Anyone feel short of breath and have feet?

Yes. I have pain which is worse at night. My shortness of breath is also worse at night. I believe my condition came from Covid because I can’t understand how neuropathy would cause shortness of breath. The neuropathic pain I have is otherworldly but I have weird neurological symptoms as well such as hyper salivating which is suffocating. No idea how it all ties together but it all started after I got Covid. Doctors have ZERO answers for me after 3 years.

Hi,
My mother in law has shortness of breath which is tied up her with neuropathy. Neuropathy can affect the major nervous systems which there are two that control the body. With both I have throat constriction among other symptoms from autonomic polyneuropathy which starts affecting my lungs and heart along with peripheral neuropathy which takes care of the things like legs and arms.
Neuropathy is the interaction between nerve and muscle and brain. For me they are corrupted signals from and to the brain and muscles mostly intermittent but some have become permanent. Worst case scenario the heart can stop instantly without warning when the neuropathy decides it wants to. I have found I have no conscious control over the problem. There is no cure or treatment for my neuropathy know to date. I just have to wait it out and hope the heart is the last organ that will be affected. Touch wood the heart is still good to go, so far! I do have an enlarged heart but always new I was big hearted anyway!
To date the worst it has been for me is paralysis when walking, unable to move the feet or legs. Reminiscent of concrete boots! Stopped dead mid stride for a few minutes, left looking and willing my feet and legs to oblige me with moving, felt like a lifetime, but just minutes. No such luck, scariest feeling so far not knowing if I'm ever going to continue moving or was that it for life. Often my left legs fails to step when commanded and the brain knows it sent the signal so continues the momentum of the stride and over I go. Fortunately the brain still learns and it now has the ability to act quickly and catch myself before kissing the ground. I'm curious why it is alway the left leg though.
I'm constantly learning just how invasive neuropathies can be. You know what it is like when the information input into a computer does not resemble what you expected out and you are left pulling your hair out until it is resolved. Same scenario, mayhem and confusion.
Cheers

Hi,
My mother in law has shortness of breath which is tied up her with neuropathy. Neuropathy can affect the major nervous systems which there are two that control the body. With both I have throat constriction among other symptoms from autonomic polyneuropathy which starts affecting my lungs and heart along with peripheral neuropathy which takes care of the things like legs and arms.
Neuropathy is the interaction between nerve and muscle and brain. For me they are corrupted signals from and to the brain and muscles mostly intermittent but some have become permanent. Worst case scenario the heart can stop instantly without warning when the neuropathy decides it wants to. I have found I have no conscious control over the problem. There is no cure or treatment for my neuropathy know to date. I just have to wait it out and hope the heart is the last organ that will be affected. Touch wood the heart is still good to go, so far! I do have an enlarged heart but always new I was big hearted anyway!
To date the worst it has been for me is paralysis when walking, unable to move the feet or legs. Reminiscent of concrete boots! Stopped dead mid stride for a few minutes, left looking and willing my feet and legs to oblige me with moving, felt like a lifetime, but just minutes. No such luck, scariest feeling so far not knowing if I'm ever going to continue moving or was that it for life. Often my left legs fails to step when commanded and the brain knows it sent the signal so continues the momentum of the stride and over I go. Fortunately the brain still learns and it now has the ability to act quickly and catch myself before kissing the ground. I'm curious why it is alway the left leg though.
I'm constantly learning just how invasive neuropathies can be. You know what it is like when the information input into a computer does not resemble what you expected out and you are left pulling your hair out until it is resolved. Same scenario, mayhem and confusion.
Cheers

I too have had weird things since I had COVID I too have had weird things since I had Covid. ranging from shortness of breath to heart, palpitations, tingling predominantly in my legs, feeling of heaviness and in coordination in my legs at times, intermittent exhaustion, for no reason and wobbliness intermittently. I am not angry at the doctors for not knowing definitively what this is. long Covid is a new phenomenon and most recently I went to a rheumatologist who very compassionately said “COVID does what Covid wants to do” and the best we could do would be to manage symptoms. I have no problem with that. It’s a whole new world post Covid. I can’t get a definitive diagnosis, but after about 10 specialist this behaves something like fiber myalgia, but doesn’t meet this full criteria, small fiber polyneuropathy, but my skin punch biopsy was negative, or Covid. Whatever it is, I’ll make modifications and we’ll do symptom management.

I too have had weird things since I had COVID I too have had weird things since I had Covid. ranging from shortness of breath to heart, palpitations, tingling predominantly in my legs, feeling of heaviness and in coordination in my legs at times, intermittent exhaustion, for no reason and wobbliness intermittently. I am not angry at the doctors for not knowing definitively what this is. long Covid is a new phenomenon and most recently I went to a rheumatologist who very compassionately said “COVID does what Covid wants to do” and the best we could do would be to manage symptoms. I have no problem with that. It’s a whole new world post Covid. I can’t get a definitive diagnosis, but after about 10 specialist this behaves something like fiber myalgia, but doesn’t meet this full criteria, small fiber polyneuropathy, but my skin punch biopsy was negative, or Covid. Whatever it is, I’ll make modifications and we’ll do symptom management.

Yes. I have pain which is worse at night. My shortness of breath is also worse at night. I believe my condition came from Covid because I can’t understand how neuropathy would cause shortness of breath. The neuropathic pain I have is otherworldly but I have weird neurological symptoms as well such as hyper salivating which is suffocating. No idea how it all ties together but it all started after I got Covid. Doctors have ZERO answers for me after 3 years.