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Comment on Physics Girl Long Covid and ME/CFS Livestream [Fundraiser + Interviews]

ME/CFS has a 5% recovery rate. I am as severe as Diana for a decade for example.

Please don’t say things like that. It insinuates that our lives are not worth living, when that choice is very personal, and having someone else say that can be very heartbreaking when you’re just living the best you can.

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Ghostalmedia@lemmy.world ⁨2⁩ ⁨months⁩ ago
Apologies for the jerks in this thread. I’m yanking those comments now since that behavior is against community rules.

As the downvotes indicate, these people are not a representation of the rest of this community’s views.

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- mecfs@lemmy.world ⁨2⁩ ⁨months⁩ ago
  thanks. appreciate it ❤️
  
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kemsat@lemmy.world ⁨2⁩ ⁨months⁩ ago
[deleted]
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- mecfs@lemmy.world ⁨2⁩ ⁨months⁩ ago
  You won’t really know until you reach those circumstances. If you had told me before I was disabled that I would be in severe pain bedridden, unable to speak and tubefed, I would have said I’d prefer to die (but part of that is thinking this would never happen to me). Now I prefer to live my limited life, and I would never give it away.
  
  I’m not denying some people would, I’m just saying its not something you should tell people with the illness.
  
  and killing yourself is a lot harder than it seems when you’re disabled, unless you have a firearm
  
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