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Hi there, I'd be interested in hearing people's experiences with Florinef for POTS. I have read the other threads as well, just trying to gain as much knowledge as I can before I decode whether to take it or not. Thanks!
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Created in 2008, Phoenix Rising is the largest and oldest forum dedicated to furthering the understanding of, and finding treatments for, complex chronic illnesses such as chronic fatigue syndrome (ME/CFS), fibromyalgia, long COVID, postural orthostatic tachycardia syndrome (POTS), mast cell activation syndrome (MCAS), and allied diseases.
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