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changes to support for people with disabilities

24 replies

hatwoman · 21/10/2010 17:40

if, like me, you feel angry about this Scope and Demos have a very good template letter to send to your mp. You put your details in, then the letter comes up, addressed to your MP, and you can edit it if you like, before sending.

[[http://e-activist.com/ea-campaign/clientcampaign.do?ea.client.id=1677&ea.campaign.id=8183
here]]

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herbietea · 21/10/2010 17:43

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2shoeprintsintheblood · 21/10/2010 18:42

well check out the sn children's topic as there is a thread in there a bout the mobility element being taken away if you are in residential care, that will affect a lot of people.
it will mean people like my dd, if when she is older she goes into residential care will never be able to come home as we will not have a WAV to bring her home.

2shoeprintsintheblood · 21/10/2010 18:44

done
will put a link in sn

sarah293 · 21/10/2010 18:52

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herbietea · 21/10/2010 18:55

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sarah293 · 21/10/2010 18:58

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herbietea · 21/10/2010 19:19

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hatwoman · 21/10/2010 19:29

herbie - it may or may not be strictly correct to say that "every" disabled person will be affected. but it's accuracy isn't really very relevant. it's pretty undisputed that an awful lot of disabled people will be affected.and it'll be the ones already in difficulty. The changes to mobility DLA as riven points out will affect those in residential care. And then the savings that are coming from changing the ESA system aren't coming from nowhere. they're coming from people who are already struggling.let's not get distracted by debating whether or not it's "every" disabled person.

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sarah293 · 21/10/2010 19:34

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herbietea · 21/10/2010 19:42

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sarah293 · 21/10/2010 19:54

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herbietea · 21/10/2010 20:10

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sarah293 · 21/10/2010 20:28

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2shoeprintsintheblood · 21/10/2010 20:56

tbh I don't see the need to argue, these cuts are going to affect a lot of people and lead to a lot of people being imprisoned in their own "homes" a lot of the cuts are unfair, but the are targeting people who have had no choice, they need defending

sarah293 · 21/10/2010 21:01

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Querelous · 22/10/2010 08:48

Thanks for the link Hatwoman. I have sent my letter to my MP adding a personal post script expressing my disgust at the rhetoric and implications of being 'work shy' applied to a lot of DLA claimants by the coalition and the media.

Also the short-sighted view that these people will be able to find work with the assistance of the proposed 'help' (I have an MA and have been job-hunting ardently for a proper job for over a year and only had 2 interviews for jobs on disabled schemes. I had been working in a care home at weekends until 6 months ago (when my husband left and I became unable to work weekends due to childcare needs for my DD now aged 4 but not yet in school).

Personally I do not recieve mobility componant only lower rate care (though was in the process of applying on reccomendation of social services).

These cuts are wretched. With a few exceptions they are being made by people with no fist hand knowledge of the situation. And we should fight them all.

Querelous · 22/10/2010 11:20

Ha ha "fist hand knowledge?" Must have been a Freudian slip!

poppyknot · 22/10/2010 13:28

Sent.

PestoEatsPumpkinsandSurfers · 22/10/2010 14:42

Thanks for alerting me to this 2Shoes, have done the email and put the link up on my FB too [hsmile]

MintyMoo · 24/10/2010 14:23

I have Dyspraxia and Fibromyalgia, am not claiming DLA as I am very fortunate not to need it at the moment. On bad days I need some help with getting out of bed, cooking etc but as I am still fairly young (20s) I am hoping it will be a while before I do need DLA. I struggled to get my current job after graduation, took me a year - Dyspraxia put people right off (Fibro dx was only a few weeks ago). I am almost 5 months in to it, prior to that I've only done bar work and shop work since I was 15. So far I have had a month off sick for the Fibro (return part time tomorrow) and around 4 half days off for brain scans, neurologist, neuropsychologist and Rheumatologist appointments. Not to mention a number of late starts/early leaves due to seeing my GP for medication, referrals etc. I'm still 6 weeks away from the end of my probation!

