Hardcore Migraine Sufferers Unite

Ta.

(Yes, once I get to the end of this, it'll be two years before they happen again).

First migraine in two years. My main trigger is blocked sinuses, so I attribute this one to a very dry September where it hardly rained at all suddenly shifting to being very rainy today.

i've been getting migraine symptoms without the headache. light sensitivity/blurry vision/aura. am i going blind?

curious about the post just above mine that mentions the change in the weather -- we just went from a long period of drought conditions to heavy rain.

Sounds like: http://en.m.wikipedia.org/wiki/Acephalgic_migraine

Barometric pressure changes can be a trigger for all sorts of migraine, including visual aura w/o headache.

That's interesting. I've noticed I often get migraines when we're in a high pressure cell, with dry air and bright skies, but my very worst migraines have been in suffocatingly hot and humid days of summer. By contrast, I seem to do fine with moderately cool, cloudy days, with or without light precipitation.

BTW I seem to recall reading somewhere that the Santa Ana winds (which are blasts of hot dry desert air funneled through the canyons and onto the southern California coastal plain) can also trigger migraines.

Many migraine sufferers in western Canada have similar problems with the chinooks.

Triggers are always personal, but barometric pressure changes are a commone one.

Ah yes, the Chinooks. The same must apply to the mistral winds in the Mediterranean I imagine

also the papyrus winds of the western arabian peninsula and the wing dings of australia.

sorry

http://en.m.wikipedia.org/wiki/Foehn_wind
http://en.m.wikipedia.org/wiki/Katabatic_wind

Yes, all those silly silly names for silly silly winds, how foolish of people to suffer from something you've never heard of.

this piece from a cluster headache sufferer is really descriptive

The headache was an unwanted guest. And my unwanted guest was a serial killer with an ice pick. When the right side of my face started to tingle, I would announce, “He’s coming.” This headache became personified. This pain took a pronoun. I planned my days around him, like how I planned my travels around snow when I lived in upstate New York. In my daily planner, I blocked out the hours between one and six. I would be occupied during those times, writing in my planner: “Down time.”

http://blog.longreads.com/2015/01/13/a-meditation-on-pain/

Cluster Headaches are such weird things. A year to the week of my last attack, I've got a "shadow" - pain in the same place as a cluster headache and with some of the same symptoms but with a lot less actual pain (say 3/10 instead of 10/10). I generally get actual cluster headaches proper every 18-24 months.

Was expecting cluster headaches in March/April but (thankfully) haven't experienced them. Ridiculously, I don't have a clear idea of when I get them (I've had them in spring and autumn) but its more or less every two years (I can actually track the last few years by checking my whinging on email).

Anyway, I've been experiencing the slightly freaky insomnia that seems to somehow precede an attack ... and it has been making me wonder if anything has changed advice-wise in the last two years?

I still use the same approach. Had 2 cluster patients in headache clinic this morning: one already on verapamil, the other I started it at a low dose. Gave them both scripts for dexamethasone and sumatriptan nasal spray.

I ordered them both CT angiograms but realized in doing so that I've got nearly 6 years experience in practice now, and have never once found an underlying structural or vascular lesion to explain cluster.

Most of my cluster patients do well, eventually stop coming to follow up appointments. I tend to run late in clinic (talk too much), keep people waiting for 20 minutes or more. If there's nothing to do but renew the prescriptions and banter about the weather, I can understand why they don't feel they need to bother.

Thanks Plasmon.

Is the nasal spray recommended over the injections?

Either/or. Nasal spray may be a little easier, plus you can aim at the affected side. Most people say it tastes gross though. But then some people don't like using injectors.

I got some zinc/magnesium/calcium supplements which I keep forgetting to take, but it occurs to me that the past 3 (?) times I actually remembered to take them I had a migraine that evening. Coincidence?

(Probably, as I haven't worked out my triggers. Certainly the last time it happened i.e. yesterday there were several other candidates, mainly stress and a weather change/getting too hot and dehydrated.)

Also tbh I'm not entirely sure these are migraines but I've been getting more and more of whatever they are lately.

I used to get infrequent and rather mild/shortlived* migraines which were unmistakeable as they came with aura, but these ones do not, so I'm not 100% sure they feel the same. However, they are approximately one-sided, come with nausea and often photophobia and/or neck pain, so I think signs point to yes.

Interestingly they also feel a lot like a more intense version of the nauseous headaches I get at certain times of the month (i.e. hormonal), which I hadn't been classing as migraines because it feels kind of insulting to use the word for something not completely debilitating, but perhaps they're all on a spectrum. Or perhaps they are 3 different things altogether. But anyway.

* at least in comparison to all the other accounts I've heard, still horrible though. it occurs to me that the thread title is "hardcore migraine sufferers unite" and I have outed myself as a very softcore migraine sufferer

I'm fairly certain that this thread can tolerate very softcore migraine sufferers ...

So, have there been any new wonder-treatments for Cluster Headaches?

Actually, getting proper ones now ... I did just think I'd had my worst ever single attack but I think that's probably just a reflection of how much I go into denial between episodes.

Anyone know anything about nerve blocks for cluster headaches? (Basically, are they effective/worth having?)

I finally found good meds. Excedrine. Pop two pills and usually they subside.

