Hello, I’m looking forward to our call. 

In 2011, I was diagnosed with Idiopathic Pulmonary Fibrosis (IPF). At the time of my diagnosis, I was given no hope for my future life. Three years later, I founded the PF Warriors as a way for patients to help other patients and families of those living with Interstitial Lung Diseases (ILD). 
Since our founding in 2014, we have grown into a global resource of over 2,000 members, addressing strategies for understanding and living with pulmonary fibrosis and other ILDs. Along with being a resource for publications and learning guides, the PF Warriors hold regular meetings and private online groups for members only, through our strong social media presence. 

The PF Warriors are the voice of the patients and families living with pulmonary fibrosis. We are the ear that listens and the shoulder to lean on, to support our community of patients, caregivers, families, and their medical teams.

We Are the Voice of The Patientb

bill@pfwarrior.com
+1 972-612-8425 (central time)
https://PFWarriors.com
 
 
Our Zoom meeting link
 
A few links about me and the PF Warriors:
Our website
Bill Vick LinkedIn Profile
Our public Facebook News Page
Bill Vick Facebook Profile
Our Twitter account
Join us!
 
Some important links for using Zoom: 
Unless you have already downloaded Zoom you will want to download the Zoom program for your desktop or mobile device. Also included, is a short video tutorial on using Zoom.