r/migraine • u/brokecracker • 13h ago
r/migraine • u/kalayna • May 13 '21
Resources
The wiki is still a work in progress, so as with the previous sticky, this highlights some resources that may be useful.
Edit - added the COVID-19 Vaccine and Migraines link since we're swapping that sticky for the Migraine World Summit announcement.
If this post looks familiar, most of it has been blatantly stolen from /u/ramma314's previous post. :)
Diagnostic Criteria
One of the most common questions that's posted is some variation of, 'Am I having migraines?'. The same is the case with 'what kind of migraine is this?'. These posts will most often be removed as they violate the rules regarding medical advice. You need to work with a medical professional to find a diagnosis. One of the better resources in the meantime (and in some cases, even at your doctor's office!) is the diagnostic criteria:
It includes information about migraine, tension and cluster headaches, and the rarer types of migraine. It also includes information about the secondary headaches - those caused by another condition. One of the key things to note about migraine is that it's a primary condition - meaning that in most cases, migraine is the diagnosis (vs. the attacks being caused by something else). As a primary diagnosis, while you may be able to identify triggers, there isn't an underlying cause such as a structural issue - that would be secondary migraine, an example of which would be chiari malformation.
Not sure if your weird symptom is migraine related? Some resources:
Website Resources
There are several websites with good information, especially if you're new to migraine. Here are a few:
American Migraine Foundation - the patient-focused side of the American Headache Society
Added Feb 2025 - the American College of Physicians (ACP)'s treatment guidelines for prevention of episodic migraine: https://www.acpjournals.org/doi/10.7326/ANNALS-24-01052
Migraine World Summit - Annual event, series of talks that are free for the first 24 hours and available for purchase (the year's event) thereafter.
They made a tools and resources list available, for both acute action and prevention, providing suggestions for some of the sub's most often asked non-med questions:
https://migraineworldsummit.com/tools/
Some key talks:
2024 - Beginner's Guide to Headache Types - If you're new and struggling with diagnosis, this talk alone may be well worth the cost of the 2024 package.
Reddit's built in search!
We get a lot of common questions, for which an FAQ on the wiki is being built to help with. For now though reddit's built in search is a great way to find common questions about almost anything. Just enter a medication, treatment, or really anything and it's likely to have a few dozen results. Don't be afraid to post or ask in our chat server (info below) if you can't find an answer with search, though you should familiarize yourself with the rules before hand. Some very commonly asked questions - those about specific meds (try searching for both the brand and generic names), the daith piercing, menstrual/hormonal migraine (there are treatments), what jobs can work with migraine, exercise induced attacks, triggers, and tips/non-drug options. Likewise, the various forms of migraine have a lot of threads.
Live chat!
An account with a verified email is required to chat. If you worry about spam and use gmail, using a +modifier is a good idea! There's no need to use the same username either.
If you run into issues, feel free to send us a modmail or ping @mods on discord. The same rules here apply in the chat server.
Migraine/pain log template!
Exactly what it sounds like! A google docs spreadsheet for recording your attacks, treatments tried, and more. To use it without a Google account you can simply print a copy. Using it with a Google account means the graphs will auto-update as you use the log; just make a copy to your own drive by selecting File -> Make a copy while signed in to your Google account. There are also apps that can do this and generate some very useful reports from your logs (always read the fine print in your EULA to understand what you are granting permission for any app/company to do with your data!). Both Migraine Buddy and N-1 Headache have a solid statistical backbone to do reports.
Common treatments list
Yet another spreadsheet! This one is a list of common preventatives (prophylactics), abortives (triptans/ergots/gepants), natural remedies, and procedures. It's a good way to track what treatments you and your doctor have tried. Plus, it's formatted to be easily printable in landscape or portrait to bring to appointments (checklist & long list respectively). Like above, the best way to use it is to make a copy to your Google drive with File -> Make a copy.
This sheet is also built by the community. The sheet called Working Sheet is where you can add anything you see missing, and then it will be neatly implemented into the two main sheets periodically. A huge thanks from all of us to everyone who has contributed!
Finding Treatment
Most often the best place to start is your family doc - they can prescribe any of the migraine meds available, including abortives (meds that stop the migraine attack) and preventives. Some people have amazing success working with a family doc, others little or none - it's often down to their experience with it themselves and/or the number of other migraine patients they see combined with what additional research they've done. Given that a referral is often needed to see a specialist and that they tend to be expensive, unless it's been determined that secondary causes of migraine should be ruled out, it can be advantageous to work with a family doc trying some of the more common interventions. A neurologist referral may be provided to rule out secondary causes or as a next step in treatment.
