I ended up on prednisone for my RA flare and am still on it, going down from 15 mg. to 14, this week, then 13 etc. I don't like to be in pain or take prednisone (is an occasional glass of wine okay?) but thank all of you for sharing your stories and realizing I and you are not alone.
Let us get well and share the love,
Originally Posted by Aletha
My name is Aletha and I joined the group for my husbands MS, and my mothers Parkinson's. I have read a lot of responses to people with RA on the LDN chat site regarding help with people that have RA. I saved a few of the stories from individuals regarding this treatment. Please let me know if you would like me to forward them.
My husband has had miraculous results for his MS with LDN. He has been on it for over 2 years and he is doing 2 sports a day. My mom has only been on LDN for about 2 months, but she says she feels better and has more energy. It might be worth looking into for RA. I don't know what kind of effect it may have on Bi-Polar, or on meds one would take for Bi-polar. But I could inquire on the LDN chat site for anyone with questions. Kindest of regards, Aletha