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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Jun242025
Greater Seattle Pulmonary Fibrosis Support Group Meeting | Virtual
Join the Greater Seattle Pulmonary Fibrosis Support Group for their monthly meetings on the last Tuesday of each month from 12:30 pm - 2:30 pm Pacific Time. All meetings are virtual using the Zoom conferencing app. Please contact David Sherry at dssherry52@icloud.com for the Zoom meeting link, or for any questions.
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Jun252025
Understanding Mold-Related Hypersensitivity Pneumonitis: Diagnosis, Treatment, and Remediation
Join us on Wednesday, June 25 at 12:00 p.m. Central Time for the next edition of the PFF Disease Education Webinar Series on the topic of mold and PF.
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Jun272025
Grief Support Group Meeting | Virtual
Join the Grief Support Group virtual meeting on Friday, June 27 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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Jul012025
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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Jul152025
Young & WILD Support Group Meeting | Virtual
Join us for the virtual Young & WILD support group meeting on July 15 at 5:00 pm Pacific Time. Please contact Rebecca Hall at youngwithpf@gmail.com for the virtual link to join the meeting or if you have any additional questions.
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Jul182025
Mayo Clinic Arizona ILD Support Group | Hybrid
Please join the Mayo Clinic Arizona ILD Support Group for their hybrid meeting on Friday, July 18 from 12:00 - 1:30 pm Mountain Time.
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Jul252025
5th Annual LDC Memorial Classic
Join us at the 5th Annual LDC Memorial Classic in Memory of Lawrence Dean Cabot Jr. on Friday, July 25th, in Fleming Island, FL. The event will include a brief opening ceremony, information about pulmonary fibrosis, a lunch meal, giveaway prizes, a raffle, and golfing, of course.
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Jul292025
Greater Seattle Pulmonary Fibrosis Support Group Meeting | Virtual
Join the Greater Seattle Pulmonary Fibrosis Support Group for their monthly meetings on the last Tuesday of each month from 12:30 pm - 2:30 pm Pacific Time. All meetings are virtual using the Zoom conferencing app. Please contact David Sherry at dssherry52@icloud.com for the Zoom meeting link, or for any questions.
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Aug022025
Breathe n Run
Lyla and Sanya Chandiramani invite you to the Breathe n Run fun run/walk on August 2nd, 2025 at 8:00 am to raise awareness for pulmonary fibrosis. Kavita Chandiramani, our beloved grandmother, lost her life to PF, inspiring us to organize "Breathe n Run." This event is open to all and serves as a platform to bring together individuals from all walks of life, united by their determination to make a difference. Breathe n Run promotes physical fitness and aims to educate the community about the impact of pulmonary fibrosis.
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Aug032025
Strike Out ILD
Join us as we lead the way toward a cure at the Strike Out ILD bowling event on Sunday, August 3rd, in Pilesgrove, NJ. The event will include a brief opening ceremony, information about pulmonary fibrosis, pizza and fountain drinks, and of course bowling.
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Aug052025
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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