Disability Model Isn’t Working

Published April 17, 2013

By John Hood

by John Hood

I’m glad to see news reporters and policy analysts devoting increasing attention to a subject Carolina Journal readers will find familiar: the role that public policy plays in discouraging work.

A key feature of the current, anemic economic “recovery” is that the share of adults who are active participants in the civilian workforce – whether employed or currently unemployed – is declining rapidly. If America had the same workforce-participation rate today as we had in January 2009, the national unemployment rate would be 11 percent – and higher than that in North Carolina. While some of the decline in participation had been explained by long-term demographic trends such as retiring Baby Boomers, there is clearly something else going on. It is evident, for example, among just the subset of workers aged 25 to 54.

Many people are starting to see rising rates of government dependency as one causal factor, particularly with regard to Social Security Disability Insurance (SSDI). Don’t take the word of this fiscal conservative for it. National Public Radio has been reporting on the phenomenon now for several weeks. Here’s an excerpt:

In the past three decades, the number of Americans who are on disability has skyrocketed. The rise has come even as medical advances have allowed many more people to remain on the job, and new laws have banned workplace discrimination against the disabled. Every month, 14 million people now get a disability check from the government. The federal government spends more money each year on cash payments for disabled former workers than it spends on food stamps and welfare combined.

A recent front-page story in The Wall Street Journal explored the issue from a different vantage point:

The unexpectedly large number of American workers who piled into the Social Security Administration's disability program during the recession and its aftermath threatens to cost the economy tens of billions a year in lost wages and diminished tax revenues.

As I wrote back in December, there are good reasons to believe that the doubling of SSDI enrollment rates over the past two decides wasn’t the result of a true doubling of actual disability rates. There is a statistical relationship between both economic performance and unemployment insurance benefits on the one hand and applications for disability on the other, for example. People become more likely to file for disability when jobs become scarce and when their UI benefits run out. Neither of those events is likely to cause people to become disabled, however.

People choose to work when they expect the real, after-tax earnings from a prospective job to exceed the value of staying out of the workforce. What value can there be in not working? Quite a lot, actually. In addition to the enjoyment of leisure time, those outside the paid workforce might derive significant value from rearing children, caring for other relatives, running households (which produces non-wage income in the form of home production of goods and services), and obtaining education (which produces higher wage income in the future, at least in theory).

Government affects the decision to work on both sides of the equation. It can reduce real, after-tax earnings by inflating the currency or increasing taxes. And it can reduce the cost of not working by offering cash or in-kind benefits that people lose when they go to work. SSDI has a particularly pernicious effect here because studies show that once someone goes on government disability, the likelihood of ever rejoining the workforce goes way down. The same can’t be said for private disability insurance, which typically has strong programs and financial incentives to see recipients recovered, retrained, and returned to the job market if possible.

I wrote about these issues at some length in a 2004 report entitled From Entitlement to Investment: Rethinking U.S. Disability Policy for the 21st Century. Noting that the share of disabled Americans with jobs actually declined after the passage of the Americans with Disabilities Act, I argued the following:

Some of the most controversial issues of the day — from education funding and health care inflation to economic growth and the future solvency of Social Security and Medicare — reflect the costs imposed on all of us by a flawed model for disability policy that focuses on rights and redistribution rather than responsibilities and the creation of wealth. This “entitlement model” for serving the nation’s disabled has smuggled concepts and principles from the civil rights era into an arena where they are largely inapplicable. It also treats too many disabled Americans as hapless and dependent wards of the state rather than as productive citizens whose value as human capital often remains untapped.

In the interest of fiscal restraint and economic growth, North Carolina and the nation need to adopt a new model that focuses on bringing as many disabled people as possible into the workforce, which will improve both their incomes and their quality of life over time. The model also requires policymakers to focus public resources on those with severe physical or mental disabilities, while discouraging the abuse of SSDI as secondary safety net for those with mild (if any) disabilities who have exhausted their UI benefits.

You can’t make the economy healthier by paying a growing share of the population not to work.

John Hood is president of the John Locke Foundation and an NC Spin Panelist

April 17, 2013 at 4:21 pm
Mary Few says:

The thought processes behind this article are tragically flawed because they fail to recognize that the writer has very little understanding of the medical and disability system.

The system is flawed, but not in the ways described here. As a former hospice nurse, I can tell you the system is incredibly arbitrary and difficult to navigate and almost everyone who applies is denied first go round even if their physician or office is skilled at filling out the forms, as most oncologists are. I must also ask, are you aware that federal disability requires a two year waiting period at which time you may or may not be able to get state disability.

You quoted the advancement in our healthcare system. While some advances have allowed people to stay in the workforce what these advances are even better at is increasing the amount of time a person stays alive. The ability to achieve a higher quantity of life, has far outpaced the ability to increase the quality of life.

Far more people with cancer live more than two years now and before you would see a lot more of these patients die before they were ever eligible to receive disability. However, living with cancer for a long time doesn't necessarily equate with living a life that allows you to work.

The chronically ill with heart, lung, liver, and kidney disease can now live longer and even be eligible for an organ transplant. While ideally everyone with a solid organ transplant could go back to work afterwards, sadly those numbers are a national average of less than 20% of transplant patients as a whole. Depending on their prior profession it can be less than 1%.

Multiple sclerosis is another disease along with rheumatoid arthritis that in its severe forms would end a life fairly quickly. Not the case any longer but living longer does not equate with the ability to work.

You also quote anti-discrimination laws. Well, they may be in place but I can assure you they are rarely upheld. In right to work states like NC all an employer has to do is come up with any reason for termination of an employee, just anything and unless the employee has it in writing or on tape the employer specifically and clearly saying something to the effect of "lets get rid of this guy b/c he is sick and running up our insurance" there will be NO consequence for the firing. This is the reality. Nice to live in the land or this is how it should be but most people live in the real world.

Are there lazy people using the system? of course there are!!! Again, here in the real world someone is always going to game the system. That doesn't mean we need to punish those in need.

I have worked with hundreds of patients over the years, who could not get disability and they were truly disabled, most by cancer, and the hardships it put upon the family when they were already facing the worst of times is disgraceful! When you work for a living and are suddenly struck by a devastating illness and you are asking for the money and help you deserve, only to be treated like a lowlife.......DISGUSTING!!!

Our advances in healthcare have done more to increase the ranks of the disabled than just about anything else. As for your anti-discrimination laws......I was terminated from a hospital no less, after pushing the issue that my chronic cancer treatment would be viewed as a pre-exsisting condition for one year even though I had no break in employer sponsored coverage....EVER!! For my entire life! Literally! There were numerous discussions between my manager and the director of nursing who discussed my healthcare issues in depth with the CEO, CFO & COO of the hospital. I had copies of the emails and they even admitted to doing it to the EEOC representative. However, the hospital was represented by a large powerful law firm in Raleigh. I even received a letter from the Director of the Raleigh office of the EEOC which states that that indeed the laws were broken and a reconciliation process needed to be completed. However, by some unknown mystery a woman who works at the EEOC under the director, obviously, was able to nullify that ruling and find in favor of the hospital without an appeal even being done.

I was able to get another job and was far from disabled at that time. I wasn't even seeking major money or anything, just a stop to what had been done and a reimbursement of my expenses.

So, make sure you understand the systems to which you are referring before you make broad assumptions.