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, 79 guest(s) and 18 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 - Combination of Rebif® and mycophenolate mofetil (Cellcept®)
 Forum FAQForum FAQ   SearchSearch   UsergroupsUsergroups   ProfileProfile   Log in to check your private messagesLog in to check your private messages   Log inLog in 


Combination of Rebif® and mycophenolate mofetil (Cellcept®)

 
Post new topic   Reply to topic    ThisIsMS.com Forum Index -> Rebif
View previous topic :: View next topic  
Author Message
Olgica
Newbie
Newbie


Joined: Mar 23, 2005
Posts: 3

PostPosted: Sun Aug 07, 2005 11:09 am    Post subject: Combination of Rebif® and mycophenolate mofetil (Cellcept®) Reply with quote

Hi!I have got MS 12 years ago.I am on Rebif since 1996.I have took it year and half.I have stoped because Rebif was experimental drug that time and it doesn't approved in my country.Rebif was so much expensive.I am on Rebif again.I am taking it already 4 years.I feel great and noone could possible that I am MS-er.I have had atack this june first time since I am on Rebif,because of that my neuro prescribed me CellCept 250mg X 2 times on day.I don't have any problems with that combination,but I was wondering do any of You take Rebif and CellCept!?Tell me if You take it how do u feel?
Back to top
View user's profile Send private message
batpere
Family Member


Joined: Nov 12, 2004
Posts: 97
Location: dallas

PostPosted: Sun Aug 07, 2005 1:18 pm    Post subject: Re: Combination of Rebif and Cellcept Reply with quote

Olgica wrote:
I am on Rebif since 1996. I have had atack this june first time since I am on Rebif, because of that my neuro prescribed me CellCept 250mg X 2 times on day. I don't have any problems with that combination,but I was wondering do any of You take Rebif and CellCept!? Tell me if You take it how do u feel?


I have been taking Avonex (same substance as Rebif, just injected in the muscle) for 7 years and the neuro added CellCept (1000mg twice a day) about a year ago because of continuing lesions. I am awaiting the results of a recent mri to see if the combination was more effective.

I don't like having to be more careful not to be around sick people because of my suppressed immune system. The physical side effects of the CellCept are very minor for me - just a slight sick-to-the-stomach feeling. I'll consider switching to Copaxone and LDN if this Avonex+CellCept still isn't enough.
Back to top
View user's profile Send private message
jazzcat
Family Member


Joined: Apr 14, 2004
Posts: 30

PostPosted: Thu Aug 25, 2005 2:09 pm    Post subject: Reply with quote

Hi all,

I haven't heard of cell-cept. What is that? I am on Rebif and have been for about 2 years. I am about to have the first MRI since my diagnosis two years ago.

Please fill me in about cell-cept.

Thanks,
jazzcat
Back to top
View user's profile Send private message
batpere
Family Member


Joined: Nov 12, 2004
Posts: 97
Location: dallas

PostPosted: Thu Sep 29, 2005 5:28 am    Post subject: Reply with quote

jazzcat wrote:
I haven't heard of cell-cept. What is that? I am on Rebif and have been for about 2 years. I am about to have the first MRI since my diagnosis two years ago.


It's an immune system suppressant that heart transplant patients take to
avoid organ transplant rejection. It comes with this warning:

WARNING: Increased susceptibility to infection and the possible development of lymphoma may result from immunosuppression. Only physicians experienced in immunosuppressive therapy and management of renal or cardiac transplant patients should use CellCept. Patients receiving the drug should be managed in facilities equipped and staffed with adequate laboratory and supportive medical resources. The physician responsible for maintenance therapy should have complete information requisite for the follow- up of the patient.

After some patients had problems, my neuro now requires blood tests
every 3 months before they will write the next rx. I'm growing
increasingly uneasy about continuing to take it. However, progression
has stopped since I added it to the Avonex I've been taking for 7 years.
Not an easy call.
Back to top
View user's profile Send private message
Display posts from previous:   
Post new topic   Reply to topic    ThisIsMS.com Forum Index -> Rebif 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: 0.10 Seconds