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The red rose has been adopted as the universal sign for Cystic Fibrosis. Apparently a young child struggled to say the name, and said "65 Roses". Various fundraisers are held through out the year which include "Bad hair Day", "Bangers n Cash", a ball with a dress theme, and "65 Roses Day". The next 65 Roses Day is scheduled for 29th May, 2009. So watch out for lapel pins and pens to help raise money and awareness for Cystic Fibrosis. My name is Genevieve. I was born in 1975, and I have a disease called Cystic Fibrosis. In this website, I talk about my personal story with CF, and complementary therapies I have used besides antibiotics. I constantly update this site with progressive updates about my life, so please make sure you come back to visit. Cystic Fibrosis is the most common life - threatening condition affecting Australian children. Today with earlier diagnosis, better understanding of the condition and better treatment of the disease, more and more children are reaching adulthood and beyond.
DISCLAIMER: None of the data or information mentioned or contained in this site is intended to be used or construed as a substitute for professional medical care and advice by your health practitioner. The author assumes no responsibility for readers use of the material and opinions expressed. Updates This site was last updated on June 3rd, 2009. You can view me and Andy riding on You Tube. This was a dressage test I did at the Victorian All Welsh show in 2007. With 38% Fev 1 lung function..;)
Thankyou to Animation Factory for their use of graphics.
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