Pickin’ of Cystic Fibrosis Benefit Concert

Featuring

Detour Bluegrass

Saturday, April 14, 2012

Zellie’s Opry House, Howard City, Michigan

Doors open at 6:00 p.m. with a pre-show at 6:10 p.m. and the concert at 7:00 p.m.

 

Zellies has donated the use of their wonderful facility for this benefit, and we thank them for their generosity. All the concerts tickets at Zellies are $5.00.

Additional donations to help find a cure for Cystic Fibrosis will be welcomed.

Check out Zellie’s site, and read more by clicking ‘Special Event Notices’ and scrolling down.

Advance tickets are available by mail on the Zellie’s site

 

 

2012 Dates Announced

The dates for the 6th Pickin’ on Cystic Fibrosis will be September 6-8, 2012. The festival raises funds for research to find a cure for Cystic Fibrosis.

Watch for a band line-up, schedule and other exciting news coming soon!

Raffle Winner

Kurt Hickman was the winner of the raffle. Here is a picture of Kurt with his prize, White River Acoustics guitar #1..

Congratulations to Kurt, and thanks to all of you who purchased tickets. Proceeds benefited Cystic Fibrosis Research.

Pickin on Cystic Fibrosis

The 2011 Pickin on Cystic Fibrosis festival in Milan, Michigan was once again plagued by rain storms.  As the winds shifted from the east to the west the rain came. It rained all day Wednesday, most of Thursday and Friday, and the festival had to be moved inside. Saturday was not much better with the threat of rain all day, but it held off until the evening. Despite the rough weather conditions the festival went on as planned. Lots of great music and a very enthusiastic, but small crowd had a great time.

It has been a very difficult couple of years trying to get this festival off the ground. We have had a lot of support from the bands that have played the festival. The fans that have weathered the storm with us have been the best. We just haven’t had cooperation from Mother Nature.

We are planning on continuing with the festival. I find it is very rare for a child with Cystic Fibrosis, or any other life threatening disease to give up. Why should we? This is not just a bluegrass festival, it is a celebration of the advancements made in the treatments of CF. There is no cure, and without events to raise money for research there never will be. I’m not willing to accept that. We will continue our efforts and do our best to build a great festival that helps add longevity to lives of those with CF.

Thank you to all that have supported our festival.

Jimmy Kittle

Pickin on Cystic Fibrosis

Raffle Tickets are Available

Guitar Raffle
Benefiting Cystic Fibrosis Research

               

 

First Prize

White River Guitar #1 OR White River Mandolin #1

White River Guitar #1

Second Prize

CD bundle of artists performing at the festival

Third Prize

GHS Accessory Pack

 

Drawing will be held September 10th at 8 pm.
at the Pickin’ on Cystic Fibrosis Bluegrass Festival

(Need not be Present to Win)

Proceeds will be donated to Hunt for a Cure supporting research for better treatments and a cure for Cystic Fibrosis

Tickets $10 each

Michigan Raffle License # R11071

The Performance Schedule is posted

You can access it from the top menu or from this link.

New Message

Please take a few minutes to read Jimmy’s new message, posted this morning.

Tickets Available Now

Advance weekend tickets for Pickin’ on Cystic Fibrosis have been printed and are available now. Tickets are $25, children under 16 are free with a paying adult. Admission at the gate will be $35 weekend, $10 Thursday evening, $15 Friday or Saturday.  You may send a self-addressed stamped envelope with a check made out to Hunt for a Cure to:

Jim Kittle
246 N. Dickinson Ave
Hesperia MI  49421

Camping reservations may be made by phoning KC Campground, 734-439-1076.

One of 30,000 Reasons for a Bluegrass Festival

Pickin on Cystic Fibrosis
Presents

Tai Clark

Tai Clark

Tai Clark

Thirty thousand children and young adults in the US are affected by Cystic Fibrosis. CF is a genetic disease that affects the lungs and digestive system. The median age of those with CF is 36 years of age. Although the treatments have improved over the past 10 years, there is no cure. Pickin on Cystic Fibrosis (POCF) is a bluegrass festival that raises money for research to find better treatments and ultimately a cure for CF.

The following is an introduction to one of those young adults with CF. We’re very proud to have her as part of our POCF family

Tai Clark makes her home McConnelsville, Ohio. Along with her family, Dad Marvin, and Mom Deana, they run the Ohio Valley Opry (OVO). Before starting the OVO the Clark’s traveled as a family band and spread their faith at Churches throughout the states.  They are a family that stands true to their faith. They are not only dealing with Tai having CF, this family has 4 girls, three of the girls have CF. Tai’s older sister Leah, and younger sister Jada, both have CF. She also has a younger sister Elaina, that does not have CF. Believe me, this requires a lot of breathing treatments and medicine just to get through the day.

Tai’s family has been singing Gospel and Country music since before she was born. In fact, just 13 days before Tai was born her mother was singing in Church. Tai says, she “can’t remember not singing”. She’s been at it her entire 20 years.

Her musical interests are singing country, bluegrass, and gospel. She likes to listen to most anything that is good. On any given day you may find her listening to Big Band, the Punch Brothers, anything from the Lonesome River Band to Merle Haggard. A few of her musical influences are Ronnie Milsap, Tammy Wynette, Alison Krauss and Dawn Sears.  You can often also catch her playing guitar or mandolin with the staff band at the Ohio Valley Opry.

Along with the daily grind of CF, Tai also has diabetes. This is quite common for those with Cystic Fibrosis. It only adds more to the daily regime of treatments and medicine. It also adds constantly watching her diet and taking insulin to remain healthy.

Through all this, Tai goes to school at Washington State College in Marietta, and is finishing her liberal arts degree.  She also works as a barista at a coffee shop in Marietta.

Tai knows she and her sisters have been fortunate, if you can call having CF fortunate. Their health has remained fairly stable. This is not the case for many that have this disease. Many have routine hospital stays throughout the year. They deal with multiple lung infections and digestive issues. Many children lose their battle with CF before they reach adulthood.

Tai Clark is a reminder for us all to be better people.  The Pickin on Cystic Fibrosis staff wish her and her family many, many years of happiness and continued good health.

The mission of Pickin on Cystic Fibrosis is to support the Hunt for a Cure organization in funding research projects for better treatments, and ultimately a cure.  We hope you take the time to visit our web sites and learn a little bit about what we do. Mostly, we hope you will visit and support our festival and our sponsors. Maybe, just maybe we can make life better for the 30,000 children and young adults like Tai.

Pickin on Cystic Fibrosis Bluegrass Festival

www.pickinoncf.com

www.huntforacure.org

September 8th, 9th, 10th 2011

KC Campgrounds
14048 Sherman Rd. Milan
Michigan 48160

The Flyer is Posted

We have posted this year’s flyer. You can access a PDF version here.

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