Welcome to the MRKH Podcast, Mind Over MRKH. MRKH affects 1 in 5000 female births, listen in to learn, connect, and be comforted by the MRKH warriors and community supporters we'll be joined by. We are a creative, resourceful, story telling and self explorative hub for all things Mayer Rokitansky Küster Hauser Syndrome.  Those with this condition have varying underdevelopment of the reproductive system. So born without or with an underdeveloped womb, cervix and vagina, usually ovaries are present and female chromosomes. (But doesn't mean to say everyone with MRKH identifies as a woman)

I'm Ellamae, I'm 29 and I was diagnosed with MRKH at 16. I am the founder and director of Va Va Womb (even though I was born without a womb) and Mind Over MRKH, I am your Podcast Host and producer - joined by MRKH warriors, friends and experts globally- to tell their stories, have their voice heard and ensure the next person diagnosed with MRKH feels less alone in their experiences. We'll be talking all things MRKH from mental health, to dealing with this new diagnosis, sex, relationships,  fertility, living child free or child less, pleasure, self acceptance, vaginal dilating and more. Find out ways you can support the work we do over on mindovermrkh.org including our future magazine, creative events, gift boxes for MRKHers that we aim to package for the next person being diagnosed  and check out our online shop too!

This Podcast is receiving regular sponsorship to keep us going strong  from our wonderful friends and U.K. Charity MRKH Connect, MRKH Connect is a UK charity designed to connect those with MRKH and provide support them and their families through events, resources and public outreach to raise awareness.  Their private Members area provides a safe space for those with MRKH from all over the world to connect and share together in a safe environment and find comfort talking with those who truly understand what having MRKH is like.

We hope as one  big MRKH Family to continue to raise funds collectively to support those diagnosed with this life changing condition that can bring so much pain and so much grief, - we just want you to know that it will also come with a fiercely magical, loyal and loving community of people just like you - you are not alone. We hope this podcast keeps you company. and if you'd like to get involved do get in touch because your story matters.