Post-COVID Syndrome is real
I had covid mid April and have had many PCS symptoms. I seem to be educating my doctors and therapists. Sometimes it feels like they think I am faking and the next time they tell me they have heard the same thing from others. I am doing everything from aqua therapy, speech therapy for the "fog" and still exhausted, headaches, fog and not sleeping well ect. I have used my short term disability at work and working thru my PTO time. I am more than frustrated. Any encouragement?
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Thank you so much for your detailed response.
I have taken glutathione and Nac orally. It doesn’t seem to help me going that route. I suspect it is because my gut is too damaged. The final stage of Covid attacked my gut. I spent twelve hours vomiting and it seems some fairly severe damage was done. I take probiotic, drink kefir etc. etc etc, to try to rebuild, but I’m still plagued with severe constipation and a locked up bowel.
I have lost about 35 lbs and I’m pretty frail now.
Now that I am FINALLY with a group that acknowledges Long Covid, I can discuss some of the things you have suggested.
Thank you.
I also have elevated alk phosphorus for over a year and just had an NP just tell me that since I have Postural orthostatic tachycardia syndrome (POTS) , I HAVE to increase my sodium intake and she thinks that will help…so I’m increasing my intake to 4 grams which is giving me a lot of icky side effects. Hopefully as my body gets used to it I will see improvement.
I meant phosphate😆