When Summer Is Hard: A Note for Parents of Children with Special Needs

Summer is supposed to be easy. For parents of children with special needs, it rarely is. You're not alone — and support is closer than you think.

5/22/20265 min read

boy in blue shirt screaming near boy in green crew-neck shirt
boy in blue shirt screaming near boy in green crew-neck shirt

When Summer Is Hard: A Note for Parents of Children with Special Needs

By Michelle Stantial, M.A., LPC-Associate | Woodlands Haven Counseling

Summer is supposed to be the easy season. No school schedules, no IEP meetings, no early mornings fighting over backpacks and routines. And yet, if you're a parent of a child with special needs, you may be reading this with a quiet, exhausted laugh — because you know that summer is often anything but easy.

You are not alone in that. And you are not failing.

The Reality of Summer When Your Child Has Special Needs

For most families, summer means more flexibility. For families raising children with autism, intellectual disabilities, cerebral palsy, or other complex needs, summer often means the sudden loss of the structure, services, and support systems that make the rest of the year manageable. Therapies slow down or pause. School-based supports disappear. The routines that took months to build get disrupted overnight. And the parent — usually the mother — is left holding it all together with very little left in reserve.

Research confirms what you already feel in your bones. Studies show that between 5–9% of parents overall experience clinical-level caregiver burnout, with significantly higher rates among parents of children with special needs. One 2025 study published in Frontiers in Psychology found that parental burnout in this population is driven by a combination of unmet caregiver needs, self-stigma — the quiet shame of admitting you're struggling — and a lack of family resilience support. Another study found that nearly 50% of the variance in parental burnout among mothers of children with special needs could be explained by the intersection of caregiver burden, limited social support, and emotional exhaustion.

In other words: what you are experiencing has a name, it has data behind it, and it is not a reflection of how much you love your child.

The Child Nobody Is Asking About

There is another person in your house this summer who may be struggling quietly — your typically developing child.

When one sibling has complex needs, the attention, energy, and family resources that flow toward that child are not evenly distributed. That is not neglect. It is reality. But research from the Sibling Support Project at the University of Washington confirms that siblings of children with special needs "have the same issues as parents, plus issues that are uniquely their own." They may feel invisible. They may feel guilty for wanting a normal summer. They may feel resentful — and then feel ashamed of the resentment.

As one researcher put it, siblings of children with disabilities often "suffer silently," because there is no space in the family's bandwidth to hold their feelings too.

This summer, your other child may be watching their friends go to the pool, to camp, to sleepovers — while your family's plans bend around therapies, meltdowns, and the unpredictable rhythms of a sibling with high needs. That child needs to be seen. They need to hear — directly, from you — that their feelings make sense, that they are not selfish for having them, and that you see them.

You cannot pour from an empty cup. Which brings us back to you.

What Burnout Actually Looks Like

Caregiver burnout does not always look like falling apart. More often it looks like this:

  • Feeling emotionally numb or detached from your child, even when you love them deeply

  • Dreading the morning before you've even opened your eyes

  • Snapping at your other children or your partner over small things

  • Feeling like you are just going through the motions — present in body, absent everywhere else

  • Losing track of who you are outside of being a caregiver

  • Telling yourself you'll ask for help when things calm down — while things never calm down

If any of that sounds familiar, please hear this: burnout is not a character flaw. It is a physiological and psychological response to sustained, unrelenting demand. Research shows that chronic caregiving stress elevates cortisol levels, compromises immune function, and significantly increases risk for depression and anxiety. Your body is not broken. It is responding exactly as a human body does when it has been running on empty for too long.

What You Can Do Right Now

You do not have to overhaul your life this summer. But small, intentional moves matter.

Give your other child something of their own. It does not have to be expensive or elaborate — a weekly one-on-one outing, a standing movie night, a walk together without the sibling. What your typically developing child needs most is your undivided attention, even briefly. Let them talk. Let them complain. Resist the urge to defend or explain. Just listen.

Name the guilt out loud. The guilt you feel about your other child, about your marriage, about your own needs — it grows in silence. Saying it aloud to a trusted person, even once, takes some of its power away.

Lower the bar on what summer needs to look like. Your family does not need to have a Pinterest summer. It needs to survive, stay connected, and find small moments of joy. That is enough.

Let someone help you. This is the hardest one. Parents of children with special needs are often so practiced at being the expert in the room — the one who knows their child's triggers, routines, and needs — that accepting help feels impossible. But isolation is one of the primary drivers of burnout. Reach out to another parent who gets it. Find a support group. Let a neighbor bring dinner.

Thinking About Fall

Here is something worth considering: fall is coming, and with it the return of school, structure, and a slightly more predictable rhythm. That transition, for many parents, brings relief — but it also surfaces everything that got pushed down during the summer. The exhaustion catches up. The grief about the year ahead sets in. The worry about a new teacher, a new classroom, a new IEP cycle begins.

Fall is often when parents finally have enough breathing room to realize just how depleted they actually are.

If you have been thinking about talking to someone — a therapist, a counselor, someone who understands what this kind of caregiving actually costs — fall is a natural and meaningful time to start. Not because you have to wait until then, but because many parents find that having something lined up for fall gives them something to hold onto through the rest of summer.

You deserve support that is just for you. Not for your child's next evaluation. Not for your family's next crisis. Just for you — the person behind the caregiving.

You Are Doing Something Hard

There is a particular kind of strength that parents of children with special needs develop over time. It is forged in waiting rooms and IEP meetings, in midnight Google searches and insurance appeals, in the hundred small negotiations that make up an ordinary Tuesday. It does not always feel like strength. It often feels like exhaustion wearing strength's clothing.

But you are doing something genuinely hard. And the fact that it is hard does not mean you are doing it wrong.

If you are in The Woodlands area or anywhere in Texas and would like to talk, I offer a free 15-minute consultation — no pressure, no commitment. Just a conversation.

Woodlands Haven Counseling Michelle Stantial, M.A., LPC-Associate Supervised by Cynthia Nava, M.S., LPC-S 📍 719 Sawdust Rd., Suite 104, The Woodlands, TX 📞 (832) 996-2888 🌐 woodlandshaven.com

Evening and Saturday appointments available. In-person and telehealth. Sliding scale spots available.

This blog post is intended for informational and supportive purposes only and does not constitute therapy or clinical advice. If you are experiencing a mental health crisis, please contact the 988 Suicide and Crisis Lifeline by calling or texting 988.

Sources & Further Reading

  • Frontiers in Psychology (2025): Caregiver burnout among mothers of children with special needs

  • Sibling Support Project, University of Washington

  • NIH/PMC: Parental burnout research and protective factors

  • Psychiatry Advisor: Emotional challenges facing siblings of children with disabilities

Woodlands Haven, PLLC

Contact

719 Sawdust Rd., Suite 104

The Woodlands, TX 77380

(832) 996-2888

Michelle@WoodlandsHaven.com