Voices: I was raised by a mother who was battling ME – it’s not just ‘being tired’, it’s a devastating, life-defining disease

When people ask me what ME is, I try to remind myself that the knot in my gut isn’t their fault. No matter how well intentioned, the accompanying question: “Is that when you’re always tired?” – and knowing how far short from the reality this falls, is something I’ll never get used to.

It sometimes feels easier to admit defeat than divulge the reality. For me, ME mostly means heartache.

ME is watching my mum struggle to walk up the stairs most days, or to shuffle to the kitchen to take her painkillers. It’s hearing her mentally strain to engage in conversation; struggling to articulate words.

It’s the days in bed, not because she’s tired – but fatigued, in a painful slumber where any light hurts her eyes. It’s making sure she’s eaten and drunk fluids, gently nudging her awake every so often from the pain-induced coma.

Dying mother gets to watch son graduate from high school in special hospital ceremony

It’s helping with school runs, looking after my younger siblings, and being on call when I’m needed. It’s feeling selfish for being healthy and frustrated at how someone else’s illness can limit my independence.

It’s knowing that walking half a mile to the local shop will mean my mum will be be bedbound for a week, but also knowing how much she’d love some fresh air and some sun on her face.

It’s a merciless elephant in the room that you can’t get rid of.

Despite all these feelings, I know I feel a fraction of her pain – and the 250,000 other people that ME affects in the UK alone. Myalgic encephalomyelitis (ME) is a chronic illness that impacts a range of the body’s functions, predominantly the nervous and immune systems.

According to ME Research UK, it is at least as disabling as multiple sclerosis, congestive heart failure and other chronic conditions as it debilitates people both physically and mentally. It can even be fatal: Merryn Crofts died last year just 10 days after her 21st birthday, after suffering with severe ME for six years and weighing less than six stone.

Receiving diagnosis is a battle. The condition has been underrepresented and misunderstood and its treatment chronically underfunded for decades.

A 2016 report, the only overview of UK funding on ME ever commissioned, concluded that despite the significant impact that ME has on the economy and its victims, research and funding remain “chronically low”, despite the fact that the economic cost of ME in 2014-15 was at least £3.3bn in the UK, according to latest research.

Harpreet Khan*, aged 53, has suffered with ME for eight years, losing her job, her social life and precious time with her family in the process. She finds it hard to describe the life-robbing symptoms: “Think about how easy it is for you to lift a hairdryer to dry your hair, now imagine that hairdryer weighs as much as a 10 ton truck. At my worst point I couldn’t get out of bed, I couldn’t move.”

A diagnosis can provide little clarity: “They haven’t a clue what to do so ply you with prescriptions, psychotherapy or whatever to avoid really looking at a person and investigating conditions,” says Khan.

Despite affecting more than twice the number of people, funding for ME is 20 times lower than for MS. Even research into male pattern baldness gets more funding – six times more, to be precise.

Managing to leave her house just once a week, Khan explains that the rest of her time is spent “paying back for the energy I used while I was out and trying to build myself up for another day”.

The lack of understanding both from medical experts and family and friends proves isolating: “You hear less and less from them, they say they don’t want to disturb you in case you’re having a bad day. They don’t realise that we need that support and to know we’re not forgotten.”

For Khan, turning to her own forms of therapy are her only respite. She is fundraising to create a wellness retreat for ME patients like her. Others are turning to alternative methods to try and ease the pain of their day-to-day lives, because there is no support elsewhere. My mum similarly uses art as an escape from the illness, but it doesn’t cure her pain.

With seven million people across the world suffering with a debilitating disease that is unknown to most, the fight to eliminate the stigma against ME is now urgent. It is time to commit to finding a cure.

*Names have been changed


Douglas Mateo

Douglas holds a position as a content writer at Neptune Pine. His academic qualifications in journalism and home science have offered her a wide base from which to line various topics. He has a proficiency in scripting articles related to the Health industry, including new findings, disease-related, or epidemic-related news. Apart from this, Douglas writes an independent blog and assists people in living healthy life.

Source Link Voices: I was raised by a mother who was battling ME – it’s not just ‘being tired’, it’s a devastating, life-defining disease