Dear friend,
Before she became a mom, Sarah Jurrens experienced the same jitters that all soon-to-be parents face. But prenatal genetic testing added yet another layer of questions.
Sarah’s baby girl, Eleanor, had cystic fibrosis. Like so many new parents who are learning about CF for the first time, Sarah’s research led her to the Cystic Fibrosis Foundation.
“I had never heard of CF, so I quickly turned to the Foundation for answers. I received tons of resources for learning about and coping with being the parent of a child with cystic fibrosis. From that point on, we were committed to helping the CF Foundation in any way we could.”
Today, because of all we have built together over the past 65 years, Eleanor is a thriving third grader who loves to swim and read – and she has the treatments she needs to help her stay healthy.
The Jurrens family understands that we must keep going until there are effective treatments – and ultimately, a cure – for all people with cystic fibrosis. That’s why the Jurrens Family Foundation has generously launched a $250,000 new monthly donor challenge.
| |
For the first 250 people to join the 65 Roses Club with a new monthly gift, the Jurrens will make a $1,000 contribution. Sarah and her family know that your new monthly gift will help ensure consistent funds for research, support programs, and sustain all that we do on the path toward achieving our mission.
Join the Jurrens family in celebrating the past 65 years by participating in the $250,000 new monthly donor challenge and be part of the 65 Roses Club today.
| |
|
|
|
|