Showing posts with label Health Policy. Show all posts
Showing posts with label Health Policy. Show all posts

Thursday, November 2, 2017

Progressive Policies Needed to Support People with Disabilities: Demand Mental Health Parity

'I have lost hope': the people with mental health problems who are being stripped of their benefits | Society | The Guardian
DailyDDoSe © November 2, 2017 

I have written and thought about this issue quite a bit. I suffered an injury that left me completely debilitated for about four months in constant, excruciating pain. 

Despite that awful experience, nothing was as awful as living with severe treatment resistant depression for most of my life. 

Just because you couldn't see my pain on an x-ray or couldn't see past a pretty smile hiding the pain inside doesn't mean it didn't exist. 

The pain consumed me. I am grateful every day for effective new meds, the treatment I received, and wonderful supportive friends who don't judge me when I have a bad day or two and need to let off some steam. 

It is critical that we not only support people while they fight their way through and back from depression and other mental health issues but we must pass progressive policies that provide equal, adequate and accessible care to people with mental health issues. 

Most people with mental health issues can live productive lives if and only if they receive proper treatment. 


Elyssa D. Durant
Research & Policy Analyst 
Columbia University, New York


'I have lost hope': the people with mental health problems who are being stripped of their benefits

Personal Independence Payments – the points-based system for disability claims – only works for people with physical disabilities, say campaigners. We meet some of those who feel they have slipped through the net


Kloey Clarke at home in Devizes, with her son Seth.

Kloey Clarke, 28, from Devizes in Wiltshire, has had severe anxiety and type II bipolar disorder for six years. "I'm scared to leave the house," says Clarke, who does not feel emotionally or physically stable enough to hold down a job and relies on her husband for care and support. "I have a constant fear of dying. I can't socialise and I can't communicate outside [the house]." For four years, Clarke depended on a Disability Living Allowance (DLA). The DLA was replaced by Personal Independence Payments (PIPs) in 2012 – and phased in from 2013 – but she was receiving them for less than a year before she was reassessed by the Department for Work and Pensions (DWP) and told she no longer qualified.
Clarke believes that the assessment for PIP is aimed at people with physical disabilities and does not account for mental illness. "I was asked if I could walk 200 metres unaided. No, I don't need a stick or an aid, but I do need my husband or someone with me. Can I talk to people face to face? I talk to my family when they visit, but can I speak to strangers? No."
She has had panic attacks as a consequence of losing her benefits, she says, and her family is now struggling financially. They have had to visit food banks twice since being rejected for PIP, but Clarke's pride has stopped her from going more frequently. "I just find it so degrading. I don't feel as if I should be there. I feel that, if I just had what I deserve, then I wouldn't need to be in that place; I wouldn't need to take food from, say, homeless people."
Clarke's marriage and her relationship with her children are suffering. "I'm useless to them, I'm not half the mum that I could be. I haven't got enough funds. The government has no idea what these types of assessments do to people with mental health [issues]; how much it takes to walk into that room and talk about something so personal and then be told you aren't ill enough."
The evidence is mounting that people with mental health problems in particular are being failed by PIPs, with claimants reporting that the new system takes no account of the needs of people with conditions ranging from schizophrenia to severe depression. Figures released by the DWP in October showed that complaints about the PIP assessment process increased by 880% last year. The number of complaints that were upheld rose similarly dramatically, by 713%.
The DLA was first introduced in 1992 by John Major's Conservative government and was paid to eligible claimants who had personal care or mobility needs as a consequence of a physical or mental disability. PIPs were introduced by the coalition government as part of the 2012 Welfare Reform Act, and have been steadily replacing the DLA since 8 April 2013. Some claimants who received indefinite DLA awards were not being reassessed, and the government then argued that it was necessary to have a system that frequently assessed people in order to determine if their needs had changed over time. In 2013, the then work and pensions secretary Iain Duncan Smith told the Daily Mail that "70% of people on it [DLA] have lifetime awards, which means no one sees you ever again. It doesn't matter if you get better or your condition worsens – it's quite ridiculous."


