This Is MS Multiple Sclerosis Community: Knowledge & Support

Welcome to the world's leading forum on Multiple Sclerosis research, support, and knowledge. For over 10 years, This is MS has provided an unbiased community dedicated to Multiple Sclerosis patients, caregivers, and affected loved ones.
It is currently Wed Jun 19, 2013 11:55 pm


All times are UTC - 8 hours [ DST ]




Post new topic Reply to topic  [ 4 posts ] 
Author Message
PostPosted: Sat Oct 08, 2011 10:08 am 
Offline
Getting to Know You...
User avatar

Joined: Thu Apr 21, 2011 3:00 pm
Posts: 18
I am 7 days in---and up to 2.0 mg and noticed several things so far--------last 3 nights I SLEPT THROUGH THE NIGHT w/o having to get up to pee or fight to go back to sleep----I feel a general sense of well-being-----------------tremors are still there, but if i stretch before exercise I even took a spin with my walker and altho it is hard, I did it---i've been wheelchair bound for 5 years and have to be honest and say my exercising has fallen way down---I am taking all the supplements suggested by joan in her "helping myself" paper written for those post ccsvi------neuro now wants me to start gilenya as I have been off tysabri due to being pre-disposed to the virus that causes pml-----my thought is to start gilenya to wave off the tysabri rebound effect, then downsize to possible copazone or just ldn. such a crap shoot----but for the moment i am feeling GOOD and want to appreciate every second of it............


Top
 Profile  
 
PostPosted: Tue Oct 11, 2011 1:46 am 
Offline
Family Member
User avatar

Joined: Tue Oct 12, 2010 3:00 pm
Posts: 31
I've always wanted to try LDN but I'm currently taking oxycodone as well as fentanyl patches and wanted to know if that meant that I couldn't take the Naltrexone would block the opiates from working properly. Any one know?


Top
 Profile  
 
PostPosted: Wed Oct 12, 2011 7:43 pm 
Offline
Family Elder
User avatar

Joined: Sun Dec 19, 2010 4:00 pm
Posts: 216
Location: USA
Definitely. I had some surgery and Fentanyl IV was used, it didn't help me at all with the pain, and I was off LDN for about a week. I received a Morphine shot in the IV post surgery and it made little difference.

I am on LDN for 3 years now. I need more surgery (eye this time) so I stopped it for two weeks this time. I feel tired and know I need my LDN fix badly. It helps with pain and is uplifting for mood too. :smile:
CD

_________________
Where there is a will, there is a way. "HOPE"

CCSVI Procedure December 2010


Top
 Profile  
 
PostPosted: Fri Oct 14, 2011 1:18 pm 
Offline
Family Elder
User avatar

Joined: Tue Oct 06, 2009 3:00 pm
Posts: 287
look it up on your search engine...i believe there is an ldn website to answer your question...

_________________
GOD BLESS.... CCSVI treatment Dr. Siskin great doc....symptom's improved for about 3 week's (gait, balance, spasticity) now back to square 1...


Top
 Profile  
 
Display posts from previous:  Sort by  
Post new topic Reply to topic  [ 4 posts ] 

All times are UTC - 8 hours [ DST ]


Related topics
 Topics   Author   Replies   Views   Last post 
There are no new unread posts for this topic. Feeling GREAT after only one month on LDN!

flora68

1

2250

Sat Mar 12, 2005 9:28 am

Mary View the latest post

There are no new unread posts for this topic. Just started at 4.5mg and feeling numb

[ Go to pageGo to page: 1, 2 ]

Mary

16

6330

Wed Jun 29, 2005 5:39 am

watergypsy View the latest post

There are no new unread posts for this topic. 10 days on LDN and feeling worse, is this normal?

Jeanief

5

3420

Mon Feb 13, 2006 11:12 am

gto_lady04 View the latest post

 


Who is online

Users browsing this forum: No registered users


You cannot post new topics in this forum
You cannot reply to topics in this forum
You cannot edit your posts in this forum
You cannot delete your posts in this forum

Search for:
Jump to:  


News News Site map Site map SitemapIndex SitemapIndex RSS Feed RSS Feed Channel list Channel list
Read hundreds of personal Multiple Sclerosis stories on Experience Project. Experience Project is an anonymous community where people connect through their life experiences, made by the same people who built This is MS. With over 30 million personal stories about every possible life experience, you can quickly find people like you!


Interesting: Secret Confessions | Dream Meanings | Ask Questions, Get Answers

Advertise on the premier multiple sclerosis forum