Friday, 14 March 2014

Have you ever….tried Medical Marijuana for migraines? New series of Q&A from YOU!

Starting right this second, every Friday from hence-forth, shall be the:  'Have you ever?' series.

Each Friday I'll post a question from a reader of this blog and hope that you, other dear readers, will answer and help out as best you can! If you want to pose a question, or ask this migraine community about anything from the best ice gel packs, to helpful apps, to how to 'come out' to your boss as a migraineur, simply send me an email at

1st question: Have you ever….. tried marijuana to treat migraines? 

 I 've suffered migraine since I was 12. I'm 28 now and the last 2 years have been very difficult, going to work feeling like sh*$ is horrible, I'd been absent many times because of it. I'm from Mexico, and it's very difficult to find good neurologists or affordable medication here in Playa del Carmen. Getting Botox is around 500usd. 

After many years of trying different pain killers, my stomach is a mess, I've become very anxious and my family and boyfriend have to deal with me and my bad days,  I have been researching about the use of Marihuana to treat migraine.
 I would love to read if you or someone in your blog have experienced with this and your thoughts about it.

Thank you so much reader 'N' for the above question. I know many of us will be able to relate to your experiences. 

So - over to you dear readers. Please leave your responses to the questions in the comments section below. 


  1. I have tried it but have found that I always have a terrible reaction to it – nausea, vertigo and sensitivity to sound

  2. Great question, I'm looking forward to seeing the responses. About half my patients who have tried it say it helps, the other half say it makes them worse!

  3. Me too! I've had lots of people ask me about this in the past so will be interesting….I'll confess I did try it once when I was much younger on a vacation and it did nothing for my pain at all!

  4. My mom was the one who encouraged me to try marijuana, so being the good daughter I am, I complied. A few times. It did not improve any of my symptoms, but it also had no negative side effects. Thus, I'd say it's worth a try. I have also tried Nabilone, which is a synthetic cannabinoid. It also didn't alleviate any symptoms.
    As a side note: I must say, I don't think my dog approved of my smoking - she glared at me the whole time. So there you have it... My mom is okay with me smoking pot. But my ten-pound dog isn't.

  5. I wrote a nice long message and it disappeared when I hit the preview button :( I will write it again. I am also (very nearly) 28 and my migraines have been a lot worse in the last two years. I have used Medical Marijuana for the last year. My old primary care doctor, and oddly enough, people at my grandparents church told me I should give it a try. I have found the most relief with a strain that is what they call at my medical dispensary here, a heavy Indica hybrid. This means that it is higher in CBDs, the non psychoactive part of marijuana, and lower in THC. The blends I usually go with are about a 70% Indica (highest in CBDs) 30% Sativa blend. I highly suggest using a vaporizer, easier on the lungs. I have found though that smoking is far more effective because it bypasses my stomach. My Neurologist said during my last appointment that pills are less effective because when you have severe nausea the stomach "goes on strike." This made a lot of sense. On my particularly bad days (most day during the winter since I live in Colorado and high altitude, cold, and barometric pressure changes are some of my biggest triggers) I smoke and use tincture (a liquid blend of marijuana and some sort of a base, most commonly glycerin) mixed into a shake. This way I can get some extra nutrients and protein and spark my appetite. I also get Botox injections, which have on;y been effective at keeping my migraines away 1/4 times now, but have helped keep some of my scarier symptoms that mimic strokes and seizures away. I am still working out proper dosing with my neurologist. Hope this was helpful! I also came across this site a few weeks ago that has a lot more detailed information if you are interested.


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