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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 |
Let's hope to see a strong support network like this in the UK sometime soon. Love to all x
My husband passed a year ago he was 32. This year in May it will be two years, id like to host a walk/run in my city in his memory does anyone know how I can get this started?
My life is very hard dealing with this disease for 8yrs it brings a toll on my every day lifestyle especially now I have a 2yr old that graceful God has blessed me with in the midst of this ugly disease I try hard each and every day to be strong for myself and my family but in actuality nobody really knows the pain we go through. I'm on 6 to 8 liters of o2 and it feels so overwhelming I am now at the point where I feel like I'm getting weaker but I'm still fighting to be strong currently in work up to be listed on the transp... read more
I was diagnosed with the disease 2009 being treat with antibiotics and last yr was worse then my Dr put me on oxygen 24/7 although its not helping that much am coughing a lot and throwing up what can I do almost giving up no happyness at all somebody help me please .
Any Organization that raises awareness about this disease deserves five stars! I was diagnosed early in 2011 and fight it and advocate every day. We can't allow another generation to be impacted by this debilitating condition.
This is a great service, communicating on IPF. Thank you. Stephen
I am a patient of lungs fibrosis. It was diagnoses Dec19-12-10
Very good information
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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