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A small study published in June suggested that almost 9% of migraineurs have facial pain during an attack. Now this is of course another of those chicken-and-egg questions, because some of those patients likely have jaw issues that are triggering migraine attacks. But others simply have migraine attacks that cause the facial pain. Read about the study from Germany, Prevalence of facial pain in migraine: a population-based study.
In fact, in rare cases, there is something rare called isolated facial migraine, where the pain in the face is the main feature of the migraine.
Sometimes treatment for the jaw is needed, such as an NTI-tss device. In other cases, when the pain is coming from the migraine attack, simply treating migraine as a whole will solve the facial pain issue as well.
What about you? Do you have facial pain during an attack? What’s it like?
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{ 51 comments… read them below or add one }
It’s interesting that you posted this today. My migraine pain has been, for the most part, under control for a while. But for the last 3 days my face has been tender to touch. I was wondering if it was sinus, but the pain goes beyond the sinus areas, plus, I’m not having any other symptoms of sinus trouble. I’ve had facial pain w/migraines before, but never without headache. Perhaps I’ll try treating it as a migraine and see it that provides relief. Either way, it’s better than the head-pounding, debilitating pain I generally associate with migraine.
Hi…just new here! i have had severe migraines for over 10 yrs now. Not fun… The last 2yrs they have become worse..the face pain, i have experienced alot of..during some of my migraines i loose all feeling in the left side of my face..then when all is done the pain starts.
Well, I took a Maxalt and the face pain went away. I’m shocked, but happy to be able to stand having anything touch my face again. Thanks for the tip, I’ll keep this in mind from now on, but at the same time, don’t want to jump right into taking medication anytime my face hurts. Always a balancing act…
I also experience face pain with migraines, mainly on the right side. Also twitches of eye lids, jaw pain and neck pain. I suffered with those symptoms for years as I had no idea they were related to migraines. Maxalt and Replax both relief those symptoms. I take Maxalt when I have time to lay down and nap. I take Relpax if I don’t have the opportunity to rest. Sometimes I only have face pain and twitching, but no accompanying “headache”. In those cases, I don’t take medication. Only if the pain is debilitating will I put strong meds in my body. The other symptoms are inconvenient, but not debilitating.
Thanks for the comments, everyone! Yes, it’s very important to “connect-the-dots” and realize which symptoms are actually connected to migraine. I’m glad this one could be of help.
Tricia – you pointed out something important. This is yet another reason migraine attacks can be mistaken for sinus headache. Important note!
For years I went to doctors complaining of sinus, jaw (tooth) and neck pain that would not arrest with over-the-counter pain relievers. The doctors thought I was nuts, as I didn’t have a sinus infection or bad teeth. I never imagined that those where migraine symptoms. I never experienced an aura, or upset stomache, or sensitivity to light or sound with my headaches. Finally my doctor put it all together and sent me to a neurologist when I complained of numbness in my cheeks, twitching eyes, and face pain. I hope you all are getting relief from your migraines.
My *eyes* hurt! I’ve been looking around the site and not seen this mentioned specifically — when I am getting a migraine, my eyes feel heavy like I want to cry. No pain initially, and no symptoms in my face or teeth (that comes later). But for years I thought I was depressed because I felt like I wanted to cry all the time. It wasn’t till I was diagnosed with migraine and noticed that the heaviness in my eyes was a precursor that went away when I took a Maxalt that I made the connection…
Hi i just recently had one of the worst migraine attacks in yrs! It lasted 8 days…hospitalized. I lost all function in my left side, was not able to speak without slurring or stuttering my words. Very scary!
They have put me on a new drug called Ralivia (tramidol). It is a pain reliever you take daily. Along with my other medication…Topomax i take daily.
Has anyone else experienced this loss of function before? Or has thier DR. mentioned this drug to you? I relize it is just release in Cananda and very new. thanks
I’ve had many such episodes. I get to the point where I can’t speak at all, and lose my memory during the time of the migraine, then I recover once the head ache goes away, usually after hospitalization and medication. Good luck to you.
