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Mental health

Caring for someone – looking after yourself too

Carers have worse health outcomes than the people they care for in some respects. What actually helps, and why asking for help is not a failure.

The invisible job

Most care in South Africa is given by family members, usually women, usually unpaid, and usually alongside other work. It is rarely described as a job, which is part of why the toll it takes goes unrecognised — by everyone including the carer.

Long-term carers have higher rates of depression, anxiety, disturbed sleep and physical ill health, and are less likely to attend to their own medical needs. This is not weakness or insufficient love; it is what sustained demand without relief does to anyone.

Signs you are running out

  • Constant exhaustion, and sleep that does not restore.
  • Irritability or anger towards the person you care for, followed by guilt.
  • Losing contact with friends, and dropping things you used to do.
  • Your own appointments, medication or symptoms going unattended.
  • Feeling trapped, resentful, or numb.
  • Drinking more, or relying on something to get through the evening.
  • Thoughts of harming yourself, or of not being able to continue.

What helps

  1. Accept specific offers, and make them specific when people ask. 'Could you sit with him on Thursday afternoon' gets a yes; 'let me know if you need anything' gets nothing.
  2. Keep your own medical appointments. Tell your clinician you are a carer — it changes what they look for and what they can point you to.
  3. Protect a small amount of time that is yours and is non-negotiable, even if it is an hour.
  4. Share the load explicitly among family. Care almost always defaults to one person unless someone divides it deliberately.
  5. Find others doing the same thing. Condition-specific support groups exist in South Africa for dementia, stroke, cancer and disability, and carers consistently report them as the thing that helped most.
  6. Learn the practical skills — safe lifting, managing medicines, what to expect next. Competence reduces fear, and back injuries end more caring arrangements than exhaustion does.
  7. Ask a social worker about respite care, home-based care services and the grants that exist. Clinics can refer.

The practical and the legal

  • Keep one list of medicines, conditions, allergies and contact numbers, and keep it where anyone stepping in can find it.
  • Sort out decision-making authority while the person can still grant it. Doing this early is far easier than the alternative.
  • Look into the Care Dependency Grant and other social grants — many eligible families never apply.
  • Tell the clinic you are the carer so you are included in appointments and instructions.

Common questions

Is it selfish to want time away?
No, and the framing is the problem. Care that continues for years only continues if the carer is sustainable. Respite is part of the care plan, not a withdrawal from it.
How do I get other family members to help?
Ask for specific tasks on specific days rather than help in general, in writing where possible. Vague appeals let everyone assume someone else is handling it; a named task on a named day is much harder to leave.
What support exists in South Africa?
Ask a clinic or hospital social worker about home-based care services, respite options and the relevant social grants. Condition-specific organisations run carer support groups, and SADAG's line is available for your own mental health, not only the person you care for.

Sources

Last reviewed 4 August 2026.