Becoming a carer for someone with Long Covid

There is no formal process which means you ‘become’ a carer.

Particularly with Long COVID, it’s often something that just happens. Family, partners and friends find themselves in the role of a carer when their loved one becomes unwell.

Often, people do not see themselves as carers, especially during the early stages. They just see themselves helping a loved one after a COVID infection. It may be difficult to accept the new title of carer. Acceptance can take time.

Watching a loved one become unwell with Long COVID can be very confusing, difficult and frightening. Many carers find themselves moving between hope, grief, frustration and acceptance, as they adjust to the changes brought by Long COVID.

It is difficult to know how long that Long COVID will last. Many carers may think that the care will be short-term, but sadly, sometimes it can last for years. Carers often find themselves wondering when their loved one will recover, whether symptoms will improve, and what the future may look like.

Long COVID is a complex illness. Often it can be confusing. With over two hundred known symptoms, when you first begin caring for someone with Long COVID, it can be difficult to understand. For example, it can take a while to understand that what looks like inactivity may be a person carefully managing their limited energy. It may be helpful to view our ‘What is Long Covid?’ webpage for further information.

It is likely that you understand your loved one’s needs better than anyone. However, Long COVID can be difficult to understand. You may both still be learning what helps, what doesn’t help, and how their needs may change.

Some ideas to think about are below.

What can I do?

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Speaking up for someone with Long COVID