Please Note: The question of COPD – will it kill you, and variations on that theme (will I recover, will I get better, etc), is addressed specifically in this post . All my COPD-specific posts are collected together here.
Note: this is a very long post, I’m afraid, so to find a specific item, use your browser’s Find function for a keyword search of this page and successive pages. This normally lives in Edit, in the toolbar, at least it does in Firefox, Opera and IE.
This post grew from my responses to Google searches that bring people to my blog, when what they’re looking for isn’t already covered. These searches generally relate to benefits, medications, Motability, ME/CFS and COPD, and for the most part, and I’ll do my best to cover them here. Note:- Benefit answers aren’t just off the top of my head, they’re properly researched, even if I already know the answer, as is anything else of which I don’t have personal knowledge.
February 10 2009 – this post is as long as it’s going to get; it’s a whisker away from 10,000 words, and this paragraph takes it past that level. In future new items will get their own individual posts. I’m reluctant to stop adding to this, as it’s my all-time most popular post, but I think it’s a matter of people being able to find information quickly. I’ve suggested, at the top, using the browser Find function, but people will still do their own thing, and scroll down, and there’s probably a limit at which they stop bothering. If you think I’m wrong, do tell me. By the way, 10,000 words is the equivalent of 20-25 A4 pages (depending on font and size), just to give it some perspective.
Obviously, by its nature, this is a work in progress, so if you have any questions about the above subjects, the areas in which I have personal experience, post a question in Comments and if I can answer it, I will. (NOTE:- Comments are moderated before being posted, so I can read them and delete them for those who require confidentiality):-
M
Can my wife work if I get DLA?
Absolutely – it matters not at all who works, even you (see below). Conversely, if they qualify, both partners can claim DLA – one person’s claim has no effect on another.
Return to work and lose your DLA?
There is no reason why working, of itself, should cost you your DLA. DLA can be paid regardless of income, wages or savings. It is paid for mobility or care – or both – and the need is not automatically obviated by working. I believe that if a claimant starts work, then that will trigger a DLA review, and THAT may result in loss of benefit, but it need not. I used to know a guy who worked and claimed Mobility Allowance, as it was before it was DLA, but his disability was incontrovertible – he’d lost a leg, and no-one can argue with that. Were I able to return to work – fat chance – then, because of the nature of my disability, I would find it very hard to justify continuing to claim DLA, and I would almost certainly be re-assessed, and lose it. The bottom line – working does not automatically prevent you claiming DLA, or retaining it if you already have it, it all depends on what’s wrong with you.
Attendance Allowance & COPD
That depends on age. Up to the age of 65 the benefit is DLA; over 65 you can no longer claim DLA but you can claim Attendance Allowance. In either case, the benefit is payable for COPD, providing it is sufficiently disabling. As with any illness, simply having it isn’t a qualification, it’s the disability that counts.
“clenil modulite”+”alcohol”
Presumably the questioner wants to know if you can drink with Clenil Modulite, a steroid inhaler. The answer is yes. Unlike oral drugs, inhaled drugs go straight to the lungs, they don’t get there via the GI tract and the blood stream, so alcohol has little/no effect. There is, though, with CM at high doses (2 puffs 4 times daily and up), the prospect of systemic side effects like those you get with oral steroids, including weight gain, which alcohol will exacerbate.
DLA medical examination uk – how to pass
It’s not a matter of passing – it’s not a driving test and there are no right or wrong answers to the questions.
The simple answer is to always tell the truth. That is, the version of the truth which is beneficial to your claim. If, say, you can walk a mile every few months on a rare good day, but usually are restricted to a short distance, then the latter is the truth in reply to the questions about how far you can walk. Actually, the question is about how many metres/yards you can walk without pain or discomfort. In my case, as pain accompanies every thing I do, the answer is zero. If it’s, in your case, say 40 yards, don’t say 10 yards, because there’s a good chance they’ll take you for a walk – they did with me (and just saying ouch, ouch, when you reach your limit won’t wash!). Basically, it’s what your normal situation is that matters – you don’t tell them about good days. That’s not dishonesty, it’s irrelevant. You don’t say how much you can do if someone helps you, either. It’s all about your unaided capabilities.
