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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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In Category: Treatments
Discussion:
VITIAMINS AND MEDICATIONS
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Hello, I was wondering what other take to help with their MS. What helps, what doesnt help, ect... Here is what I am currently taking;
One-A-Days Womens Multivitamin, B-12(bottle reads 'promotes energy metabolism& nervous system health', Provigil(for engery), Gabapentin(for pain..doesnt seem to help AT ALL), and my once a week shot, Avonex.
So what you think? Any advice, suggestions? I have not been feeling good and need some help.
Take care! -Jen
Posted on 05/15/08, 07:05 pm
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Reply #1 - 05/15/08  11:04pm
" Hello Jen I started out taking avonex for 2 years and had to switch to ribif 44mcg three times it seemed to slow the progression of my disabilities. You should check out a web site called patients like me. It has alot of good info about what kind of medications -that people with MS are taking. Take care Greg "
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Reply #2 - 05/19/08  10:16pm
" I also take B-12 for energy, etc. I did a lot of reading about it before. I learned that B-12 is not completely digeted (?) into your body's system. I found a few sites that sell B-12 Patches. The vitamin is absorbed completely. You wear a new patch 1x/week for 24 hours.
Hope this will help you. "
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Reply #3 - 05/19/08  11:21pm
" Thx for that information helps me out. I really want to look in the B-12 info Chrissy gave me. "
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Reply #4 - 05/20/08  7:25am
" or do sublingual B12 "
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Reply #5 - 05/20/08  1:14pm
" I take so many vitamins that my table looks like it could be a health food store.
Vitamin D, B, flax oil, calcium 2-aep. B12 injections weekly (many years), glyconutrients, glucosamine sulphate & salba.
That's what I recall right now (keep a list to keep track.) "
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Reply #6 - 05/20/08  1:52pm
" Darcie, do the B12 shots seems to help?? What about the other stuff you take, do you feel better after taking all of those? Thx "
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Reply #7 - 05/20/08  7:22pm
" Well, all I can say about B12 is that by injection it goes directly into your bloodstream.
I get an injection Tues. & do sublingual on w/ends as well. I think the B12 is why I've stayed in remission for many years & I have had some small improvements as well.
Never done steriods & don't have a neuro.

Bye for now,
Lorna "
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Reply #8 - 05/20/08  10:23pm
" For the past couple of months, I've been doing this vitamin therapy I found in a book my dad bought right after my dx. It's quite expensive & I'm not sure if it is helping, but if nothing else, i have more energy during the day...
DHA 300mg, 2xdaily; Co-Q10 100mg, 2xdaily; Vit E 400IU; Vit C 500mg, 2xdaily; Alpha lipoic acid 200mg; N-acetyl cysteine 400mg, 2xdaily; Acetyl-L carnitine 400mg, 2xdaily; Phosphatidylserine 100mg, 2xdaily; Ginko biloba 65mg; Vit D 400IU; B1 50mg; B3 50mg; B6 50mg; Folic Acid 400mcg, 2xdaily; AND B12 500mcg, 2xdaily.

I'm on Copaxone shots too. "
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Reply #9 - 05/21/08  11:04am
" Have you heard about low dose naltrexone? Go to ldn.org for info.

Lorna "
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Reply #10 - 05/26/08  8:29pm
" i bought this fantastic book shortly after i was diagnosed, based on a recommendation. i'm not sure if any of you have it, but it's the 'Prescription for Nutritional Healing' It has MS in it, as well as every other ailment known to man. :) i just starting taking vitamins for my MS and some of the symptoms i have.

i literally starting taking things yesterday, so i'll let you know how it goes. "
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