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DiscussionSmall Fiber Neuropathy biopsy test results
Neuropathy | Last Active: Feb 15 2:46pm | Replies (36)Comment receiving replies
Replies to "Hi Robyn, I appreciate your sharing very much. I know for sure I don't have POTS...."
@rnlorena I had a lot of those cardiac tests you mention also. It was the tilt table/autonomics testing my neurologist did that diagnosed the POTS. All the cardiac testing just concluded “tachycardia”, basically. I hear from so many people that it’s extremely difficult for them to get into Mayo. It was very simple for me. I wonder if it has to do with insurance. I just called, shared with them that I was looking for a second opinion and requested a specific doctor (based on my online research of the providers at Mayo). One thing worth mentioning is that my insurance does not require a referral. I can choose my specialists, as long as they are in network, without a referral. Maybe insurance is the difference? Which Mayo would you look to get into? I live in Phoenix and am very lucky that they’re practically in my backyard.