3 thoughts on “#StopPOTS & Feel Free To Share

  1. It’s interesting that you found out that POTs isn’t rare. I have EDS (and probably POTs). I asked my doctor about it, and he said “What’s that?” Ugh. I wish if it wasn’t rare, that doctors would be trained to recognize it.


    • Ya POTS isn’t rare at all. POTS is also not new, but newly identified. Because POTS was just named and identified in the late 20th century knowledge and understanding has been slowly gaining in the medical professions.


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