Multiple sclerosis (MS) is a chronic disease which affects the brain and spinal cord. MS can cause a variety of symptoms, including changes in sensation, visual...
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Teva Manufactures vinegar.
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Does anyone else feel like Copaxone is nothing more than vinegar? That's how i feel because i've been on it for 2 months and already had a relapse and it's lasted twice as long as my first 2 attacks since January. It's also different symptoms and i have 10 new lesions. Am i wrong in thinking this stuff is supposed to be helping me? Not coinciding with the worsening of my disease.
Posted on 05/15/08, 01:05 pm |
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Hi,
Don't give up... Copaxone works very slowly I started to see big difference at 6 months.. call Shared Solutions and talk to nurse ask her "what average time is to see some improvements. My neuro and Shared had different views on time factors 
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I call it Nail Polish Remover
if you read the ingredients.. they're in the same family. squirt some on your nails and see if it doesn't take off the nail polish
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Copaxone takes about 6 months to really become effective. Most docs give it 6 months to a year to determine if it is an effective treatment method for a patient.
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i am so sorry. you are too young not to get help from this. i guess you have to hang in there.
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well the first couple of months i was on copaxone i got a lot more lesions...then it settled down and i haven't had an attack in 6 months
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I am a 3 month CX user and feel the same way. My symptoms went away with REBIf at 4 months and now they are returning slowly and weak but they are coming back stronger. I knew this when I decided to take this drug that you have a LUL time. I just pray that I don't get new lesions.
10 new lesions are a lot and I would be aggressive at your decision to hold off for that 4-6 month mark or start deciding your next move just in case. I am researching mal-absorption with exzemaparent because I am very low vit.s and Ldn because some use it with Cx I have not research that yet and doing it with my doc. just be aggressive, goodluck
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