MitoAction Energy Walk — Syracuse, NY

Join us this September 15, 2024 at Green Lakes State Park to help us to raise awareness and funds for mito—one step at a time!

Sunday, September 15, 2024
Green Lakes State Park, Fayetteville, NY

Gather your team and get ready to go for a walk all together while raising awareness for mitochondrialRelated to the mitochondria. disease! Whether you walk as an individual, create a team or volunteer, you’re making a difference in the lives of patients and families who rely on us. Your fundraising helps MitoAction change the future of health for every mito patient, here and around the world.

Hosted by the Payne family in honor of their daughter Caroline, Energy Walk Syracuse has raised over $55,000 to raise awareness and support families impacted by mitochondrial disease.

This family event offers support, friendship, and fun for everyone! The day’s highlights include:

• Musical entertainment
• Food & Refreshments
• Unique raffle items
• Kids’ arts & crafts
• Sponsor activities
• Team & individual awards
• And so much more!

Schedule of Events

9:00 am – The Party Starts: On-site Registration/Check-in and festivities begin!
9:00 am – 12:00 pm – face painting and glitter tattoos with The Face Paint Lady, FPL Entertainment, as well as games, raffles, music, character visits, and food and beverage sales.
9:00 am – 10:00 am – Bluey & Bingo visit!
9:45 am – Fun Run Group 1 begins
10:00 am – Runners begin
10:10 am – Walkers begin
11:00 am – 12:00pm – Otto the Orange & Bubble Man Productions visit!
11:50 am – Fun Run Group 2 begins
12:00 am – Raffle Drawing
1:00 pm – Event Ends

2024 Energy Walk Photos

Meet Caroline

Caroline Hope Payne was born 8 weeks premature in 2010, weighing only 2 lbs., 4 oz., resulting in a 47 day stay in the NICU. She is a twin and during pregnancy we discovered she had slow Doppler flow, poor growth, and a hole in her heart. The doctors told us that she would not make it, while her sister was thriving. Two days before the twins were born, the sonogram showed that she had reverse Doppler flow, which caused an immediate admission to the hospital. Regardless, Caroline came out shaking a fist and making the doctors laugh!

In her newborn and toddler years, she missed all the typical milestones and wasn’t gaining weight. At 8 months old, she started physical, occupational, and speech therapy. When Caroline was around 3 years old, I noticed a story on Facebook about a girl with mitochondrial disease that had many of the same symptoms that Caroline seemed to have. I asked the pediatrician about mitochondrial disease and she said it wasn’t something we needed to worry about.

Caroline had a brain MRI at 3 years old which came back showing no issues. But, then in January 2016, when Caroline was 5, a new MRI showed a “significant enlargement” in her brain that was diagnosed quickly as “probably a brain tumor.” This was cause for more testing and of course, more panic. Over a period of 3 days, we met with neurologists, oncologists, radiologists and a pediatric neuro surgeon. More and more doctors weighed in and determined that maybe it wasn’t a tumor after all. Our neurologist ordered a series of tests and diagnosed her with a probable metabolic or genetic condition.

After another EEG, MRI, and multiple other tests, we were referred to the Center for Development, Behavior, and Genetics at Upstate University Hospital in February 2016 for an evaluation of a possible mitochondrial disorder.

On March 17, 2016, Caroline was officially diagnosed with mitochondrial disease with 2 mutationsgenetic variant, genetic change (ND-1 and ATP-8), as well as Leber’s Hereditary Optic Neuropathy.

Caroline is now 10 and a half years old and the smallest of 4 girls in our family. However, she likes to point out that she is 1 minute older than her twin sister! She makes friends and impressions everywhere we go. At school, she is often called “The Mayor.” She still receives physical and occupational therapyTreatments aimed at helping someone complete certain daily tasks of daily living and deals with a heart condition and poor vision. She tires easily, but she doesn’t let that stop her from living life fiercely! She loves to read and watch cooking shows. She is a cheerleader on a special needs cheer team at an all-star gym.

She continues to meet milestones, but on her own timeline. “Though she be but little” – she is a fighter and continues to persevere! Our “Tiny Liney” as we often call her continues to remind us that now matter her size, she is BIG and so is the impact she continues to make on everyone she meets.