Three boys with Duchenne muscular dystrophy need donors’ help so that their life-saving treatment can continue
Thirteen-year-old Kevin, sixteen-year-old Ralf, and eight-year-old Henri can fight [...]
Permanent donors to the Children’s Foundation save the lives of hundreds of children: every donation really counts!
Even a small permanent donation makes a big [...]
Rare Disease Day conference 2025 – registration open
On 21 February 2025, everyone is invited to [...]
Supporting a little Myroslav, who has a rare skin disease
Content of the support: We help buy the skincare products [...]
Loviise, living with achondroplasia, gains 5.5 centimeters in height from treatment
Three-year-old Loviise has a rare condition called achondroplasia, [...]