“English, which
can express the thoughts of Hamlet and the tragedy of Lear, has no words for
the shiver and the headache. It has all grown one way. The merest
schoolgirl, when she falls in love, has Shakespeare or Keats to speak her mind
for her; but let a sufferer try to describe a pain in his head to a doctor and
language at once runs dry.”
Virigina Woolf, On
Being Ill, 1926
One of the most frustrating aspects of living with migraine is that no one else can see it. I've attempted to dramatize a migraine in my Introduction page, mainly to evoke and hook in readers. But over the years I’ve so often wished that my leg would
turn green and fall off during a migraine, not because I crave sympathy, but
because then I wouldn’t be thought a neurotic hypochondriac. It would also
solve the problem that Virgina Woolf, a migraineur, rather eloquently points
out: that describing one's pain and illness is an impossible task. But it is one I nevertheless
set an array of migraine and headache sufferers. I asked them to tell me what
their migraines felt like. Their responses reveal not only what an individual
and varied condition this is – but what a very real one it is. Even if no legs turn green and fall off.
I think Virgina Woolf would be most
impressed.
“Every single morning I wake up with pain in the
left side of my head. It feels like a vice has been attached to one half of my
head and it’s being squeezed tighter and tighter, as the day goes on the right
side joins in. This then feeling like a tight belt has also been wrapped around
my forehead and is being pulled tight. I get this every single day but
in addition to this, usually 3-5 times a week, I get a migraine
attack too. This feels like someone has buried a chainsaw right into the left hand side of my head!!!”
Mandi Howard, aged
45, Hemicrania Continua, New Daily Persistent Headache and
Chronic Migraine sufferer since July 2010.
Fran, aged 28, aka Skulls and Ponies, very bravely taped herself on the verge of a migraine and described not only how it feels but how she treats attacks. Check out her blog for other useful migraine posts. Fran has suffered with migraines for 8 years.
Migraine Movie from Fran Swaine on Vimeo.
“It's
like having a black cloak around my head, a heavy, throbbing haze of confusion,
pain, clumsiness and vertigo which can vary from leaving me wobbly to stumbling
around, or having to lay completely still and unable to care for myself. I have
the most bizarre auras, tinnitus, double vision, facial/teeth pain, ear ache
and absences which I can only describe as something similar to silent epilepsy.
Some days I find walking more than a few meters impossible, I am so exhausted
by the pain. It isolates you physically and emotionally but it still remains an invisible
illness.”
Annie,
aged 43, Chronic with Basilar &
Vestibular Migraine.
Migraines
commenced at 12 years old.
They began out of
no-where when I was around 17 as a once a week, want to blow your
head off with a shot gun, puking
everywhere, kind of deal. Then they transformed into something less severe but
more common, eventually becoming something I had to feel every single day.
Imagine those
little toy wind up monkeys that bang symbols together. Imagine that sound from
the moment you wake up every day of your life, to the moment you go back to
sleep. I don't really get sensitive to light anymore and I'm fairly strong now so
I still try to get on with my life but the one thing you can't avoid when out
is babies and little kids screaming and crying, it makes me think my head might
actually blow up, especially if I can't escape like when I'm waiting to see the
doctor, it's unbearable.
In my last job a colleague
thought it was funny to hit his keys on my desk every time he went past
thinking it wound me up, I tried to tell him it wasn't winding me up - it was
hurting me, but it didn't seem to make a difference to him. I think it's high-pitched
sounds I really, really can't cope with.
Maggie Austin, aged
24, Chronic Migraine Variant Without Aura. First migraine 7 years ago.
Occipital
Neuralgia feels like something has the nerve near the base of my neck and is
slowly twisting it as tightly as possible through a mangle which has tiny nails
all over it, and makes you feel like both sides of your head are caving in very
slowly and your eyes are being pushed together! Trimeginal Neuralgia, for me,
varies. On a low pain day I just get a constant feeling of a dull pain on the left
side of my face and it’s the whole left side, teeth, ear, cheek and eye. But on
a high pain day, it’s like someone has sewn a long icicle into my cheek that
wont melt and just gets colder and colder and more painful and the stress it
causes makes me chew the inside of my mouth so I have holes inside my cheek
that are also sore.
