Help us cure our children
These are our children
This is Celeste, 5 years old. Celeste is a very happy and lively girl, who unfortunately has a mutation on the SATB2 gene. This leads to that she learns things more slowly and that she can’t do what other children in her age can.
You can help us in the work to cure Celeste!
What do we do to help the children?
Cure
We drive and support research related to SATB2 syndrome.
We call this initiative CureSATB2.
Care
We optimise SATB2 syndrome management within the European healthcare system.
Support
We provide support to families affected by SATB2 syndrome worldwide and address issues specific to European families.
Awareness
We raise awareness about SATB2 syndrome and share available resources within scientific communities worldwide and within European healthcare.
We drive and support research related to SATB2 syndrome.
We call this initiative CureSATB2.
Care
We optimise SATB2 syndrome management within the European healthcare system.
Support
We provide support to families affected by SATB2 syndrome worldwide and address issues specific to European families.
Awareness
We raise awareness about SATB2 syndrome and share available resources within scientific communities worldwide and within European healthcare.
