partners
We are looking to join forces with like-minded individuals and organizations to expand our mission. We believe that by working together, we can make a meaningful difference for families impacted by pulmonary fibrosis. Our mission is to create a supportive, compassionate network that provides resources, emotional support, and practical assistance to those affected by this life-altering disease. We invite you to join us in this vital work.
A breath of fresh air.
We’re proud to share that our partnership with the American Lung Association (ALA) in the fight against pulmonary fibrosis has reached an exciting milestone. At the 12th Annual Irv Feldman Texas Hold ’Em Tournament, we proudly displayed the new Learning to Live with PF workbook—a powerful resource developed in collaboration with the ALA.
Our ongoing relationship with Danielle Trojenik, Executive Director of Greater Chicago ALA, has been central to this effort. Her leadership and shared commitment to supporting the pulmonary fibrosis community continue to inspire our work.
The Learning to Live with PF workbook is designed to support patients, families, and caregivers affected by pulmonary fibrosis.
This milestone marks an important step forward in our shared mission, and we look ahead with hope and determination. Click below to access the Learning to Live with PF workbook.
Pictured (left to right): Kristina Gromala ALA Development Manager; Mitchell Feldman, FFF President; Anita Oruche ALA Chief Engagement Officer
Pictured (left to right): Mitchell Feldman, President; Mara Feldman-Fox, Treasurer; Danielle Trojenik, Executive Director of Greater Chicago ALA; Laurence Feldman, Vice President.
VISION
1
EXPAND
We will expand nationally and want to work with you to bring our tournaments to your city.
2
CONNECT
We will increase awareness and fundraising through joint social media initiatives and outreach.
3
FUND
We will fund new and existing programs that are aligned with our mission in supporting families.
Learning to Live with PF Navigator Pilot Program
We’re excited to launch the Lung HelpLine Initiative with the American Lung Association (ALA), offering personalized support to patients and families affected by pulmonary fibrosis (PF). At its core is the Learning to Live with PF workbook—a 50+ page guide covering everything from understanding PF and building a healthcare team to managing symptoms and living well with PF.
Through this initiative, new callers to the ALA Lung HelpLine receive the workbook, and Lung Health Navigators provide follow-up calls to guide them through it, offering tailored support every step of the way.
Together, we’ll spread the word through social media, flyers, and outreach at the Irv Feldman Casino & Poker Night—making it easier for those with PF to get the help and resources they need.
Click below to access the Learning to Live with PF workbook.
$60,000 Awarded to 25 Projects Across 11 States
In response to the pandemic this funding provided essential support, including food, cleaning supplies, medication, caregiving assistance, care packages, and other essentials to those battling pulmonary fibrosis. Together, we helped families and caregivers navigate some of their toughest times—showing the power of community in moments of crisis.
Interested in partnership opportunities? We want to hear from you.
Achievements
The Feldman Family Foundation has surpassed incredible milestones and achieved growing successes to directly support families affected by pulmonary fibrosis.
Since 2013, the Feldman Family Foundation has proudly hosted annual poker tournaments in honor of our father, Irv Feldman, who bravely battled pulmonary fibrosis. These events have featured stellar prizes, including luxurious getaways and unforgettable experiences, with 1st place tournament winners earning a ticket to compete in the World Poker Tournament in Las Vegas. The funds raised from these events have been directly channeled to support families, provide essential supplies, and enhance education and awareness about pulmonary fibrosis. With your support, we can achieve even greater things.
Patient education
Educated families using the Interstitial Lung Disease (ILD) Family Tree that is used in pulmonologists offices nationwide.
Community Service Grants
Provided grants to PF patients during the COVID-19 pandemic
Individual supports
Connected local PF patients in Illinois with Personal Protective Equipment (PPE), Supplies, and Patient Education.
Medical Guides
Provided access to guides in effectively cleaning oxygen supplies during COVID-19 when PF patients were at an extreme disadvantage.
Diagnosis
Helped fund the Clinician Toolkit used for early diagnosis of Interstitial Lung Disease (ILD).
