Exciting news today! The Breathe for Bea Foundation was featured on the front page of the Carver Reporter today, as well on their website. The story talks about the inspiration behind our Foundation – Ashley “Bea” Briggs – and how we hope to help and support other individuals and families who are fighting Cystic Fibrosis.
Continue reading “Breathe for Bea Foundation is in the News!”
Today truly is a good day for a good day! The Breathe for Bea Foundation is officially incorporated as a non-profit organization! We are extremely excited and want to thank each and everyone of you that has shown us love and support since Bea’s passing in early 2017, and continues to do so. We are truly grateful.
Continue reading “The Breathe for Bea Foundation is a Reality”
Thanks for visiting the Breathe for Bea Foundation blog. Here we share stories about our cherished Ashley “Bea” Briggs, recent Travel for Bea adventures, event updates and recaps, what’s going on at the Foundation, personal experiences with Cystic Fibrosis, and a whole lot more.
If you are interested in writing for the Breathe for Bea Foundation blog, please contact Jesse DaCosta at [email protected].