Ok so Ive started my own little self treatment plan whilst I way to see the neuro as Ive been having a horrible relapse for the last month and dont see neuro till April 30th.
What Vitamins and supplements do you take? And how has it affected your MS symptoms?
Ive just started taking:
Vitamin D (With Calcium and Folic Acid in - from Midwife cause Ive just had baby)
Hi I take a few vitamins and supplements, I take ; 1000mg Codliver oil capsule
100mg Co Q10
25mcg Vit D3
1000mg Calcium
500mg Magnesium
300mg Chlorella
I’ve just started taking Co Q10 after reading about how it is used by the brain cells, to keep them healthy and keeps us more alert. I feel well, but I don’t have relapses I’m PPMS. Hope you soon start to feel better.
I take 5000iu of Vitamin D3 every day and 600mg of Alpha Lipoic Acid as well. I ran out of alpha lipoic a few weeks ago and stopped taking it and I noticed my pins and needles was much worse, went back on it and seems to have made a difference.
I tried Cod Liver Oil capsules for a while, but I didn’t like burping up the horrible taste all day. I also tried garlic capsules, they are supposed to have no anti-social after effects. Not for me, phew! I just take a multivitamin once a day.
@ Bill… I seem to be getting on ok so far with the baclofen… but im only at 20mg a daytrying to see what difference a minimal dose will make. No real tiredness…
Fish oils - hate oily fish Vitamin d -not enough sun and can’t get enough from diet Magnesium - fabulous sorted out my stiff legs Probiotics - don’t take but going to start - put on shopping list Min xx
Vitamin A -10,000 IU (Now Foods), - I take this for dry skin but it is made from Fish oils so cant’ be bad.
I really don’t know of taking these makes a difference but at least it is something I can do and gives me an element of control. Was anyone ever told what they should be taking. This lot is just guess work but Alpha Lipoic Acid looks interesting. I well seek that out and give it a go too. Why are we not given this stuff on prescription? We are spending a fortune. I asked my GP about vitamin D suplements a few year ago and they only prescibe that if you have a deficiency.
Skin & hair capsules (nothing to do with MS, but does contain additional amounts of some of the other stuff already noted - e.g. the oils & vitamin D).
I’ve occasionally taken Gingko and CQ10, but couldn’t notice any benefit from either of those (not that I’d swear there is from any of the others), so I didn’t persevere with them long term.
Apart from the Vitamin D, I sometimes wonder if I’m wasting my money. But as I’ve been doing quite well, and not had a relapse in some time, I’m reluctant to change anything, in case something in my cocktail is doing the trick. It does get pricey taking all this stuff, all the time, though.
I’d never thought about the possibility of it interfering with DMDs, but I’m not on them anyway.
But since diagnosis, I’ve always avoided echinacea, or anything reputedly “immune boosting”. I don’t know if the claims made for such supplements are even true. But I don’t think I want my immune system to be any more fired-up than it already is, so I don’t take the chance. Ginseng is another one I won’t take (distinct from gingko, which may be of some benefit, and I don’t think is an immune booster).