Coaching Pole Vault is My Passion – and Has Nothing to do with Cystic Fibrosis
I grew up playing sports with my brothers – anything they did, I followed them and tried it out. Unfortunately – and
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I grew up playing sports with my brothers – anything they did, I followed them and tried it out. Unfortunately – and
Eight years ago, today, I was granted the gift of life – I was saved with a bilateral lung transplant. April 18th
Quarantine. Social distancing. Isolation. These words are very familiar to those of us living with chronic illnesses. I am 63-years-old, eight years
The Emotional Rollercoaster Ride of Transplant “Dry Runs” To sum it up: dry runs are devastating If you are reading my blog,
Aging Out of the ‘Life Expectancy’ for Someone Living with Cystic Fibrosis Have you ever had a doctor tell you how long
Seven Years Post-Transplant Seven years ago, on April 18, I received a new set of lungs from my donor, Chris. He gave
This year to honor my lung transplant donor, Chris, I decided to do something spontaneous and fun. April 18th marked the 7
No matter who you are, your life is full of options. Remember that. It’s crucial, for without options, we lose hope. I
In this installment of Jerry Unplugged: A Cystic Fibrosis Podcast, Jerry sits down with Chris McEwan and Mike Hill from
In his latest podcast, Jerry Cahill sits down with Storm Johnson, a 22-year-old CFer who is currently recovering from a double
We all have hopes and dreams, but too many of us never accomplish them. Why? Fear, procrastination, health problems – there are
Life is not a controlled experience whether you have a chronic disease like CF or not. But, as human beings, we desperately
When I was a child, I was embarrassed for anyone to know I had cystic fibrosis. I just wanted to be
I’m 61 from Brooklyn, New York and I’m a cyclist, a double lung transplant recipient and I also happen to have cystic
When living with cystic fibrosis, knowing your mutation is key, but it doesn’t have to be the sole focus of living your