POTS or Addison's Disease?
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Hello,
I am concerned that I have POTS syndrome. I was diagnosed with Addison's Disease and put on Florinef. I began to get much better, but never fully well, and about a month ago I began to regress and experience both new and old symptoms. My GP told me that she thinks I have POTS syndrome and referred me to a neurologist, who I will see in December. My GP put me on propranolol for now, which I began today. I am a 19 year old female and I am wondering what anyone with POTS thinks of this. These are my most concerning symptoms: low blood pressure, nearly fainting while standing, tunnel vision upon standing, extreme fatigue (bsolutely zero energy), headache, dizziness, purplish feet, always cold, dull lower back ache, occasional tingling sensation in fingers & scalp, occasional numbness in leg and feet while using restroom.
I would greatly appreaciate any advice or feedback.
Thanks,
Bre
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