My Great Strides Story
Carolyn Vache
Fundraising for Denver Great Strides 2026
Carolyn Vache
Dear Family & Friends,
It’s Great Strides time of year again!
As most of you know, our grandson, Greyson, has Cystic Fibrosis. He was diagnosed with CF at two weeks old and he began therapeutic treatments right away. Today Greyson is an active 9½ year old boy who loves going to 4th grade, and he builds incredible Lego kits and is taking gymnastics too!
The Cystic Fibrosis Foundation’s largest national fundraising event is Great Strides, with walks being held throughout the United States! Great Strides Denver is on Sunday, May 9th, at 9 am at Sloan's Lake Park, 1700 N Sheridan Blvd, Denver, CO 80212. We would love to have you join Team Super G for this easy walk. Last year Team Super G raised over $25,000! And with your help we will do it again!
The Cystic Fibrosis Foundation’s mission is to cure cystic fibrosis and raise awareness about this rare, genetic, life-threatening disease that makes it difficult to breathe and affects many other organs. The Foundation leads the way in research and drug development. Nearly every Cystic Fibrosis drug on the market today has been researched and developed by the Foundation.
We virtually attended the CF Foundation Annual Meeting where we listened to the renowned Dr. Michael Boyle, the President and CEO of the foundation discuss the new five year strategic plan. This plan includes developing transformative genetic therapy approaches for every person living with CF and a plan to pioneer a genetic cure for CF. It’s truly amazing what is happening in the research world!
The Cystic Fibrosis Foundation has been called “the greatest story in medicine” due to its groundbreaking approach to raising funds that are allowing the life changing treatments for those with CF and moving toward a cure for this life-threatening disease. Sadly, about 8% of people with CF have nonsense genes for which there are no or very limited therapies. The CF Foundation is committed to finding a cure for all people that suffer from this disease.
You can be a part of this exciting journey that helps make these miracles possible, as we turn the corner into genetic treatments and the path to a cure. Please join Team Super G and the CF Foundation to find a cure to help all people with Cystic Fibrosis live longer, healthier lives and to pursue their dreams. If you are unable to attend the walk and would like to support the CF Foundation, please consider a donation. Any amount will make a difference.
Click on the Register button above to sign up for the walk and the Donate button above to make a donation.
Thank you,
Carolyn & Dan Vaché
It’s Great Strides time of year again!
As most of you know, our grandson, Greyson, has Cystic Fibrosis. He was diagnosed with CF at two weeks old and he began therapeutic treatments right away. Today Greyson is an active 9½ year old boy who loves going to 4th grade, and he builds incredible Lego kits and is taking gymnastics too!
The Cystic Fibrosis Foundation’s largest national fundraising event is Great Strides, with walks being held throughout the United States! Great Strides Denver is on Sunday, May 9th, at 9 am at Sloan's Lake Park, 1700 N Sheridan Blvd, Denver, CO 80212. We would love to have you join Team Super G for this easy walk. Last year Team Super G raised over $25,000! And with your help we will do it again!
The Cystic Fibrosis Foundation’s mission is to cure cystic fibrosis and raise awareness about this rare, genetic, life-threatening disease that makes it difficult to breathe and affects many other organs. The Foundation leads the way in research and drug development. Nearly every Cystic Fibrosis drug on the market today has been researched and developed by the Foundation.
We virtually attended the CF Foundation Annual Meeting where we listened to the renowned Dr. Michael Boyle, the President and CEO of the foundation discuss the new five year strategic plan. This plan includes developing transformative genetic therapy approaches for every person living with CF and a plan to pioneer a genetic cure for CF. It’s truly amazing what is happening in the research world!
The Cystic Fibrosis Foundation has been called “the greatest story in medicine” due to its groundbreaking approach to raising funds that are allowing the life changing treatments for those with CF and moving toward a cure for this life-threatening disease. Sadly, about 8% of people with CF have nonsense genes for which there are no or very limited therapies. The CF Foundation is committed to finding a cure for all people that suffer from this disease.
You can be a part of this exciting journey that helps make these miracles possible, as we turn the corner into genetic treatments and the path to a cure. Please join Team Super G and the CF Foundation to find a cure to help all people with Cystic Fibrosis live longer, healthier lives and to pursue their dreams. If you are unable to attend the walk and would like to support the CF Foundation, please consider a donation. Any amount will make a difference.
Click on the Register button above to sign up for the walk and the Donate button above to make a donation.
Thank you,
Carolyn & Dan Vaché
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