New Member Introductions Welcome to our community! Come in and introduce yourself to other members!!


advertisement
Reply
 
Thread Tools Display Modes
Old 02-06-2012, 04:24 PM #1
mammy mammy is offline
New Member
 
Join Date: Feb 2012
Posts: 1
10 yr Member
mammy mammy is offline
New Member
 
Join Date: Feb 2012
Posts: 1
10 yr Member
Default spinal myoclonus

hello I am new to this site I am asking for info on behalf of my hubby, hes in his early forties and has had cancer twice [two different types] He has a damaged nervious system due to the treatment, he also has myoclonic jerks, ataxia, an essential tremor and now has been hospitalised twice for 4 weeks total in the last 9weeks with what the doctor says is spinal myoclonus but at first they thought it was epilespy as when he fits they look like epileptic fits he has in excess of 5 a day does anyone have any info on this they can share with me and what kind of treatment they have had?
mammy is offline   Reply With QuoteReply With Quote

advertisement
Old 02-06-2012, 05:02 PM #2
ginnie ginnie is offline
Elder
 
Join Date: Aug 2010
Location: Anna Maria Island Florida
Posts: 6,278
10 yr Member
ginnie ginnie is offline
Elder
 
Join Date: Aug 2010
Location: Anna Maria Island Florida
Posts: 6,278
10 yr Member
Default Hello Mammy

Welcome to Neuro Talk. I hope that there will be alot of people to help you with the problems your husband has. You are both experiencing alot of stress with all this trouble, and its good your sought help. I do not know about this particular condition. There are those that may however have experience with this kind of trouble. I am so sorry you have had to through all this with cancer, and then the side problems due to the treatments. Please do look into any of the site here that deal with brain issues. You are welcome to join into any conversation too. Please be at ease here, there is lots of compassion and helpful information. If you need to talk I am here for you. Thre is also a cancer forum that may provide some help. There is a search bar at the top of the page. Just tap in what condition, and it will lead you to that forum. I have been here several years, and I still get confused a bit, so don't worry if you wind up on another site. There will be more people to help direct you. In the meantime I will keep you in my thoughts and prayers. I try to make new people feel comfortable and weclome. ginnie
ginnie is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Rrae (02-07-2012)
Old 02-07-2012, 12:22 AM #3
Rrae's Avatar
Rrae Rrae is offline
Grand Magnate
 
Join Date: Nov 2009
Location: i thought it was in my left pocket
Posts: 4,117
10 yr Member
Rrae Rrae is offline
Grand Magnate
Rrae's Avatar
 
Join Date: Nov 2009
Location: i thought it was in my left pocket
Posts: 4,117
10 yr Member
Smile Hello Mammy

Welcome to NT!

I'm sorry to hear what you and your husband are going thru. You'll find very caring people here with lots of support and understanding.
Try checking into the Epilepsy forum. It has alot of great people there and good information. Here's the shortcut link to get you there:
http://neurotalk.psychcentral.com/fo...sprune=-1&f=11

It's so good that you are here.
I hope to see you around the forums

Caring,
Rae

Rrae is offline   Reply With QuoteReply With Quote
Old 02-07-2012, 02:38 AM #4
Darlene's Avatar
Darlene Darlene is offline
Legendary
 
Join Date: Sep 2006
Location: Once a Texan, always a Texan.
Posts: 11,976
15 yr Member
Darlene Darlene is offline
Legendary
Darlene's Avatar
 
Join Date: Sep 2006
Location: Once a Texan, always a Texan.
Posts: 11,976
15 yr Member
Wink Nice to meet you!!


mammy,

Hello and welcome, happy to see you have come to be with us, it a great place to be. As you can see we have a great number and caring fellow members here, welcome to a supportive and relaxing place. Have fun looking into the different forums. Our shoulders are here for support in many ways.

I agree with Rrae on the epilepsy forum then again also check in the following forum on spinal myoclonus:

http://neurotalk.psychcentral.com/forum65.html

Again welcome, looking forward to seeing you around. My thoughts and prayers are with you.

Darlene
__________________

.

"Life without God is like an unsharpened pencil -- it has no point.
Darlene 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
Does anyone have SPINAL MYOCLONUS or PALATAL MYOCLONUS? Topsie Movement Disorders 28 12-01-2015 06:12 AM
spinal myoclonus...questions? k4gypsyrose Movement Disorders 3 07-30-2011 01:09 PM
Spinal Myoclonus and Palatal Myoclonus??? Topsie Reflex Sympathetic Dystrophy (RSD and CRPS) 15 06-16-2011 04:42 PM
Spinal Myoclonus and Multiple Sclerosis howard50 Multiple Sclerosis 8 05-22-2009 04:43 PM


All times are GMT -5. The time now is 08:13 AM.

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.