Just Breathe Foundation

Just Breathe Foundation Our mission is to make the lives of individuals and their families battling cystic fibrosis (CF) more manageable.

We provide funds to applicants in Western New York struggling with the financial hardships the disease causes. Our goal as a foundation is to be able to assist as many people living with cystic fibrosis as possible and continue to raise awareness of the disease through our local events. Our vision is that one day we can alleviate all of the financial stressors that burden anyone dealing with CF. This includes assisting hospitalized patients in need of “CF tune-ups”, purchases of medical equipment, and/or travel expenses to reach appropriate care. For instance, if an individual with CF came to us in need of financial assistance for a lung transplant, our goal would be to pay 100% of the costs associated with this process.

It’s Giving Tuesday! Your generosity is what allows us to continue supporting local CF families. As we go into the holid...
11/29/2022

It’s Giving Tuesday!

Your generosity is what allows us to continue supporting local CF families. As we go into the holiday season, please consider donating to Just Breathe!

https://justbreathecf.org/product/donate/

Go pick up this beauty  today!! A dollar from the sale of each Peanut Butter Fluff donut goes to Just Breathe Foundation...
03/31/2022

Go pick up this beauty today!! A dollar from the sale of each Peanut Butter Fluff donut goes to Just Breathe Foundation💜🍩

A great cure for the Monday blues? Knowing that  is making a special donut for JBF to be sold from Thursday 3/31 to Sund...
03/28/2022

A great cure for the Monday blues? Knowing that is making a special donut for JBF to be sold from Thursday 3/31 to Sunday 4/3😍

A portion from the sale of each Peanut Butter Fluff donut will go directly to the Just Breathe Foundation 💜

As we reflect on the 12 Days of Giving, we wanted to leave you with a note from the JBF Board:While Covid has hindered o...
12/22/2021

As we reflect on the 12 Days of Giving, we wanted to leave you with a note from the JBF Board:

While Covid has hindered our ability to host Just Breathe events, it hasn’t dampened our ability to support CF patients and families in need thanks to the support and generosity of all of you.

When JBF became a 501c3 in 2013 it legitimized the cause. What started as a small fundraiser for Jenna snowballed into a foundation that has gifted over $200,000 to CF patients across Western New York.

We never could have imagined the impact that JBF would have on the local CF community, and we cannot imagine a better way to honor Jenna’s legacy.

Thank you to all who have supported Just Breathe throughout the years and to those were able to donate to JBF during the 12 Days of Giving. Wishing you and your families a very Merry Christmas and all the best in 2022!

All our best,
The Just Breathe Foundation Board

This holiday season we are doing a “12 Days of Giving” for Just Breathe Foundation. Each day we want to share a part of ...
12/21/2021

This holiday season we are doing a “12 Days of Giving” for Just Breathe Foundation. Each day we want to share a part of who we are as a foundation, and we hope each day that someone is inspired to donate. This year has been hard for everyone, and especially for the CF community. In order to help the families that we do on the scale that we do, we rely on the support and generosity from all of you.

justbreathecf.org/donate

Day 12: Anthony Simonetti, Just Breathe Foundation President and proud brother of CFer Jenna Simonetti

The last couple of years have been a challenge and a change for everyone. As we near the second Christmas with the world having to wear masks and worry about catching covid, I can't help to think that this is the life my sister Jenna and all of the individuals who have lived with CF have been accustomed to their entire existence. It helps to put everything into perspective and reminds me how difficult living with cystic fibrosis can be.

As most of us already know, Jenna passed away last October. The Just Breathe Foundation had decided end to our annual Christmas Ball prior to Covid and Jenna taking a turn for the worse. This marks the second Christmas without the CF Ball and without Jenna's presence lighting up the room. It seems almost impossible to think about how things could be so different from two years ago.

One thing that hasn't changed is the mission of the Just Breathe Foundation. We must still come together as a community to help support those still here today living with Cystic Fibrosis and bring awareness to more people about the impact that CF has on the individuals and families who are affected by Cystic Fibrosis. I ask everyone to do what they can to continue to support the CF community the remainder of the giving season.

