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  1. To everyone **PLEASE READ**
  2. To those that had intro's on the old site...
  3. Andrew
  4. Cyndi
  5. Diana
  6. Gwenllian
  7. Ian
  8. Karen
  9. Nancy
  10. Patricia
  11. Terri
  12. Trev
  13. Andrew
  14. Suzie (Witho)
  15. Capabayan (Elizabeth)
  16. A bit of history...
  17. Another bit of history
  18. New Member
  19. Trish
  20. Hello
  21. New member
  22. Debbie
  23. Richard's First WG Story
  24. I am a family member of a WG survivor
  25. My mother has WG
  26. About me and suggestions for "alternative" help from other Weggies
  27. Hello out there!
  28. Peter
  29. I'm a Newbee
  30. Newbie
  31. Marcy's story
  32. new to this forum
  33. Tingling feet
  34. ROGER A new member, from the U.K.
  35. 13 years, 232 days -- and counting....
  36. Newbie to the forum
  37. New to the site
  38. New member and new to the world of forums
  39. My father has Wegener's--new to forum
  40. New To Group
  41. Just getting started
  42. solomagnum
  43. My husband has WG
  44. What what your Doctor's "a-ha!" test?
  45. Another new member to site, but 2 Year WGer
  46. 20 Years of Wegener's
  47. An eye story
  48. weggie's storry
  49. Grandson diagnosed...
  50. New Member
  51. Follow up to Eye Story
  52. Newly Dx'd with WG
  53. Newly diagnosed, too
  54. Husband Newly Diagnosed, Quick Downward Spiral
  55. A couple of questions
  56. New to the Club
  57. Diagnosed 3 weeks ago, only out of hospital for a week
  58. Saw the Rheumy again today
  59. Tammy
  60. Big thankyou to Andrew and other members
  61. Diagnosed WG in June 08
  62. new menber
  63. new menber
  64. Lucky, I Guess
  65. An introduction
  66. Just let me get this off my chest
  67. "We're Not Exactly Sure What's Going On..."
  68. I am looking for help right now.....
  69. Not me but brother n law has WGD
  70. Hi Everyone
  71. Beware not to drop Prednisolone too much
  72. My Toastmasters Speech
  73. Gums
  74. New to WG
  75. second episode of Wegeners
  76. Hello - I'm Jonathan
  77. New to the forum
  78. family member has wg
  79. Diagnosed May 2007
  80. Diagnosed yesterday, still in hospital, new member!
  81. New here! Diagnosed 1/08 Still rough!
  82. Glad to be diagnosed
  83. New Forum Member
  84. Blood Work Pointing to WG - No Active Symptoms
  85. seeing a neuroligist tomorrow.
  86. Dumpy
  87. Hair has gone frizzy!!!!!
  88. Diagnosed January 2009
  89. I'm new here...
  90. Shirina
  91. diagnosed Jan 2009 also
  92. saw my rheumy
  93. My WG story
  94. Mike: 27 years without WG
  95. Wondering
  96. New Member
  97. Granddaughter Has WG
  98. Just Joined
  99. Diagnosis
  100. just joined
  101. Just Diagnosed
  102. living with WG
  103. New member intro
  104. Derek. New member
  105. Hi, I'm new here. Here's My Story.
  106. bloodtansfusion
  107. hematologist
  108. My Mother has been diagnosed
  109. New Member
  110. A miracle baby.Ivelirsse's story.
  111. New Here
  112. Newly diagnosed
  113. I'm New Here
  114. A last maybe some answers!!!!!!!
  115. So, as it turns out, I have this disease...
  116. New Here!
  117. Greenish toe?????? OMG!
  118. sorry i've not been on for a while.
  119. My WG's story (I hope it isn't too long)
  120. Final Days
  121. Genetic Link
  122. New guy
  123. Hello, new to the forum.
  124. Update on Ivelisse
  125. how am i supposed to feel.
  126. started on cellcept today.
