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  1. Home
  2. What we do
  3. ME or Chronic Fatigue Syndrome
  4. Helpful support and resources

Carers, friends and family

Living with ME/CFS or Long Covid can affect not only the individual but also the people around them. Family members, friends and carers often play an important role in providing practical, emotional and day-to-day support.

Because these conditions can fluctuate and are often invisible to others, it can sometimes be difficult for loved ones to fully understand the impact symptoms have on daily life. Access to reliable information can help everyone feel more informed, supported and connected.

Understanding ME/CFS and Long Covid

Learning about the condition can help family members, friends and carers better understand symptoms such as fatigue, post-exertional malaise (PEM), brain fog, sleep difficulties and fluctuating levels of function.

What are ME/CFS and Long Covid?

Supporting Someone You Care About

Providing support may involve:

  • Understanding the importance of pacing and energy management
  • Respecting changing symptoms and limitations
  • Helping with practical tasks and daily activities
  • Listening without judgement
  • Supporting healthcare, education or workplace discussions

Small adjustments and understanding can make a significant difference.

Looking After Yourself as a Carer

Supporting someone with a long-term condition can be rewarding but can also be physically and emotionally demanding.

Carers are encouraged to:

  • Recognise their own support needs
  • Take breaks where possible
  • Access information and advice
  • Seek help when they need it

Looking after your own wellbeing is an important part of providing sustainable support to others.

Young Carers and Family Life

Children and young people may also take on caring responsibilities when a family member has ME/CFS or Long Covid. Accessing appropriate support and understanding can help young carers balance family responsibilities, education and their own wellbeing.

ME/CFS and Long Covid can affect the whole family. Understanding, flexibility and open communication can help create a supportive environment for everyone involved, while ensuring that carers, family members and friends also receive the support they need.

Further Information

Carers, family, and friends – Action for ME – visit the Action for M.E website to find out more about carers, family and friends of someone living with these conditions.

In this section

  • What is ME or Chronic Fatigue Syndrome?
  • Pacing and energy management
  • Sleep
  • Diet and Nutrition
  • Working with ME/CFS
  • Understanding Post-Exertional Malaise (PEM)
  • Symptoms of ME, CFS or Long Covid
  • Getting a diagnosis
  • Severe and very severe ME
  • Explaining ME/CFS or Long Covid to others
  • Children, young people and Long Covid
  • Carers, friends and family
  • What is Long Covid?
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