Tramadol may be new in Canada but it’s been in the US for many years. (I googled and the way you spelled it only comes up as a “common misspelling of Tramadol”). It’s called Ultram here. It can cause dependence like Vicodin, so be careful. Here is some info: http://en.wikipedia.org/wiki/Tramadol
Yes, losing function as you mention Lisa is possible with migraine. However, as you probably know it’s important to rule out other possibilities (such as stroke) before giving a diagnosis of migraine (even if there is pre-exisisting migraine).
It would be wise to get another opinion – both on the symptoms and the treatment. There are a variety of treatments available, and I think you would be wise to get a migraine specialist to hear about your medical history.
I have an apt. with a nuroligist ( i know spelled that wrong) In two mths…..the doctor i seen in the hospital tried telling me i was too wrong to develope symptoms of a stroke, that brought an argument on….As a nurse i see stroke patients alot and age is not a factor.I have suffered from migraines since i was a child and seen many doctors….now my daughter is having them…do not want to see her go through what i am. Thank you Christine for the info….
Its good to realise I am not on my own. My migraines are definitely food related but not always sure which food – sometimes I can tolerate something and another time I can’t. I wonder if anyone has the same progression as me. If I eat something that will trigger an attack it takes about 8-12 hours before I start to feel the symptoms; first upset tummy and neck ache; then the headache starts and by 24 hours later using sick. Feel totally wiped out for the next 24 hours then start to come round. Does anyone else suffer for so long?
Yes, people do sometimes have a “delayed reaction” when it comes to food triggers. And yes, erica, the length of your symptoms is not at all unusual – I wish I could say it was! Sometimes things last even longer.
And yes, sometimes the same thing can trigger or not trigger an attack. This is likely because of the “full bathtub” – it’s not one thing triggering the attack, but a number of things. One the “bathtub is full”, it just takes one more thing for it to overflow….
It is hard to understand triggers. Some are very consistent at triggering a migraine, and some aren’t. I journaled pretty extensively for a year, and I’m still not sure what all my triggers are. James, that is a very good explanation about the bathtub being full. It makes perfect sense to me. I am a long time runner. That explains why running will sometimes trigger a migraine, and sometimes not. This site is very helpful to me – thanks everyone!
Thanks James for commenting on my posting. Bathtub effect sounds sensible. In this way of thinking I also think that eating too much can trigger a migraine. As if you can only tolerate one sort of food at a time and only a certain amount.
Thanks everyone for your post and information. Migraine is horrible but at least I don’t feel like there is something to be too scared about, not something happening only to me.
It hurts to see the right side of my face sagging; and sometimes it’s only my left foot that feels cold. The sagging started yesterday; I started taking Naproxen E- Mylan 500 (2x/day) on Friday and I don’t know if I am having some side effects; I have to have someone to read to the info inside the box–too small. I understand the spelling difficulties of Tricia because I am also haing them. My brain is telling me that I have typed that letter and find on the screen that I haven’t. I was a spelling champion at school and a fast typist, but now, sometimes I don’t care anymiore if my fingers aren’t punching the right keys.
Arora, you bring up a good issue – I have been experiencing noticeable memory loss the past 6 months or so. As a project manager, I work in a very fast paced environment. I’m in meetings all day and I have to remember a lot of details. I’m not sure if it’s side effects of medication (Maxalt and Relpax), or if the migraine pain distracts me, or if migraines cause memory loss. I have started to take notes extensively. Even looking back on the notes, I can’t recall hearing the information (who said it and in what context). I look back on emails that I sent and I honestly don’t remember sending them. I feel like I have Alzheimers. The memory loss is beyond what I consider normal and it worries me.
Hi all,
This is all very interesting reading, i recently began feeling strange sensations on the left hand side of my face, my mouth felt like it was sagging a bit and i felt like i was slurring my speech and my left eye felt watery, i think i have got it down to happening when i have fizzy drinks.
