Imagine for a moment you’re having a dream.
In this dream you’re trapped in a room with no doors, no window and no light.
It’s pitch black.
But there’s someone else in the room.
Someone who’s wearing night vision goggles whilst you remain in the dark.
What you can’t see is their firm grip on a metal baseball bat, ready to swing.
You’re hit in the head and drop to the floor. The attack causes dizziness, vertigo, and confusion.
Eventually you vomit from the intense pain. Your speech is slurred. You can’t concentrate.
You frantically search around this small dark room, feeling only solid concrete in every direction.
There is no escape.
Some time passes… it could have been hours or even days.
Just as you can begin to rise to your feet, you are struck again in the head.
The attack leaves you completely debilitated. Worse than the first.
The pain is so intense you feel you might pass out… but somehow you don’t. Cruelly, you’re left conscious with all the pain.
Your head is spinning. You feel pins and needs in your fingers and your face.
Bright lights which aren’t really there, blind your vision.
You beg for it to stop.
But it won’t.
***
This is how a migraine attack has been described to others without migraine.
It’s a nightmare that you don’t wake up from.
Only it’s worse.
No one believes you.
Contents
The reality that people with migraine face
- Migraine is not just a bad headache, it is a neurological disease diagnosed by an extended set of criteria which include, but are not limited to, nausea, vomiting, sensitivity to light and sensitivity to sound in addition to moderate or severe head pain.[i]
- Migraine is more common than asthma, epilepsy and diabetes combined.[ii]
- According to the World Health Organisation, a severe migraine attack is among the most disabling illnesses, comparable to dementia, quadriplegia and active psychosis.[iii]
- Like autism, there is a spectrum of migraine disability. Some people have one attack or less per year. Some attacks are far more disabling than others. People can have migraine symptoms every day. It is estimated that 2% of the world’s population have migraine or related symptoms on at least 8 days a month.[iv]
- You can be smart, take your prescribed medication and still fail repeatedly to improve your condition. Research in the US found that around just 1 in 20 patients with chronic migraine are correctly diagnosed and treated by their doctor.[v]
- Migraine is not a psychological disorder or personality type.
- The stigma for chronic migraine is greater than that of epilepsy.[vi]
- The general public understanding of migraine is poor. Migraine Awareness Week in the UK and National Migraine & Headache Awareness Month in the US are not for profit initiatives to improve the awareness, research and advocacy for migraine patients.
- There is no cure for migraine. Treatments are available but nothing works for everyone. A treatment is considered effective if it can reduce the frequency or severity of migraine by at least 50%.[vii]
- In rare cases, migraine can be life-threatening. Each year people with chronic migraine are lost to suicide. Attacks are also known to induce a stroke in susceptible patients which in very rare cases has led to death.[viii]
- Those with migraine are often discriminated against. Migraine patients can experience social ostracism, isolation and job loss as a result of their migraine condition.[ix]
- Migraine is complex and multifactorial. Many things can trigger a migraine in different people including:[x]
- Sleep factors: lack of sleep, poor quality sleep or sleep schedule changes.
- Strong emotions: such as distress, grief or anxiety.
- Monthly hormonal fluctuations.
- Odor: strong smells, incense, cigarette smoke, perfume and chemical smells.
- Visual stressors: including fluorescent lights, bright sunlight, exposure to bright computer screens for extended periods of time or flashing lights.
- Neck pain: including discomfort, stiffness or pain in your neck or upper back area and the shoulders.
- Hunger: including missing meals, low blood sugar levels, hypoglycemia or getting too hungry.
- Dietary factors: There are many potential dietary factors. Not all affect everyone. Common foods listed as triggers include nitrites (processed meats) and MSG (monosodium glutamate), chocolate, aged cheese, red wine, beer, citrus fruits, cured meats such as bacon, hot dogs, aspartame and ice cream.
Over time, migraine can take everything.
Many of us with migraine need all we have to deal with the physical suffering and mental stress caused from constant and debilitating attacks.
When I’m at my weakest and most vulnerable from another attack, I’m forced to face another unexpected monster.
Discrimination and ridicule.
I’m told things like: “Why did you leave work? It’s just a bad headache. You don’t see me leaving when I get a headache.”
It’s difficult to describe the frustration and disappointment from such a patronizing statement.
If I wasn’t so exhausted from the recent attack, I’d be angrier.
Cancer patients who have both migraine and cancer have said that of the two conditions, they found migraine more difficult.
