Welcome to This Is MS!

     Modules
· Home
· Content
· Downloads
· Encyclopedia
· FAQ
· Feedback
· Forums
· Journal
· Private Messages
· Recommend Us
· Search
· Site_Map
· Stories Archive
· Submit News
· Surveys
· Top 10
· Topics
· Web Links
· Your Account

     Google
Google
Web
This is MS
These ads help pay for the upkeep of our site. They are automatically served by Google and are not affiliated with This is MS.

     Languages
Select Interface Language:


     Who's Online
There are currently, 38 guest(s) and 4 member(s) that are online.

You are Anonymous user. You can register for free by clicking here

     Next Step

From the creators of This is MS comes Experience Project

EP is a community where members connect through shared life experiences-- like MS--and so much more. You are not defined by any one thing, so be your true self and find others just like you at Experience Project.

Get started by sharing your Multiple Sclerosis story.


     Donations

To remain unbiased, This is MS does not accept corporate sponsorships.

Therefore, we must rely on our users to help support us. Please donate to our upkeep if you have the means. Thank you!


ThisIsMS.com :: View topic - Copax+
 Forum FAQForum FAQ   SearchSearch   UsergroupsUsergroups   ProfileProfile   Log in to check your private messagesLog in to check your private messages   Log inLog in 


Copax+

 
Post new topic   Reply to topic    ThisIsMS.com Forum Index -> Regimens
View previous topic :: View next topic  
Author Message
OneEyeBlind
Family Member


Joined: Jan 15, 2004
Posts: 88
Location: New Jersey, USA

PostPosted: Wed Sep 08, 2004 8:47 am    Post subject: Copax+ Reply with quote

Hey everybody,

Copaxone
Multi-vitamin
Vitamin D+calcium
[b]B Complex
(for energy) and B12 (for overall mental health)

I had a bout with ON in 6/03. I was diagnosed in 7/04 after a year of waiting and testing.

I started Copaxone on 8/30/04. Since I am only a week and a half into my C therapy I cannot really say if its working. I do feel the need to sleep in the afternoons and do not have as much energy as I used to. But with a FT job, a home and 3 kids it's hard to find the time to rest.

Hope everyone out there is well and wish you all the best!
_________________
Karen (OneEyeBlind) Wink

* I don't suffer from insanity, I enjoy it!
Back to top
View user's profile Send private message
Xenova
Family Member


Joined: May 21, 2004
Posts: 71
Location: Louisiana, USA

PostPosted: Wed Sep 08, 2004 12:58 pm    Post subject: Reply with quote

I don't know if you are expecting C to help your symptoms but it isn't prescribed for that purpose. It is prescribed to slow MS progression. Sleep and fatigue could be an effect of C but it is also a prevalent symptom of MS. You may want to ask your physician for his/her recommendations to fight fatigue. There are good medicines both prescribed and over-the-counter that will deal with the fatigue.
Back to top
View user's profile Send private message
teachk
Getting to Know You...


Joined: Aug 03, 2004
Posts: 11

PostPosted: Thu Sep 09, 2004 4:46 pm    Post subject: Reply with quote

I found that I had less fatigue with Copaxone than with the interferon drugs. I actually feel that I have more energy. I have been on Copaxone since 7/17/04. Xenova keep the faith. I truly think you will start to feel better. Do check with you Dr. about anti fatigue meds. Amatadine is one of them. I started taking it in March. You can build up a tolerance for it. I would like to go off and see if I still have the fatigue like I had in the spring. Best of health!
Back to top
View user's profile Send private message
OneEyeBlind
Family Member


Joined: Jan 15, 2004
Posts: 88
Location: New Jersey, USA

PostPosted: Wed Oct 06, 2004 7:23 am    Post subject: Reply with quote

Thanks for responding. I do acutally feel I have more energy since being on the Copaxone. I still feel a need to rest in the afternoons but I don't feel dead tired all the time. I am a little over one month into my treatment at this time.
_________________
Karen (OneEyeBlind) Wink

* I don't suffer from insanity, I enjoy it!
Back to top
View user's profile Send private message
Stoli
Getting to Know You...


