This profile has not been claimed by the business owner or representative.
Claim this business to update business information, get appointment requests, engage visitors with web chat, and more!
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 |
My mother passed away a week ago and she had pulmonary fibrosis. I miss her more than anything but I know she is no longer suffering and that God is taking care of her now. If anyone can direct me to the site for helping cope with her death please post the link. Thanks have a blessed day!
I just lost my husband to this dreadful disease. Started with shortness of breath and escalated in a relatively time. By the time it was diagnosed the condition was chronic. It's like breathing with cement in your lungs. Honey I love you. RIP.
Great program, informative, educational, great people!!
Some times I just want my dad back but not like he was very sick man p f took him 24 daysdayfastest in Gainesville ga I did not like him on all the pumps and other things he dies on the 3 of Julia year ago please hug. Your sick person you will miss it love all of your support this is his pic
A very good page.
my husband died may,19, 2014 3 months ago from this disease, it happened so fast we didn't even know he had it and never heard of it, he had a heart transplant in 2005 and lived through lung cancer he was diagnoised with cancer in 2008 and was in remission from 2010 to 2014 and he went into hospital on may 14, 2014 and was gone 4 days later, they had to put him on ventilator the first night and his oxyegen level was at 54% without oxygen help, they told me that the radiation from the cancer is what caused the fibrosis, is th... read more
A place for me to know that my Dad is not alone.
I Lost my dad last 6months ago. Suffering from Lung Disease Fibrosis. Treatment is from India The Global hospitals & Health City Chennai. He was feeling Better at India Since 4years he was in continuous using Oxygen Gas Cylinder & Oxygen Machine. Please what ever it was i am missing alot my Dad . For more details you can ask me +923002669398 Raja.
It's nice to know that others are still here after 5 years or more as you always hear the bad news & not the good. I'm going to fight to the end living life to the full.
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.
Need help? Contact us.
Speak with a specialist to learn how you can grow with Birdeye. We are reachable at profiles@birdeye.com