Royal Childrens Hospital
My little boy Wade who is 19 month old has Cystic Fibrosis
I am doing a charity run for the research of his condition for the Royal Children’s Hospital, where he spends quite a bit of time.
About Cystic Fibrosis
Cystic Fibrosis is a life-limiting disorder which severely affects lung function and digestion. As yet, there is no cure.
However with early detection and treatment, the quality of life and the longevity of those with Cystic Fibrosis can be greatly improved.
This is why medical research into Cystic Fibrosis such as that undertaken by The Royal Children’s Hospital, Melbourne is vitally important.
Here is a link for donations, if you can it would be much appreciated http://rchfoundation.com.au/ian_smith_8