
TO CURE A ROSE FOUNDATION
At To Cure A Rose Foundation, we’re on a mission to make genetic treatments faster, more affordable, and within reach—so that the next child born with a rare disease can receive a customized drug within days of diagnosis. Hope is not a wish. It’s a plan.
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2021
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AUSTIN
To Cure A Rose | Fighting for Children Like Rose to Cure HNRNPH2 Fighting for children like Rose. We develop therapeutics for children with rare genetic diseases and we need your help. To Cure a Rose Foundation began in 2021 after Casey McPherson39s daughter Rose was diagnosed with an ultrarare genetic disease HNRNPH2. Rose lost her ability to talk walking is difficult and she continues to retreat into a world away from her family.
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🌹✨ Grab your tickets now for the Rose Gala — happening August 9th at the stunning Omni Barton Creek Resort in Austin, TX. It will be an inspiring evening of purpose and celebration, raising critical funds to accelerate treatments for rare genetic diseases. Enjoy a night of dinner, dancing, and powerful stories that remind us why this mission matters.
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