I spoke to my dad who is an optician and he suggested it could be migraine related, although i’ve never suffered from what i think of as a migraine – headaches, trouble with looking at bright light etc, from reading all of this it seems very likely now. Does anyone else get it but not get other effects like a headache? I’ve also had a few issues with my memory recently but dont know if this is down to just being busy at work, i’m not taking any meds that i could put it down to, but can this be an affect of a migraine that affects the face too?
Hi Everyone! I have just recently returned from the migraine pain clinic in Calgary alberta. Had med changes, I have been taken off the tramadol which i am very happy about…..had very bad side affects with these….d/c the t4′s, :0) and lowered my dose of topomax i am now on amitryplyne nightly BIG improvement on my daily migraines! and only for pain i am on an anti inflamitory called naproxen….helps alot…….no rebound headaches from this at all!!
i do want to thank Christine for your info I took that with me and discussed it with my specialist and she agreed with my concerns! so a big thanks to you!! Lisa
interesting reads forsure. I sit here for the last 2 days my right side is tingling and numb. Half right down the middle of my lips, nose etc. No headache. I get migrains that last anywhere up to 8 days. Just feel all doped up just to get through my headache which dibilitates me. I can get it on half of my face, starting the back of my neck then up and around. then i have a 24 hr reprive then bang on the other side. VERY frustrating. Have been suffering for 28yrs to my recollection.
My migraines are definitely related to food intolerances. Have just come across a brilliant book by Dr. Lamar Gibbons called Self Help Way to treat Colitis and other IBS. I know we don’t necesarily have IBS but the food intolerances are the same and I haven’t had a migraine for over a week!!!!! Certainly worth a look especially if food triggers your migraines.
This is so ironic. I live in rural central IL. I am about 3hrs from the
Diamond Headache Clinic in Chicago. I have had migraines for about 20 years, finally ending up on disability. I talk about my headaches by year, because they change. The only consistency is that about March/April, usually around the time change, I get a migraine that lasts for about 2 months. This year, however, they never stopped. I have facial pain, but I have it all the time, especially in my forhead area. I finally made an appointment and had the awesome expreience of not only seeing a Dr. at the Diamond clinic, but he immediately put me in the hospital in Chicago. They have a 37 bed unit at a nearby hospital. I was there for 5 days. My Dr. changed all my medications. I have only been home for a couple weeks, but already my facial pain is gone.
He told me that some of the meds would take a few weeks to completly reach their level in my body. I have high hopes (and total faith in my Dr.) that I will finally find som relief. I would like to say that personally, I feel that when a person has suffered from severe migraines for a long period of time, there is something that changes in our brains. I don’t believe that I will ever be headache free, but I now have hope that I am being taken seriously and have a chance of a more normal life.
Sandra W.
I am so thankful I have found this forum. To be able to read everyone’s comments is so helpful. I have been having trouble for years (typically in the fall) that tends to be different but the same if you know what I mean. I had shingles in my right ear which spread down my face in 1978, which started a landslide of lifelong events. I had an allergic reaction to compozine and suffered lock jaw for 6 hours the next year. I now have constant ringing in my ears! I was institutionalized for depression several times over the next 10 years usually in the fall of the year. Not to list all the following years events, but in 2006 I had an heart ablation and was put on heart medications for an irregular heart beat. Last fall I had Bell’s Palsey on the right side of my face. The droopy face, slurred speech, slobbering, my eye would not close, was absolutely horrible. This fall it has been the migraine symptoms with dizziness that has lasted for over a month now. I can’t look up, I can’t look down! I went to the school nurse and she put me on an antibiotic for an inner ear infection and sinus infection. I wasn’t getting better so I finally I went to see my ENT and he said I didn’t have an infection, that it sounded like migraines to him. The light went on!!! I started putting the puzzle together. First, it is genetic! My mother and sisters have had them all their lives. The time of the year also seems to be a factor. This year I have been trying to work but I can’t concentrate. I just feel crappy! I just want to sleep! My face tingling is really beginning to bother me! In my 55 years, I have been diagnosed with a number of things but I think they all boil down to this: Migraines! The comment I read about foods rang true because the first symptom I had was I noticed my gut was bloated. I became constipated and things have gone down hill since. The more I research this, the more I realize I need to clean my system out. I read somewhere that when your stomach gets out of balance it can cause your brain to get squirrely too! Go figure!!!
