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lisabev

172 profile views
1 reviews

Review for Pulmonary Fibrosis Foundation, Chicago, IL, USA

Rating: 5 stars  

My father was diagnosed with Pulmonary Fibrosis in October 2010. At that time we never heard of this disease. After my father's diagnosis we began to research IPF and was horrified to learn that there is no cure and very little awareness. I am saddened to say that my father lost his battle from IPF On December 21, 2010. After my father's passing my family embarked on a mission to raise funds and awareness for this disease. We have since held two fundraising walks in memory of my father and have combined raised a total of $30,000. This would not have been possible without the help and support of the Pulmonary Fibrosis Foundation. The Pulmonary Fibrosis Foundation is a wonderful foundation that works extremly hard to fight the battle to find a cure for this unforgiving disease. The staff is amazing and so supportive from organizing a fundraising event to allowing people to connect with others that have been touched by this disease. The Pulmonary Fibrosis Foundation IS A GREAT NON PROFIT!

Would you volunteer for this group again?

Definitely

For the time you spent, how much of an impact did you feel your work or activity had?

Life-changing

Did the organization use your time wisely?

Very Well

Would you recommend this group to a friend?

Definitely

When was your last experience with this nonprofit?

2012

Role:  Volunteer