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ANNUAL "TRAILS OF HOPE" HORSEBACK TRAIL RIDE
FOR CYSTIC FIBROSIS AND AVA CROW

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ANNUAL HORSEBACK TRAILRIDE FOR AVA CROW AND CYSTIC FIBROSIS
FIRST OF ALL... A BIG THANK-YOU TO ALL WHO PARTICIPATE IN OUR ANNUAL TRAILS OF HOPE  TRAIL RIDE
PLEASE CHECK BACK HERE OFTEN FOR NEWS OF THE ANNUAL "TRAILS OF HOPE RIDE".
SOME OF OUR TRAIL RIDE PICTURES ON YOUTUBE 

AwpeE.jpg (17357 bytes)AVA CROW- DAUGHTER OF ROBYN AND DAVID CROW:

SEE AVA'S YOUTUBE VIDEO
Ava was diagnosed with Cystic Fibrosisis, the devastating genetic disease that affects tens of thousands of children and young adults in the United
States.  CF is a progressive disease which attacks both the digestive and respiratory systems.  
The diagnosis brought many changes to Ava's life to include a regimen of treatment that includes taking medication before all meals and the daily use of a
nebulizer and  special airway clearance vest to breakup any mucus in her lungs before it builds.  These
treatments will increase Ava's quality of life and
extend her life but they are not a cure for thedisease.    Research and care supported by the CysticFibrosis Foundation is making a huge difference in
extending the quality of life for those with CF.However, at this time advances in medicine for CF are outpacing the available funding. We continue to lose precious lives to CF every day. That's why your help is needed now more than ever to ensure that a cure is found sooner - rather than later. To learn more aboutCF and the CF Foundation, visit www.cff.org or call(800) FIGHT CF.