Guest guest Posted October 15, 2005 Report Share Posted October 15, 2005 Hi everybody, I'm a French woman of 53. I have been diagnosed with pemphigoid in 1996 and since then I am trying to find the right medecine to help me.I tried all the immunossuppressants available in France but no one worked. The only thing that works is prednisone but, because of the side effects, I try not to take it except when I can't stand the pain anylonger. I have just joined the group and would like to get in touch with persons with pemphigoid or other autoimmune disease who takes LDN. Any information would be welcome. Thank you! Josy Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 16, 2005 Report Share Posted October 16, 2005 --- In low dose naltrexone , " painterjosy " <painterjosy@y...> wrote: > > Hi everybody, > I'm a French woman of 53. I have been diagnosed with pemphigoid in > 1996 and since then I am trying to find the right medecine to help > me.I tried all the immunossuppressants available in France but no one > worked. The only thing that works is prednisone but, because of the > side effects, I try not to take it except when I can't stand the pain > anylonger. > I have just joined the group and would like to get in touch with > persons with pemphigoid or other autoimmune disease who takes LDN. > Any information would be welcome. > Thank you! > Josy > ========= You may be the first person on the board with Pemphigoid. There may be someone here with it and I just missed them some how. I was chronic progressive MS for 14 years and 4.5mg LDN halted my MS and has kept the disease progresson halted for a little over 2 years now. I learned alot just by going back to the very beginning posts of this board. I took my time and read through about the first year of posts. Try to get LDN, I think you'll be glad you tried it. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 17, 2005 Report Share Posted October 17, 2005 -Thank you for your reply § If you remember who has pemphigoid on this board I'd be thankful to get his/her name. I'm going to ask my derm When I see him on the 19th of nov. God bless you. Josy -- In low dose naltrexone , " Bren " <TwisterAlley2@w...> wrote: > > > > > > > Hi everybody, > > I'm a French woman of 53. I have been diagnosed with pemphigoid in > > 1996 and since then I am trying to find the right medecine to help > > me.I tried all the immunossuppressants available in France but no one > > worked. The only thing that works is prednisone but, because of the > > side effects, I try not to take it except when I can't stand the pain > > anylonger. > > I have just joined the group and would like to get in touch with > > persons with pemphigoid or other autoimmune disease who takes LDN. > > Any information would be welcome. > > Thank you! > > Josy > > > ========= > > You may be the first person on the board with Pemphigoid. There may be someone here with it and I just missed them some how. I was chronic progressive MS for 14 years and 4.5mg LDN halted my MS and has kept the disease progresson halted for a little over 2 years now. I learned alot just by going back to the very beginning posts of this board. I took my time and read through about the first year of posts. Try to get LDN, I think you'll be glad you tried it. > > > Quote Link to comment Share on other sites More sharing options...
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