Questions to ask your child's neurosurgeon

A checklist of practical questions to bring to your child's appointments

Important. This is a general guide. Your child's situation is unique. Do not let this replace the conversations with your child's medical team.

When you're sitting in the consulting room facing a neurosurgical diagnosis for your child, it's easy to forget the questions you wanted to ask. This page is a checklist you can bring with you — print it, save it on your phone, or read it before the appointment. Not every question will fit every situation; pick the ones that matter to you.

Understanding the diagnosis

  • What exactly is the diagnosis, in plain language?
  • How sure are you of the diagnosis? Are more tests needed?
  • What caused this in my child, if we know?
  • Is this condition common or rare?
  • Will it get worse if we wait?
  • Can you draw it for me or show me on the scan?

Choosing the treatment

  • What are the treatment options for my child?
  • Which option are you recommending and why?
  • What happens if we decide not to operate, or to wait?
  • How many of these operations do you and your team do each year?
  • Is there a second opinion you would recommend we get?
  • How urgent is this — can we take time to decide?

The operation

  • How long does the operation usually take?
  • Will my child have a scar, and where will it be?
  • Will my child's hair need to be shaved?
  • What are the main risks of this operation, and how often do they happen?
  • What can go wrong, and what do you do if it does?
  • Who will be in the operating room? Will you do the operation yourself?
  • How will I be updated during the surgery?

Hospital stay and immediate recovery

  • How many nights will my child be in the hospital?
  • Will my child be in intensive care after the surgery?
  • Can I stay with my child overnight?
  • What will pain control look like? Will my child be uncomfortable?
  • When will my child be able to eat and drink again?
  • When will the wound dressing come off, and how do we care for it at home?

Going home and life afterwards

  • What activities can my child do safely after going home? Sports? Swimming? Air travel?
  • When can my child go back to school or nursery?
  • What restrictions are temporary and what are long-term?
  • Will my child need any medications at home? For how long?
  • What is the follow-up schedule? When is the first appointment after surgery?
  • Who do I call if I have a concern between appointments, and what number do I use after hours?
  • What signs at home should make us go to the emergency department?

The long-term outlook

  • What is the long-term outlook for a child like mine?
  • Will this affect my child's development, learning, or behaviour?
  • Will my child need other specialists — physiotherapy, speech therapy, eye doctor, neurology?
  • How often will my child need scans, and what kind?
  • Will this affect my child's ability to participate in normal life as an adult?
  • Is there a parent support group or family network we can join?

Practical and family questions

  • How should we explain this to my child (in language they can understand)?
  • How should we explain it to siblings, grandparents, school?
  • Is there a social worker, child-life specialist, or psychologist who can help our family?
  • Are there financial or insurance questions we should ask the hospital about?
  • Are there reputable websites or books you would recommend?
  • Are there things on the internet you would specifically warn us NOT to read?