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@beanie300

@johnbishop thank you for these resources. It is an option but my insurance will only cover it if my doctor sends me there. He was actually going to send me to the MN clinic for my POTS testing but they couldn’t see me for 6 months so my doctor sent me elsewhere instead.

I am on medications. I am currently on Bupropion for anxiety, Fluoxetine for depression, (been on both of those since about 16 so I am fairly certain they aren’t the cause of fatigue), Ranitidine and Cetirizine (antihistamines to help counteract the dermatographia and hives), and Hydroxyzine as needed to help supliment the other antihistamines. I only take that one like once or twice a month though when I am breaking out really bad.

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Replies to "@johnbishop thank you for these resources. It is an option but my insurance will only cover..."

Hi @beanie300, there is another active discussion that may be helpful for you to read through and meet others who may have some of the same symptoms.

Groups > Just Want to Talk > Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) treatments
-- https://connect.mayoclinic.org/discussion/myalgic-encephalomyelitis-chronic-fatigue-syndrome-me-cfs-treatments/

John