Showing posts with label myalgic encephalomyelitis. Show all posts
Showing posts with label myalgic encephalomyelitis. Show all posts

Monday, 7 August 2017

Library

This is a library of information and files about the British benefit system. They are specifically aimed to help people with Myalgic Encephalomyelitis, Fibromyalgia, Post Viral Syndrome, and similar conditions, but anyone can access them.

Currently the focus is on Employment & Support Allowance, but Personal Independance Payment and Universal Credit information will be added and adapted as and when it becomes appropriate.

For those who do have the conditions these files and posts are aimed at, you can join our Facebook group for additional help.

We have experience with these forms, and are very happy to offer you advice. We also have a Helper System, whereby we can either check over your forms before you send them off, or help you to fill them in.

Because we specifically wish the group to remain on topic, we also have a social group where we can share woes and jokes:
(Note, it is not a dating group).

As documents and posts are added to the site, links to each one will be added below:


ESA:

- What is ESA? Explains ESA, Contributions Based ESA, Income Related ESA, Work Related Activity Group, Support Group, payment rates, and outlines the process of application.
- ESA50 Download tthe ESA50 (the long questionnaire) as a PDF
- Filling in the ESA50 A helping guide to completing the ESA application form. 
- ESA50 Example Answers for M.E. & FM This post goes through each question, suggesting M.E. and Fibro specific answers. You should hopefully be able to find answers that meet your circumstances here. 
- ESA Descriptors. Descriptors are used to score your application for ESA. 
- 3 Ways into the Support Group & the ESA Suport Group Descriptors. Meeting any one of these will place you in the Support Group. 
- Special Circumstances Explains in simple terms how you may be exempt from filling in the ESA50 and / or having to do the medical assessment (work related activity assessment)
- Regulations 29 & 35 This is the legislation to use if you should be exempt from filling in the ESA50 and / or having to do the medical assessment (work related activity assessment).
- The Physical / Mental Dilema Explains how physical and mental health symptoms are taken into consideration.
- I Can But I Can't Explains how to fill in the form for tasks that you can sometimes, but not always, do.
- Aids & Appliances Talks about how Decision Makers can assume the use of aids and appliances you do not own.
- Supporting Evidence Talks about how a decision is made, the different types of evidence, and discusses how to write supporting letters. 
- Assessment Centres Check that you will be able to cope with the centre you've been assigned.
- What to expect from the Work Capability Assessment If you're looking for the part about home medicals, it's right at the end.
- Questions You May be Asked A post copied from dwpexamination outlining the type of questions you may be asked, and how to understand them, in the Work Capability Assessment.
- Work Capability Assessment Centres A list of UK centres. 
- Work Capability Assessment List of Questions The list of questions you may be asked in the WCA and how to answer them. 
- Challenging a Decision. Describes what to do if you don't agree with a decision. Use the GL24 to Request a Reconsideration of to Appeal, for ESA, or DLA. 
- Work Related Activity - Explains what the Work Related Activity Group is, and gives ideas as to what you can do.
- Sanctions Explained What are "sanctions"? When are they applied? How much will I lose?
- Tidbits of ESA Advice Anything extra that doesn't fit in the other posts.
-
Document for requesting reconsideration Description's in the title ;)

Other Material:

- Work Capability Assessment described by Joyce Drummond Joyce Drummond is a nurse who worked for Atos performing assessments for ESA.
- SYMPTOM SECTION of the International Consensus Criteria for M.E. Useful to help fill in the ESA50
- International Consensus Criteria for M.E. Useful to include as supporting evidence if you have an official diagnosis. 
- Canadian Consensus Criteria for M.E. The symptom section, plus a download of the whole available. 
- 'About your illness and disability' example answer How I answered this section of the ESA50
- Why you need to save information you find Explains why it's important to save information you find that could help with your claims
- GL24 Word Version (Use this to request a reconsideration or appeal of ESA or DLA).
- GL24 PDF Version (Use this to request a reconsideration or appeal of ESA or DLA).
- Request for Reconsideration Example The document shows you the format I used to make a reconsideration request after I was turned down for DLA.


Monday, 7 October 2013

Filling in the ESA50

When you apply for ESA you will eventually be sent the ESA50 form (unless you fall under the special circumstances). Most people find the ESA50's arrival very stressful. The fact that it has a time limit on returning it, makes it even worse. Most conditions only require someone to fill in a few sections on the form, but people with M.E. have something to enter in many sections, which is one of the reasons we tend to need more help.

Having help through the process makes it a lot less stressful. Make sure you pick the right person to help you though. A friend of family member is probably not the right person, unless they understand how the DWP operates and what a Decision Maker will be looking for. There are a number of organisations who may be able to help you. A few such organisations include:
  • The Citizens Advice Bureau
  • DIAL
  • Mind - The Mental Health Charity
  • the Civil Legal Aid Agency

You can also join our group on Facebook. We've helped a number of people who have M.E. with their ESA50 forms. We offer help filling in the form to people with M.E. and similar conditions, and will check through your form when you have filled it in to look for anything obvious that might go against you.

I suggest going through the guide below first, as it is exactly what I'll be suggesting on the group. If you find it helps, a comment is always appreciated.


One of the most important parts of your ESA application is the supporting evidence. So, my advise is that when you start considering applying for ESA, you actually put in place as much supporting evidence as you can first.

Once you have the form, don't let it panic you. Panic and stress affect your cognitive abilities, so deep breaths. You will have been given four weeks to return it. It essentially has 20 sections. So, theoretically you can take it one section a day, and still return it in time. The wa8 days spaced apart) without too much stress.

I recommend completing the form on a computer, so that you can amend any errors. If you choose, you can complete the actual form they sent you by hand afterwards.

I have three rules:
  1. Don't be afraid to be totally honest. Most people, particularly people with M.E., have either got so used to playing down the things they suffer from, or have been ill for so long that they've forgotten what normal was, that it can become quite emotional to fill in this form.
  2. Give yourself breaks, in which you reward yourself somehow. Letting this process make your health worse is a big no no.
  3. Start the working on the form as soon as you get it. The longer you leave it, the more stressful it becomes.

First Session

1) Fill in:
  • your personal details.
  • if you do not want the DWP to phone you do not put your phone numbers on the form. (Personally I advise leaving it off).
  • any dates you cannot make an appointment.
  • the details for your doctors, and specialists. Your doctors surgery should be able to provide you with details of specialists if you're uncertain of them. If you've more than one specialist (most people with M.E. do), add the information of the other specialists on another page.
  • at the back of the form on page 10 fill in any details about any cancer treatment you're receiving.

2) At the end of page 3 there is a box which asks if there is any help you need for the face to face assessment. Unless anything obvious springs immediately to mind, scroll past this for now. It is usually easiest to fill this in as you go through the other questions; they tend to stimulate ideas. We will come back to it later anyway.

3) Also scoot past the big box on page 5 asking about your illness or disabilities.

4) Completing the section about your medication shouldn't be a problem. Remember to include anything you take regularly that is not prescribed by your GP (vitamins, minerals, herbal remedies, etc).

5) Completing the section about hospital, clinic or special treatment, also should not be a problem. Treat it as a table, for example:
Counselling with MIND - for severe anxiety and PTSD - one hour - every two weeks
Physiotherapy (Solihull Hospital) -
for the problems with my hypermobility - 40 minutes - once a week
Osteopathy (Burntwood Osteopathic Clinic) -
for back pain - half hour - as needed

Include any up coming appointments you have that could lead to further treatment. For example:
I'm awaiting appointments with the balance clinic, and a date for an MRI of my head and spine.

6) If any of your problems are due to drugs, alcohol, or other substances, do fill that section in. Don't be mistaken though, this section is referring to MISUSE only. Side effects from medications your GP or specialists have given you, do not go in this section.

