  185. Hunger
  186. Update on Jeff
  187. MNDA Annual Conference and AGM Forum Photo
  188. shaving whit ALS.....
  189. MND Awareness
  190. Paddling to raise awareness
  191. How do you .............??
  192. Iberian cruise
  193. RESUSCITATION form. thoughts ?
  194. At last, i'm getting some support
  195. Still no Diagnosis
  196. Tests
  197. Bed sores
  198. Possible TV appearance
  199. Hard times
  200. Professional help.
  201. Update on health and a new bungalow
  202. Latest from Jeff in Liverpool
  203. World’s smallest text-to-speech device
  204. Thumb Print
  205. Chris Woodhead Foundation (Providing care and support MND).
  206. Moving back to the UK
  207. Confirmed
  208. Food supplements
  209. shower chair
  210. Living or Dying?
  211. Be Prepared !
  212. Jaded John Campaign
  213. upstairs
  214. Seventy als patients. Not a single ventilator. Can anyone help?
  215. What happens now?
  216. Tests tests and more tests
  217. Proloquo2go
  218. Can You Help Produce Some Guidance?
  219. ventilator fear
  220. Marijuana
  221. describing the pain
  222. What would you do?
  223. convene
  224. inconsiderate people
  225. Happy Christmas!
  226. Donate body to medical research during Christmas holidays URGENT
  227. Mnd, now that it is over
  228. My Brave Lady Finally Loses The Fight
  229. MND Connect - Phone line problems
  230. Not A Good Start To 2012
  231. NONI juice................. any one know?
  232. Jumpy legs/Cramps
  233. Waiting time for Peg fittings?
  234. rig
  235. How many MRI scans do you need
  236. Pregabalin
  237. jaded johns west wing
  238. Mucus plug
  239. New home
  240. Chromosone 9
  241. ALS Wave
  242. Care Centres
  243. Is information "sugar coated"
  244. My wonderful friend Jeff has gone with grace and dignity
  245. Cogane
  246. Advice on NIV
  247. Sorry feel like a rant
  248. Freezing cold feet and lower legs
  249. stay warm
  250. How Long Between First Symptom and DX?

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