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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Mar262026
Grief Support Group Meeting | Virtual
Join the Grief Support Group virtual meeting on Thursday, March 26 from 1:00 pm - 2:00 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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Mar272026
New Port Richey Pulmonary Fibrosis Community Support Group | In-Person
Join the New Port Richey Pulmonary Fibrosis Support Group for their meeting on Friday, March 27 from 11:30 am - 12:30 pm Eastern Time. For additional information, please contact Cheri Cline at chericline.cc@gmail.com.
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Apr072026
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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Apr072026
BSLMC PF Support Group Meeting | Virtual
Join the BSLMC PF Support Group for their meeting on Tuesday, April 7 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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Apr162026
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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Apr182026
PFF Walk - Tampa
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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Apr232026
MUSC Interstitial Lung Disease Support Group Meeting | Hybrid
Join the MUSC Interstitial Lung Disease Support Group for their meeting on Thursday, April 23, from 10:00 am - 11:00 am EST. Please contact Naomi Nielson at nielsonn@musc.edu or 843-876-1888 for any questions regarding this meeting.
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Apr282026
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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May052026
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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May052026
BSLMC PF Support Group Meeting | Virtual
Join the BSLMC PF Support Group for their meeting on Tuesday, May 5 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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May212026
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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