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!!!



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

The Coalition for Pulmonary Fibrosis is the nation's largest nonprofit organization representing the PF community.
www.coalitionforpf.org or (888) 222-8541

Flaming and/or SPAM will not be tolerated.

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