Help Us Support Declan’s Education, Advocacy, and Essential Needs

Our son, Declan, is a bright, loving 5-year-old with big dreams — and big challenges. Declan lives with autism, cerebral palsy, developmental delay, epilepsy, hearing loss, and speech delay. Despite everything he faces, he lights up every room with his smile, determination, and loving heart.

Sadly, instead of receiving the support he needs at school, Declan has been repeatedly removed from class, sent home early, and even suspended for behaviors directly tied to his disabilities. At just five years old, he’s already spending more time excluded from learning than included with his peers. This is not fair, and it is not the education he deserves.

We have done everything we can to advocate for Declan, but the school system is failing him. To make sure his rights are protected and his needs are met, we now need to hire a special education attorney to stand beside us. Legal representation is critical to ensure Declan receives the free, appropriate public education he is entitled to under federal law.

But Declan’s needs extend beyond the school system. He also requires devices and supports that are costly but essential for his safety, communication, and independence. Funds from this campaign will go toward:

Attorney fees for special education legal representation,

Therapies and educational supports not being provided at school,

Communication technology (AAC device/speech-generating device),

Mobility support (wheelchair or adaptive equipment),

Service dog training to assist with safety and independence,

Other therapeutic and medical supports related to his epilepsy and disabilities.

Our goal is to raise $$$ to ensure Declan has both the legal advocacy and the life-changing tools he needs. Every dollar raised goes directly toward fighting for his rights and giving him the best chance to learn, communicate, and thrive.

From the bottom of our hearts, thank you for standing with Declan. Whether you donate, share, or simply send your support, you are making a difference in our son’s life.

With gratitude,

Sean and Stephanie Burrows