|Wolfram Syndrome – Our journey
Spreading the word in the Rare Disease Day supplement in The Guardian 28th February 2020
|What Mother’s Day Means to Me!
A blog written for Genetic Disorders UK by Tracy Lynch CEO and Co-Founder WSUK- March 2017
|Dursley teenager with extremely rare genetic disorder to raise funds for charity in SainsburysWednesday 3rd August 2016Georgina Carolan is fundraising and has managed to get a newspaper article about it as well. Well done Georgina.|