I really appreciate all the helpful comments from fellow sufferers. I hope I can help some one however, I don’t really know much at this point.
In the last 3 weeks the right side of my face has started to annoy me. It doesn’t hurt unless I made a facial expression or touch it. It starts under my cheek bone and up to my hairline and its on the side of my face. It does not go into my nose or eye. It is sensitive to the touch and really starting to annoy me. It is a very slight pain but still annoying especially when touched.
I do suffer from migranes and have since an accident over 40 hears ago. My migranes have tapered off the older I get. I have about 2 a year now.. Sometimes bad (thick tounge, slurred speech, distorted vision, severe headache, numbness to left side of face and mouth, numbness of left hand ect) and sometimes not bad at all but we all know the difference between a headache and a migrane no matter how severe it is. My migranes have all the symptoms of a stroke. Except I can smile and I can lift my arms.
My question is: Do you think my facial tenderness is caused from a migrane? I have had it for about 3 weeks now. I did have a sinus cold about a month ago and I did have a large tooth on that side fixed and it was giving me fits. I have had that tooth xrayed twice and it has since not been bothering me and xrays show nothing is wrong with it.
I’m just wondering if I should see a dr. (dont want to, just went before this all started) or any advice?
I have never heard of migranes lasting so long and I dont take any meds for this at all.
Hi there……I found this herbal migraine pill and thought hey why not?? What can it hurt? RIGHT???
Well it has testimonials from many others with migraines…..it states…works within 20min or your money back…hmmm.
So i thought i would give it a try…on the instruction for those who are severe to take 2 daily so that is what i have been doing.
Has been 2 wks now….and i normally am one of those people who wake with headache or migraine symptoms in the morning hrs and it takes atleast 3 to 4 hrs to disapate ….it has been 6 days FREE of symptoms in the morning!! <:0)
And even having the beginning of a minor migraine the other evening i took my evening pill it leveled off enough that a exedrin helped.
These herbals are called…."" BELL Master Herbaslist MIGRAID Headache Relief"" I found them at our Local NUTTERS heath food store.
Maybe they can help some of you too!
thought my face pain was fibromialgia or congestion – doubted migraine diagnosis – i thought migraine was a headache with sensitivity to light (which i don’t have) – until i found this site. new migraine sufferer – diagnosed yesterday, this is not good.
so, i’m a breast cancer survivor and i had a scare – i’m glad it’s migraine and not a brain tumor, which got ruled out on wednesday
so… i’m goig to continue checking in – need all the info / experience/ expertise from all here, to deal with this.
thanks to all – i know i sound crappy, feeling crappy, but THIS TOO SHALL PASS !
I was recently diagnosed with cluster headaches about 3 months ago.I have tried many different medications and found one that worked.The headaches are much better,but my teeth on that side of my face hurts and i cant figure out why this pain is coming from my teeth when the headaches are better.Does anyone have any suggestions?
At first my teeth start hurting, then it travels up both sides of my jaw, and when it does my hearing is effected. It seems as if my hearing is muffled. About 5 to 10min later I have a migraine, I can feel the temporal part of my head throbbing and once I get over the migraine, my jaws are tired (kind of like if you have been chewing a peice of gum for a long time).
I have been a migraine sufferer for over 30 years. I take Topamax 100mg to help control them, i have been on it for about 6 years. Without it my migraines last months at a time. I still get them occasionally from food triggers. I find red dye #40, dark chocolate, MSG. to be the worse. The FDA still does not feel red dye #40 is a problem.
I have problems with remembering words when trying to talk to people and have trouble reading books, the letters jump around, has anyone else had that?
Regarding the letters jumping when you read: There are some people with this problem who get relief by using colored filters over the page they are reading. A friend of mine did research on this and had assembled a collection of tinted plastic cover sheets. Different people are helped by different colore filters. There is a word for this condition, but I cannot recall it.
