2008 - 50 Events in 50 States

 

Ohio

 


 

A Barn Sale

 

Ohio Style

 

Vicki Mountain hosts her Seventh Annual Barn in memory of Lawrence Bray.  The event starts October 10th at 12pm and ends October 12th at 3pm. 

You can donate items, peruse the preused, or just come out and support.

For more information contact the Foundation:
pulmonaryfibrosisinfo

@yahoo.com
312-587-9272

 

 

Invite your friends via Facebook!

 


 

 


 

 

 


 


Dad in Maui 2006

Christine Poleon to Run Marathon in
Honor of her Father, Robert Poleon

In December of 2006 my father, Robert Poleon was diagnosed with idiopathic pulmonary fibrosis. It is a lung disease of unknown origin. Although there are treatments, there is no cure at this time.

To raise awareness and funds for research, I am training to run my first marathon in January. I am asking friends, family and corporate sponsors to donate money for each mile I run in training, weekend races and "The Marathon." The website will have a tally of miles on a monthly basis. You can donate based on the miles I log. Challenge me to do more for donations. Or simply donate an amount of your choosing.

Pennies, nickels, dimes and dollar bills will all make a difference. The funds you donate will go directly to The Pulmonary Fibrosis Foundation. Cash gifts are deductible from federal income tax up to 50% of your gross income, with a 5 year carry over. You will receive a receipt for your tax records.

Check donations may be mailed to:
Pulmonary Fibrosis Foundation
1332 North Halsted Street, Suite 201
Chicago, Illinois 60622

To donate on line click below:
http://www.active.com/donate/pulmonaryfibrosis/robertjpoleon

 

This isn't just about awareness or money. It is about hope. Hope he will one day walk me down the aisle. Hope he will one day hold my first born child.

Thank you for your support!

Christine

As of 8.20.07 22 miles and counting!

 

   

 

Smarty Pants Theater Co.

Fred Leeds & Matt Derda Will Present a Benefit Performance to Raise Funds for the Pulmonary Fibrosis Foundation's Research Program to Find a Cure for Pulmonary Fibrosis
at
The Shoe Factory Antique Mall
120 E. South Street.
Lebanon, Ohio 45036

The performances will begin at 7:00 PM on January 19th & 20th, 2007

There will be a social hour with beverages served from 6:00 PM - 7:00 PM.
This will be an opportunity to meet the artists
and make donations to this worthy cause.

The program will involve improvisations, stand up comics, sketches and other acts.

Ticket are $10.00 to benefit the fight against Pulmonary Fibrosis

For more information call Matt Derda at 513-850-3574

or

Krysten Knievel, Events Coordinator

Pulmonary Fibrosis Foundation
1332 N. Halsted St. Suite 201
Chicago, IL 60622

312.587.9272


  7th Flying Pig Marathon

Sunday, May 1, 2005

 In memory of Tom Murray who passed away from Pulmonary Fibrosis on December 4,  2003

Support the fight against Pulmonary Fibrosis. There are more than 200,000 people in the United States who are suffering from this deadly disease. Of these 40,000 die every year. Only through research which is fully supported by the Foundation will a cure be found. The Flying Pig Marathon is an annual full 26.2 mile marathon. I have been running for many years and have ran in the Boston Marathon, New York and several others. I also have had a setback. Last September I suffered a stroke, combine that with rotator cuff surgery recently, I feel fortunate to walk this year's event. I will be joined by my wife, Diane, and two of her sister's Ellie and Kathy. Two of my brother-in-laws (Joe and Tom G.) will also be competing in running the event. We have another sister-in-law who will be walking the 1/2 marathon portion.  You might say this is a family event.  

Donations may be sent to the Pulmonary Fibrosis Foundation at 1332 N. Halsted St. Chicago, IL 60622

312.587.9272

 

Dad was never one to complain so we didn’t realize the seriousness of his health.  He went in for back surgery on November 4 expecting to come home the following day. Three weeks later, after numerous tests Dad was diagnosed with “end stage Pulmonary Fibrosis”, a disease whose cause is unknown and a disease for which there is no known cure.  The hospital presented us with two options: a nursing home or we care for him at home.   There was only one option, Dad was coming home. Before his discharge, we had a family meeting to ensure that we had round the clock care.  After Dad was home for two days, we realized that a schedule wasn’t necessary.   The family was always there, waiting to hear his next words, wanting just one more minute with him.  Meanwhile, mom was back cooking for an army. 

Dad was a kind and gentle man who was always concerned about others. He never wanted anyone to fuss over him. He was authentically interested and involved with each and every one of us.  He worried that his illness was keeping us from our work and our families.  He worried about mom and how hard it would be on her. During his last days we noticed a tenderness between our parents, that was always there, we were just too busy with our everyday lives to notice. Even when we thought Dad was most likely feeling very miserable he always managed to make us laugh. His Irish wit was unmatched. He entertained the grandchildren, nurses and visitors at the hospital. Whenever the grandchildren entered the room, his face would light up. We shared many many tears but also much laughter during his last week at home. Thanksgiving Day dad was home. We all gathered around his bed hanging on every little gesture, smile and word.  It was a struggle for Dad to talk and we could tell he had something to say. The room grew deafly silent while we waited for Dad to speak. He whispered two words, “Thank You”. Dad we just want to say.... Thank You! This is just the type of man he was, never expecting anything from anyone and always appreciative.  

This past Thanksgiving will be the most meaningful to all of the Murray’s.  Although it was very sad, we have great comfort in being a part of this family. We have been blessed to have the opportunity to care for the man who has provided everything to us.  After Dad passed, Mom gathered the family and led us in a prayer.   At the end of the prayer Mom said, “I have always told you to make the most of your hellos to help you through the good-bye’s”. Dad with this we are saying good-bye, and although we’re going to dearly miss you, I know that you are watching over us and that everything is the way God meant it to be.  

Tom Quinlan

Tom Quinlan is the son in law to Tom Murray tomquinlan@insightbb.com