Jonathan Kremer has the rare genetic defect MOPD type 1 (microcephalic osteodysplastic primordial short stature), which means he has a rare form of short stature. His head is much too small and his brain and bones are malformed.
The parents hope that various therapies will have a positive effect on the motor and speech development of their almost three-year-old son. However, many of these therapies are only subsidized to a limited extent or not at all by the health insurance company. The family is therefore happy if they can finance them through donations.
Bettina und Elina Dörfler GbR
Help for Jonathan Kremer.