Cancer you can see. It leads to more deaths. Cancer immediately unites the sympathy and support of loved ones.
Migraine on the other hand is met with skepticism, stigma and discrimination.
Migraines don’t kill as many people as cancer but they can destroy everything worth living for.
Migraine has broken up marriages, families, relationships and careers.
If you’re reading this letter from someone who shared it with you, it’s because I don’t want our relationship to fall apart. You’re important to me:
I’m sharing this letter with you because I care about you and our relationship.
This isn’t a request for pity or sympathy.
I’m simply asking that you try to understand:
…I’m not trying to get out of the housework.
…I’m not taking the day off work to go shopping.
…I’m not trying to avoid your friends’ events.
I’m simply doing the best I can with what I’ve been dealt. There’s always someone worse off than myself and I’m grateful for what health and support I do have.
But I didn’t ask for this.
This is one of the most complex and challenging battles life has thrown me.
Help make the fight easier by removing the guilt and shame.
When it’s all said and done, few things matter more than our friends and family. What impact do you want to have on others around you?
You’re health too may some day fail.
If it does, you can only hope that you receive the support that is being asked from you now.
With your patience, understanding and support, I might just be able to make it out of that dark room.
The more awareness and understanding we have the more we can reduce the unnecessary stigma and discrimination of those with migraine and other debilitating neurological diseases.
Resources for employees with migraine:
Migraine Trust open letter for an employee with migraine (UK)
Article References
[i] Lipton, Richard B., et al. “Migraine prevalence, disease burden, and the need for preventive therapy.” Neurology 68.5 (2007): 343-349.[ii] Headache Disorders – not respected, not resourced. All-Party Parliamentary Group on Primary Headache Disorders. 2010.[iii] Shapiro RE and Goadsby PJ. The long drought: the dearth of public funding for headache research. Cephalalgia. 2007;27(9):991-4.[iv] Natoli JL et al. Global prevalence of chronic migraine: a systematic review. Cephalalgia. 2010 May;30(5):599-609.[v] Lipton, Richard B., et al. “Barriers to the diagnosis and treatment of migraine: effects of sex, income, and headache features.” Headache: The Journal of Head and Face Pain 53.1 (2013): 81-92.[vi] Young, William B., et al. “The stigma of migraine.” PloS one 8.1 (2013): e54074.[vii] Kaniecki R, Lucas S (2004). “Treatment of primary headache: preventive treatment of migraine”. Standards of care for headache diagnosis and treatment. Chicago: National Headache Foundation. pp. 40–52.[viii] Agostoni, E., et al. “Migraine and stroke.” Neurological Sciences 25.3 (2004): s123-s125.[ix] Diamond, Merle. “The impact of migraine on the health and well-being of women.” Journal of Women’s Health 16.9 (2007): 1269-1280.[x] Pavlovic, JM; Buse, DC; Sollars, CM; Haut, S; Lipton, RB (2014). “Trigger factors and premonitory features of migraine attacks: summary of studies.”. Headache. 54 (10): 1670–9.
thank you for putting this into words.
I hope it helps Rxandra.
Thank you, Carl. Beautifully done.
My pleasure Janine. I tried to do justice to the prison that migraine can trap us in.
iNCREDIBLE.
Thank you so much for creating this website with life saving and life changing content. I don’t know what I would do without it, along with Paula’s – Migraine Again…..I have found support from you, where we share this connected "unfortunate" hand that we’ve been dealt. I will share this letter with as many as possible in hopes they find compassion and understanding.
Thank you Carl, you’re an Angel.
Thank you for your kind feedback Karla.
Well said – it’s a good start in trying to describe it all. Made me a bit emotional actually. Just goes to show how ‘used’ to coping with it all you get or have to get. It’s been a long road – 38 years now and I’m in a much, much better place than I was years ago but they still haunt me a few times a year. My daily meds have definitely helped I believe in lessening the frequency and the potency of attacks. I wouldn’t wish these on my worst enemy and that really is saying something I can assure you. I hope you and yours part company soon Carl x
Thank you for the well wishes Caitriona. And you’re right, this is only a start in trying to describe it all. Books are written about it. No short article can do justice to the impact of migraine.
thank you, earth angel.
My pleasure Gina. I hope it helps.
please read this well written article carefully. it is an insight to a very serious neurological disorder.
