Just after his first birthday the doctors in Amsterdam diagnosed Seb with a very rare genetic disease. At which point Ben and Rebecca made the tough decision to leave Amsterdam and return to the UK to be near family and to get the treatment Seb needs.
While there is no 'cure' for the disease, Seb will undergo chemotherapy and a bone marrow transplant to stop the disease from progressing and to significantly change his life expectancy.
Unfortuantely, Seb 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, Seb is a very happy boy and continues to smile and laugh every day.
We at KidKraft have formed this page to support Ben, Rebecca and Seb Armstrong in their fight. For every dollar donated, KidKraft will match it- up to $7600 USD.
Thanks in advance for your kindness and generosity.