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I am a 22 year old female who has recently been diagnosed with POTS. Unfortunately this has hit me like a train with all my symptoms appearing quickly within 3months. I use a walker and wheelchair to prevent me from getting hurt. I'm allergic to the midodrine so I'm currently unable to take my beta blockers. Working on a FND diagnoses
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Ehlers-Danlos Syndrome (EDS)
Disorders of The Nervous System
Midodrine
Postural Orthostatic Tachycardia Syndrome (POTS)
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☝ 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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