Breathe Believe

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Breathe Believe "Giving those affected by Cystic Fibrosis reason to BELIEVE"

✨SAVE THE DATE: Friday, December 4th✨We’re back… and so excited to be bringing back one of our favorite annual events th...
10/07/2026

✨SAVE THE DATE: Friday, December 4th✨

We’re back… and so excited to be bringing back one of our favorite annual events this year!! Grab your friends, your ugliest sweaters and come kick off the holiday season with a fun-filled evening while helping in the fight against Cystic Fibrosis. You won’t want to miss it. πŸ’œπŸŽ„

Breathe Believe Ugly Sweater Party!
πŸ“… December 4th, 2026
πŸ“ Patrizia’s of Westbury

Full details coming soon- Stay tuned!

We can’t wait to celebrate with you all again! πŸ’œ

We are sad to announce that the walk has been CANCELLED this weekend due to the weather. We were looking forward to seei...
09/24/2026

We are sad to announce that the walk has been CANCELLED this weekend due to the weather. We were looking forward to seeing you all… but happy to share we have other events already in the works and can’t wait to share them soon! Stay tuned πŸ’œ As always, thank you all for your constant and ongoing support of Breathe Believe and our fight against CF.

Join Us! After a few years, Team Breathe Believe will be making a debut and walking in CFF Great Strides and would love ...
09/12/2026

Join Us! After a few years, Team Breathe Believe will be making a debut and walking in CFF Great Strides and would love for you to join us. Details as follows, please let us know if you have any questions. We just ask all our supporters to wear any Breathe Believe t-shirt you have from over the years- if not, let us know and we will try to find some sizes πŸ’œ We hope to see many of you there !

25 whole years have come and gone but no matter the time that passes, we will ALWAYS REMEMBER πŸ’™ The heroes, those we los...
09/11/2026

25 whole years have come and gone but no matter the time that passes, we will ALWAYS REMEMBER πŸ’™ The heroes, those we lost and their families left behind are forever in our hearts! So much has changed in those years, but we cannot forget how we all came together... united as one in those days following... We will NEVER forget πŸ‡ΊπŸ‡Έ

09/10/2026

We are providing up to $7.3 million to support Ride Therapeutics’ work to identify potential delivery vehicles that could help carry genetic therapies into the lungs of people with cystic fibrosis.

Genetic therapies have the potential to benefit all people with CF, regardless of their mutations. But first, researchers need a safe and effective way to get those therapies into the right lung cells.

Using AI-powered technology, Ride will test millions of tiny particles, called nanoparticles, and identify the ones that could transport a genetic therapy into the lung cells of people with CF. These nanoparticles act like protective carriers, helping genetic therapies reach their target while protecting them from the body’s natural defenses. This investment is part of our mission to pursue groundbreaking research and advance new treatment possibilities for every person with CF.

Happy September πŸ‚πŸ’›
09/01/2026

Happy September πŸ‚πŸ’›

08/25/2026

You don't need to be a cystic fibrosis expert to make a difference in the life of a student with CF.

When educators understand the unique challenges their students with CF may face, they can help create an environment where students feel supported and empowered to thrive academically and emotionally.

Happy August β˜€οΈ Hoping this month brings you all the happiness and finishes your summer off on a great note πŸ’œ
08/01/2026

Happy August β˜€οΈ Hoping this month brings you all the happiness and finishes your summer off on a great note πŸ’œ

Today is 65 Roses Day (6/5) 🌹 The β€œ65 Roses” story dates back to 1965 when an observant 4-year-old, hearing the name of ...
06/06/2026

Today is 65 Roses Day (6/5) 🌹 The β€œ65 Roses” story dates back to 1965 when an observant 4-year-old, hearing the name of his disease for the first time, pronounced cystic fibrosis as β€œ65 Roses.” Today, β€œ65 Roses” is a term often used by young children with cystic fibrosis to pronounce the name of their disease. Although, 65 roses sounds pretty and is easier to say, it certainly doesn’t make living with this ugly disease any easier πŸ’œ

cysticfibrosis cfawareness cysticfibrosisawareness

π‡πŽπ– πƒπŽ π˜πŽπ” 𝐆𝐄𝐓 π‚π˜π’π“πˆπ‚ π…πˆππ‘πŽπ’πˆπ’?CF is a genetic disease. To have CF, you must inherit two copies of the CFTR gene that co...
05/12/2026

π‡πŽπ– πƒπŽ π˜πŽπ” 𝐆𝐄𝐓 π‚π˜π’π“πˆπ‚ π…πˆππ‘πŽπ’πˆπ’?

CF is a genetic disease. To have CF, you must inherit two copies of the CFTR gene that contain mutations - one copy from each parent. That means that each parent must either have CF or be a carrier of a CFTR gene mutation.
When two people who are carriers have a child, there is a 25 percent chance of having a child with CF.
When one parent has CF and one parent is a carrier, there is a 50 percent chance of having a child with CF.

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Westbury, NY

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