Thank you for visiting my fundraising page for children with Cockayne Syndrome and their families!!
    My name is Natasha Belston and I am a very happy little girl that suffers from a rare genetic condition that leaves me unable to do many things that you can do.  My condition is classified as a type of dwarfism with mild to severe retardation, I can only be in the sun for a little bit or I will sunburn, I age very fast, also known as progeria, and they say that I do not see or hear well at all.  I do wear contacts to help with my vision, but do not wear hearing aids. I am unable to walk, talk, crawl, or even sit up on my own right now and I am 15 months old!!  They also say that our average life span for children with my syndrome is only 4-7 years. Although I have many complex medical issues in my life, I always smile and enjoy spending lots of time on the floor.  Thank you for reading about me and please consider making a donation to help support research, and educate people on this rare syndrome!!  I would love you to join us at our !st ever National Walk-A-Thon at Woodland Park in Kalispell MT on Saturday May24th at 10:00 am to walk with us and spread the word about Cockayne Syndrome and to just enjoy a great day with family!!   If you would like to talk to me please contact me at jenniferbelston@gmail.com