Monday, May 28, 2012

10 years of migraines non-stop

By Dinny Thursday, October 08, 2009

It's my 10 year anniversary and I started a blog, and would appreciate anyone checking it out as I'm feeling more and more isolated as the years go by. Please feel free to give me feedback and comments. http://chronicpain911.wordpress.com/   Thanks much.

Nancy Harris Bonk, Health Guide
10/ 9/09 3:21pm

Hello, and welcome to MyMigraineConnection.com!

 

It is important to know you are not alone in Migraine disease, which as you said can be so isolating. You may be able to find lots of support here too. 

 

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

Anonymous
J
10/13/09 1:00pm

Hi Dinny,

I have had migraines for years and years, too.  I'm not saying the following to compete, only to highlight that I understand.  Mine started when I was 8 years old, and I am now 47.  I had a year of vomiting starting around 7 years old, which medicine now knows in children is a precursor to migraine headaches.  I understand your isolation very well.  I am on disability for major depression also, but would be getting out more if not for the almost constant migraines I have almost always had.  I used to work, and just had to work in spite of them.  When I went on disability, I was able to finally stay in bed with them, which was such a relief, but there is the isolation.

 

I have finally found doctor who does occipital nerve blocks -- and if you haven't had one and are interested, or have had one and it hasn't worked well, make sure you find a doctor who does them at the base of the skull by the spine, that is the atlas vertebra, not one who does them somewhere directly on the skull.  You will get the maximum benefit if they are done at the root of the nerve by the atlas.  I have found that this procedure has helped prevent more headaches than any medicine preventative, and wish I could have had it 15 years ago before my headaches got so very, very severe.  I have also had a supra-orbital nerve block, which has helped some, but I'm not sure of the doctor's competence who performed that block.  I think it needs to be redone, as the doctor said afterward that he was used to doing them for eyelid repair, not migraine prevention.  He could have confessed his ignorance beforehand because I think it makes a difference in terms of the medication mix / ratios, and I wasted my time and money (I pay 20%).

 

I'm thinking you might want to discuss your isolation, or maybe relieve your isolation more than discuss what we've all done for our migraines.  I can tell you I totally relate to what you're saying.  I wish I had more to say that sounded hopeful but I'm in pain so much (between occipital blocks) that I can't get myself out of the door.

 

I hope that knowing someone else is in your shoes and understands is helpful.

 

Please tell us more about what you're experiencing, thinking, and feeling, and want to talk about more.

 

J

Anonymous
dinny lynn
10/29/09 5:12pm

Wow, I never would have made it as long as you have in that shape.

 

I've just slowly gone down hill and was pretty dibilated for over 10 years. I know it probably won't go away either. I'm fairly functional these days, but go through tough periods from time to time. It's hard to feel truly happy and grateful for the life I have, when I've lost so much of who I am. I do try to be happy and grateful, probably about 85%, but there's a lot that's gone and will never be due to the migraines and a lot I've robbed my husband of also.

By Dinny— Last Modified: 10/29/09, First Published: 10/08/09