The big differences between PIP and DLA claims arise from the assessment criteria. DLA is based on an individual's condition and the needs arising from this, while entitlement to PIP is assessed using a points-based system. Claimants are typically invited to a face-to-face assessment in a private consultation room, but are sometimes assessed in their homes. People score points according to their ability to complete a number of everyday activities, such as washing and cooking, and whether they need aids and appliances or help from another person to do so. According to Full Fact, an independent factchecking charity, between October 2013 and October 2016, 22% of DLA claimants with mental health conditions had their benefits reduced when they were reassessed for PIP, and a further 25% lost them altogether.
Many of the people I speak to say the PIP assessments do not take into account the effect their mental health conditions have on their lives. Some say that, even though they are physically capable of preparing a meal, driving a car, or dressing and washing themselves, the ability to do these things changes all the time. This is especially the case with conditions such as clinical depression or bipolar disorder, when, on some days, a person may find it difficult to get out of bed.
Daniel O'Connor, 64, from Glasgow, has led a tough life. He has severe depression and adjustment disorder, and has twice attempted to end his life. O'Connor had been receiving DLA for nearly 22 years when, this year, his application for a PIP was rejected. Since then, he has experienced financial hardship and says his condition has worsened. O'Connor says he felt as if he wasn't being listened to at his PIP assessment and recalls telling the assessor that on some days he struggles to get out of bed because his depression is so debilitating. However, his assessor dismissed his story, citing the fact that he could drive as evidence of his ability to carry out everyday tasks. "We got to discussing a previous suicide attempt I had [made]," he says. In the final moments of the interview, the assessor asked him seven times if he was going to go out of the door, there and then, and kill himself. O'Connor adds he found himself in the position of having to placate the assessor. "It seems to me that her concerns were not about me; her concerns were about what the reflection would be on her if I did go out of the door and kill myself."
Rejected PIP applicants have the right to appeal the decisions made by the DWP, and statistics from the Ministry of Justice show that 65% of appeals are ruled in favour of the claimant. Campaigners say this demonstrates a systemic ineptitude in the way the assessment criteria are being interpreted.

Alison Smith with her husband, Mark, at home in Beverley. Photograph: Darren O'Brien/Guzelian

Alison Smith, 55, from Beverley in Yorkshire, cares for her husband, Mark, who has bipolar disorder. Mark "is unable to go out without someone with him or socialise", she says. He can go for days without washing, dressing or eating. He will neglect his medication if not reminded and has self-harmed. The couple have lost other benefits, including their housing benefit, since losing PIP and they have been relying on a lump sum from Alison's pension to get by.
Alison had a difficult time at her husband's appointment. "The woman who did the assessment was horrible. She wouldn't let Mark speak. When he tried to say anything, she kept saying: 'No, I'm not interested in that – I need to go through what's on this computer.' They don't look at the mental illness side of things. Mark has the [physical] ability to make a sandwich, but he doesn't have the mental ability to do it."
"Often, we hear from people with mental health problems who tell us that they dread the face-to-face assessments," says Paul Spencer, policy and campaigns manager at the mental health charity Mind. Spencer adds that, as well as reforms to the Work Capability Assessment, used to determine one's eligibility for Employment Support Allowance (ESA), "we also urgently need the government to overhaul the PIP assessment process to make sure it is fit for purpose – and delivered by people who really understand how someone's mental health problem can affect their daily life".
Lorna Crofta's story illustrates this lack of understanding. Crofta, 53, from Worcester, has had severe mental health problems since childhood. She was awarded DLA for three years and then invited to apply for PIP this year. Her application was refused because she failed to attend her assessment – she had received a diagnosis of bowel cancer and the assessment was scheduled just before an operation to have a tumour removed. "I had come to a complete standstill physically, and that had an additional impact on my mental health. I hadn't even opened my post for weeks and had gone beyond thinking in a rational manner about anything. I would not have been able to handle someone being in my house." Crofta says she has been living in poverty all her life. Even before losing her DLA, she says, the benefit wasn't allowing her to do much apart from securing basic subsistence. "My life is just existing between one appointment and the next. I have lost hope. I dread how much worse things will be if my appeal is turned down."

