Help I was on DLA had interview with ... - Fibromyalgia Acti...

Fibromyalgia Action UK

59,987 members67,154 posts

Help I was on DLA had interview with atos and placed on ESA with not having to sign on or support to go to work

Fedupman profile image
13 Replies

I've now recieved another booklet to fill in for limited cspabillity to work its only been a few months since I was last at a face to face with atos is this normal

Written by
Fedupman profile image
Fedupman
To view profiles and participate in discussions please or .
13 Replies
linlit profile image
linlit

what group were you placed in wrag or support group

lin

Fedupman profile image
Fedupman in reply tolinlit

Support group in march now recieved this form to see if I qualify for ESA I'm confused I already get Esa

linlit profile image
linlit in reply toFedupman

phone dwp to find out what is going on

lin

ausalison profile image
ausalison in reply toFedupman

Same here. I am in the Support Group and have now received ESA form to complete by end of January 2014. I am confused but will contact DWP. You are not alone :D

Royalspec01 profile image
Royalspec01 in reply toFedupman

the first thing id do is ring them and explain to them that you have just been assessed and have been put into support group and in receipt of their payment,...as this could be some breakdown in their internal communications. try not to worry to much as it could be that simple, as far as im aware the support group allows you two years before your next medical. If you have a negative response then seek advice from CAB HOPE THIS HELPS

MrsP-C profile image
MrsP-C

Hi FedUpMan! (love it!). I'm afraid to say this is the system! I have received Incapacity Benefit (or whatever they want to call it now) for the past 6 years. The system dictates that they send out a new form every 8-10 months for you to complete and return to enable your benefit to remain unchanged. This, I know, is really stressful and painful (especially if your Fibro is in your hands) but "its the system". My advice is to be totally honest when completing your form. Do not be an optimist (like me). Don't put "sometimes" on the form. If it happens to you even once then put it down. Take a copy of your form before you post it off so that you have the details to refresh your memory when your next form comes. My last form had to be submitted last September (only 8 months since my previous form) and, as yet, I have not had a decision! When I called DWP they told me that Atos had an "uncontrollable backlog and would be getting to me when they can!". I joked with the lady that I'll probably receive my next form before my previous one has even been looked at! Although, looked at is an understatement. I believe they must glance at the check boxes and see if it fits their criteria. I can tell you that they do not read through the paragraphs you write them in further details or explanations as I have been testing this myself over the past few years. My last form stated I was considering suicide (I would never - that's the optimist in me again). They don't care, they're not medically trained, they are a "call centre" for the Government. I find it extremely frustrating that we are entitled to our benefit but still get stressed out filling in the form because you feel like a fraud. Please remember the actual fraudsters don't give it a second thought, they know exactly what to put on their forms to cheat the system. Just clearly state your condition, give your symptoms, your medications and the impact it has upon your life. No-one who experiences Fibro would wish it upon anyone else as it's such a debilitating illness which has very little research done for it and so can feel hopeless. You're not alone. Most importantly of all, it's not all in your head!! If you told someone you had MS you'd get understanding and support. The symptoms can be extremely similar but because its a new(isn) condition everyone thinks you're just swinging the lead. You are not. If you've paid into the system during your life then you are entitled to look for support when you are unable to function properly. Good luck. Keep me posted?

bobchewie profile image
bobchewie

Isn't the DWP doing the assessing noe by using google.

Libbyloo2005 profile image
Libbyloo2005

Hi,

I was put in support group in May & received another form to fill in before Christmas. I called the DWP to ask why and was told its the new system with everybody's claim being reviewed every 3 months - 3 years! I could understand it if I was in WRAG group but not support group. I haven't miraculously improved since May! Ridiculous!

mufos profile image
mufos

Hi, it seems nothing is normal, i think they just pull a few names out the hat every day, and pester them, they gave me a real hard time last year , and like a lot of people i had to appeal, it was so stressful, they keep asking more and more from me, i simply didnt know what to put and how to put it, surly just being on Morphne should tell them somthing. Any way at the moment i am waiting for an apointment, they said they would pay for a taxi, back in october last year, when all i wanted was a home visit, as traveling is is painful for me, But i am still waiting to here from them, and to be honset the longer they take the better, i get so upset by it, as do many of you , i know. So just fill it in again and send it back, you never know you might not get pulled out the hat again for a while , good luck any way, and dont let them wear you down. Regards Mufos

esagestapo profile image
esagestapo

Atos does not work to any set pattern, they can send out review forms any time they like. Follow the advice given here and keep a copy for reference because you will be filling out these forms for as long as you are claiming ESA.

Mdaisy profile image
Mdaisy

Hello Fedupman,

If you would like some information that may help you complete your ESA50 application, please email me info@fibroaction.org. I would be happy to help :)

healthunlocked.com/fibroact...

I look forward to your email

Best Wishes

Emma :)

FibroAction Administrator

lumely profile image
lumely

Have you being officially diagnose with FMS, if yes try to see your Dr and ask weather he/she can explain how you are affected every day to day, if not ask your Dr for an official diagnosis But guess what Atos are very crafty, try not to do every thing they ask you to do , because they will turn round saying that you can manage. As far as any move or day to day activity you do curse you pain to me thats' not a normal life.Try to ask for help with filling the forms. good Luck.

Kirby profile image
Kirby

Hi Fedupman

You can be reassessed from anything between 3 months to 3 years. This is how the DWP operate now. The best thing to do once you fill out a form once is to photocopy it for the next time so it won't be such a chore.

Best wishes

Not what you're looking for?

You may also like...

Help with DLA, ESA, ATOS and appeals please?

Please can someone help me? I am getting into a right mess with all of these forms and I really...
helen01 profile image

atos interview said i will go to support group

Hi does anyone know what this means please, i went to the ATOS interview and they said i will go...
sharron1 profile image

ESA stopped because I was too ill to go to the Atos medical :( what should I do next?

Hi Everyone, In November I recieved an appointment for an Atos work capability medical...

not been on for a bit, but oh my God. i need to let all this out or i will self combust! i have had fibro for many years, along with

arthritis and 2 heart conditions (neither one very serious).my daughter is supposed to be my carer,...
mimsysmum profile image

I went to the esa medical assessment on they 7 the march 2017 will I pass the esa and go go in the support group

I went to the esa medical assessment on they 7 the march 2017 will I go in the support group and...