Pulmonary Fibrosis Support Group of Minnesota

Pulmonary Fibrosis Support Group of Minnesota Support Group for Twin Cities-based Pulmonary Fibrosis patients, families and friends We meet once a month, meeting information will be posted.

A support group for Twin Cities-based Pulmonary Fibrosis patients, families and friends. Any and all are welcome! While we are not officially affiliated with any particular organizations, we work closely with the University of Minnesota ILD Clinic, American Lung Association MN Chapter and Pulmonary Fibrosis Foundation based out of Chicago.

10/25/2025
09/01/2025

September is Pulmonary Fibrosis Awareness Month!
Join the walk on September 28th from 9:30-12:30 at Central Park in Roseville, MN!

Pulmonary Fibrosis Warriors, family, friends and supporters! Mark your calendar for the PF walk on September 28th at Cen...
05/06/2025

Pulmonary Fibrosis Warriors, family, friends and supporters! Mark your calendar for the PF walk on September 28th at Central Park in Roseville, MN, from 9:30am -12:30pm. See you there!

12/23/2024

The Pulmonary Fibrosis Support Group of MN wishes you and your family a Very Happy Holiday Season filled with hope!

04/15/2024

Hosting a Facebook fundraiser? We are delighted to announce our fun new Facebook fundraiser initiative for the PFF. Create excitement with your Facebook fundraiser using our Birthday Bingo for PFF cards!

Here's how it works. There are three different level bingo cards that correspond to different fundraising amounts: $500, $1,000, and $2,000. You get to choose the level that you'd like to do. Once you've downloaded the graphic and uploaded it onto your Facebook fundraiser page, you can mark it off every time a generous donor contributes an amount that fills one of the bingo spaces. It's that simple! And the most exciting part? When you complete the entire bingo card, we'll send you a surprise PFF promotional item as a heartfelt thank you for your invaluable support! πŸ˜ŠπŸ’™

To use a Birthday Bingo for PFF card for your Facebook fundraiser, please click the following link and scroll down to the middle of the page to download your chosen level card. For any questions, please visit the following website to contact our team at https://www.pulmonaryfibrosis.org/get-involved/events/fundraise-with-team-pff/fundraising-on-facebook

01/01/2024

The PFSG-MN wishes you a Happy New Year of hope for new treatments and a cure!

12/24/2023

The PFSG-MN wishes you and your family a Happy Holiday Season!

12/11/2023

REMINDER! πŸ”” Patients, caregivers, and family members are invited to join United Therapeutics and the Pulmonary Fibrosis Foundation for an industry hosted webinar at 1:30 p.m. CT on Wednesday, December 13. This presentation will focus on how a patient is diagnosed with pulmonary hypertension associated with interstitial lung disease (PH-ILD). Presenters will discuss the tests that are performed at diagnosis.

This is the second webinar in the Industry Hosted webinar series. Even if you were unable to join the first webinar on October 31, which defined PH-ILD, discussed how ILD progresses to PH-ILD, and reviewed symptoms of PH-ILD that patients may experience, we encourage you to attend this webinar!

Register now at https://register.gotowebinar.com/register/4864196995506072153

12/11/2023

Minnesota Vikings Latest News

12/11/2023

πŸ””πŸ“° Our official news recap of the PFF Summit is now live across the web!

The conference, which took place Nov. 9-11, returned to its in-person format for the first time since 2019. Over three days, the PFF Summit brought together more than 800 healthcare experts, physicians, researchers, patients, caregivers, and industry leaders from 43 states and 16 countries in an exchange of knowledge, experiences, and insights on PF research and care.

β€œIn an atmosphere of collaboration and shared purpose, the PFF Summit 2023 provided an unparalleled opportunity for medical professionals and patients to engage in impactful discussions, exploring the latest advancements and strategies in managing and treating PF and ILD,” said Dr. Franck Rahaghi, President, CEO and Chief Medical Officer for the PFF. β€œTogether, we are making progress in our mission to find a cure for these devastating diseases.”

Read all about it in our official press release at https://www.pulmonaryfibrosis.org/about-us/news-and-media/news/article/2023/12/08/pulmonary-fibrosis-foundation-s-pff-summit-2023-advances-research--urges-clinical-trial-participation-to-accelerate-new-therapies

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P. O. Box 390498
Minneapolis, MN
55439

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