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Post-COVID Neuropathy/Yale paper

Posted by jeindc @jeindc, Oct 1 11:12am

I'm cross-posting this to the post/long COVID group since others there have posted post-COVID neuropathy. One day those of us w/ post-COVID will be understood and they'll find prevention or help. https://www.yalemedicine.org/news/when-nerve-pain-and-numbness-are-linked-to-long-covid

Interested in more discussions like this? Go to the Post-COVID Recovery & COVID-19 Support Group.

kellysmail2016 | @kellysmail2016 | Oct 11 8:26pm
In reply to @mlee5309 "Suicide pods are absolutely real and I only know this because I’ve had mental illness way..." + (show)
@mlee5309

Suicide pods are absolutely real and I only know this because I’ve had mental illness way longer than physical. First person ever to use one was last week. Worked perfectly according to the witness. But then they arrested the creator. Can’t be cutting into Pfizer’s business I guess. I’m almost 52 going on 300 which was another thing you said that I say all the time when I look in the mirror. I’ve also said I can’t believe a condition like this could exist with so much pain and have no remedy yet not label me terminal. I could eat Tide Pods I suppose but I think Gain Flings would provide the coroner with a much needed fragrance boost

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Ahhhh.. so damn funny. I use Gain Original. Best smell ever!!! Damn Pfizer. Aren’t they rich enough! I know my “Drug Stand”
As I call my night stand now, is paying a few salaries out there. Hell my one inhaler (and there are 18 other meds sitting here) is $500 without insurance. Symbacort. I haven’t looked up the others yet. When I first starting getting really sick, I looked up my symptoms to see what popped up. Always knew LC was there but thought other shit as well. PH popped up. Pulmonary Hypertension. My ECHO showed my pulmonary arterial systolic pressure is 31 mmHg. That says when you read actual medical literature that is from accredited hospitals that is the low end of PH. So I joined the MyPH CHAT and really loved some of the people on there. My Cardiologist said he doesn’t think so. Neither does my pulmonologist. So I , embarrassingly let everyone know I wasn’t in their club anymore. lol. They let me stay since I was still sick and half of them think Covid did it to them. Imagine that. So now I have two clubs I can rant to. Hunh! 😬

REPLY
1 reply
mlee5309 | @mlee5309 | Oct 11 8:35pm
In reply to @kellysmail2016 "Ahhhh.. so damn funny. I use Gain Original. Best smell ever!!! Damn Pfizer. Aren’t they rich..." + (show)
@kellysmail2016

Ahhhh.. so damn funny. I use Gain Original. Best smell ever!!! Damn Pfizer. Aren’t they rich enough! I know my “Drug Stand”
As I call my night stand now, is paying a few salaries out there. Hell my one inhaler (and there are 18 other meds sitting here) is $500 without insurance. Symbacort. I haven’t looked up the others yet. When I first starting getting really sick, I looked up my symptoms to see what popped up. Always knew LC was there but thought other shit as well. PH popped up. Pulmonary Hypertension. My ECHO showed my pulmonary arterial systolic pressure is 31 mmHg. That says when you read actual medical literature that is from accredited hospitals that is the low end of PH. So I joined the MyPH CHAT and really loved some of the people on there. My Cardiologist said he doesn’t think so. Neither does my pulmonologist. So I , embarrassingly let everyone know I wasn’t in their club anymore. lol. They let me stay since I was still sick and half of them think Covid did it to them. Imagine that. So now I have two clubs I can rant to. Hunh! 😬

Jump to this post

Covid ailments, symptoms, medications, side effects et al probably will allow us onto nearly every group on here. Although I still haven’t found a group of hyper salivaters. Far from my most painful symptom but definitely one of the most annoying. This typed discussion would have taken me 14 years to articulate factoring in spit takes

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1 reply
kellysmail2016 | @kellysmail2016 | Oct 11 8:44pm
In reply to @mlee5309 "Covid ailments, symptoms, medications, side effects et al probably will allow us onto nearly every group..." + (show)
@mlee5309

Covid ailments, symptoms, medications, side effects et al probably will allow us onto nearly every group on here. Although I still haven’t found a group of hyper salivaters. Far from my most painful symptom but definitely one of the most annoying. This typed discussion would have taken me 14 years to articulate factoring in spit takes

Jump to this post

Omg. I’m lovin’ it. I didn’t even have to pay an admission fee. Hell, if you can’t work, you can charge a fee to all of us for a comedy show. And for that spit running down your face, I feel for you. My mouth gets so dry that I think my lungs start to even dry out. Seriously. Funny thing is I have swollen Saliva Glands. Size of golf balls. I guess they are hoarding all my spit!!

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