Doc not sure what to do? Dr. Messoud Ashina did a MWS talk this year about the 10 step treatment plan that was developed for GPs and other practitioners to use, primarily geared for migraine with and without aura and chronic migraine. Printing and sharing this with your doc might be a good place to start: https://pubmed.ncbi.nlm.nih.gov/34145431/
Likely in response to this, the NHS published the following:
https://headaches.org/2022/01/19/national-headache-foundation-position-statement-on-the-treatment-of-migraine/ (link is broken)
/mod hat off
My personal take on this is that hopefully your doctor is well-versed. The 10-step treatment plan is, I think, a good place to start for clinicians unfamiliar, but it's not a substitute for doing the learning to be able to move away from an algorithm and treat the patient in front of them.
/mod hat back on!
At this point it's probably good to note that neurologists are not, by definition, migraine specialists. In fact, neurologists often only receive a handful of ours on the entire 200+ headache disorders. As with family doctors, some will be amazing resources for your migraine treatment and others not so much. But they can do the neuro exam and ruling out of secondary causes. Exhausted both? There are still options!
Migraine Specialists
A migraine specialist is just that - a doc, most often a neurologist, who has sought out additional training specific to migraine. There are organizations that offer exams to demonstrate that additional knowledge. Some places to find them:
MRF is no longer. UCNS is it!
United Council for Neurologic Subspecialties
Migraine & Headache Australia - Headaches and Pain Clinics
Telehealth
There's a serious shortage of specialists, and one of the good things to come of the pandemic is the wider availability of specialized telemedicine. As resources for other countries are brought to our attention they'll be added.
US:
Canada:
Crisis support.
Past the live chat we don't have subreddit specific crisis support, for now at least. There are a lot of resources on and off reddit though.
One of the biggest resource on reddit is the crisis hotlines list. It's maintained by the /r/suicidewatch community and has a world wide list of crisis lines. Virtually all of which are open 24/7 and completely anonymous. They also have an FAQ which discusses what using one of the hotlines is like.
For medical related help most insurance companies offer a nurse help line. These are great for questions about medication interactions or to determine the best course of action if nothing is helping. If your symptoms or pain is different than normal, they will always suggest immediate medical attention such as an ER trip.
r/migraine • u/kalayna • May 25 '26
UPDATE to the 16 May Rules Update - App Devs, Anyone Doing Market Research, etc. Will Want to Read
edit - the new bit is a... ranty. To those here just to check in, my apologies.
Y'all.
Seriously.
The sheer number of app devs who have continued to waste mod time and continue spamming in comments after being warned is mind-boggling.
I believe that this community deserves good tools. HOWEVER, this community is not here to be sold to, and just like the post that preceded this, the people who can't stop spamming are rarely community members first, and devs second. They're here because you are the market. Since last week's post I had given a lot of thought to a periodic 'promote your stuff!' post to strike a balance, but after spending far too much of my holiday cleaning up spam-droppings... I'm feeling less than charitable. o.O
Spammers. If we warn you and you keep spamming, it won't just be you that's banned. It will be any mention of your product regardless of who posts it.
Astroturfing? Instant permaban - you and your product. Why?
You should not spam in any way, especially through private message. You should not hide your affiliation to your project or site, or lie about who you are or why you like something.
Here's a copypasta of the previous post, all of which still applies:
(If you were looking for the Summit pinned post, it's here.)
We're currently seeing multiple posts - or people that know promotion isn't permitted and trying to sneak it in via comments - promoting apps and/or doing market research daily. Most of the people hoping to benefit from this community have never made any effort to participate in it.
Promotion has always been in the the rules, and surveys/research have always required pre-approval from the mod team (though we recently had to update to not approving any because I'm the only active mod and simply don't have time to review in addition to everything else).
With all of the above in mind and all of the attempts to circumvent or flat-out argue about removals, it's time to formalize things:
Promoting your new app and/or doing market research (what don't you like/what works for you/what is missing in other <whatever>) is not permitted in this subreddit. The same goes for asking for feedback. Yes, this includes the ever popular 'hey I did a thing but it's against the rules to promote here, so if you're interested, send me a pm!'. If you're thinking about sending a modmail to ask to be an exception with less than 6 months of active participation in this subreddit, don't (even then it may not be approved).
I will be updating rules, sidebar, and filters over the course of the weekend.
Because of the lack of participation for most of these users and the number of users that have attempted to get around this, this will be one of the rare times when suspensions will be issued on first strike, rather than warnings first.
