You don't have to figure this out in the right order.
Common Ground is a plain-language guide for parents and guardians of autistic children — what autism is, what the research actually shows, what helps day to day, and how to find the services your state owes your family.
Five things worth knowing on day one
A diagnosis doesn't change who your kid is. It changes what you know about how they experience the world, and it unlocks doors — school services, insurance coverage, state programs — that were closed without it.
Early intervention for children under three doesn't require an autism diagnosis, and in every state you can refer your own child without a doctor's note. Waiting for an evaluation appointment is not a reason to wait for help.
Most state Medicaid waiver programs have waiting lists measured in years. Getting on the list costs nothing and you can decline services later. This is the single most common regret parents report.
Requests to schools must be in writing to start legal timelines. Start a folder — evaluations, IEPs, letters, denial notices, doctor's notes. You will need it more than once.
Autistic adults were autistic children. Their accounts of what helped and what hurt are some of the most useful information you will get, and often free.
Caregiver burnout is real and common. Respite care exists, it's often state-funded, and using it is not a failure. Look for it before you're desperate.
Cinco cosas que conviene saber el primer día
Un diagnóstico no cambia quién es su hijo. Cambia lo que usted sabe sobre cómo vive el mundo, y abre puertas — servicios escolares, cobertura del seguro, programas estatales — que estaban cerradas sin él.
La intervención temprana para menores de tres años no exige un diagnóstico de autismo, y en todos los estados usted mismo puede referir a su hijo sin orden médica. Esperar la cita de evaluación no es motivo para esperar la ayuda.
Casi todos los programas estatales de exención (waiver) de Medicaid tienen listas de espera de años. Apuntarse no cuesta nada y siempre puede rechazar los servicios después. Es el arrepentimiento más común entre los padres.
Las solicitudes a la escuela deben hacerse por escrito para activar los plazos legales. Arme una carpeta: evaluaciones, IEP, cartas, negativas, informes médicos. La va a necesitar más de una vez.
Los adultos autistas fueron niños autistas. Lo que cuentan sobre qué les ayudó y qué les hizo daño es de la información más útil que va a recibir, y suele ser gratis.
El agotamiento del cuidador es real y frecuente. Existe el cuidado de relevo (respite), muchas veces financiado por el estado, y usarlo no es un fracaso. Búsquelo antes de estar desesperado.
If you are worried right now
Urgent help
988 — call or text the Suicide & Crisis Lifeline, 24/7, for mental health crises of any kind, including for caregivers. Some areas can dispatch a mobile crisis team instead of police.
911 — if your child is missing. Say the words "autistic and may not respond to their name," and mention water: wandering toward water is the leading cause of death after elopement. Ask your local department whether they keep a voluntary registry for residents with disabilities.
If a crisis feels close for you as a caregiver, talking to your own doctor or a counselor is a reasonable next step, and one a lot of parents in this position take.
Both lines offer interpreters. You can say the name of your language in English and wait to be connected.