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Insight: Oct 16

This week SBS discusses managing chronic fatigue syndrome.

This week on SBS Insight explores what it’s like to have chronic fatigue syndrome and if there is no cure, what is the best way to manage it? Chronic Fatigue Syndrome,

At 20 years old, Adele Clydesdale had just climbed Mount Kilimanjaro; she was starting her second year of university and playing in the Victorian Netball League.

So when she got glandular fever, she didn’t think much of it. She knew plenty of people who’d had it in high school and they always recovered quickly.

But even when test results revealed the glandular fever was out of her system, Adele was still unwell and her symptoms were getting worse. She was increasingly fatigued, couldn’t string sentences together and had extreme body pain.

At six months, it was confirmed Adele had chronic fatigue syndrome, a diagnosis she found quite confronting.

“I felt like there was quite a stigma around it and when I tried to share it with my peers and friends, there was that perception that ‘I get tired too, maybe I’ve got chronic fatigue as well’”, she tells Insight host Jenny Brockie.

Chronic Fatigue Syndrome (CFS) is estimated to affect between 0.2-2 per cent of the population in Australia, yet very little is known about this condition*.

Otherwise known as Myalgic Encephalomyelitis or ME, it is an illness characterised by profound fatigue, not relieved by sleep or rest and worsened with activity.

Patients will commonly experience muscle and joint pain, impaired memory and concentration and gastrointestinal disorders. However, the most defining indicator of CFS is Post Exertional Malaise (PEM) – when a certain level of cognitive or physical exertion will exacerbate a patient’s symptoms. There are currently no proven treatments for CFS which means many are left without answers.

Ketra Wooding, 33, has been unwell for eight years and with such severe symptoms she has been living in a nursing home for seven of those years.

She recalls when her doctor diagnosed her: “I said to him, ‘how long is this going to last?’ And he said it’ll probably be five to seven months, and I was devastated. I’m so glad I didn’t know how long it really was going to be.”

Tuesday, 8:30pm on SBS.

One Response

  1. I have Fibromyalgia and CFS is one of my many symptoms. I can no longer work as a child care worker. In the morning I feel like I have not slept at all, I need to have rest breaks alot.

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