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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 |
They diagnosed my mom with PF two years ago ,she is only 53 years old ,i need support on how to deal with this disease and how to help her feel better ,she is sad and depressed,she is on a transplant process but she has been in the hospital for the last few days really sick,thanks a lot
helping to deal with life since husband was diagnosed just a month ago...thank you i just wish there was more help in my area than there is...mobile,alabama
This page is a really good resource and support for those who live with pulmonary fibrosis and those who have had loved ones lose the battle of pf. My mother was diagnosed in December 2013 and passed away in May 2015. Crazy how little we knew about this disease. We were not prepared and want to make a difference . We as siblings have started the "Give Air " foundation to help raise awareness and funds . We want to make a difference . Please check it out and if at all possible donate so we can help find a cure for this horrif... read more
Gracias por la información a sido muy útil pero tengo que usar traductor, tengo año y medio que me diagnosticaron la enfermedad de fibrosis pulmonar ahora me duele las articulaciones de piernas codos u manos dedos voy a checar un reumatólogo me cuido con inhaladores, corticoides y oxigeno 16 horas al día ya vivo a nivel del mar me dicen que es todo lo que se puede hacer que opinan?
Wife of 34 years has been diagnosed with IPF as of 10-05-2015. We will fight it as long as it Takes ! Where's the headquarters for the IPF foundation?
Gracias por dar información sobre esta enfermedad mi madre fallecido por fibrosis pulmonar aquí en Ecuador no hay especialistas en esto y mi madre padecia supuestamente de resfriado fuerte no fue ya al final de la etapa de esta enfermedad que le dijeron que era fibrosis pulmonar fue duro el verla a mi madre es esta etapa de su vida el dolor que sentia hoy mamá ya descansa pero talvez si se ubiera sabido desde un principio de la enfermedad talvez si se ubiera podido hacer algo más poreso creo necesario que las personas sepan ... read more
I'm glad I found this page, I was recently diagnosed with pf
What a wonderful page that I've been following since my father was diagnosed with IPF a few years ago. He always was a fixer and jack of all trades. But this disease couldn't be fixed and he lost his battle this past Monday. Thank you to everyone at the foundation spreading awareness of this horrible disease. Prayers to finding a cure with all your hard work and dedication.
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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