# MRKH: The Rare Condition That No One Talks About, with Natalia Shvarts

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Text version: https://stenobird.com/podcast/womenkind-collective-3653569/mrkh-the-rare-condition-that-no-one-talks-about-with-natalia-shvarts.md
Podcast: [WomenKind Collective](https://stenobird.com/podcast/womenkind-collective-3653569)
Published: 2026-07-04T21:00:00+00:00
Episode link: https://shows.acast.com/womenkind-collective/episodes/mrkh-with-natalia-svarts
Audio file: https://sphinx.acast.com/p/open/s/660030ee8d6ad80016ba0381/e/6a429a0fc2fe1c7f49be1906/media.mp3
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JSON: https://stenobird.com/v1/public/podcasts/womenkind-collective-3653569/episodes/mrkh-the-rare-condition-that-no-one-talks-about-with-natalia-shvarts
Duration seconds: 3933

## Resource

Link to Pre Order: Tackling Gender Bias in The Healthcare System. What Patient stories Teach Us About Implementing Systemic Change:  https://www.waterstones.com/book/tackling-gender-bias-in-the-healthcare-system/louise-hockings-thompson/jinty-sheerin/9781805018810 She was 16 years old, newly separated from her home country, when she received a diagnosis that would reshape everything she thought she knew about herself, her body, and her place in the world. Natalia Shvarts was born with Mayer-Rokitansky-Küster-Hauser Syndrome, MRKH , a rare condition affecting over 10,000 women in the UK, where the vagina and uterus are underdeveloped or absent. It would take years, and a memoir, to find her way home to herself. In this episode, we sit down with Natalia, solicitor, speaker, MRKH advocate, and author of I Don't Matter: In Search of Home , for an honest, unflinching conversation about what it means to be told, as a teenager, that your body is different, and to spend years rebuilding your identity from that moment on. We explore the diagnosis itself, what Natalia was told at sixteen and how she made sense of it; what MRKH actually is and why it remains so widely undiagnosed; the profound question she found herself asking in those early years: "If real women bleed, what even was I?" ; navigating vaginal dilation as a teenager, largely alone and without adequate support; where gender bias shows up in MRKH care and how the medical system fails women with the condition; the loneliness, secrecy and shame that surrounded her diagnosis and her family's reaction to it; entering the UK's first womb transplant trial and the moment she made the decision to withdraw; the link between her diagnosis, people pleasing, and finding herself in a relationship involving coercive control;…

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## Transcript

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