If you have Ehlers-Danlos Syndrome you may also have POTS or another form of Dysautonomia. But what does this mean? Here I discuss in very basics what POTS is like, how to get diagnosed and as always - from the perspective of living in Ireland. Find the support group I mention here: IrishDysautonomiaAwareness (it's linked on their public page).
[Disclaimer: As always -I am not a medical professional and speak only from a patient perspective. As I note in all of my videos, only a trained rheumatologist can diagnose EDS and HSD, and give you advice on what tests and treatments are best suited to your unique case. My advice is simply on what treatments exist out there, and where to access care and support. For further information see www.eds4ire.ie]
13 сен 2024
