This page contains information on book resources available for parents of premature babies.
Learn about the definition of and the causes and medical conditions associated with prematurity.
Babies can feel pain. Learn about ways pain in newborns and babies can be assessed and techniques that can help ease pain.
Information for parents about hereditary multiple osteochondromas (previously called hereditary multiple exostoses), a genetic condition that causes growths (bumps) on the bones.
Learn about the supports available to families coping with pregnancy and infant loss, including perinatal palliative care.
Congenital cytomegalovirus (cCMV) occurs when a fetus is infected with a virus called cytomegalovirus. Learn more about how cCMV happens, the signs and symptoms of cCMV and how it is diagnosed and treated.
If you are infected with HIV and pregnant, learn how certain medicines can lower the risk of passing HIV on to your baby.
Learn about newborn nutrition, routine care and everyday health issues as well as some common physical and emotional adjustments to life after pregnancy.
Learn about the common causes of chronic lung disease in premature babies and the ways to diagnose and treat it.
Discover how to help your teenager manage their diabetes and how it will affect their day-to-day lives.
Learn all about your newborn baby's eyesight, hearing, and senses of taste, touch and smell.
Learn about cleft lip and cleft palate and its impact on a baby's feeding, hearing, teeth and speech.
Learn about possible outcomes for premature babies.
Very premature babies are at risk for metabolic bone disease, a condition that affects their bone health and increases the risk of fractures.
Learn about what a premature baby needs to eat and how they can get proper nutrition.
Learn about respiratory distress syndrome, a common condition in very premature babies.
Read about the symptoms of neonatal withdrawal syndromes and approaches to treatment.
Genetic counselling is a process that provides information and support to individuals and families at risk of, or with, a genetic condition.
22q11DS is a genetic condition with a wide range of symptoms. Learn about some of the more common medical features of 22q11DS.
Learn about making sleep time easier and safer for your newborn baby.
Read about the causes, diagnosis and treatment of neonatal seizures.
Information for parents about trisomy 13, a rare genetic condition that causes developmental delay and affects many different organ systems.
Babies, children and adults all need iron to keep their bodies healthy. Discover sources of iron and how to get enough.
Learn about common growths, called infantile hemangiomas. Also, learn when they are tested and treated by doctors.
