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Pulmonary Fibrosis Foundation

4.6

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

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WeekdayScheduleStatus
Mon9:00 a.m. to 6:00 p.m.
Tue9:00 a.m. to 6:00 p.m.
Wed9:00 a.m. to 6:00 p.m.
Thu9:00 a.m. to 6:00 p.m.
Fri9:00 a.m. to 6:00 p.m.
SatClosed
SunClosed
4.6171 reviews
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Sandra Koch-Humphreys's profile image
Sandra Koch-Humphreys 
8 years ago

My was was diagnosed with this on April 5th. I'm learning much as I can about this disease. Feel free to message me . I know it's going to be a long rough road I know I have to put my trust in God. 

Pauline Inez Borge Clark's profile image
Pauline Inez Borge Clark 
8 years ago

Im 39 and just diagnosed with pulmanary fibrosis. Im very scared and im looking for any info or support. Thank you. Im in maine wondering if anyone knows any support groups 

Mike Holaway's profile image
Mike Holaway 
8 years ago

I think that IPF &copd has kicked my butt and broke me from the expensive meds and all the pain and coughing and wheezing slowly dieing of a suck diese these sites help friends and knowing im not alone in this im in bad shape need a cure bad god bless all 

Edwin Sebastiani's profile image
Edwin Sebastiani 
8 years ago

hopefully they find a cure for my mother, its devastating seeing my mother go tru this � 

Kenneth Wisecarver Jr's profile image
Kenneth Wisecarver Jr 
8 years ago

My wife had your page she like reading what other people said she likes there story she passed away 6 mouth with this disease 

Neetu Kapoor's profile image
Neetu Kapoor 
8 years ago

My mom gt diagnosed wth this dreadful disease in march 2016.n nw she's on oxygen 24/7..we are jus praying fr a miracle to happen.plzz pray fr her..to God. 

Debbie Tryan Herndon's profile image
Debbie Tryan Herndon 
8 years ago

A great organization supporting patients, caregivers, and research for PFF�� 

Liz Burnside's profile image
Liz Burnside 
8 years ago

It is a great site and I feel so comfortable saying what I feel as I know I'm not judged. Thank you for these forum 

Joei Bujnowski's profile image
Joei Bujnowski 
8 years ago

God bless all you are suffering 

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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