I just joined the new discussion board forums over at the Lupus Foundation of America, which looks like it’s going to be a great resource for folks with lupus.
I posted in the introduction thread, but I really hesitated before doing it. I looked around and all the posts are by people diagnosed with lupus. There is no forum for spouses or friends and family. There is a forum for men, but it’s for men who have lupus.
Am I spinning my wheels here? Or is it just too early to judge?
There is a new category in the LFA message boards.
It’s called “Caregivers of People Living with Lupus.”
We hope you find this helpful.
http://www.lupus.org/messageboards
Jeff,
I read your posts over at the LFA website as well as your blogs here. I have lupus and have been married 8 years, so your posts really hit home with me. My husband also joined the forum at LFA. Hopefully we can all get to know each other…nice to “meet” you.
~Lynn
Wick: You are fabulous! The messageboards are looking great.
THanks for the complement. Much appreciated. Now if I can figure out how to add things like blog log and blog catolaog to it will be a miracle
Chronic Chick: You’ll get it. It just takes a little time, and a good book on CSS. Your site looks great!