With my
migraines, I feel I have two. The first one goes right across my forehead like
a skin tightening feeling, and it feels rock hard and this is the only migraine
I get where I feel very sick and do actually throw up. Blinking and any
movements of my eyes hurt and makes the pain worse. The only thing I can do is
sleep to not make it worse. My second migraine, my big migraine if you like,
only appears on the right hand side and sometimes where the pain is so bad
parts of my head, the size of a small tomato, swell up and a lump will appear
and I am unable to lift my head off my pillow and feel very dizzy. My head
feels 100 times heavier than what it is, but the pain I can't quite put my
finger on. It can feel like very sore pins n needles and that I have taken a
large whack to the head several times. Almost like a concussion!
Mel Browning, aged 40, Occipital Neuralgia for 3 years, Migraine and Trigeminal Neuralgia since February
2012.
“I feel like I’ve had a stroke. I can’t move my right hand side at all, I can’t even speak properly. I am helpless. Then there is the pain – it is shooting, stable, shooting, moving around. One moment it is on the right side of my head, then the left, then the back of my head, and all the time I have this heavy numb feeling down my right.”
Basilar Migraine sufferer for 5 years.
During
a migraine I feel very drained and tired and all I can think about is lying
down and trying to sleep. My head feels really heavy and my neck can no longer
support it so if I’m not lying down, I am normally leaning my head against
anything handy - walls, desks, tables, lamp posts etc. It feels like my brain is expanding, there is so much
pressure on my skull. I
find it hard to have my eyes open, they feel dry, my eye sockets hurt and
bright lights feel painful. My brain stops making connections. I feel stupid
and slow and find it tiring to talk. I feel completely spaced out and it feels
like things are happening around me but I’m not really part of the real world.
I am very sensitive to noise and smell and can often feel dizzy and nauseous.
My whole body feels very sensitive and achey, similar to when you have the flu.
I often have freezing cold hands and feet but a really hot head so ice packs
and hot water bottles are simultaneously used. The only thing I can do when I
have a migraine is hide away from all stimuli and lie down in a dark room away
from sound, light and distraction and just wait it for it to pass. Sometimes I can sleep, but sometimes
I just lie there in a zoned out state for hours. When I’m recovering
from a migraine I feel like I’ve been hit by a bus and feel completely bruised
and battered and very drained and tired.
Fiona
Russell, aged 31, 8 years as a Migraine sufferer.
“The first sign of an impending
migraine is a slight feeling of unease and disorientation. My limbs then
start to feel heavy and tingly and a slight numbness almost imperceptibly
spreads up my arms. My mouth feels strangely dry. Then comes the
dreaded black spinning penny in my blind spot accompanied by cartoon stars on
the periphery and searing, burning sunbeams across my central line of sight.
A vice-like grip envelops my head
and an amazing volcanic pressure builds behind my eyes. Finally, the
blurred vision is such that I am lying at the bottom of a rippling pond looking
upwards at the world. There is no option but to hunker down for the next
couple of hours. Suddenly everything clears and I am overwhelmed by a
sense of energy and euphoria....”
Owen, aged 35, Migraine with Aura for 6
years.
Thank you so much to the lovely, brave migraineurs who shared their incredible stories and descriptions. Next time you meet someone who tells you
they suffer with migraine, why don’t you ask them what it feels like?
FACT:
A migraine is usually made up of 4 phases: Prodrome/Premonitory phase, Aura, Headache and then Postrdome. This is why my task of
asking for a simple description of a migraine was a tricky one! Not all
migraineurs suffer from each phase - but recognising and understanding them can be crucial in managing migraine.
Coming Up: Next I asked these
same migraineurs to show me what a migraine LOOKS like…a brave few took
pictures….this time I joined in!
Migraine Awareness Week!
(2-7th September 2012)
If you suffer from Migraine, or any
of the other conditions mentioned above, you can find help at:
The Migraine Trust National Migraine Centre
The Migraine Trust National Migraine Centre
Wow - it's interesting to hear other people's stories. I focused purely on the headache part of my migraine but the other phases are just insane. Perhaps more manageable - although after an awful migraine I'd say the postdromal phase is the worst. It's exhausting and you are constantly on the verge of getting another migraine. You feel like you want to wrap yourself in cotton wool!
