Story
Dear Family, Friends and Colleagues
Thank you for visiting my webpage. I would like to ask for your support once again to help Jake and other children suffering with AADC deficiency...
As in previous years, I will again be undertaking a 10 mile walk with my son Alex, in the grounds of Royal Russell School, South Croydon on Sunday 8th June 2008 in aid of AADC Research.
My best friend's 10 year old youngest son Jake was born with AADC (Aromatic Amino Acid Decarboxylase) deficiency, which is an extremely rare brain disease. AADC is a genetically inherited neurological disorder affecting the brains ability to produce neurotransmitters, dopamine and serotonin; two of the most essential neurotransmitters needed for every day living!
The severity of symptoms experienced by each affected child varies, but the majority of children show minimal motor development in the absence of treatment. You can visit www.aadcresearch.org if you would like to know more
As most of you know this is a charity very close to my heart because Jake and his family are very close friends of our family. My son Alexander is very fond of Jake and has known him for many years.
With your help
I am hoping to raise a total of £1,000 for further Research in to AADC...
Please dig deep and sponsor me on-line.
Many thanks for your support.
Ayeda and Alexander x
The picture to the left is Jake with singer Gabrielle. Gabrielle will be there this year to support this wonderful cause. If you would like to join the walk and meet her please contact lisa@aadcresearch.org for a sponsor pack.
Donating through this site is simple, fast and totally secure. It is also the most efficient way to sponsor me: The AADC Research Trust will receive your money faster and, if you are a UK taxpayer, an extra 28% in tax will be added to your gift at no cost to you.
