Here I am on Inspire!

I live in a spectacular place in the Pacific Northwest albeit a bit far from the expert medical I have needed for my fibromuscular dysplasia. I am isolated here and although I have many loving friends, I have a rare disease and sometimes don't know if I have done anything about FMD except to put out the fire--when I had my renal artery by-pass surgery. Should I have more than a nephrologist and vascular surgeon following me? They aren't looking for FMD anywhere else but in my carotids, because I complain about my right ear making those post-surgical booming noises. Enough complaining--I guess I can complain to you guys because you KNOW. I love it that you're there. Thank you!

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