Every year, we arrange several different camps for children, adolescents and adults with congenital heart defects. The activities are adapted so that the participants can experience the joy of movement without putting their hearts at risk. Of course, as a parent, you are always welcome to participate!
We offer support to affected families, both emotionally and financially. As the fear and worry is often overwhelming for parents of heart children, we hold support groups. For particularly hard-hit families, we can provide support in connection with treatment and habilitation. Parents who lose a child due to a congenital heart defect can also receive a funeral allowance.
Please don’t hesitate to contact us for further information!
Linda Sundberg
Generalsekreterare
linda.sundberg@hjartebarnsfonden.se08-442 46 55