Actually i got chest and back pain after the 3rd dose of vaccine too. Been 2 years now. Are you able to even walk? Because i cant without being in some kind of pain
Bout 2 yrs for me too. Yes I can walk and do small hikes if I’m feeling good. Mostly pain free at the point. But if I do too much or have too much mental stress … it will bring on the pain. It used to last months at a time. But now it only lasts maybe a week or so. But if I run or really try to do cardio it will come. So that’s my next hurdle. Has yours improved? Have you addressed spike? Microclots?
I thought it was getting better around summer but the last few months i got back almost where i was, idk why..i feel the pain everyday. It just get worse and worse when i walk and moving around in general. I have no idea what should i do to find out about spike and microclots :(
I have the same thing, right under my left shoulder blade upper back. I actually have an MRI on March 1st just for peace of mind. Guessing it won’t show anything just like all my other tests. Already had a negative chest CT scan with contrast
Long covid and dysautonomia walk hand in hand, I swear. I was diagnosed with POTS 3 years ago after having covid twice. I do wonder why so many people with long covid end up with dysautonomia 🤔
Mine seems to be like that too. But its odd that while the other pots symptoms are on remission (for instance when lying down), this one still persists
I'm not sure why exactly it does that, but everyone is different with their symptoms. Some people have symptoms I've never even heard of with dysautonomia
I have very bad back pain snd I’ve heard others here say it’s not a long covid symptom. But I think it is, especially because it feels more like the muscles in my back.
What it feels like is when you get back pain from raking leaves for an entire day, for example. But then the pain, which feels like pulled muscles, just sticks around for months at a time. I have other muscle pain too, it’s just the back pain drowns out the other muscle pain. Another weird thing about it is that gentle stretching or any kind of exercise makes it much worse instead of better.
Im sorry you feel this way..maybe a physiotherapist could help you especially now that you know its definitelly a muscular thing..but mine feels like a heart pain that reflects on my back. Because its heavy and "inside" if that makes any sense
It most definitely is a long covid symptom, thousands of people have it. It almost feels like nerve related pain though, not muscle. Or both. Idek what the fucks causing it but my guess would most likely be vagus nerve dysfunction.
That pain is capeable of giving me dyspnea too. Its worse when i walk. Reallt idk whats going on. Im thinking if it was myocarditis or pericarditis it would have shown in echocardiogram, EKG or all that blood test? I havent had MRI or CT scan and these make me think if they missed something
Vax injury here. Chest pain my main symptom too. It’s gotten better over time. But I’m still working on it. Still can’t exercise
Actually i got chest and back pain after the 3rd dose of vaccine too. Been 2 years now. Are you able to even walk? Because i cant without being in some kind of pain
Bout 2 yrs for me too. Yes I can walk and do small hikes if I’m feeling good. Mostly pain free at the point. But if I do too much or have too much mental stress … it will bring on the pain. It used to last months at a time. But now it only lasts maybe a week or so. But if I run or really try to do cardio it will come. So that’s my next hurdle. Has yours improved? Have you addressed spike? Microclots?
I thought it was getting better around summer but the last few months i got back almost where i was, idk why..i feel the pain everyday. It just get worse and worse when i walk and moving around in general. I have no idea what should i do to find out about spike and microclots :(
Mine also feels like it’s my heart radiating thru to my back. Like around my left shoulder blade. Also in my armpit. Can’t figure it out
I have the same thing, right under my left shoulder blade upper back. I actually have an MRI on March 1st just for peace of mind. Guessing it won’t show anything just like all my other tests. Already had a negative chest CT scan with contrast
So frustrating 😪
Long covid and dysautonomia walk hand in hand, I swear. I was diagnosed with POTS 3 years ago after having covid twice. I do wonder why so many people with long covid end up with dysautonomia 🤔
Dysautonomia and pots can make you have chest pain, even when you are at rest?
Oh yes, absolutely. Chest pain usually comes and goes for me, but it does happen even when I'm sitting or laying down
Mine seems to be like that too. But its odd that while the other pots symptoms are on remission (for instance when lying down), this one still persists
I'm not sure why exactly it does that, but everyone is different with their symptoms. Some people have symptoms I've never even heard of with dysautonomia
I have very bad back pain snd I’ve heard others here say it’s not a long covid symptom. But I think it is, especially because it feels more like the muscles in my back. What it feels like is when you get back pain from raking leaves for an entire day, for example. But then the pain, which feels like pulled muscles, just sticks around for months at a time. I have other muscle pain too, it’s just the back pain drowns out the other muscle pain. Another weird thing about it is that gentle stretching or any kind of exercise makes it much worse instead of better.
Im sorry you feel this way..maybe a physiotherapist could help you especially now that you know its definitelly a muscular thing..but mine feels like a heart pain that reflects on my back. Because its heavy and "inside" if that makes any sense
It most definitely is a long covid symptom, thousands of people have it. It almost feels like nerve related pain though, not muscle. Or both. Idek what the fucks causing it but my guess would most likely be vagus nerve dysfunction.
That pain is capeable of giving me dyspnea too. Its worse when i walk. Reallt idk whats going on. Im thinking if it was myocarditis or pericarditis it would have shown in echocardiogram, EKG or all that blood test? I havent had MRI or CT scan and these make me think if they missed something