In partnership with Rockinghorse Children’s Charity

On this page
- What is this information about?
- Why have I been given this information?
- What does the Paediatric Oncology Psychology Service do?
- Who is in the team?
- What do paediatric oncology psychologists do?
- What happens during a psychology appointment?
- How has this service helped other people?
- Where can I look for more information and resources?
- Who can I contact for further information and advice?
What is this information about?
This information is about the Paediatric Oncology Psychology Service. It tells you who the team are and what support we offer as a service.
Why have I been given this information?
It is normal for families to feel overwhelmed or struggle with the impact of a cancer diagnosis and treatment. The Paediatric Oncology Service are here to listen and support you, emotionally and psychologically, if you feel you need it.
You may find that you have already been given a lot of information and are not ready to read this yet. Please do not feel you have to look at this information now, but you may find it helpful to keep it in a safe place so you can find out more about the service later on.
The service contact details are at the end of this information.
What does the Paediatric Oncology Psychology Service do?
We offer support to children and young people up to 19 years old, and their families, to help cope with the emotional and psychological impact of cancer diagnosis and treatment.
The service offers psychology assessment and therapy. This can start as soon as diagnosis is given, anytime throughout the treatment plan or after treatment finishes.
Who is in the team?
The team includes:

Dr Alice Emond
Principal Clinical Psychologist and Service Lead

Dr Meg Montgomery
Clinical Psychologist

Dr Hannah Smith
Rockinghorse Senior Counselling Psychologist

Aimee Sullivan
Service Administrator
We are based on level 9 oncology daycare.
What do paediatric oncology psychologists do?
We work with you and your family to help you to understand and cope with the cancer diagnosis or treatment.
We create a support plan together with you and your family.
Things that we can support you with include:
- Understanding and managing your wellbeing
- Coping with the impact of diagnosis and treatment
- Managing medical procedures and treatment side-effects
- Understanding and coping with difficult thoughts, feelings and behaviours
- Changes around school and work
- Difficult memories from experiences with treatment
- Living life alongside treatment
We work together with other people who are looking after you. This includes your team of doctors, nurses and other healthcare staff at the Alex and at your main treatment hospital.
We also work with other people who are important to you: this includes people at your school, nursery, or charities.
What happens during a psychology appointment?
Wellbeing assessments
All families are offered two routine family wellbeing assessments.
Wellbeing assessments are open to all family members. These sessions are with a psychologist, and they assess how you are coping with treatment and what other support might be helpful.
Other support could include self-help resources, individual or family referrals to our service, or signposting to other services.
Therapy referrals
If your child or member of the family needs some psychology support, they can be referred to the psychology team for some therapy sessions. This includes siblings, parents or carers.
Referrals for a patient’s siblings, parents or carers can be made directly by families themselves, your medical team, or other professionals. Referrals for therapy will always be discussed first with whoever the referral is for.
Following an assessment, we can offer six to 12 sessions of 50 minutes each, which can be in person, by video or telephone. We try to link in with any medical appointments with the oncology daycare department to reduce your visits to the hospital.
How has this service helped other people?
“It’s really helped my son to understand his sister’s condition and his own feelings.” (sibling)
“(The psychologist) allowed our child to discuss how they were feeling and come to terms with their treatment changes.” (Parent of a child on treatment)
“I feel I have taken time to reflect, and this has given me the tools and space to continue processing and dealing with what’s to come.” (Parent of a child off treatment)
Where can I look for more information and resources?
We are not a crisis mental health service. If you have urgent mental health concerns, please visit A&E or call the Sussex mental health line via NHS 111.
Teens Unite
Support and information for young people who have experienced a cancer diagnosis and their families
Young Minds
Resources for young people and parents/carers to support with general mental health and wellbeing
Brighton and Hove e-wellbeing
Resources and local community-based information
If you would like further resources, please contact our team directly.



Who can I contact for further information and advice?
To make a direct referral or enquiry about our service
administrator
01273 696955
Ext. 62406
This leaflet is intended for patients receiving care in Brighton and Hove.
The information in this leaflet is for guidance purposes only and is in no way intended to replace professional clinical advice by a qualified practitioner.
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