Hi everyone! Long time no speak.
Just out of curiosity, what vitamins/supplements does everyone take? I only take Vitamin D at the moment. Feel like I should be taking others.....
I am just happy to be here. I was diagnosed back in 2012 but my doctor believed that I had it most of my life. I am only treating the MS with vitamins and supplements. I used to be on Ocrevus for a few years. My health is doing well. I only struggle with pain and fatigue but they are being treated ...
If any of you comes across my half finished post on vitamins and supplements please return it as it has been swallowed up and I haven’t the energy to repeat it at the moment.
Mmm I methinks have a steep learning curve for understanding this web site - it’s has to be age related!
Random thought - W...
Hi all,
I see so many people with MS taking vitamins and supplements and I was wondering how you all decided what to take? Just your own research or advise from a professional?
Hi. My real name is Anna and I was diagnosed three months ago, just before my 44th birthday. I've only had one relapse, but it was big, knocked me flat on my butt, and even after steriods, and now ocrevys, I'm still feeling it. I was always pretty healthy, no smoking, drinking, recreational subst...
My daughter has recently been diagnosed with MS and wants to follow the Wahl's protocol as well as take the DMT drug. However I'm worried that she may be stimulating the immune system while the drugs are repressing it. The MS diet eliminates as much as possible dairy,refined sugar,legumes and glut...
Hi everyone, I've been reading through what seems like a zillion threads here trying to determine what vitamins and supplements everyone takes. If you have a moment could you please post here what you take, dosage etc . I'm currently taking supplements as advised by the site Overcoming Multiple Scle...
Just need some help, I've been taking 1000 I.U for ages, but I've been told to start taking 4000 I.U but I couldn't find any 4000 so got 3000 I.U, does any one else take vitamin D with 3000 I.U, just wanna check I'm doing the right thing. Thanks guys
Hello everybody
I was diagnosed in 2016 with MS. The disease started with the symptom of numbness of the soles and feeling of heat. I made injections with Copaxone until 2023. For 1 year I have been in the Coimbra Protocol with a dose of 90,000 units of Vitamin D3, of course under the guidance of th...
How does everyone deal with the idea of supplements?
Do you get your Vitamin D?
Have you tried things like creatine, B12 and Lion's mane?
I'm currently taking all of these, and Magnesium.
I've found Vit D to be really beneficial when it comes to feeling tired etc.
Has anyone discovered any other su...