Psilocybin and LSD appear to have promise with migraines/cluster headaches.

https://www.ncbi.nlm.nih.gov/pubmed/16801660

http://www.thedailybeast.com/articles/2014/02/05/longtime-sufferers-of-cluster-headaches-find-relief-in-psychedelics.html

Thanks all. Oxygen does help (though I sometimes wonder if it just delays the pain). Sumatriptan works - it works well/speedily as an injection but less so as a tablet (though I still think it has some value). I don't like to take it for long periods of time, though.

Shitting hell. Five cluster attacks so far today (two possibly rebounds from using Oxygen).

Have been pondering last week's "Doctor in the House" about Cluster Headaches. The premise: a GP spends longer than the ten minutes they would allocate in a typical surgery to consider an illness. The GP appeared to insinuate that the headaches were a "life-style" issue and that the treatment should involve a reduction in stress and a change in diet. No mention was made of the specific symptoms or the recommended treatments (Oxygen, Sumatriptan injections) - and there's definitely an argument that what was being shown wasn't strictly a Cluster Headache.

I've experienced Cluster Headaches for 26 or so years, covering a variety of stress levels (from not at all stressed to mildly stressed) and from "skinny" to n"ot-so-skinny" aw well as a variety of diets (all, for the most part, healthy. Found myself highly irritated by the suggestion that the pain is a result of my "life-style" ...

i've been getting what i've called "tension headaches" more regularly in the last few years. they feel like a hangover without the nausea

- pounding headache, often on one side
- neck pain/tension
- nasal congestion

usually lasts til evening. on some rare occasions it lasts thru the night and into the next day. they are awful but i have no idea what they are or how to deal w them :/

physiotherapy might help

Cluster headaches aren't typically tied to stress. They happen more often in people who smoke and drink (and supposedly, have "leonine facies"). I encourage my cluster patients to quit smoking and drink only in moderation if at all, but that's about the only lifestyle advice I give them. I'm not aware of any association with diet.

Tracer, your headaches sound like migraines -- unilateral and throbbing. Migraine often produces pain in the neck / back of the head (occipitonuchal pain) and autonomic symptoms in the face like sinus congestion. Migraine headaches aren't necessarily severe, and the associated migrainous symptoms (sensitivity to light, sound etc, and nausea or dizziness) can be mild and sometimes manifest mostly as fatigue and a need to rest. As long as they resolve completely, it should be safe to treat them symptomatically. You could see a doctor and try a triptan for acute treatment, or if you want to manage them on your own you could take a large dose of ibuprofen (800 mg) plus some hydration +/- caffeine and if possible sleep.

thank plasmon!

https://splinternews.com/why-working-women-with-migraines-suffer-in-silence-1820243253

The cluster headaches are about, two years to the week since my last lot.

At the point of finishing my last cluster, I was prescribed Sumatriptan and Oxygen and had the offer of a Nerve Block "next time".

I don't get on with Verapimil.

Any new developments in the last two years?

Not sure why I wrote "about" - I meant "back".

i have been getting what i term my "Saturday headaches". i attribute them to stress at work. they are truly terrible - i am floored until around 5pm no matter how many ibuprofen i take, coffee, water etc.

my working theory is that extreme shifts between stress and non-stress exacerbates them. for instance, the last one happened when i worked like crazy on a Friday and went straight to the pub afterwards, then zoomed home to put kids to bed. i only had a pint and a half. so it wasn't a hangover. but i think there's something about the whiplash of those two modes that is stripping my gears.

sounds like you are onto something -- how does your nervous system feel? are you sleeping? are you jumpy? i haven't had a migraine in a long time but have grown increasingly (painfully) aware of the relationship between stress and somatic/physical symptoms :(

i never, ever get enough sleep but it's not insomnia it's just staying up too late :/

IANAD but if you make an effort to get enough sleep, it could really make a difference and maybe even solve your prob!

yep :/

Change in pattern does give me migraine attacks. So days off: lots of migraine. Go on a day trip? Migraine. It's not food but stress that gives me migraines. :-(

Hmm. Had a nerve block in the hope of seeing off Cluster Headaches for the next 8 weeks or so (the rest of the episode) ... and it worked ... for 36 hours.

:-(((((

today's my day for complaining on ilx. migraines suck. i've had this one about 24 hours, which means i've got at least 12 to go.

I get them very rarely, and when I do they are largely silent - I've only ever had one full-blown migraine, so at least I do know what's it's like to have a real one, but I had an intermediate one on Wednesday for the first time in maybe 3 years and it fucking sucked. It started off as a silent migraine with my right eye just completely aura-ed out couldn't see anything but shimmering then that wore off and I felt like someone was stabbing me in my eye for a few hours til it stopped hurting enough I could go to bed. I had some cocodamol and weed and turned all the lights off which may or may not have helped at all. Woke up the next day with a sore eye but it was gone by lunchtime thank fuck.

I get them once every week or two. i used to take imitrex but it made me have them three or four times a week so now i take nothing. it's not really sustainable, i need to start on something to prevent them.

Having a quick scroll through this thread ... Plasmon is a hero!

UK question: are Sumatriptan injections and Oxygen cylinders available? Bit worried about Brexit and the Covid world breaking me during the next cluster ...

What is plasmon? is that Aimovig?

Plasmon is a contributor to this thread. A neurologist, if I recall correctly? But genuinely appreciated.