Esa assessment.

[Littlemole43]

I have my assessment on the 21st December I really don't know what to expect as I didn't have one for my pip . I have read other peoples posts and I'm quite concerned because there is no way I can possibly work . my crps is getting worse just when it is as bad as it's ever been the pain escalates even more . I'm in remission from skin cancer and suffer from lymphedema from the result of having lymph nodes removed . I suppose I'm looking for some reassurance .

[RAYJAYC]

Hi

Rather than repeating myself; take a look at the PIP Claim/assessment post next to yours. The same applies for an ESA assessment! Different questions but fundamentally the same....

Good luck..

RJC

[Littlemole43 in reply to RAYJAYC]

Thankyou was helpful

[Bananas5]

Is this a reassessment? Meaning you have had one before? Or is this your first time?

Quite important as DWP have changed their rules.

x

[Littlemole43 in reply to Bananas5]

It's my first

[Cb1963]

hi littlemole,43,now i know the ESA medical can be daunting for you,but if your receiving pip that should stand you in good stead if your receiving pip already,I suppose firstly if your in the work related group this might mean the dwp are seeing if your fit to work which probably mean you go onto JSA,however if your already in the supported group this medical should really be just a informal discussion on how your day to day activities (or lack of them in your case) affect you,and being in remission,will count for you,but try to get an outside source of help to guide you through the DWP criteria as if you make a simple mistake it could be your undoing of your claim,your local council should have a help/advice centre,which sometimes baffles me as they are ultimately funded by local government fighting against our government,so take your time over the next two weeks,have a plan of attack,don't get in a panic,and hopefully you'll get the correct and proper decision,but definitely get some support otherwise you'll just worry,and its nice to have some help when your head feels like its going to explode with the constant bombardment of letters,so be calm and best wishes

[Littlemole43 in reply to Cb1963]

Omg I wouldn't know where to start , I can't go out on my own so how or where would I begin, it sounds ridiculous I know but the only time I can get out is Sunday which is my husband's only day off, my sister in-law comes up on a Saturday if she isn't busy but unfortunately she seems to be busy every week lately. I sound like a fumbling fool now don't I , any suggestions anyone ? All idea's gratefully received. . ⏳

[RAYJAYC in reply to Littlemole43]

You can request a home visit if you're never able to leave your home.

[Mina786]

Hi. If you passed PIP I wouldn'tsay the ESA would be any harder. Many like myself with chronic pain and long term health conditions have passed Esa and not PIP . However , to help your case . I would suggest most definitely getting in touch with a local welfare rights officer . Either in local authority or Citizens advice . I'm pretty sure they can come with you. Also send any letters from GP/ specialist/ anyone who helps you, in addition to proof of treatments for supporting evidence .

Welfare rights officer would be able to break it down for you in terms of points and also draft a letter for you.

Amend the PIP evidence you sent so yu don't have much work.

Hopefully you will pass. As it's all in black in white , with factual evidence of your health conditions .

Don't give up what your entitled to.

Good luck xx

[De33]

Hi, I went for my assessment and I don't want to frighten you, but it was not good! The assessment itself is ok, however be aware they assess you from entering the building. Every step is counted, how you speak, what you say, all has an impact. I have three consultants all saying I was not fit to work and yet the assessment scored me 0 points and stopped benefit, which was ESA. The report stated I was articulate and didn't show signs of mental health etc. I live with chronic pain which effects my daily life and have to take all the strong meds to get me out of my bed... there was no mention of the amount of medication I take to get me on my feet etc. I feel that if I presented myself dirty and not properly clothed and spoke slang would I have been given credit! The system is so wrong and not fair to people who have worked hard all their lives but have a very unfortunate illness that is not visible to the eye!

[Littlemole43 in reply to De33]

Don't worry you haven't scared me mine is visible it's bad I can't walk far , I use a walking stick and if I'm taken out I'm have to be in a wheelchair . I'm already receiving pip and didn't have an assessment for that . I had an appointment with a pain specialist at the rivers private hospital and will be having treatment in jan/Feb. I will be having injections all the way along my main nerve line from my back along my hip and down my leg .I'm not scared just didn't know what to expect , thank you for the information .