Beaners Bunch
Dear Friends and family,
Hey everybody! It’s time once again for Great Strides Walk for Cystic Fibrosis. This is our 36th year of participating in this very worthwhile cause! Would you consider joining our team Beaner’s Bunch this year on May 18th at Buffalo Island Park at 10:00. am? If you would rather have us walk for you, that’s great too. A donation in any amount helps the CF Foundation find new and better treatments for people with CF. Since Beaners passing in 2011, remarkable breakthroughs have been discovered in medicines that are extending the lives of CF patients. However, this is still not a cure, sadly, and the effects only last as long as the drug is taken. Also, there are still many patients whose CF mutation makes them ineligible for these new drugs, so more needs to be done. Right now, the most curative treatment for them is a lung transplant, and shortened life span. That is unacceptable. Every person born with cystic fibrosis deserves to live a long, and healthy life. We won’t rest until there’s a cure. Until it’s done. We are so thankful for the workings of the CF Foundation.
Will you help us to help them?
Thank you, Larry and Carol
Hey everybody! It’s time once again for Great Strides Walk for Cystic Fibrosis. This is our 36th year of participating in this very worthwhile cause! Would you consider joining our team Beaner’s Bunch this year on May 18th at Buffalo Island Park at 10:00. am? If you would rather have us walk for you, that’s great too. A donation in any amount helps the CF Foundation find new and better treatments for people with CF. Since Beaners passing in 2011, remarkable breakthroughs have been discovered in medicines that are extending the lives of CF patients. However, this is still not a cure, sadly, and the effects only last as long as the drug is taken. Also, there are still many patients whose CF mutation makes them ineligible for these new drugs, so more needs to be done. Right now, the most curative treatment for them is a lung transplant, and shortened life span. That is unacceptable. Every person born with cystic fibrosis deserves to live a long, and healthy life. We won’t rest until there’s a cure. Until it’s done. We are so thankful for the workings of the CF Foundation.
Will you help us to help them?
Thank you, Larry and Carol
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