in 2020 I was finally diagnosed with endometriosis. It took 7 years of going to different doctors who all told me I was faking it. Now the doctor that diagnosed me isn't really doing anything to help with the pain. I went to a new doctor who also diagnosed me with Vulvodynia and she suspects I also have Lichen Sclerosus. Does anyone have any advice on how to deal with the pain? I'm currently on multiple medications to help with the pain, but I was wondering if there were any more ways to treat it?
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