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Hi all, I’m not looking for a specific question to be answered. I’m looking for connection with others who have experienced POTS. Living with POTS has a big effect on my life & what I’m able to do and it’s hard for others to understand. I am hoping to help others and be helped by others through compassion & empathy.
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Postural Orthostatic Tachycardia Syndrome (POTS)
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I don't know what area you live in but if you look up dysautonomia International and look up where you live you will be able to find groups on Facebook that could possibly help you out!
☝ This content is generated by our users and it is not a substitute for professional medical advice. Please consult with your physician before making any medical decision
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