LOWE SYNDROME ASSOCIATION INC
The LSA is an international organization dedicated to helping children with Lowe syndrome and their Founded in 1983, the LSA is an international, non-profit organization made up of parents, friends, professionals, and others who are interested in helping children with Lowe syndrome and their families. Lowe syndrome is a rare genetic condition affecting males that results in multiple physical and medical challenges. There is no cure yet today, but many of the symptoms can be treated effectively. With the help of the LSA, researchers have added significantly to the body of knowledge about Lowe syndrome, and parents have benefited greatly from the mutual support and information provided by the organization.
Founded
1983
1300
Web
lowesyndrome.org
Address
Cincinnati
Lowe Syndrome Association Welcome to your full resource for meaningful information and most importantly help. Family Support Research Medical Answers The Lowe syndrome Association Unites 232 Families 26 Countries 1700 Friends . .
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1. What are some effective strategies for raising awareness about Lowe syndrome within local communities and schools to foster support for affected families?
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Brooklyn Simmons
2 days ago
Odpovědí v diskuzi
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2. In what ways can the Lowe Syndrome Association enhance collaboration with medical researchers to improve treatment options and outcomes for children with Lowe syndrome?
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Brooklyn Simmons
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Together, we can make a real impact in communities around the world. Help us bring hope and support.
🎉 Amazing work, Lowe Syndrome Association! Your dedication to supporting families and advancing research is truly inspiring. Together we can make a difference! 💪❤️
Brooklyn Simmons
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🌟 Grateful for the Lowe Syndrome Association's commitment to helping families navigate the challenges of Lowe syndrome. Your support means the world! #HopeAndSupport 🌈
Brooklyn Simmons
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