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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 |
RecommendedSo many people get misdiagnosed with this horrific disease, My Mother was diagnosed with ipf in July 2018 but had breathing issues since 2010, diagnosis consisted of bronchitis, pneumonia, asthma, SHE MEVER SMOKED a day in her life... she passed away 3 weeks ago on January 6, 2020! Prayers for all the patients and caregivers, it’s a frustrating disease and extremely debilitating! My Mother couldn’t walk 5 feet without gasping, then it was 1 step would render her breathless...it was heartbreaking to see her have to suffer Res... read more
Finding out the latest treatments and you are not alone in your search. Thank you.
My brother passed from this awful disease and since I have found that there is not enough funds and research!!! How can you donate with a check and know that it is safe?
https://www.gofundme.com/f/qjz7r-inogen-oxygen-machine…
The most comprehensive website for pulmonary fibrosis information.
brings awareness to those whom do not know about this disease. Also brings patient, caregiver, etc... a place to talk to others
A good source for information about my newly diagnosed lung disease, Pulmonary Fibrosis.
Very informative,,, there’s still so much we don’t know about this terrible disease !! Prayers for research ,, for dedicated scientists and for all sufferers of this dread disease !!
Great organization for resources in dealing with this disease.
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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