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Group meeting once a month or more, and got some responses back about making it a zoom. That's perfectly fine with me please let me know if you're interested.
For the people in my area if you still want to meet up, I would love that as well. Because since I was diagnosed with Lupus and 53 other diagnosis all my family & friends abandoned me.
TYIA
I'll join, too, Lastreet, if at all possible.😘
I'll join the Zoom. I'm in Maryland so meeting up would be hard to do at the moment.
Hey 👋 thats tough !
Unfortunately I believe its because Family and Friends truly do not understand about the Diseases we have ? They want to and try to support us but I know even with myself they just don’t get it because they can’t see it, its not like a cast on a broken arm. If I don’t want to go anywhere or say I’m not feeling well, they still ask me “ well whats wrong “ Hello, right Lol !
If I get my computer up and running I can Zoom ?
I don’t know your name or where your at but I understand
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