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General information

If your child is suffering from a terminal illness that is likely to be life-limiting, you will. find useful information below.

For ease of reading, the term "child" also refers to adolescents and young adults in the following explanations.

"Children are not just small adults." Children with an incurable, life-limiting illness have special needs in hospice and palliative care. In these cases, care always focuses on the entire family – that is, not only the sick child but also their parents and siblings. Whenever possible, the top priority is to provide care at home.

The following points provide information on how hospice and palliative care for children differs from adult facilities, and what special offers are available:

  • If desired, hospice and palliative care for children can begin as early as the time of diagnosis, often accompanying the child and the family for a long time, up to and beyond the child’s death.
  • Care and support always involve the whole family, with siblings included and their needs being taken into account.
  • Age, illness and stage of development are being considered when providing care.
  • Children may be affected by a wide range of diseases, including many rare conditions and some types of tumours.
  • Children have specific wishes and needs that vary by age – babies for example have different needs than 17-year-olds.
  • Illnesses often last a long time, and symptoms may change over time.
  • For rare diseases, little may be known about how they progress and their treatment.
  • In general, care is provided over a longer period of time than it is for adults.

Contents and principles of hospice and palliative care for children:

  • Pediatric hospice and palliative care should be available to all children and their families who need it, regardless of the family's financial means.
  • A team of members of various professional groups with special training in pediatric palliative care looks after the child and their family. Volunteer companions are involved in the care.
  • Where possible, the child’s family home should be the child’s primary place of care.
  • Every child should have access to professional medical, psychological, and physical treatment for pain and symptoms around the clock, 365 days a year.
  • Care should be tailored to the child's age, stage of development, needs and abilities.
  • Children should be allowed to participate in decisions about their care in accordance with their age and development.
  • In any medical decision, the child's best interests are the most important consideration.
  • The legal guardians, as well as the child and their siblings, must be given comprehensive information appropriate to their age and stage of development.
  • Respite offers for the family, even if only on an hourly or daily basis, are important and should be offered both at home and outside the home.
  • Grief counselling must be offered from the time of diagnosis, throughout the illness, at death and for as long as needed afterwards.

Further information can be found under the following link:

Website Kinder-Hospiz Österreich

The expert framework for hospice and palliative care for children, adolescents and young adults outlines all four specialised services and which services are available. You can find more information at the following link:

Website - Hospice and palliative care - Ministry of Social Affairs

Last update: July 2, 2025

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