 

Second Session

We're going to go through all the questions in the Physical Functions section. That isn't as scary as it sounds. We're looking at the text boxes that accompany each question.

Before embarking on this task you need to decide whether you are going to fill in the form according to your average days, or your worst days. Personally I recommend filling it in according to your worst days. We will cover this better later, but you need to make the decision in order to know how you're going to answer these questions.

What I'm going to instruct you to do is described more fully in this blog post.

For each question, consider these things carefully:
  • severe discomfort.
  • pain.
  • breathlessness.
  • extreme fatigue.
  • repeatability.
  • reliability.
  • safety.
If you can do the activity, does it cause you discomfort, or severe discomfort?
If you can do the activity, does it cause you pain?
If you can do the activity, does it make you breathless?
If you can do the activity, does it cause you fatigue or extreme fatigue?

If you can do the activity, how often / soon can you repeat it?
If you can do the activity, can you do it to a reliable level?
If you can do the activity, can you do it safely?


Some examples of how to use the above points:
  • I cannot walk 50 metres repeatedly or safely, without undue discomfort, pain, and extreme fatigue.
  • I cannot remain stationary, standing in one place, for more than 40 seconds, without severe discomfort, pain, and extreme fatigue, reliably, repeatedly, or safely, due to Postural Tachycardia Syndrome.
  • At times I can raise both arms, but most often it is with severe discomfort and pain, often causing extreme fatigue. I cannot ever raise both arms repeatedly, or reliably.

Third Session

Now we'll go back through those questions, one by one, and see if we can add any more personalising information to each question. If you have a recent example you can use, it can help to use that too. Don't feel you are restricted to my guidelines; if something occurs to you that is outside my suggestions, do make note of it.

Try and keep it all concise; remember, the Decision Maker has less than half an hour to look through your case.

1. Moving around and using steps
State whether:
  • you use a wheelchair, or walking aid.
  • you have any physical problems with your hips, legs, knees, ankles, or feet.
  • you suffer from pain or discomfort in your legs.
  • you know why you suffer from that pain or discomfort.
  • you have problems with walking, for example, you stumble or fall, or have balance problems.
The answer from my form:
"I use a wheelchair for long outings, and a walking stick for shorter walks. I have Hypermobility that affects my hips and knees with a lot of pain. Fibromyalgia and sciatica also cause pain in my leg muscles. I can never walk any distance without significant pain and discomfort. I suffer ticks that cause me to stumble and fall, sometimes as frequently as once a minute (I'm soon having an MRI to pinpoint the cause of these ticks)."


1. Going up or down two steps
State whether:
  • you use a wheelchair, or walking aid.
  • you have any physical problems with your hips, legs, knees, ankles, or feet.
  • you suffer from pain or discomfort in your legs.
  • you know why you suffer from that pain or discomfort.
  • you have problems with walking, for example, you stumble or fall, or have balance problems.
Yep, I'm asking you to repeat things. (The more a Decision Maker sees it, the more likely it is to sink in).

My example:
"When I use a wheelchair I cannot use steps or stairs at all. When I walk with the stick I also need a banister to help me use steps. I have hypermobility that affects my knees, making it very painful for me to use steps. In my home I usually crawl slowly up stairs, and come down slowly on my bottom, because of the risk of me falling. My most recent fall down the stairs was three weeks ago. I have an appointment with an Occupational Health Therapist whom I'm hoping will be able to provide me with some aids."


2. Standing and Sitting
State whether:
  • you use a wheelchair, or aid for remaining in a stationary position.
  • you have any physical problems with your hips, legs, knees, ankles, feet, or lower back - even your arms if relevant.
  • you suffer from pain or discomfort in your legs or lower back.
  • you know why you suffer from that pain or discomfort.
My example:
"I suffer discomfort remaining in a stationary position, which at times can cause me to pass out (I recently passed out in the post office queue) I can never remain standing in a stationary position for more than 30 seconds without experiencing this discomfort. The stick I walk with has a seat on it, so that I can avoid standing in queues. (I am waiting for an appointment at the Balance Clinic to test whether I have Postural Tachycardia Syndrome). This problem also means I need to have my feet raised when sitting, though I can sit for a few minutes being affected.

I also suffer with lower back pain (you have an MRI from 2002 showing a disc bulge and arthritis around L4 and L5). This again causes problems with standing, but it also causes problems with sitting; I need to shift my seated position every 15 minutes due to severe pain."



3. Reaching
State whether:
  • you use any aids for reaching.
  • you have any physical adaptations for reaching.
  • reaching can cause you discomfort or pain.
  • you know why you suffer from that pain or discomfort.

Consider both reaching out in front of you, and reaching up above you.

My example:
"I have two problems raising my arms. The probable Postural Tachycardia Syndrome causes me to become light headed when I raise either arm. Upper back pain and neck pain, caused by my back problems, are exacerbated by extreme movement of my arms."


4. Picking up and moving things
State whether:
  • you have problems holding your arms up to the sides.
  • you have problems with coordination.
  • having problems with reaching affects your ability to pick up and move things.
  • you are limited in the amount of weight you can lift.
  • why you suffer that limitation, if you know why.
My example:
"I would struggle to lift both arms to lift the box in the example, because of the probably Postural Tachycardia Syndrome causing me to become light headed when I raise either arm. On my very worst days extreme fatigue affects my ability to lift objects."


5 Manual Dexterity (using your hands)
State whether:
  • you have any physical problems with your hands and/or fingers.
  • you suffer from pain or discomfort in your hands and/or fingers.
  • you know why you suffer from that pain or discomfort.
My example:
"Due to Fibromyalgia I suffer agonising pain in my fingers and hands, approximately one in four days, therefore have problems pressing buttons, picking up objects, typing, using a computer mouse. I have Carpel Tunnel Syndrome in both hands which causes shooting pains in my hands. The injection to treat Carpel Tunnel has cause further problems when any pressure is placed on the thumb of my right hand."


6. Communicating with people
State whether:
  • you have difficulties with speech.
  • you have difficulties holding a pen, or writing.
  • you have difficulties typing on a keyboard.
  • you know what causes those difficulties.
  • you have cognitive difficulties that affect your ability to construct sentences.
My example:
"Fatigue often causes my words to become confused and muddled up, and my speech to be slurred. This causes problems with conveying messages. People often assume I'm drunk."


7. Other people communicating with you
State whether:
  • you have a problem hearing.
  • why you have that problem, if you know.
  • you have a problem with your sight that affects your ability to lipread (if you've a problem with hearing).
  • you have problems reading.
  • you have a cognitive problem that affects your ability to understand people.
My example:
"I suffer from constant tinnitus that fluctuates in volume depending upon how fatigued I am. Fatigue affects my ability to follow conversation. I also suffer a lot of sensitivity to sound that causes significant headaches, as I wear earplugs - which of course then means I cannot hear people speaking at a normal volume."


8. Getting around safely
State whether:
  • you have a problem with your sight.
  • you have a guide dog, or need a person to guide you.
  • you wear glasses or use contact lenses.
  • you have a cognitive problem that affects how you understand what you see.
I don't have a personal example for this, but for the sake of argument:
"I have tunnel vision which affects my ability to judge what is happening in my surroundings. This causes me problems with tasks such as crossing the road, and means that I cannot drive."


9. Controlling your bowels and bladder and using a collective device
State whether:
  • you suffer urinary incontinence during the day.
  • you suffer urinary incontinence during the night.
  • you suffer fecal incontinence during the day.
  • you suffer fecal incontinence during the night.
  • you use incontinence pads or something similar.
  • you use a collecting device.
  • you have problems getting to the bathroom in time at night.
  • you have a colostomy, an ileostomy, or a urostomy.
  • you have problems getting to the bathroom in time at all.
  • you have to discard clothing because of these problems.
  • the frequency with which you need to discard clothing.
I also suggest:
  • you suffer with irregular heavy periods.
My example:
"I suffer IBS. During the loose stool phase I often have accidents. During the constipation phase I use Movicol, which causes extremely loose stool, and again, I often have accidents. I also suffer with very irregular heavy periods, which make a big mess when they arrive; I'm usually unaware that it has happened until someone brings my attention to stains on my clothing. I usually need to discard at least one pair of underwear per month."

