‘Cruel’ disease robbed little girl of speech and movement months after she learnt to walk and talk
Ben Stewart is fighting to raise funds for research into Rett Syndrome, a rare
Menu
Ben Stewart is fighting to raise funds for research into Rett Syndrome, a rare
Navigating the clinical care system for children and adults with Rett Syndrome in the
The family of a girl left “locked in” by a rare syndrome has raised
The debacle of Altrincham’s 24M Health and Wellbeing Centre is well known – but
This week at Reverse Rett, we have been fortunate to be able to welcome
Jonathan Paton’s daughter, Abby was diagnosed with Rett Syndrome in September last year. Despite