Have you been diagnosed with **Pulmonary Fibrosis?**

Got questions? Need answers?



Do you know a loved one with **pulmonary fibrosis?**
Have you lost a loved one to **pulmonary fibrosis?**


Then this is the group for you!!

Whether you are the PF patient, or have a loved one with PF, or have lost a loved one to this disease, our group can help you unravel and understand the complexities of this disease.

Together we can grow and learn more about **PF** through the help and comfort of each other.

Just so you know we are a fun group of people. Our board discusses pf, treatments, what works for us, how to deal with symptoms, etc... BUT we also discuss our families, grandchildren/children, politics, jokes, humorous stories, and we like to discuss tv shows.

Anything can be discussed in this group as long as it is civil!!!
Flaming and/or SPAM will not be tolerated.


***Any medical concerns should be directed to your physician or your pulmonologist. Information shared is not medical advice.***

Pulmonary Fibrosis Foundation
http://www.pulmonaryfibrosis.org
or 312-587-9272

Join us on facebook - http://www.facebook.com/PulmonaryFibrosisFoundation

Join us on twitter - @PFFORG

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