From Keri:
Our family participates in many fundraisers for the Cystic Fibrosis Foundation and we do our best to raise money to fight this disease. One of the newest drugs on the market is called "Kalydeco." It is the first drug available that targets the underlying cause of CF. While this drug only helps 4% of the CF population, the CF Foundation is working on another drug similar to Kalydeco that will help Taylor and those with her gene mutations. We can't wait for the day when this drug is available for Taylor.
We take each day as it comes. We have a lot of hope for the future for Taylor and the other children and adults affected with cystic fibrosis. We absolutely believe that one day CF will stand for CURE FOUND!
If you would like to donate to our cause, please visit our Great Strides website at http://fightcf.cff.org/goto/keriking
To view Taylor's videos regarding her life, please visit
http://www.youtube.com/watch? v=rAYiYbWhMV0 - 2014 videohttp://www.youtube.com/watch? v=Umnpt5LpYhs - 2013 video
http://www.youtube.com/watch? v=i5zRg1-jKUY - 2012 video
For more information about cystic fibrosis, please visit their website at: www.cff.org
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