Attend a Foundation Event
Attending or supporting an event is a great way to get involved and learn more about the Pulmonary Fibrosis Foundation's programs and services, to educate yourself and others about pulmonary fibrosis (PF), and to connect with other PF advocates.
Contact information on this page is solely intended for patients, caregivers and family members who are looking to connect to an event. Contact information should not be used for business purposes at this time.
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Sep022026
Women & ILD Support Group Meeting | Virtual
Join the Women & ILD Support Group's virtual meeting on Wednesday, September 2 from 1 pm - 2 pm Eastern Time. To receive the virtual meeting information, please contact Jennifer H Singley, MEd, NCC at jennifer@wescoe.org or call 484-553-6340.
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Sep092026
Nebraska Medicine PF Support Group
Join the Nebraska Pulmonary Fibrosis Support Group virtual meeting on Wednesday, September 9 at 2:00 pm Central Time. To receive the virtual meeting information, please contact Cait Kinder at Pfsupportgroup@nebraskamed.com.
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Sep122026
2026 MN Walk to Breathe
The Pulmonary Fibrosis Support Group of Minnesota (PFSG-MN) is excited to host our Third Annual PFF MN Walk to Breathe. The walk will include a brief opening ceremony, information about pulmonary fibrosis, and a walk at Central Park Roseville.
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Sep122026
The Govie Classic
The Govie Classic, presented by Family Golf and Learning Center, is an event in memory of Kevin Bittner to support the Pulmonary Fibrosis Foundation.
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Sep132026
Metro Detroit Pulmonary Fibrosis Community Walk 2026
Join us as we walk together toward a cure at the Metro Detroit Pulmonary Fibrosis Walk on Sunday, September 13th, in Detroit, MI. The walk will include a brief opening ceremony, information about pulmonary fibrosis, and a walk at The Corner Ballpark. Gather your friends and family to join us as we raise funds and awareness for the Pulmonary Fibrosis Foundation.
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Sep142026
Central Valley Pulmonary Fibrosis Support Group - Sacramento Meeting | Hybrid
Join the Central Valley Pulmonary Fibrosis (CVPF) Support Group - Sacramento on Monday, September 14 from 2:00 p.m. - 3:30 p.m. PT. Family members, friends, and caregivers are welcomed!
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Sep172026
PFF Voices | Virtual
This is a virtual support group open to all members of the pulmonary fibrosis community, whether it be patients with PF, caregivers, loved ones, or lung transplant recipients. Join this group to learn more about the disease, hear from others experiences, and discuss concerns you may have.
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Sep192026
PFF Walk - Chicago
The PFF Walk brings people together to raise funds, build awareness, and breathe hope into the pulmonary fibrosis (PF) and interstitial lung disease (ILD) community. By walking with us, you're joining thousands of individuals across the country to accelerate research, empower our community, and transform care so that everyone with PF and ILD can live a better life.
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Sep222026
PFF Lung Transplant Community Support Group Meeting | Virtual
The PFF Lung Transplant Community Support Group is intended for those who have had, or are awaiting, a lung transplant due to pulmonary fibrosis, are interested in learning about a lung transplant, or are caring for an individual who has had or is awaiting a lung transplant. This group provides an opportunity for discussion and dialogue around transplant-related challenges and celebrations.
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Sep252026
New Port Richey Pulmonary Fibrosis Community Support Group | In-Person
Join the New Port Richey Pulmonary Fibrosis Community Support Group for an in-person educational class on Friday, September 25, from 11:30 a.m. – 12:30 p.m. Eastern Time. For additional information, please contact Cheri Cline at chericline.cc@gmail.com.
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Sep262026
Richmond Pulmonary Fibrosis Awareness Walk 2026
Join us as we walk together toward a cure at the Richmond Pulmonary Fibrosis Awareness Walk on September 26th, in Sandston, VA. The walk will include a brief opening ceremony, information about pulmonary fibrosis, and a walk at Taylor Farm Park. Gather your friends and family to join us as we raise funds and awareness for the Pulmonary Fibrosis Foundation.
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Sep262026
A Community Gathering for Pulmonary Fibrosis
Join Care Center Network (CCN) members University of Michigan, Henry Ford Health System, and Corewell Health for an ILD patient education event. Participants must register to attend!
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