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Does anyone know how much is spent globally on male pattern baldness every year? Oh I do, it’s $52 Billion. What about Erectile Disfunction research? $2 Billion. What about Endometriosis/Adenomyosis research every year? Oh I know that too. It’s $27 million. Who has had enough besides me?
Endometriosis and Adenomyosis aren’t treated like real diseases and never have been. You shouldn’t have to have cancer, ALS or broken bones to matter. Many people say the pain of Endometriosis and Adenomyosis is on par with being shot. Not to mention, I, like so many others will never have kids because of it. 5 miscarriages, 2 failed IVF rounds and the only thing that continues is the suffering. I have had 2 surgeries and the pain continues. I’ve had enough. Who is up for a rally March 1st, 2026 for more Endometriosis/Adenomyosis research? If you or any woman in your life has been affected by this invisible disease, please try to be there. Let’s fucking do this.
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Telfair Square, 118 Barnard St,Savannah, Georgia, United States
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Concerts, fests, parties, meetups - all the happenings, one place.
