I’m so sorry, I can’t remember what strength, it was about seven years ago, about a year after my diagnosis, when I went straight to a diagnosis of SPMS. Having been told by my abrupt and somewhat disinterested neurologist there was no cure and no treatment. I felt I had nothing to lose by giving it a try. I think I probably took it for around six months.
I’m SPMS too, so in the absence of any official medication to deal with ‘progressive’ types of MS, I’m looking for an alternative way to try to improve things myself.
(…it often feels like the medical profession has written-off the very idea of trying to help?!!)
If I find something by happy accident, I’ll be only too pleased to let everyone know, so wish me luck
Sorry to post this so late on in the day, but this is my first day trying Serrapeptase.
The initial plan for the first 7 days is to try:
2 x serrapeptase 80units first thing in the morning
2 x serrapeptase 80units early evening
…both times, tablets to be taken on an empty stomach
I’ll review dosage after 1st week and either increase/decrease/keep the same for following week depending on whether I’m experiencing any effect at all