Lorna Crofta in Worcester. Photograph: David Sillitoe for the Guardian

The shadow work and pensions secretary, Debbie Abrahams, has seen first-hand some of the hardships disabled people are facing as a result of the government's welfare reforms. "The number of cases I get, not just in my constituency but right across the country, is shameful – and shameful on the country as a whole," she says, from her constituency office in Oldham. The system, she argues, is designed to put people off and to stop them claiming, "and, unfortunately, it's working". Abrahams adds that the assessors need to be held to account: "The fact that two-thirds of assessments are overturned on appeal just shows the fact that it is a warped system."
The DWP responds: "PIP looks specifically at how someone's life is affected by mental health, unlike the old system, which did not sufficiently recognise mental health problems." They add that there are now more people with a mental health condition receiving the higher rates of PIP than their DLA equivalents. "PIP ensures that mental health conditions are given the same recognition as physical ones. It does this by considering how impairments affect a person's life, rather than labelling individuals on the basis of a condition."


In February, the DWP was advised by judges at the Tribunals Service (the branch of the Ministry of Justice that oversees tribunals and adjudications) to award more points on the mobility assessment of the claim if people suffer from "overwhelming psychological distress". However, because of concerns that these changes would cost an extra £3.7bn by 2022, the government enacted legislation reversing the judgment: it altered the mobility criteria to exclude people who had psychological distress – specifically, psychological distress caused by following the route of a familiar or unfamiliar journey when travelling alone. The move will mean that 292,500 claimants will no longer be entitled to any mobility component, which could affect people with a wide range of conditions including learning disabilities, autism, schizophrenia, anxiety conditions, social phobias and early-stage dementia. The government argued that the judgment had "interpreted the assessment criteria for PIP in ways that are different to what was originally intended".
In April, Valerie Grant, 73, killed herself after her severely autistic son was told he did not qualify for disability benefits. Her death came after a UN report, published in November 2016, concluded that the UK government has failed to uphold the rights of disabled people, a verdict the UN reached again this August. Areas of concern highlighted in the UN's report are high levels of poverty for disabled people and their families and reduced standards of living as a result of multiple welfare reforms and benefit cuts. One of the welfare reforms highlighted for criticism is the criteria used to assess people for PIPs.
In response to the UN's findings, the DWP said: "We're disappointed that this report does not accurately reflect the evidence we gave to the UN, and fails to recognise all the progress we've made to empower disabled people in all aspects of their lives." It added that the government spends over £50bn a year to support disabled people and those with health problems and that "it is encouraging that almost 600,000 disabled people have moved into work in the UK over the last four years".
Abrahams says that Labour, if elected to government, would aim to scrap both the Work Capability Assessment, the ESA and the PIP assessment, and devise a system that doesn't look for ways to stop someone's support. She says: "First of all, we should recognise and value what our social security system is for, and I make it absolutely clear it should be like the NHS. It is there for everyone in their time of need and we should value it." In the meantime, disabled people will have to continue to battle the DWP for access to benefits.
O'Connor says he has experienced financial hardship since losing his benefit, but that has been mitigated by the fact that he is approaching state pension age, and the fact that he receives money from private pensions. "I'm very lucky that I'm in a situation where I will not be made homeless, but, even if I was, I still wouldn't give up. They could sanction me to death, but I will not be doing their job for them; I will not be killing myself."
In the UK, the Samaritans can be contacted on 116 123. In the US, the National Suicide Prevention Lifeline is 1-800-273-8255. In Australia, the crisis support service Lifeline is 13 11 14. Other international suicide helplines can be found at www.befrienders.org.


