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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 lost my mother Oct 23, 2001 at the age of 54 to this disease. It took two years to be diagnosed at which time one lung was functioning at 50% and the other at 25%. And there was nothing they could do for her. When she passed she only 1 lung functioning at 25%.
SEEKING MORE INFO...HUSBAND JUST DX WITH IPF...JUST STARTED OXYGEN...LOOKING FOR FOLKS IN SEATTLE AREA...GREAT BLOG!!!
I just got diagnosed with pf in January. Ive spent weeks in the hospital, was on a ventilator for nine days! They are telling me my rheumatoid arthritis is causing it! Its very scary, but after reading some of these posts I feel some better about it! Thank you for this site!♡
I have seen my mom suffering . Thanks to God and the doctor that she is stable today and out of it.
I have IPF diagnosis in 2007 I went through the process for Double Lung transplanting end of 2013-2014. I was ready to be added to the list was just waiting on my last test results one of many I had for over a year. It disqualified me in November 2014 . I would love to talk with everyone that is going through this giving me your point of view what is and is not working for you. Thank You.
Great information and fantastic uplifting posts. I'm so glad there is a place both Families and those affected with this disease can go.
Informative & encouraging Facebook page about diagnosis, treatments and fundraising efforts for a cure.
I love you all ...I think about all of us dealing with this disease...I love know there are more people with this...but I also struggle with science...why haven't they done more with this since there is no cure no stopping or reversing...I wish that thing get better for us all...maybe some more trials that will actual work for us ...Big HUGS☀️
I love this site. There aren't many places to go for information, encouragent, and to be encouraging to other people. Although it is heartbreaking to read some of the stories, it is so encouraging to see the strength of the human spirit, and the blessing we receive while fighting this disease. Don't give up the fight!
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 at 9:00 a.m.
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