Aa
New Group for Sarcoidosis
Hello everyone. I was diagnosed with sarcoidosis this year and find it hard to believe the lack of information on the subject. I plan on doing as much research as possible on this disease, as I'm finding that even my doctors need prompting sometimes and I wanted to start a support group for those suffering from sarcoidosis. Please check out my sarcoidosis support group under user groups and join me in the fight to educate others about this little known, though sometimes tragic disease.
Best Answer
Thank you very much for your reply. Do you have sarcoidosis or do you just know about it through your research on autoimmune diseases?
Misty
Misty
Hi.
I would just like to say, goodluck in your new forum.
Hopefully you can promote, and help people, with sarcoidosis.
I wish you well, and am pleased that more awareness, is being raised about this disease.
Good Luck
Nicola
I would just like to say, goodluck in your new forum.
Hopefully you can promote, and help people, with sarcoidosis.
I wish you well, and am pleased that more awareness, is being raised about this disease.
Good Luck
Nicola
Have an Answer?
You are reading content posted in the Autoimmune Disorders Community
A list of national and international resources and hotlines to help connect you to needed health and medical services.
Herpes sores blister, then burst, scab and heal.
Herpes spreads by oral, vaginal and anal sex.
STIs are the most common cause of genital sores.
Condoms are the most effective way to prevent HIV and STDs.
PrEP is used by people with high risk to prevent HIV infection.
I dont have sarcoidosis, but i have a very close friend who has this condition.
But the hospital which deals with this for him, doesnt know much about,it and are very backward on information.
I am very interested, in information, and treatment into this condition.
Any help i would appreciate .
Good Luck. and Welldone in your new forum.
Nicola