@@nailpolishqueen1919 I’ve seen it infrequently, but have seen it. I’ve not seen it be permanent for anyone though, and it wouldn’t really make sense that it would be because it is cleared completely by the body. However, it can take 5-6 months for complete clearance.

@@meandcadasil7093 yes cadasil has a very obvious and stand out pattern though. The appearance is typically is very easily differentiated from other causes and patterns.

@@Neuralgroover, I agree that the pattern is distinctive, yet so many people are still misdiagnosed as having MS (many doctors still unaware of CADASIL). The pattern and location of white matter lesions alone, however, is not enough to make a diagnosis of CADASIL. Taking a thorough family history; understanding the range of symptoms; the significance of symmetrical pattern of confluent white matter lesions; and knowing that there is a Notch3 mutation genetic test available, will help to decrease the incorrect diagnoses of MS. Intesrestingly, though, there are documented cases of people with a dual diagnosis of CADASIL and MS.

@@meandcadasil7093 all excellent points, and I agree with 100% of that.👍

@@John--nj4lp some people do get migraine aura without headache, which we call a migraine equivalent syndrome. However, we typically get a brain MRI and MRA for either migraine aura without headache or exertional migraine, so I would still suggest discussing with your doctor.👍

Same October 11th for me 🥹

@@danimavs517 hopefully you’ve had a good headache specialist trying different things and had the proper evaluations. Never give up!

@@tarikhelo4269 not necessarily. There are a lot of good treatments, just need to get in with someone who knows how to treat it, like a headache specialist. I’ve seen a lot of people improve from it for sure. In fact, I’d say more do than don’t.

@@grantlawrence611 try to maximize your volume. It’s really loud when I play back the video on my devices, so not sure why it wouldn’t be as loud.

@@Neuralgroover thanks

@@Jaydacator make sure you have a good headache specialist that doesn’t give up and keeps trying different types of options. There are many different angles to try to treat it!

It can look the same, but typically demyelination has a bigger and more extensive appearance and has some characteristic patterns, locations, etc. to it.

No I don’t, but we do see a fair amount of referrals from the VA.

The link to the blog discussing these devices in greater detail works for me in the KZbin video description, not sure why it’s not working for you. You can also go the website in my bio and type in neuromodulation or GammaCore in the search bar and it will also bring up the blog discussing them in more detail.

Sorry to hear that! Hope you’re recovering well.

I suffer from migraines what brand do you use and how much mg?

​@@iyana03 vitamoment, magnesiumcitrat 250g pack. (german brand)

@@iyana03 Vitamoment magnesium citrate (german brand)

I'm wondering too please? 😊

Pls tell me the dose that you taken

I’ve only been struggling with this for a few months, so I can only imagine what you’re dealing with. Praying that you find the strength and encouragement to keep going.

Im on 7 years. Gabapentin helped me some. It severely affects my sleep aswell.

@@smithcoffee8 make sure you have a good headache specialist that doesn’t give up and keeps trying different types of options. There are many different angles to try to treat it!

Yes, some people can respond to those diets. Here's a blog I wrote on some of these migraine diets. virtualheadachespecialist.com/migraine-and-headache-diets/

Tyvm

Good question! Glycine is actually an amino acid which acts as an inhibitory (blocks overactivity) neurotransmitter in the central nervous system. It helps regulate brain activity by inhibiting the transmission of signals between nerve cells.

Thank you kindly, dear. I will pass this along to my grandchild. He suffers migraines. I suggested riboflavin, omega 3, CO q 10 and now magnesium. You are doing a wonderful public service by sharing your knowledge. Some folks can’t get out to see a dr for various reasons so we very much appreciate hearing tid bits. I read pubmed too but some things seem complicated and it takes me a whole month to get it, eg glutamate dominant and how the supps may help block the receptors. I keep reading a bunch of times before I finally get it. Anyway, thank you for helping society. You make us smile knowing the kindness spread through the world. I wish you peace health and happiness.☮️🌎☮️

@@Tad-For-Global-Peace thanks, I appreciate that! I just hope the videos help someone because there’s a lot of unnecessary suffering out there and not enough headache specialists.

Please help me I had allergic sinus and migraine fo several years.please suggeste me which type of magnesium I have to take.magnesium citrate or magnesium nitrate or only magnesium with no combination.

Hi, I’ve read all are good but Glycinate is best. Please use pubmed for medical readings! Good luck friend

Hi, I just want to tell you you were not alone. I have been diagnosed with vestibular migraines. I used to get migraines when I was younger, but then they switched to a new form of migraine called vestibular migraine, which is kind of common so I know what it’s like to be doing nothing and suddenly get a quick dizzy spell that last a couple seconds. It’s really scary and I’m sorry you’re going through that. With vestibular migraines, there can be head pain or no head pain, and you could be dizzy during the migraine after the migraine or before the migraine. Sometimes you can get earful, tinnitus, ear, pressure, ear pain because the migraine is affecting your entire vestibular system. I also have BPPV but that is something I’m not too concerned about because I just need a certain head movement position to re-position the crystals in my ear and it’s known that those who have vestibular migraines it’s common to also have BPPV. I had an MRI done recently and it showed white lesions so that’s why I’m here trying to learn about it. I hate that there is a connection between dementia and strokes with people who have migraines kind of makes me worry to be honest, but there’s nothing I could do about it. I don’t have high blood pressure, diabetes, or high cholesterol, but those white lesions are from migraine versus plaque. I believe I hope I’m waiting to see my doctor to talk about the results of the MRI. Please see Dr. Michael Teixido Here on KZbin. He has a great channel that discusses migraine and vestibular migraines and all the other balances diseases, etc. he’s great.

Migraines can have certain kinds of predome auras that happen before someone gets a migraine with or without pain, depending on where the spreading depression is some people get a visual aura, some people can get a sensory aura where they feel tingles, etc. and then some people could get a motor aura where they get paralyzed, and some people can also get an aura where they get confused and they can’t talk.

I’m one of those people that have a migraine without aura.