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</div><img alt="" media_type="3" src="https://d2g8igdw686xgo.cloudfront.net/92578023_1753302400363354_r.jpeg" width="100%" />
<div>Hi, my name is Olga Kurpita, and I’m the parent of a beautiful 4-year-old boy named Jonathan who faces more challenges in a single day than many of us can imagine in a lifetime.
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<div>My son is <strong>non-verbal</strong> and has been diagnosed with <strong>severe Autism, genetic mitochondrial dysfunction, neurodevelopmental delay, sensory processing disorder, and OCD</strong>. Every day is a battle for him — from struggling to communicate basic needs to processing the world around him in ways that most therapies have failed to reach. Ohio’s disability Medicaid has played a large role in assisting us with Jonathan's medical bills. However, Medicaid does not cover the majority of the treatments that create lasting change. We pay each pediatric therapy intensive and any therapies outside of PT/OT/speech out of pocket. And so far, we’ve done our absolute best to address these multi-thousand-dollar expenses. We’ve tried so many resources over the past three years — countless local specialists, early intervention programs, and alternative therapies. While we've seen slight progress, it's been minimal. We’ve poured everything we have into giving him the best support possible, but we know in our heart there’s more out there that could truly make a difference.
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<div><strong>That’s why I’m reaching out today.</strong>
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<div><strong>A New Hope in New York</strong>
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<div>After extensive research and speaking to other families, I found a highly respected doctor Robert Melillo, in New York who is a world expert in Neurodevelopmental Disorders. His Melillo Method™ is used to identify brain imbalances and treat many symptoms of mental, attention, behavioral, and learning disorders. This revolutionary approach is paired with diet and nutritional counseling and lifestyle modification to help promote brain and body balance, correcting the underlying problems common to the entire spectrum of seemingly disparate childhood or adult neurological dysfunctions. This intensive program offers a comprehensive, cutting-edge neurological evaluation and intensive therapy program tailored to children just like my son.
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<div>A full neurological examination and consultation
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<div>Visual and auditory processing tests
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<div>Cognitive and developmental testing tailored to his abilities
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<div>Advanced diagnostics like qEEG brain mapping
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<div>Daily therapy sessions using tools such as:
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<div>Cold Laser Therapy with Melillo Method Protocols
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<div>Transcranial stimulation
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<div>Virtual Reality-based neurofeedback
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<div>Rezzimaxx vibration therapy
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<div>Most importantly, one-on-one work with a leading expert who understands the complexity of his condition
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<div>This is a chance at real progress, connection, and relief — for him, and for our family.
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<div><strong>How You Can Help</strong>
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<div>We’re seeking to raise <strong>$30,000 to cover:</strong>
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<div>The full cost of the intensive therapy program
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<div>Travel expenses to and from New York
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<div>Lodging and meals during the stay
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<div>Any necessary follow-up equipment or therapies recommended by the doctor
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<div>Every donation, no matter how small, helps bring us closer to giving my son the chance to experience the world more comfortably — and maybe even speak his first words.
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<div>Your support means everything to us, and we are so grateful for your kindness, prayers, and hope.
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<div><strong>If you can, please take a moment to contribute or share the GoFundMe link with your friend and community.</strong> Your kindness and generosity will help ease the financial burden we are facing.
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<div>Thank you for considering helping Jonathan. Together, we can make a difference in our lives.
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<div>From the bottom of my heart — thank you.
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Anonymous

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Still $14,380 to go. Help us build momentum.