It appears you have not yet Signed Up with our community. To Sign Up for free, please click here....

Multiple Sclerosis Message Board


Post New Thread   Closed Thread
LinkBack Thread Tools Search this Thread
Old 08-02-2005, 08:35 AM   #1
Join Date: Jul 2005
Location: Houston, TX
Posts: 67
jennypash HB User

Hi All. I am in the process of starting copaxone injections. I am just waiting for the medication to arrive at my house. I got this injector thing yesterday from the company. Its spring loaded or something. I am scared to death of a daily injection but if it is what i need to do to battle this, then I will do it. My question is - do any of you know about this injector or use it? I would think it would make it eaiser than putting the needle in yourself - which is how I assumed it was done. Also - how has copaxone worked for you?


Sponsors Lightbulb
Old 08-02-2005, 08:41 AM   #2
Join Date: Jun 2005
Posts: 92
djpihavems HB User
Re: Copaxone

In my opinion, the auto injector just hurts more. If it is the visual of the needle that upsets you, then you might need it. But, it doesn't make the shot itself any easier.

I know it's hard to believe at first, but you will get used to it. And honestly, doing the shot every day actually makes it easier. I used to take Avonex and the buildup between shots made me a basket case.

It just becomes part of your daily routine.

Some advice... make sure you take the shot out of the fridge a few hours before you use it, so it can come up to room temp. Don't shoot into the fronts of your legs. It hurts and leaves bruises. I don't shoot into my arms either, especially in the summer when you want to wear sleveless. The tummy and the butt are the easiest places to shoot. Learn how to do the shot yourself, so you don't have to depend on someone else to always be there.

Old 08-02-2005, 01:23 PM   #3
Katie M
Junior Member
Join Date: Jul 2005
Location: East central F.L.
Posts: 14
Katie M HB User
Re: Copaxone

Hi, I've been on copaxone for 3 months. I've never used the auto inject, but have it handy just in case. It looks alittle complicated to me. I would love to get to the place where I can give my own injections, but my husband gives them for now. In all truthfulness, I not sure I will ever be able to do it on my own. The shot may sting and welt some, alot like a bee sting, but for me, it doesn't start untill about 5 sec after the shot itself is over. I've never found the needle to be painful. The belly and butt is definatly the easiest to tolerate in my opinion also. I've never had any other problems from copaxone then the bee sting feeling. I wish you luck.

Old 08-03-2005, 08:01 AM   #4
Senior Member
Join Date: Jul 2003
Location: Salt Lake City, UT, USA
Posts: 206
painsucks HB User
Re: Copaxone

Hi Jenny,

I've been on Copaxone for 5 months now. I use the auto-inject thing every day because I really didn't want to have look at the needle when I poked myself with it! I messed up a couple of shots early on, like I forgot to pull the red cap thing off the injector so when I pushed the trigger all the medication just squirted into the bottom of the injector, nice huh?! But now I'd consider myself a pro, it only takes me a couple of minutes to prepare and give myself the injection each day. I do it at night, part of my getting ready for bed routine. I actually take 5 of the shots out of the refrigerator at a time and put them in my little blue packet and keep them in my bathroom medicine cabinet. This way I don't forget to take it out of the fridge every day. But on those days when I do forget, I've got a funny method of "microwaving" the injection...I put the syringe under my boob! I guess gravity and old age are good for something sometimes! Everyone has already said, the hip and the tummy are the best sites, hurt the least and don't leave lumps or bruises. My legs always seem to bleed and bruise and my arms get lumps so I don't like to do it there. I do think the Copaxone is helping me, I haven't had a really bad flare up since March and that for me is a very good thing! You'll get used to doing this, it will just be like brushing your teeth after a while. Hang in there and keep us posted on how you do. Good luck.

Closed Thread

Similar Threads
Thread Thread Starter Board Replies Last Post
MS and Chronic Hives on Copaxone wtorrens Multiple Sclerosis 30 12-04-2011 07:02 PM
Diagnosis Confirmed Yesterday- Questions about Copaxone LLCRGD Multiple Sclerosis 18 11-07-2008 05:31 AM
Copaxone & Hives or Bad Reactions Shelly7630 Multiple Sclerosis 62 08-13-2008 04:06 PM
Neuro Appt and Copaxone quest? oceangirl19 Multiple Sclerosis 6 09-13-2007 03:50 PM
This or that...Avonex or Copaxone midwestdeb Multiple Sclerosis 11 05-24-2007 02:12 PM
copaxone and requested please MSNik Multiple Sclerosis 5 03-31-2007 05:39 PM
copaxone use while pregnant?? locket Multiple Sclerosis 2 03-10-2006 11:32 AM
Avonex vs. Copaxone crystal22 Multiple Sclerosis 12 12-11-2005 06:04 AM
Copaxone and menopause early onset pcmuphy Multiple Sclerosis 1 06-15-2003 10:30 PM
Ladies...Using Copaxone and Menstruating Brandysmom Multiple Sclerosis 0 12-08-2001 07:13 AM

Thread Tools Search this Thread
Search this Thread:

Advanced Search

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 Off
HTML code is Off
Trackbacks are Off
Pingbacks are Off
Refbacks are Off

Sign Up Today!

Ask our community of thousands of members your health questions, and learn from others experiences. Join the conversation!

I want my free account

All times are GMT -7. The time now is 01:49 PM.

Site owned and operated by HealthBoards.comô
© 1998-2018 HealthBoards.comô All rights reserved.
Do not copy or redistribute in any form!