Paul Delaney
Hi everyone! We’ll, we’re doing it again! "Paddle for CF" this year along with our “Great Strides” walk. They’re both on the same day and same location…Huntington Beach! Our amazing friend Jim Roesler is leading us on the Paddle event right on the beach and on the water. The Great Strides walk will be right next door on the HB boardwalk. We would love to have you join us for either a paddle in the water or a comfortable walk at the beach. Pick one or both…either way, it’s guaranteed to be a great time.
This will be our 22nd Great Strides and our 4th Paddle for CF event. Yep, 22 years!! I want to thank everyone for your support over these past 22 years! Your prayers, encouragement, love, and friendship have made this journey much easier than we thought possible. Thank you!!
As most of you know my son Braeden has Cystic Fibrosis (CF). You wouldn’t know it by looking at him, he’s a picture of good health. But deep inside, CF is still doing its thing. It can be heartbreaking at times, but when we look back at how blessed we’ve been with Brae’s overall health, and with all the support we’ve received over the years from our family, friends, and friends of friends, we’re lifted right back up. Thank you for that!
Braeden is in his final year of college attending UCI. So far so good, and I think it’s been helpful that his sister (Shae) is attending UCI too!
The CF Foundation continues to make great strides each year and we’re getting so close to a cure; we can taste it. This is because of all your support and generosity over the past years. You’re part of helping the world find a cure for a life shortening disease and in your lifetime! What a wonderful gift to be a part of. But even though we’re really close, we’re not there just yet. We still have a ways to go and unfortunately the science that gets us there costs more money than you can imagine. Always $$$$$$ and lots of it!
So, if you’re in a position (and only in a position) to help us out this year, no matter what the amount is, I’m hoping you’ll support all the families affected by this terrible disease.
There are thousands of kids just like Braeden fighting for, and deserving a longer life, a better quality of life, and someday hopefully a cure. The CF Foundation is making those things happen. Children with CF are not only living longer, but they’re also living a lot better. The research hasn't reached a plateau; it's truly advancing. We’re soooooo close!!!
Please join us in our battle to raise funds in support of the research that will one day change the lives of those with Cystic Fibrosis and their families. Please help us change the meaning of CF to:
CURE FOUND!!!!
Thank you for all that you can do!
All the best, love, and Blessings,
Paul (Braeden’s Dad)
This will be our 22nd Great Strides and our 4th Paddle for CF event. Yep, 22 years!! I want to thank everyone for your support over these past 22 years! Your prayers, encouragement, love, and friendship have made this journey much easier than we thought possible. Thank you!!
As most of you know my son Braeden has Cystic Fibrosis (CF). You wouldn’t know it by looking at him, he’s a picture of good health. But deep inside, CF is still doing its thing. It can be heartbreaking at times, but when we look back at how blessed we’ve been with Brae’s overall health, and with all the support we’ve received over the years from our family, friends, and friends of friends, we’re lifted right back up. Thank you for that!
Braeden is in his final year of college attending UCI. So far so good, and I think it’s been helpful that his sister (Shae) is attending UCI too!
The CF Foundation continues to make great strides each year and we’re getting so close to a cure; we can taste it. This is because of all your support and generosity over the past years. You’re part of helping the world find a cure for a life shortening disease and in your lifetime! What a wonderful gift to be a part of. But even though we’re really close, we’re not there just yet. We still have a ways to go and unfortunately the science that gets us there costs more money than you can imagine. Always $$$$$$ and lots of it!
So, if you’re in a position (and only in a position) to help us out this year, no matter what the amount is, I’m hoping you’ll support all the families affected by this terrible disease.
There are thousands of kids just like Braeden fighting for, and deserving a longer life, a better quality of life, and someday hopefully a cure. The CF Foundation is making those things happen. Children with CF are not only living longer, but they’re also living a lot better. The research hasn't reached a plateau; it's truly advancing. We’re soooooo close!!!
Please join us in our battle to raise funds in support of the research that will one day change the lives of those with Cystic Fibrosis and their families. Please help us change the meaning of CF to:
CURE FOUND!!!!
Thank you for all that you can do!
All the best, love, and Blessings,
Paul (Braeden’s Dad)
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