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Watching this after getting some respite from the whole shebang. Started 6 hours ago. The whole course, auras, blind spots, everything. Felt the urge to yeet out my right eye

i see a kinda blurry spot, looks a bit like when there’s a spot of water on a window. Sometimes the visual seems to be outside of my field of vision? i also get kinda weirded out and it feels a bit unreal or something. Anyone here with the same symptoms? To add on; I’ve had regular headaches my whole life, maybe two days a week. maybe every two weeks i get a really strong headache, usually a neck massage and a nap helps, but painkillers etc. dont’t. I’ve had a migraine with the visuals a few times during my whole life, and after that i get a strong headache. Now i’ve had the visual and disoriented part without the headache a couple of times during the last month or so. Someone else with the same thing?

Ooh I dk I don't like these type of headaches they don't make u feel good I'm over 65 just now starting getting them last one was bout 34 yrs old

Wondering about serotonin syndrome and if you have it from taking say SSRI’s (relpax) is still psilocybin safe??

Thank you

If I have a single cup more one day than usual, the next day I'm very likely to have a migraine. Deviation definitely plays a role for me and consuming too much in general makes it likely that even waking up a few hours later on a week-end means a day wasted to migraine due to suddenly not getting my fix.

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this is absolute bullish*t!, I did't even know suck thing existed until I saw this video, I had these problems but I was smart enough to clear my path and all the necessary stuff and get out of that situation very very quickly on a piece of paper!, bro... come on don't be stupid you can't stay in this situation for too long, close this garbage and get back to your work, watching these bullish*t content would of course make your situation worse. if you believe in so

The 1st lady describes exactly how I feel.. Like someone blowing up a balloon that my skull can't accommodate. I first had this 6 years ago and for some reason I've just started again with it

Sadly, so, SO true 😢I have had Elhers-Danlos Syndrome, PoTS, Sjogren’s, Hypothyroidism and Spondyloarthritis - the first syndrome, from birth. I’m 74 and was only formally diagnosed at 63! One of the major symptoms is pain and chronic migraine, since the age of 11. I’m totally and utterly exhausted. Thank you for this.

Hi thank you for this information I always go through hearing all of that I suffer from migraines sometimes very bad but I’ll get up smile do my household chores take medication and continue because I always hear from my family exactly what you are saying.

It’s truly a living nightmare.. iv been dealing with cluster headaches for abt 15 years now n I get abt 4 to 6 attacks in 24 hours for abt a month to 3 months thn thy disappear for a few months.. lately iv been getting them from June to august n then again November to February. I hate thm so much. Thy last from 15 mins to abt 45 mins. The worst is when I’m around people n I get an attack. It hard to explain to people how painful it is n I feel lik my family gets annoyed by me when I get attacks. Thers been times Wer I wanted to put a bullet in my head n end the pain.

Interested but cant understand because of sound. Gou should redo this one.

Recently I have developed symptoms like migraine with aura with severe neck pain. After 1week with severe headache my whole body got numb and speech became like a baby only for 30minutes. MRI shows hemorrhage in cerebellum. But doctors couldn't identify whether it is migrain or stroke. They give me topiramate , flunarazine , pixotifen ,aspirin, atorvastatin. Now I'm sleeping day and night because of medicines.

Excellent video! I was recently diagnosed with migraines. My symptoms are headaches, teeth pain (mainly my molars), neck pain, eye pain & ear pain.

Thank u for sharing ❤️

Also got another question can you get it from different water? BC it started when the kitchen broke and we were going to replace it it's all taken out but we don't have enough money so we use a different water

Curious does this go along with vestibular migraine? It have vm and very bad anxiety, because of the dizziness that comes with vm.

How can a individual find out if this is damaged?

