あなたはちょうど蕁麻疹色素症と診断された人にどのアドバイスをしますか?

蕁麻疹色素症で診断されたばかりの人々に対する蕁麻疹色素症の経験を持つ人々からのアドバイスを参照してください

元の


I don't have much advice because there isn't much to offer. When I was seeing a Dr regularly I felt like a chronically ill patient and it took a toll on my psych. I opted to skip the annual exams, the multiple tests that were required yearly, multiple medications that weren't adding value to my life. I have not seen a Dr for this in 5+yrs and I'm fine. I treat with over the counter allergy meds and I get through life just fine. I pray endlessly for this to self resolve and for Drs and researchers to discover a treatment and cure.

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