Unlike in the past, you don’t apply for the components of DLA (they used to be separate benefits, Attendance Allowance and Mobility Allowance), you submit a blanket application and wait and see what you get.
A medical examination is pretty standard, to verify your disability, and if you take a lot of medication for your condition, you may think it’s a good idea to reduce it or just not take it – I couldn’t possibly comment. I would suggest, though, that you insist on being examined at home. My personal view is that if you are well enough to go trekking off across town – or further if you live in a rural area – then that might adversely influence how you are perceived.
If you are asked to perform any actions that you feel would be harmful, then refuse. I can’t kneel, for example, and if asked to demonstrate that, or climb stairs, or bend down – anything, in fact, that involves bending my knees beyond an absolute minimum, I would refuse, because it would damage my knees, the ligaments, and leg muscles, and I’d be even more disabled for weeks. They cannot refuse your benefit on the grounds of your refusal; you are within your rights to refuse to injure yourself. Explain, though, just don’t say no.
If you have a mental illness, then you may want to take a close friend with you who can speak for you, or seek a benefits advocate, if you feel it would be difficult for you to properly explain your situation. In fact, I would suggest that anyone does this if the claim is turned down and goes to appeal. One thing you should not do, at appeal, is come up with new stuff that you should have told them in the first place, it just makes them suspicious. Unless, of course, your condition has deteriorated in the meantime. And one thing to bear in mind is that most rejected claims are granted on appeal.
Appeals are a pain in the butt. I’ve never been to one, but I understand that you’re pretty much treated as if you’re lying. My advice is to be firm with them but, no matter how justified you might feel, never lose your temper. A favourite tactic is to repeatedly ask the same question. My advice is that asking twice is acceptable, more than that is not, and a polite “We’ve covered that at length, can we move on? would be perfectly in order.
I’m sorry I can’t be more precise than this, but everyone’s experience of the application process is different. I’ve never had any problems with benefits, though I’m wary of applying for the middle care rate (I already get lower care and higher mobility), as every time you apply you’re reassessed, and that’s risky.
I also know, very well (this isn’t hearsay from the Daily Mail!), a woman who is little more than a hypochondriac, yet in her time she has managed to get every disability benefit available, including direct payments to hire her own care staff. Go figure.
One final though – fill in the downloadable application form from here . That way you’ll have a copy of everything. Also, you may find it easier to type your answers on separate sheets of paper. This is acceptable as long as your name and NI number is at the top of each sheet, and you show the numbers of the questions your answers relate to. I also date and sign each page, but that’s not a requirement.
Clenil Modulite gains weight
Not necessarily. Like any other steroid, it all depends on the dose. As I say above, at high doses with this high-strength inhaler (2 puffs 4 times a day), you get pretty much the same systemic effects as with oral steroids like Prednisolone (Prednisone in the US), including weight gain, and you should carry a steroid card. Clenil Modulite is a replacement for Becloforte, and contains the same drug with a CFC-free propellant, so you should expect the same side-effects. In addition I’m convinced that it causes increased sputum production, which is not a good thing.
Tesco website access issues
For a major player in the online retail market, Tesco’s website is pretty rubbish. The only way to ensure proper functionality in all areas is to access it via Internet Explorer – it malfunctions badly and unpredictably with Firefox, though it seems OK with Opera.
How long am I contracted to my motability
I’m not entirely certain what the questioner is asking, but the standard period for DLA-based contracts (HP or lease), is three years.
Help, I can’t get d.l.a. and I’m ill
A common complaint sadly, but being ill isn’t a qualification for DLA – being disabled by your illness is – the two are quite different. There is some advice about DLA above, and also elsewhere on this blog – type DLA into the search box at top right, and the titles of the posts it throws up will show which are relevant (DLA also cops up in posts which aren’t about benefits. In addition, if you’re in the same position, post a comment and I’ll see if I can help. Comments are moderated before they appear, so if you want confidentiality say so, and I’ll delete your personal details.










