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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 like this site found I had IPF a year ago, love all the new insights
I am still learing about this disease. I have copd and pulmonary fibrosis.but i am a fighter
I lost my sister to PF 10 years ago after having a severe pneumonia it gave her PF gave her 2-5 yrs she died after 3 yrs.
I never heard of this aweful disease until my dad was diagnosed back in 2006 (I believe) then it took his life in 2011..doctors called it idiopathic on how he got this. He survived a massive heart attack n 2 cancers n this is what killed him...it was heart breaking but loved taking care of him!! God, I miss him sooo much!! At last he's breathing again!!
My sistet in law lost her life to this disease 9 yrs ago. It was a long and hard struggle for her, and really hard for my brother. He would have done anything for her, especially to make her life better and easier. We miss you Susie!
I have recently been diagnosed and in need of information and group support.
The one and only voice taking a stand on curing Pulmonary Fibrosis!
Some day some how we will find a cure to this terrible disease that has no cure. Let's start a fund raising campaign for stem cell research to rejuvenate lung tissue. We are too capable a nation not to find a cure!
We are celebrating Alice's four year anniversary of her lung transplant. All is going well and we thank the entire team at MGH for such a successful outcome and their work in keeping our hope alive.
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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