Great to be back virtually @uiccom for another successful #MRKH syndrome patient panel! Pairing didactic education about #MRKH with patient lived experience is the best. Panelists & I loved sharing our experiences with students today. Ty @Sneheyicantweet for co-hosting! @BYMRKH
In 2020 I felt so low that I couldn’t see how I’d ever be able to live a successful life with MRKH in tow…
2 years later I’m at uni, working 2 jobs, and I’m a global advocate with my own charity for the condition that once made me feel so broken. There is always hope⭐️
#mystory
@kateonthinice Hi are you still looking for stories around this topic? I would be happy to have a chat to you as someone who was diagnosed with a rare infertility condition but turned my life around and now globally advocate for the condition
We are super proud to have been able to support this article written by the lovely Priya @stylistmagazine about @vicslanexo story! Our stories help us shine a light on how MRKH can impact us and importantly the value of support in our journey. https://t.co/tzJUtXhh5l
Today is International MRKH Awareness Day… I am a part of the 1 in 5000 women born with MRKH Syndrome, a rare infertility diagnosis affecting the reproductive organs. Head to https://t.co/SP4NeZFaMn to read my story 💕 #mrkh#infertility#women#story