A new autism diagnosis, for a child or for yourself, can bring relief, questions, and many feelings at once. All of these are normal. A diagnosis is a starting point for understanding and support, not a final verdict on what someone can do.
Early steps usually include learning what autism means for this person, asking the diagnosing professional what supports they recommend, and finding out which services you may be eligible for.
Things to consider
- Ask for a written copy of the evaluation and its recommendations.
- Ask which services are recommended and how to get referrals.
- For children under 3, ask about your state’s early intervention program; for school-age children, ask the school about an evaluation for special education services.
- Check what your health coverage or Medicaid may cover.
- Look after yourself too — connection with other families or autistic adults can help.
Who to talk to
The diagnosing clinician, your primary care provider, and — for children — your state early intervention program or school district.