Hey all, thank you so much for all the info, will definitely make use of your suggestions. It means so much to be in contact with fellow spondys, we live in Namibia, Africa, so there's not a lot of info, doctors or support, in fact there's no support groups or Rheumys in Namibia. This site is a life-safer and gives us hope, makes one feel 'n little less alone. Thank you so much once again.


Janine

Wife of AS sufferer & Lupus (in remission)