Story
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I met this lovely little girl this week and she Is absolutely gorgeous. She is fun loving and tough and is very brave.
She wants/needs to raise as much money for Muscular Dystrophy so that the money raised can help others.
Here is her story:
Carmela is a very happy, bright and funny little girl with a zest for life but she struggles with daily obstacles. She has L-CMD (Muscular Dystrophy) which is a progressive muscle wasting disease which unfortunately will affect her heart and lungs and most likely not make adult life.
Carmela enjoys the fast lane such as whizzing down the hills on the back of mummy’s bike and being as active as possible doing fast funfair rides. She is very sociable and is always smiling and pretty much anything excites her. But there are days she gets upset because she can’t keep up with her friends or she is fed up of falling over.
As a family we want to help Carmela and other children with L-CMD to stay strong and fight for a cure but we need the help of others to make this happen.
Please show your support and join us in raising money for Muscular Dystrophy UK so that research into this rare condition can happen. You can either donate to this page or start your own fundraising challenge by clicking in the button above.
Let’s stand up to Muscular Dystrophy together.
I met this lovely little girl this week and she Is absolutely gorgeous. She is fun loving and tough and is very brave.
She wants/needs to raise as much money for Muscular Dystrophy so that the money raised can help others.
Here is her story:
Carmela is a very happy, bright and funny little girl with a zest for life but she struggles with daily obstacles. She has L-CMD (Muscular Dystrophy) which is a progressive muscle wasting disease which unfortunately will affect her heart and lungs and most likely not make adult life.
Carmela enjoys the fast lane such as whizzing down the hills on the back of mummy’s bike and being as active as possible doing fast funfair rides. She is very sociable and is always smiling and pretty much anything excites her. But there are days she gets upset because she can’t keep up with her friends or she is fed up of falling over.
As a family we want to help Carmela and other children with L-CMD to stay strong and fight for a cure but we need the help of others to make this happen.
Please show your support and join us in raising money for Muscular Dystrophy UK so that research into this rare condition can happen. You can either donate to this page or start your own fundraising challenge by clicking in the button above.
Let’s stand up to Muscular Dystrophy together.