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Anybody belong to any of the Parkinson's friends/familiy support groups? Any recommendations?
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My husband's father was diagnosed and my husband recently found out that - after seeming to plateau - it's gotten very, very bad.
We're planning on looking into support groups online, and I've already seen a few resources, but I was wondering if anybody had been to any of the support groups or recommended any in particular. It looks like a number of groups haven't been meeting since Covid, so I'm trying to cover all our bases in asking around.
Thanks muchly for any advice!
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