Also, you've probably noticed I'm the primary one handling approvals/removals, and that there are updates the sub could use that have not been done. In addition to chronic migraine and adulting in general I have what totals up to nearly 2 full time jobs and am usually also taking college classes, so there is a lot going on, and running this sub in a way that rules are enforced and the sub itself is enhanced and we're able to provide space for the community to be active in helping with research opportunities takes a lot more time than the above workload allows. To that end, I'd love to add 2 or 3 new mods to the team that can consistently (meaning most weeks) offer a couple of hours to running/maintaining the subreddit. That can be:
Working on the FAQ: at one point there was an effort to build something of an 'intro to migraine' resource
Fielding research/survey reviews: even better if you are or have been part of the research community (someone did offer this before; if you're still interested please reach out!)
Post / comment reviews: If you're a regular/semi-regular visitor and don't mind doing some cleanup while you browse, this is one of the easiest ways to ensure that community standards are upheld
I've held off on posting this because I had big plans to set up an awesome form to fill out, but for all of the above reasons that has not happened. SO! If you're interested, please send us a modmail with answers to the following questions:
Why you're interested
What you think mods do
Previous modding experience
What you're interested in helping with
Your time zone / location
How much time you can reasonably and consistently pitch in to help
Optional: Anything else we should know about you? Any ideas for the sub you'd like to implement?
As long as the above isn't struck through feel free to send a message if you're interested. It may take a bit to hear back because busy, but unless we get hundreds of apps we'll follow up to set up a chat with u/ramma314 and myself so we can get to know you a bit. If we do get hundreds of apps we'll update here that we either can't get back to everyone or that we'll be copypasta-ing replies specifically for that reason.
r/migraine • u/uzuis4thwifee • 16h ago
Having to run errands with a migraine
rizatriptan✔️
cooling patch on forehead✔️
sunglasses✔️
only one eye open at a time✔️
caffeine✔️
r/migraine • u/cheater00 • 1h ago
Ginger powder: works for me
I'm a triptan user, normally when I have a migraine I need a dose of sumatriptan or zolmitriptan. The latter works somewhat less and is slower. Recently I saw a short by Dr Greger on YT talking about a good-looking study that said a 1/8 teaspoon of ginger powder in water works just as well as sumatriptan, or even better.
I didn't believe it so I started trying it since then. Just drink a glass of it every day. Same amount. I don't measure it exactly, I just do it by eye with a normal teaspoon.
I haven't had migraines since. It works well. Sometimes I get a slight very very low level "i might be getting a migraine" kind of feeling, but it never actually turns into a migraine.
I'm not using any special medicinal version, just normal organic ginger powder I've been using for cooking. That specific packet is probably like 15 years old already. It's not fresh by any means. It still works perfectly fine. I don't use any special water, I literally just put like 1-2 fingers of cold tap water in a small glass (like a hotel breakfast juice glass) and then dump the powder in it, swirl it around so it absorbs into the water, and down it all like that.
I searched this sub and there's previous discussion, going back as far as 10 years ago. People suggest all forms of ginger, including candy, candied, powder, capsules, fresh, etc. Apparently all of it works but for me the powder is the easiest way to get it all in one go.
Some people report it doesn't help them, some people say it's hit and miss. So it's definitely a personal thing.
https://www.reddit.com/r/migraine/comments/cw1si4/ginger_as_a_substitute_for_triptans/
https://www.reddit.com/r/migraine/comments/1211wim/chiming_in_on_ginger_it_works/
https://www.reddit.com/r/migraine/comments/1akd9nq/ginger_for_migraines/
https://www.reddit.com/r/migraine/comments/sci2h5/ginger_capsules_as_abortive_med/
https://www.reddit.com/r/migraine/comments/4ykxdp/shout_out_to_ginger/
https://www.reddit.com/r/migraine/comments/1brjqr3/ginger_root_powder/
There's also someone for whom eating ginger stopped working. They were doing fresh, raw ginger.
https://www.reddit.com/r/migraine/comments/1e83lbq/ginger_doesnt_work_anymore/
I hope this helps someone here, especially given how expensive triptans can be.
r/migraine • u/Gh0stwhale • 2h ago
The fries and coke cure works!!
I woke up with a wicked headache and nothing I did would fix it. I did everything right and my head was still throbbing.
