Harrisons Fund

Campaigns & Appeals

Every now and again someone comes up with a fabulous idea and we just have to grab it with both hands and run as far as we can with it! You will find all our favourite and most exciting campaigns and events here. Why not have a look or even pick one and get involved?

Epsom Blue Hair Brunch
24/06/2018

This year's Epsom Blue Hair Brunch will be held on Sunday the 24th of June at St Martin's Junior and Infant school in Epsom. To buy tickets for this amazing Brunch please click here to go to their website.

more info >

Birthday For A Birthday Campaign

Everyone loves birthdays!

A Birthday for a Birthday

Could you spare a birthday to give a child with Duchenne another one? Giving up just one of your birthdays can help us fund research into a cure and hopefully extend the lives of children with Duchenne. Kids born with Duchenne don't get  to have as many birthdays as they should. We are working to change that! 

more info >

Most people hope to have at least seventy birthdays in their lifetime which can mean a lot of presents. Some of the birthday presents you receive you may absolutely love, but there will be those which end up being donated to charity shops or  regifted, or sold on eBay.  Children with Duchenne, a life limiting disease, sadly do not live to be 70,  so they have a lot less birthdays than most people. For most of the kids with Duchenne, their life span is merely 20 years. 

Duchenne Muscular Dystrophy is 100% fatal. Most children with it are usually in a wheelchair by the age of 12. One in 3,500 boys is born with it, and in the UK 2,500 kids have it at the moment. You can have it, no matter where you are or what your ethnic background is. A third of all cases start in the womb, with no warning before the baby is born. Girls can also get Duchenne with around 1% of Duchenne births being female. Most kids with it die in their late teens or early twenties·

It leads to respiratory failure, heart failure, and other debilitating orthopaedic complications. Although we know a lot about how Duchenne is caused, current treatments are pretty limited. Steroids and daily stretching are what most doctors recommend, but they have their drawbacks and don't prevent debilitating muscle contractures.

One of the projects that we are raising funds for is research into anti fibrotic drugs to alleviate these contractures so why not get involved and make a difference.

Decide to give up your birthday and instead donate the cost of your celebrations and ask your friends to donate to Harrison's Fund instead of giving you a present? You can set up your fundraising page here and you won't even have to get sweaty or dirty to feel good!! We will then send you some great tips to help make your fundraising the best it can possibly be. Thank you xx

tweety-pie

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OF DUCHENNE CHARITIES

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