If you have these symptoms would love your input.

People have different symptoms depending on which organs or tissues the virus damaged or where it is still hiding. What has helped me the most with extreme fatigue and other symptoms is antivirals. Valacyclovir, starting 0.5 g three times a day, and then, as weeks pass, increasing to 1 g three times a day. You will know if it is going to help you within 1-2 months, after you reach 3 g a day. Let me know if you want me to expand.

I have had the same success with Valacyclovir improving my symptoms significantly. For me 1 gm twice a day seems to give me symptom relief. Sooo good to be able to have some sort of normalcy again.

Yes - I have the debilitating fatigue that is one of the primary symptoms for so may of us long haulers. I can SO relate about docs knowing nothing in terms of treatment. My PCP and pulmonologist both individually diagnosed me with Long Covid but I have to constantly advocate for my own health and treatment options. I've learned a lot from listening to other long haulers and what has helped them with specific symptoms that I also have. Nothing has helped my chronic fatigue except time. For me, I think micro-clots may be one of the major contributors to my fatigue. (I have 50+ other symptoms I am battling .) I recently started taking nattokinase after hearing from some other long haulers that it helped their fatigue. It's a natural supplement which 's a blood thinner and there's also some evidence that it degrades spike protein. Fingers crossed it works for me.

Chronic fatigue, when I saw that I thought Thyroid. Have you had your Thyroid Panels run? As your doctor to test your TSH, T3-Free, T4-Free, TPO Antibodies. You could have hypothyroidism. I had similar symptoms and had my thyroid levels checked and lo and behold I have Hypothyroidism and Hashimoto’s. I was exhausted and would fall asleep right after dinner in the evening, which isn’t me at all. Once I got my diagnosis, I began taking medication, Synthroid and I started on a nighter dose of 125 mcg and took along with it another drug called Cytomel 5 mcg. Now since my levels have come down, I’m only taking 75 mcg of Cytomel. I have my blood levels checked every 3 months and if my levels are in the normal range, no need to alter medications. Look into having this done and I would bet you will need medication too. Good luck on your health journey.

Yes - I have the debilitating fatigue that is one of the primary symptoms for so may of us long haulers. I can SO relate about docs knowing nothing in terms of treatment. My PCP and pulmonologist both individually diagnosed me with Long Covid but I have to constantly advocate for my own health and treatment options. I've learned a lot from listening to other long haulers and what has helped them with specific symptoms that I also have. Nothing has helped my chronic fatigue except time. For me, I think micro-clots may be one of the major contributors to my fatigue. (I have 50+ other symptoms I am battling .) I recently started taking nattokinase after hearing from some other long haulers that it helped their fatigue. It's a natural supplement which 's a blood thinner and there's also some evidence that it degrades spike protein. Fingers crossed it works for me.

One of the many, many doctors I've visited suggested thyroid issues. He prescribed two thyroid meds which didn't improve my fatigue or other symptoms. After several months, blood tests indicated the meds had damaged my thyroid. I of coursed ceased the meds.

I'm so sorry. I don't presume to know what foods to avoid or which abs to ask for. I've had LH since 2020-- I know. A long time.
I went thru covid clinic, multiple doctors. Finally found an immunologist who helped enormously.

Do you mind sharing your Doctor's info and contact as majority of us with LC have yet to have any relief of any sort and doctors who are careless and just don't now what to do.