dianna haze
@diannahaze
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Tweeting through the hazy brain fog of Severe Long Covid. (Chronically ill alter-ego of @thephysicsgirl)
Joined June 2023
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RT @ProperChels34: One of my closest friends in the community. If you are German, or know anything that could help regarding this post, ple…
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RT @tink_ina: Tobias has been deteriorating extremely fast and he can now barely communicate with me over text. My dad and I have the past…
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RT @LauraMiers: After Covid disabled me in early 2020, I was entirely bed-bound for approximately 2 years, believing I was terminally ill,…
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@admiral_th @modernainjury @ThePOTSPostman It’s hard enough not to push once you’ve had the disease for a while and understand it better. It’s nearly impossible when you first get it and don’t understand what’s going on with your body. 😢
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@katiamek @modernainjury @ThePOTSPostman I recently did, yes. I had a minor cold about 2 months ago. I actually got a lot less sick than normal which was very surprising.
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@modernainjury @ThePOTSPostman But it was all fast. I went from COVID to very severe in 5 months. And in between pushing too hard, I was resting really hard. I think preexisting MCAS maybe made me deteriorate quickly.
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@finnishgunners I understand it. I was there. It’s hard to be positive, or even kind when your whole life is just pain and fear.
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It’s hard enough for us to get hate from people who don’t believe long covid or MECFS is real. Criticism from others in the community is almost worse. I only have empathy and love for you all. What you’re going through is so f***ing hard. ❤️🩹❤️🩹❤️🩹
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That said, the stellate ganglion block treatment helped my recovery. I’m not a doctor though! I cannot recommend that or any other treatments to anyone because what worked for me may not work for others.
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@GoreLloyd @MissMollyAu I missed my husband too. And he missed me. Even though he was my full time caregiver 😢. I understand.
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