I get it always on back of left eye few days before period. Hurts a lot

For forty years, I have had visual aura without headache. Usually two or three times a year. In 1986 I fell on the tennis court and suffered a contra coup injury. Hospitalized x 3 days. Extreme dizziness, vertigo, nystagmus (eyes twitching), loss taste and smell. Following this head injury I had a flurry of the visual auras, sometimes more than one in a day. That quieted down and they settled into rarity. I started keep track and had about 4 per year since 2023 so to get my attention they may have come more often. This summer I had four such visual migraines in a 4 week period. Each lasted les than 30 minutes and each classic. No headache but I felt like I had a hangover after. Didn't feel right. Also, not at the same time, but twice since June 1, I also had BPPV which lasted three to four days. I had dizziness (rolling over in bed, changing position) but also the disassociation the doctor described. I felt like I was looking down on the room from a great height. My ears itched constantly even though I had just been to the ENT to have the wax removed (I have small ear canals and make a lot of wax). I have hearing loss in one ear but don't know if that is age related (age 85 in September). I haven't had a real headache for 54 years and can't remember ever having a frank migraine like others (including my husband) describe. But my ears feel "full" and so does my head. Esp behind my eyes and in the occipital region. I have AVMs of the bowel and can't take Nsaids but am wondering if I should take Tylenol even though the headache is so mild I can get along without anything. This has been one of the most informative lectures I have ever heard. Thank you so much Dr. Teixido.

A man with a crippling migraine condition is useless to even a woman with an equally crippling migraine condition.I believe a total lack of physical intimacy itself can be a contributor of migraine.My two untreated concussions at age 12 and 13 I believe made my rare migraine condition into a life destroying one of visual snow,chronic pains and constant pre migraine,migraine and post migraine symptoms.I have PTSD because I had to go through the last eight years of my schooling like this starting in 1972.I wont elaborate to much on my hermit miserable life I will just say psychiatry and neurology never failed to disappoint from age 21 to the present age of almost 65.An undateable even friendless life is not living but has been profitable for the pill pushers. I do have the memories of talking to pretty therapists for what thats worth....Once at age 21 I attended a Day treatment Unit in a town I needed to drive to for over a half hour daily for six months.I did not feel alert enough to drive in the first place,but they insisted I take Thorazine and the fact that the drug was making me fall asleep at the wheel did not concern them at all.That was evil.I have to hide the facts that, I'm on disability,don't drive and live at home, from everyone especially any woman Id be interested in. It was embarrassing enough when I was younger now I see I lost in life and medicine like educators before them had zero actual interest in ever helping me or recognizing the trap I have been in.What do women want?Look at CZcams and despair.

1. Cold sugar free Red Bull through a straw. 2. 100 mg Sumtiriptian. 3. Eye mask. 4. Phillips Evo Oxygen generator. 5. Deep breathing from the belly up through the stomach, up thru the throat, pushing my breath up to the top of my head and hold it. 5. Try tor relax between the shocks. 6. Sumtrpitian shot knocks them up within 10 mins if i have access to one.

my migraines are getting worse, i am in pain all the time. I am sorry to hear what you are going through. I like the idea of a support group

Thank you for this informative video. I trained my own service dog to help with three vestibular disorders as well as agoraphobia and it has been life changing. While Skidboot knows many tasks, from picking up dropped items, retrieval of items, deep pressure therapy, crowd control/providing a buffer, as well as several other tasks, he doesn’t provide any heavy mobility tasks due to his size (he’s a border collie). However, as you mentioned in the video, even smaller dogs can help with proprioception. Touching him, the feel of the leash or pullstrap in my hand, all help with proprioception.

Migraines are a disability and people need to realise that

Ty

As someone who suffers this was very interesting! This resonated so so much with me! Thank you so much from London 🙏🏻

is there a difference between nerve block under ultrasound and without ?

Hi I was wondering if chocolate causes migraines for everyone diagnosed with them?

I have had VM for 11 years after a concussion mine is 24/7 no meds have helped what else can I do?? 😢

I started getting depressed really bad in 2016. I got a headache in 2012-2013 then in 2014 it when away for 8 months then came back. At that point I had done great in school for 8 months and could actually focus and then it came and by that point I had given up. I’m not sure what subform that could fall under, but this is really interesting I really hate that other people have this, but it’s nice not to feel so alone.

