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  • Life Outside of Hospital
  1. Family Support
  2. On treatment
  3. Life outside of hospital

Life Outside of Hospital

The day to day life for a child with cancer, and their carers can be very difficult. There are many challenges to be faced and it’s normal to feel overwhelmed.

 

Your child may be experiencing distressing emotions about their cancer diagnosis, side effects from treatment and mood changes from the effects of medications. It is very important that carers of children with cancer look after themselves during this time. Knowing what to expect and who to get support from can help the family cope throughout treatment. 

Social workers assigned to you by your hospital should be able to connect you to support services and we have collated a range of options through our Related Support Services page.

The Cancer Council Victoria has also developed a resource area regarding life during and after treatment with information regarding the following:

  • Nutrition and diet
  • Fatigue
  • Blood counts
  • Hair loss
  • Mouth and dental care
  • Physical activity
  • Pain
  • Caring for a child with cancer
  • Play time for the child with cancer
  • Practical issues (finance, child care, travel, insurance)

Cancer at school

Starting day-care, pre-school or primary school is a big step for any child. If your child is also managing cancer treatment it will be important to share information regarding their care with appropriate staff and maintain regular communication regarding how your child is coping both at home and in care. 

The Cancer Council Victoria’s Cancer in the school community pack is designed to be shared with your child’s school and is available to order for free or downloadable as a PDF from the site. The American Cancer Society also has a useful article regarding returning to school. 

The Royal Children’s Hospital Melbourne has produced a What do I tell my friends and  classmates at school?  Which is designed to help children and parents discuss communicating the disease to peers. They have also developed the Chronic illness and school page with guidelines on how to coordinate support from medical carers and schools. 

Read next: After Treatment

More information

Visit our Related support services page for an extensive list of information and resources.

Published: 20th August, 2019

Updated: 10th March, 2022

Author: Karina May

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Neuroblastoma Australia Level 1, 441 Pacific Highway, Crows Nest, NSW 2065,
+61 02 9056 5076, [email protected]