Long COVID

This video shares a basic overview of long COVID and helpful resources for those dealing with the condition or post COVID POTS.
To learn more about long COVID and find clinics, visit the link below!
longcovidalliance.org/what-is...

[@karendale9926]

So grateful for your channel. ❤

[@DysautonomiaInformationNetwork]

Thank you so much. We are glad to hear you are finding the videos helpful. All the best.

[@elyserose8210]

its how i got dysautonomia. i had an ICPET and was started on pyridostigmine to try and help. the ICPET sucked but gave a lot of insight to my hemodynamic status while exercising, arterial and venous blood gasses, and pulmonary function

[@davidrogers3920]

The CFS Recovery group on TH-cam and Facebook have also seen there can be a common cause and cure in CFS, POTS, ME, MCAS, Dysautonomia and Long Covid. But as Lauren said, you should go to your doctor first and get tests done. If the test results are all "normal", then the CFS Recovery group's approach may help you.

[@DysautonomiaInformationNetwork]

Yes, getting tested and seen by a doctor is the first step. What will help greatly depends on the symptoms the person is dealing with. As the video on our channel about POTS by Dr. Raj details, treating the specific symptom is sometimes just as important as the overall diagnosis. That's an important point especially when it comes to Long-COVID because so many symptoms cross diagnosis of different disorders.

[@anjolotito385]

My case, I have dysautonomia post covid 🥲🥲🥲 …