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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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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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
National Walk Day
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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Sep262026
Seattle Walk for Pulmonary Fibrosis 2026
Join us as we walk together toward a cure at the Seattle Walk for Pulmonary Fibrosis on September 26th, in Seattle, WA. The walk will include a brief opening ceremony, information about pulmonary fibrosis, and a walk at Seward 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
2026 Seattle Walk for Pulmonary Fibrosis
Join us as we walk together toward a cure at the Seattle Walk for Pulmonary Fibrosis on September 26th, in Seattle, WA. The walk will include a brief opening ceremony, information about pulmonary fibrosis, and a walk at Seward Park. Gather your friends and family to join us as we raise funds and awareness for the Pulmonary Fibrosis Foundation.
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Sep292026
Greater Seattle Pulmonary Fibrosis Support Group Meeting | Virtual
Join the Greater Seattle Pulmonary Fibrosis Support Group virtual meeting on Tuesday, September 29 from from 12:30 pm - 2:30 pm PT. Please contact David Sherry at dssherry52@icloud.com for the Zoom meeting link, or for any questions.
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Oct062026
PFF Caring Conversations Support Group Meeting | Virtual
Are you caring for a person who is living with pulmonary fibrosis? This monthly support group provides a safe and welcoming space for caregivers to connect, share experiences, and gain valuable insights. Each month, we gather to discuss topics that matter most to you, offering support and understanding in the journey of caring for a loved one with pulmonary fibrosis.
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Oct062026
The Villages Pulmonary Fibrosis Support Group | In-Person
Join the in person meeting for the The Villages Pulmonary Fibrosis Support Group on Tuesday, October 6 at 9:00am ET. This meeting will take place at The Villages Lake Miona Recreation Center in The Villages, Florida. For more information, please contact Support Group Leader, Laura Golden. Email: Laura.goldengirl@yahoo.com / Phone Number: 832-595-4652
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Oct062026
BSLMC PF Support Group Meeting | Virtual
Join the BSLMC PF Support Group for their meeting on Tuesday, October 6 at 12:00 pm CST. This group meets virtually. Please contact PulmonaryFibrosis@bcm.edu or call 832-355-3339 for any questions regarding this meeting.
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Oct132026
Central Valley Pulmonary Fibrosis Support Group - Sacramento Meeting | In-person
Join the in person meeting for the Central Valley Pulmonary Fibrosis (CVPF) Support Group - Sacramento on Tuesday, August 11 from 2:00 p.m. - 3:30 p.m. PT. This will be an open group discussion at Kyles Temple AME Zion Church in Sacramento, CA. Family members, friends, and caregivers are welcomed!
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