Welcome to Mickey Hofmeister's Page
Mickey Hofmeister
Mickey Hofmeister
You’re so fine… you’re so fine… Hey Mickey!
I am truly honored to be recognized alongside some incredible professionals in our community as one of Richmond's Finest by the Cystic Fibrosis Foundation.
My family has spent more than 30 years volunteering with the CF Foundation, and I especially want to give a shout‑out to Suzanne Nolan (aka “Aunt Suzy”). I’m excited to continue this tradition and do my part to help make the Foundation’s mission of curing cystic fibrosis a reality.
As part of accepting this honor, I have committed to raising $4,000 leading up to our celebration at the annual Brewers Ball. Any donation—big or small—makes a real impact, and I encourage you to consider supporting this cause. You can truly be part of ending this disease in our lifetime.
If you do donate, don’t forget to check whether your employer offers a matching gift program—it’s an easy way to double your impact!
Looking for a Brewers Ball ticket?
You’re in the right place—you can purchase tickets directly through me on this page. The Brewers Ball is an incredible evening that brings together honorees, supporters, the Foundation, and those living with CF for a night of networking, unlimited food and beverages, and continued fundraising toward a cure.
Why This Matters
Nearly 40,000 people in the United States have cystic fibrosis: a progressive, genetic disease that affects the lungs, pancreas, and other organs. Sixty years ago, children with CF usually did not live long enough to attend elementary school. Today, because of Foundation-supported research and care, the median survival age of people with CF is over 50. Working alongside the CF community, the CF Foundation has fostered the development of more than a dozen CF treatments and helped add decades of life for people with CF. Yet, many people with CF do not benefit from existing therapies. Our vision is a cure for every person with cystic fibrosis – a life free from the burden of this disease – and we will not leave anyone behind.
To learn more about CF and the CF Foundation, visit www.cff.org. Together, we can make a difference in the lives of those with cystic fibrosis. Thank you for supporting the mission of the CF Foundation!
I am truly honored to be recognized alongside some incredible professionals in our community as one of Richmond's Finest by the Cystic Fibrosis Foundation.
My family has spent more than 30 years volunteering with the CF Foundation, and I especially want to give a shout‑out to Suzanne Nolan (aka “Aunt Suzy”). I’m excited to continue this tradition and do my part to help make the Foundation’s mission of curing cystic fibrosis a reality.
As part of accepting this honor, I have committed to raising $4,000 leading up to our celebration at the annual Brewers Ball. Any donation—big or small—makes a real impact, and I encourage you to consider supporting this cause. You can truly be part of ending this disease in our lifetime.
If you do donate, don’t forget to check whether your employer offers a matching gift program—it’s an easy way to double your impact!
Looking for a Brewers Ball ticket?
You’re in the right place—you can purchase tickets directly through me on this page. The Brewers Ball is an incredible evening that brings together honorees, supporters, the Foundation, and those living with CF for a night of networking, unlimited food and beverages, and continued fundraising toward a cure.
Why This Matters
Nearly 40,000 people in the United States have cystic fibrosis: a progressive, genetic disease that affects the lungs, pancreas, and other organs. Sixty years ago, children with CF usually did not live long enough to attend elementary school. Today, because of Foundation-supported research and care, the median survival age of people with CF is over 50. Working alongside the CF community, the CF Foundation has fostered the development of more than a dozen CF treatments and helped add decades of life for people with CF. Yet, many people with CF do not benefit from existing therapies. Our vision is a cure for every person with cystic fibrosis – a life free from the burden of this disease – and we will not leave anyone behind.
To learn more about CF and the CF Foundation, visit www.cff.org. Together, we can make a difference in the lives of those with cystic fibrosis. Thank you for supporting the mission of the CF Foundation!
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