International FOXP1 Foundation

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Our mission is to build a global community that empowers and supports families and individuals with FOXP1 syndrome by sharing knowledge, inspiring hope, supporting research, and raising awareness. Our mission is to build a global community that empowers and supports families and individuals with FOXP1 syndrome by sharing knowledge, inspiring hope, encouraging research, and raising awareness.

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854079051

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Mendenhall

Address: PO Box 846, MendenhallWeb: Sign in to see organisation websiteFacebook: InternationalFOXP1FoundationRevenue: 145384ICO: 854079051

HOME | FOXP1 Foundation HOME FOXP1 SYNDROME RESEARCH FAMILIES ABOUT US GET INVOLVED More Advancing ResearchEmpowering Families Now Hiring Executive Director Click Here for More Information FOXP1 syndrome is a rare genetic disorder characterized by delays in early motor and language milestones mildtosevere intellectual deficits speech and language impairment and behavior abnormalities. The International FOXP1 Foundation is committed to building a global community that empowers and supports families and individuals with FOXP1 syndrome by sharing knowledge inspiring hope encouraging research and raising awareness. INFORMATION AND RESOURCES While there is still so much unknown and no real changes in our daytoday life with the diagnosis it was a relief to have an answer and explanation for everything about Joey that had felt off. It is amazing to feel the support from the other families and to know we are not alone.

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Michael

It's inspiring to see how this foundation is making a difference for families affected by FOXP1 syndrome. Let's keep raising awareness and advocating for our loved ones! 🌟 #JoinTheFOXP1Family

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Victor

1. What strategies can the International FOXP1 Foundation implement to raise awareness and educate the public about FOXP1 syndrome effectively?

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Hannah

2. In what ways can families affected by FOXP1 syndrome share their experiences to inspire hope and foster community support among other diagnosed families?

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International FOXP1 Foundation

Make a difference. Participate in research - https://rare-x. org/foxp1/ RARE-X is a secure, patient-reported data platform that collects information about your child’s genetics, symptoms, medical history, and daily experiences — directly from you.

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Mark

So proud to support the International FOXP1 Foundation! Together, we can shine a light on FOXP1 syndrome and help families feel less alone in their journey. 💙 #FOXP1Awareness

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International FOXP1 Foundation

✅ Sign up for your newsletter here: 🔗 https://www. foxp1. org/join-us.

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Birth Defects, Genetic Diseases Research Category

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63. International FOXP1 Foundation

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