Thanks for visiting the Breathe for Bea Foundation blog. Here we share stories about our cherished Ashley “Bea” Briggs, the latest on what’s going on at the Foundation, event updates and recaps, 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].
The Breathe for Bea Foundation has been very busy lately – we’ve sent out eight care packages in the past 30 days! Three more are going out today and another is going out next week. Many, many thanks to everyone for your support and very generous donations. Without you none of this would be possible and we are incredibly grateful. Together we are ALL making a difference.
Continue reading “Care Packages Galore!”
This past Monday, April 15th, the Breathe for Bea Foundation held its first fundraiser of the year, a private Glassware Paint Party evening hosted by Kreativ Drinking at Monte Christos Restaurant in Plymouth, MA. The event was a big success and we had a great turnout!
Continue reading “Event Recap – Breathe for Bea Glassware Paint Party 2019”
We’ve been really busy here at the Foundation since the start of the new year! Aside from opening up our scholarship program for the 2019 fall semester and getting numerous applications for assistance, our care packages continue to be a big hit with the Cystic Fibrosis community. We have received a number of requests in the first few weeks of 2019, and recently sent out a care package to an 8 year old girl in Michigan, another to Ohio to an 18 year old girl, and one to Florida to a 53 year old woman. We hope to be able to fulfill many more as the year goes on.
Continue reading “2019 is Off to a Busy Start!”
While the Breathe for Bea Foundation’s financial assistance programs are geared towards helping cover prescription costs, hospital/doctor bills, un-reimbursed medical equipment, hotel expenses incurred while a child or spouse is in the hospital, etc., we occassionally receive requests for other things. A few weeks ago, the Foundation received an application for financial assistance from a mom in New York named Erin who described to us that her son Tyler, who has Cystic Fibrosis, loves to stay active and that one of his favorite things to do is ski. She was hoping for a grant from the Foundation to help cover the cost of a ski club that Tyler wanted to join.
Continue reading “Meet Tyler from New York who Loves to Ski!”
We are very excited to announce our inaugural Breathe for Bea Scholarship recipients! Our scholarship program honors the memory of our cherished Ashley “Bea” Briggs, who never let Cystic Fibrosis stop her from pursuing her dreams. It was her spirit and determination that drove the Foundation to establish our scholarship program this year, so that we could help others who are living with CF achieve their dreams of a higher education too.
Continue reading “2018 Breathe for Bea Scholarship Recipients”
Over the weekend, on Saturday, September 8th, 2018, the 1st Annual Breathe for Bea Cornhole Tournament took place at the Ted Willams Camp in Lakeville, MA. Seasoned cornhole veterans, along with more casual players just looking to come out and support the cause, gathered to remember and the honor the life of Ashley “Bea” Briggs, as well to raise funds for the Breathe for Bea Foundation – funds that allow us to help make the lives of CF patients and families who are battling Cystic Fibrosis, a bit more manageable.
Continue reading “Event Recap – 1st Annual Breathe for Bea Cornhole Tournament”
The Breathe for Bea Foundation has sure been busy in recent weeks! Thanks to your generous donations, we were able to send out hospital care packages to CF patients all across the United States. You allowed us to be able to make it a “Good Day for a Good Day” for Karson in South Carolina, Bryce in Kentucky, Tyler in Ohio, and Dawn in Wisconsin!
Continue reading “More Care Packages Delivered!”
This past Saturday, August 18th, 2018, friends and family of Ashley “Bea” Briggs gathered for a great day of fun – and some competition – at the 2nd Annual Breathe for Bea Volleyball Tournament. Her incredible spirit and love for the game were both celebrated, and we were also able to raise some funds for the Foundation which will allow us to continue to help and support individuals and families affected by Cystic Fibrosis. Just like last year, team slots filled up quick and we had an amazing turnout, with many donning Ashley’s favorite color blue!
Continue reading “Event Recap – 2nd Annual Breathe for Bea Volleyball Tournament”
The Breathe for Bea Foundation recently sent out its seventh care package, this time to a young man named Aaron in Illinois. Aaron is 29 years old, and has been battling Cystic Fibrosis since he was diagnosed at the age of two. We received a request for a care package from his cousin Wendy, who let us know that Aaron had been in and out of hospitals countless times over the years and had been recently admitted to the hospital in St. Louis, Missouri. She mentioned that he loves hunting and fishing, so we got to work on putting together a care package for him in hopes of bringing a little extra sunshine to his stay. I think we succeeded!
Continue reading “Care Package Number Seven is Delivered to Illinois!”
A few weeks ago, I ran the Tough Mudder in Charlton, Massachusetts with a few other members of Team Beastrong, and I’m so glad I pushed myself into doing it again this year. This was a hard decision for me and I was dreading it the entire week prior to the event. You see, my sister Ashley / Bea had participated in three of them before she passed away a year ago in March; Cystic Fibrosis never stopped her from doing things like the Tough Mudder. She always pushed me to try new things and I knew it would be hard to do it without her. However, with the help of some friends, we created a team to run it in honor of her.
Continue reading “Event Recap – Tough Mudder Boston 2018”