CHASING CONNOR'S CURE
"In February 2016, our beautiful son Connor was diagnosed with a form of Muscular Dystrophy called Duchenne.
Duchenne attacks the muscles and in most cases mobility is lost by the age of 10. It will eventually attack the lungs and heart which will lead to shortened life expectancy.
Unfortunately, today it has no cure. However, we are on a mission to #endduchenne by raising vital funds and awareness to accelerate finding a cure to save Connor and boys like him".
Matthew & Emma Crawford
Connor's Parents
MEET CONNOR
This is Connor; a gorgeous, boisterous, fun loving, fancy dress wearing and rather loud 7 year old boy from Tonbridge, Kent. Chasing Connor's Cure was founded shortly after Connor was diagnosed with DMD with the ambition to accelerate the search for treatments and to find a cure for this cruel, life limiting disease. Please help us on our journey and follow us on social media and subscribe to our newsletters to be kept up to date with events, and our mission to #endduchenne.
Our charity events so far...
To date, we have raised an awesome £200,000 helping to fund FIVE new research projects totalling more than £610,000
VIEW OUR SOCIAL MEDIA ACTIVITY
Help US on OUR MISSION TO
END DUCHENNE
If you would like to get involved on our mission to end Duchenne by helping to raise awareness and vital funds, we'd absolutely love to hear from you. Please get in touch.
