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 😊
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...
Of the many theories I studied, cognitive behavioral therapy is very good at stress reduction and it is my first choice for a therapy for clients with chronic disease. According to Pahlavanzadeh, Abbasi and Alimohammadi (2017), psychological aspects are one of the factors that could influence the qu...
just wondering if anyone takes nerve pain supplements. Been taking Ginger Root and Magnesium for a month or so now. But find my pain levels have increased since taking the,. Has anyone expereinced similar with the supplements mentioned? just not sure if things are getting worse or I have to go throu...
Is anyone else not taking meds right now? I tried ocrevus and copaxone… both of them made me worse.. which made me not take medication other then vitamin D.. going on over 2 years now with nothing.. MRIs also have been stable
Neuro said it would take ~30 mins, but it was no surprise that it actually took over an hour (brain and whole spine).
I was glad I'd listened to some of the noises on a youtube video first - I felt a bit weird doing that and my scanner made a few different [continuous] noises as well as the knocks a...
Hey friends, I’m just a bit frustrated at the moment and am seeking some solidarity and maybe advice from those who have been through what I’m dealing with 🌸 I started taking gabapentin last year to help manage my pain, despite the fact that it wasn’t managing my pain at all, I was discouraged from...
My partner was diagnosed with MS earlier this year and declined any medications except vitamin d3 supplement, shes had two lots of optic neuritis. Any advice?
Hello all,
I have a tingling feeling in my feet. I have tried various creams, compression socks and Vitamins in hopes to reduce the symptoms.
Does anybody else get pins and needles feeling in their feet or other parts of their body, and have found ways to cope?