Our story begins on 5 December 2013 in the city of Tangier, Morocco, with the birth of my first child, Iyad, who was very small in height and weight. For two years, many paediatricians were unable to diagnose Iyad’s condition, so we moved to the capital, Rabat, to no avail. Then we went to Valdemoro,…

“We were told nothing could be done, but with the right people and bold decisions, we changed the outcome.” – Jonathan At just two years old, George was diagnosed with a rare liver cancer – rhabdomyosarcoma – and an ultra-rare genetic condition, Mosaic Variegated Aneuploidy (MVA) Syndrome. With determination and the support of experts like…