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2025 Amina Deserves a Normal Life Your Support Matters En Franais We are reaching out to you with hope and urgency. Amina is a bright and courageous child battling an incredibly rare condition known as bilateral congenital femoral deficiency CFD Type 2 and bilateral humeroradial synostosis with ulnar aplasia. This condition affects only 1 in 100000 individuals and without treatment it severely impacts their quality of life. There is hope however.