Tuesday, December 16, 2008
Senators file Nick's Law
Also, Senator Patrick Anderson, R-Enid, refiled Nick's Law as SB 36. Senator Mary Easley, D-Tulsa, refiled Nick's Law as SB 46.
These three senators filed their bills shows a bi-partisan approach to address the need for insurance coverage for medically necessary treatments of autism.
Friday, December 12, 2008
We’re in this together
We’re in this together
Point of View Health coverage
BY DAVID BLATTPublished: November 16, 2008
With more than one in five non-elderly Oklahomans lacking health insurance and health care costs posing an ever-growing burden on businesses and families, identifying options to expand access to health insurance coverage is likely to be a major priority for Oklahoma policymakers during next year’s legislative session. This fall, legislators and others have been working as part of a House task force aimed at developing recommendations to chart a path forward.
We believe Oklahoma can best move forward by building upon the foundations of our mixed private-public health care system and upon programs and policies adopted in recent years. In particular, the state should continue to expand the Insure Oklahoma program, which provides a public subsidy for low-income employees and their spouses to purchase employer-sponsored insurance when that is offered, or to buy in directly to a public product when employer-sponsored coverage is unavailable.
Insure Oklahoma represents a flexible public-private partnership that can help small and medium-sized businesses provide coverage to their employees. While enrollment in Insure Oklahoma has been slow to grow, real progress seems likely if and when Oklahoma receives federal approval to move ahead with expanding the program to firms with up to 250 employees and employees up to 250 percent of the poverty level. At the same time, the Legislature should consider expanding eligibility for traditional Medicaid to adults below the poverty level. This would help cover a population that has very high rates of uninsured and often finds even the subsidized cost-sharing obligations of the Insure Oklahoma program to be unaffordable.
While recent policy initiatives are moving Oklahoma in the right direction, we must be extremely careful that efforts to expand coverage don’t come at the expense of eroding the quality of health insurance in the group and individual markets. Some are tempted to relax coverage standards and offer more choices for bare-bones, low-cost coverage. This is seen as especially attractive to the young and healthy, who currently may only be offered more benefits than they want at a cost they cannot afford or choose not to pay.
The basic problem with this approach is that affordable coverage for those with the greatest health care needs — especially women of child-bearing age, persons with chronic physical and mental health conditions and older workers — can only remain available is if there is a large, diverse pool that includes younger, healthier individuals. If that population is pulled out of the risk pool by the availability of bare-bone products, we could easily descend into a downward spiral where those who most need health care will be unable to find or afford it. That won’t solve our uninsured problem and it certainly won’t make us a healthier state.
Real solutions to the crisis of the uninsured in Oklahoma will occur only if everyone — the public and private sectors, young and old, high-income and low-income, healthy and sick — is working together toward our common goals of affordable, quality care.
Blatt is director of policy for the Oklahoma Policy Institute ( http://www.okpolicy.org/).
Wednesday, December 10, 2008
Oklahoman OP/Ed - Cost benefit Analysis needed
OUR VIEWS: Insurance mandates
Published: December 10, 2008
With two months to go before the start of the next legislative session, one of the loudest issues that will come before lawmakers is already making noise.
It’s the issue of forcing health insurance policies to cover autism treatments. Taking a larger view, it’s the issue of adding mandates to policies that make them more expensive and thus harder to afford by those already struggling to get coverage.
Battle lines on this issue were drawn in the 2008 session, in a tussle between the forces of emotion and the forces of reason. Back then we termed it a classic case of the irresistible force meeting the immovable object.
Parents of children with autism have a champion in state Sen. Jay Paul Gumm, D-Durant, who approaches the issue with almost evangelistic fervor. If he’s the good guy in this deal (and we don’t necessarily believe he is), then the men in black hats are Republican House members who believe the mandate train must be held up if not derailed.
Gumm says momentum is building for "Nick’s Law,” the mandate bill named for an Edmond boy who is autistic. Last year, Gumm couldn’t get a hearing for the bill in the Republican-controlled House, despite intense lobbying from the parent group and Gumm’s emotion-choked arguments.
A possible compromise — passing this mandate in exchange for a bill restricting future mandates — went nowhere. This reasonable approach may face just as much opposition as before. Gumm now has the burden of getting his bill through a Senate that will be controlled by Republicans for the first time in history.
The autism mandate would be the 37th the state forces on policyholders. Estimates on what the autism mandate would cost vary wildly — so much so that it’s difficult to believe either side’s numbers.
Nevertheless, mandates do add to the cost of insurance, and that reduces the number of people who can afford insurance in a state with a chronic uninsured problem.
Rep. Doug Cox, R-Grove, is a physician who initially supported Nick’s Law. He now opposes it on the basis of not wishing to worsen the uninsured problem.
