Mission Accomplished (and a hug from Kelly)

Simon Hughes is raising money for Ehlers-Danlos Support UK
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Ride 24 - Newcastle to London 2015 · 22 August 2015 to 23 August 2015 ·

Ehlers-Danlos Support UK improves quality of life for people living with the Ehlers-Danlos syndromes (EDS). We work across the UK to support, advise and inform those living with the condition and the medical professionals working with them.

Story

Thanks for taking the time to visit my JustGiving page.

My daughter, Kelly, is one of thousands of sufferers of EDS which can manifest itself in many ways, from "just" stretchy skin to extreme pain in joints, chronic insomnia, digestive problems etc. an extract from www.ehlers-danlos.org describes it best.

Ehlers-Danlos syndrome (EDS) is a genetic disorder in which the structure of connective tissue is abnormal due to a gene mutation. This results in abnormally fragile and hyper-extensible tissues throughout the body which can lead to a range of multi-systemic symptoms; the effect on the body is widespread and not limited to one body system.

There are different types of the condition and a vast spectrum of symptoms are experienced by our community. Although many lead full and active lives, EDS can lead to physical disability and some rarer types can be life limiting. There is a lack of knowledge about EDS in the medical profession and it is therefore often misdiagnosed or overlooked.

Donation summary

Total
£2,696.40
+ £488.88 Gift Aid
Online
£2,696.40
Offline
£0.00

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