Several neurologist never did a small fiber neuropathy skin test so I will request this and see IF BCBS will approve to have this done.

Thank you for the additional info and links!! I will review them tomorrow and get back with you on those links.

I just can not understand why so many doctors in the U.S have no idea what is going on regarding so many people with these symptoms. It seems to me so many doctors do not want to be bothered with difficult cases.

I feel so let down, betrayed, ignored and pushed to the side by so many doctors.

I wish Mayo would accept more patients who have many ANS symptoms in order to help us get the correct diagnosis and help us with some sort of remedy or action plan to live with these horrible debilitating symptoms.

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