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I am considering going to the Mayo Clinic here in Minnesota to finish my testing for Mitochondrial Disease. Has anyone else been to Mayo in Rochester for mito? What was your experience like? Would you recommend Mayo for adult mito testing? I would greatly appreciate stories of both good and bad experiences. If you had a bad experience that you are comfortable sharing, please send me a PM. I'm weighing the pros and cons of doing testing at a hospital nearby vs. travelling to a place like the Cleveland Clinic. Thanks so much! Rachel