If this is your problem, the fix is immediate and cheap, and has no side effects!!!
I just started using organic raw unfiltered apple cider vinegar with mother
i bought it at a health food store. 1 tablespoon in a glass of water 3 times a day (can sweeten if needed) I have suffered migraines all my life.
they are GONE…GONE…..GONE.
the trace minerals ..probably magnesium did the trick…..and as an added benefit my arthritis pain disappeared in 2 days.
I recently started getting facial migranes when eating at Macdonalds. Found out it was the mustard!! Wonder if it is GMO foods. GMO the great experiment!!
Hi, I just stumbled onto this site and found it interesting what each person had to say about their migranes experiences. I’m not sure at this time if thats what I’m having. I’ve been to the er twice with severe head pain. I have had meds given to me just to numb the pain but not total relief. I’m waiting for a ct scan to rule out other conditions. My only concern is that everything I’ve read about migranes they usually only last up to 72hours. I’ve had a headache for well over a month. My symtoms are very migrane related but length is longer. Just wondering if theres anyone out there that can give me some answers.
New to forum. Have suffered from migraine attacks since 1999, I’m thirty now, they started when I was nineteen. The first one that I experienced, I was driving my car home after a day at work, where I had to leave because the pain in my head was so intense. Anyway, I blacked out and ended up coming to in the oncoming lane of traffic, over 50 miles away from home. Scared me to death, needless to say. Now, I have other symptoms other than just extreme pain in my head. My face hurts, ALL THE TIME, to the touch. I also have a very peculiar, constant pain in my neck and upper shoulder area, my neck crunches when I move it just slightly, and the real kicker….I can be just sitting, doing nothing, and my neck will have a “rubber band” sensation-like that of a rubber band popping inside it, and then from the area in which that occurred, a burning that spreads up to the top of my scalp, paralyzing the side of my body on which it happened….my head feels too heavy for my shoulders. Puking happens during some of the episodes, a feeling of being shut off from reality, and the auras and hallucinations are there with just about every attack..I even get the blurry vision.
I have been to my GP and they did xrays, over three years ago, said that my spine in the cervical area of my back had “lost its curve.” No advice to follow up with any other physician, except chiropractic….which I did recently, because the pain is so much that I cannot function anymore. Been to urgent care twice in the last three months because I wished truly that I was dead, couldn’t get out of bed because I was in so much pain…last time, the urgent care physician suggested a neurologist to find out what’s going on. So I have set up an appt. I have taken Midrin, Flexeril, Butylbital, and nothing seems to help. This last time, they gave me Maxalt, and so far I have had to take one dose, it has helped a bit.
I am a pre-k teacher and have the two most beautiful, wonderful children in the world of my own, and I just want my life back. If anyone out there has gone through this, please let me hear from you!
Just an afterthought…there’s a song from Pink Floyd that mentions “the swollen head blues”……this is a feeling I can relate to.
hi sarah i have jut read your forum, sounds very similar to mine. To cut a very long story short i was diagnosed with occipital neuralgia in january this year, neck always crunches, burning feeling ect. I have a steriod injection in both sides of the occipital nerve and has proved to be really good. I hope this is some sort of help or that you have found someting to help you by now.
I have had a migraine for the better part of 2 weeks now, whith a few hours of relief here and there. It’s a low grade headache, not if full bloom, but the left side of my face hurts really bad. All the teeth on the left side hurt like cold air on an exposed nerve. As soon as I get my next check, I am going to see if I can get a dentist to pull all my teeth. I can’t take the pain anymore.
Hello Sherry
I have been suffering with a migraine since March but didn’t know it, Like you it started off with my teeth hurting,then my head and neck,pain was so bad that i went to the dentist thinking it was my teeth, i had an xray and it turns out my teeth are fine.
Went to the hospital as i could not take the pain anymore as it has been painful for me everyday and starting to get me down. I was told by my consultant that i am suffering from facial migraines i thought he was going mad as i had never heard of facial migraines before.
I am hopeful now and keeping my fingers crossed that it will finally get sorted out.
