I am seeing my MS nurse on 1st July, just that I thought I would try and sort myself out so they can see I am keen not to be affected or reliant on anyone, don’t know if it’s denial. So also look at local council website, thank you.
Hi, over the 17 years I have had this chronic disability, I have had marvellous help from OT visits, physios, district nurses and other bods.
Yes, they can offer lots of gadgets and things to keep you safer at home and out and about…but with the cuts, there isnt as much on offer and sometimes,we have to buy our own things.
Best thing to do is ask Social Services for an assessment.
thank you for your response. I will look into an assessment, think I have one on the 1st July as just a week out of hospital (2 month stay) gggrrrrr… Seems like mine has come on suddenly, which is scary but more aware of it now. Any top tips would be great for this newbie xx