SMS Research Foundation

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The mission of the Smith-Magenis Syndrome Research Foundation is to advance scientific research leading to innovative treatment options for people living with SMS. The mission of the SMS Research Foundation is to advance scientific research leading to innovative treatment options for people living with Smith-Magenis Syndrome (SMS). Since our founding in 2010, we have been singularly focused on investing in scientific research that will lead to life-changing therapeutics for this rare and complex genetic syndrome.

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2010

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3700

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Georgetown

Address: PO Box 661, GeorgetownWeb: Sign in to see organisation websiteFacebook: SmithMagenisResearchFoundationEmployees: 1Volunteers: 40Revenue: 280717ICO: 272906662

Smith-Magenis Syndrome Research Foundation Watch Now Aarons Story In the most loving and articulate way SMSRF board member Jennifer Sauer and her husband Brian open up about the challenges and complexities of raising their son Aaron with SmithMagenis Syndrome SMS. New Style Same Mission Introducing SMSRFs new visual identity designed to blend tradition with innovation. New SMS Research Findings Were excited to share the latest findings on the RAI1 gene pivotal in brain development explored through innovative studies in mice marmosets and human cells. Exciting News.

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SMS Research Foundation

Have you gotten your β€˜I Love Someone with SMS’ decal. This exclusive design is still available so you can proudly spread SMS awareness while supporting innovative research. πŸ”— Get your decal today at smsresearchfoundation.

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Emily

So inspired by the work SMSRF is doing! Understanding Smith-Magenis Syndrome is crucial, and I love how you're pushing for innovative treatments. Keep it up! ❀️

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Emil

What are some innovative treatment options currently being explored for Smith-Magenis Syndrome, and how can the community support these efforts?

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Grace

Jennifer and Brian's story really touched my heart. Thank you for sharing the challenges and triumphs of raising Aaron. It helps us all understand and support families affected by SMS better! 🌟

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Lucas

How can we enhance awareness and understanding of Smith-Magenis Syndrome among healthcare professionals and the general public?

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SMS Research Foundation

Strength and tenderness – together, they create an unstoppable force. This community is driven by both as we fight for individuals with SMS. πŸ’œ #ShareMyStrengthSaturday #SMSRF #smithmagenissyndrome #SMS #smsresearchfoundation.

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Motivated by the compassion of Jesus Christ, our Mission is to provide transitional housing with education, support services and community partnerships for women and women with children in Scott County.

46. SMS Research Foundation

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The Canavan Research Foundation is dedicated to eradicating genetic brain diseases, including Canavan, Alzheimer's, Parkinson's, and MS.

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The Malan Syndrome Foundation's global mission is to improve the lives of affected individuals.

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Smith-Magenis Syndrome Australia Ltd (au)

Australian parents, who have children diagnosed with Smith-Magenis Syndrome (SMS), with the desire to raise awareness and help support our SMS community.

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THE SMITH-MAGENIS SYNDROME (SMS) FOUNDATION UK CIO (uk)

Official Smith-Magenis Syndrome Foundation UK - Facebook Page.

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