I too have this problem, if you have tried an otc sinus med with no relief then see your general practitioner and get an antibiotic as it is probably a sinus infection
Have you tried taking a decongestant like Sudafed? When my teeth ache, if I take a Sudafed I can often stave off a migraine (I know this because I have waited too long at times an then only Maxalt will help). The person who mentioned muffled hearing — if your ears are congested, it can go to your sinuses and either can trigger a migraine.
Hi. I am new to this cite. I just discovered it today. I am sitting at my desk with ringing in my ears, jaw/teeth pain, and difficulty concentrating. Even while typing this, I have to correct every other word. I am 44 years old and have been diagnosed with Basilar Type Migraines. I have doubted if that was a correct diagnosis. However, this cite has helped me alot. My symptoms are those above then it progressively worsens until I cannot even speak. I just sit and stare. I can hear people talking to me, but I cannot physically respond. These episodes last anywhere from 3o mins. to 2 hours. Sometimes I just “run slow” which means I have to concentrate very hard to understand someone’s words and have to take my time to respond. I even say words that make no sense. Does anyone else have these problems associated with their migraines. I do not get a headache very often afterwards, but the pressure in my head is very noticeable.
hi im new here
ive suffered with migraine’s since i was in my teens….my mum is a chronic sufferer too. I used to get a bright light followed by blurred vision then feelin sick. Now i seem to be getting them in my face, along my cheek bones from my temple on both sides of my face, ive had my sinuses checked last week as ive also had nose problems and it isnt that, I have found this web site very usefull. I was just wondering if eye strain can be a cause of any of these symptoms??
thanks
Got my first migraine when I was 10. Was 9 o’clock at night, I was sleeping, when I woke to severe pain on my right hand side of my head and vomiting.
30 years on, I still suffer terribly from this affliction. I had several migraine episodes where the right hand side of my face went numb … scary thing is … when I went to lie down, I went blind in my right eye for 6 minutes.
I was referred to a neurologist but I have never gone. To afraid to find out if it’s something more then just a migraine. Yes they have gotten extremely bad, and I can be bed ridden for months.
I know wear sun glasses inside and out as my eyes as so sensitive to light. Maximelt doesn’t work, nothing does. To tired now. Just tired of this constant pain.
I have suffered with migraines for 32 years! I am only now, beginning to understand them. Thanks to a fabulous neurologist! I have tried almost every prescription,OTC, and herbal medicine known to man! I recently had botox injections and they seem to be helping, far from a cure. My migraines occur nearly daily and have worsened in symptoms and severity. I have the facial pain, ear, tooth, neck pain, vomitting,sweating,dizziness,vertigo, nausea, etc! I was told I had atypical trigeminal neuralgia,and begged for root canals, sinus surgey, anything! I was desperate enough to break down and go o Topamax, which I despised! I felt brain dead! I am following an antimigraine diet,that is crazy strict, but at this point I would try ANY THING! I am happy to find this forum, and wish the best and pain free days for all of you!
Hello there,
I know the thread is a bit old, but I was wondering if someone could help me.
I’m relatively young, about to turn 26, but for a couple of years now, I’ve had this symptom when I touch the outside of my left nostril, I get a burst of pain on the left side of my brain.
It feels like a migraine, a strong headache, but stops when I remove my finger.
Is it this face migraine you guys are all talking about here?
Is there a nerve running close to the nose which could trigger this pain? Please advise, I really don’t know what I got, and haven’t met anyone who had the same symptoms.
Thank you very much!
Hi,
I realize I’m coming in very late in this thread, but just found your article after a quick search. I have suffered with migraines since childhood and experience intense accompanying facial pain. It’s always on the right side, goes from the neck area along the jaw, eye socket, temple and up to the top of the head. It’s excrutiating at times. I’ve only taken Imitrex for my migraines and that gets rid of the migraine within an hour. Since losing my health insurance, I’ve been taking the generic version…not fun. The side effects are pretty awful (body/flu-like aches, weird panicky feeling), but it does get rid of the migraine after about an hour or so.
