The 8th Annual Adult Prom will be postponed to April 30, 2022 at the Peek n' Peak in Clymer, NY from 7pm until midnight. The cost of the ticket will be $75 per person. This will include open bar, snacks, photo booth, professional photographer, and more. All tickets purchased for the 2020 event will still be good for the event. Remaining tickets will go on sale January 1, 2022 at noon. We only have 150 tickets remaining for the event so we expect them to sell out fast. If you reserved a room or a condo, please reach out to the Peek n' Peak to move your reservation. They are expecting your call.

The Adult Prom will be held in both Main Lodge and The Retreat, with shuttles running between them. You will be placed at a table if you purchase a seat ticket at either venue but you are more than welcome to be at either venue to dance, take pictures, and mingle. Just know that you will have a chair at a table. We will have both venues setup the same way for photographers, photo booths, and DJ.

Charlee with her parents at The Adult Prom 2014 at the historic Riverside Inn, Cambridge PA.

Charlee Elizabeth Cook is the eight-year old daughter of Samantha McKissock and Ryan Cook who was diagnosed with cystic fibrosis when she was 1 month old. Cystic fibrosis is a chronic disease that affects the lungs and digestive system. People with cystic fibrosis produce mucus that is abnormally thick and sticky that can obstruct the airways causing severe breathing problems and bacterial infections in the lungs. This disease occurs in 1 in 2500-3500 Caucasian newborns and less in other ethnic groups.

At this stage in Charlee's disease, due to the large amount of mucus her body creates her pancreas is no longer functioning. She now has to, and will always have to take enzymes prior to every meal she eats to do the work of the pancreas- aid in digestion. She also will have to undergo chest physical therapy multiple times a day for the rest of her life. This consists of percussion on her chest, side and back to loosen and break up mucus that damages and causes lung failure.

Charlee make dealing with this disease as easy as possible. She is a beautiful, loving, happy little girl. She is always happy and smiling, and making others do the same. You would never know looking at her of her diagnosis. Thanks to all of the support, fundraisers, donations and her amazing doctor team at children's hospital...we have HOPE. Thank you!

Visit Claire's Place Foundation for the inspiration behind the flash mob!

Help us reach our goal of over $100,000 in the fight against Cystic Fibrosis!