March 25th holds a special place in my heart. It is recognized as National Cerebral Palsy Awareness Day, and this year marks the 20th anniversary of its establishment. This day is more than just a date on the calendar it is a day of recognition, love, strength, and awareness. It’s a day where we celebrate not only individuals living with cerebral palsy, but also the caregivers, families, and support systems who walk this journey alongside them every single day.
On this day people wear green to show their support and to honor the resilience and strength of those affected by cerebral palsy. Green represents growth, hope, and renewal and for many of us, that is exactly what this journey has required.
Cerebral palsy is deeply personal to me because my son has it. Before his diagnosis in 2007 I had never even heard of cerebral palsy. Like many parents I was suddenly introduced to a world I knew nothing about. Even after doctors explained it to me I found myself overwhelmed and still searching for answers. I had to do my own research just to begin understanding what this diagnosis meant for my child and for our lives.
Nineteen years later, I am still learning.
That’s one thing people don’t always realize, this journey doesn’t come with a manual. As your child grows, new challenges, questions, and milestones arise. You learn, adjust, and grow right alongside them.
My son is affected on his right side which is known as hemiplegia cerebral palsy. In his case he is unable to walk and is nonverbal. He uses a wheelchair and depends on us completely for his daily care. Our life looks different from many others but that doesn’t make it any less meaningful or filled with love.
One of the most important things I’ve learned is that cerebral palsy is not the same for everyone. It is not a one-size-fits-all diagnosis. Some individuals are able to walk independently or with assistance. Some can communicate verbally or with devices. Many can do things that others may not expect. And in some cases, like my son’s, individuals require full support for everyday living.
Every story is different. Every journey is unique. And every single one deserves to be seen, heard, and valued.
I’ll be honest, sometimes I feel like cerebral palsy doesn’t receive as much awareness or attention as other diagnoses. But what gives me strength is the community. I have met some truly incredible parents and caregivers who advocate tirelessly. They make sure the world knows that our children are here, that they matter, and that their stories deserve to be told.
This journey has taught me patience, strength, resilience, and a kind of love that runs deeper than words can explain. My son has shown me what it means to fight every day, to keep going, and to find joy in moments others might overlook.
So on March 25th, I wear green not just for awareness but for my son. For his strength. For his journey. For every milestone, big or small. And for every family walking a similar path.
Let this day be a reminder:
Our children matter.
Their lives matter.
Their stories matter.
And they deserve to be seen every single day.
