Meet Our First Hospital Care Package Recipient!

We wanted to share with you all an example of where your generous donations and support of the Breathe for Bea Foundation goes towards. Meet Blake,  a local four year old boy from Massachusetts who was diagnosed with Cystic Fibrosis at three weeks old. Blake was admitted into the hospital a couple of weeks ago for a 14 day clean out. His parents Josh and Ashley reached out to our Foundation to let us know about Blake’s impending hospital stay, and what some of his favorite things are, including Paw Patrol and superheroes! Armed with this information, our Beastrong team went to work on putting together our first hospital care package for Blake to help try and make his stay a little more comfortable.

Hospital Care Package Recipient Blake

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Event Recap – Celebrating Ashley’s / Bea’s 31st Birthday

Being the incredibly thoughful person that she was, Ashley / Bea would often plan birthday festivities for others. Now, in her honor, we make sure to plan a special night to honor hers. So, for the second year in a row, a large group of family and friends descended upon East Bay Grille in Plymouth, Massachusetts on March 24th, 2018 to celebrate Bea’s birthday.

Ashley's 31st birthday tribute

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Event Recap – 2018 Mayflower Brewing St. Pats 5K

In January 2017, I was asked to run a 5K with a group of friends. I was told that “there’s beer at the end!” Ok, sure, I might run for beer I said. But, I still hesitated to actually register. Then Ashley / Bea went into the hospital, and her sister Emily said to me, “run it with me, run for Bea”. Knowing how Ashley grabbed life by the horns and didn’t let Cystic Fibrosis stop her, I signed up for the Mayflower Brewery St. Pats 5K for Bea. Little did I know what the following weeks would bring, just how much that first 5K race would change me, and how much it would mean to me.

team beastrong 2018 mayflower st pats 5k recap

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Today is a Good Day for a Good Day!

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].