Siponimod reviews
Hi all, hope it’s okay to ask for people’s opinions.
I was offered Siponimod a couple of years ago, apparently as an asthmatic it’s the only one I can have.
At the time I turned it down due to the lowered immune system, UTI risks, eye issues risk, etc. the ones listed are because of a history of issues with them. I also have fibromyalgia and a long list of other issues.
My ms increases after illness the last being an infected and perforated gallbladder, which I knew nothing about.
With this last increase in ms symptoms I’m now debating starting Siponimod and would love to hear people’s opinions on it?
My father stopped taking arsenic in the 1950’s and lived a good life without medication, but I know we are all different.
I hope I can read your opinions, I’m in a tough place right now.

Hi. I've been taking siponimod for 2 years now. I must admit I was scared about taking it but I needn't have worried. I've had no side effects and have been absolutely fine. I know quite a few other people with MS on it and they've been ok too. You have a nurse for the first month to monitor things + they work for the drugs company I think). I have to have blood tests every 3 months to check for any risks associated with it but again there's not been any problems. It's meant to slow progression down by a third.
Works great for me. No problems for two years.