What they're actually looking for in this one is whether you need to discard clothing due to the severity of the incontinence (hence my suggestion of periods).


10. Staying conscious when awake
(This is where you explain about brain fog).
State whether:
  • you pass out.
  • you black out.
  • you have fits.
  • you suffer Diabetic hypos.
  • you remain conscious but lose awareness.
  • you fall asleep unpredictably.
  • you know what causes the above.
  • you know how regular these are.
  • you suffer from brain fog (cognitive dysfunction) - and describe it if you do, as it isn't a particularly well recognised or understood symptom.
My example:
"Due to probably Postural Tachycardia Syndrome I pass out any time I have to remain standing in a stationary position. This also happens when sitting without my legs raised, though is less frequent. I have severe anxiety attacks, during which I lose awareness, often regaining awareness in unusual places and covered in self inflicted wounds. The severe fatigue caused by M.E. affects my ability to think and function to a degree that I am completely unsafe to be left alone."

Fourth Session

Now that you've filled in the text boxes for the first set of questions it should be fairly quick and easy to go through the tick boxes without dilemma over what the right answers are for you. Don't over estimate your abilities, but make sure any negative answers are explained in text.

Try to avoid ticking "it varies". I have been informed, though how reliable the source was I'm unsure, that ticking "it varies" automatically scores you zero for that section. If you're filling in the text sections as per your worst day, remember to tick the boxes in conjunction with your worst days also.

 

Fifth Session

We're now going to do pretty much the same for the Mental, cognitive and intellectual functions section, first looking at the text boxes that accompany each question first.

For each question, consider these things carefully:
  • variability
  • repeatability.
  • reliability.
  • safety.
  • severe discomfort.
  • pain.
  • breathlessness.
  • extreme fatigue.
If you can do the activity, does your ability to do it vary.
If you can do the activity, how often / soon can you repeat it?
If you can do the activity, can you do it to a reliable level?
If you can do the activity, can you do it safely?

If you can do the activity, does it cause you discomfort, or severe discomfort?
If you can do the activity, does it cause you pain?
If you can do the activity, does it make you breathless?
If you can do the activity, does it cause you fatigue or extreme fatigue?

Some examples of how to use the above points:
  • I can not repeatedly learn how to do tasks, due to extreme cognitive fatigue.
  • I can not reliably finish tasks I start, due to extreme fatigue.
  • I can not cope reliably or repeatedly cope with varying types of change.
  • I can reliably or repeatedly behave appropriately with other people. Social interaction causes me severe fatigue.

Sixth Session

Now we'll go back through those questions, one by one, and see if we can add any more personal information to each question. If you have a recent example you can use, it can help to use that too. Don't feel you are restricted to my guidelines; if something occurs to you that is outside my suggestions, do make note of it.

11. Learning how to do tasks
State whether:
  • you are dyslexic (People with M.E. often suffer with 'acquired dyslexia').
  • you suffer from another learning difficulty.
  • your learning abilities are affected by fatigue.
  • your memory affects your ability to learn new tasks.
  • your ability to learn tasks varies depending upon the task.
My example:
"I have problems learning new tasks because of my memory. With simple tasks, I usually cannot remember how to do them when I have to try doing them for myself. With more complex tasks, by the time I am several steps into learning the task I cannot remember how it started."


12. Awareness of hazards or danger

State whether:
  • you have sensory problems that may affect this.
  • you have a problem that affects your coordination.
  • you suffer from loss of awareness at times.
  • you experience variations in your perception that may affect this.
  • your levels of fatigue may affect this.
  • your awareness of hazards or danger varies.
My example:
"Hypermobility affects my coordination, often leading me to bump into things without realising I'm going to. When I have anxiety attacks (two or three times a week) I lose awareness, regaining awareness in unfamiliar places. My awareness of hazards and danger vary according to how fatigued I am."


13. Starting and finish tasks
State whether:
  • you frequently fail to finish tasks you start.
  • you have sensory, cognitive, or learning problems that affect your ability to focus.
  • you don't take care of your personal hygiene as often as expected.
  • your ability to start and finish tasks varies.
  • you know the reason for the above.
Part of my example:
"I frequently fail to take care of my personal hygiene. For example, I usually shower once a week. I am unable to climb into a bath because of my lower back problems, but cannot stand in the shower because the probable Postural Tachycardia Syndrome. As such I have to sit down to shower. Washing my hair is a trail due to the issues I have raising my arms. I have problems with the water hitting me, because my skin is very sensitive, so I usually have a headache after a shower. Plus it's very exhausting, so I usually have to go back to bed after showering."


14. Coping with changes
State whether:
  • you can't cope with small changes.
  • you can't cope with big changes.
  • there is a reason for the difference in your coping abilities.
  • if change causes you significant stress.
  • your ability to cope with change varies.
My example:
"I can cope with changes to official appointments, provided I have some warning, for example if a counselling or doctors appointment is changed a few days in advance. I have to rest a lot for any appointment though, so if it's cancelled a few hours or minutes beforehand I find it very distressing. I cope a less with social changes. Again, I have to rest and prepare a lot in order to engage in social engagement, a lot more so than for a doctor's appointment. As such, if such an event is cancelled it can cause me to become more depressed for a long time. I cannot cope with sudden change at all; for example, unsolicited phone calls or someone knocking on the front door. Such events are likely to cause a panic attack, due to issues related to my PTSD.

I was recently supposed to have an appointment with my fatigue specialist. When we arrived we had been logged in to see the wrong doctor by accident. This lead to me crying in the appointment. The panic attack kicked in in the car on the way home. I was then exhausted for 10 days afterwards."



15. Going out
State whether:
  • you can cope with going out.
  • you need to rest or prepare to go out.
  • using any aids or appliances to go out has an emotional impact on you.
  • you need someone with you in order to go out.
  • your ability to cope with going out varies.
My example:
"Issues with PTSD mean that I cannot go out alone to somewhere I am not familiar with. I can cope with trips to places like the doctor's surgery, because I know there is someone I know at the other end who will make me feel safe. Going out in general causes high levels of anxiety, which in turns causes me severe fatigue."


16. Coping with social situations
State whether:
  • you suffer from social phobia or agoraphobia.
  • you can cope with meeting friends.
  • you can cope with meeting strangers.
  • you can cope with an official venue (ie, doctor's surgery or hospital).
  • you can cope with visiting a friends house.
  • you can cope with socialising in your own home.
  • you can cope with strangers being in your own home.
  • you can cope with officials being in your home.
  • any neurological or cognitive problems you have that affect your social interaction abilities.
  • any specific issues you have with social situations.
  • if your ability to cope with social situations varies.
  • you have any form of authority complex.
My example:
"Leaving the house makes me very anxious. I very much enjoy social activities when friends visit me, but visiting people elsewhere is a problem. Specifically, I become claustrophobic in crowds. I struggle with certain types of noise, needing to wear earplugs to cope. My partner recently took me to a bowling alley; I was already very anxious, but the noise in the place caused me a panic attack - when I regained awareness I was sitting on a pavement in an unknown location."


17. Behaving appropriately
State whether:
  • you have a behavioural problem that affects your behaviour towards other people.
  • people often misunderstand what you say.
  • you avoid social situations because of people not understanding you.
My example:
"When I'm fatigued I become impatient and snap at people. When I'm not fatigued people still frequently become upset with the way in which I communicate. I do not know why, but this problem is all the time."



