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.
Joined: Apr 21, 2008 Posts: 217 Location: New Brunswick, Canada
Posted: Sat May 10, 2008 11:59 am Post subject: First injection of Copaxone
Completed! Didn't use the autoinjector... just did the needle with the nurse here, all by myself! Didn't hurt at all (tummy injection). After, the medicine burned a little, but overall it wasn't bad. I didn't even ice/heat before or after, and if the injections are like this each time, I don't think I'd need to bother with that.
What can I say? I'm proud! I've had a long standing fear of piercing my own skin, but that was nothing! _________________ Dx RRMS March 5, 2008.
Joined: Sep 30, 2007 Posts: 120 Location: Charlotte, North Carolina
Posted: Sat May 10, 2008 7:21 pm Post subject:
Nenu,
Glad to hear you are on one of the CRABs. I take Rebif myself. You are braver than I lass, it took me almost a year to switch from the auto injector to just the syringe. Definately easier that way. Hope everything stays copacetic with your shots.
Joined: Apr 21, 2008 Posts: 217 Location: New Brunswick, Canada
Posted: Sat May 10, 2008 7:47 pm Post subject:
Thanks for the head's up. I'm going to try each one free of cold/heat/pills first week and see how each site reacts without outside interference. From what the nurse told me, the autoinjector is more painful than only the syringe. So that's a plus! Besides, if I learn early not to rely on the autoinjector, it makes things easier if I plan to travel or be anywhere where I need to take my meds... because I can just leave the a.j. at home.
Jack, no move... long story, basically the people who put in the offer could not get a mortgage, their bank messed up and told them they were preapproved, and then came back and said oopsie, actually you aren't, wewps! So yeah. I had to cancel my apt. I had gone to see and was accepted for, basically start back at square one, and that threw me into a bout of complete stress (plus my nana's funeral this mo. and having to face my shots today), and I basically went into relapse with symptoms. NOT FUN!
But I'm doing a lot better these last couple of days. Still symptoms, but they seem to be clearing up some
Edit to include Jack's name, which admittedly I'll probably forget because my mind's horrible like that! :p ~ Laura ~ _________________ Dx RRMS March 5, 2008.
Joined: Apr 21, 2008 Posts: 217 Location: New Brunswick, Canada
Posted: Sat May 10, 2008 9:41 pm Post subject:
Yes, I discussed that with my nurse today... definitely am keeping an eye out for it, but it was explained that choosing different injection sites is the key to helping prevent it.
While that would suck, living with the symptoms and thought of disease progression sucks more _________________ Dx RRMS March 5, 2008.
Joined: Nov 24, 2007 Posts: 69 Location: South Germany
Posted: Mon May 26, 2008 6:54 am Post subject:
The great thing about the auto-injector is you can jab one-handed in many more places than two-handed. So when your stomach is full of bumps, you can start on hips and thighs. Just a thought for the future. _________________ Bibo ergo sum
Can you believe I've been injecting either Rebif or Copaxone now for 9 years and I STILL can't manage a manual injection, so hats off to you
Just a word of warning, all the Copaxone nurses say that blurb about lipoatrophy being to do with rotating sites but I am sceptical. I have very extensive lipo on legs/hips but I was absolutely disciplined about rotating. I drew up a chart with over 50 sites on it and I always stuck (sorry for the pun!) to those sites in sequence, yet I still ended up lipoatrophied.
It didn't really start until I was on Copaxone for more than 2 years.
I just keep remembering how ill I was off Copaxone, and how my legs were not working properly. Now my legs won't win any beauty competitions but they work. That wins hands down for me.
Joined: Apr 21, 2008 Posts: 217 Location: New Brunswick, Canada
Posted: Mon May 26, 2008 1:40 pm Post subject:
Surprisingly I haven't been ill on Copaxone. Thankfully. I am really hoping this drug works for me. It seems to be the easiest of the bunch to manage the side effects of. _________________ Dx RRMS March 5, 2008.
I starrted with Avonex, that's a scary needle to jab yourself with, but at least it was just 1 x per week.
I switched to Betaseron last year for 6 months and was sick the whole time.
I've been on Copax for 6 weeks now, I've really no side effects to speak of.
Do want to warn you about the thighs though. I bruise and redden there.
I'm going to experiment with technique, AI vs manual etc.
Also, as an aside, the nurse who trained me to inject works for my neuro, does all of his injection training. Most of what she told me I heard or read before except that she advises rubbing the injection site vigorously with the alcohol wipe for a full minute before the shot.
The purpose is to bring additional blood flow to the area to help disperse the drug more quickly, so it doesn't hang around the site long enough to cause severe reactions.
Joined: Apr 21, 2008 Posts: 217 Location: New Brunswick, Canada
Posted: Mon May 26, 2008 9:27 pm Post subject:
Sorry this thread was 'bumped' so to speak, and I'm actually on injection number 16 or so now.
As far as the injections go... tummy is painful (site reaction), arms are EASY, thighs are odd... right thigh seems to consistently have a lump after injection for up to 24 hours after, left thigh has no issues, hip/bum area is TOUGH to reach (I have to turn myself into a human pretzel to reach it) but really no discomfort there compared to the stomach.
The stomach seems to be the most pain from the medicine after injection of all the sites. I do that injection site on Saturday, so when I return to work, hopefully I won't be working Saturdays, because I'd like it if this site were on a day I didn't have to work _________________ Dx RRMS March 5, 2008.
Posted: Tue May 27, 2008 4:04 pm Post subject: Good job!
Good job Nenu!
I have been on Copaxone for 8 years and it is a good drug.
Some helpful tidbits - be careful about using the back of your arms - lipo seems to occur here more than anyone else.
Try very hard not to directly hit a vein. You will know when you have - you will flush head to toe and feel warm and short of breath. Don't worry it only lasts 15 minutes or so. Just lie down and let it run its course.
Joined: Apr 21, 2008 Posts: 217 Location: New Brunswick, Canada
Posted: Tue May 27, 2008 4:48 pm Post subject:
Oh yeah, I am very careful about avoiding the veins, which I can see quite well on my legs at least. Fact my right leg has a ton of them that I can see.
Makes picking a spot rather tricky. _________________ Dx RRMS March 5, 2008.
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!