It’s been a very long time since I’ve written anything in this blog… but I thought it was high time to start a series of posts about my current life with fibromyalgia. So, what even is fibromyalgia? Let’s break it down a bit.
- It’s also known as Fibromyalgia Syndrome, FM, FMS, or just ‘fibro’.
- The word itself comes from fibro-, meaning ‘fibrous tissues’, myo-, ‘muscle’, and algos, ‘pain’, which translates to ‘pain of the muscles and connective tissues’.
- Fibromyalgia is a chronic pain condition, meaning that the pain is long-term.
- It is characterised by two traits known as hyperalgesia – feeling a pain stimulus more intensely and longer than normal; and allodynia – feeling non-pain stimuli (like pressure or cold) as pain.
- It has much in common with, and clusters together with Chronic Fatigue Syndrome, Irritable Bowel Syndrome, Depression, Anxiety, Restless Leg Syndrome, Myofascial Pain Syndrome and Temporomandibular Joint Dysfunction – but is recognised as distinct from all of these.
This is just scratching the surface, though, as fibromyalgia has a whole galaxy of other symptoms aside from pain. These can include (but are not limited to): severe fatigue, cognitive impairment, joint stiffness, limb weakness, chronic headaches, digestive difficulties, body temperature fluctuations, skin tingling and muscle twitching. On top of this, there is no known cause, no cure, no widely accepted treatment – and as one consultant rheumatologist helpfully told me, “if you put 100 doctors in a room, you’d have 100 different opinions about whether it is even real or not”.
It certainly feels real.
Medical definitions and lists of symptoms are all very well, but it can be very difficult to understand what it is actually to live with such a nebulous condition. So I plan to explore and explain my experiences in this ‘Life With Fibromyalgia’ series, and I hope it offers some insight into a widely misunderstood illness.