Almost forty years with MS, myself (but who’s counting.)
Always choosing treatment with as few drugs as possible. Never took steroids as I was mis-diagnosed for such a long time. I had already stopped working by then.)
Only drug that I now use, has been shown to limit MS progression – (something called
low dose naltrexone.) No needles and very inexpensive, when used in a liquid method.
For info online, check ldninfo.org.
only side effect with LDN, (sleep disturbance, for a few days)