Joined: Sep 14, 2004
Posts: 16
Location: Australia

PostPosted: Thu Oct 21, 2004 6:52 pm    Post subject: Reply with quote

It took about 2 months for me to notice an improvement; that was abpout 18 months ago and all had been good up to about 3 weeks ago. Feeling like a great big sloth - very fatigued ! Hopefully it will pass quickly !
Good Luck
Stoli
Back to top
View user's profile Send private message
OneEyeBlind
Family Member


Joined: Jan 15, 2004
Posts: 88
Location: New Jersey, USA

PostPosted: Wed Jan 05, 2005 9:07 am    Post subject: Reply with quote

Stoli,

I am 4 months into my copaxone and I am feeling much better. I got thru the holidays with little fatigue.

I hope your fatigue is improved. If you read this please write back to tell me how you are doing.

Be well,
_________________
Karen (OneEyeBlind) Wink

* I don't suffer from insanity, I enjoy it!
Back to top
View user's profile Send private message
Stoli
Getting to Know You...


Joined: Sep 14, 2004
Posts: 16
Location: Australia

PostPosted: Wed Jan 05, 2005 4:04 pm    Post subject: Reply with quote

Mr. Green Well hello there Karen

I am so glad to hear that you are feeling much better, I hope your positive karma rubs off on the rest of us !

After 18months on copax. I seem to be only OK. At first I felt a lot better-but I was also very good with the Swank diet. Now my will power has slipped, my energy levels are low. Don't know if it is the change in diet or MS. Now that xmas is over I will have to give it another try.

The heat (summer here) isn't helping but this fatigue issue has been around since winter. I really hope this isn't what it will be like forever more, I'm not sure i'm ready to deal with that possibility yet. Sheesh, I'm only 36 I'm meant to be able to walk up stairs - not move around like an 80 year old needing a hip relacement !

Take care of yourself.....
Stoli
Back to top
View user's profile Send private message
PattiNJ
Newbie
Newbie


Joined: Nov 16, 2007
Posts: 3
Location: New Jersey

PostPosted: Wed Nov 28, 2007 9:16 pm    Post subject: Copaxone Reply with quote

I have been on this drug after having a go=round with avonex. The Avon. left me with frequent episodes, so I dropped it and went to Copaxone. It has been three years since I started, and I have not had an episode. The MS is still here, I walk with a walker and use a transport chair to get out, but I do not feel I am getting worse. I am interested in seeing if Walkaide will help me. Short of a miracle, I am positive I'm not too bad. Be well my firnds, PattiNJ
Back to top
View user's profile Send private message Send e-mail
Display posts from previous:   
Post new topic   Reply to topic    ThisIsMS.com Forum Index -> Regimens All times are GMT - 6 Hours
Page 1 of 1

 
Jump to:  
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
You cannot vote in polls in this forum





We encourage you to also visit our Multiple Sclerosis story and support community on Experience Project. Experience Project is a vast and powerful community where people connect anonymously through life experiences. It's made by the same people who built This is MS, on the premise that no one life experience-- like having MS-- defines a person. It now covers over 2 million life stories. Find and share yours!

Experience Project: I have Multiple Sclerosis


Anonymous Confessions | Free Dream Interpretations | Ask Any Question
Site Map

This site does not offer medical advice. All treatment decisions should always be made with the full consent of your physician.


All logos and trademarks in this site are property of their respective owners. The comments are property of their posters, quoted articles are © referenced source, all the rest © 2002-8 by thisisMS.com.
PHP-Nuke Copyright © 2005 by Francisco Burzi. This is free software, and you may redistribute it under the GPL. PHP-Nuke comes with absolutely no warranty, for details, see the license.
Page Generation: 0.11 Seconds