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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 need all the information I can get to understand IPF
Such an amazing foundation! Can't wait to help raise money and help find answers to so many questions!
Sí, me encanta que se muevan los hilos de la investigación y que la gente colabore para buscar una posible cura a esta horrible enfermedad. Yo la padezco y agradezco mucho todo tipo de ayuda y también me gustaría poner mi granito de arena pero no se como hacerlo.
Our world changed 2years ago when we found out my dad had pulmonary fibrosis.I remember him saying lace calm down at least it's not stage 4 cancer or worst we can deal with this.The truth is this is just as bad and I wouldn't wish this on anyone can you imagine not being able to do something as simple as breathing your own body does it involuntarily but with this disease you can't,he goes the 14th about his double lung transplant I just pray he gets them in time.Its great to know there is actually a support group for this it... read more
My mom found a suppliment that helped stop the lung part of it.serracore NK
First learned about Pulmonary Fibrosis beginning of December 1994. While my grandfather / father was taken from this. I remember back than only having limited resources to what it was. Now people have more knowledge of it. Support groups, across the globe.
UCLA the Best place to go, Westwood, Ca, Dr Sammy Wite& Dr. Ross
We're so grateful for this page, allowing patients and caregivers opportunity to interact with others dealing with the same issues. This PFF page reminds us that we are not alone in this fight, this is an awesome resource and blessing!
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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