18. Eating and drinking
State whether:
  • you need someone to cut up your food.
  • you need food liquidised.
  • you need someone to place food in your mouth.
  • you need someone to manoeuvre drinks to your mouth.
  • you take nourishment via a tube.
  • you having difficulty eating for any reason.
  • you particularly dislike eating.
  • you have an eating disorder.
  • you purge.
My example:
"With a Fibro flare my hands are in so much pain that my partner has to cut my food for me. With an M.E. relapse all glands become swollen, and my throat very sore, which makes swallowing food difficult."
 

Seventh Session

Now we'll return to the section on Page 5: 'About your illnesses or disabilities'. Having gone through all the other questions you are now probably a lot more aware of the symptoms attributed to your various conditions than you were at the beginning of this procedure.

I tend to over populate this area, so only include what you feel is necessary and appropriate. You can find my version of this answer here. The reason I have put this personal information here is that it can hopefully inspire you to remember symptoms that you may have forgotten or wouldn't have thought to include.

It was very hard to admit to many of the things in that document when I first wrote it. The way I persuaded myself to face reality is by understanding that no one who mattered to me would see it (until I put it online anyway). There is no shame in suffering the things we suffer. We didn't choose to be ill. So take a deep breath and be honest with yourself.

If you do find this section particularly traumatic, come join the group and I'll hold your cyber-hand with your while you complete it.

Anyway, I approach this section with five sections:

1) In the first section I list the conditions with which I suffer. Beneath these I bullet point the symptoms each condition causes, and then bullet points further information such as any aids or appliances I use, methods I use to cope with the condition, and how it may have affected me. (This is what the DWP are seeking).

2) Describes what my life was like before I was ill, and how different it is now. (The DWP does not ask this of you).

3) Describes what good days and bad days, and the approximate ratio of each. (The DWP does not ask for this, but it's important for fluctuating conditions).

4) State which type of day I am describing throughout my form. (The DWP doesn't request this, but again, it's important for people with fluctuating conditions).

5) If you have had help willing in the form, make sure you state it on the form - help includes using guides like this one. (Again, the DWP doesn't ask this, but they'll assume you have all the skills required to fill the form in if you do not do this).
 

Eighth Session

We can now return to page 3 and list any help you may need for the assessment. Going through the form will hopefully have triggered all appropriate ideas. Just in case though, here are a few you may require:
  • I will require disabled parking outside the centre.
  • If the assessment centre is not on a ground floor I will need a lift or escalator.
  • I cannot use public transport.
  • I may require somewhere to lie down while I wait for the assessment.
  • I may require a dark quiet room while I wait for my assessment.

On page 17 list any supporting documents you are including, and any you're expecting to send on later. Make sure each piece of supporting evidence has your name, date of birth and National Insurance number somewhere visible on every page.

Tick the box to confirm you're sending additional evidence.

And fill in the details on Page 18. Sign it when you have printed it out. (I forgot to sign a form once; they still accepted it).

 Aaaaaand ... relax!

 
Some people send the form by recorded delivery to the DWP, because of their infamous ability to lose documents 'in the post'. However, because forms are received by the post office, and not the actual DWP, there is no one to sign for recorded delivery when it arrives, so it's essentially meaningless to send it that way. As such I recommend using the pre-paid envelope they send you with the form, and phoning a few days later to make sure your form has been received. Allow 10 days before panicking. And always keep a copy!



ESA50 Example Answers for M.E. / Fibro

A full guide to filling in the ESA50 (big ESA questionnaire) is here. This post is for people who have M.E., Fibro, or similar conditions, to give you some extra gentle prods in the right direction. So, use the other guide, but as you reach each section, consider whether any of the phrases / questions below apply to you. Do not forget to enter information about any other conditions you have, too! (For example, because M.E. is my main problem, I nearly always forget to put information about my back problems on forms).

If you can suggest any additional sentences for any of the questions on the form, please do not hesitate to contact us through the group. Please remember that these are in reference to M.E. and Fibro specifically, though.

Beware any benefit cheats - I am throwing wild cards into these suggestions, which will be blazingly obvious to any trained medical professional. If you're a genuine claimant you need not worry about the wildcards, as you will only be using sentences that honestly apply to yourself.

On Page 3, there is a box that says "Tell us about any help you would need if you have to go for a face-to-face assessment."
  • I am unable to use public transport.
  • I would require an assessment on the ground floor, or a building with a lift, because I cannot use stairs.
  • I would require parking at the front of the assessment centre, as I cannot walk further than 50 metres.
  • I would require a ramp at the entrance of the building, as I use a wheelchair.
  • I would require seating at reception, as I cannot remain standing, for the queue to register.
  • Ideally I would wait in a darkened room as I am very sensitive to light, but if this is unavailable I will cover my head / wear sunglasses in the centre.
  • Ideally I wait in a silent room as I am very sensitive to sound, but if this is unavailable I will wear earplugs / ear defenders. Please bring this to the attention of the assessor, as I may not hear him / her when they call me for my assessment.
  • I require seats with no arms as I need to raise my legs from the floor.
  • I require seats with no arms as I need to lie down while I await assessment.





Question 1: Moving Around & Using Steps

  • Orthostatic Intolerance / Orthostatic Hypotension / Postural Hypotension / Postural Tachycardia Syndrome affects me when I'm walking, so I am unable to walk many steps without needing to sit / lie down. (If OI does not affect your walking, do not use it in this section).
  • Post Exertional Malaise affects me very quickly, so I am unable to walk many steps without needing to pause to rest.
  • It is too painful, due to pain in the muscles of my legs, caused by M.E. / Fibro, for me to walk more than 50 metres.
  • It is too painful, due to pain in the muscles of my legs, caused by M.E. / Fibro, for me to raise my legs to use steps.
  • I cannot walk any distance unaided due to dizziness / vertigo.
  • I cannot mount any steps unaided, due to dizziness / vertigo.
  • My balance is too poor to walk 50 metres unaided.
  • My balance is too poor to walk up any steps unaided.
  • I cannot walk due to weakness in my legs.
  • I cannot use steps due to weakness in my legs.
  • I usually / often / sometimes crawl up the stairs in my house.
  • I use a stick to walk with, because it helps reduce pain.
  • I use a stick to walk with, because it helps with my balance.
  • I use a stick that has a seat on it, so that I can avoid passing out because of Orthostatic Intolerance / Orthostatic Hypotension / Postural Hypotension / Postural Tachycardia Syndrome.
Incidentally, many people with M.E. and Fibro do not know that they have Orthostatic Intolerance. Do you find that when you remain in a stationary position (standing, some people suffer it when sitting with feet down, too) that you become light headed, slightly nauseous, kind of sweaty palms, and just generally don't feel right? Is it alleviated by raising your legs? If yes, then you need to be tested for it (most doctor's aren't familiar with it, so it's useful to print out information about it for them). For now though, on your ESA50 refer to it as becoming light headed or feeling like you will pass out. (The reason I keep using three names for it is because different specialists seem to know it by different names. The last one, "Postural Tachycardia Syndrome" isn't the same as the others, but they are part of Postural Tachycardia Syndrome). Complicated, isn't it!

Likewise, in case you're unaware of what Post Exertional Malaise is: It literally means "illness after activity". Illness usually being exhaustion or extreme fatigue, in this case. People with M.E. generally have to be very careful how much activity they undertake, as they will pay for it later. We pace what we do, because we have limited energy resources. That nasty payback later (which varies a little from patient to patient) is the Post Exertional Malaise.

If you're unfamiliar with both of the things I've just described, I highly recommend you do some reading about M.E., starting with the symptom section of the International Consensus Criteria for M.E..



