Living with MRKH …

is not easy and so many of us wish there was more awareness of conditions like ours both publicly and more importantly, in the medical community.

Having to describe your own diagnosis to a doctor who has never heard of it can be triggering and difficult and it can be hard to express what MRKH means.

It’s complex and complicated and also, individual.

This is why articles like this are so important.

Articles that shine a light and draw attention to it by drawing on information from the community through the work of @mollymarymcglynn and her 2023 film Fitting In, a must see in our eyes as the only MRKH film and one based on Molly’s own experience, to the work of advocates like the lovely @ally__hensley peer organisations of which we are delighted to be featured along with our community peers @beautifulyoumrkh, @sumaavicoaching and @mrkhstars who are just some of the amazing peer support networks available.

Thank you Catherine Gianaro @catherine.gianaro for your thoughtful article 💜

Read the article in full here – https://chicagohealthonline.com/living-with-mrkh/