Rett research is at a turning point. With an FDA-approved treatment, two gene therapy trials underway, and more approaches in the pipeline, progress is accelerating like never before. In this video, CEO Laura Hameed shares how IRSF is meeting the moment by advancing science, empowering families, and building the partnerships needed to turn possibility into reality. Watch now and hear why she believes hope for families living with #rettsyndrome has never been stronger. | International Rett Syndro
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Rett research is at a turning point. With an FDA-approved treatment, two gene therapy trials underway, and more approaches in the pipeline, progress is accelerating like
International Rett Syndrome Foundation. . Rett research is at a turning point. With an FDA-approved treatment, two gene therapy trials underway, and more approaches in the pipeline, progress is accelerating like never before. In this video, CEO Laura Hameed shares how IRSF is meeting the moment by advancing science, empowering families, and ...
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Rett research is at a turning point. With an FDA-approved treatment, two gene therapy trials underway, and more approaches in the pipeline, progress is accelerating like never before. In this video, CEO Laura Hameed shares how IRSF is meeting the moment—by advancing science, empowering families, and building the partnerships needed to turn possibility into reality. Watch now and hear why she believes hope for families living with #Rettsyndrome has never been stronger. | International Rett Syndro
Rett research is at a turning point. With an FDA-approved treatment, two gene therapy trials underway, and more approaches in the pipeline, progress is accelerating like never before. In this video, CEO Laura Hameed shares how IRSF is meeting the moment—by advancing science, empowering families, and building the partnerships needed to turn possibility into reality. Watch now and hear why she believes hope for families living with #Rettsyndrome has never been stronger. | International Rett Syndro
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83 reactions · 19 shares | We’re going back to our official name International Rett Syndrome Foundation (IRSF), while continuing our commitment to Rett syndrome research and families. You can still find us at www.rettsyndrome.org, but we’re going back to our IRSF to better reflect our vision to create a WORLD without Rett syndrome. | International Rett Syndrome Foundation | Facebook
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83 reactions · 19 shares | We’re going back to our official name International Rett Syndrome Foundation (IRSF), while continuing our commitment to Rett syndrome research and families. You can still find us at www.rettsyndrome.org, but we’re going back to our IRSF to better reflect our vision to create a WORLD without Rett syndrome. | International Rett Syndrome Foundation | Facebook
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Rett research is at a turning point. With an FDA-approved treatment, two gene therapy trials underway, and more approaches in the pipeline, progress is accelerating like never before. In this video, CEO Laura Hameed shares how IRSF is meeting the moment—by advancing science, empowering families, and building the partnerships needed to turn possibility into reality. Watch now and hear why she believes hope for families living with #Rettsyndrome has never been stronger. | International Rett Syndro
Rett research is at a turning point. With an FDA-approved treatment, …
387 views1 month ago
FacebookInternational Rett Syndrome Foundation
#rettsyndrome | International Rett Syndrome Foundation
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83 reactions · 19 shares | We’re going back to our official name International Rett Syndrome Foundation (IRSF), while continuing our commitment to Rett syndrome research and families. You can still find us at www.rettsyndrome.org, but we’re going back to our IRSF to better reflect our vision to create a WORLD without Rett syndrome. | International Rett Syndrome Foundation | Facebook
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47 reactions · 24 shares | Basic Research finds ways to fix the biology of Rett syndrome through drug compounds or gene therapy, which leads to developing medicines or procedures used to treat Rett syndrome. Rettsyndrome.org is committed to accelerating research to treat and cure Rett syndrome. #OVERPOWERRETT | International Rett Syndrome Foundation | Facebook
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49 reactions · 17 shares | Thank you to those who have completed the Rett Syndrome Burden of Illness Survey! 185 people have become part of a conversation that will lead to more support, more treatment, more services.  But we still need your voice to reach our goal of 375. Join us. https://voicesofrett.org. Parents and Caregivers: Please email bgibson@rettsyndrome.org for an access code. | International Rett Syndrome Foundation | Facebook
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