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#1 | ||
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Senior Member
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Hi,
Congrats on doing your first Copaxone shot. I've been on it for 4 years now and so far so good, antijinx. ![]()
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He is your friend, your partner, your defender, your dog. You are his life, his love, his leader. He will be yours, faithful and true to the last beat of his heart. You owe it to him to be worthy of such devotion. Anonymous |
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#2 | |||
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Member
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Another member of the C Club. I heard Jennifer wasn't allowed in.
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"Thanks for this!" says: | Debbie D (12-05-2008) |
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#3 | |||
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Senior Member
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In the beginning (I'm always tempted to say, "God said, 'Let there be light. And there was light.'"), it stung for quite a while. Then sometimes thereafter it would sting just a little bit or not at all and there would be a few weeks where it would sting like it did in the beginning. I have no clue why it went that way, but maybe it depended on the batch.
Good for YOU for getting through it. It's certainly a mindset change. I couldn't handle it at first because it made me feel like I was sick--like the syringe was a visible sign of me being ill. Ugh... I got over that and moved to just disliking the injections! LOL
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A Hairy Chicken Is Better Than A Hairy Hand! |
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"Thanks for this!" says: | Debbie D (12-05-2008) |
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#4 | |||
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Magnate
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Congratulations!
![]() I took Copaxone for five years, and it seems that after awhile it would sting only occasionally. I'm numb on my left side, so it's a relief when I do left-sided Betaseron injections because I don't feel a thing. ![]()
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Mair . |
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"Thanks for this!" says: | Debbie D (12-05-2008) |
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#5 | |||
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Magnate
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I'm past the 6 month point on Copaxone, and I find the sting now only lasts a couple minutes for me. At first it was lasting 20-25 minutes.
I never pre-medicated or applied heat/cold. I also do my shots manually however.
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2004 to present - Trigeminal Neuralgia 2007 to present - Burning Mouth Syndrome March 2008 - Multiple Sclerosis DX 05/2008 - Relapse 05/2008 to 02/2009 - Copaxone 10/2011 - Relapse - Optic Neuritis developed 9/2012 - Relapse - Balance issues 1 sided 8/2012 - Erythema Nodosum - diagnosed 10/2012, reaction to Topiramate (Topamax) April 7/14 - Raynaud's Syndrome DX |
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"Thanks for this!" says: | Debbie D (12-05-2008) |
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#6 | |||
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Senior Member
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The Dimpled One brings up a good point--manual injections.
You might want to do some manual injections every once in a while. One day you'll find yourself somewhere and you'll have left the blooming Autoinflictor home. So you'll HAVE to do a manual injection. It's very different staring at the needle going into your skin than putting the Autoinflictor there and pressing the button whilst grimacing. ![]()
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A Hairy Chicken Is Better Than A Hairy Hand! |
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"Thanks for this!" says: | Debbie D (12-05-2008) |
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#7 | |||
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Elder
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Not to mention that the manual injections are easier than using the autoinflictor. You can control how quickly you inject, and doing manual injections is a lot more gentle to your skin. You dont have a harpoon blasting thru your skin.
I just passed my 1yr C-versary (Copaxone anniversary) I dont think I had made it to the six month anniversary before I switched to doing manual injections. So much easier, and really a lot less painful...still itches like crazy on my left leg a lot for some reason tho.
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~ Never do anything that you wouldn't want to explain to the paramedics. ~ Author Unknown ~ ~ "Animals have two functions in society. To taste good and to fit well." ~ Greg Proops, actor ~ |
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"Thanks for this!" says: | Debbie D (12-05-2008) |
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#8 | |||
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Elder
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Thanks everyone. We did practice manual injections on a small ball, but it's probably a good idea to do a few manually. How do you know how far to put the needle in?
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Instant Karma's gonna get you-gonna knock you right in the head...John Lennon |
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