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September 2022

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38<br />

Wanstead Village Directory<br />

Tired of fatigue?<br />

Based in Wanstead, the East London ME/CFS Support Group has been<br />

a lifeline for those living with chronic fatigue syndrome. Long COVID<br />

sufferers, like Tim Armitage’s wife, are also invited to join them<br />

My wife, Sally, has had ME for the<br />

last six years. The effects of her<br />

condition are varied. There’s<br />

extreme fatigue, where doing even light<br />

work around the house or ‘just popping<br />

to the shops’ can wipe her out, muscle<br />

aches and weakness, sleep disturbance<br />

and cognitive dysfunction, where facts and<br />

figures that were once readily available are<br />

now difficult to remember.<br />

After activity more strenuous than a short<br />

stroll, she experiences post-exertion malaise,<br />

meaning that at any time, from a few hours<br />

later to the next couple of days, she is<br />

exhausted. Her symptoms become more<br />

intense with no amount of sleep lessening the<br />

effects. She calls this payback!<br />

Then, in 2020, she caught COVID.<br />

This worsened her existing problems and<br />

added new ones on top. She now suffers from<br />

regular migraine attacks and an altered sense<br />

of taste and smell.<br />

As a family with two teenagers, we’ve adapted.<br />

She and I used to be a partnership, splitting<br />

household jobs equally, but now most things<br />

fall to me. As someone who was always on the<br />

go, my wife has found this difficult. It’s one of<br />

many things that’s changed.<br />

We have to limit social activities, dog walks<br />

and holidays. Everything is planned with<br />

precision. Public transport is often not an<br />

option and I have to drive and drop her close<br />

to the door. We also limit the time spent<br />

somewhere so she doesn’t get too tired, and<br />

sometimes I’ll go out with the kids on my own<br />

so she can rest at home. It’s not how we would<br />

choose life to be, but, unfortunately, it’s our<br />

new reality.<br />

My wife likens living with ME to a smartphone<br />

that can’t be fully charged. Even if it’s plugged<br />

in all night, by morning it’s still only at 25%.<br />

And by lunchtime, it’s empty.<br />

This forces her to make micro decisions about<br />

how she spends what little energy she has and<br />

how to programme in small periods of rest<br />

for recharging, simply to make it to the end of<br />

the day.<br />

One thing that has kept her sane has been the<br />

ME support group she came across in 2018.<br />

They meet monthly, on Saturday afternoons<br />

at the Wanstead House Community Centre.<br />

They have been a lifeline. The informal drop-in<br />

group share their experiences and knowledge<br />

of having ME.<br />

My wife wants to spread the word to anyone<br />

suffering from either ME or Long COVID that<br />

there is a supportive, local group waiting to<br />

help and listen to those who need it.<br />

The East London ME/CFS Support Group<br />

will meet on 10 <strong>September</strong>, 15 October<br />

and 26 November at Wanstead House,<br />

21 The Green, E11 2NT between 2.30pm and<br />

5pm (free; donations welcome). For more<br />

information, call 07957 152 566<br />

To advertise, call 020 8819 6645 or visit wnstd.com

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