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Post-COVID Neuropathy/Yale paper
Post-COVID Recovery & COVID-19 | Last Active: Oct 11 8:44pm | Replies (53)Comment receiving replies
I have that too, @mlee5309 ! Ditto about who said to see whom. It is with the inside my mouth 'rash'. Eating in particular activates even more excess saliva. I'm seeing an ENT for the tinnitus and the saliva - since one doc thought it was sinus related. (I've had "sinus issues" my whole life. THIS is entirely different.) My first question to the ENT will be what they are finding that is with post-COVID patients - and if they are reading nothing (when the appt. was made, I was not given answers) I might just spend a shorter time there.
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That’s wild. Eating does the opposite for me. It suppresses it for a few hours for me before the tidal wave begins. Problem is my IBS only allows for one meal a day around 10:30am because it takes me nearly 12 hours to digest that or at least feel like that. I’ll throw in one more discovery in this process. I’ve had constipation issues my whole life. Always told to get a colonoscopy. Nothing ever came back wrong. I started getting B12 shots at the beginning of my neuropathy symptoms and my constipation has improved significantly. I’m about 52 now and have seen docs for constipation for 30+ years. Not one ever mentioned B12 as a solution. But Linzess and all the other bullshit RXs they were all in. Hard not to be jaded