😢😢😢😢😢😢 i suffering cluster Headache right now....i dont know what to do...i only take pain reliever everyday...it almost one month plzzz help me what to do

It,s 1 o'clock here, I just happened to get in on the dizziness and vertigo program. Thanks for sharing.

My migraines started at 18, and every year when it gets cold or too hot I am almost sure to get migraines. For a month or two, everyday around 10 AM and recently it started at night also, wakes me up automatically and torture starts. It took me 20 years to find a right doctor who correctly diagnosed my runny nose brutal headache as migraine actually. I was prescribed preventive medicine which would fail mostly, then Headset tablet as SOS. I am 38 now and I couldn't enjoy my youth much because of my migraine as I would have to stay home for most part of the year. Too much running also gives me migraine. I inherited it from my mother who got it from her mother, who got it from her father. Even after taking Headset tablet, it takes me 45 minutes and those minutes are terrifying. When I had no such medicine, it took 4-5 hours for body to automatically vomit and get normal again.My head would be ringing for rest of the day. Other people can't understand its effect, specially folks at job.

Will tell my head, stop it! You're over reacting!

Sleep machine, Maxalt pills, mouth guard, tumeric tea for inflammation, regular massage, fresh cool air in the bush all help me.

Dis me and employer is giving me hell.

Hi I also suffer with migraine headaches and yes chocolate does trigger your migraine I love chocolate I would eat very small amounts and after take my medication I enjoy listening to all the topics on migraine.

My grandmother, my older sister, me and my younger brother is suffering from it. It's an absolute torture and the worst thing that other people think that I'm just being over-dramatic about a simple headache. WHICH I'M NOT!

Had to stop halfway through to wipe tears from eyes so I could see the screen - thank you so much for sharing your experience and insights

Your joking... right? Every issue has a month now.. its pretty stupid. At what point does it just become a joke, because i think we are there.

You see i don't have my period yet so i can't have this. WHY IS THIS HEADACHE IN THE BACK TOP OF MY HEAD

So much completely useless information. I have chronic migraines, averaging 27 migraines per month. Rebound headaches are constantly a problem, though i always stay well under the recommended dosages. I detoxed for two hellish months and it did nothing. Corticosteroids work much better and faster. The doctor mentioned triptans causing rebound headaches but ergots do as well. My best strategy to reduce rebound headaches is to take half doses of ergotamine and take the other half if the migraine isn't relieved. Also taking low doses (4mg, 4mg, 2mg, 2mg) of Dexamethasone when relief medications completely fail makes them act sparkly new again. Switching relief meds, such as from ergotamine to Sumatriptan (after 24 hours) never works. Rebounding on one is the same as rebounding on all. CGRP inhibitors suck, especially when rebounding. Obviously this is my story and everybody responds very differently. Testing what works and doesn't is best.

I have these n it's awful

Could taking medication for ear pain associated with hyperacusis calm the ear nerves and help with this condition?

I have hyperacusis and have been dealing with this for 15 years. The symptoms you describe about pain in the ear and going down through the teeth and side/back of neck are exactly what I experience when I have a loud noise event. I’ve been researching hyperacusis for many years and the only thing that’s been suggested is sound therapy. I’m wondering if there is a correlation with my ear pain, which you describe as an ear migraine, and my symptoms. I also appreciate your advice on foods that could trigger migraines. It couldn’t hurt for me to try a nutrition approach to my hyperacusis. Any thoughts would be appreciated. Thank you.

I have csf leak by my nose and mouth some oil type liquid comes from past 2 years when I get up I get faint I feel my ears sound quality decreased even my brain x ray shows some liquid passing all over and cause maxillary sinustis but here in India doctors are so rude they not listen your talk and suggest medicine and what my life is hell now I lose intrest in everything day by day and going to s*ci*e soon....

luckily, I have never had migraines, but it was heart-wrenching to hear about these experiences. what a wonderful couple; I wish them all the best. it’s fantastic to hear that psychedelics were helpful. i hope for the best for them and all sufferers.

Thank you