It’s 5PM, I have to go to work in a bit, and so I stopped by to get a Mcdonalds small fry and coke…
After the first few fries I instantly felt better. I guess I needed the salt but omg I feel great and I’m so relieved to not have to work with a migraine
r/migraine • u/Adorable_Art539 • 4h ago
Crying is one of my worst trigger
When I get upset and cry it will cause a horrible migraine. I was at the emergency vet for hours yesterday and convinced my dog was about to die, and naturally of course I was crying, and this morning I woke up with a migraine (also didn’t get a lot of sleep) and so far I’ve done —
IM toradol injection
Rizatriotan
Nurtec
Zofran
IM toradol and Rizatriptan did help for a few hours, but then I was still in a lot of discomfort again so I took a nurtec about 4 hours later.
I am still in pain and have nausea.
Just popped another Riza..
r/migraine • u/BlackberrySuperb7168 • 6h ago
Personal home remedy
Ok so I live in the States but on a vacation ten years ago I discovered a British otc med called migraleve that worked for me as well as a prescription. Unfortunately one of the ingredients is not otc in the USA.
So I did a little online research and the medication was very similar to meclazine which is sold as bonine or non drowsy Dramamine
So my home remedy is this. Right when I detect it coming on I take a meclizine along with a single Excedrin pill and a single Aleve. I take them with some regular (not diet or zero) cola. I personally think the caffeine helps some and the insulin reaction from the sugar helps metabolise things quickly.
I have shared this with some friends and they also say it works. Best is that you literally can get everything from a dollar store.
Good luck
r/migraine • u/backtonov • 5h ago
Weekly check in
How is it going for everyone this week?
I’m feeling doom and despair but was wondering how everyone else is doing too.
r/migraine • u/Zealousideal_Cap7782 • 8h ago
Ubrelvy or Nurtec
Curious if anyone has tried both and had more success with one than the other?
I used to take sumatriptan but started to have side effects so I was switched to Rizatriptan. I had no side effects with Rizatriptan and it worked very well. Recently, it has been giving me the same side effects that sumatriptan once did. My dr said to stop the Rizatriptan and to consider Ubrelvy or Nurtec. Just wanted some insight before I ask my dr for the prescription!
r/migraine • u/ChickenMythic • 19h ago
How do u all deal with unsollicited advice?
Today is another shitday
Not one, not two but three different people felt the need to hand out tons of unsollicited bullshit generic advice om how I should get rid of my migraines and how to treat them.
I just feel so disrespected. I have had this condition over 25 years. Do you really think you have a better idea of how my migraines work than me?
Anyone else run into this? Do you get frustrated? How to reply politely in a way that says: fuck you, not interested and shut up.
By the way - non of these are migraine patients themselves. I would actually enjoy talking to them about migraines
r/migraine • u/Loud-Distribution744 • 59m ago
Migraine - double panda oil
Hi all,
Ever since I started working, I have been experiencing debilitating migraine. While I try to avoid pills, I had come across this pepper mint oil two years ago.
My colleague used it and had apparently bought it from Malaysia. She gave me one bottle and now I’ve run out of it. Can’t find it in Indian markets
Can the kind reddit community pls suggest good substitutes for this available in India?
r/migraine • u/Embarrassed_Box7242 • 23h ago
Migraine Police Vent
I hate when people ask how I function with a migraine and that it’s probably just a headache.
I had childhood absence epilepsy and it’s common to have migraines as a result, so I’ve had them since I was a kid. They don’t make me cry anymore but I feel sick and people talking make my head spin. No I can’t sleep it off bc I can HEAR everything twice as loud. But YES I do have migraines. I’m not sure why people like to compare “oh but mine make me so sick I need to be on bedrest for days”; while I’m sorry about that, this has always been my life. So yes, I’ve come to live with it and just take it because life goes on with or without me.
r/migraine • u/RiTFWx • 12h ago
Premonition/something is not right aka I know my body is going to give me a migraine soon
Hey all — new here, migraines for 37 years, currently under good control with ubrelvy and some preventatives.
Sometimes I get a spidey sense that I’m going to have a migraine and take my CGRP. This used to happen when my only rescue drug was indocin and it never worked. I have never gotten a migraine after a spidey sense and taking a CGRP.
Does anyone else experience this? It feels like existential dread coupled with vague fatigue and irritability.
r/migraine • u/Kind-Leader-7845 • 14h ago
Does anyone see something similar to this when they have theirs? NSFW
Does anyone see something similar to this when they have theirs? It's not literally double but this sort of disorientation when looking at ppl
r/migraine • u/Kmkgoodworks • 20h ago
Vyepti🤞🧠
Got my first infusion yesterday so far feeling good!🥰
r/migraine • u/Ryley1890 • 1h ago
Lidocaine injections
Hi all. For about a year and a but now I've been getting 12 weekly lidocaine injections to try numb the pain. Never normally have issues but after yesterday's treatment the back of my head is still swollen and my neck is uncomfortable to move. This time around they did add steroids to the treatment as the usual lidocaine had become ineffective.
