Spastic Paraplegia Foundation, Inc.
Hereditary Spastic Paraplegia #hsp & Primary Lateral Sclerosis #pls together we are #HSPandPLS The Spastic Paraplegia Foundation is committed to promoting research to find cures for Hereditary Spastic Paraplegia and Primary Lateral Sclerosis, to educating people and their families affected by these conditions to help them live full and productive lives and to creating opportunities for mutual support and sharing.
Founded
2002
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Spastic Paraplegia Foundation - Hereditary Spastic Paraplegia & Primary Lateral SclerosisF Rare Disease Day is February 28 2025 Rowan has SPG4 After being diagnosed with HSP I found the SPF website and attended their annual conference. It was great to learn about HSP PLS and meet others like me. We have multiple committees for anyone to join Education Ambassadors Fundraising Marketing Advocacy and SPF Kids Join our newest outreach effort What is it. Welcome to Spastic Paraplegia Foundation Inc.
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Great news from Oregon! A federal judge has just ruled that sex education programs, which include important discussions on gender identity, must continue to receive grant funding. This is a huge win for inclusive education and ensuring every student feels represented! 🌈📚 #InclusivityMatters #EducationForAll
Judge in Oregon bars feds from halting grant funding for sex ed that involves gender identity
Oregon Live
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