Jarrow ME sufferer speaks out about life in lockdown to help others dealing with self-isolation
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Jarrow resident Nicola Corr, was only in her 30s when she was diagnosed with Myalgic Encephalomyelitis (ME) in 2009.
Until then she had led an active social life and was enjoying a career as a teacher for primary school pupils with learning difficulties and autism.
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Hide AdHer life changed dramatically when she began to develop symptoms and she was forced to retire at 36 and move in with her mother for support.
“The biggest change is how small my world became very quickly,” said Nicola, now 45.
“Rather than being the main person in the family giving support, I rely on them for support now.”
In Tyne and Wear there are around 4,500 people living with the neurological condition, which affects people’s ability to recover normally after any physical and mental activity.
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Hide AdNow housebound, many of the services Nicola has come to rely on such as supermarket deliveries and carers disappeared overnight due to the coronavirus pandemic.
But she still believes her condition has given her a rare advantage to others who are struggling with the sudden disruption to their daily lives.
“The sudden decline in availability for having groceries delivered is the major issue we have faced,” she said.
“As I am housebound and bedbound more than half the time, the lockdown has meant very little change to me personally. I think like many others with ME being housebound for many years has given us a strange advantage over those who have suddenly had a huge change to their daily routines.”
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Hide AdFor ME Awareness Month throughout May, charity Action for M.E is encouraging people with the condition to share their insight and experience of living with uncertainty and isolation to help shine a spotlight on the hidden condition.
Nicola said: “For those who are struggling with isolation I would encourage them to make an effort to keep in touch with friends and family in whatever way appeals to them.
“Social media has been my window to the outside world for so long, and life would be a lot harder and more lonely without it. Finding a new 'normal' and routine of some kind really can help to keep you from going insane.”
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In light of the pandemic, Action for M.E set up an Crisis, Support and Advocacy Service to help people in urgent need with things such as shopping, medication collections, peer-support and advice on welfare changes.
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Hide AdChief executive, Sonya Chowdhury commented: “We have been contacted by people with ME in truly desperate situations.
“So far, we have seen a three-fold increase in requests for urgent support – all at a time when our income is expected to drop by at least 50%. Like many other organisations and charities, we made the difficult decision to furlough several staff. We are continuing to make critical decisions to ensure we are here for people with ME now and in the future.”
Anyone living with or caring for someone with ME can contact [email protected] or call 0117 927 9551 for support.