Thursday, August 30, 2007

U.S. Uninsured Rate Climbs Again

By Daniel C. Vock, Stateline.org Staff Writer

Forty-seven million Americans went without health insurance in 2006, an increase of 2.2 million people from the year before, according to a report issued by the U.S. Census Bureau Tuesday (Aug. 28). It marks the sixthconsecutive year the ranks of the uninsured have grown.

For the second year in a row, the percentage of children without medical coverage also increased. The Census Bureau estimates 8.7 million kids – or 11.7 percent – had no insurance, an increase of 700,000 over the year before.

Advocacy groups immediately seized on the numbers to back their call for an expansion of the State Children’s Health Insurance Program (SCHIP), a joint state-federal venture for families who make too much to qualify for Medicaid.

“The huge number of uninsured Americans exceeds the cumulative population of 24 states plus the District of Columbia. This epidemic of uninsurance has reached crisis proportions, and Americans want to see the problem solved,” said Kathleen Stoll, health policy director of Families USA, a group pushing for a large expansion of SCHIP...

To read the complete article and for related stories click:
Stateline.org

Wednesday, August 29, 2007

Autistic basketball sensation's inspiring year

Jason McElwain, 18, discusses how one night transformed his life.
— John Springer, contributor for TODAY
2007 MSNBC Interactive

After he stunned everyone by coming off the bench to score 20 points in four minutes in a high-school basketball game [last year], autistic teen-ager Jason McElwain says he hopes his story is still inspiring others to set goals and achieve their dreams.

"What more can you want?" the 18-year-old Rochester, N.Y.-area boy said in an interview on TODAY Thursday morning, as he recounted his year in the spotlight, which included a meeting with President Bush. "My life has changed from going to just an ordinary kid with autism to someone who is a hero."

Jason, then 17, was thrust into the spotlight when Greece Athena High School basketball coach Jim Johnson decided to send him onto the floor for a little play in the team's final regular season game against Spencerport on Feb. 16, 2006. Jason had never made the team but stayed on as team manager, and Coach Johnson thought a little playing time would be a fitting show of gratitude for his dedication...

..."I never thought he would come this far," Debbie McElwain said of her son's disability, which was diagnosed when he was 2 1/2. "When your child is diagnosed with severe autism, you just want him to speak. Jason had most of the autistic symptoms of severe autism. It was just one hurdle after the next ... You just want him to say one word, because wants an autistic child says the first word, you are on a roll."

Jason's been on a roll ever since the big game, which his team won.

"I just hope more people are aware of autism, the disease autism," he said, "and that people know more about it and get the treatment they need with their children, early in life like my loving mother [did]."

Marked primarily by impaired social interaction and diminished communication skills, autism is a developmental disability believed to be caused by both genetic and environmental factors. Last week, the U.S. Centers for Disease Control issued a report estimating that one in 150 children born in this country are autistic — much more prevalent than previously thought.


To read the complete article and to watch the video, click here:
MSNBC Interactive

Living with disabilities: Aging parents face unknown

The Daily Herald
Monday, August 27, 2007

Randy DeRose has his eye on a Harley-Davidson.

With slicked-back hair and an easy smile, Randy has been doing his best to earn one since his brother gave him his first ride. But even if he meets his reading and writing marks, it's not going to happen.

Arms weakened by Down syndrome, the 40-year-old would never be able to hold up a 700-pound motorcycle, never mind the rest. But it's a goal to work toward, says his mother Lena DeRose, and Randy, the youngest of six children, is always up for a challenge.

The 84-year-old Springville mother should know. She has had her son by her side since the day four decades ago when she told off a doctor for suggesting she leave her newborn in the care of the state. "I said 'How can you insult me like that?' "

Facing the ravages of age, including death, groundbreaking parents like Lena are among the first who have to ask themselves what will happen to their 40 and even 50-year-old mentally disabled sons or daughters once they aren't around.

When Randy was born, mentally disabled infants rarely felt the embrace of a mother or father, says Kathy Edwards, director of Recreation and Habilitation Services in Provo.

"Doctors would go to parents and say 'Don't look at them, don't touch them, take them to the training school,' " Edwards said.

The state Training School in American Fork -- now known at the Developmental Center -- took in many children during the early years of it's 75-year history, almost regardless of the level of mental disability. The center now houses about 250 people who are considered extremely disabled.

But that first generation of defiant parents shunned the Training School, did look at their children, did touch them, and by all accounts provided a good life, a life that is now coming to an end.

And so Lena, whose husband died two years ago, struggles to find a reasonable solution for her son...


