Ridiculous Atos HCP comments

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Re: Ridiculous Atos HCP comments

Postby sheppeyescapee » Wed Feb 15, 2012 8:42 pm

Sure! :lol:
J - 28,student,married to the lovely Em and live with 2 cats Bilbo and Pippin. Diagnosed with Aspergers, Dyspraxia, Dyslexia, EDS-HM, Mild Asthma, Chronic Pain, Chronic Fatigue, POTS, Syncope
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Re: Ridiculous Atos HCP comments

Postby Ldyalb » Wed Feb 22, 2012 4:30 pm

I also had 'How long have you had Hypermobility Syndrome for?'. She also asked me how long I'd had Dyspraxia for as well which is equally a stupid question.

But the best bit? At the end of the medical:

'Ok I need to check if you have a pulse now' :duh:

I'd been talking to her for 20 mins - I didn't drop dead at any point. Of course I had a pulse!!!

Amazingly I actually passed the medical and am in the WRAG. Still waiting on the DLA decision!
Dyspraxia - Dx Jan 2010, borderline ASD as well plus strong Dyscalculia overlap.

Fibromyalgia - Dx Jan 2011.

Hypermobility - Dx May 2011
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Re: Ridiculous Atos HCP comments

Postby trekster » Sat Feb 25, 2012 8:45 pm

good luck with the DLA application.
Alexis

Aspergers, Fibro, OCD, C-PTSD, insomnia, dyslexia, raynauds, mild carpel tunnel, gluten and dairy intolerance
part time wheelchair user.

HMS diagnosis 27/9/11

Feel free to PM me about adult autism social groups in the Bristol and Bath area.
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Re: Ridiculous Atos HCP comments

Postby zornna » Thu Mar 08, 2012 12:33 am

finaly got my report back so here's some more ridiculous comments :wall:

her hands and fingers can lock and grip can be affected as part of her condition. Overall she is unlikely to have any signifficant functional problems picking up and moving things

goes to the local shops alone, but is always accompanied, due to fear of falling and struggling and being left

can manage to cook, but aviods the use of hot pans due to problems with locking fingers
18 years of random falls, subluxes, and having many bendy party tricks was finally dignosed as having BJHS, still fighting for some help from GP, but after all this time I realise that I'm neither weird or alone :-)
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Re: Ridiculous Atos HCP comments

Postby roseyglow » Sat Mar 10, 2012 5:49 pm

:shock:

and these are the "Professionals" that make decisions that can ruin lives :(

Seems so very wrong, am dreading applying.
Ehlers Danlos Type 1/3, Erythromelalgia, Degenerative Discs, Peripheral neuropathy, Gastroparesis, Multiple Hernias and Prolapses but somehow still smiling x
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Re: Ridiculous Atos HCP comments

Postby barkingmad » Wed Mar 28, 2012 8:53 am

Oh my goodness.

We didnt have room in this newsletter but perhaps Hannah should use the best in a booklet with stickman pictures!

Like the others said ' These are health professionals!' I would have died if I had written some of the stuff on this thread! :(
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Re: Ridiculous Atos HCP comments

Postby shen » Wed Mar 28, 2012 5:34 pm

This isn't about me, but i do want to share what the ATOS wrote on my friends report.

He is an amputee and they wrote

'has no probelms using busses ..... when he gets on a bus, in order to remain comfortable, he has to take his stump off' :lol:
♬ ... If this is paradise ... ♬
♬ ... I wish I had a lawnmower ... ♬
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Re: Ridiculous Atos HCP comments

Postby sheppeyescapee » Wed Mar 28, 2012 8:48 pm

Lol :lol:
J - 28,student,married to the lovely Em and live with 2 cats Bilbo and Pippin. Diagnosed with Aspergers, Dyspraxia, Dyslexia, EDS-HM, Mild Asthma, Chronic Pain, Chronic Fatigue, POTS, Syncope
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Re: Ridiculous Atos HCP comments

Postby star gazer » Thu Mar 29, 2012 12:55 am

it really beggars belief. I'm sure a book of ridiculous coments could be written!
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Re: Ridiculous Atos HCP comments

Postby suew » Tue May 29, 2012 8:10 pm

when did I get Hypermobility syndrome ? cant remember when I caught it may have been at primary school !!!
no mobility issues - no muscle wastage , doc didnt mention severe calcaneal deviation at all or swelling so big couldnt do shoes up !
normal stairs - umm no live in a cottage with stairs so narrow and steep they dont comply with building regs, havent been up them for ages.
descibe a normal day - he replied that I said I dont go to work .....
needless to say I am challenging these points and more , including the fact that my name wasn't written on any pages of the report except the front , Im sure it wasn't even my report he sent in as I surely didnt recognise the person he was talking about. :D
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Re: Ridiculous Atos HCP comments

Postby mazza111 » Tue May 29, 2012 9:53 pm

Aww come on guys at least they mentioned your wobby bits in the report, even if they didn't quite get it :lol:

Which Stacey, no examination of knees and no mention of any hypermobile bits in the report.

She goes to the pub regularly <--- don't think she's been in a pub for about 2 years :liar:

She wore make up and had a clear complection --- errr, she wore no make up and was admitted to hospital soon after the medical for psoriasis treatment as she was covered from head to toe in it.

I'm looking forward to reading the reports on the wobbly bits if/when she gets the next medical :lol:
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Re: Ridiculous Atos HCP comments

Postby suew » Wed Jun 06, 2012 7:33 pm

:wall:
this one not directly from Atos but from complaints dept at disability and carers service , in reply to my complaint letter about reusal of dla and atos report

'the DM does not dispute that you have medical conditions that restrict you,however the available evidence does not demonstrate that your needs are severe enough to meet entitlement criteria'
hmmm :shock: so im ill but not quite ill enough! it seems not being able to walk isnt such a big deal after all !!
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Re: Ridiculous Atos HCP comments

Postby sirenmoonbee » Sun Jun 24, 2012 11:57 am

Due for my third assessment soon, I truly wonder what gems they will come up with next. This time i will be going in with a right femur that has been broken and rotated and fixed with plates and screws. Ave recovery is 18mths not a bendy though this can be much much longer as my bones never heal in the correct time frame.
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Re: Ridiculous Atos HCP comments

Postby cracker » Sun Jul 01, 2012 8:13 pm

roseyglow wrote::shock:

and these are the "Professionals" that make decisions that can ruin lives :(

Seems so very wrong, am dreading applying.

i agree with you hun. they can ruin lives & knock peoples conifedence. :wall:
some of the things they come out with is unbleliveable. :shock: :cussing:
i dread it when i get the dreaded brown envalope land on my doormat :shock:
Diagnosed with HMS July 2011. at age 31by my physio & HMS EDS3 & pots the 28 March 2013 age 32 by Prof Grahame.
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