Colette's Great North Run 2017 page

Participants: Sue Boyd
Participants: Sue Boyd
Great North Run 2017 · 10 September 2017 ·
Thanks for taking the time to visit my JustGiving page.
I have decided to take part in the Great North Run 2017, for the first time this year! I've heard it's a terrific event, and like the London Marathon raises millions of pounds through participant fundraising each year. I enjoy a challenge; and training to run 13 miles without stopping (hopefully) is certainly that! I like setting myself personal challenges, but nothing comes close to giving you the motivation to get on and do it than knowing that through your personal endeavours you are raising money for a worthwhile cause.
This year I have decided to support Genetic Disorders UK. This is for personal reasons. Everyone that knows my family and I, will know that our daughter, Ella has autism (ASD) and severe learning disabilities. What they may not know is that we have recently discovered that the reason for Ella's difficulties is because she has a genetic disorder; PTEN Harmatoma Tumour Syndrome (PHTS). PHTS is a spectrum of disorders caused by germline mutations of the PTEN gene. All patients are born with macrocephaly (very large heads); learning disabilities are common and there is predisposition to develop certain types of tumour.
Genetic Disorders UK is a registered charity with a vision to improve the lives of individuals and families affected by genetic disorders.
While individual genetic disorders are rare, it is thought that there are currently more than 6,000 diagnosed disorders and new disorders are being identified every day. It is estimated that 1 in 25 children is affected by a genetic disorder. This means that in the UK, 30,000 babies and children are newly diagnosed each year and more than half a million children and adults are living with a genetic disorder.
Through fundraising donations the charity can provide support to families. Their mission to become the leading source of information and support for both those affected by a genetic disorder, and the charities and patient groups that support them. Extra money can therefore be channelled, into much needed grants for disorder-specific charities.
Thank you for taking the time to read my story, and many thanks for donating.
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