Question 2: Standing & Sitting
  • I am unable to remain in a stationary standing position for more than ## minutes, due to Orthostatic Intolerance / Orthostatic Hypotension / Postural Hypotension / Postural Tachycardia Syndrome.
  • Orthostatic Intolerance / Orthostatic Hypotension / Postural Hypotension / Postural Tachycardia Syndrome last caused me to pass out from a standing position on ##/##/####.
  • I struggle badly from Post Exertional Malaise. As such I am frequently so exhausted that I cannot sit up at all, let alone move from one seat to another.
  • I am unable to remain in a stationary standing position due to lack of strength in my legs.
  • I am unable to remain in a stationary standing position due to dizziness / vertigo causing me to fall.
  • I am unable to remain in an upright seated position due to weakness.
  • I am unable to move from one seat to another without help, due to weakness in my arms and legs. I cannot lift my own body.
  • I am unable to remain in a seated upright position without my legs raised in front of me, due to Orthostatic Intolerance / Orthostatic Hypotension / Postural Hypotension / Postural Tachycardia Syndrome.
  • I am unable to remain in any position, whether seated or standing, for more than ## minutes due to discomfort.
  • I use a stick with attached seat because I am unable to remain in a standing position due to Orthostatic Intolerance / Orthostatic Hypotension / Postural Hypotension / Postural Tachycardia Syndrome.


Question 3: Reaching
  • I am unable to raise my arms above my head due to Orthostatic Intolerance / Orthostatic Hypotension / Postural Hypotension / Postural Tachycardia Syndrome.
  •  I am unable to raise my arms as if to a upper shirt pocket, due to Orthostatic Intolerance / Orthostatic Hypotension / Postural Hypotension / Postural Tachycardia Syndrome.
  • I am unable to raise my arms above my head due to weakness.
  • I am unable to raise my arms as if to an upper shirt pocket, due to weakness.
  • I am unable to raise my arms above my head due to pain in the muscles.
  • I am unable to raise my arms as if to an upper shirt pocket, due to pain in the muscles.
  • I am unable to raise my arms above my head as it causes / exacerbates my dizziness / vertigo.
  • I suffer badly from Post Exertional Malaise. As such my arms often feel too heavy to lift above my head.
  • I suffer badly from Post Exertional Malaise. As such my arms often feel too heavy to lift them as if to a shift pocket.


Question 4: Picking up & Moving Things
  • I am unable to pick up either a half litre or a litre carton due to extreme pain and / or stiffness in my hands.
  • I am unable to pick up either a half litre or a litre carton due to disorientation caused by extreme fatigue.
  • I am unable to pick up a large object such as an empty box, because I cannot hold my arms out to the side due to pain in the muscles.
  • I am unable to pick up a large object such as an empty box, because I cannot hold my arms out to the side due to extreme fatigue making them feel very heavy.
  • I am unable to pick up a large object such as an empty box, because I cannot hold my arms out to the side due to weakness.
  • I am unable to pick up a large object such as an empty box, because I cannot hold my arms out to the side due to pain in the muscles.
  • I am unable to pick up and move an object from one place to another due to a lack of co-ordination caused by extreme fatigue.
  • I cannot bend to pick up a large object such as a box, from the floor, due to pain in my legs.
  • I cannot bend to pick up a large object such as a box, from the floor, due to vertigo / dizziness.


Question 5:  Manual Dexterity (Using Your Hands)
  • I cannot *pick example from form* due to pain and / or stiffness in the muscles of my hands.
  • The ability to use my hands is severely affected when I am exhausted, because I become very unco-ordinated.


Question 6: Communicating With People
  • I am frequently so exhausted that my speech becomes very slurred, and I cannot formulate a coherent sentence (with written, typed, or spoken) due to struggling to find the required words.
  • When I'm extremely fatigued I am unable communicate sensibly in a verbal manner.
  • When I'm extremely fatigued I am unable to communicate sensibly in writing.
  • When I'm extremely fatigued I am unable to communicate sensibly by typing.
  • I am often / frequently / never able to communicate by typing due to severe pain in my hands.
  • I am often / frequently / never able to write due to severe pain in my hands.
  • I am often / frequently / never able to speak due to severe pain caused by TMJ (Temporomandibular Joint Disorder).


Question 7: Other People Communicating With You
  • I frequently struggle to understand what people are saying to me due because of tinnitus.
  • I frequently become confused when people talk to me, because when I'm extremely confused my audio processing is fairly / moderately / severely affected.
  • When I'm extremely fatigued I struggle to follow words on a screen.
  • When I'm extremely fatigued I struggle to read more than a few sentences / paragraphs / pages.


Question 8: Getting Around Safely
  • Severe fatigue affects my cognitive ability to problem solve. As such I struggle to find my way around somewhere unfamiliar.
  • Severe fatigue affects my cognitive ability to problem solve. As such I struggle to find my way around somewhere unfamiliar without it causing further exhaustion.


Question 9:  Controlling your Bowels & Bladder, and Using a Collecting Device
  • I am often unable to get to the bathroom when I need to, due to extreme weakness. As such I use incontinence pads.
  • I often have urinary incontinence accidents.
  • I often have incontinence accidents from my bowels.
  • The medication I am taking for #### causes unpredictable loose stools, so I often suffer incontinence which may stain my clothing.
  • The medication I am taking for ##### causes urinary urgency, so I often suffer urinary incontinence because I cannot reach a toilet quickly enough.
  • I often suffer incontinence at night / in my sleep.
You can include problems with menstrual cycles that are difficult to control or may stain your clothing, in this section too.



Question 10:  Staying Conscious When Awake
  • CFS affects my sleep pattern and Circadian Rhythm severely. I need to sleep approximately ### in each 24 hour cycle. My personal body's most comfortable rhythm is to wake at ####, sleep at ####, with #### rest / sleep periods in between. 
  • On worst days I will sleep straight through several days at a time.
  • I am constantly at risk of passing out due to Orthostatic Intolerance / Orthostatic Hypertension / Postural Hypotension / Postural Tachycardia Syndrome. The last time I passed out due to this was #####.
  • When I am extremely fatigued my cognitive function is severely affected, to such a degree that I am at risk of having accidents, or performing acts that are dangerous. My ability to process information is reduced by approximately ##%. [This is what we call brainfog; most health professionals are unfamiliar with this colloquial term we sufferers use].


Question 11: Learning how to do Tasks
  • Extreme fatigue affects my cognitive ability. As such I find it difficult to follow the steps taken when learning a new task.


Question 12: Awareness of Hazards & Danger
  • When I am extremely fatigued my cognitive ability to process the information surrounding me is reduced by approximately ##%. As such I am at high risk of not processing a hazard or danger before it happens.


Question 13: Starting & Finishing Tasks
  • Severe exhaustion significantly affects my cognitive ability and memory. As such when I attempt to learn a new task, I am unable to remember the beginning of the process when I'm in the middle, let alone when I've reached the end.  
  • I am unable to perform two sequential personal tasks (ie, brushing my teeth and washing my face), one after the other without taking a rest break in between the two tasks.


Question 14: Coping With Changes
  •  Because any activity causes me severe Post Exertional Malaise I have to prepare myself a lot in advance. I usually have to rest before an activity, and then again after an activity. As such, if an activity is re-scheduled it can be detrimental to my health. If it is brought forward, I will be unprepared for it, and may have to cancel due to not being physically and cognitively ready. If it is moved backwards it can be upsetting, as I will have wasted valuable days resting in preparation for the activity.
  • Small changes, such as a doctor's appointment running late can affect me severely due to the immense amount of stimulation in waiting rooms (a lot of sound, light that I cannot hide from, etc).
  • There is no such thing as a small change to my routine, because every activity I undertake must be prepared for carefully due to needing to pace and use my energy extremely carefully. For example, if I visit my GP for ten minutes in the week, I will need to rest in a darkened silent room, for several days in order to return to what is 'normal' for me.

