Katie has been diagnosed with an rare autoimmune disease called Juvenile Dermatomyositis.
Canterbury
Katie is a seven year old girl who recently became very ill very quickly but her normal GP could not find out what was wrong with her for over 2 months.Then when she got too bad her mother Tiffany a single parent with another girl Hollie got so worried and upset that she could not get any answers for why her little girl was in so much pain when she moved and why she was stiff that's when Tiffany took her to the hospital to find out what was going on.Tiffany had been told it was Glandular Fever to start with but within 2 days of Katie being in hospital they found out she had Juvenile Dermatomyositis which only 3 in 1 million children in the world get diagnosed with each year.
So I am putting this Give a Little together for people to help Tiffany and her little girl be able to afford all the things Katie needs to make her live comfortable until she is able to walk properly again without any pain or stiffness.
I'm involved just because I have seen what Tiffany and Katie have been through over the last couple of months and how much Tiffany could be helped with the cost of the items required for Katie to be happy.
Thank you so much for contributing to Katie's recovery. Bless you and your family x
Thank you so much for contributing to Katie's recovery. Bless you and your family. x
Thank you so much for contributing to Katie's recovery. Bless you and your family. x
Thank you so much for contributing to Katie's recovery. Bless you and your family. x
Thank you so much for contributing to Katie's recovery. Bless you and your family. x
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