After finally getting diagnosed with PCOS, I’m still overthinking the body hair part
At first, the thing I noticed most was how chaotic my hair growth became...crazy body hair but thinning scalp...Then my periods became irregular, often lasting more than two weeks with very heavy bleeding and painful cramps. Eventually I decided to get checked.
My doctor was actually very professional. They asked about my menstrual cycle, symptoms, weight changes, and body hair growth, then did bloodwork and an ultrasound. The results showed elevated testosterone levels and cysts on my ovaries, and that’s how I was diagnosed.
I’m also currently taking medications prescribed by my doctor, mainly Metformin and Spironolactone. I also read a journal article saying that spearmint might help with ovulation and reducing hirsutism. Besides using my sister’s ulike ipl, I’ve also started eating spearmint leaves every day, usually two leaves daily.
I’m honestly scared that people will realize I have PCOS, and I still haven’t told my family. (My sister doesn't live with us.)
For those of you who also struggle with PCOS-related body hair, how have you dealt with it?