Many parents of disabled children feel under pressure or stressed. Managing stress might help you to feel more in control.
Emotional and practical support can help too.
"I can’t sleep."
"I can’t eat."
"I’m eating too much."
"I can't focus or remember things."
"I can’t talk to my partner."
"I’m drinking too much."
"I feel like no one understands what I’m going through."
"I feel like I can’t cope."
If you care for a disabled child, you can have an assessment to see what support might help make your life easier. This is called a carer's assessment, also known as a parent carer’s assessment.
Accepting that your life has changed will help. Some parents cope with these extra pressures by:
Has anyone offered to make things easier? This could be looking after your child while you have a bath or go shopping. Ask for help if you need it.
Support could be a parents group, nursery, a friend you can talk to or respite care.
Other parents in the same situation may understand and be able to help you.
Respite care, also called short breaks for carers, is temporary care that lets you take a break from looking after a disabled adult or child. It does not affect your benefits.
Respite care is there to support your wellbeing and health, allowing you to care for a disabled person. You do not need to wait until you’re struggling.
Getting some rest, looking after your mental health and asking for support can help you and your family manage.
If you can, try taking a little time off. Try relaxing by:
Being a parent can be hard. Looking after your mental health and wellbeing is important. Everyone manages their mental health differently.
If you need support, here are some things you could try:
Talk to your doctor about getting treatment and support.
Discuss what’s affecting you. Tell your GP if you’re stressed, depressed or if you feel like you’re not coping. You could prepare for your appointment by writing down what you want to say. You could talk about:
Last reviewed by Scope on: 22/07/2024
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