Thankyou all for your posts
Hi midchild. First, Id like to say I hope your surgery in 2 weeks time goes well.
Im interested in the fact you couldnt sleep on your good side after your posterior op, Ive never even considered that I might not be able to do that, I really hope I can. Can I ask if you were in less pain after the 2 weeks then?
I have had back problems for a long time, Ive had 2 slipped discs, have crumbling of discs and a bit of a curved spine, plus when I had a lumber puncture when I was being tested for M.S, there was a sudden panic because the needle was in and something in my back wasnt where it was supposed to be, caused the medical staff to run off and get more equipment in a panic, but Im really not sure what that was all about haha....sleeping on my back hurts within a very short time and anytime at all Ive woken on my back Im in pain, as if the back has " seized up" so Im really hoping I can sleep on my side! Im going to try your suggestion tonight about messing about with the pillows a bit and see what I can sort though.
Hi Glynis. Im so sorry about losing your son

. Such a young age.
I know you totally understand my concerns about doing this when caring for a disabled adult . It really is a worry. Ive not had good experiences with Social Services. I had to fight for every little bit of help Ive ever had with my Daughter, which isnt much to be honest. We had an hour a week before I moved here, none since moving here. Once when S.S finally sent someone out from the Adult Learning difficulties team to interview us at our old home, to see about possibly taking my daughter out for an hour a week, I was told they couldnt take her oit because she has petite mal epilepsy, and has " absence" seizures, and their staff would be in danger if she " fell on them".

.
Finally we got the hour a day, but all they did was take her to walk to a cafe, have a coffee and walk back. So really, no help has ever been given. Shes never been to a " centre" to learn living skills, or to any groups, nothing at all. She was statmented at school and had a special needs teacher for an hour and that was every day, but since leaving school, nothing really at all. Everything seemed to stop when she left school. So Im fighting here for what I HOPE is going to be more than an hour a week of something for her. Someone said to once that its because shes got a "borderline disability". Shes disabled enough that she needs help, but not disabled enough for Some people to realise that.
Yep thats very true what you said about Mum, I was thinking the exact same thing, it might do her some good to be out here for a week. She did care for my Dad for years before he died, but he cared for her too. She did sometimes moan that he was a lot to cope with at times, but I think that when someone takes a lot of your time, you miss them even more. It might give her a purpose, to care for someone again for a while? Having said that, shes very unsteady on her feet and her eyesight isn't good, so would be limited in what she can do, but Im not going to say that to her, bless her.
I think Im going to ask for a walker, sounds like a very helpful thing to have. Yep Im lucky im in a bungalow, there are 7 steps up to the front door ( why build a bungalow for disabled/elderly people then put loads of steps to the front door!) but theres a back entrance I can go in with no steps. Thanks for all your help and suggestions, I do appreciate it a lot
Zauberflote, the image youve put in my mind of you with your apron and all your stuff hanging off your walker made me smile

And Im certainly going to try all that if I can get a walker! But what are the tennis balls for the back legs?