Question 15: Going Out
  • Severe fatigue affects my cognitive ability, as such planning a journey.
  • Severe fatigue affects my cognitive ability, as such, navigating a new place are too difficult.
  • Severe fatigue affects my cognitive ability, as such planning a journey and navigating a new place are too difficult.
  • I cannot walk to my nearest shops.
  • I cannot drive.
  • I cannot use public transport due to over stimulation.
  • Fatigue affects my ability to drive. As such I cannot reliably and repeatedly drive myself anywhere.
  • I need someone with me when I leave the house, because I become fatigued very quickly, so can place myself in danger.
  • I need someone with me when I leave the house as I need to use a wheelchair, which I cannot self-propel.


Question 16: Coping With Social Situations
  • I become anxious about meeting new people, because most people do not understand that severe fatigue affects my speech and cognitive ability. So people often think that I am drunk or slow.
  • I become anxious about meeting people I do know, because I know that any activity will have a knock on affect which can last for days or even weeks.


Question 17: Behaving Appropriately
  • I often fall asleep in social situations, which some people do not like.
  • When I am fatigued my cognitive ability is severely affected. It takes me a lot longer to process information around me, situational and conversational. It often gives the impression that I am not listening, or not interested in what people are saying or what is happening.
  • When I become fatigued I experience a lot of pain, which causes me to become very grumpy. This always has a negative affect on social situations.


Question 18: Eating & Drinking
  • I need help to eat and drink because my hands are too painful to hold cutlery or a drinking receptacle.
  • I need to be prompted to eat and drink because my memory is so poor that I often forget to eat.
  • My memory is very poor so I need someone to keep track of when I eat and drink.
  • I cannot plan a meal due to my cognitive abilities being affected by severe fatigue.
  • I cannot chew food due to TMJ (Temporomandibular Joint Disorder).
  • I cannot swallow food or drink due to extreme weakness.


Thursday, 3 October 2013

Regulations 29 & 35

Regulations 29 and 35 are otherwise known as 'special circumstances'. The legislation below is explained in this post.


Regulation 29

Entitles you to be placed in the WRAG because work carries a substantial risk (of being made more ill) to you or another person.

Exceptional circumstances
29.

(1) A claimant who does not have limited capability for work as determined in accordance with the limited capability for work assessment is to be treated as having limited capability for work if paragraph (2) applies to the claimant.

(2) Subject to paragraph (3), This paragraph applies if—
(a) the claimant is suffering from a life threatening disease in relation to which—
(i)
there is medical evidence that the disease is uncontrollable, or uncontrolled, by a recognised therapeutic procedure; and
(ii)
in the case of a disease that is uncontrolled, there is a reasonable cause for it not to be controlled by a recognised therapeutic procedure; or

(b) the claimant suffers from some specific disease or bodily or mental disablement and, by reasons of such disease or disablement, there would be a substantial risk to the mental or physical health of any person if the claimant were found not to have limited capability for work

(3) Paragraph (2)(b) does not apply where the risk could be reduced by a significant amount by—

(a) reasonable adjustments being made in the claimant’s workplace; or
(b) the claimant taking medication to manage the claimant’s condition where such medication has been prescribed for the claimant by a registered medical practitioner treating the claimant.

Regulation 35

Entitles you to be placed in the Support Group because work-related activity (ie what you have to do if you are in the WRAG) carries a substantial risk (of being made more ill) to you or another person. Certain claimants to be treated as having limited capability for work-related activity

35.

(1) A claimant is to be treated as having limited capability for work-related activity if—
(a) the claimant is terminally ill;

(b) the claimant is-
(i) receiving treatment for cancer by way of chemotherapy or radiotherapy;
(ii) likely to receive such treatment within six months after the date of the determination of capability for work-related activity; or
(iii) recovering from such treatment, and the Secretary of State is satisfied that the claimant should be treated as having limited capability for work-related activity; or

(c)
in the case of a woman, she is pregnant and there is a serious risk of damage to her health or to the health of her unborn child if she does not refrain from work-related activity.


(2) A claimant who does not have limited capability for work-related activity as determined in accordance with regulation 34(1) is to be treated as having limited capability for work-related activity if—
(a) the claimant suffers from some specific disease or bodily or mental disablement; and

(b) by reasons of such disease or disablement, there would be a substantial risk to the mental or physical health of any person if the claimant were found not to have limited capability for work-related activity.

Friday, 27 September 2013

What to expect from the Work Capability Assessment

When you apply for ESA, you may have to undergo what a lot of people colloquially refer to as 'the medical'.

The DWP call it the Work Capability Assessment (WCA). That's exactly what it's doing; assessing how capable you are of work, not assessing how ill or disabled you are.

Naively, when I first underwent this in 2003 I believed that they had my interest at heart (that our government looks after us), that they wanted to assess how ill I was, as opposed to how capable of work I was, and that when they referred to 'work' they were referring to the job I used to do. This is why I failed. Lack of understanding. So I advise to be prepared, and know what you're expecting and what is expected of you.

You will be sent a letter inviting you to attend the WCA. It will give you the date of the assessment, and the location. You may well find that the assessment centre they expect you to attend is over an hour's journey for you. They may have included a route for you to use to get there, using public transport, too.

If the assessment centre does appear to be in an unreasonable location for you, contact the DWP to discuss it. There may be one that isn't any nearer, but is more convenient for you to get to; the assessment may be able to be rearranged for you. You can view a list of assessment centres here.

If the date they have scheduled your assessment for is inconvenient, again, contact them to reschedule it.

If you are given a morning appointment, and you find morning's impossible to function (as many people with M.E. do), you might want to contact them and ask for an afternoon appointment. Make it clear why you are rescheduling. Then when you get to the actual assessment, again, make it clear, so that it is noted that you cannot function in the morning. On the other hand though; if an assessor can see how badly you function in the morning, it may help you to score more points on the assessment.

The public transport itineraries they send people are usually totally ridiculous. The one they sent me would have taken six hours, with a 40 minute wait at one station, and a walk across a city. None of it was at all possible. The public transport agenda is essentially their first way of tripping people up. A lot of assumptions are made if you are able to use public transport, for example that you have planning skills, you do not suffer from social phobia or anxiety, you can deal appropriately with people you do not know, etc.

Ideally you will arrange for someone to drive you to the assessment centre. The assessment centre may offer to pay a little towards the fuel. Otherwise you may be able to agree with the assessment centre for them to pay a portion of a taxi fee. If neither of these are possible for you, some areas have voluntary drivers; your Citizens Advice Bureau is most likely to have this list.

Of course, if you can drive, then you may drive yourself there. Again, the assessment centre may pay a little towards the fuel. There are a few things to consider in doing so though:
  • Do you normally need to rest before and after driving that distance? - it will be assumed that you do not.
  • Are you able to drive the same distance every day? - it will be assumed that you can.
  • Are you able to fill your car with fuel, or does someone else usually do that for you? - it will be assumed that you have the manual dexterity and strength to lift the fuel pump nozzle.

Joyce Drummond, who worked for Atos for a while, has given a very insightful account of what to expect from the WCA. I highly recommend reading it for further observations that I may not have made here.

In Joyce's account she states that at the centre she worked in they did not use security cameras to assess people as they approached the assessment centre. However, we've heard so many accounts of people believing this has happened, that it's best to assume they do.

The assessor will ask you where you parked. Your answer will be used, in part, to assess your mobility (how far you can walk). Most centre's do not have parking available nearby. I personally choose to be dropped off outside - even if there are double yellow (or red) lines there. I cannot walk far reliably, repeatedly or safely, so I don't want to mislead them into thinking that I can.

