Rocklahoma Signed Guitar Auction; Help Ryan Cunningham Live His Dream

Ryan Cunningham (left) is an 8 year old bundle of fun from Dunedin, Florida. Ryan is a huge fan of 80's music!  He was born with Cystic Fibrosis, a horrible disease that attacks the lungs, preventing them from clearing out mucus and disturbs the digestive track. Ryan is forced to take more than 30 pills a day and is often forced to drink protein shakes. He has frequent hospital stays and has to go through daily respiratory therapy. Ryan dreams of attending Rocklahoma and meeting all his favorite rock heroes.

Catch the Fever Music Festivals, Bigg Time Entertainment, Inc., Just Having Fun Productions, Great White, Nelson and Keel are going to make this happen.

Bigg Time Entertainment, Inc. is proud to coordinate this venture.

Just Having Fun Productions, Great White and Nelson is graciously providing airlines tickets for Ryan and his parents Dave & Cathy.

Catch the Fever Music Festivals is kindly providing hotel accommodations and all access passes.

Keel spoke with their endorser, Dean Guitars, and convinced them to donate a guitar for auction.

A guitar signed by Great White, Nelson, Kix and Keel as well as others performing at Rocklahoma 2009 will be auctioned to raise money for miscellaneous expenses of Cunningham’s journey to Rocklahoma as well as the Cystic Fibrosis Foundation www.cff.org. Click here to bid on the donated Dean guitar - and be sure to act fast!

If you wish to donate toward Ryan’s dream of attending Rocklahoma and the Cystic Fibrosis Foundation, PayPal donations to RocklahomaForRyan@att.net

Comments

[Chessie]

I cross-posted this to my Facebook page. :) I just wish I could send something to help.

>^..^<

[Christian]

It sure would be sad if the guitar sells for $150 or something.

[Aunt Debbie]

Ryan is my nephew who I am very proud of. This little guy has gone through so much in his young life with alot of hospital stays and the all treatments he has had to endure. I hoping he gets alot of response not just for him but also for the Cystic Fibrosis Foundation.

[JARED List]

I have cystic fibrosis, and i have to do therapies, take over 30 pills a day, and am constantly trying to get my 4,000 calories everyday, life isn't easy with CF. I got a wish granted from make-a-wish, and i was thinking ryan could do the same thing. I wish ryan the best of luck, and know thAT WE ARE CLOSE TO A CURE and we just have to keep praying for it to come.I am 14 years old and if you believe you can, you will.