September 2022
You also want an ePaper? Increase the reach of your titles
YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.
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