  127. New to WG
  128. Found a youtube video about Wegener's
  129. Josh's story
  130. My Sisterís Story:
  131. Raj
  132. Just diagnosed
  133. CanadianGuy... really???
  134. Sound familiar?
  135. marion
  136. What can I expect?
  137. My Roommate and I!
  138. New Member/New to Wegener's
  139. Newly Diagnosed
  140. My Story...
  141. just diag. with WG
  142. Hello! ~=]
  143. Still Waiting Diagnosis Confirmation
  144. life is still a rollercoaster after 3 yrs!
  145. Im new and this is my story..
  146. 13 year old just diagnosed
  147. Hi members
  148. Hi There
  149. An optimistic story
  150. New member and just diagnosed
  151. pediatric rheumotologist
  152. New Here
  153. Here for my daughter
  154. this is my story
  155. I got my first CT Scan today
  156. New to all this but day by day I am hoping to win out!
  157. Vikings fan diagnosed in June 2009
  158. I started Chemotherapy this week!
  159. Just a normal day
  160. lab results
  161. This is new to me.
  162. This is new to me.
  163. lado123
  164. hello there.
  165. G'day fellow Wegies
  166. My WG experience
  167. Mom of Newly Diagnosed 18 Year Old -- HELP!
  168. My husband's story
  169. From undiagnosed to climbing Mt. Everest!
  170. Long road
  171. a long road,BUT FINALLY IN REMISSION
  172. Do I have Wegs or don't I?
  173. Hello from Melbourne :)
  174. Hello from Melbourne Australia
  175. Looking for advice from Canada
  176. Hello from central Texas.
  177. Good morning from Scotland
  178. The Curse of Kimbangu- A Scotsman's tale....
  179. my sister....
  180. Elevated Antiproteinase 3
  181. looking for help for my mother
  182. Trying to conquer my puter
  183. Still on puter
  184. Hello from another newbie
  185. Eyesight going blurry sympton of?
  186. Finally getting off Preds
  187. My Spouse has Wegeners
  188. Hi from New Zealand
  189. Many of us are Heading toward remission
  190. Newly Diagnosed
  191. Diagnosed, but lucky (I hope)
  192. Big HELLO from CROATIA
  193. Katie Got A New Kidney!
  194. Newly Diagnosed in NYC
  195. Almost Famous
  196. Diagnosed in Decemember 2009
  197. fairly new member
  198. What a week
  199. Well, here's the deal with me then...
  200. my sister
  201. When in Doubt Kiss your Dog
  202. Hi Everyone! I'm New
  203. 15yo Son diagnosed last week with WG
  204. Sudden Severe Dry Eye Symptoms Due To An Acute Infammation Of The Tear Glands
  205. Multiple skin cancers due to Wegeners?
  206. Merry Xmas you have Wegners 2009
  207. New and Scared
  208. New From California
  209. WG & Its effects on my Lungs & what has it done to yours
  210. CT scan
  211. Next Drug?
  212. hello everyone
  213. JanW's surgery went well!
  214. Breaking free of the cotton candy web of denial...
  215. Waiting on confirmation of disease, very scared, confused.
  216. New WG patient
  217. New to the group
  218. Off Preds Starting Taper of Immuran
  219. My wife got busy
  220. Microdermabrasion
  221. Hello
  222. Hello and Brief Introduction
  223. Hello, yet another newbie!
  224. Another WG Newbie...(we should have a convention)
  225. Hello and very nervous
  226. Kansas, USA Wegener's Gal
  227. Hello
  228. Hello
  229. hi everyone
  230. Hi everyone
  231. Hello - my 14 year old son was recently diagnosed
  232. 17 years old, diagnosed three months ago
  233. I'm glad I'm not alone, and happy I found you!
  234. So Happy to Find This Website
  235. Hi! I'm new :)
  236. my 8 year old son in hospital now.
  237. any info on treatment of trachea stenosis
  238. hi everyone im ian from scotland
  239. 30-year Survivor
  240. New to the site
  241. Starting my Diet tomorrow!
  242. New from Perth, Western Australia
  243. does anyone have a problem with skin fungus/
  244. Arrrgggg! Its got me..... or is it I got it?
  245. Newly Diagnosed
  246. wegeners and your diet
  247. Finally decided to reach out...
  248. hello all
  249. a weggies poem
  250. janene