We believe the first thing the Legislature should do vis-a-vis mandates is to pass a law requiring a cost-benefit analysis for all future mandates. That analysis should not be funded by the state. Absent a consensus on the cost of any particular mandate, it’s folly to keep adding dollars to policy premiums.
Monday, December 8, 2008
Lawmaker proposed mandate waiver
Lawmaker proposes mandate waiver
The Edmond Sun
December 06, 2008 01:02 am
— OKLAHOMA CITY (AP) — Legislation that would waive state health insurance mandates and permit insurers to create inexpensive “bare-bones” health insurance policies could significantly reduce the number of uninsured Oklahomans, a physician and state lawmaker said Friday.
Rep. Doug Cox, R-Grove, an emergency medicine physician at Integris Grove General Hospital, said he is drafting a measure that would waive a variety of mandated coverage for people in their 20s and 30s whose major health expense is accidental injuries.
Cox said he believes mandates drive up the cost of health insurance and make it unaffordable for many Oklahomans. Oklahoma has an estimated 600,000 uninsured residents, including 85,000 under the age of 18.
“Younger people are for the most part healthy,” Cox said. “It’s also the age range where they don’t really have the excess cash to use to buy things like insurance policies. So, let’s offer them a bare-bones policy.”
Cox’s proposal received the support of Insurance Commission Kim Holland, who said she endorses the plan to evaluate the state’s mandated coverage and develop affordable health insurance policies.
“I think it’s appropriate to take a second look and say, ‘Wow, do people really need all this,’” Holland said. “Affordability is the No. 1 reason that people say they don’t have insurance. We have to come up with more affordable health insurance options.”
Every state imposes health insurance mandates on insurers. Minnesota has the most with 64 and Idaho the least with just 15.
Oklahoma has 36 health insurance mandates for such procedures as immunizations for children, mammograms, breast reconstruction and prostate cancer screening. Some mandates, such as maternal health, are imposed by federal law and cannot be waived, Holland said.
Lawmakers plan to consider another mandate to cover the diagnosis and treatment of autism when the Legislature convenes in February.
Cox said waiving state mandates would allow health insurers to create high-deductible accident policies for young people. State-mandated coverage would still apply to people 40 and over, he said.
“As you get older, preventative tests become more important,” he said. “I think it will have some impact. Young people just don’t see the value of insurance. Young people don’t see the value until they need it — and then it’s too late.”
Holland said 70 percent of young adults aged 19-34 in Oklahoma do not have health insurance. “They’re young. They’re invincible. They’re looking at the immediate. They’re not thinking long-term,” she said. Holland said her agency is interested in developing insurance products to help people manage their health from a young age.
“There are ways that we can construct low-cost plans for them,” she said.
A health insurance mandate is a requirement that an insurer or health plan cover or offer coverage for health care providers, benefits and patient populations.
The Council for Affordable Health Insurance, a research and advocacy association of insurance carriers based in Alexandria, Va., says mandates make health insurance more comprehensive as well as more expensive by requiring insurers to pay for care consumers previously paid for out of their own pockets.
CAHI estimates that mandated benefits increase the cost of basic health coverage from a little less than 20 percent to more than 50 percent, depending on the state and its mandates.
Saturday, December 6, 2008
Nick’s Law is Oklahoma Senate Bill 1


Nick’s Law is Oklahoma Senate Bill 1
By Bailey Dabney, Publisher
CLAREMORE DAILY PROGRESS
December 4, 2008 December 04, 2008 04:19 pm
— With health insurance, most Americans can reasonably expect their plan to pay for treatments that heal them when they are sick.
After all, that’s what insurance is for. Our premiums are due and are paid even when we are not sick.
If your child is autistic you still pay the premiums, but don’t be expecting a whole lot of care. It’s been argued that illegal aliens get better care than autistic citizens.
With a little help, that may be changing. Nick’s Law, or Senate Bill 1, would stop insurers from denying necessary care for autistics.
Opponents say that insurance premiums would have to go so high that more Oklahomans would lose their health insurance.
The facts don’t support that argument. According the Bill’s sponsor, Senator Jay Paul Gumm (D, Durant), an actuarial study revealed a cost per policy holder of $1.66 per month.
Senator Gumm believes he has the bipartisan support and the votes needed to pass it in both chambers, if it will be allowed to come up for a vote.
In April, Tulsa Representative Ron Peterson blocked hearing of the bill in the House. Peterson used to make his living in the insurance business. The largest sector of his financial support came from the insurance and pharmaceutical industries, both of which have seemingly waged war on the families of autistics for years.
He also blocked passage of Steffanie’s Law, a bill requiring coverage for certain cancer victims. Steffanie Collings, of Noble, died March 13th with $450,000 in medical bills.
Representative Peterson chose not to seek re-election after the current term, so his blockade should now be lifted.
