Louise Scott
Louise's page
Fundraising for Action Duchenne
Story
Hi Everyone!
Running for Jude.
This year I have decided to take on the challenge of running the 2019 London Landmark's Half Marathon.
I am running on behalf of Action Duchenne.
Action Duchenne plays a huge role in the life of my best friend Sammy and her son Jude. In 2012, Jude was diagnosed with Duchenne Muscular Dystrophy (DMD).
Duchenne muscular dystropohy is a rare and complex genetic muscle wasting condition, many of those living with Duchenne lose the ability to walk in early adolescence and often live into their late twenties. Although mostly inherited Duchenne can affect anyone from any family at any time. There is currently no cure for Duchenne Muscular Dystrophy.
Action Duchenne work tirelessly to raise money and awareness of the condition and their work has helped further research into treatment and a cure. With your help and support i hope to raise lots of money for this amazing Charity.
I am going to be regularly posting updates on my training, with any additional events i sign up to also on behalf of Action Duchenne.
If you would like more information on Duchenne Muscular Dystrophy and the work of Action Duchenne, please click on the following link https://www.actionduchenne.org
Many heartfelt thanks for reading my page and donating money to this great cause!
Love
Lou
X
Thanks for taking the time to visit my JustGiving page.
Donating through JustGiving is simple, fast and totally secure. Your details are safe with JustGiving - they'll never sell them on or send unwanted emails. Once you donate, they'll send your money directly to the charity. So it's the most efficient way to donate - saving time and cutting costs for the charity.
Running for Jude.
This year I have decided to take on the challenge of running the 2019 London Landmark's Half Marathon.
I am running on behalf of Action Duchenne.
Action Duchenne plays a huge role in the life of my best friend Sammy and her son Jude. In 2012, Jude was diagnosed with Duchenne Muscular Dystrophy (DMD).
Duchenne muscular dystropohy is a rare and complex genetic muscle wasting condition, many of those living with Duchenne lose the ability to walk in early adolescence and often live into their late twenties. Although mostly inherited Duchenne can affect anyone from any family at any time. There is currently no cure for Duchenne Muscular Dystrophy.
Action Duchenne work tirelessly to raise money and awareness of the condition and their work has helped further research into treatment and a cure. With your help and support i hope to raise lots of money for this amazing Charity.
I am going to be regularly posting updates on my training, with any additional events i sign up to also on behalf of Action Duchenne.
If you would like more information on Duchenne Muscular Dystrophy and the work of Action Duchenne, please click on the following link https://www.actionduchenne.org
Many heartfelt thanks for reading my page and donating money to this great cause!
Love
Lou
X
Thanks for taking the time to visit my JustGiving page.
Donating through JustGiving is simple, fast and totally secure. Your details are safe with JustGiving - they'll never sell them on or send unwanted emails. Once you donate, they'll send your money directly to the charity. So it's the most efficient way to donate - saving time and cutting costs for the charity.
