Worked example by condition

PIP answers for hearing loss

A worked example showing how each of the 12 PIP activities can be described for someone with hearing loss or deafness. Every answer is written in the first person, in the plain wording assessors look for, and each one weaves in the reliability factors that decide how an activity scores.

How hearing loss affects a PIP claim

The hardest thing about putting hearing loss on a form is that most people, including some assessors, believe hearing aids fix it. They do not. Aids make sound louder, not clearer, and they lift the background as much as the voice you are trying to follow. So a person with aids in both ears may manage a quiet conversation one to one, facing the other person, and still lose almost everything in a busy room, on a bus, at a till, or when two people speak at once. If you are deaf you may rely on lipreading, on seeing faces, or on British Sign Language, and none of that works when someone speaks from behind you, covers their mouth or turns away.

What gets left off forms is the amount of guessing and the cost of it. Filling in the gaps from a few caught words, watching mouths, working out from context what was probably said, is relentless concentration, and by the middle of the afternoon there is nothing left, so you follow even less. Then there are the consequences: telephone calls you cannot take, appointment reminders left on voicemail that you never hear, appointments missed, instructions from a nurse or pharmacist half understood, and someone else having to relay or interpret so that you know what you have been told. Many people also live with tinnitus that sits on top of whatever they are trying to hear and gets louder when they are tired. Add all of that up and the usual result is withdrawal: turning down invitations, leaving the group, going quiet.

The reliability rules are what turn that into an answer the form can use. An activity only counts as something you can do if you can do it safely, to an acceptable standard, repeatedly and in a reasonable time. Hearing a single sentence in a quiet room is not the same as following a real conversation to an acceptable standard, and passing a hearing test in a soundproof booth says nothing about a kitchen with an extractor fan running. Say what you can follow, where, with whom, and for how long before the effort runs out. Hearing aids are an aid that the form recognises for talking, listening and understanding, so it is worth stating plainly that you wear them and, just as plainly, what you still cannot follow with them in.

The example below does exactly that. It also answers honestly on the activities that hearing loss genuinely does not touch, because a form that only claims what is true reads as far more credible than one that stretches every question. The DWP always makes the final decision, but describing your day accurately gives your form the strongest chance of being understood.

How your health condition affects youPIP2 · Q9
9. Talking, listening and understanding
Does your condition affect you talking, listening and understanding? (Put a cross in one box below)
✓ Yes
Tell us about the difficulties you have with talking, listening and understanding and how you manage them.
I wear hearing aids in both ears and have done for years, but they do not give me normal hearing back. They make sound louder rather than clearer, so they bring up the background as much as the voice I am trying to follow. In a quiet room, one to one, with the light on the other person's face, I can hold a conversation, and I am lipreading as much as listening to do it. Anywhere else I lose most of what is said. If a television is on, if there is traffic or an extractor fan, or if two people speak at once, speech turns into noise. I catch a word here and there and guess the rest, and I get it wrong. I cannot use a telephone at all, so I never hear an appointment reminder or a call from the surgery, and I have missed appointments because of it. If someone speaks to me from behind, or covers their mouth, I do not know they are talking to me. My wife comes to every appointment and repeats what the doctor has said facing me, slowly, because otherwise I come away not knowing what I have been told, and she makes and takes my phone calls for me. Concentrating this hard is exhausting and by the afternoon I have nothing left, so I follow even less. I also have constant tinnitus that gets worse when I am tired and sits on top of whatever I am trying to hear. Even with my aids in, I cannot take in anything detailed or complicated without someone there to go through it with me.
★ Suggested descriptor · 9c · 4 points
Hearing aids are an aid the form counts, so say that you wear them and then say plainly what you still cannot follow with them in, and who has to relay or interpret for you.
How your health condition affects youPIP2 · Q11
11. Mixing with other people
Does your condition affect you mixing with other people? (Put a cross in one box below)
✓ Yes
Tell us about the difficulties you have with mixing with other people and how you manage them.
Being around people has become very hard since my hearing got worse, and it is not because I do not want company. In any group I cannot follow who is speaking or what has been said. People talk across each other, they laugh at something I have missed, and by the time I have found the right face to look at the subject has changed. I used to nod along and pretend I had understood, until I answered the wrong question twice at a family birthday and could see people deciding I was rude or confused. Now I mostly stop going. I have turned down every invitation this year apart from close family, and I have stopped going to the club I went to for eleven years. When I do go somewhere I need my wife with me. She sits where I can see her, tells me who is talking and repeats the important parts facing me so that I can lipread her. Without someone doing that I sit at the edge of the room for an hour, say nothing, and ask to go home. I cannot start a conversation with anyone new, because I never get the first few words and I am too embarrassed to keep asking a stranger to repeat themselves, so I avoid it. It leaves me low and very isolated, and there are weeks when the only person I have a proper conversation with is my wife. I can be in a room full of people, but I cannot actually engage with them to any decent standard unless someone is there to relay what is going on.
★ Suggested descriptor · 11c · 4 points
This activity is about engaging with people rather than hearing them, so describe the support you need in company, and the invitations and groups you have given up.
The other activities

What to cover for each one. Your paid form writes the full answers for you.

Q3

Preparing food

What to mention

Describe what you cannot hear in a kitchen and why it matters for safety: a timer, a pan boiling over, a hob left on behind you, or a smoke alarm sounding while your back is turned. Mention any vibrating timer, flashing alert or alarm pad you rely on, and anyone who looks in on you while you cook. Say plainly whether you could prepare and cook a simple meal safely on your own without those things.