^ed 

Tuesday, March 28, 2017

Reality Check: 47 Million Underinsured and Uninsured in America

I am one of them: here's my DailyDDoSe March 28, 2017


We live in a society where no one accepts responsibility for their mistakes; no one is held accountable
for their actions; and one EVER, EVER says they are sorry.

Let me show you a small glimpse inside the typical day of the 47 million uninsured and underinsured in the wealthiest nation in the world: The United States of America.

As someone who spent years as one of the 47 million (source RWJF.org) I spent day after day after day doing the same thing without any result or consequence.

I can only offer
you a glimpse into day in the life because there is no room to sit in my car with all the files, medical records and appeal documents.

I believe my apartment may actually be a fire hazard...

This was my daily update posted at 7:30am:

As for my most recent insurance dispute (2008) little jas changed and I feel I have done everything humanly possible to
protect health care providers who are NOT providing health...

I cannot clean up the slack for my every underqualified, health care provider (who did NOT provide adequate care to my patients or myself). However I feel I have no other choice than
to share what I have learned...

Having been on both sides if the proverbial couch, I have the perspective
that is both enlightening and scary at the same time.

Sometimes I try to look at this fight, (I meant to say this life) objectively.

I can see my own future, and I can see where it is taking me. I know how it will end it I don't thinks I can
keep up the
pace.

It is amazing at how far we will go to have nothing at all.

I have come this far, and on some level I almost enjoy the dance.

No.

On some level, I actually love the
dance.

No. I won't give up now. Because without this turmoil, this means an end to this demonstration project of futility and determination, amd without that I am nothing at all. I can't lose what I never had.

I won't be another sell-out; mostly because I don't know how.

I am the voice of perseverence. I am one of 47 million Americans with sunstandard medical care.

And today I am I am still fighting the good fight.

This battle; this challenge; this half won war has come to define me. And without that, I am really nothing at all.

As someone once told me, if you don't stand for something, you'll fall for anything. I've already fallen, but I sure as shit stand for something.

So for now, I write. Maybe later, I will listen. And if there is any justice left in this world, maybe someday I will actually live.

Just me,

Elyssa D. Durant, Ed.M., ABD
Research & Policy Analyst

^ed 

Friday, August 30, 2013

UNWRITTEN: Harry and Louise: Adding Insult to Injury?

Harry & Louise: Adding Insult to Injury? 

My first spring back in New York, we used to joke about J-School: Were they trying to tweak our skills turning us into experts in public journalism or public relations.

I took my first graduate level class in public journalism on the 4th floor at the infamous J-School located inside the cool steel gates separating surrounding Morningside Heights. 116th street from the homeless and the winos’ asking everyone all the passer by's for money just before we walked through the iron gates leading to the Ivory Tower. 

The blocks surrounding 116th-120th where only the young and the talented get ready to take their place in society. 

We would pass the men living on the streets each day, enter through the solid stone doors that were 12 ft tall, and write about them.  With such eloquence you would hardly know they were homeless at all.  We exploited them.

Just like Tuskegee exploited the Blacks, and the Army exploits the young and the rudderless, we exploited the sick irony of paying more per credit than they earned in one year on Veterans benefits or disability.  

We disgust me.  

But Karma is a bitch, because less than 2 years later there I was, sleeping in the law school stacks; showering in the indoor pool...  gym because I “looked good enough to pass through the gates.”  I had that Ivy League pedigree. The would-have-been Harvard Law student—maybe even have had it paid in full had I been a boy or born to a different mother.

What the fuck did they know?   That cute little Jewish Girl from Long Island, the one from a "good" family... the Harvard Legacy with the beautiful mother always dripping in jewels and fur from her latest boyfriend or husband—that little girl was me.

I should have been the perfect example of how a power player in the making the benefits from good breeding.  No one ever needed to know that beneath it all I worked my ass off to get into College and ultimately get a scholarship into the top ranked program in Sociology and Social Policy to effect change.  The fact that I dropped out of high school at 16 could remain my dirty little secret. 

