advertisement
Reply
 
Thread Tools Display Modes
Old 07-10-2009, 03:04 PM #1
suzyqz_2007's Avatar
suzyqz_2007 suzyqz_2007 is offline
Member
 
Join Date: Jan 2008
Location: Houston, Texas
Posts: 643
15 yr Member
suzyqz_2007 suzyqz_2007 is offline
Member
suzyqz_2007's Avatar
 
Join Date: Jan 2008
Location: Houston, Texas
Posts: 643
15 yr Member
Default switching from copaxone to avonex

I was taking copaxone but having bad site reactions & it really didn't seem to be helping me any so my neuro wants me to start avonex, (I'm waiting on the nurse to call so that she can come out and teach me, though it might be next week sometime)

The thought of the needle and no auto injector really has me stressing out, not to mention the flu like syptoms that it could cause. Am I worrying too much? What can I expect? Ohhhhhhh I hate needles and I hate this freakin' disease!
__________________

.


Dx'd RRMS July 2007


suzyqz_2007 is offline   Reply With QuoteReply With Quote

advertisement
Old 07-10-2009, 04:18 PM #2
Dejibo's Avatar
Dejibo Dejibo is offline
Elder
 
Join Date: Jan 2008
Location: New Hampshire
Posts: 7,332
15 yr Member
Dejibo Dejibo is offline
Elder
Dejibo's Avatar
 
Join Date: Jan 2008
Location: New Hampshire
Posts: 7,332
15 yr Member
Default

I have done Beta, and got kicked over to Copaxone. I have never taken Avonex, so I cant help you there, but I did want to step forward, and offer up a hug.

Changing to any new drug is so stressful. hang in there.
__________________
RRMS 3/26/07
.

Betaseron 5/18/07
.

Elevated LFTs Beta DC 7/07
Copaxone 8/7/07
.



.
Dejibo is offline   Reply With QuoteReply With Quote
Old 07-10-2009, 05:07 PM #3
MdotDdot MdotDdot is offline
Junior Member
 
Join Date: Jul 2009
Posts: 32
10 yr Member
MdotDdot MdotDdot is offline
Junior Member
 
Join Date: Jul 2009
Posts: 32
10 yr Member
Default

you will feel flu-like: sore muscles, warm, achy for about a day afterward. using the injections are okay once you get used to it. if it is troublesome, then get your doc to write you a script for smaller 25gauge needles. and at least it's only once a week!
MdotDdot is offline   Reply With QuoteReply With Quote
Old 07-10-2009, 05:26 PM #4
SallyC's Avatar
SallyC SallyC is offline
In Remembrance
 
Join Date: Sep 2006
Location: SW Ohio
Posts: 17,844
15 yr Member
SallyC SallyC is offline
In Remembrance
SallyC's Avatar
 
Join Date: Sep 2006
Location: SW Ohio
Posts: 17,844
15 yr Member
Default

It was the other way around for me, Suz. I left Avonex because of the side effects and went to Copaxone. I had no site reactions to it, but had too many exacerbations, so now I'm on LDN..

Not all PwMS have the major flu sx with Avonex, as I had, so Good luck.
__________________
~Love, Sally
.





"The best way out is always through". Robert Frost



~If The World Didn't Suck, We Would All Fall Off~
SallyC is offline   Reply With QuoteReply With Quote
Old 07-10-2009, 05:37 PM #5
Lady's Avatar
Lady Lady is offline
Senior Member
 
Join Date: Aug 2006
Location: East Coast USA
Posts: 1,174
15 yr Member
Lady Lady is offline
Senior Member
Lady's Avatar
 
Join Date: Aug 2006
Location: East Coast USA
Posts: 1,174
15 yr Member
Default

Hi,
I did Avonex before Copaxone. I found it is best to start with 1/4 of the dosage, if your Neuro permits. Then go to 1/2 a dosage, when ready. Then up to full dosage.

This way you see how your body tolerates it. Some people don't get the flu, some pre-medicate, or medicate every few hours. Maybe pick a day of the week when you will be staying at home, so you can treat any symptoms you get, if any.

The needle is intimidating, but truthfully, injecting into the muscle, never gave me a skin reaction. I learned to dart it in, if that helps you. Count to three, and just do it. It is over quickly.

It didn't agree with me, but so many people have no problems with Avonex. I hope you are one of them, and that it helps you. Good Luck.
__________________
LADY

May happiness be at your door. May it knock early, stay late, and leave the gift of good health behind.


"Life is what it is". We can only focus on controlling those things we can control, we must let go of the things we can't.
Lady 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
going from Avonex to Copaxone slskckjebw Multiple Sclerosis 12 05-06-2011 07:17 PM
Switching DMDs FinLady Multiple Sclerosis 6 04-04-2009 11:54 AM
Switching from Betaseron to Copaxone FaithS Multiple Sclerosis 15 07-31-2008 12:10 PM
Avonex/Rebif to Copaxone? the Bird Multiple Sclerosis 1 02-05-2008 11:11 PM
Switching AD? Viriatus Depression 1 05-03-2007 03:40 PM


All times are GMT -5. The time now is 02:56 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.