Help Satya raise money

Mutations in ASH1L gene is an ultra rare genetic condition affecting nearly 70 families globally and my son Kautik(aged 9) is one of them. ASH1L related disorders is known to cause neurodevelopmental disorders like Autism, ADHD, Memory Deficits, Intellectual disability and other conditions like seizures/epilepsy, Feeding and Speech disorders, GI Disturbances, Hearing & Vision impairments, Brain size & structure malformations, Hypotonia/Dystonia, Musculoskeletal Deformities and Heart abnormalities. With your support, Care4ASH1L will work towards fostering ASH1L research to find a cure and improve the quality of the lives of the ASH1L Warriors. Thank You!