<a href="https://instagram.com/mrkh_nigeria_">Elizabeth </a>is an MRKH advocate in Nigeria, one of the first women with MRKH in Nigeria to raise awareness and form a support network. Elizabeth is 26 and was only officially diagnosed with MRKH last year.&nbsp;Read a short blog from Elizabeth she did for MRKH Connect <a href="https://mrkhconnect.co.uk/indeed-we-are-warriors/">here</a> and listen to the full episode to hear her story!
This Podcast is sponsored by our wonderful friends <a href="//mrkhconnect.com">@MRKHCONNECT </a>who are raise funds to connect, research and fund MRKH support and awareness.&nbsp;
<a href="https://open.spotify.com/episode/09vfUqPZ1lXtcjsOYysrno?si=iE8WkueVRj2mIlx6BZTg7Q">Listen to our full trailer here!&nbsp;</a>
Find out more about<a href="//mindovermrkh.org"> Mind Over MRKH</a>

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THE MRKH PODCAST

Mayer Rokitanksy Küster Hauser Syndrome

Bought to you by Ellamae, founder and director of Va Va Womb and MindOverMRKH.org for the MRKH community, by the MRKH community.

MRKH is a congenital condition that 1 in 5000 female babies are born with.

This podcast is about ALL THINGS MRKH, the people that live with it, the experts that can help us understand our bodies more. Think worldwide MRKH voices.

Expect real, honest, raw content with plenty of resources and regular unique episodes!

This is a podcast for the community, by the community. 
Sponsorship: MRKH Connect