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Autism Day by Day — the guide I needed when I was you. · Jul 24, 2026

Breaking is Not An Option

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Donna Ross-Jones · Autism Day by Day — the guide I needed when I was you.

There were days when my standard for success was not noble.

Nobody died today.

Good day.

That is not a joke, except sometimes you laugh because the alternative is to sit down on the floor and never get back up.

That is the kind of thing autism mothers understand about each other without explanation.

When another mom said, “We might crack sometimes, but we don’t break,” it stopped me. Not because it was poetic. Because every autism mother I know understood it immediately. We know the sound of cracking.

We know what it feels like when the pressure has been sitting on the same place for too many years. We know the private moments nobody sees. The phone calls made from parked cars. The paperwork spread across kitchen tables. The meetings where we were polite because polite got us further than screaming, even when screaming would have been the more honest response.

We know the beam does not break because it is never allowed to.

There are children under it.

There are adults under it.

There are futures under it.

There are siblings under it.

There are housing payments, school, therapy, recreational and staff schedules, medication refills, IEPs, IPPs, service denials, transition plans, dental appointments, doctor appointments, crisis plans, and the quiet lingering ever present terror of what happens when we are no longer here to hold up the ceiling.

So we crack. Then we keep holding.

That is what this mom and I were really talking about.

Not inspiration. Not strength in the shiny, social media way. The other kind. The kind you do because there is no one else in the room.

“We might crack sometimes, but we don’t break.”

That sentence has stayed with me because it carries the whole truth of our lives in eight words.

It does not pretend we are fine.

It does not pretend we are unshakable.

It does not call us warriors, which I have never liked because most of us did not volunteer for battle. We were drafted. We were handed a diagnosis, a system, a child we loved more than language could hold, and a world that expected us to figure it out while acting grateful for every crumb of help.

So yes.

We cracked. Of course we cracked.

What kind of woman would not crack under the weight of loving a child the world keeps misunderstanding?

The mom I was talking to was Susan, she founded Bright Path for Autism because families need guidance through transition. That word — transition — sounds so clean when systems use it. So organized. So reasonable.

Transition.

As if a child becoming an adult with autism is a hallway with signs on the wall.

This way to services.

This way to housing.

This way to employment.

This way to dignity.

Anyone who has lived it knows better. Transition is often a cliff. And many parents arrive at the edge still holding the wrong map. I know that cliff. I was pushed off it years ago and told to learn how to fly on the way down.

Single mother. Business owner. Autism advocate. Sole financial provider. One child needing full-time support. Another child needing a mother who was not always available in the ways they deserved. A company to run. A household to hold together. A system to learn because nobody handed me the real instructions.

There were days when my standard for success was not noble. Nobody died today. Good day. That is not a joke, except sometimes you laugh because the alternative is to sit down on the floor and never get back up. That is the kind of thing autism mothers understand about each other without explanation. We do not need the softened version. We do not need the speech.

We do not need someone telling us how strong we are when what we actually need is a trained provider who shows up, a system that works, a school that tells the truth, a regional center that does not make families beg for what their children are entitled to receive, and a public that understands our children are not problems to be hidden.

There is a particular anger that comes with doing this work for decades.

Not bitterness.

Anger.

Clean anger.

Earned anger.

The kind that comes from looking around after twenty-five, thirty, forty years of advocacy and realizing the systems should be better by now.

They should be.

That sentence sits in me hard.

The systems should be better by now.

Parents should not still be finding out too late that a diploma can end services.

Families should not still be walking into transition without understanding what disappears at twenty-two.

Mothers should not still be translating every system to every other system because nobody built a bridge.

We should not still be asking exhausted parents to become legal researchers, case managers, behavior specialists, benefits coordinators, housing planners, crisis responders, employment developers, transportation experts, and emotional shock absorbers.

But here we are.

Still building the bridge while standing over the canyon.

That is why conversations like the one I had with Susan matter.

Because something happens when two autism mothers talk without performing for anyone.

The room changes.

You do not have to explain the math.

You do not have to prove the weight.

You do not have to say, “I love my child,” before saying, “I am tired.”

She knows.

You do not have to dress up the truth so nobody misunderstands it.

She understands.

You can say the hard thing, the real thing, the sentence that would make someone outside this life uncomfortable, and another mother will not flinch.

That is rare. It is also holy. Because most of the time, mothers like us are managing translation.

We translate our children to the world.

We translate systems to our children.

We translate professionals to staff.

We translate behavior into meaning.

We translate fear into plans.

We translate exhaustion into calendars.

We translate love into structure.

And then, after all of that, we are expected to translate ourselves into something palatable.

Not too angry.

Not too honest.

Not too tired.

Not too demanding.

Not too much.

I am 67 years old.

I am done making the truth smaller so it can fit into rooms that were never built for families like mine.

Susan’s work matters because families need people who know the path. Not in theory. Not from a brochure. Not from a conference panel where everyone nods and nothing changes.

From lived experience.

From the cracked beam.

From the mother who knows where the floor gave out and came back to mark the hole for the next family. That is what autism mothers do when we are at our best. We leave markings. Not because we had an easy road. Because we did not.

We say, “Watch this corner.”

We say, “Ask for this in writing.”

We say, “Do not let them rush you.”

We say, “Start planning earlier than you think.”

We say, “Your child is not done becoming.”

We say, “Do not confuse services on paper with support in real life.”

We say, “Love brought you here. Strategy is what builds the future.”

And sometimes we say nothing. Sometimes we just sit across from each other and let the truth breathe. Because the truth is, we are tired.

We are proud.

We are grateful.

We are angry.

We are still laughing at things no one else would find funny.

We are still fighting battles that should have been solved before our children became adults.

We are still here.

Cracked, maybe.

Not broken.

There is a difference.

I think about the beams in old houses. The ones that have held too much for too long. If you look closely, you can see the stress lines. You can see where the weight gathered. You can see the places where time left its mark.

But the house is still standing. Not because the beam was untouched. Because it kept doing its job. That is not something to romanticize. It is something to respect. And it is something to relieve whenever possible. Because no beam should have to hold forever without support. That is the part I want the world to understand about autism mothers.

Do not admire our strength and then leave us under the weight.

Do not call us amazing when what we need is access.

Do not call us resilient when what we need is staffing.

Do not praise our advocacy while keeping the doors locked.

Do not turn our survival into a compliment.

Help change what keeps requiring it.

The next time you sit with a mother raising a child with autism — especially one moving into adulthood — resist the urge to fix her with advice.

Ask a better question.

“What are you carrying right now that nobody sees?”

Then listen. Not to answer. To witness.

That is where connection begins.

That is where one cracked beam recognizes another.

And for a moment, the ceiling feels less heavy. Because some of us were not invited into this club. We were drafted.

But we stayed.

And somehow, God help us, we built something beautiful anyway.

P.S. Susan Tatem founded Bright Path for Autism to help families navigate the transition years with more clarity and support. I am grateful for every mother who turns what nearly broke her into a path another family can walk with fewer wounds.

This is the guide I needed when I was you.

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