I don't think they will, if it helps. Fingers crossed for you.I'm dreading Wednesday, what's the chances of these despicable twats reducing payments for those on ESA but not in the 'support group' to a rediculous £73 a week?
The overturn rate at tribunal is very high, and they appear very fair.well they say i have to go to tribunal there is no second chance
with phone interviews even if its there fault (i wont take that lying down) it
takes from
3-6 months to appeal ,paper work in the post.
nice to hear can`t understand why the dwp are being so vile and nastyThe overturn rate at tribunal is very high, and they appear very fair.
Because sadly many of the staff, not all- some are some good people trying to do their best still - have bought into the lies that people on benefits are scroungers, or are afraid for their own jobs.nice to hear can`t understand why the dwp are being so vile and nasty
it really starts to make me miss trust them, thank god for Violentpandas
e mail, i would really have lost heart, plus the support on here
You qualified for support group before - and from what you have said that hasn't changed. Please hold on to that.I'm dreading Wednesday, what's the chances of these despicable twats reducing payments for those on ESA but not in the 'support group' to a rediculous £73 a week?
please keep fighting. Wishing you strength xwell they say i have to go to tribunal there is no second chance
with phone interviews even if its there fault (i wont take that lying down) it
takes from
3-6 months to appeal ,paper work in the post.
well they say i have to go to tribunal there is no second chance
with phone interviews even if its there fault (i wont take that lying down) it
takes from
3-6 months to appeal ,paper work in the post.
Take them to your local job centre and get copies of the originals authorised (an office stamp & signature) , ask for a pre-paid envelope and post the copies off yourself - much better than depending on the internal post systemI can't remember whether I have to send original documents or not! And if I do will they send them back?
nice to hear can`t understand why the dwp are being so vile and nasty
it really starts to make me miss trust them, thank god for Violentpandas
e mail, i would really have lost heart, plus the support on here
nice to hear can`t understand why the dwp are being so vile and nasty
The DWP has probably asked your Dr about you and, seeing as they don't see you all of every day, want you to answer the question, instead of them doing it amd getting it very wrong indeed.just got a letter from Doctors asking to list my daily living
activitys and how my health affects me from atos but i am
going to tribunal ?
ViolentPanda? Come in please, when you've woken up again.atos sent the letter the day before the DWP had made there
decision I remember thinking thats odd, did not take any notice
but today got another letter from the doctors, prompting me to
reply i would ring atos but have very little phone credit its turning
into an agathar christe novel.
just got a letter from Doctors asking to list my daily living
activitys and how my health affects me from atos but i am
going to tribunal ?
A win for one is a win for all, as it can help to change case law.Great generosity of time and support here Urbz. Solidarity.
Thanks both. I've calmed down a bit now. My cortisol levels must have gone through the roof, I'll pay for that later eh ViolentPanda? I've try to stay clear of the DWP because any contact with them enrages me so much.
I've never appealed my WRAG decision because I thought that they might stick me on JSA and my last DLA award has lapsed because I was too ill to handle filling out another form. DWP win win eh? Cunts.
My claim is not about the money, we're used to not having any. I just want them to leave me alone especially now as we're engaged in a major battle with Children's Services over their lack of support regarding a two year old that we've given a home to under a Special Guardianship Order. I just can't fight on too many fronts.
I've got a letter from the Rheumatologist confirming my diagnosis for the diseases outlined above and a letter from the Podiatrist confirming that I have an inoperable broken Navicular in my left foot, an old tree surgery injury which makes walking incredibly painful. My left hand, I'm left-handed, is fucked through arthritis and so writing is nigh on impossible and I've had an arthroscopy on my right knee though both my knees are fucked. I've got arthritis in both hands and all my major joints are riddled with it really.
I can't get any pain relief because I've got Stevens-Johnson Syndrome and I'm allergic to NSAIDs. Co-Codamol in the quantity that I'd need to take gives me constipation.(Too much information.)
Any part of my body that isn't suffering with arthritis is generally useless due to the ME and if that isn't affecting me then the Fibromyalgia gets the rest. Tbh it's impossible for me to tell where one condition stops and the next starts. Then there's the depression, symptomatic and inherent in the diseases, constant exhaustion, lack of sleep, memory lapses and problems with vision, hearing and concentration.
Should I be/am I likely to be put in the Support Group? I seriously doubt it, these are all somatic manifestations so far as the DWP are concerned aren't they? I reckon we're fucked and we'll have problems paying the rent soon let alone anything else. Angry? You bet your fucking life I'm angry.