ReplyDeleteThank you so much for putting these together! It's reassuring to know I'm not crazy, but I feel so bad for those who suffer. It's ironic how alone I feel when experiencing a migraine, yet I know there are millions who feel the same misery. To all, I pray for relief from and understanding of such a debilitating illness.
ReplyDeleteGreat blog and collation of experiences. They perfectly display that the experience of migraine is really so individual and varied. Some migraines can pass in hours, others last for days, if not a week, some just roll on back to back continuously. But the one common thread throughout all the experiences is that they are incredibly debilitating.
ReplyDeleteI've only ever experienced a few migraines in my life. The first one when I was 17. I was replacing a lightbulb and hadn't switched off the lamp at the mains, as I put the bulb in the flash of light suddenly coming on triggered a severe pain behind my eyes. What ensued over the next two days was the single worst pain I've ever felt, like my head was being crushed. My eyes wouldn't focus, I was vomiting continually. A doctor had to be called and I was given an injection in my bum(!) which worked almost immediately this was followed by some foul tasting powder I had drink over the next few months to stop the migraine reoccuring.
ReplyDeleteWhen I was at uni in my final year, I began getting zig zag shaped "aura" and the migraines began again. It sounds weird but I also used to get a "shrinking" feeling. Hard to explain but a bit like Alice in Wonderland after she drank the shrinking potion!! A feeling of shrinking then expanding. Safe to say I thought I was going crackers!
I haven't had a true migraine for several years now and the doctor feels I've simply "grown out of them" That's fine by me. Such a debilitating illness.
Hi! Wow that sounds horrible! Fingers crossed you wont get that again - as I"m sure you know what you experienced actually has a name - Alice In Wonderland Syndrome (AIWS) where things visually seem distorted...as CS Lewis was a migraineur many people think he got the inspiration from his auras... I like to think we migraineurs have super cool, genius creative brains! :)
DeleteWhat a great blog, it's interesting reading other peoples experiences. I never understood how debilitating migraines were until it happened to me. Thank you for putting this together. xx
ReplyDeleteThank YOU for your fabulous contribution xx
DeleteI get it where it feels like my skull is expanding and it often hurts deeply in between my eyes or in the eyes themselves. I often feel dizzy or disoriented during this and sometimes get a stiff neck as well. I have also had tension headaches. When I get the expanding feeling wearing a bicycle helmet tightly helps relieve the pressure feeling, though I'm sure I look silly in my pjs and a bike helmet, its worth it.
ReplyDeleteHey Sheena, happy new year! Well, I must say I've never heard of anyone actually putting on a bicycle helmet before - you might have to take a picture for me..... but as you say if it helps go for it!! Hope 2013 brings you many headache free days! x
DeleteHi all... its horrible....my pain starts very slowly.. it was a worm and heavy feeling in my head and neck joint... then its moving around.. from staring point to full head suddenly itz strikes more heavy and hot flush in head.. between two eyes. Itz worse.. and i feel like someone striking a nail in my eyes chicks and teeth... its worsen and worsen...until i tried cefaly headband. its really works a lot. My throbbing headache are gone. i feel relaxed and suggested it for other migraine suffer.
ReplyDeleteThis is fantastic! I'm so tired of clinical terms like "discomfort" and "tender"... I have a few different types of migraine attacks:
ReplyDelete(1) My brain is a washcloth being wrung out
(2) My skull is in a vice - this is generally the more "mild" type where I can still do things, it just feels awful.
(3) My brain is suddenly claustrophobic and is trying to escape my skull
(4) My brain has been replaced by a ball that rolls back and forth whenever I move and somehow stabs the side of my head if I move too fast
(5) Ice Pick migraines - sudden and over quickly
I have issues with a lot of medication and get "rebound" migraines when I'm on something. I can sometimes stop them with Advil gel caps (since I normally feel them coming on) but since I get several in a row, this only works for the first few. Also, since there are liver issues in my family, I don't like taking medication. If I don't "catch" a migraine before it gets worse, I get the usual light/noise sensitivity, exhaustion, dizziness, and nausea that many people mention - I also get a sort of numb pain down my arm.
Thank you for setting this blog up and giving us a space to share symptoms. It often feels like I'm losing my mind when they get bad.