Hello,
I’ve been recently diagnosed and been told to take vitamin D tablets. What else do you take? I’ve also been taking lions mane and found that super helpful.
Hi all, does anyone else have illness after illness? I’m not a poorly person and never have been but this last month or so I’ve had an infection, then Covid and now I’m ill again. Not used to this at all! I already take the recommended dose of vitamin D and multi vitamins. When I’m feeling poorly it...
So I was thinking of upping my intake of vitamins and a like through supplementing with super greens (a powder that can be mixed into a shake) does anyone else supplement their diet I any way? Are there things I should avoid?
PS I forgot to mention magnesium. You said you were starting it. For me I take it at night and I don’t wake up with leg cramps that I used to get before I started the magnesium.I started with 400mg but now take 600mg in two separate pills ( 400 + 200mg) because I still got some leg cramps with 400mg...
I’m going to Turkey in September. I don’t take any controlled meds but do take a lot of prescribed. Do I need to get anything from my dr to prove anything?
The most important thing to keep in mind about diet is that it is viewed as an ‘add on’ to scientific/medical treatment. It is also imperative to get medical advice from your health care team on any steps you wish to pursue. When you have a team they see all of your underlying conditions as well ...
Hi,
I just wanted to know if anyone had any recommendations regarding any supplements or vitamins or diet? I'm aware it's all a bit different for everyone but I figured any advice would be a start and would be greatly appreciated.
My MS nurse just suggested vitamin d which I have and I do take so...
I have had Primary Progressive M.S. for 30 yrs. and the only info. I got from my Neurologist was to make sure I took my Vitamin D. I have had only 2 Drs. since I was diagnosed. One retired and the other left our Province of Manitoba. Now, I only see a Nurse and diet has not come up yet.
So I had my first dose of KESIMPTA yesterday. Injection went well so quick and easy. After effects started 4 hours or so later and were a little more troublesome I had horrendous chills that made my body convulse. Then became so hot and sweaty. Suffice to say it wasn’t a fun first night. Once I’d sl...
Just wondering if anyone else on Tysabri notices an increase in joint pains/aches after the infusions? If so, have you found any supplements that help like magnesium etc.? Thanks 😊