See Alike in...

Alike App

Browser

swaghetti.girl

596d

I've been diagnosed with LS since I was 3 years old. I was prescribed the classic creams, my symptoms lessened, and I stopped. Then, when I was 18 and became sexually active, I realized that I had had a flare up worsening for years. As a child I never fully understood what a flare up meant; I always thought certain symptoms were just a part of life. I believe that my lack of treating my flare up interruption in my vaginal development as a whole, with clitoral and labial fusing. Basically, I don't have a clitoral hood or a labia minora. My clitorus is underneath my fused hood and can never come out, so I can't feel anything there. I never knew any of this was abnormal until i became sexually active, and now it is most likely irreversible. Has anyone else experienced clitoral fusion? Have you been able to manage your symptoms and how? I have been looking into surgery but it seems very risky.

☝ 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

Thank you! Your submission has been received!
Oops! Something went wrong while submitting the form.

Want to chat or share? Download the Alike app now and get complete access to Alike.health's unique features.

Find people who are
experiencing a similar
medical reality

100% Free
100%
Free

Download Alike for the full experience

JOIN

View All

Bupropion

night sweats

paranoid

Valium

sertraline

palpitations

Anxiety (Including GAD)

Depression

palpitations

Depression

Valium

Bupropion