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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
230 E Ohio St, Ste 304, Chicago, IL, 60611, United States
Get directionsWeekday | Schedule | Status |
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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 |
My mother, Theresa Rose, passed away in 2005 from PF. Today would have been her 83 bday. Our story is nothing new. By the time she was properly diagnosed there was not much recourse. RESEARCH PLEASE!
I lost my mother this year to this horrible disease she had just turned 49 in march. We weren't given much hope from the beginning. Watching my mother fight and suffer with this diseased was really hard and painful. I hope and pray that a cure is found. Awareness is very important and I will do my best to be part of it.
Not only are the amazing at promoting awareness, providing education and supporting research, they offer a compassionate community.
I like it because it keep us informed on pertinent information local and far away it's a place to connect to people that are going through what you are. This disease is a horrible experience but it help to have someone or a group fighting for the same goal.
Pulmonary Fibrosis Foundation has a 4.6 star rating with 171 reviews.
Pulmonary Fibrosis Foundation is closed now. It will open at 9:00 a.m.
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