just to say my father enjoyed reading this,and did have astroke 12 years ago,allso suffers from emphysema,copd,hypertension its that bad that is doctor cant controle it properly,allso hiyatas hernia and acid reflux,panic attacks,infections,cant win, filled in ib50 about 5 weeks ago waiting to here from atos health care, he never thought that he would ever would have to call this labour goverment a shitehouse and uncareing loads of robing bast^rds picking on the disabled,cant believe it, even the dwp said its negible only 1 percent on the fiddle and they are catching more and more all the time,but who can we turn to the tories are the same. he as allso just been told that he might have or could have artheritas,not that the doctor would say that he does have,i dont think the doctor dare say that he does have,im afraid that my farther is afraid of being disabled now as do all the other genuin disabled people.
Hi John,
COPD should be manageable, with the right meds. If your father’s not not already attending the chest clinic at your local hospital, he should be – he may well get better meds there. Some GPs also have an odd idea of what constitutes adequate medication for COPD – the last post in the list below is what I take. The thing to bear in mind, though, is that “manageable” doesn’t equal normal – with COPD normal lung function, no matter what the medication, can never be regained.
Check out these posts too:-
http://ronsrants.wordpress.com/2009/01/29/a-bed-wedge-for-copd/
http://ronsrants.wordpress.com/2009/01/31/a-tip-to-alleviate-acid-reflux-gerd-in-copd/
http://ronsrants.wordpress.com/2009/01/16/copd-meds-and-potassium-deficiency/
http://ronsrants.wordpress.com/2008/12/24/copd-and-calcium-antagonists-a-personal-view/
http://ronsrants.wordpress.com/2008/10/05/copd-and-acid-reflux/
http://ronsrants.wordpress.com/2008/06/06/drugs-for-copd/
my father says thanx for the links, is med for copd is ventolin,clenilmodulite,serevent.and spiriva,but still as days were he is gasping for breath allso at nights were he as to take is sprays ,allso panick attacks its quite frightning to see him this way allso as i said he had a stroke 12 years ago and is disabled down is right side, from is daughter emma
is it worth putting down about a minor learning difficulty on a DLA claim form? my partner is trying to claim DLA and whilst filling out the claim form i noticed that an example of an illness/disability was learning difficulties. my partner cannot read or write very well and always asks me to fill in any forms, write any letters and read his mail. is it worth putting this on the claim form as he hasn’t been diagnosed with it but we are very aware of it in everyday situations?
Put down anything that seems appropriate – it may help. Just one thing, though – is it genuine, diagnosed, learning difficulties or plain, old-fashioned illiteracy? I used to work as an adult literacy tutor, and I know from experience that there’s a lot more illiteracy than most people suspect. There’s also another reason for asking – you may be asked for supporting evidence of learning difficulty and/or the DWP will check it out for themselves. If you’re sure, then yes, go ahead.
If, though, it is illiteracy, then there is probably an adult literacy scheme somewhere in your area, if your partner is interested – from experience, with a good tutor, fluency in both reading and writing can be achieved in a year.
Hi I really need to know if your national insurance contributions are paid if you recieve DLA. I recieved higher rate in the past and i was told that it would cover my stamp to but now I am getting told i owe them payments because my stamp isnt up to date. Any ideas?
If there is any NI credit it’ll be with Incapacity Benefit (or Income Support), not DLA, the mobility component of which is related to the degree of disability whether you work or not .
Whether there actually is any NI credit with IB seems to be a secret! I’ve tried all the search terms I can think of on Google and come up blank. If you’re getting IB the best thing to do is talk to the office that administers your benefit. Logic suggests that if one is on long-term disability benefit, like IB, then there would be a NI credit built-in but, sadly, logic has nothing to do with benefits.
I am too ill to work and I have just been diagnosed as having fibromyalgia. Is it recognised as an illness? could I claim?
Hi Liz,
The important for a successful DLA claim is how disabled you are.
You’ll find a link to download a DLA form, along with some advice about claiming, on this page http://ronsrants.wordpress.com/2009/07/07/claiming-dla-and-esa-some-tips/ .