And to this day, no one has ever come forward to expose that little truth.  Probably because so few people know—Maybe three or four  So would I reveal such an embarrassing little detail of my life and risk my reputation on something I should have left behind me over twenty years ago?

Because it matters.   

No one needed to know.  I can get by well enough on my looks, I speak quite eloquently, and usually appear normal to most, but it is an important little factoid because people constantly judge ME based upon who they think I am – either the girl with the wealthy parents, or a lazy too stupid too get off welfare. 

It matters because what appears to be and what is are often two very different things.  I am in fact, an Ivy League Alumnus.  I did in fact get a full scholarship into the PhD program in Public Policy at a leading University. 

I am in fact unable to find employment and live on a ridiculous monthly allowance from Social Security (Supplemental Security Income) the lowest of the low.  I am so far beneath the poverty level (already ridiculous) that I often wonder how I manage to live at all. 

So that "legacy," the access I once had to the Ivory tower on the 4th floor we wrote is now gone.  Not because they didn't like my work-- they loved it!  Solid A in Public Journalism. 

Well if I were in New York today, I would most likely be one of the people o the streets.  Actually, I would probably be sitting across the street at the Bookstore just so I could stay close to the vast amounts of wisdom and philosophy within the hollowed halls as classes break for the summer. I would be watching people go in and out and be envious that they had the one thing that I don't: access.  

So I made it through the very Same J-School where Pat Buchanan refused to speak to his Alma-mater because he once punched someone in the face on the 5th floor.  I made it through despite the fact that I often times slept in my car in the middle of winter because I could not afford gas for the commute and eventually lost my apartment.  I made it through having no electricity and frozen water pipes.

The question is: can I make it through this?  I paid my dues. I deserve a chance.  Dammit, I deserve a do-over.  I deserve a job.   I deserve a little credit. 

Will our policy decision be based upon our need for reform or the ability to perform?

We used to joke about all the sell-out Journalist who give up on reporting the news to become speech writers for politicians.  How people like Pat Buchanan (a J-School alum) became so skilled at using their words to  sell ideas in such a way that people actually believed the propaganda they were sinning.

I have given much thought to this... the only people who are more arrogant and self serving than politicians and academics are reporters!

I think they become addicted to the their own power to manipulate people and they are willing to trade a little tarnished idealism for power and inflated self-esteem.

I am not one of those people. I care enough about the issues to take the time to examine them from all angles-- and I fell that the massive amount of money being spent by agencies that I hold in deep respect launching a counter-attack on the insurance companies and their ad execs will have serve to damage their reputation.  I chose to volunteer with these agencies because I believe they are well informed and do a great job to involve the everyday average Americans like myself in the political process. 

By spending $750,000 on advertising, these groups now seem to be on the same level as the Insurance Industry and others who exploit the poor and infirm at the mercy of the healthcare marketplace. 

So I take issue with this campaign.  Let Rick Scott be heard.  Using such tactics will make the good guys no better than the Insurance Companies that exploit us all.

Are these ads showing us: how to reform or how to perform?

The large amount of funds being thrown (public or private) being spent on media fluff, and emotional being spent on media propaganda and 'skittles' on both sides of the healthcare debate.

I am offended by the huge amounts of money being spent on propaganda and skittles by both sides of the healthcare debate. Excessive, exorbitant monies being spent to manipulate the public through misleading ads, expert analyses, media alerts~ this is insulting at best.

Real dollars being used to manipulate the public about real issues: the sick; the poor; the ignorant... We are selling bad data and information to those who need it the most.

Talk about adding insult to injury?  I do hope HCAN, HealthJustice and others will reconsider this campaign.  I am one foot soldier who is unwilling to participate in this one.

Bottom line is this: we need to stop manipulating images and perceptions about the reality of healthcare, education, and social welfare in the United States.  All is not well in America.  Not well at all.  And I am here to prove it!

Elyssa D. Durant, Ed.M.
United States of America