Thank you Gina
I have had clinical migraine for 31 years and see the best neurologist in Chicago. (,preventatives, meds, injections, BOTOX, etc)!
I am now at the point of no return and have finally been accepted into an inpatient procedure that I’d happy to share with those who are at the ends of their rope. I M me or text and I’ll be happy to fill you in! All the best, edye
If things improve for you, please share your case study at https://www.migrainepal.com/casestudies/ where we are collecting case studies of patients who recover or achieve remission for the benefit of others.
I’m in the same boat as you’ve been in Edye and I would love to know how your latest treatment has gone as well as what the procedure was. I’m doing the Botox and treating with BP meds, etc. I still wake up with them and I’m in a battle 2 to 4 days out of every week. The fact that I have two little girls at home and I’m stuck in bed on somedays just gives me such a heavy guilt bc I’m missing out on so much.
My heart brakes for those who suffer from this. Praying that through Our Great Physician that a cure is in site!
Me too Kim!
I’m very hopeful given what I’ve seen from new research. Exciting times are ahead.
Carl! This brought me to tears…thank you for helping get through to someone with your beautiful description and powerful message. I have been hurt deeply by being misunderstood, called a hypochondriac, and the shame of being accused of doing this to myself because I am not making "healthy choices"….this all while desperate in pain every single day with no where to turn to. I’m grateful to stumble across this blog because I shared this letter with someone very important to me…someone that loves me unconditionally but simply hasn’t understood over the years how bad my chronic/hemiplegic migraines truly are. I want you to know that I am shocked with the reaction I received from them today. They told me it was the wake up call they needed and helped them snap out of it and they wanted to offer their support. I am still surprised but with tears of frustration and happiness…perhaps my journey will be now less painful with my people on my side instead of against me. Thanks again Carl.
I’m humbled by your comments Chandra. The fact that is has helped make a difference for you means the world to me. I wish you the very best and thank you for such a warm and encouraging note!
Warm regards,
Carl
Rose
hi i suffer with chronic migraines for weeks, no pain killers that can help them. I have uncontrolled shaking hands, and arms unable to drink, feed or dress myself. When i do have these migraines i am not able to speak a sentence i just ramble words over and over, not nowing birthday dates, simple tasks sleep for days in and out of consciousness. Decreased control over body movements, mobility weakness, help needed to go to the toilet and shower. I was frustrated crying, feeling down and depressed until i found this aboriginal temporary curer a table called GUM GUM Tables which is controlling my chronic Migraines.
Glad to hear you have found relief of some kind Rosemary. Take care and I hope things continue to improve for you in the new year. Best wishes, Carl.
Hi Rosemary,
I see that you mentioned shaky hands as one of your symptoms. I sometimes experience this before, during, or after migraines, and when I mentioned it to the doctor they couldn’t explain it. Do you know why you experienced this? Is this a common symptom for migraineurs?
Motor weakness isn’t uncommon.
Migraine affects the brainstem and nervous system which can lead to a whole range of unusual and inconsistent symptoms across the population of migraine patients and even within the same patient across different attacks.
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Thank you for expressing something that I have tried and failed to put into words many, many, many times
My pleasure Megan. Glad you found it helpful.
I never knew I was in 1 in 20 Americans who are correctly medicated
I take Amytriptylin for preventative medicine and Zolmatriptin (excuse my spelling) for treatment when I get one. At this point im from chronic to 1 or two a month.
Great result George!
Over time as you start embedding effective healthy behaviors and habits and building resilience you might look at transitioning the preventative with natural prevention strategies and tactics.
Hi Jake, it’s only 1 in 20 who tick all three of these:
1) See a doctor
2) get accurately diagnosed
3) receive guideline recommended treatment.
And yes, it’s scary.
I am totally perplexed about this issue. I suffer around 6 or 7 severe migraines every year. If you suffer from migraines in South Africa you simply walk into any Pharmacy and they will sell you a special migraine cocktail for less than $2, consisting of a combination of 3 to 5 tablets and capsules, specially formulated for migraines. Taking this cocktail would cure the migraine withing 60 minutes and you will be back to normal in two hours. (The head still needs some time to realign after the pain has gone). I now live in Australia and there is nothing any Pharmacy or Doctor has managed to give me or prescribe me that works.
