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Groundwork.

My child was just diagnosed. What now?

Short answer

In the first weeks, do three things and let the rest wait: get on the waitlists, because they are long; tell two people who will not need managing; and sleep. The feelings you are having, including the ones you think are shameful, are a normal response to a genuine load. Grief alongside love is not a contradiction and is reported by almost every parent. You do not have to become an expert this month.

What the first months actually feel like

Relief and grief at once, and guilt about both. Relief because there is finally a name, guilt because the relief feels disloyal. Grief for a version of the future you had pictured, guilt because your child is right there and has not gone anywhere.

Then, quite quickly, a job you did not apply for. Referrals, waitlists, school meetings, insurance, acronyms. Many parents describe becoming an administrator of a system when what they wanted was to be a parent, and the loss in that is real even though nobody counts it.

A practical order for the first three months

  1. Join the waitlists now. They are the long pole. You can change your mind about a service later; you cannot get the months back.
  2. Find out what your school district is obliged to provide and start that paperwork, because it runs on its own slow clock.
  3. Tell two people. Not everyone. Two who will not need you to manage their reaction.
  4. Postpone the reading binge. A week of research at 1am will not change the outcome and will cost you sleep you cannot afford.
  5. Decide nothing large yet. Not about school, moving, work, or your relationship. Almost no decision made in the first six weeks is a better decision than the same one made in the fourth month.

The parts nobody warns you about

The thing that is actually about you

Everything in the system points at your child. Almost nothing points at you, and when you do start talking about yourself, most conversations get redirected back to them within a minute. That happens to these parents constantly, and it is why so many of them stop talking.

You are allowed to need an hour that is about you. Not about strategies for your child. About what you are carrying. That is the work I do here, and it is separate from anything to do with your child's care, which belongs to the professionals handling it.

What I am not

I am a coach. I do not diagnose, treat, or direct any part of your child's care, and I will not second guess the people who do. What I bring is forty eight weeks of field training with autistic children, which means you will not have to explain the world you have just walked into.

Common questions

Is it normal to grieve after an autism diagnosis?

Yes, and it is extremely common. Parents report grief for an imagined future alongside undiminished love for their actual child. The guilt about the grief is usually heavier than the grief.

What should I do first after a diagnosis?

Get on waitlists, start the school paperwork, tell two people, and sleep. Postpone large decisions and the research binge. Nothing important is lost by taking the first month slowly.

Why am I so tired when the diagnosis has not changed anything?

Because the load changed even though your child did not. Parent burnout in this situation is a recognised pattern: exhaustion that sleep does not fix, emotional flatness, and lost joy in parenting.

Not sure if this is for you?

The first call is free, it runs about 15 to 20 minutes, and its only job is to work out whether I am the right person. If I am not, I will say so and point you somewhere better.

Book the free call

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