Remember that the vast majority of us who get frustrated with or complain about having to wear masks and washing hands more, and fear catching a virus that will get us sick and maybe even kill us, that this is the reality and norm for most individuals that live with the awful disease we call cystic fibrosis.

This holiday season we are doing a “12 Days of Giving” for Just Breathe Foundation. Each day we want to share a part of ...
12/20/2021

This holiday season we are doing a “12 Days of Giving” for Just Breathe Foundation. Each day we want to share a part of who we are as a foundation, and we hope each day that someone is inspired to donate. This year has been hard for everyone, and especially for the CF community. In order to help the families that we do on the scale that we do, we rely on the support and generosity from all of you.

justbreathecf.org/donate

Day 11: Amanda Bergeron, a mother with CF, tells us her story

“I just breathe, for me. But most importantly, for my kids. Parker, 9 and Giana, 18. Anyone else would think this sounds kind of dumb, actually putting thought into a process of the body that is seemingly so automatic. Breathing. In and out. All day and night and even when you’re sleeping. To most it goes without a second thought while the business of life and the day overcrowd the mind.

About 4 years ago there was a time, that for me, breathing in and out were the only two thoughts in my head that kept me alive. It took all of my mental and physical effort just to breathe. This was during my struggle to hold out living until I got my lung transplant as I watched my life being stolen from me. With the assistance of the Just breathe Foundation they helped make all of this possible. I had never even heard of the foundation. And one day when I was at a clinic appointment to discuss my upcoming trip to Pittsburgh to be evaluated for transplant I had voiced my concern about the travel costs, gas, food, lodging etc. and the weeklong stay once I got there. And how I was going to be able to have all of this under control in time to leave. I was told about the Just Breathe Foundation And given a brochure and an application form.

What happened next was really a gift from god, in human form. They were able to assist me in providing financial aid not only for my trip, but also lodging, gas and food. Most importantly for me however, was peace of mind. The ability to make the plans and know for certain I would be able to leave home and travel the five hours to Pittsburgh in peace. With the certainty that everything was all under control. And I only had to focus on breathing.

Fast forward four years, now I’m well and healthy and did in fact get the life saving double lung transplant that I needed, but now, the just breathe foundation has become a lifeline. And has assisted me multiple times in securing financial aid for my routine trips back and forth to Pittsburgh for all of my followup care. Now and in future.

I truly appreciate all the kindness and generosity of the people who yearly donate to a cause so worthy, But also SO very important for so many of us who fight daily to keep up the balance of our health and family as well as manage finances and still somehow stay sane though it all. I very deeply appreciate and value all of the people with the foundation, who I’ve come to know as very dedicated friends through all the years. As I know that they all have a more personal connection to all of us as this illness has directly and personally affected each one of them in some way.”

This holiday season we are doing a “12 Days of Giving” for Just Breathe Foundation. Each day we want to share a part of ...
12/19/2021

This holiday season we are doing a “12 Days of Giving” for Just Breathe Foundation. Each day we want to share a part of who we are as a foundation, and we hope each day that someone is inspired to donate. This year has been hard for everyone, and especially for the CF community. In order to help the families that we do on the scale that we do, we rely on the support and generosity from all of you.

justbreathecf.org/donate

Day 10: Nicole tells us about her and her husband Chris’s experience with the Just Breathe Foundation

“My husband Chris (38) has CF and was diagnosed as a baby. A couple years ago there was a very tough period that he was in and out of the hospital every 2-3 weeks for tune-ups. It became second nature for our son, Benjamin, to spend time there visiting him. He knows it is a part of our normalcy that daddy has this disease and does medicine to help keep him healthy. He knows he does not have the disease but he supports his daddy so much. The Just Breathe Foundation is a foundation that provides assistance financially to people with Cystic Fibrosis. During this rough time, it was a struggle for our family in many ways. I was trying to work as much as I could while being in the hospital for him and taking care of our son. Just Breathe helped relieve some burden financially when there was so much else we were worrying about. For the past 2 years my husband has been on Trikafta which has been nothing short of a god sent miracle. It has given him his health back, which he does not take for granted any day. It has given us our life back. The support of the foundation when we needed it for our family is something we will always, always be so appreciative of. We thank the Simonetti family for starting this foundation for the CF community. It will forever be something we are grateful for, and will forever keep the spirit of our beloved friend Jenna alive.”