For pictures, video, and to read the complete article click:
The Daily Herald

Tuesday, August 28, 2007

On a "Mission from ADAPT," Disability Activists Blow into the Windy City to Attack Segregation

More than 500 ADAPT activists from around the country will converge in Chicago September 8th-13th to take action against a crisis in Illinois that is the poster child for a larger national problem. The crisis is directly caused by a record of bad decisions made by Illinois state officials, and the institutional bias built into the way the nation's long term care system is funded.

ADAPT will assure that Gov. Blagojevich knows that his plans to reopen a state institution for persons with developmental disabilities and his lack of support for Money Follows the Person legislation are actions of segregation and in violation of the U.S. Supreme Court's Olmstead decision. ADAPT will also challenge the Illinois Congressional delegation to take a leadership role nationally in eliminating the institutional bias so people with disabilities and older Americans can live at home with dignity.

Currently, Illinois ranks 41st in the nation for providing the community-based services that will allow disabled and older citizens to stay in their own homes. Illinois' long record of being in the bottom ten states puts it among the worst when it comes to human rights in general and disability rights in particular.

"It turns my stomach to know that my state, historically a home of civil rights in America for people of color, is the same state that is one of the worst civil rights performers in regard to people with disabilities,"
said Chicago native Larry Biondi, an organizer with Chicago ADAPT. "I'm ashamed of Illinois' record of institutionalizing people with disabilities. Right now there almost 20,000 people who have said they want to get out of Illinois' nursing homes- nursing homes they never wanted to go into in the first place. But they were forced to go there by the institutional bias in Medicaid funding, and the state's failure to act in accordance with federal law- law that clearly states that people should receive services in '...the most integrated setting,' which is clearly the community!"

While in Chicago, ADAPT will hold a national housing forum that will be attended by HUD Fair Housing Assistant Secretary Kim Kendrick, and state and local officials. At the forum, ADAPT will reveal its national housing agenda; take testimony from people across the country who have had difficulty finding affordable, accessible, integrated housing; and distribute information on pending visitability legislation, and the redirection of HUD's 811 Supportive Housing program funds to projects that are integrated. Currently, the 811 program primarily funds segregated housing situations for people with disabilities.

"As we have begun to make progress in getting people out of institutions, and preventing people from being forced into institutions, the lack of affordable, accessible, integrated housing in typical neighborhoods has become glaringly apparent," said Beto Berrera, a member of Chicago ADAPT and a Chicago housing expert. "We are hosting this national housing forum so that federal officials can hear just how bad the situation is, and to gain their support in working with us to right this wrong."

ADAPT will send a clear message to the Governor of Illinois, the nation's medical community, and Congress that supporting the incarceration of people in institutions for the 'crime' of disability will not be tolerated. In the classic Chicago movie, The Blues Brothers, Jake and Elwood Blues came to Chicago on a mission from God. ADAPT is coming to Chicago on a mission, too....a mission to "Free Our People!"

CLICK FOR MORE INFORMATION on ADAPT.

Monday, August 27, 2007

Monday Round up Blog

Joseph P. Kennedy, Jr. Foundation 2008 Professional and Parent Public Policy Fellowships
The Joseph P. Kennedy, Jr. Foundation is seeking outstanding professionals working in the field of inclusive services and supports for people with intellectual and developmental disabilities and parents or close family members of a person with intellectual and developmental disabilities for an intensive one-year Public Policy Fellowship in Washington, D.C.

During this year-long Fellowship, the successful applicant will learn how legislation is initiated, developed, and passed by the Congress, or how programs are administered and regulations promulgated by federal agencies. Fellows will also participate in an advocacy training workshop, national disability policy seminars and the intensive week-long Bioethics course at Georgetown University's Kennedy Institute of Ethics. Former Public Policy Fellows describe the Fellowship as a major turning point in their lives, not just careers.

The coming year offers exciting opportunities to contribute to policy and program or legislative development in key areas such as special education, health and mental health care for persons with mental retardation, child care, housing, justice, child welfare and other areas related to improving the quality of life for individuals with intellectual disabilities.

We seek professionals, parents, and other family members with outstanding experience in:
State or national level advocacy for persons with intellectual and developmental disabilities and their families;
vocational rehabilitation, education, child care, child welfare, law, employment, community organizing, housing or development of inclusive community supports and services;
health or mental health care for people with intellectual and developmental disabilities; or
development of family training or family support services.

Application deadline: September 14, 2007
Anticipated start date: January 2008
Please go to www.jpkf.org for more information.



