I see your comments about Nursing Support and which is great to hear about. Like I said before have asked for help many times but get fobbed off with ,you’ll need to be assessed and any possible MS drugs might have to be paid for. What’s happened to my Country and where my Ancestors reach back to the 4th Century, through the Plantagenets too. Trying to stay alive is a real struggle because one lives alone with MS. Even my MS Consultant messes me around and where it’s been over three years since we had a chat. Yes I know about the Covid thing, but there’s still ,say Skype or their own. There’s a layer of professionals that earn big money, yet do very little for it. I once received a lot ,travelled the World, yet never forgot who I was or what my responsibilities were. This is one of the major faults with the NHS, they’ve become unaccountable and more money won’t fix that. Any real tips on how to get help for me and my poorly Wife would be appreciated and without those damn assessments. I still proud.