Q4

Eating and drinking

What to mention

Hearing loss does not usually touch this one, because it is about cutting food up, getting it to your mouth, chewing and swallowing. What counts is needing someone to cut food up or feed you, a physical difficulty holding cutlery, or needing to be reminded to eat at all, which for most people comes from another condition rather than the hearing. If you have something else going on that does that, describe it here in its own right. If eating and drinking are fine for you, leave this one alone.

Q5

Managing your treatments

What to mention

Explain how much of managing treatment happens by voice: dosage instructions from a pharmacist, a nurse explaining a change over the phone, reminders left as voicemail. Mention who telephones the surgery for you, who comes in to repeat what you are told, and any review or appointment you have missed because you never heard the call. Describe what happens to your medication when that support is not there.

Q6

Washing and bathing

What to mention

This question is about washing yourself, so hearing alone rarely reaches it. What counts is needing an aid or another person to wash and bathe safely, or not being able to be left alone in the bathroom, and that is worth saying if taking your aids out leaves you hearing nothing at all and someone has to stay in the house or check on you. Say plainly what the risk is and who covers it. If you wash and bathe on your own without help, leave this one alone.

Q7

Using the toilet and managing incontinence

What to mention

This one is about getting on and off the toilet, cleaning yourself and controlling your bladder and bowel, none of which hearing normally affects. What counts is needing a rail, a raised seat or another person, or having accidents you have to manage with pads or a change of clothes. If a second condition causes any of that, describe it here rather than leaving it out because your main claim is about hearing. If none of it applies to you, leave this one alone.

Q8

Dressing and undressing

What to mention

Hearing does not usually come into dressing, so only claim this if something genuinely reaches it. What counts is needing an aid or help with buttons, zips, shoes and socks, taking far longer than you should, or needing prompting to dress or to change into clean clothes. Anything to do with fitting or managing hearing aids belongs under managing your treatments, not here. If you dress and undress without help, leave this one alone.

Q10

Reading

What to mention

This question is about taking in written information, and ordinary glasses do not count as an aid, so hearing loss on its own usually does not reach it. What does count is being deaf from birth or early childhood with British Sign Language as your first language, so that written English is genuinely hard and somebody has to go through letters and forms with you and explain what they mean. If that is you, say so plainly. If you can read and understand letters yourself, leave this one alone and keep your spoken difficulties under talking, listening and understanding.

Q12

Managing money

What to mention

Hearing loss does not usually affect the sums themselves. What can count is missing information in a phone call with the bank or at a counter, so if you have had to hand money matters to someone else because of that, describe it and say what would happen without them. Be careful to keep it honest: not hearing the bank is a hearing difficulty, and it belongs under talking, listening and understanding unless it has genuinely taken the money out of your hands. If money is genuinely fine for you, leave this one alone.

Q13

Planning and following a journey

What to mention

Describe what happens when a journey stops going to plan: a platform change over a tannoy, a cancellation called out on a bus, a driver or guard giving directions you cannot hear. Explain whether you need someone with you on an unfamiliar route because of that, and what you have done when you have been left stranded. Keep this to following and completing the journey, not how far you can walk.

Q14

Moving around

What to mention

This activity is only about standing and physically walking, so hearing on its own does not limit it and most people will say they can walk more than 200 metres. What counts is a physical or balance problem that shortens the distance, so if your hearing loss comes with vertigo, Meniere's or unsteadiness that makes you stop or hold on to something, put the distance and what stops you here. Having to be extra careful crossing roads because you cannot hear traffic belongs under planning and following a journey. If walking is genuinely fine, leave this one alone.

Your own answers, for every activity

The tips above are general pointers. Your paid form gives you a full, ready-to-copy answer for all 12 activities, written from your exact conditions, medication, aids and bad days, not a general example. This is a worked example for hearing loss; yours is written for you. £99.99 one-off.

How to use this example

This is a worked example, not a script. It shows one honest way a person with hearing loss might describe an ordinary week, so you can see the level of detail and the plain wording that assessors are trained to look for. Please do not copy it word for word. Your own answers should reflect your hearing, the situations you genuinely cannot follow, the aids you actually wear and the help you actually get or go without, because that is what the assessment is about and that is what makes an answer ring true.

Notice that not every activity has to be claimed. Hearing loss hits a small number of activities hard rather than touching all twelve, and being honest about what it does not change makes the difficulties you do describe far more believable. If your hearing loss comes with dizziness, balance problems or another condition, describe that in the activity it really affects rather than forcing it into this one. If you would rather start from your own words, tell us about your health and we will write your answers from your own conditions, in the same first-person style, ready for you to read, edit and copy onto your PIP2 claim form or AR1 review form.

K
Karol Slusarczyk
Founder, FillMyPIP · t/a Benefits Expert · ICO:00014179042

I have spent years helping people describe their conditions accurately on PIP forms, and I built FillMyPIP from that experience. I wrote this worked example to show, honestly, the kind of detail and wording that helps an assessor understand what hearing loss is actually like day to day. I am not a solicitor, a doctor or a DWP employee, and this is guidance, not legal or medical advice.

Now generate YOURS

Tell us about your hearing loss in your own words and we will write one full activity for you, free, before you pay anything.

Fill my form - free preview →