My endless pain: living with fibromyalgia

I live with a little understood, often invisible, medical condition that means my life is a bit of a rollercoaster. I never know from one week to the next, or even one day to the next, how I will be.

Take the last month. I’ve had a couple of fairly good weeks, where I have been able to get out and about and do a few things extra, like meet up with friends. However, this also has its payback and for a few days I’ve been stuck in bed unable to leave the house.

This yo-yoing of symptoms is typical of the experience of a fibromyalgia sufferer. It is one of the most common chronic pain conditions in the world, has an estimated one million sufferers in the UK – and yet it is shrouded in mystery. Last week it entered the public consciousness when the Desert Island Discs presenter Kirsty Young said she would be taking time off because she has the condition. Last year, Lady Gaga revealed she was a sufferer.

My fibromyalgia started when I was 24, shortly after the birth of my daughter in November 1993. It took until May 2005 to get a diagnosis. In those 12 years, I was told that my symptoms were due to various types of arthritis, depression and, more than once, that they were all in my head. It was a very frustrating time, especially when all the tests and x-rays kept coming back clear.

hen I finally did get my diagnosis it was a huge relief to have a name for what I was experiencing. However, that relief was tempered when I soon began to realise that many people do not consider fibromyalgia to be a real illness. If a condition does not have a medical test to confirm it, then that condition does not exist, they believe.

My main symptoms are severe, widespread pain, chronic fatigue, cognitive dysfunction and memory problems (we call it “fibro fog”), sleep problems and irritable bowel syndrome – but there are many more that affect me to varying degrees. Like many people with fibromyalgia I can look much better than I feel – and the condition is often described as an invisible illness for this reason. Because you do not look ill, or there is no obvious cause for the symptoms, people may not believe that you are as ill as you say you are – and this disbelief can come from medical professionals, family and friends, as well as from complete strangers.

Most of the time I use crutches for walking, or my mobility scooter for longer distances. My balance and spatial awareness are very poor, so I might stagger, stumble and fall if I do not use them. People tend to think you either need to use a walking aid or you do not. But with fibromyalgia you may need it one day, then not the next.

hen I finally did get my diagnosis it was a huge relief to have a name for what I was experiencing. However, that relief was tempered when I soon began to realise that many people do not consider fibromyalgia to be a real illness. If a condition does not have a medical test to confirm it, then that condition does not exist, they believe.

My main symptoms are severe, widespread pain, chronic fatigue, cognitive dysfunction and memory problems (we call it “fibro fog”), sleep problems and irritable bowel syndrome – but there are many more that affect me to varying degrees. Like many people with fibromyalgia I can look much better than I feel – and the condition is often described as an invisible illness for this reason. Because you do not look ill, or there is no obvious cause for the symptoms, people may not believe that you are as ill as you say you are – and this disbelief can come from medical professionals, family and friends, as well as from complete strangers.

Most of the time I use crutches for walking, or my mobility scooter for longer distances. My balance and spatial awareness are very poor, so I might stagger, stumble and fall if I do not use them. People tend to think you either need to use a walking aid or you do not. But with fibromyalgia you may need it one day, then not the next.

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