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Macbeth

Updated 4mo ago

Seeking Diagnosis for POTS and EDS - Any Tips?

Hi POTS peoples! How many of you also have been diagnosed with EDS? And if you were, how did you get that diagnosed? I’m currently seeking a diagnosis, and I’ve found it’s very common to have both

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AI-generated answer based on the text from previous posts and comments

Some individuals have shared their experiences of being diagnosed with both POTS and EDS. One person was unofficially diagnosed by a physical therapist many years ago but wasn't able to get officially...See More

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_opaline_

4mo

Hi, I have both as well as MCAS, it’s very common to have all three together as well as some of the other comorbidities like migraines, GI issues, and interestingly enough even mental health issues and neurodivergence
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Macbeth

4mo

that is interesting, my sister has mcas and pots as well, and we think Eds. I also have a ton of GI issues and just had an endoscopy and everything
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Watermelon2003

4mo

I have EDS and POTS lovely. I was diagnosed by rheumatology and gene testing. Big hugs and hope you get sorted soon sweetheart x

The content in this post is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition.

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