David Visser, son of Jeroen and Maaike Visser, is 2 months old.
Just after his first montly anniversary the doctors in Amsterdam diagnosed David with a very rare genetic disease. At that point Jeroen and Maaike made the decision to do anything in their power to get the treatment that he needs.
While there is no 'cure' for the disease, David will undergo chemotherapy and a bone marrow transplant to stop the disease from progressing and to significantly change his life expectancy.
Unfortuantely, David will require continued treatments throughout his childhood to limit the damage that the disease has already inflicted and that the transplant cannot reverse.
Despite all of these problems and the treatments that he is going through, David is a very happy boy and continues to smile and laugh every day.
Thanks in advance for your kindness and generosity.