Monday, June 16, 2008

Michigan Shmichigan

I’ve been doing some research lately, and have discovered that there are no support groups in Michigan and no clinical trials. I find this hard to believe, as I can’t be the only one in the State of Michigan who has Lupus. This just doesn’t make sense.

Anyone know why this is?

Has anyone started their own support groups or anything like that in their respective states? If I wanted to, how would I go about doing this?

No comments:

Post a Comment