Jenson had his 1st birthday on 9th December 2013 and it was on this day that we were devastated to learn that our little baby boy has Duchenne Muscular Dystrophy. This is a disease that through time will slowly take away Jenson’s mobility, leaving him in a wheel chair. His ultimate fate will be his loss of life because his heart and lungs will eventually cease to work. As you can imagine our world has been rocked and there is no cure for this condition and we feel so helpless.
Jenson’s Journey has been set up to raise awareness of Duchenne Muscular Dystrophy and to tell you his story. We are very focused on setting up a charity for Jenson and obviously are looking for any help to raise awareness and to raise much needed funds, which can be used to help with research, that hopefully will eradicate this disease and save many boys like Jenson.
Your help is greatly needed.
Please get in touch if you can help.
Our first objective is complete – ‘Jenson’s Journey’ charity is now very much alive, by following Jenson on Facebook, his website or twitter, we can update you on our progress. Thanks for reading and hopefully our hope will someday become a reality when a cure is found.
Twitter – jenson’s journey@jensons_family
Email – email@example.com
Facebook – Jenson’s Journey