I'm sure this subject has been discussed to death, for that I can only apologise.
For a couple of years now, doing a little research on my own, I think that I may have what a Work Psychologist I saw 01/2012 called a neuro diverse condition. I thought it might be Aspergers, it might be ADD possibly Dyspraxia. I'm by no means an expert nor a diagonistician. I could be completely wrong and, as i suspect my GP thinks (but doesn't say), lazy!
When I first saw the Work Psychologist (a dwp person, i don't know much about the specific role as I'd never heard of them before) I was on JSA. Since then I started on the Work Programme which I am still on. She claimed she could test for Aspergers but relented to saying she could do some kind of test to see if I might have ADD. I realise that makes no sense, but it involved answering a load of puzzles like remembering number sequences backwards and spotting patterns and stuff. From what I could understand she said it was highly likely. I have yet to get an official diagnosis as such facilities are not local to me and I find travelling around cities rather scary. There is now a chance the local CMHT might do one.
However the Work Programme treated me badly. They ignored the information regarding my mental health (even though no formal diagnosis) and refused to accept even the possibility of such problems - of any kind. I was told that without a support worker present they wouldn't countenance any such possibility. I made a complaint and have since changed advisers. Though the replacement is better they still admit they can't do anything. Basically the WP is rubbish. I was told that the main problem was because I was on JSA and that I should claim ESA.
To cut a long and predictable story short that's what I did, six months later I have, unsurprisingly, failed the WCA. I've sent the GL24 form back to lodge an appeal. I'm not sure how that will work but I'm told that doing so reinstates my benefit until such time as they decide whether to change their mind (I doubt it, let's be honest). In the meantime I have to persuade my GP I need help.
I suppose my point in posting is just to hear what other people think. I haven't found my GP to be terribly helpful or sympathetic and the system certainly isn't. ESA should be employment support, but it seems to work on the basis that, in order to get into the WRAG (my stated goal, i don't claim to be deserving of the support group) you need to also qualify for the support group. This doesn't make much sense to me. As a result I feel guilty as if I'm swinging the lead. But on the other hand, I just can't cope with the DWP. I find life difficult and I find dealing with society at times very hard. All the stuff you've heard before no doubt.
I can't say for certain I'm an aspie/add/whatever, so I could be wrong. But just trying to get support and be taken seriously is horrendous. It's enough to make you ill even if you aren't. If anyone has any advice I'd be grateful, thanks.
[quote]...the mental health partnership involved to chase up the appointment (she made 2 months ago). Unfortunately there seems to be a huge waiting list for about a year. No tribunal is going to wait a year[/quote]
I tried explaining that (before contacting the mental heatlh ppl) that I could get to tribunal before I'm seen for a diagnosis and that if I fail the tribunal then that's it.
I don't think I did misunderstand, what you said above means that your assessment wait is affecting you getting benefits, therefore you need to write to them telling you that your tribunal is going to be severely impacted as you won't have a diagnosis by then, and therefore your benefits will be cut. Copy that to the tribunal people/DWP.
I still think you should spell out clearly in writing to your GP what the situation is and ask for her response in writing. Face-to-face is a lot harder and in writing you have proof and it's harder for them to ignore. You can always then complain to the practice manager or NHS PALS with copies of your written evidence.
Yes I understand you now. I suppose I could try, though I don't think it's going to make any difference. The person I spoke to was helpful adn they are trying to set up an assessment service closer to home, which is great. However this seems to be the problem. It's also not helped, I suspect, by NHS cuts and service changes.
As for the GP. I really don't know. I'm goign to see what the CAB has to say. I doubt they would, but if they could directly explain to the GP that would really help. I suspect they would pay more attention to them asking because of who they are, compared to me, as merely the patient.
I've complained to PALS before. Our practice manager, IMO, simply hasn't a clue. We are merged with another surgery and we are getting the rough end fo the stick IMO. I've had to see several different doctors over the years abotu this. They don't like that, I can tell, but I have no choice.
[quote]...the mental health partnership involved to chase up the appointment (she made 2 months ago). Unfortunately there seems to be a huge waiting list for about a year. No tribunal is going to wait a year[/quote]
I tried explaining that (before contacting the mental heatlh ppl) that I could get to tribunal before I'm seen for a diagnosis and that if I fail the tribunal then that's it.
I don't think I did misunderstand, what you said above means that your assessment wait is affecting you getting benefits, therefore you need to write to them telling you that your tribunal is going to be severely impacted as you won't have a diagnosis by then, and therefore your benefits will be cut. Copy that to the tribunal people/DWP.
I still think you should spell out clearly in writing to your GP what the situation is and ask for her response in writing. Face-to-face is a lot harder and in writing you have proof and it's harder for them to ignore. You can always then complain to the practice manager or NHS PALS with copies of your written evidence.
Yes I understand you now. I suppose I could try, though I don't think it's going to make any difference. The person I spoke to was helpful adn they are trying to set up an assessment service closer to home, which is great. However this seems to be the problem. It's also not helped, I suspect, by NHS cuts and service changes.
As for the GP. I really don't know. I'm goign to see what the CAB has to say. I doubt they would, but if they could directly explain to the GP that would really help. I suspect they would pay more attention to them asking because of who they are, compared to me, as merely the patient.
I've complained to PALS before. Our practice manager, IMO, simply hasn't a clue. We are merged with another surgery and we are getting the rough end fo the stick IMO. I've had to see several different doctors over the years abotu this. They don't like that, I can tell, but I have no choice.
