CRUSH RETT SYNDROME

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Crush Rett Syndrome's mission to is to raise awareness and funds for research to cure Rett Syndrome. Crush Rett Syndrome's mission is to raise awareness for Rett Syndrome and funds for effective treatments and ultimately a cure for Rett Syndrome. No salaries are being paid for any positions at this time so that we can direct all raised funds toward our mission. More than 350,000 people are afflicted with Rett Syndrome worldwide. We are working hard to give all of them a second chance at a normal life by accelerating the timeline for a cure that will reverse the symptoms.

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2016

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Gilbert

Address: 602 E Rawhide Ave, GilbertWeb: Sign in to see organisation websiteFacebook: CrushRettSyndromeVolunteers: 4Revenue: 217991ICO: 811809941

Crush Rett Syndrome - Raising Awareness & Funds to Cure Rett Syndrome OUR PASSION Raising awareness and funds to CRUSH Rett Syndrome out of existence. Give Back to Get More Join the team of families caregivers medical professionals and researchers that are going to cure Rett Syndrome Mission We are dedicated to providing energy passion and inspiration to raise awareness and funds accelerating the progress to find treatments and a cure for Rett Syndrome. We will make Rett Syndrome the first reversible neurological disorder to be cured. Events Our fundraising events are planned to enable the maximum exposure to our cause so that we can grow our network of kindhearted individuals and businesses that can help us reach our goal for a cure.

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Catherine

What strategies do you think would be most effective in increasing community engagement and awareness for Rett Syndrome?

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Michael

Just ordered my Puravida bracelet! 🌟 Proud to support such a meaningful cause and help lift families in need. Together, we can make a difference! 🙌 #CrushRett #Awareness

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CRUSH RETT SYNDROME

Thank you for following along this month. We will continue to post updates about the progress of Rett syndrome research the human clinical trials. Stay strong and continue the fight to crush Rett syndrome.

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CRUSH RETT SYNDROME

The 2nd adult patient dosed in Taysha's gene therapy trial is reporting positive results. “The two adult patients dosed with TSHA-102 have different mutations in their MECP2 gene that manifest in different phenotypes and clinical severity. Following treatment, both patients experienced improvement in key clinical domains impacting activities of daily living, including breathing dysrhythmia, autonomic function, socialization, and gross and fine motor skills.

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Simone

Incredible work being done here! 💖 Let's come together to raise awareness and funds to CRUSH Rett Syndrome for good! 💪 #CrushRett #CureRett

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Emil

How can collaborations between NGOs and local businesses enhance fundraising efforts for causes like Crush Rett Syndrome?

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Fund Raising and/or Fund Distribution Category

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