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Hello, and welcome to MyMigraineConnection.com!

So you don't feel totally alone here are some quick facts about Migraine disease. Migraine itself is the 12^th most disabling disorder in the US. There are almost 38 million Migraineurs in the US too. I know that isn't much comfort, but it does help to know you are not alone.

Migraine specialists are experts in treating patients with Migraine and headache disorders and are the doctors you want to see. Neurologists treat so many different conditions, like stroke, MS and epilepsy, it is hard for them to be experts in any one area. Migraine specialists devote their entire practice to Migraine and headache - only. We have have a list of patient recommended specialists you can see HERE.

This article may further help you see what the difference is between a neurologist and a real Migraine specialist. It might mean you have to travel a bit, but to get your life back it will be well worth it. Migraine and Headache Specialists - What's So Special? 

Thank you for creating a SharePost. SharePosts are a form of blogging, and there are many things you can do with them. You can share an experience, suggest something that's helped you, use SharePosts as a Migraine and headache journal, and many other things.

We also have a discussion forum that you may want to check out. Especially if you have questions or are looking for information, you may find the interaction on the forum to be quite helpful. To get to the forum, just look for the orange box marked "Manage" and click on the Migraine Forums link. Because our forums are maintained by a third party, you'll need to register for the forum. You can use the same information you used to create your community log-in if you like. If you want to go directly to the forum, you can click HERE.

Along with your personal "My Home" page and the discussion forum, you'll find links to a great deal of helpful information and a spot to sign up for our free newsletter on the main page of our site, http://www.MyMigraineConnection.com.

If you have any questions, please feel free to post them to the forum or send me a message through my profile.

Welcome again,

Nancy Bonk
MyMigraineConnection.com Expert

So sorry to hear about your situation.  I have BTDT also, migs since age 12, have 2 kids age 17 and 6, am now 47.

I take Relpax when I get an aura or begin to feel the mig "tickling" one side of my head.  My neuro is putting me on Lexapro as soon as I can get them delivered cheaply from Canada--hopefully this week.  I used Lexapro 2 years ago for about 6 months and it significantly reduced my migs. The neuro seems to think I may have low serotonin, so the Lexapro helps increase that.  I'm not depressed, but I do get rather cranky when I get migs often! I went off it because it dampened my libido so much.  But the migs are back and I need to work on controlling them better.

The Relpax is a real blessing.  Only side effects are achy neck and shoulders and tiredness, but that beats a mig hands-down.

I have only tried those meds above and Imitrex, which stopped working for me after about 10 uses.  It's a bummer, because Imitrex is generic and a lot cheaper than Relpax now.

Good luck and God bless!