If you believe that a health plan should not be required to cover treatments for Autistic patients, do you also believe that they should not cover cancer treatments? Apparently Rep. Peterson does. Would you support politicians who allow health plans discontinue insulin for diabetics? How about antibiotics for ear infections? Hernia surgery? Aids? What condition is next?
Claremore’s own Representative Tad Jones (R, Claremore) is now the House Floor Leader, an influential position to say the least. Our Senator, Sean Burrage has already pledged his support of Nick’s Law, and voted for it in the spring.
The ball will likely end up in Rep. Jones’ hands.
Will the former quarterback and new House Floor Leader exert his considerable influence or fumble? Let’s hope he gives Nick’s Law the chance to be voted on.
Copyright © 1999-2008 cnhi, inc.
Thursday, December 4, 2008
Momentum, Editorial Support Grows for “Nick’s Law”
The State of
OFFICE OF SENATOR JAY PAUL GUMM
Atoka,
December 4, 2008
FOR IMMEDIATE RELEASE
Contact: Senator Jay Paul Gumm
State Capitol: (405) 521-5586
Durant Office: (580) 924-4717
Momentum, Editorial Support Grows for “Nick’s Law”
Even Editorial Opposition Admits “Bill Will be Hard to Stop”
(For digital audio, go to http://www.oksenate.gov/ and select “News”)
“I continue to hear from more families and child advocates who know this bill is the right thing to do,” said Senator Jay Paul Gumm, author of Nick’s Law. “Since the legislation was first introduced, we’ve seen a growing number of newspapers throughout the state voice editorial support for the measure.”
Autism is the fastest growing developmental disability in the
To date, newspapers in
In 2008, the measure repeatedly passed the Oklahoma Senate with bipartisan support. Gumm, a Democrat from Durant, said there was bipartisan support in the House of Representatives, as well. A small group of House Republicans, led by now-former Rep. Ron Peterson worked to prevent even a vote on the bill.
“I’ve said it repeatedly: Autism strikes families from all walks of life, families from both political parties,” he said. “Conservative Republican lawmakers in other states have written, fought for and passed similar legislation. High-profile Republican governors already being talked about as presidential candidates have signed into law similar legislation.”
Gumm said
In a national Associated Press story by medical writer Lindsey Tanner, a study published in the
According to the story, these families endure health care costs that put “unprecedented financial strain” on families. Further, the report notes that when compared with parents of children with chronic health care needs other than autism, those with autistic children are three times more likely to have quit jobs or cut back on work hours to care for their children.
These families pay more for their children’s health care, spend more time providing or arranging for that care and are more likely to have financial challenges. Lost wages and high health care costs compound the struggles of these families, often leading to divorce.
“Every shred of evidence points to the fact that bills like Nick’s Law do make a huge difference in the lives of these children and their families and are unquestionably ‘pro-family,’” Gumm said. “This bill is not a complete solution – no one has claimed it is – but it is the foundation on which we can build while ultimately saving taxpayers’ dollars.
“To do nothing, is to condemn these children to a lifetime locked behind the walls of autism. To do nothing condemns these parents to a lifetime of unprecedented financial struggles. To do nothing condemns taxpayers to eventually picking up the tab. To do nothing is unconscionable.”
Monday, December 1, 2008
Study: Autism puts Unprecedented Financial Strain on Families

Monday , December 01, 2008
More than half a million U.S. children have autism with costly health care needs that often put an unprecedented financial strain on their families, national data show.
Compared with parents whose youngsters have chronic health care needs but not autism, those with autistic children are three times more likely to have to quit their jobs or reduce work hours to care for their kids. They pay more for their kids' health needs, spend more time providing or arranging for that care, and are more likely to have money difficulties, the study found.
"This is the first national survey that looked at the impact on families of having kids with special health care needs," said lead author Michael Kogan, a researcher with the government's Maternal and Child Health Bureau.
The results are from a nationally representative 2005-06 survey of nearly 40,000 children with special health care needs. These children have a broad range of chronic conditions, including physical and mental illness, requiring more extensive than usual medical care.
A total of 2,088 children with special health needs had autism, which translates to about 535,000 kids aged 3 to 17 nationwide, the study authors said. The study appears in December's Pediatrics, being released Monday.
Jacquie Mace, whose 12-year-old son, Austin, has autism, said the study presents a "very realistic" picture of the challenges affected families face.
Mace said she spends "easily $15,000 to $20,000 out of pocket" yearly on supplies for behavior treatment she provides for her son. She's still working to pay off a $7,000 bill for dental work Austin had last year. He has to be sedated and hospitalized for dental care because he can't sit still in a chair, Mace explained. Austin's health insurance doesn't cover any of it, she said.
Some states require insurers to cover certain autism treatment while similar proposed measures are pending in others, including Illinois.
Mace hasn't had to quit her job helping local families find autism resources, but knows of many parents who've had to leave work to care for their autistic kids.