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The Dragonfly

Anyone else on Copaxone

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The Dragonfly

Hi everyone!

 

I have been using copaxone for three weeks. I don't mind the injections everyday, actually i get a kick out of finding new spots, so i can play dot-to-dot on my body, light humour, gotta keep that going. :penguin2:

 

What has started out fine I now get welts on my thighs. So stopped injecting into there, i now do my tummy, arms and buttocks. Again don't mind that but i spent the entire of last night scratching my injection site from yesterday on my left arm, huge welt there. Welt and redness there before scratching. Really itchy and i am using shear determination right now to not scratch. Did my tummy today, no problems. I am just running out of spots and kinda worried. I have been rotating them all aswell.

 

Has anyone else had this much trouble and what did you do to relieve it?

 

Thank you

 

Jennifer x

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Chaos

I have been injecting Copraxone for about 7 years. Never really had any problems apart from lumps under the skin where I inject in my stomach.

I would suggest for the itching feeling you are experiencing putting ice cubes on the injection site. Put the ice cubes in a bag first so when they melt you don't have water everywhere.

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The Dragonfly

Hi Chaos,

 

As one does with MS, I forgot I asked this question. Thank you for answering.

 

I have been icing and it has helped a bit. I still get the welts, and I bruise very badly on my thighs. Think I might have to stop doing it there completely. I read that the lumps and itching is normal so I will persevere.

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Rama

Hi,

 

I was on Copaxone for about 3 months. I didn't get itching but did get lumps on my thighs which were very tender. If I had continued on the Copaxone I think I would have stopped injecting into my thighs. I never tried injecting into my arms. Only areas that I found ok were stomach and buttocks. If you are okay with these sites I would stick with them.

 

By the way I stopped taking it because I have now been diagnosed as SPMS and I am hoping to get on a trial for SPMS and one of the criteria is you are not taking any DMDs. Weren't doing me any good anyway.

 

Gill x

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The Dragonfly

Ah, interesting Gill. My stomach and buttocks are my best areas, guess more fat....haha. Arms are ok. The last few on my thigh have been drawing up blood after I take the needle out, I'll stop there I think.

 

I'll give it a year and see how it goes. I have permanent numbness and a weird irky feeling that I can't explain in three fingers on each hand. Extreme tiredness still and my legs are like weights, hope the copaxone helps.

 

Jen x

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Rama

I hope it works for you Jen.

 

X

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