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Pulmonary Fibrosis Foundation
- Healthcare
- Chicago, IL
About this business
The mission of the Pulmonary Fibrosis Foundation is to find a cure for idiopathic pulmonary fibrosis (IPF) by funding research, advocating for pulmonary fibrosis issues, promoting disease awareness, and providing a compassionate environment for supporting patients and their loved ones. We aim to accomplish this by working with the medical community to drive new research, increasing research funding, representing the needs of our constituents in Washington DC through national advocacy, and developing caring relationships with... read more
Location details
230 E Ohio St, Ste 304, Chicago, IL, 60611, United States
Get directions| Weekday | Schedule | Status |
|---|---|---|
| Mon | 9:00 a.m. to 6:00 p.m. | |
| Tue | 9:00 a.m. to 6:00 p.m. | |
| Wed | 9:00 a.m. to 6:00 p.m. | |
| Thu | 9:00 a.m. to 6:00 p.m. | |
| Fri | 9:00 a.m. to 6:00 p.m. | |
| Sat | Closed | |
| Sun | Closed |
RecommendedThey do amazing work for people with IPF
información actualizada y casos reales para aprender
do you have PF or have a loved one with PF, just received the diagnosis absolutely read their website. caregivers/Care Partners you are not forgotten at the PFF. There are groups for you to join in, even from your own home. PFF is there for All!
They are a leader in advocacy for pulmonary fibrosis. They are the light house in the ocean of challenges!
La información aportada a los afectad@s. Estoy compartiendo los posts nuevos acerca de investigaciones sobre PF... Y también los posts divulgativos. Me parece una información fiable y útil.
The Pulmonary Fibrosis Foundation lets us know we are not alone as a loved one with the disease or as a caregiver. The disease is so rare that there are no support groups in our geographic area. We drive two hours to see my husband’s pulmonologist. My husband’s best friend since junior high and he were diagnosed with PF in 2017, totally unrelated. But, his friend lives in Ohio and we live in Wyoming. We are planning to join an online support group as symptoms have become more evident. This photo of my husband John shows how ... read more
I'm new to the site but what I have read is very encouraging hearing other people experiencing with IPF
My Dad passed away from his 8 month battle with IPF in February. He was misdiagnosed with allergies for years (5), before they found out what it really was. I'm thankful for this foundation but I wish they could find a cure for this awful disease.
Just diagnosed in July and recovering from an open lung biopsy. Trying to stay positive but very scared about my future. Joining this site for info and support.
Frequently asked questions about Pulmonary Fibrosis Foundation
How is Pulmonary Fibrosis Foundation rated?
Pulmonary Fibrosis Foundation has a 4.6 star rating with 171 reviews.
When is Pulmonary Fibrosis Foundation open?
Pulmonary Fibrosis Foundation is closed now. It will open tomorrow at 9:00 a.m.
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