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A caregiver’s role is challenging, especially if you need to balance a job, family and housework on top of caring for your loved one living with dementia. You may think you can or should do everything by yourself, or may want things to be done well with very good outcomes. This is understandable, as the stakes are high in caregiving. However, it is not always possible to have things done perfectly as a caregiver, and expecting this may increase the likelihood of burnout.


Even if things are going well, some caregivers may think that they are not doing enough. Feeling guilty happens when expectations are not met, and when the person who worked for certain outcomes attributes the results they find unsatisfying to themselves. They may also feel guilty about their own emotions; for example, caregivers may sometimes struggle with feelings of not wanting to be a caregiver in the first place or wanting free time for themselves.

As a caregiver, it is always a good idea to remind yourself at least once a day about:

  • How much help you are providing a person you care for
  • How your intentions come from love, care, and compassion for your loved one

Doing this will not only motivate you to improve your caregiving skills; but also give you a sense of fulfilment as an individual, for the present and future.


It is natural to feel frustrated, trapped and angry at the situations you may find yourself in as a caregiver. However, showing these emotions to your loved one living with dementia or other persons in your life may not be a helpful way to manage the situation.

However, it is just as unhealthy to keep these feelings to yourself. If you feel angry and frustrated, do not ignore these emotions. Find healthy and positive ways to let off steam. Consider trying some of these options to let go of anger and frustration in a safe way:

  1. Join a support group for caregivers. It can provide opportunities for you to share your feelings openly. Group members will understand how you feel and no one will make you feel guilty. They may even offer practical, effective advice or solutions. Research also shows that support groups can help caregivers deal with their situations better.
  2.  Make an appointment with a therapist, family counsellor or spiritual advisor.
  3. Keep a journal to express and write down your feelings.
  4. Exercise e.g. take a walk to cool down.
  5. Other creative methods, such as: going to a private corner or room and take out your anger on a big pillow.
Support and understanding are essential. It may be useful to seek advice and solace from other caregivers going through the same experience.


Caregiving can be emotionally demanding and may trigger negative emotions such as the ones mentioned above. Sometimes, these negative emotions can lead to depression which will put the well-being of you and your loved ones at risk.

It is already good in and of itself to make time for yourself, get some respite, and talk to a professional, family, or friend for you to express your emotions. In light of how depression can increase the risk of developing illnesses such as heart disease and put others around you at risk, however, it is even more important that you take the time to care for yourself.

If you have five or more of these symptoms for more than two weeks, you may have depression. Make an appointment and talk to a doctor, psychiatrist or psychologist.

If caregivers are experiencing stress symptoms, here are some ways to manage them:

To avoid burnout, set aside time for yourself

Make and keep doctors’ appointments to maintain your own health

Join a caregiver support group to expand your network

Make use of respite care opportunities – you must rest so that you can care for your loved one better

Talk to a professional, friend or family member about the challenges you face and explore ways to manage your stress

Coping With These Emotional Burdens

You may feel alone and that you are the only one dealing with these feelings. However, you are not alone. Every caregiver faces the following problems at some point:

Dependency & Isolation

As persons living with dementia become more dependent on their caregivers, the caregivers sometimes fear being isolated from the community. More than ever, respite and support are coping techniques every caregiver needs as building blocks for their emotional support network. Many caregivers may feel bad asking for help. However, caregivers who are able to develop personal and social support will more likely cope better.

Knowing When to Seek Help

“Why doesn’t anyone ask how I am doing?”

 It is easy to feel invisible next to a person living with dementia. Many caregivers say that nobody asks about their situation as everyone else is focused on the person living with dementia. These feelings should not be allowed to build up, as mental health experts advise.

Support groups, religious and spiritual advisers, or mental health counsellors can always advise caregivers on the many positive ways to seek help when needed.

Also, seek professional help immediately if you are:

  • Drinking more alcohol than usual
  • Using unhelpful coping methods
  • Often taking prescription drugs without a doctor’s advice
  • Suffering from skin rashes, back aches, colds, or a flu that does not go away
  • Unable to focus or think clearly
  • Feeling tired and do not want to do anything
  • Feeling worthless, guilty, or sad most of the time
  • Having fear and anxiety
  • Having thoughts of inflicting harm on themselves or their loved ones living with dementia
  • Experiencing the points above for two weeks or longer

Some Tips for Dealing with Physical and Emotional Burdens

Live one day at a time

Make a list of important tasks and prioritise them, think of ways to make your work easier, allow some things to be left undone

When handling a difficult task, make it easier by listening to music

Find time for regular exercise; this will help you keep fit, increase your physical stamina, and keep you feeling more energised

Focus on getting relaxing sleep instead of more sleep

Take short rests in the day to get enough sleep

Set aside time for meditation, reflection or prayer

Do deep breathing exercises and meditate to free your mind of troubles

Take care of your self-esteem; remember that you have skills and talents

Remember that you have limitations, and continually acknowledge them

Set goals; remember that you may not be able to do everything like before

Have a balanced diet

Make time for yourself

Treat yourself to a massage once in a while

Keep in contact with friends and take part in interesting activities

Let friends or family know that you welcome help; allow them to help with respite care

When you visit the doctor, talk about your caregiving responsibilities, not just your loved one’s symptoms

Share your concerns with a friend

Join a support group, or start one to share ideas and resources

Use respite care services in the community

Speak openly and honestly to people who should be doing more to help

Make a list of tasks and assign specific ones to people who offer to help

Know that you do not have to feel guilty about your emotions, and that simply acknowledging them is okay. It is natural and human to experience them.

Express your anger and frustration by writing down your feelings

Allow yourself to cry

Remind yourself that you are doing something important for the person in your care

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  1. (2019, December 9). Ministry of Health. Your Guide to Understanding Dementia. Retrieved on 24 March, 2021, from 
  2. (N.d.). Alzheimer’s Disease International. Dementia statistics. Retrieved 24 March, 2021, from

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A Caregiver’s Guide to Avoid Burnout

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