Kelly first came to us in 2013, shortly after her three-year-old son Felix received his diagnosis. After months of testing Felix was finally diagnosed with Phelan McDermid Syndrome, a rare genetic disorder caused by the deletion of terminal chromosome twenty-two Q-13. The disorder affects speech, mobility and cognitive development and means that Felix will need 24-hour care for the rest of his life. We gave Kelly emotional and financial support to help her.
Share Kelly's Story
If you need financial support like Kelly then visit the link below for more informationFinancial Help
See how you can help colleagues in need