advertisement
Reply
 
Thread Tools Display Modes
Old 11-01-2010, 08:56 PM #1
m3guitar m3guitar is offline
Junior Member
 
Join Date: Sep 2008
Posts: 8
15 yr Member
m3guitar m3guitar is offline
Junior Member
 
Join Date: Sep 2008
Posts: 8
15 yr Member
Red face Upcoming MVD

Hi,
I'm Mark from Missouri. I first was diagnosed 7 years ago. I did the drug therepy which worked for 6 months and then had the GK. It worked for 6 years but left my face numb with constant pressure. The tn came back recently and I've opted for the mvd because the side-effects are too restricting from the trileptal. My surgery is in two weeks and I find the prospect pretty scary. I'm convinced if it works it will all be worth it.
Thanks, Mark
m3guitar is offline   Reply With QuoteReply With Quote

advertisement
Old 11-02-2010, 09:18 AM #2
Mylastnerve Mylastnerve is offline
Member
 
Join Date: Nov 2007
Posts: 126
15 yr Member
Mylastnerve Mylastnerve is offline
Member
 
Join Date: Nov 2007
Posts: 126
15 yr Member
Default Welcome!

Dear Mark,
Welcome to the forum )
There are some folks on this forum who have had MVDs, including myself. It is a bold step that you are taking, to try to get rid of this beast. I remember my fears before the surgery, you know, worrying about the worst outcome, etc. I was so happy to wake up on the other side of the surgery, doing fine...so try not to worry too much. I will be here, as well as the other folks on this forum, to help you through.
I encourage you to continue with this thread, or start a new one, so that we can track your progress and help you as you journey down this road. In the meantime, if you felt like telling us a bit more about you, and your TN story, that would be great, so that we can get to know you better.
Lily
Mylastnerve is offline   Reply With QuoteReply With Quote
Old 12-01-2010, 09:05 PM #3
m3guitar m3guitar is offline
Junior Member
 
Join Date: Sep 2008
Posts: 8
15 yr Member
m3guitar m3guitar is offline
Junior Member
 
Join Date: Sep 2008
Posts: 8
15 yr Member
Thumbs up MVD Success

Quote:
Originally Posted by Mylastnerve View Post
Dear Mark,
Welcome to the forum )
There are some folks on this forum who have had MVDs, including myself. It is a bold step that you are taking, to try to get rid of this beast. I remember my fears before the surgery, you know, worrying about the worst outcome, etc. I was so happy to wake up on the other side of the surgery, doing fine...so try not to worry too much. I will be here, as well as the other folks on this forum, to help you through.
I encourage you to continue with this thread, or start a new one, so that we can track your progress and help you as you journey down this road. In the meantime, if you felt like telling us a bit more about you, and your TN story, that would be great, so that we can get to know you better.
Lily
Hi Lily,
I had my mvd on Nov. 17 and this is the first day without terrible headaches. My left ear is still completely stopped up but I think this will also improve. I am totally without TN PAIN and it is wonderful. My neuro still has me on Lyrica at a dose of 2 capsules twice a day. I'm still not sure why. Sorry I haven't been back for a while. I found a site called livingwithtn.org that is wonderful.
I'm homebound for a few more weeks so please reply as I have plenty of time. Thank you, Mark
m3guitar is offline   Reply With QuoteReply With Quote
Old 12-02-2010, 12:25 PM #4
ladynbraids ladynbraids is offline
Junior Member
 
Join Date: Nov 2010
Location: Arkansas
Posts: 8
10 yr Member
ladynbraids ladynbraids is offline
Junior Member
 
Join Date: Nov 2010
Location: Arkansas
Posts: 8
10 yr Member
Default

Hi Mark!

We are neighbors...Arkansas here.. and had our MVD's on the same day. Mine was done in Pittsburgh. Today, is also the first day for me that my headache is better.

A big high-five for having a successful MVD. I know exactly how you feel as I've been shock free for 15 days now since waking up from surgery. I was completely taken off all TN meds 5 days following surgery.

Maybe we can care notes on days that something might be up. Like have you felt any sensations at times in the Trigeminal Nerve area?

All my best,
Judy
ladynbraids is offline   Reply With QuoteReply With Quote
Old 12-02-2010, 06:15 PM #5
Mylastnerve Mylastnerve is offline
Member
 
Join Date: Nov 2007
Posts: 126
15 yr Member
Mylastnerve Mylastnerve is offline
Member
 
Join Date: Nov 2007
Posts: 126
15 yr Member
Default

Hi Mark,
I think that I have spoken with you on LWTN - you play the slide guitar? My name is Lily there. I am SO glad to hear that the TN pain is gone - if I remember right, they found a good sized compression when they got in there? I am so very glad for people who have successful outcomes - I hope that it stays this way, and that you get your life back. The headaches will come and go, and that feeling in your ear will go away - I had it too, my NS said that the nerve to the ear is close to the MVD site, and that it literally pulls back, which makes the ear fullness feeling happen. I have a titanium plate, and I swear that I can feel the storms come in now - the hole in my head just ACHES. But that is no big deal.
Ladyinbraids,
Wow, I am so happy for you too -this is double good luck! remind me to schedule all future surgeries on Nov. 17! I am just so happy for your outcome! Yay!
Things will slowly improve from here, and you will get your energy levels back to normal soon. I remember that it took some time.
Hugs to all,
Lily
Mylastnerve is offline   Reply With QuoteReply With Quote
Reply


Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off


Similar Threads
Thread Thread Starter Forum Replies Last Post
Upcoming Dr. Visit - Please help! MartyD19 Peripheral Neuropathy 5 09-18-2010 05:28 PM
Upcoming Trial hugg724 SCS & Pain Pumps 8 08-31-2010 12:39 PM
Another problem......with upcoming CT scan whirlwind123 Myasthenia Gravis 6 04-27-2009 02:30 PM
Upcoming trip to UCSF dshue Peripheral Neuropathy 0 03-14-2009 10:29 PM
Upcoming TNA Events Jeanc Trigeminal Neuralgia 0 02-15-2007 07:22 PM


All times are GMT -5. The time now is 12:48 PM.

Powered by vBulletin • Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise v2.7.1 (Lite) - vBulletin Mods & Addons Copyright © 2024 DragonByte Technologies Ltd.
 

NeuroTalk Forums

Helping support those with neurological and related conditions.

 

The material on this site is for informational purposes only,
and is not a substitute for medical advice, diagnosis or treatment
provided by a qualified health care provider.


Always consult your doctor before trying anything you read here.