The Maddi Foundation - Help us beat SPG15

Maddi is fighting a rare form of MND. Please support our journey to a cure. Donate today 🙏🙏 We fund research to help develop treatments and hope ultimately to find a cure for Spastic Paraplegia Type 15 or SPG15.We aim to raise awareness of SPG15 disease by connecting clinicians, researchers and patients together and at Public Events.
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💖 Every bit of support counts! Together, we can raise awareness and bring hope to those affected by SPG15. Let's help Maddi and others like her! 💪✨ #FightMND #MaddiFoundation
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Incredible work being done by The Maddi Foundation! 🌟 Let's come together and donate to fund vital research for SPG15. Your contribution can help make a difference in the lives of so many! 🙏❤️ #CureSPG15 #HopeForMaddi
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Poslední diskuze

1. What strategies can NGOs like The Maddi Foundation implement to raise awareness and funding for rare diseases, particularly those like SPG15 that often go unnoticed?
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2. How can advancements in gene therapy for conditions like SPG15 contribute to broader research and treatment strategies for other genetic disorders?
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Help us beat SPG15 The Maddi Foundation is changing the path of rare disease. By working on finding a cure for SPG15 it could lead to more understanding of new ways to treat other diseases. ITV INTERVIEW WITH MADDI We would like to thank SPF for their help alongside The University of Sheffield for their hard work The Charity Our MissionEstablished in 2016 as the Save Our Maddi Appeal the Maddi Foundation emerged in response to Madeleine Thurgoods diagnosis of Hereditary Spastic Paraplegia 15 SPG15. CoFounder Carina Thurgood Maddis mother passionately advocated for raising awareness of SPG15 driving the Foundations commitment to advancing research and developing Gene Therapy for this rare genetic disease.

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