I recently had a severe migraine attack but had unfortunately used my last cocktail a few weeks prior (I bring them over from South Africa whenever I get the opportunity). My wife eventually had to take me to Emergency at the local hospital at 4:30 am where the doctor gave me an injection and I was put on a drip. Because my 3 hours stay in Emergency stretched into the next shift the relief doctor was the one that discharged me soon after he clocked in. The two doctors charged $250 each, which Medicare paid for, and my wife paid a $335 non-refundable admission fee to the emergency ward. ($835 all up)
It is so sad. It goes further than this. I used to get these cocktails made up here in Australia with the help of my GP who prescribed two of the tablets for me that I needed to make up the cocktail. After the first round of 30 cocktails I went back to my GP for another prescription, only to be told that those particular tablets, or anything similar are no longer available in Australia. This was some 8 years ago. Since then I have been subjected to the imports again, and they have never let me down.
I would consider us migraine sufferers as a minority group; yet in a time where minorities these days seem to have the upper hand, this is something nobody seems to want anything to do with. If the cocktails I have been taking have any detrimental effect on my health, it is yet to be discovered after some 25 years of taking them. Is it that the people in Government Health Departments don’t suffer from migraines?
It is something many people hide… due in some part to stigma and discrimination. Because it’s an invisible illness the public remain skeptical about it and there we are yet to have any big meaningful public awareness campaigns. At least in Australia or South Africa. This may change soon and people are working on it. Until then, it’s unlikely migraine will be given the resources, support or education it deserves.
Well said! Well said! Thank you!
Thank you Cassie, I hope it helps.
Warm regards, Carl
Carl I can’t believe how accurate your description of a migraine is! I have tried for years to put it into words. Unfortunately, I have lost friends and family to this monster. I will be using your letter and spreading this website around. It’s great!
Thanks again!
Thank you so much Deb!
I hope this helps and shows others that there are many people who are smart, resourceful and who follow the directions of their doctor and still battle with migraine.
Thank you for this Carl. It’s so hard to explain what we go through and it’s so difficult for people to relate. I have never pretended I had a migraine, but I have pretended to be ok when I am not countless times.
I have had cancer and yes, the initial fright of the diagnosis is probably not comparable to anything else. However, with most cancer diagnoses, there’s a plan and a timeline and eventually you are more or less done. With migraine, you don’t see the light at the end of the tunnel. You get hopeful with a treatment plan only to see your hopes squashed time and time again. To me it’s been the hardest thing I have ever had to endured. No question about it. It crashes your spirit and your sense of self unlike anything else. It’s hard to keep positive but it’s so important to never give up and keep on fighting and trying everything. CGRP is quite promising, hopefully it works for most of us.
Thank you,
Maria.
Thank you Maria for sharing your experience. It’s amazing to hear from someone like you whose been through so much and still has the strength to persevere and remain hopeful.
We have a bright future ahead with many new treatment options arriving soon.
thank you carl, for giving up thought to people to think about the feelings of people with migraine attack before commenting on them.
My pleasure 🙂
I had no idea that a migraine is a neurological disease. My wife gets them and the way she describes them makes me worry for her. What’s the best way to help someone who is having a migraine?
Encourage her to learn about migraine and her triggers. It gives her more control and confidence. Migraine can be managed. I’m living proof but it takes time and patience while learning. Often it’s two steps forwards one step back. For you, simply ask her “how can I help?” when she is having an attack. It’s awful during an attack. Sometimes just being there for her is enough.
Hi Carl,
Thanks for elaborating all the details with perfection, if someone asked me about what is a migraine earlier, for a very long time I would not be able to explain them (though I am having a migraine for 9 years )This article gives my feelings powerful words. A doctor told me after a certain period migraine goes on its own. Is this true?
I’m glad this helped David. I guess it depends on how long you wait. Most people in their 80s don’t have migraine…. but who wants to wait until then? I’ve found that the people who recover from chronic migraine earlier in life take an active role in their own self-management and care. That doesn’t mean becoming your own doctor, it means partnering with them on an even ground where you have made the effort to learn about migraine, your condition and self manage what you can control to the extent that you can.
Thanks. I was looking for something to explain to my family and friends what I go through. Unfortunately this is the reality.
It is, unfortunately. I’m glad this helped.
Great letter, thank you.
Just before I had to give up my job because of migraine, I finally found a way to make people understand. I explained that the pain is worse than childbirth (which I’ve experienced) and lasts for longer.
Even men with wives who’ve had children understand that. It shocks them. You can see it in their faces, proving that they just didn’t understand migraine before (thought it was a bit of a headache).