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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 |
RecommendedThey are Amazing , I have learned so much from them,My Momma just lost her battle from Pulmonary fibrosis August 14,2018, I miss her so much💙💚💙💚💙
I lost my husband with this disease on May 12th of 2018 he had started having artery problems and they kept telling us he has wheezing in the lungs was finally told by a lung doctor that he has this disease he gave him 3 months. And he lived two and a half years put him on hospice and I have found out so much information through a friend now who lost his wife the same way prayers go out to all as this was so horrible to watch he was 50 lb when he died I am going to stay up with this site prayers to all of y'all and let's try... read more
Outstanding support for pulmonary fibrosis patients, families, and caregivers! PFF assists local support groups too.
My father passed away Friday July 13th after being diagnosed one week before. We had never even heard of this disease. He was 73.
My father was misdiagnosed for having asthma for 40 years. Two years ago we found a good specialist that correctly diagnosed him with Pulmonary Fibrosis. He passed away last October, at home. Always get a second opinion on any long term illness!
My Dad passed away 11/20/17 from this disease. He was diagnosed just 18 months prior. Initially we thought it was caused by environment, but in his final days we learned it is hereditary.(?) Praying a cure can be found through genetic testing and no one else in our family has to face this ugly disease.
I was diagnosed 2 years ago on meds but very scared try to walk everyday. My dad died a horrible death from this disease. I know there is no cure and don't want to die like that. It helps to hear other stories guess I am lucky I am75.
My husband passed away Wednesday from this horrible disease but I found mant articles that helped us understand about it.
You have an incredible site that helped me from the start of my journey through miracle gift of transplant. THANK YOU�
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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