Do something amazing... Skydive for charity
Muscular Dystrophy UK
07771374836 / 01446761116
Book a Skydive
This is an opportunity to complete a solo parachute jump and put yourself in control of the skydive. You will have one day of training for the jump. You will make a solo parachute jump from 3,500 feet on the next jumping day. Your parachute will deploy (open) automatically as soon as you leave the aircraft and you will navigate yourself back to the dropzone for landing.
Please be aware that there are more restrictions than tandem skydives, for example maximum age 54, height/weight restriction but it is more fun!
To read more about static line please see here.
Jump for Free
Minimum Raised £395
BEST PRICE in the UK, never beaten on price with our PRICE GUARANTEE! We'll beat any like for like Tandem Skydive by £10
Call our office to book!
Why jump for us?
Please jump for Muscular Dystrophy UK because we need your help to fight.
Muscular Dystrophy UK is the leading UK charity focusing on muscular dystrophy and other related conditions. We are dedicated to beating muscular dystrophy and other related conditions by finding treatments and cures and to improving the lives of everyone affected by them.
For a fundraising pack and sponsor form please contact Regional Development Manager Laura Crouch.
Muscular dystrophy and related neuromuscular conditions are regarded as rare and, in many cases, even ultra-rare conditions. There are currently no efficient treatments or cures available for most of these conditions. Research, however, advances fast and a number of clinical trials to test the clinical benefit of promising technology are under way.
Over more than 50 years, the charity has contributed to crucial scientific breakthroughs in the field of muscular dystrophy and related neuromuscular conditions such as: laying the foundations for the promising technology of 'exon skipping' which is currently being tested in clinical trials for boys with Duchenne muscular dystrophy, and funding work that has led to a scientific breakthrough in finding a treatment for mitochondrial myopathy, which is now close to clinical trial.
Scientists and clinicians are beginning to express cautious optimism that treatments might become a reality in the near future, but to do this we need to continue to fund research. We aim to find treatments and ultimately cures for muscular dystrophy and related neuromuscular conditions and improve the lives of everyone affected by them and we need your help to do this.
Our work has five main focuses:
- we fund world-class research to find effective treatments and cures
- we provide practical information, advice and emotional support for individuals with muscular dystrophy and other related conditions, their carers and families
- we campaign to bring about change and raise awareness of muscular dystrophy and other related conditions
- we award grants towards the cost of specialist equipment, such as powered wheelchairs
- we provide specialist education and development for health professionals.
We rely almost entirely on voluntary donations and legacies to fund our work. Dedicated volunteers,companies, trusts and foundations help us to raise money to fund our vital work.