12/18/2021
12/18/2021

This holiday season we are doing a “12 Days of Giving” for Just Breathe Foundation. Each day we want to share a part of who we are as a foundation, and we hope each day that someone is inspired to donate. This year has been hard for everyone, and especially for the CF community. In order to help the families that we do on the scale that we do, we rely on the support and generosity from all of you.

justbreathecf.org/donate

Day 9: Leo, our very opinionated unofficial board member

Leo has grown up around Just Breathe and lost his incredible Aunt Jenna to CF in 2020. He is an incredible kid that has graciously shared this video with everyone to tell us

We hope to eventually live in world where no lives are lost to CF 💜

Liz Anthony

This holiday season we are doing a “12 Days of Giving” for Just Breathe Foundation. Each day we want to share a part of ...
12/17/2021

This holiday season we are doing a “12 Days of Giving” for Just Breathe Foundation. Each day we want to share a part of who we are as a foundation, and we hope each day that someone is inspired to donate. This year has been hard for everyone, and especially for the CF community. In order to help the families that we do on the scale that we do, we rely on the support and generosity from all of you.

Day 8: Christie tells us her story about being a mom to CFer Gavin

Having a child with cf is not only an incredible job, but can also feel lonely and desperate. Regular appointments, incredible life changing meds, and hospital stays caused our family serious financial burdens. A friend suggested we partner with the Just Breathe Foundation, and what an incredible experience. Their love and compassion, and most of all understanding, have helped us get through some of our most challenging times. Whether we've need help with rent, utilities, or a new appliance, the Just Breathe Foundation has helped us push through every single time. We could never fully put into words the gratude we feel towards the amazing women and men who operate it, and we will forever be grateful to have known such a strong, amazing woman, Jenna.

Justbreathecf.org/donate

Justbreathecf.org/donateThis holiday season we are doing a “12 Days of Giving” for Just Breathe Foundation. Each day we ...
12/16/2021

Justbreathecf.org/donate

This holiday season we are doing a “12 Days of Giving” for Just Breathe Foundation. Each day we want to share a part of who we are as a foundation, and we hope each day that someone is inspired to donate. This year has been hard for everyone, and especially for the CF community. In order to help the families that we do on the scale that we do, we rely on the support and generosity from all of you.

Day 7: Board member & CFer Kyle Schuhart tells us about his JBF experience

Hi my name is Kyle Schuhart. I’m a 27-year-old resident of Fairport, NY and I have Cystic Fibrosis. I found out about the Just Breathe Foundation a few years back when I was having trouble affording some medical bills I had racked up from hospital stays that us CFer’s call “tune-ups” which consist of being in the hospital for 2-3 weeks at a time receiving IV antibiotics to get our lungs back into working order when we get sick. I applied for help and the Just Breathe Foundation generously help me get out of the medical debt I was facing. I wouldn’t have been able to do it without them. A few years later I had the opportunity to join the Board of Directors for the foundation and I couldn’t think of a better way to pay back the help they had given me previously. As part of the Board I am able to see how far our help really stretches to people like me who were and are in need. Since the Covid outbreak it has been hard as you can imagine to put together a fundraiser to bring in funds for the foundation. Just because it’s hard to bring funding in though doesn’t mean CF patients stop seeking help, and they shouldn’t have to. We want to continue to help as many patients as possible that reach out to us, and right now the only way to do that is to reach out to all of you for support. I hope that many of you will find us to be a worthy cause to donate to during this giving season. Thank you!

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Rochester, NY
146XX (14604=DOWNTOWN)

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