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Does anyone I know here have MS? My recently diagnosed mom is suffering with frequent, severely painful MS “hugs,” and we’re looking for some home treatments. Any advice is deeply appreciated.
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Sorry, pal, that sucks. More like spasms or continuous pressure? I get a tight belt like thing around my diaphragm (not MS but neuro issue) it helps if I get all clothes or blankets away from my torso and is better lying down than upright, probably things you already tried but sending non MS hugs.
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Spasms ramping up to continuous pressure and breathlessness. I’ll ask her if it’s better lying down! <3
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Sounds different than my weird thing, hope she gets some relief!!
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I follow a Warhammer channel called MS Paints. He has a very cool community on Discord. He’s very open about it in his videos.
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Wait he paints and has ms?
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Yup. He talks about how much he can or can’t do and issues that come from having MS.
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