Stay tuned for the PFF Summit 2019 program.

To view the PFF Summit 2017 program, click here. The PFF Summit 2017 program included breakout sessions that were designed to suit the needs of different categories of attendees. However, sessions were open to all attendees who were interested. A majority of the sessions were recorded and can be found on our YouTube channel.


Pie In The Face for PF

Many of you may be wondering and many may already know what sparked this passion in me to promote pulmonary fibrosis awareness. Its simple, my child.

Pie (Pulmonary Illness Extinction) Persons are challenged to put a pie in their face within 48 hours of nomination. When challenge is completed, donation is made!

My daughter was diagnosed with idiopathic pulmonary fibrosis August of 2013 and was told she had 2-5 years to live. I have always given to many charities/causes over the years but now its personal. When my daughter was diagnosed I had little knowledge of the impact of this disease and as an RN my initial thoughts were" I can fix this." 

The more research I did, the more I realized the seriousness of this disease and how so little is known about it and its causes. My emotions have gone from denial to anger, because no parent should lose a child before themselves. I know many have and my heart has always gone out to them because I could not even imagine what they must have been going through and now I see myself in those same shoes.

As a Christian I pray everyday for a miracle, as a nurse I pray for a cure, as a mother I pray for not only for my child, but for everyone affected by this dreadful disease. All I am asking is for support to my cause. If you cannot donate, please share for awareness and last but definitely not least pray.  For updates, please visit our Facebook page.

Thank you,

United States of America