The buildings vary, but most of them do not have the assessment centre on the ground floor. One of my experiences was thus:
I arrived at the assessment centre. Two security guards watched me get out of my partners car. One made notes. After I had reached the door and presented my papers I was asked whether I could use the stairs. I said that I could not, and asked to use the lift. I was told that if I could not use the stairs then I could not go up to the assessment centre in case there was a fire. I started to panic, so the other security guard rephrased, asking whether I'd be able to push myself to use the stairs in case of a fire. So that I could get to the centre, I said that if there was a fire I'd have no choice, even if it meant going down on my bum. I was assessed as being able to use stairs, on the basis of that conversation.
That was a dirty trick. At the time I knew no better. If anyone plays a trick like that on you, don't fall for it. If you can use the stairs fair enough, but if you can't, don't be forced to put yourself in a position that causes you pain and/or discomfort. If they prevent you from going upstairs, they are forfeiting the assessment, not you. If you've mentioned on your ESA50 that you have a problem using stairs then they should not have scheduled you to be assessed at a centre that is inaccessible to people who cannot use stairs. What I should have done was ask my partner if he could go up to the centre and explain the situation. I believe I could have insisted upon an assessment downstairs, even if that meant rescheduling it for another date and location.

And that is one of the keys for the whole of the assessment; don't do anything that causes you pain or discomfort. As soon as you feel anything tell them - because they cannot know if you don't do so.

Once you arrive at the assessment centre you need to go to reception to book yourself in and prove you are who you say you are. At my last assessment they played another dirty trick here; three receptionists sat behind the desk giggling and gossipping while a queue built up. I sat on the floor to start with (if you have Orthostatic Intolerance too, you'll understand why), but moved to some chairs after five minutes, to lie down.

If there is a queue when you arrive, I recommend you take a photo of your watch, or preferably a clock on their wall; a screen print of your phone if necessary. The reason I suggest this is because that half an hours queue at the reception desk made me late for the assessment. They later used this as an excuse to send me home without the assessment. Not turning up for an assessment can result in your benefit being revoked.

At the desk they ask you for three forms of ID. I totally forgot to take any one time, so just emptied my entire purse at the lady, which she accepted. So I believe that several things with your name on will be fine. If you usually have trouble remaining standing, you can request a seat while you're at the desk.

If you accept the expenses form, bare in mind that they will be assessing your manual dexterity when you fill it in, and how legible your handwriting is. If you have to submit it in another room, they'll also be assessing your mobility. As such, if your condition is fluctuating, make sure that the assessor knows (once you meet them) what the difference is between these actions and how they would be when you've become fatigued.

Everything you do and say is being watched. From the moment you step into the assessment centre the type of chair you choose to sit in is noted, how you sit in it, whether you fidget, rock, talk to yourself, etc, is all being noted. If you stand or pace, your mobility is assessed. If you use your phone or have brought a book to read, or a book of puzzles, your manual dexterity and concentration are being assessed. Judgements are made according to what you are wearing, and how well groomed you are (not particularly correctly in my experience). Joyce Drummond mentioned that they even make note of whether someone's eyebrows are waxed. I couldn't help wondering how they know.

For most people it isn't particularly unfair that their actions in the waiting room are assessed. The problem for people with M.E. and similar conditions is the fact that our conditions fluctuate. For some of us they fluctuate on a hour by hour basis, others it can be month by month. So, until we actually speak to the assessor to explain where we are in our fluctuations, judgements really should not be made. I've heard of people's assessments not taking place though, because of observations that have been made in the waiting room. (To be fair, though, in these cases the decision has gone in the claimant's favour).

Usually you will be expected to wait a while before you meet your assessor. You may be assessed by a nurse, a physiotherapist or a doctor. Technically speaking the rules state that neurological conditions should be assessed by a doctor. Despite NICE and WHO recognising M.E. as being a neurological condition, the DWP and Atos do not. If your personal condition has been recognised as being neurological you can therefore insist upon being assessed by a doctor. Personally, since we're not seeking treatment from these people, I don't really see that it makes a difference.

The assessor will come to the waiting room and call you by name. They will be assessing, at first, how well you hear them, then they'll assess whether you make eye contact and to some extent your manual dexterity and social behaviour when they offer to shake you by the hand. As you walk with them to the assessment room they are assessing your mobility from whether you walk straight, stumble, bump into doorways, etc.

If you usually use a walking aid or wheelchair, take it with you. The assessor may ask you if they were prescribed or if you bought them. Whichever is your answer, make sure you explain clearly what your reasons are for using it. If there are other aids or appliances you use at home that you believe may help the decision, you could bring them in, or take a photograph to add to the evidence.

You can take someone in to the assessment with you. This person can make notes on the assessment, provided that you allow the assessor to make a photocopy of these notes before you leave. You can have the assessment recorded by prior arrangement. If you want your assessment recorded, you simply phone the DWP and request it. There are not many recorders available throughout Atos as an organisation, so making this request can cause the date of your assessment to be postponed. You can also have home assessments recorded, again, by prior arrangement.

Once you're in the assessment you will be invited to sit down. If the type of chair you are given to sit in is one you are normally uncomfortable in, make sure you mention this to the assessor. If they offer you another chair, don't be fooled into carrying it across the room if it will cause you any discomfort or pain, whether that would be immediate or later.

To every question you are asked, understand that they are making various judgements. For example:
  • how much do you need to move around for whatever the question was in reference to.
  • how much do you need to move your hands?
  • how much do you need to walk?
  • how much responsibility does it require?
  • how much prior organisation?
  • how much social interaction does it require?
  • how much social interaction with strangers?

For example, they ask you whether you have any pets. If you simply answer 'yes', it will be assumed that you have a cat or a dog. From that they assume that the animal is fed on the ground, so you must be able to squat (bend the knees) and open a tin (manual dexterity). They will also assume you walk the dog daily. Even if you specify that your pet is not a cat or dog, an amount of responsibility and organisation is assumed, since you will assumably be feeding and watering the animal every day. They do not ask you how many pets you've accidentally maimed or killed. As such, if you have a pet in your household, which you are not responsible for, either do not tell them that it is your pet, or tell them who takes care of it.


There is also a physical section to the assessment. You will be asked to perform certain movements, some of which you will need to get up onto a couch for. If anything the assessor asks you to do, including climbing on to the couch, causes you discomfort or pain, or usually would, make it absolutely clear to them. If you know that something will cause you discomfort or pain, you can refuse to do it. If they try to talk over you (as one of my assessor's did continuously), say it to them again afterwards.

Once the assessment is over, you should hear what the result is within 4 to 6 weeks. If it seems to be taking forever, phone the DWP to find out what is why. 

Under some circumstances you may be able to arrange for the medical assessment to take place in your home, usually by a visiting doctor. The two scenarios I know of this happening are:
  1. By submitting a letter from your GP or a specialist stating that attending the WCA will be detrimental to your health, or that of someone else.
  2. When the medical assessment has been cancelled at your detriment, they may offer you a home assessment instead. (This happened to me).
Getting the DWP to agree to a Work Capability Assessment at home is infamously difficult. Simply requesting one yourself rarely works, no matter how hard you state your case. To illustrate how difficult it is; a close friend of mine was in hospital in a neurological unit when she was called for re-assessment. The DWP refused to give her a home/hospital assessment, so she was taken to the assessment centre in an ambulance, and carried in on a stretcher.

The home assessment is very similar to that performed in the assessment centre's. You are asked very similar questions. You are still asked to perform certain movements. The main difference is that the assessor can see for themselves the evidence around your home as to your state.


Useful Links

A comprehensive look at the WCA questions and how to answer them, written by Michelle.

A list of the questions you'll be asked in the WCA.

Friday, 30 August 2013

SYMPTOM SECTION International Consensus Criteria for M.E.

Adult and Pediatric ● Clinical and Research

Myalgic encephalomyelitis is an acquired neurological disease with complex global dysfunctions. Pathological dysregulation of the nervous, immune and endocrine systems, with impaired cellular energy metabolism and ion transport are prominent features. Although signs and symptoms are dynamically interactive and causally connected, the criteria are grouped by regions of pathophysiology to provide general focus.

