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BoneDustWoman

242d

I was seen at the nearest Long Covid clinic by a Dr who has been studying and treating long covid since 2020, and she formally diagnosed me with ME/CFS. She's connecting me with a support group and PT to treat my dysautonomia (with the explicit caution to the PT against overexertion), and she's ordering more specific blood work to check more thoroughly for vitamin deficiencies and immune-related inflammation. It's such a relief to feel like my health care is now being led by someone who understands what I'm going through and what will improve my well-being, even if she can't cure me.

☝ This content is generated by our users and it is not a substitute for professional medical advice. Please consult with your physician before making any medical decision

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