Thanks so much for the article! I
I have had migraines for yrs. But lately my face hurts sooo bad! I can’t remember my face being this bad. All behind me eyes,down the sides of my nose and the top of my head feels like it will blow off. Sometimes this with my eye and nose hurting so bad is just on one side. I press on them so Hard it is a wonder I have not done damage. The last one I had hurt so bad my blood pressure went up and stayed up. I also had a nosebleed on the side that was hurting so bad. This has never happened. It really scared me. Any comments or help. Noone really understands unless they have had migranes. They can just take one aspirin and get over theirs. Someone who has had some of these symptoms please comment and HELP! Oi
Hi Linda,
I get facial pain with my migraines (my jaw hurts, feels almost like an ear ache or toothache), but what you’re describing could be a sinus infection or maybe even TMJ. You might want to see a doctor to have it confirmed. I often get a rapid heart rate with my migraines (I have high blood pressure and take a beta blocker). Nosebleeds can be an indication of a sinus infection, but they can also indicate blood pressure problems. Both of these issues need to be looked into by a physician. Most medical experts suggest that, even if you’ve experienced regular and even chronic heachaches, if you are experiencing new or different types of headaches it’s important to be seen by a doctor asap. Best of luck to you!
Hi
I’ve lost function in the left side of my face. I went to see the doctor and he confirmed it was migraine. For those who have experienced it, will my face come back to normal? Thank you.
I have been experiencing severe headaches on the right side of my face since I turned 30. I am now 34.
Mine seem to be triggered by changes in atmospheric pressure. I had my first one after a flight from the northeastern US back home to Louisiana. I didn’t have another one for a while, but now I have one every time a cool front comes through. Like I said, they are only on the right side of my face. It’s a throbbing, pounding pain that seems to be centered just above my right eye in the middle of my right eyebrow. My whole face swells up and droops and my vision is affected. I also experience nausea and vomiting and light sensitivity as well. It hurts to open my eyes and to blink. It feels like the whole right side of my mouth on the top and bottom are full of cavities and it hurts to chew. You could literally draw a line down the center of my face as to where the pain is. It involves the entire right side of my face. The last time I had one, I couldn’t get out of bed no matter what medicine I took. I lost an entire day due to the headache. I don’t see auras and don’t hallucinate, although I know that not everyone who has migraines experiences those symptoms either. They also seem to be triggered my hormones and seem to occur more around my periods. I went to the dentist and my teeth were fine. I really am not sure if it’s sinus polyps or facial migraines.
I have been alternating Allegra D and Zyrtec D, which I have to get from behind the pharmacy counter. I take one for a month and then switch to the other when one stops working. I take one every day with breakfast and my headaches are much more manageable. I only have one on occasion as opposed to almost daily and they are nowhere near as severe. I am able to function normally while taking these meds. In Louisiana, the weather is always changing and little fronts, whether warm or cool, always seem to be passing through.
I have been reading these blogs and I find them helpful. I just went out and bought a whole bunch of produce to give the diet change a try. I don’t eat a lot of meat anyway, so cutting that out isn’t that big of a deal. It’s cutting out the sugar and milk that will be more of an issue. I’m becoming a lacto ovo vegan (I think that’s what they call it)–not eating eggs, wheat, msg, wine, milk, soy protein, sugar, or meat of any kind. If a food lists sugar, wheat, or soy in the first 3 ingredients, I won’t eat it. It’s gonna be tough though, especially during my period when I crave chocolate like crazy. I know I should give up coffee, but I’ve had it every morning for the past 30 years and that’ll be extremely tough. For now, instead of using a dairy creamer or milk and sugar, I’m gonna try goat milk and truvia. Hopefully it won’t be too hard to stick to, I would like to stop taking the Allegra D and Zyrtec D altogether. I feel foggy-headed all the time and am not sure if it’s from the meds or the migraines or both. I find it hard to concentrate. I have always loved to read and now find that I have to re-read the same things over and over to comprehend it. My mind seems to wander a lot.
Hopefully the change in diet will help. Thanks to everyone for your comments.