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

Got questions? Need answers?

Then this is the group for you!!

If you are the pf patient, or have a loved one with pf, this 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.

***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.

Take care,


Jennifer
Owner, PF Yahoo boards

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