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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 |
I walked yesterday with 800+ other participants. Each of us we're there to show our support for a loved one. I was there with a good friend who lost her husband to this disease about 2 years ago. Keep up the good work PFF!
It was a beautiful day, great walk, and a very emotional time. �. Thank you for everyone who supported me.
Diagnosed in 2015. Currently on Esbriet and doing well. Fortunately I am a responder. For some that is not possible. Please continue doing the research it takes to find the cure for this dreadful and life changing disease. Thank you to those that support to make a difference and to all you PF/IPF warriors.
I have a very dear friend who has this disease and I'm amazed that I had never heard about it before. I've learned so much from this site and have shared this with my friend. Where she lives there is very little support.
I thank God for this page, I am 44 and was diagnosed with this terrible disease in the last year, and no one has even began to treat me for this condition. So I appreciate all the information you give us. thank you so much!
I find the page is very useful. It is useful because it shares new advancements, often propel patients to get to a recognized lung center. I was on medicare and they took care of all my expenses. I now go to Baylor Center and my doctor here has been excellent. If you want to give your father a great gift, get to a lung center.
My family lost our brave, strong and precious mother. Her strength fighting this disease was inspiring to everyone who knew her. She's finally at peace and rest.
Thank you for helping with awareness and research. Thank you for the web page where we can support each other. What a great organization!
They diagnosed my mom on Nov 7 2016 she passed away on Feb 4 2017. My Aunt (my mother's sister was diagnosed on April 4th. She passed away on May 3rd.
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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