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← Return to CIDP diagnosis after severe GBS long ago, where do I start?
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CIDP diagnosis after severe GBS long ago, where do I start?
Neuropathy | Last Active: 5 days ago | Replies (9)Comment receiving replies
@slkanowitz ,
What an encouraging letter! Made ME feel better and I'm not even part of this thread. I agree with what you said, to my limited ability to really understand, not having had GBS, Lupus, or Covid. Have enough else, though, including CIDP, and it's true that the people on Connect are kind and helpful. The moderators are without equal ~~ really fantastic! It's a website you can trust. ~ Barb
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Hi Barb @bjk3,
Thank you for your comments, you're a sweet kid! I'm sorry to hear you have CIDP and hope the available treatments give you back some of your lost functions or at least stop/slow down the symptoms. For me it's a hopeful situation. Life is hard enough without something like this on top of aging to slow us down. Your help is much appreciated.