(Photos courtesy of Slice of Columbus)
Join us on Wednesday, September 12, for Slice of Columbus! Proceeds benefit Nationwide Children’s Hospital.
Slice of Columbus is Ohio’s LARGEST pizza event — and it’s all for a great cause. On Wednesday, September 12, in the Columbus Commons, you can enjoy pizza, entertainment and community from 5 to 9 p.m.
Enjoy pizza samples from numerous local shops, and then vote for your favorites in the People’s Choice Award! While you’re savoring pizza, there will be live music by The Conspiracy Band.
Slice of Columbus is a family friendly night, full of children’s activities and fun. There’ll be putt putt, face painting, arts and crafts, bouncy houses and more!
Act now; buy your tickets today online! Purchase your tickets in advance to take advantage of early bird pricing. All tickets include unlimited pizza and entertainment.
|Youth (6-17 years)||$8||$10|
|Adult (18+ years)||$15||$18|
|VIP Youth (6-17 years)**||$20||$25|
|VIP Adult (18+ years)**||$75||$85|
Children 5 and under are FREE.
* Family Package includes 2 adults (18+), up to 3 children (6-17 years) and 5 Pepsi products (soft drinks and water).
** VIP section allows for private tent access, no pizza lines, complimentary Pepsi products (soft drinks and bottled water), complimentary craft beer and wine (21+), complimentary snacks and sides (salads, bread sticks, desserts, etc.), and free parking with ticket purchased prior to September 7.
Your participation in Slice of Columbus helps kids just like Kaleb and Mia!
Kaleb and Mia both had their first seizure in January of 2013, within just three weeks of each other. Tests determined that Mia and Kaleb both had epilepsy. However, their neurologist in Florida wanted to do further testing since the anti-epileptic drugs were not working.
In August of 2013, the Diaz family had genetic testing done. In November 2013, they received their diagnosis; both Mia and Kaleb had Batten disease.
Batten disease is a progressive neurological disease. Currently, there is no cure. Patients with Batten’s experience cognitive impairment, loss of developmental milestones, epilepsy and sight impairments. Life expectancy for those with Batten disease is 8 to 12 years old. Researchers at Nationwide Children’s are working to slow down the regression of the disease and move closer toward finding a cure.
A few months into treatment at Nationwide Children’s, her family noticed that the seizures were shorter in duration, not as intense and not as frequent.
It’s been a little over three years since Mia’s first infusion and she hasn’t had a seizure in over two years. She is still able to eat by mouth and retains her vision. Mia loves being her friends and going to the playground. She loves Chick Fil A, swimming, riding roller coasters and jet skiing.
With there being limited spots in the trial, Kaleb began treatment 19 months after Mia.
In the words of his mother, Barbara, “He is able to give those amazing cuddles that only he knows how to give. He is taking steps in his gait trainer and able to eat by mouth again. He is happy and getting stronger each day.” Kaleb loves music, being outdoors, swimming, Mickey Mouse and Nutella.
Every other week, Mia and Kaleb are admitted for infusions and stay overnight each time. They also come in for therapy and to see their specialists in neurology, pulmonology, GI and optometry.
“To our family, Nationwide Children’s means hope. It’s a place that has provided us optimism in a time when we thought all hope was gone. Because of Nationwide Children’s, we get to make more memories and we get to enjoy more time with our children. I can honestly say that Mia and Kaleb are still enjoying life and that they wouldn’t be here today without the enzyme replacement therapy — a treatment that wouldn’t be possible without research,” says Barbara, Mia and Kaleb’s mother.