Boomer Esiason Foundation

Boomer Esiason Foundation We are a group of passionate, dedicated individuals who work every day to raise money, awareness, and support for the cystic fibrosis community.

💙 It's Friday, and this week we're honored to share Charlee's story, as told by her mom, Krista McEmery Casey."Charlee...
08/21/2026

💙 It's Friday, and this week we're honored to share Charlee's story, as told by her mom, Krista McEmery Casey.

"Charlee was diagnosed with cystic fibrosis before she was even born. She spent her first month in the NICU after developing meconium ileus and having surgery at just 24 hours old. Since then, there has been no slowing her down!

Today, Charlee loves softball and swimming, and she approaches life with incredible determination. Whether she's taking on a new sport or facing daily CF treatments, she meets every challenge with strength, resilience, and a smile. She is our CF warrior, and we couldn't be more proud." 💙

Charlee reminds us that cystic fibrosis is only one part of her story. Her courage, joy, and unstoppable spirit inspire everyone around her.

Thank you, Krista, for sharing your family's journey, and thank you, Charlee, for showing our community what resilience looks like. We can't wait to see all you'll accomplish. 💙

25 BEF babies 💙🍼Three years ago, we launched our IVF program with a vision: to help people with CF build the families th...
08/20/2026

25 BEF babies 💙🍼

Three years ago, we launched our IVF program with a vision: to help people with CF build the families they had once dreamed of. Today, we’re celebrating an incredible milestone… 25 BEF babies have been born! ✨

We’re so proud of how far this program has come and, most importantly, of all the families we’ve had the privilege of supporting and those we continue to help build.

Here’s a look at just some of the beautiful babies born through the program! 💙 These little faces represent the hope, love, and possibilities this program was created to provide.

We’re incredibly grateful to our partners at Kindbody and Boston IVF for helping make this program possible and for helping us change the lives of so many families in the CF community.

Here’s to the first 25 babies and to all the families still to come!

💙 It's Friday, and this week we're honored to share Bennett's story, as told by his mom, Megan Jones Holland."This is ...
08/14/2026

💙 It's Friday, and this week we're honored to share Bennett's story, as told by his mom, Megan Jones Holland.

"This is Bennett, almost 16, and he's my CFer! Bennett was diagnosed at just 6 weeks old after an abnormal newborn screening. He is double Delta F508 and lives life to the fullest! This year, he started pole vaulting for his high school track team, and he also plays soccer for his high school. He is smart, kind, and loves with his whole heart. He is my hero!" 💙

Bennett is a wonderful reminder that cystic fibrosis is only one part of a person's story. His determination, adventurous spirit, and compassionate heart shine through in everything he does, from competing in sports to supporting those around him.

Thank you, Megan, for sharing your family's journey, and thank you, Bennett, for inspiring our community with your strength, resilience, and heart. We can't wait to see all the incredible things you'll accomplish both on and off the field. 💙

💙 It's Friday, and this week we're honored to share Bear's story, as told by his mom, Caitlin Hargrove."This is Bear! ...
08/14/2026

💙 It's Friday, and this week we're honored to share Bear's story, as told by his mom, Caitlin Hargrove.

"This is Bear! He's 7 years old and lives a very full life with CF. Bear was diagnosed just before his 5th birthday and is the only person in the CF registry with his two mutations. He's had a lot of ups and downs over the years but is always a trooper. Bear runs cross country, does taekwondo, and is learning tennis. Most importantly, Bear is just about the kindest human you'll ever meet." 💙

Bear reminds us that every cystic fibrosis journey is unique. Through every challenge, he continues to face life with courage, determination, and an incredibly kind heart. Whether he's crossing the finish line, practicing taekwondo, or learning something new on the tennis court, Bear shows us what it means to embrace life with resilience and joy.

Thank you, Caitlin, for sharing your family's journey, and thank you, Bear, for inspiring our community with your strength, perseverance, and kindness. Your story is a beautiful reminder that some of the greatest strength comes from the biggest hearts. 💙

💙 It’s Friday, and this week we’re honored to share Mya Wheelock’s story, as told by her mom, Katie.“Mya wears a mask....
08/07/2026

💙 It’s Friday, and this week we’re honored to share Mya Wheelock’s story, as told by her mom, Katie.

“Mya wears a mask.

At home, she wears it during her breathing treatments—morning and night—as she uses her vest and nebulizer to help keep her lungs strong. It’s part of her routine, preparing her for school, sports, and everything else life brings.

On the softball field, she wears another mask.

As a catcher, Mya sees everything. She calls the pitches, protects home plate, and snaps her glove shut with a loud POP! Every three months, she checks in at the clinic, tuning up her body the same way she sharpens her skills on the field.

Different masks. Same brave girl.

