Guest guest Posted August 27, 2001 Report Share Posted August 27, 2001 Hi all - I am very happy to have found this site and to slowly start connecting with people with more experience in the day to day living with MSA. My father is in the process of being diagnosed, but his doctors are leaning more and more towards MSA. I suppose what I initially need to know is what can I do to help him?? Does anybody have experiences with altenative therapy, counselling or excercise that they found to be usefull and supportive? In adwance thank you. Cathrine Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 31, 2005 Report Share Posted May 31, 2005 --- Kurt wrote: > Hello all, I am new to this group. My sister in law > was just diagnosed > with Neurosarcoidosis, and I would like to know what > we can do for > her. Apparently it is progressing quite quickly and > I would like to > know what we can expect and what to do. > Im now researching this (how I came about you all). > Is there a support group here in South Carolina > (Myrtle Beach area)? > Thank you and God Bless. > > Kurt > Kurt- Sorry to here about your sister in law. One place you may want her to call is National Jewish hospital in Denver, Colo ().ask for there lung line. They do a lot of research on Sarcoids, and will tell u all u ever needed to know about it.. Also the Univ Of North Carolina at Chapel Hill hospital is doing a study on Sarcaids and they were looking for volunteers, so she may want to look into that. > Hope this info helps- ( A former Carolinian myself) > > > __________________________________ Discover Yahoo! Stay in touch with email, IM, photo sharing and more. Check it out! http://discover.yahoo.com/stayintouch.html Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.