Tomorrow could be interesting/fun LOL. Hubby's community support is coming to see him, it has been over 3 weeks since the last visit and he is not happy about the time span, to be quite honest neither am I.
She used to call and see him once a week then once a fortnight, and if you have read back to some of my previous posts on this thread you will see, it has never really be a happy situation from the start.
She comes out with stupid comments when she calls, like "Why have you been asleep at this time of day". I have given her a lot of print offs from here to read, not sure if she has or not. There is another guy who comes with her on alternate visits, though it does seem to be on most visits now, who does understand PTSD.
Our issue now is that she/they have cut there visits short, from the an hour down to 25 mins last time. Its as if now that I am not working, they are leaving it all to me. ER no, they are the professional they are the ones who are supposed to be working with him at home, along side his therapy sessions. Even hubby's therapist was shocked that they are doing this, he did not seem happy about the way they are now handling this.
So tomorrow, hubby has decided to put this to them. To find out just what there plan is, as he was told that once his therapy ended, she/they would start doing more with him, but nothing was mentioned about it being cut back. He feels that she is not really interested or even knowledgeable enough to work with him, though her colleague is trying to teach her. He feels as if she is wasting his time and hers, as all that happens now is, she calls for about 30 mins, has a quick chat about how he has been the last few weeks, arranges another time to call and see him, then leaves.
Not much point in any of this really, nothing they can tell us about any of this that I have not already learnt from here, more like me teaching them. MMM maybe I should put in an Invoice for the time and effort I have spent educating our so called professionals here in the UK.
Wonder what the going rate is for private consultations, might find out, then send them the bill. So how about I send them one for all the time I have put into caring for my husband when they should have been here. All those breakdowns I have had to deal with alone, all time off work I have taken, unpaid, when he has been too ill to be left alone. All the sleepless nights I have had, due to nightmares and flashbacks. This list goes on, but you get the picture.
So for a rough guess, we have to be talking a good few thousand £ here :rofl:. Yea right, as if they would pay me for doing there job, they could not afford my prices.
There is another way to look at this, as in the knowledge and experience most carers have is priceless, free to be shared with those who need and appreciate it, but not affordable for those who THINK they know better than some of those closest to their sufferer.
So tomorrow hubby decides whether to ditch his so called support or not, not up to me, but I think I already know what he will do, as long as they let him speak, and not talk him out of anything THEY do not agree with.
Oh and I promise to keep the Doberman on a tight leash. :thumbs-up
Amethist