The Nina Foundation has been founded to aid scientists and professionals financially to do further research on the Angelman syndrome.

A big problem for children affected by the Angelman Syndrome is that little to no scientific research has been done as (in every country) only a few hundred children with this syndrome exist. These children really need a correct analysis of which therapy would be the most effective, for example physiotherapy, speech therapy, medication, education, etc.

Please support this charity by donations and thereby give the children with Angelman Syndrome some hope, that the scientific research will bring the answers and possible therapies. 

Please also view our brochure.