more than a party
ShamRockin' for a Cure is organized by an incredible volunteer committee dedicated to making CF stand for Cure Found. Working alongside the CF Foundation, this group secures sponsors, auction items, in-kind donations, volunteers, and more. Interested in learning how to get involved? Contact us.
When our son Gavin was diagnosed at age 2 1/2 with cystic fibrosis (CF), we didn’t have any idea what it was. We knew it was bad, but the panic really set in when we found out it was a genetic disease because I was already 6 months pregnant with our second child. We were shocked when our unborn son, Jake, was diagnosed with CF through amniocentesis two weeks later. We gave ourselves a few weeks to recover from this double diagnosis, but quickly decided to find a way to save our boys. We knew we had to build an army of people to help – we couldn’t do it on our own – so we named ourselves The Baker Boys’ Battalion, rolled up our sleeves, and went to work.
ShamRockin' for a Cure was launched in 2009 when our close friends came up with the idea to throw a fun party while helping the fight against cystic fibrosis. From the stage of Ameris Bank Amphitheatre, we've watched our army of friends and family grow to epic proportions. ShamRockin' has become our symbol of strength and hope... and has raised more than $2.9 million since inception!
We are so grateful to the battalion of supporters that stand behind our family and the other CF families like us. Gavin, Jake, and the other 30,000 people in the US fighting this disease deserve to live a full, healthy life and because you’ve joined the Baker Boys’ Battalion, they have a very real chance of seeing that actually happen.
xoxo, Pam Baker
in loving memory
OF JON BAKER
Jon, co-founder of ShamRockin', lost his battle to cancer in 2021. He was an incredible father, husband, brother, son, friend, cousin, leader, advisor, coach, and more. Jon was always the life of the party and his life was full of family, friends, fast cars and fun adventures.
We will raise a glass this year, and every year, to honor his larger than life energy that will always surround us.
The mission of the Cystic Fibrosis Foundation is to cure cystic fibrosis and to provide all people with CF the opportunity to lead long, fulfilling lives by funding research and drug development, partnering with the CF community, and advancing high-quality, specialized care.
Founded in 1955, the Cystic Fibrosis Foundation is the world’s leader in the search for a cure for cystic fibrosis. The Foundation was started by parents desperate to save their children’s lives. Their drive and determination to prolong life has resulted in tremendous strides, accelerating innovative research and drug development, as well as advancing care and advocacy. People with CF are now reaching milestones once thought not possible. Yet not everyone can benefit from existing treatments. We believe every person with CF should have the chance to live a long, healthy life – a life free of cystic fibrosis. Together, we will make CF stand for Cure Found.
"We are driven by a dream that one day – every person with cystic fibrosis will have a chance to live a long, healthy life."