I worry that if I lost my job I would seriously struggle to find another. I worry that Remploy, the government funded organisation to help people with disabilities and health conditions find and keep work will have it's funding removed. I worry that others who are worse off than me will struggle to find work, will be told they are fit to work when they aren't and will have their quality of life seriously damaged. My DP is a civil servant in the Fast Stream so I worry that if he loses his job I'll have to quit mine and move back home as I can't afford to live in London on my salary - especially if my income is reduced due to having to go part-time or having prolonged periods of sickness.

I hate this implication that anyone with a disability is workshy or a benefit cheat. I hate this idea that just because some people with disabilities can do great things (like paralympic athletes etc) it means those of us who don't are too lazy or have the wrong attitude and we're 'disabling' ourselves by thinking we can't do things when in fact we can. My employers have actually been great lately but people who are sick for large amounts of time, people who need extensive adaptions to do a job are not as attractive to employers as those who don't on the whole. Especially not in the recession!

When I was dx with Dyspraxia my DP thought it was great I was finally diagnosed (as an adult) as it meant I would easily find a job as people would want me to fill their 'quotas' [hhmm]

People seem to think that Disability is some kind of amazing free ticket - you automatically get a job because you're disabled and will sue anyone who turns you down for one under the DDA/Equality Act, you don't even have to apply for DLA or ESA, your Dr just tells SS and they fall over themselves to offer you thousands of pounds a year in benefits. Motability cars are some kind of free for all where people who are on incapacity benefit for 'blisters' or 'bad back' get a nice, completely free, new car every 3 years. They don't realise how hard it is for people with disabilities, they don't know how hard people who look after people who are sick or disabled have to work. They think GP's just diagnose anyone who walks through their door with ADHD etc if asked to so their parents can claim benefits. They assume anyone with a learning difficulty is thick, but of course, they can push trolleys or stack shelves so it's ok.

My DP said that at his work, under the previous government, they had diversity training (one of his colleagues is blind and has a guide dog in the office) and were told that the Civil Service considered adaptions for disabled people as just as reasonable as someone who wasn't disabled asking for a light bulb in a dark room with no windows to enable them to do their job. If only everyone else thought the same way!

I am going to get off my soap box and write to my MP now...

NutmegSprinkles · 25/10/2010 01:12

It makes sense for the DWP to assess couples on their household income - surely that's what a committed relationship is about, sticking together in sickness and in health.

The one year limit for contributory ESA just brings it into line with other benefits - I know women who have claimed it for years even though they have a DH on a high salary. Yet other couples who were on income-based benefits have always had them when if one partner's wage is too high.

poppyknot · 25/10/2010 14:00

From the Andrew Marr show yeterday interview with Douglas (not Danny!) Alexander.

ANDREW MARR:

So where in your area, the welfare area, would you make cuts?

DOUGLAS ALEXANDER:

Well I've said for example on disability living allowance, we need to rewrite the rules and we will work with the government to support them as they rewrite those rules to make sure that we transfer people in a more fair and equitable way. Secondly, I've said that we should look at the transition that's already happening from incapacity benefit to employment support allowance. So those are two clear examples where I think we should do more.

'Rewrite the rules?' So make it nigh impossible to claim maybe?

knowyourrights · 18/02/2011 23:10

The RNIB in conjunction with MIND have a letter which you can copy to your MP against the proposed changes to esa. Please forward to anyone and everyone you think might be interested!

www.rnib.org.uk/getinvolved/camp ... nd_IB.aspx

cory · 19/02/2011 10:58

Don't quite get herbie's argument. My dh works for the council, where they are currently debating whether to axe jobs (which will almost certainly mean his) or simply do 10% pay cuts. In any case, I'd be surprised if dh's department lasts much longer. I still don't see these situations as parallel: dh can try to get another job, but for a disabled person changes in DLA may well mean the difference between being able to do any job and never working again. For a disabled person in a residential home, cutting the mobility component may mean confining them to four walls forever after. Dh can move, my paralysed MIL can't. And even if he does end up unemployed, it is a lot cheaper to be live if you are able bodied. So I am quite happy to support this appeal without asking any DLA claimers for reciprocation in an area that is more immediately urgent to me.

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