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Real members of MyEndometriosisTeam have posted questions and answers that support our community guidelines, and should not be taken as medical advice. Looking for the latest medically reviewed content by doctors and experts? Visit our resource section.

Hey Ladies,what Is Your Experience On Lupron?

A MyEndometriosisTeam Member asked a question 💭
Harare,Zimbabwe
July 14, 2024
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A MyEndometriosisTeam Member

Omg worst drug they ever put me on! Didn't help and also gave me what's called lupron brain. I couldn't think or function. It was terrible!

July 14, 2024
A MyEndometriosisTeam Member

Seriously stay away from it!! It's still causing effects on me and I haven't been on it since like 2010!

November 11, 2024
A MyEndometriosisTeam Member

STAY AWAY FROM ALL GnRH agonists!! This includes Orilissa (Lupron in pill form), Myfembree, Synarel, Dienogest!

July 14, 2024
A MyEndometriosisTeam Member

I pray you don't have lasting effects like me. My brain is still not the same. Its like I get a fog just out if the blue amd it just happens anytime!

3 days ago
A MyEndometriosisTeam Member

Hmm, after extensive surgery for bowel, pelvic and diaghramatic endo, they put me on leuprolide for 3 months. Put me in menopause- hot flashes, weak and achy bones and joints, brain fog, mood swings, tingling limbs, palpitations, dizziness. I've been off it for a month but still have the effects. Doctor said it might last for a couple more months. I'm keen to stay off meds now and try natural ways to manage the endo

4 days ago

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