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Tahnee Richards

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In Memory of Lindon Matthew Crellin - My Cousin

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Hi there,
 
Myself and Dakota have decided to make a difference by taking part in The Color Run and raising money for charity.

I have chosen Cystic Fibrosis because it is an illness that has affected my family severely, i have lost two cousins to CF and although the loss of any family member or even a friend to any kind of illness is very sad, i have seen my cousin go through so much to reach the age he did, he was a fighter, so strong and courageous and fought till the very end, when he was well he was a happy, full of life guy, he never seemed to let CF control him.

We want to help do our part in finding a cure so those suffering from CF can have a chance at a long, pain free life and for the families of those with CF can look forward to one day knowing that their loved ones may have their pain and suffering gone, this doesn't help those who have lost their battle already but i dont think anyone should give up hope because their loved ones are no longer here, i believe those no longer here would want us all to keep fighting for a cure for those still fighting.
 
Please support my efforts by making a secure online donation and a message of support.
 
we would also really appreciate it if you could 'Like' and share my page above or comment below so more people know about it.  
 
Click 'Donate Now' to make a secure online donation and help me reach my target. I would welcome any contribution, great or small, that you could make!
 
Thanks so much for your support!

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Cystic Fibrosis Western Australia

Cystic Fibrosis (CF) is one of the most common life-limiting recessive genetic conditions affecting Australians today. CF mainly affects the respiraoty and digestive system, making it difficult to beathe and digest food. People with CF often need to take up to 40 tablets per day, maintain intensive daily physio and visit the hospital on a regular basis in order to stay as healthy as possible. Your support will help Cystic Fibrosis WA to provide essential services for people who are living with CF and funding for critical CF research projects. Please help us to achieve our vision of “Lives unaffected by CF”.

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