![](../images/friendraiser_uploads/10503.1530927420.custom.jpg)
My Great Strides Story
**Join Us in Supporting Cystic Fibrosis!**
Every breath matters for those with cystic fibrosis? Meet Trevor, our son, who has CF and lives his life to the fullest.
Trevor's journey with cystic fibrosis has taught us the true meaning of courage. He approaches each day with a smile and an unwavering spirit. But he's not alone. Thanks to advancements in research and treatment, Trevor and countless others living with cystic fibrosis have hope for a brighter future.
However, there's still work to be done. Cystic fibrosis remains a life-limiting genetic condition, and we need your help to continue making strides towards better treatments and, ultimately, a cure.
Your support can make a real difference in the lives of individuals like Trevor. By donating today, you're not just giving money—you're giving hope. Hope for a life without limitations. Hope for more moments with loved ones. Hope for a future where cystic fibrosis is no longer a barrier to living life to the fullest.
**How You Can Help:**
- Get involved in raising awareness for cystic fibrosis in your community
Every contribution, no matter how big or small, brings us one step closer to a world where cystic fibrosis is a thing of the past.
Thank you for standing with us in the fight against cystic fibrosis. Together, we can make a difference!
With gratitude,
Karen.Rob & Trevor
---
Feel free to personalize it further to better fit Trevor's story and your fundraising goals. Let me know if you need any more assistance!
You can support me!
By supporting my fundraising goal, you have an opportunity in your lifetime to be part of ending this disease. Please consider joining us and help make medical history.
Connect With Us
IMPORTANT NOTE ON ATTENDANCE AT FOUNDATION EVENTS:
Updated July 5th, 2023
The CF Foundation is committed to ensuring the health and wellbeing of individuals attending Foundation events. Individuals attending CF Foundation events must abide by the Foundation's Event Attendance Policy www.cff.org/attendancepolicy, which includes guidance for event attendees living with cystic fibrosis.