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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 lost my father in 1996. He had PF. Last week they told my brother he has it. I have dermatomyositis. I am a "candidate" also. I pray he reaches out to you. He keeps to himself and says he's "fine". Thank you.
I have Pulmonary Fibrosis..I am on oxygen and handle it well...cannot have a lung transplant because of my age. So I keep my oxygen near...
Am so scared of this they call me i hate this with passion
I lost my beloved husband 5 years ago this month to this insidious disease We had never heard of it either . It presented with just a dry cough in Sept of 2008 ....a very perceptive GP had a feeling that not all was well and sent him for a CT scan ....by Dec he was on 24/7 Oxygen and meds . We were told in March 2009 he had 18 months . Despite amazing care and support , that was true . He died peacefully at home where I had been blessed to care for him throughout . It still hurts .
My mother was diagnosed with pulmonary fibrosis recently.I am really worry and want to know how i can help her. She is a very strong woman but in this moment, she is afraid with this bad news. I really appreciate all the councils you can give me.
I am thrilled to be a small part of this important Organization. I had a transplant 11 years ago and I just want to give back to others when I can.
Any fellow IPF patients in Australia on this page? Thanks for all your inspirational stories. My Dad has just been diagnosed but together we are aiming for him to live for another 5000 days. Day 8 and counting!
I'm going to be looking to you for support as I deal with this dreadful diagnosis....
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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