It is likely that a child with epilepsy will need to have regular clinic visits to review progress and lifestyle. Learn what happens during a clinic visit.
After scoliosis surgery, clinic visits are required to ensure proper healing and growth. Learn about the frequency of these visits and what to expect.
Learn what will happen during follow-up visits after your child's leukemia treatment ends.
An overview of seizures and epilepsy, with information about treatment options.
Find out what happens at clinic visits during follow-up treatment when your child is back at home after receiving treatment for a brain tumour.
Learn what happens at follow-up clinic visits after brain tumour treatment for your child has ended.
Siblings may receive less attention at times because the needs of a child with epilepsy take over. Helping siblings cope is an important aspect of family life as well.
Learn about the SickKids interprofessional outpatient clinic for newborn babies to assist in the diagnosis and non-operative treatment of DDH.
Most people with epilepsy can have full social, sexual and family lives. Read about issues surrounding sex and reproduction for those with epilepsy.
DEE-SWAS is a rare epilepsy syndrome that can affect children aged two to 12. Learn about the symptoms, diagnosis and treatment of DEE-SWAS.
Sudden unexpected death in epilepsy (SUDEP) is rare in people with epilepsy. However, it is important to be aware of the risk factors and how to prevent it in your child.
Find out how epilepsy is diagnosed and what questions to ask to make sure you understand the diagnosis.
Read about the causes and treatments for reflex epilepsy, a rare condition in which seizures are set off by specific stimuli such as flashing lights.
Read about the types of epilepsy and the suggested treatments.
Read about the causes and symptoms of absence epilepsy and how the condition is treated.
Read about options for a teen attending college or university while coping with epilepsy.
A teenager with epilepsy will need to transfer management of their epilepsy to an adult care setting. Find out about transitioning smoothly from paediatric to adult care.
Find out how to make travel and time away at camp safe and enjoyable for a child with epilepsy.
Read about the causes, diagnosis and treatment of neonatal seizures.
Learn about the diabetes care team, who is involved and what to expect during clinic visits.
A detailed list of epilepsy organizations, research and books. A wide range of topics is covered, including guides for families and the ketogenic diet.
Most parents of children living with epilepsy are concerned about aspects of their child’s behaviour. Varying behaviors can be expected from a child with epilepsy. Learn about causes of behavioural changes and how to manage them.
The prognosis of an illness is a forecast of how it will develop and the outcome after treatment. Read about the factors that affect the prognosis of a child with epilepsy.