Is this normal for the added steroids and has anyone had any experience like this
r/migraine • u/EnderDragoon • 13h ago
Start crossing fingers
9+ hours of BO, Cologne, joint atrophy and recycled air. The clamping is already crawling up the back of my neck, headed directly for the back of my left eye.
r/migraine • u/alex_mattson_ • 11h ago
Anyone else afraid of a brain bleed?
All the symptoms of a brain bleed sounds just like my migraines, and my family has hustory with brain injuries/bleeds. I don’t easily go to the er because i’ve learned to deal with the pain. My grandma had a brain bleed, thought it was just a migraine and ignored it.
r/migraine • u/TreTreeTree • 4h ago
Postdrome experiences
Just for some background. I luckily do not typically have ongoing migraines, and over the last 2 - 3 years I've had 4 or 5 large scale migraines that have basically put me out of action for a week and this usually includes a period of postdrome (where I just feel like a blob and get the typical; dizziness, head tightness, vision blur, nausea).
This time around 6 days ago now I unfortunately made the stupid decision to drink quite heavy and had a bad hangover which turned into a migraine and now I think I am in the postdrome phase but honestly it can be hard to tell when the symptoms feel like a sinusoidal wave. I plan on going to my doctor (once again) but was wondering if anyone has any tips and I know there are a lot of posts about postdrome I am sort of asking for the sake of having people to talk to about this!
Would really appreciate hearing any tips to make it through postdrome or even just commenting and letting me know that you made it through would mean the world to me. I'm currently in that state of mind where I feel like it's never going to end (although it has in the past) and It's going to impact my work, my life, etc, etc. I try to avoid spiraling but it get's tough when it feels like days later your symptoms haven't really gotten much better.
P.S. I tried Maccas Coke and Fries and it was awesome in the moment but unfortunately was no permanent magic remedy
r/migraine • u/onlychappals • 57m ago
Migraine
Hi all,
Ever since I started working, I have been experiencing debilitating migraine. While I try to avoid pills, I had come across this pepper mint oil two years ago.
My colleague used it and had apparently bought it from Malaysia. She gave me one bottle and now I’ve run out of it. Can’t find it in Indian markets
Can this kind reddit community pls suggest good substitutes for this?
r/migraine • u/ComprehensiveAnt4549 • 14h ago
Pregnancy and sumatriptan
I am one of those people who have had migraines for over 15 years and always knew they wouldn’t improve during pregnancy (although my family doctor assured me they would). Well they haven’t and I have been on rizatriptan my entire life and switched to sumatriptan shortly after my pregnancy started.
I have done my research, talked to pharmacists and drs and although I continue to take them, and will have to because I simply cannot function without, I would like to hear from other people who took them during pregnancy!
I have read there is no risk for neurodevelopment but this is at the top of my fears! Probably just pregnancy anxiety getting to me, but if you took them, and your kids are older, how are they? Every one of my pharmacists just say “no evidence of disorders because no studies have been done.”
I have read almost every forum about sumatriptan and pregnancy and know lots of people have taken it, but I would like to hear how your kids are now! TIA!
r/migraine • u/Kiy_the_ghost • 16h ago
Doctor recommended I go to the ER for migraine
So I’ve had chronic migraines for the past 3 or so years, and I’ve just recently been able to go to doctors to try to help them.
But right now I’ve had a migraine for the past 3 and a half weeks, and have been switching around my preventative medications (propranolol and amitriptyline) and safety medications, but none of the safety medications have worked(I’ve tried sumitriptan, nurtec, and maxalt), so my doctor recommended going to the ER to see if they can get rid of it. I was wondering if that would actually work? Because it would probably be expensive and I’ve already tried so many things.
r/migraine • u/Solid_Yesterday_4409 • 8h ago
Chopped my hair off and now I can sorta wear pony tails
So before my hair was down to my hips but a couple days ago I got it cut to my shoulder and I can wear my hair up for a few hours now!
Haven’t noticed any big difference with it down contributing to my migraines but ponytails were always a trigger for me before
r/migraine • u/Kennam320 • 23h ago
End of the line
I’ve decided I am done searching for remedies and giving up on. Hope that I will ever get better now I do not need a wellness check. I just mean I am going to live with my fate of having migraines and work my life around them instead of fighting it. I do not have the energy to get excited about one more pill or online remedy or Facebook group that’s going to help cure me I’ve just come to a resolve that this is my life and it’s still a good life in spite of these headaches.