A patient will meet the criteria for post-exertional neuroimmune exhaustion (A), at least one symptom from three neurological impairment categories (B), at least one symptom from three immune/gastro-intestinal/genitourinary impairment categories (C), and at least one symptom from energy metabolism/transport impairments (D).


A. Post-Exertional Neuroimmune Exhaustion (PENE pen׳-e) Compulsory 

This cardinal feature is a pathological inability to produce sufficient energy on demand with prominent symptoms primarily in the neuroimmune regions. Characteristics are:

1. Marked, rapid physical and/or cognitive fatigability in response to exertion, which may be minimal such as activities of daily living or simple mental tasks, can be debilitating and cause a relapse.

2. Post-exertional symptom exacerbation: e.g. acute flu-like symptoms, pain and worsening of other symptoms

3. Post-exertional exhaustion may occur immediately after activity or be delayed by hours or days. 4. Recovery period is prolonged, usually taking 24 hours or longer. A relapse can last days, weeks or longer. 5. Low threshold of physical and mental fatigability (lack of stamina) results in a substantial reduction in pre-illness activity level.

Operational Notes: For a diagnosis of ME, symptom severity must result in a significant reduction of a patient’s premorbid activity level. Mild (an approximate 50% reduction in pre-illness activity level), moderate (mostly housebound), severe (mostly bedridden), or very severe (totally bedridden and need help with basic functions). There may be marked fluctuation of symptom severity and hierarchy from day to day or hour to hour. Consider activity, context and interactive effects. Recovery time: e.g. Regardless of a patient’s recovery time from reading for 1⁄2 hour, it will take much longer to recover from grocery shopping for 1⁄2 hour and even longer if repeated the next day – if able. Those who rest before an activity or have adjusted their activity level to their limited energy may have shorter recovery periods than those who do not pace their activities adequately. Impact: e.g. An outstanding athlete could have a 50% reduction in his/her pre-illness activity level and is still more active than a sedentary person.


B. Neurological Impairments At least One Symptom from three of the following four symptom categories

1. Neurocognitive Impairments

a. Difficulty processing information: slowed thought, impaired concentration e.g. confusion, disorientation, cognitive overload, difficulty with making decisions, slowed speech, acquired or exertional dyslexia

b. Short-term memory loss: e.g. difficulty remembering what one wanted to say, what one was saying, retrieving words, recalling information, poor working memory
 
2. Pain

a. Headaches: e.g. chronic, generalized headaches often involve aching of the eyes, behind the eyes or back of the head that may be associated with cervical muscle tension; migraine; tension headaches

b. Significant pain can be experienced in muscles, muscle-tendon junctions, joints, abdomen or chest. It is non-inflammatory in nature and often migrates. e.g. generalized hyperalgesia, widespread pain (may meet fibromyalgia criteria), myofascial or radiating pain


3. Sleep Disturbance

a. Disturbed sleep patterns: e.g. insomnia, prolonged sleep including naps, sleeping most of the day and being awake most of the night, frequent awakenings, awaking much earlier than before illness onset, vivid dreams/nightmares

b. Unrefreshed sleep: e.g. awaken feeling exhausted regardless of duration of sleep, day-time sleepiness


4. Neurosensory, Perceptual and Motor Disturbances 

a. Neurosensory and perceptual: e.g. inability to focus vision, sensitivity to light, noise, vibration, odour, taste and touch; impaired depth perception

b. Motor: e.g. muscle weakness, twitching, poor coordination, feeling unsteady on feet, ataxia

Notes: Neurocognitive impairments, reported or observed, become more pronounced with fatigue.

Overload phenomena may be evident when two tasks are performed simultaneously. Abnormal reaction to light – fluctuation or reduced accommodation responses of the pupils with retention of reaction. Sleep disturbances are typically expressed by prolonged sleep, sometimes extreme, in the acute phase and often evolve into marked sleep reversal in the chronic stage. Motor disturbances may not be evident in mild or moderate cases but abnormal tandem gait and positive Romberg test may be observed in severe cases.


C. Immune, Gastro-intestinal & Genitourinary Impairments

At least One Symptom from three of the following five symptom categories

1. Flu-like symptoms may be recurrent or chronic and typically activate or worsen with exertion.
e.g. sore throat, sinusitis, cervical and/or axillary lymph nodes may enlarge or be tender on palpitation

2. Susceptibility to viral infections with prolonged recovery periods

3. Gastro-intestinal tract: e.g. nausea, abdominal pain, bloating, irritable bowel syndrome

4. Genitourinary:e.g.urinaryurgencyorfrequency,nocturia

5. Sensitivities to food, medications, odours or chemicals

Notes: Sore throat, tender lymph nodes, and flu-like symptoms obviously are not specific to ME but their activation in reaction to exertion is abnormal. The throat may feel sore, dry and scratchy. Faucial injection and crimson crescents may be seen in the tonsillar fossae, which are an indication of immuneactivation.


D. Energy Production/Transportation Impairments: At least One Symptom

1. Cardiovascular: e.g. inability to tolerate an upright position – orthostatic intolerance, neurally mediated hypotension, postural orthostatic tachycardia syndrome, palpitations with or without cardiac arrhythmias, light-headedness/dizziness

2. Respiratory: e.g. air hunger, laboured breathing, fatigue of chest wall muscles
3. Loss of thermostatic stability: e.g. subnormal body temperature, marked diurnal fluctuations; sweating episodes, recurrent feelings of feverishness with or without low grade fever, cold extremities

4. Intolerance of extremes of temperature

Notes: Orthostatic intolerance may be delayed by several minutes. Patients who have orthostatic intolerance may exhibit mottling of extremities, extreme pallor or Raynaud’s Phenomenon. In the chronic phase, moons of finger nails may recede.


Paediatric Considerations

Symptoms may progress more slowly in children than in teenagers or adults. In addition to post- exertional neuroimmune exhaustion, the most prominent symptoms tend to be neurological: headaches, cognitive impairments, and sleep disturbances.

1. Headaches: Severe or chronic headaches are often debilitating. Migraine may be accompanied by a rapid drop in temperature, shaking, vomiting, diarrhoea and severe weakness.

2. Neurocognitive Impairments: Difficulty focusing eyes and reading are common. Children may become dyslexic, which may only be evident when fatigued. Slow processing of information makes it difficult to follow auditory instructions or take notes. All cognitive impairments worsen with physical or mental exertion. Young people will not be able to maintain a full school program. 3. Pain may seem erratic and migrate quickly. Joint hyper-mobility is common.
Notes: Fluctuation and severity hierarchy of numerous prominent symptoms tend to vary more rapidly and dramatically than in adults.

Classification ____ Myalgic Encephalomyelitis ____ Atypical Myalgic Encephalomyelitis: meets criteria for post-exertional neuroimmune exhaustion but has two or less than required of the remaining criterial symptoms. Pain or sleep disturbance may be absent in rare cases.

Exclusions: As in all diagnoses, exclusion of alternate explanatory diagnoses is achieved by the patient’s history, physical examination, and laboratory/biomarker testing as indicated. It is possible to have more than one disease but it is important that each one is identified and treated. Primary psychiatric disorders, somatoform disorder and substance abuse are excluded.


Paediatric: ‘primary’ school phobia.

Co-morbid Entities: Fibromyalgia, Myofascial Pain Syndrome, Temporomandibular Joint Syndrome, Irritable Bowel Syndrome, Interstitial Cystitis, Raynaud’s Phenomenon, Prolapsed Mitral Valve, Migraines, Allergies, Multiple Chemical Sensitivities, Hashimoto’s Thyroiditis, Sicca Syndrome, Reactive Depression. Migraine and irritable bowel syndrome may precede ME but then become associated with it. Fibromyalgia overlaps.