Help to transform our extraordinary hospital into something even better.
View: 525
Download: 2
Flare-ups are a very common part of having long term pain, even when you are getting better. Flare-ups can disrupt your normal daily activities and may last from a few days to several weeks. Having a flare-up can make you feel down, disappointed and very frustrated.
Flare-ups can be caused by many things such as:
Sometimes there does not seem to be a trigger, they can just happen.
Flare-ups are very common but the good news is what you do during a flare-up can make a big difference to the impact on your life, the length of time it lasts and how often they might happen.
Remember that flare-ups are only short term problems.
Do not stop everything and rest. The longer you stop the harder it is to get going again.
Follow your flare-up plan as soon as you notice the signs that a flare-up might be happening. A personal action plan for flare-ups helps you know what to do to stay confident and in control.
Remember to ask for help or advice from people who have helped you before such as doctors, therapists, nurses, teachers friends and family.
Noticing what is happening when a flare-up starts can provide the first step to managing things effectively. This includes the physical and emotional changes that happen with a flare-up, and also what you and others do to cope with it.
For example: your pain feels worse, you notice increasing or new areas of sensitivity, you feel more tired than usual, you are not sleeping so well, you feel more irritable, your mood seems lower, you feel overwhelmed or anxious.
Put your own examples here:
For example: spending more time in your room, having longer lay-ins, choosing not to see friends or join in with family activities, cutting out sport or clubs, missing more school or falling behind with homework. You may notice you are moving or walking differently, or resting more.
Put your own examples here:
For example: you are looking pale, you move differently or guard a part of your body, you seem more tired, sleeping in the day, you are short tempered, you have difficulty getting up in the morning, you are missing more school than usual or spending more time in your room, you are choosing not to do things, you seem less talkative or tearful, you are relying on others to help you more than usual.
Put examples from your family and friends here:
Looking at your day to day life may help you understand why a flare-up has happened, and give you clues to help you recover. Not all flare-ups are linked to recent events and sometimes it is hard to find a reason. However, the questions below can still help you get back on track.
When a flare-up happens it is easy to forget all the information you have learned about managing pain and what has helped before.
When pain or other symptoms flare-up the brain focuses on the problem, and you are more likely to think about the difficulties it causes. This restricts access to other more creative or reflective parts of the brain, making it harder to remember new information or positive things you have achieved.
To help you get back to a more balanced view it helps to remind yourself about pain management ideas:
Using the information from steps 1 to 3 you can now create your own plan to help you when you experience a flare-up (or set-back).
In the first column write down things you and other people notice about you when you have a flare-up. This includes what you feel and do (how your behaviour changes) and what happens. You may want to add things that other people do (like bringing you food in bed for example).
Next to each item, in the right hand column, fill in some ideas that you and other people can do to help you work through the flare-up with confidence. There are some examples to help you at the top of the plan.
Signs of a flare-up | Action |
Noticing more pain and tiredness | Planning in some regular rests each day and prioritising pacing activities |
Falling behind with school work | Letting school know as soon as possible and talking to teachers about a plan to help you catch up |
Please note: this is a generic information sheet relating to care at Sheffield Children’s NHS FT. These details may not reflect treatment at other hospitals. This information is not intended as a substitute for professional medical care. Always follow your healthcare professionals’ instructions. If this resource relates to medicines, please read it alongside the medicine manufacturer’s patient information leaflet. If this information has been translated into another language from English, efforts have been made to maintain accuracy, but there may still be some translation errors. If you are unsure about any of the guidance in this resource or have specific questions about how it relates to your child, always ask your healthcare professional for further advice.
Resource number: CME5
Resource Type: Article
Western Bank
Sheffield
S10 2TH
United Kingdom
Switchboard: 0114 271 7000
We’ve got a special MRI scanner just for teddies so children can see what it’s like before they have a scan.
Help to transform our extraordinary hospital into something even better.