There’s also a link to get an ESA form there too.
Note that DLA and ESA are unrelated benefits – you can claim one without the other.
Hi Ron,
I was diagnosed with CFS last year. Determined to get better I did a staged return to work and built up to 4 days in the office with 1 day working from home. Didn’t do much else though and 2/3 weekends out of 4, I’d just sit around at home trying to recuperate for the week ahead.
Sometimes, not often, I’d have a good phase when I was able to do more outside work then suffer the consequences with the delayed fatigue, malaise etc. For example, I had a week off at the end of August and did a couple of longish walks. 4/5 miles perhaps. I felt unwell returning to work and have recently had a bit of a relapse. So now I’m off work for a bit and the most I can manage is a short shuffle to the corner shop, and I’ve only done that twice in the last 9 days.
I had an ATP profile test done recently. The results were a bit of a shocker to be honest. They show badly impaired mitochondrial function with a disability rating of 25/100 – a rating of 30 would mean I was able to do 2/3 hrs office work with breaks, rarely leaving the house.
The test results show a high cell free DNA score of 22ug per ml (I think). This seems to indicate my body’s been making energy in a rather costly way and tissue damage is occuring as a result. In short the disability rating is the amount of energy I have to spend, if I go over it I will end up paying for it in unpleasant ways.
Several people on the ME boards have mentioned these results will help with a DLA claim, however, it never occurred to me that I would be eligible because I’m working.
This week I’ll be picking up 7 prescription items and have had the expense of taxis to go pick up stuff from the chemist. When I am more well, I would just walk / bus / walk, but in this relapse phase that’s simply not a good idea. I think I probably could push myself and do it but it would make me feel very unwell – nauseous, faint, strong compulsion to lie down & recover. No pain though for which I’m very grateful.
Given the cost involved with the medication and the necessity of having to get taxis at the moment to just do the essential stuff, DLA would really be useful. I’m worried reading the other posts that it would be very hard to fill in the forms as my clinical level of ability is greater than my bio-chemical level of ability. Plus it fluctuates so greatly. There is no ‘normal’.
Apologies for the long post, are you able to recommend anything. Should I just not bother if it’s going to be too much hassle?
Regards,
Sue
Hi Sue,
Just a quickie – I’m on my way out – but DLA is payable whether you work or not. The mobility component anyway – not sure about care but logic suggests not. One caveat, though – DLA depends on demonstrable disability, not numbers. The bottom line is how well you can walk (and you may be asked to prove it – I was).
Have a look at this post http://ronsrants.wordpress.com/2009/07/07/claiming-dla-and-esa-some-tips/ there’s some useful advice and also a link to download a DLA application. Personally, I don’t find the form difficult. But then, I spent much of my working life filling forms for HM Customs and for foreign consulates, and compared to that, benefits forms are a breeze. Anyway, if you have any problems, you know where I am.
Oh – an important point. The DLA people (or anyone else involved in benefits), are not your enemies, no matter what you might read elsewhere – they’re just normal people doing a thankless job. Be nice to them, and they’ll be nice to you – that’s my experience anyway.
And be aware that almost everyone is having problems claiming right now, from what I’ve heard, so don’t be disheartened if you’re turned down – it doesn’t end there, and many cases are successful on appeal.
hi ron,ive been on the lower rate dla i am now 69 and was diagnosed with copd and emphysemia have i any chance of getting the middle rate of dla,thanks rita
Hi Rita,
Sorry for the delay – having a bad spell. There’s absolutely not reason why you shouldn’t reapply. You may even get the higher rate mobility. Before you do though, you need to make sure your GP, and any consultant, will support your claim. If they will, you’re in with a chance.
These days, sadly, a chance is all it is. There are no guarantees, I’m afraid – judging by the comments on some of the posts here, DLA is getting harder to claim successfully. Doesn’t mean you shouldn’t try, though.
Oh, almost forgot – make sure you’re adequately medicated – they do take that into account though, personally, I think that’s bugger all to do with them.
Ron.