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If you’re the parent or caregiver of someone on the autism spectrum, you’ve probably felt whiplashed by recent headlines. On one hand, you’re hearing promises that the federal government will solve autism’s causes by September. On the other hand, you’re reading about research funding cuts and scientists speaking out against misleading claims. As families who’ve […]
If you’ve been feeling a knot in your stomach lately about news reports mentioning “budget cuts” and “Medicaid reductions,” you’re not alone. As parents and caregivers of individuals with developmental and intellectual disabilities, we know that behind every policy headline is a real family wondering: Will my loved one still have the support they need? […]
You love fiercely. You’ve moved mountains for your family member. You’ve learned medical terms you never expected to know, advocated in rooms where you felt out of place, and found strength you didn’t know you had. If you’re here reading this, it’s probably because that same love that drives you is also whispering: “There has […]
Right now, you might be sitting with this diagnosis, feeling like the ground has shifted beneath your feet. Maybe you’re questioning everything, or feeling protective, or even relieved to finally have answers. Whether this news came suddenly or you’ve been expecting it for a while, whatever you’re feeling is exactly right for where you are […]
Have you ever watched someone you love struggle with something that used to be effortless? Maybe it was your father pausing at the checkbook, pencil hovering, confusion clouding his eyes. Or your sister taking twice as long to button her coat, frustration tightening her features. Or maybe it was yourself, realizing one ordinary Tuesday that […]
It’s 3 AM. You’ve finally fallen asleep after helping your loved one through another difficult evening when the soft call comes again. As you rise, for the third time tonight, you catch your reflection. The person looking back appears more exhausted than you’re ready to admit. When was the last time you slept through the […]
Dear Friends, Colleagues, and Community Members, As I look at the photograph of our dedicated team gathered together… I’m filled with immense pride and gratitude. Twenty years ago, Community Direct Services began with a simple yet powerful vision. To provide personalized, compassionate care that truly empowers individuals with mental and physical disabilities to live with […]
As a parent of a child with special needs, you’ve mastered the art of multitasking. Medication schedules, therapy appointments, doctor visits, school meetings. Each day brings a new logistical puzzle. Many parents tell us they’ve memorized phone numbers of specialists they never imagined they’d need and can recite insurance codes in their sleep. What if […]
As a parent of a child with disabilities, you already know what it means to be a fierce advocate. You’ve mastered medical terminology, navigated complex systems, and fought tirelessly for your child’s needs. Now, there’s another challenge on the horizon. Proposed Medicaid cuts in 2025 that could fundamentally alter the support your family depends on. […]
Ever notice how you’re constantly building bridges between what your loved one needs and what’s actually available through existing support systems? That space, what we call “The Care Gap”, has been widening for many families lately. The distance between ideal care and available resources grows larger. Forcing you to construct increasingly complex bridges to span […]