Mya just turned 13 and will be starting 8th grade this fall. She is pancreas sufficient, and her CF mutations are incredibly rare. But no matter what CF brings her way, Mya never quits. CF will not be something that brings her down.” 💙

Whether she’s completing a breathing treatment or stepping behind the plate, Mya shows the same determination, discipline, and strength. CF is part of her routine, but it doesn’t define what she can accomplish.

Thank you, Katie, for sharing Mya’s story with our community, and thank you, Mya, for reminding us what it looks like to keep showing up, keep competing, and keep moving forward. We can’t wait to see what 8th grade and the next softball season have in store for you! 🥎💙

💙 It's Friday, and this week we're honored to share Avery's story, as told by her mom, Jamie Nurnberg."Avery Hastings,...
08/07/2026

💙 It's Friday, and this week we're honored to share Avery's story, as told by her mom, Jamie Nurnberg.

"Avery Hastings, 14, is living her best life with CF. She started CFTR modulator therapy the day after she turned 2 with Kalydeco, and she is now on her third drug study trial and thriving! She competes in ranch rodeos, is a catcher on an elite travel softball team, and earned a 3.5+ GPA during her freshman year of high school. Avery hopes to pursue a career in nursing someday. She is kind, strong, and my hero!" 💙

Avery is proof that a cystic fibrosis diagnosis is just one part of her story. Her determination, compassion, and drive inspire everyone around her, whether she's competing in the arena, behind the plate, or working toward her future goals.

Thank you, Jamie, for sharing your family's journey, and thank you, Avery, for showing our community what strength, perseverance, and hope look like. We can't wait to see all the incredible things your future holds. 💙

💙 It's Friday, and this week we're honored to share Atlas' story, as told by his mom, Kennedy Guenin."This is my sweet...
07/31/2026

💙 It's Friday, and this week we're honored to share Atlas' story, as told by his mom, Kennedy Guenin.

"This is my sweet CFer, Atlas. He is 4 and doesn't let his CF define him. He loves being outside, riding his bike, hiking, and playing on his swing set. He is super social and loves making friends with everyone." 🩷

Atlas reminds us that a cystic fibrosis diagnosis is only one part of who he is. His adventurous spirit, kind heart, and love for exploring the world shine far brighter than his diagnosis ever could.

Thank you, Kennedy, for sharing your family's journey, and thank you, Atlas, for inspiring our community with your resilience, joy, and unstoppable spirit. Your story is a wonderful reminder to embrace every adventure and cherish every moment. 💙

07/29/2026

☀️ Build your perfect Summer Snackle Box with Kate Sneddon!

Wherever summer takes you, pack a mix of carbs, protein, fruits or veggies, healthy fats, and a favorite treat to keep you fueled for every adventure. 💜

This , remember: there's no one right way to snack, build your box with foods you love that fit your summer plans.

👇 What's in your snackle box?
🥨 Favorite crunchy snack
🍓 Must-have fruit
🧀 Go-to protein
🍪 Favorite treat

"💙 It's Friday, and this week we're honored to share Ariana's story, as told by her mom, Tiffany Casale."My sweet girl...
07/24/2026

"💙 It's Friday, and this week we're honored to share Ariana's story, as told by her mom, Tiffany Casale.

"My sweet girl, Ariana. 💜 She doesn't know she has cystic fibrosis yet. To her, daily medications, vest treatments, extra salt, and clinic visits are just a normal part of life. She doesn't see herself as different, she simply wakes up each day with a smile and a happy heart."

Ariana's joy is a beautiful reminder that courage doesn't always look extraordinary. Sometimes, it's found in the everyday moments, in the laughter of a child, and in the love of a family navigating life with strength and hope.

Thank you, Tiffany, for sharing your family's journey, and thank you, Ariana, for inspiring our community with your bright spirit. Your story reminds us to celebrate every smile, every milestone, and every day. 💙

07/21/2026

What if the biggest challenge in your life became the reason you discovered your greatest passions? 💙

As a BEF Ambassador, Emily Brown is showing what's possible while living with cystic fibrosis. Her journey has inspired a love for nutrition, a commitment to fitness, and the determination to keep reaching for new goals. From competing in collegiate track to crossing the finish line of the New York City Half Marathon, every achievement is a reminder that progress comes from perseverance.

Whether it's lifting weights, going for a run, or simply celebrating another step forward, every victory matters.

Thank you, Emily, for sharing your story and reminding the CF community that strength isn't measured by the obstacles you face, but by the courage to keep moving forward. 💙

Address

483 10th Avenue
New York, NY
10018

Opening Hours

Monday 9am - 5pm
Tuesday 9am - 5pm
Wednesday 9am - 5pm
Thursday 9am - 5pm
Friday 9am - 5pm

Website

Alerts

Be the first to know and let us send you an email when Boomer Esiason Foundation posts news and promotions. Your email address will not be used for any other purpose, and you can unsubscribe at any time.

Contact The Organization

Send a message to Boomer Esiason Foundation:

Shortcuts

Featured

Share

Category