Your doctor cannot be absolutely certain about what will happen to your child following a diagnosis of an DIPG. They can give you an estimate, based on the tumour type and current situation, but they may not be able to predict other factors, such as how well your child might respond to treatment.
Prognosis is often an ongoing process, revised at different stages in your child's journey.
Different people approach their prognosis in different ways.
There is no right or wrong answer as to whether or when to receive such information. It is entirely up to you whether or when you want to speak to your doctor about your child's prognosis.
The survival rate given below is not meant to represent how long a person will live past those intervals. For example, someone who has survived for two years after diagnosis may live as long as any other healthy person, depending on their circumstances.
It is important to remember that statistics and averages cannot tell you what will happen to you specifically. You can find a general overview of prognosis for DIPG below.
Our Brain Tumour Information Pack has been designed to help you cope after diagnosis and support you during this difficult time. It can help to guide you through the healthcare system, answer your questions, and reassure you that you're not alone so that you feel confident when discussing treatment and care options with your medical team.
Unfortunately, we're currently unable to send Information Packs by post. All the information contained in the pack can be found in the email you'll receive after completing this form.