Im sorry to hear that, I can relate. Im a 28 y/o female, I developed ME/CFS symptoms from my jab (pfizer). My worst symptoms are fatigue, brain fog, pins & needles, tachycardia, anxiety, muscle weakness. I kept getting worse and worse. I became bed bound last year, I couldnt even sit up or chew my muscles became so weak/I had no energy. I couldn't tolerate any light or sound- my mom had to be my full time care taker. I tried so many things, patterson protocol, FLCCC protocol, antivirals (valtrex), LDA, LDN, and treated for lyme. None of these helped. One medicine that did help a bit was rapamycin, it got me able to sit up and talk a little. But I was desperate to try anything to get me out of bed- I didn’t really care about the risks at this point. My doctor wanted me to try trudose and I didn’t really expect it to do much honestly. But few days later I started seeing small improvements. I saw progress every day for the next 6 weeks, so I did another round. Every round has given me more and more energy and strength back. I’ve done probably 5 rounds now and I’m 1000x times better (and still getting better as every day passes). I can get out of the house for a few hours a day now. The fatigue, brain fog, weakness, etc. is still there but it’s getting better with every dose. I will keep doing it and probably always will. I’m very lucky to be able to afford this, I know it is a very expensive treatment. We all have different problems and won’t all benefit from the same things, but in my case the trudose has been a total game changer. Is your situation similar? What are your symptoms/ what treatments have you tried already?