I think quite a few people on here have tried it with success.

I tried it. I did 3 rounds over 9 months. It did not help me.

does anyone know how it's supposed to work? I've seen it as a possible treatment for essential tremor so it obviously has a neurological effect.

I have tried Botox and it has been very effective for me. Every three months I get the injections. I am sensitive to most meds but botox never caused rebound or any side effect

I have been getting BOTOX injections for my Migraines since 2008 (before it was FDA approved).
It has saved my life! I was able to go back to work, and function somewhat.
Oh, I still take preventative meds (Topamax), and sometimes Fioricet and/or Maxalt. But, at least I'm not being hospitalized or on disability anymore.
g
Give it a chance. It reduced my pain and frequency.

Where exactly is the Botox injection? Is it on the scalp or the forehead? I am wondering where is the actual injection site and is it very painful? Thanks in advance.

Hi, I am a chronic Migraine Patient and I get the Botox as well. I have been getting them for about 2-3 years now and it really helps. You get the injections all around your head and neck area. I also got the injections around my eyes, temples, and forhead. I am not going to lie, to me it hurts. Now not bad but it does hurt. I get a slight headache pain for about a week after but then I';m good for the next 3 months. When I'm due for my next series of injections, I guess my head knows and I start getting small or slight migraines until I go to the dr. But I do recommend the Botox. Before I was getting more than 15 a month and now I maybe get 5. So it has helped. Just please try to find a neurologist that is very familiar with Botox and is licensed. Not all Neurologists are liccensed to give Botox.

I hope this helps. And good luck.

Pacheco,

Thanks for taking the time to reply and explain about the Botox injections. The thought of a needle going in to my forehead and neck and head is terrifying to me but I will think about it. It is probably worth the temporary pain of the needle to get some relief from the Migraines. You are really brave. Have a beautiful day! :-)

I had it several years ago....it's a tiny needle, lick a pin prick. Am I right everyone? It didn't work for me and my insurance wouldn't pay for it anyhow. My neurologist compared it to "When Harry Met Sally" - you'll know right away if it works for you.

It is worth a try, especially if your insurance pays a hefty portion of the expense. I did the botox treatment for a year. It was helpful in some respects, but my number of migraines did not decrease (20-24 days a month). It did help with light and noise sensitivity. You owe it to yourself to see if it's something that will help you.

I have had botox for the past few years. It is hit or miss for me. When it works I have great weeks where my migraines are very minimal.
The shots however for me are painful especially if I'm particularly tight that day (which I usually am, especially my neck muscles)
The neurologist said for me to use an over the pain numbing spray next time before to help. Has anyone else tried this? I think I'm going to.

I'm getting this done tomorrow... and nervous as hell about this.

For me, this is a last resort. We've tried everything else... I'm either allergic to everything or it doesn't work.

Jade...did you have the botox? Did it help?

I'm seeing my neurologist today about starting Botox. I hope we have finished with everything the insurance wanted before I could start the shots. I'm hoping to get shots really soon too.

I had the Botox on the 18th of September.

First, the shots were -insanely- painful, especially on my face, and I bled quite badly. My blood pressure, usually 120/84, must have been high, as I was nervous and stressed about the procedure. My neuro said he'd never seen anyone bleed like that before.

When it was finally over, I went home and then went to bed, in more pain than I've ever experienced. My migraine raged out of control for 7 days. I have returned to my pre-botox pain level, and am afraid.... 2-4 weeks, they said, for it to kick in... it's been 2. Nothing. My work is getting annoyed, and wanting my doctor to start talking about return-to-work, but I *can't* yet. I can't even think my way through a crossword puzzle!

So, I'm worried I'll lose my job. I mean, if I do, I do.... as long as we get my health in order... but I just never thought I'd be.... HERE.

yikes that sounds awful Jade. Hope it settles soon and you are able to return to work.