Running out of injection sites

A board to discuss the Multiple Sclerosis modifying drug Copaxone
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annad
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Running out of injection sites

Post by annad »

Hi to all!
Has anyone had to stop using copaxone because they ran out of injection sites?
I am running out of 'fat' to inject into and I don't get the full amount injected into me. I've also stopped using my arms as a site as it's just too darn painful.
Not sure if it's doing anything for me anyway.
thanks!
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Zelda
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Post by Zelda »

annad

My neurologist told me, that in 4 – 5 months, Copaxone is going to be available in pills. Until then … hang in there.
LR1234
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Post by LR1234 »

Zelda, If that was true you could buy copaxone now. It is made up of 4 amino acids that are readily available in all health food stores! so I don't think they can make copaxone an oral pill. However there are oral pills of other drugs coming this May.
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annad
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Post by annad »

Thanks!
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Zelda
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Post by Zelda »

LR1234

Maybe you know something that my neurologist doesn’t? In that case, we’ll just have to wait and see.
Wonderfulworld
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Post by Wonderfulworld »

Hi Annad
have you got a low BMI? I was very thin for a while when on the Best Bet Diet and I was working out a lot. I ran out of viable injection sites. I know it's a solution not many would be comfortable with but I put on half a stone and suddenly it became an awful lot easier to keep on injecting.
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globab
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Post by globab »

i am a heavier lady, and have run out of spots...
even though i have a fair amount of fat on my body, it is still painful as heck on upper arms, and legs... so i dont do those, I use mainly belly....
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tld723
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Post by tld723 »

Have you tried adjusting the depth of the needle? That helped me immensely!
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joeymia
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Post by joeymia »

so what happens if inject into muscle? besides pain does the medicine still work?
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