Postural Orthostatic Tachycardia Syndrome (POTS)
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Has anyone heard of POTS? After a lil over 2 years and 3 Ablations and many trips to the Emergency Room I was diagnosed with POTS. My cardiologist said there is no cure. He put me on new medication to take with other cardiac medication called Digoxin. I have only had 1 does of it so far but I can already say this is gonna be a very long road getting used to this new medication. The nausea is unreal, dizziness, sleeplessness but even with all these symptoms I can say my heart hasn’t been over 120 so Digoxin is doing what it’s supposed to do. I just have to get used to the side effects of a new medication.
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peter01729 Elefantaflaca44
Posted
My Autonomic Nervous System was permanently damaged by the beta blocker Bisoprolol, so I a under the care of an Autonomic Neurologist now.
Whilst I dont qualify for the POTS symptom, I do for its close relative Orthostatic Hypotension. I feel so desperately ill now only OK if I stay in bed and dont eat anything.
A good forum for POTS is DINET Dysautonomia Information Network,
Elefantaflaca44 peter01729
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