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.

To ensure that your event is listed on the PFF calendar, please submit your listing at least two weeks in advance of the event date. Please also note that due to a high level of submissions, we are unable to post listings that are more than 12 weeks in advance of the event. Please allow 1-5 business days for your event to appear on the calendar. 

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.

Submit an event

  • Let's Talk Cough

    On October 28, 2026, the Asthma and Allergy Foundation of America (AAFA), COPD Foundation, Global Allergy & Airways Patient Platform (GAAPP), and the Pulmonary Fibrosis Foundation (PFF) will host the Let’s Talk Cough initiative, a groundbreaking joint effort to highlight the lived experience of chronic cough.

    12:00 AM UTC Standard Time
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  • Nov
    03
    2026

    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.

    Virtual
    1:00 AM - 2:00 PM CST
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  • Nov
    03
    2026

    The Villages Pulmonary Fibrosis Support Group | In-Person

    Join the in person meeting for the The Villages Pulmonary Fibrosis Support Group on Tuesday, November 3 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

    The Villages, Florida
    9:00 AM - 10:00 AM EST
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  • Nov
    03
    2026

    BSLMC PF Support Group Meeting | Virtual

    Join the BSLMC PF Support Group for their meeting on Tuesday, November 3 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.

    12:00 PM - 1:00 PM CST
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  • Nov
    04
    2026

    Women & ILD Support Group Meeting | Virtual

    Join the Women & ILD Support Group's virtual meeting on Wednesday, November 4 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.

    1:00 PM - 2:00 PM EST
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  • Nov
    09
    2026

    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, Monday, November 9 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!

    Sacramento, CA
    2:00 PM - 3:30 PM PST
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  • Nov
    11
    2026

    Nebraska Medicine PF Support Group

    Join the Nebraska Pulmonary Fibrosis Support Group virtual meeting on Wednesday, November 11 at 12:00 pm Central Time. To receive the virtual meeting information, please contact Cait Kinder at Pfsupportgroup@nebraskamed.com.

    12:00 PM - 1:00 PM CST
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  • Nov
    13
    2026

    MUSC Interstitial Lung Disease Support Group Meeting | Hybrid

    Join the MUSC Interstitial Lung Disease Support Group for their meeting on Friday, November 13, 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.

    Mount Pleasant, SC 29464
    10:00 AM - 11:00 AM EST
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  • Nov
    15
    2026

    2026 Arizona Community Walk for Pulmonary Fibrosis

    Register now for the 2026 Arizona Community Walk for Pulmonary Fibrosis on November 15th at Steele Indian School Park in Phoenix, AZ. The walk will include a brief opening ceremony, information about pulmonary fibrosis, and a walk at Steele Indian School Park. Gather your friends and family to join us as we raise funds and awareness for the Pulmonary Fibrosis Foundation.

    Phoenix, AZ 85012
    9:00 AM - 12:00 PM MST
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  • Nov
    19
    2026

    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.

    Virtual
    1:00 PM - 2:00 PM CST
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  • Nov
    23
    2026

    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 Monday, November 23 from 11:30 a.m. – 12:30 p.m. Eastern Time. For additional information, please contact Cheri Cline at chericline.cc@gmail.com.

    New Port Richey, FL 34652
    11:30 AM - 12:30 PM EST
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  • Nov
    24
    2026

    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.

    Virtual
    1:00 PM - 2:00 PM CST
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