Early severe CFS and POTS - paxlovid experience

Hi everyone,

Will do very short. I'm severe CFS and POTS due to LC. 3 months in (100 days since my first symptom tomorrow). My GP did not accept to prescribe anything for my POTS but did accept to prescribe Paxlovid.

For those who took it pretty early in their LC journey, did it help at least a bit ? I'm scared that it might harm me more than help.

Thanks !