Questions to ask your child's neurologist

Appointments can move fast and it's easy to forget what you wanted to ask. Print this page or save it as a PDF, tick the ones that matter to you, and take it along.

Understanding the diagnosis

What is the diagnosis (or the working diagnosis), in plain terms?
What is causing it — and do we know the cause yet?
Is genetic testing relevant for my child, and what could it change?
What does this mean for my child's development and future?

Tests and results

What did the EEG / MRI / blood or genetic tests actually show?
Are any further tests needed, and why?
Can I have copies of the reports for my records?

Treatment and medicines

What are the treatment options, and what are the goals of treatment?
Why this particular medicine — and are there any we should avoid for this condition?
What side effects should we watch for, and what monitoring is needed?
What should we do if a seizure or episode lasts too long (our rescue plan)?
Are non-medicine options (such as diet or therapy) relevant?

Day-to-day and support

How will my child's development, learning and behaviour be supported and monitored?
What should school or nursery know, and is any extra support available?
Who do we contact, and how, if things change or we're worried?
What are the warning signs that need urgent attention?

Looking ahead

Are there clinical trials or specialist centres relevant to my child's diagnosis?
When is our next review, and what should we expect by then?
Is a second opinion or educational review worthwhile at this stage?

Zatay Medical provides independent educational reviews only. Our reports are not a diagnosis, treatment, or prescription, and do not replace care from your treating physician.