Roadmap to Cures 2.0

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Rett Syndrome Research Trust

Rett Syndrome Research Trust

Ай бұрын

The genetic medicine revolution is here!

Пікірлер: 3
@bruceeyers9819
@bruceeyers9819 Ай бұрын
Exciting times.looking forward to the October conference. Excellent short summary thanks.i am a medical doctor with a Rett granddaughter.
@daviddemarco7499
@daviddemarco7499 Ай бұрын
I'm hearing the same exact things that I was hearing before April 2, 2009 when my Daughter Rebecca died of Rett syndrome. All we have to do is fund your research.
@miracle4molly665
@miracle4molly665 24 күн бұрын
I am sorry to hear about your daughter Rebecca. My daughter Molly currently lives with Rett and thanks to RSRT (who we fundraise for), clinical trials are underway for a cure! My daughter is 12 and while she may not get a cure in her lifetime (though we are hopeful), if we can stop future girls and boys from having Rett Syndrome, I am all for it.
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