HOW COMMON ARE MARITAL DIFFICULTIES IN FAMILIES OF CHILDREN WITH DOWN SYNDROME?
LARGE POPULATION-BASED STUDY PUBLISHED IN THE AMERICAN JOURNAL ON MENTAL RETARDATION TAKES A LOOK AT DIVORCE AMONG PARENTS OF CHILDREN BORN WITH DOWN SYNDROME-While Down syndrome is well-studied, there have been gaps in research, on the focus on families. A large-scale population study-one of the first with an epidemiological approach-studied families of 647 children with Down Syndrome and 361,154 of comparison children who did not have any disabilities, and found that divorce in families of children born with Down Syndrome is not as common as thought of, but is higher in cases of less educated parents and those living in rural areas. The findings from the study can be used to counsel parents of newborns about the risks and timing of possible marital discord during the first few years of the child's birth, as well as to develop special programs for families in rural areas.
Click to read "Divorce in Families of Children with Down Syndrome: A Population-Based Study" by Richard C. Urbano and Robert M. Hodapp in the American Journal on Mental Retardation (Volume 112, No. 4).
Click to learn more about AJMR.



Self-Advocacy: Know Yourself, Know What You Need, Know How to Get It-Link:
Self-advocacy is the ability to understand and effectively communicate one's needs to other individuals. Learning to become an effective self-advocate, especially for individuals with a hidden handicap such as dyslexia, is all about educating the people around you.
"Engaging Parents in Education: Lessons from Five Parental Information and Resource Centers" is a new publication of the US Department of Education, the second to be published in its "Innovations in Education" series. Its purpose is to explain "how to" strategies used by Parent Information Resource Centers (PIRCs)* to improve or expand their parental involvement programs in public schools. Topics addressed in the publication include:
Making Education-related Information Available and Understandable
Getting in Touch with Parents Statewide
Connecting With Hard-to-Reach Parents
Promoting Cross-stakeholder Communication
Moving From Information to Action
Assessing Local Needs Related to Parent Involvement
Training Parent Liaisons
Training Parents for Leadership
Training Parents and Educators to Function in Teams

PRESUME COMPETENCE:Challenging Conventional Wisdom About People with Disabilities

Copyright 2007, Kathie Snow, Disability is Natural
This is the first of three articles on this issue. The second article will focus on disability organizations/systems; the third explores the inadvertent perpetuation of the “presumed incompetence” mentality in advocacy efforts.
Within our judicial system, a person is presumed innocent. At trial, the person charged with breaking the law doesn’t even have to take the stand to defend himself; it’s up to the prosecution to present evidence which shows the defendant is guilty beyond a reasonable doubt.

Similarly, in every day interchanges, we meet new people at work, in a store, or in other activities, and we generally presume they’re competent. We presume, for example, that someone labeled “teacher,” “doctor,” “cashier,” or “mother” is competent in the role. Sometimes, once we get to know someone better, we might discover he/she is more/less competent in some areas than others, which is true for all of us! (The late, great Ann Landers once cautioned us to remember that 50 percent of all doctors graduated in the lower half of their class—and the same is true for any other category of graduates.) But like the judicial counterpart of “presumed innocent,” our initial reaction to others is to presume competence. And there are many other instances where similar positive presumptions are made about a business, situation, organization, etc. It seems that, in general, we initially presume the positive, unless and until we receive information to the contrary.

The same is not always true, however, for individuals who happen to have disabilities. As a result of long-standing mythical and erroneous perceptions, when we encounter a person with a disability, positive presumptions and attitudes may be instantly replaced by negative stereotypes and prejudice (yes, we prejudge), and the person with a disability is presumed incompetent. The guilt-by-association mentality may also kick in, so the person’s parents may also be presumed incompetent. (I was once told that my family was dysfunctional, our daughter was dysfunctional, and my husband and I were dysfunctional because of our son’s disability!)

There is no proof that the presence of a disability automatically confers an incompetent status. And many negative consequences result from our erroneous, unfair, and prejudicial presumptions. Children and adults with disabilities are segregated from the mainstream and isolated in special programs for treatments, interventions, and services. They may be prevented from engaging in the ordinary experiences most of us take for granted. Low expectations are the norm. Hopes and dreams are stripped away by physicians, educators, services providers, and even parents, as in, “People with ______ will never ________.”

But have we ever given the person the opportunity to try? Has a child had the opportunity to be in general ed classes or be involved in ordinary (and inclusive) activities in the community with whatever supports and accommodations are needed? Has an adult had the opportunity to have a real job, live on his/her own, and/or be responsible for his/her own life, with whatever supports and accommodations are needed? Has a child or adult had the opportunity to experiment with AT devices (such as power wheelchairs, communication devices, etc.)?

Traditionally, we’ve presumed incompetence and forced a person with a disability to prove she’s competent before allowing her to be in a general ed classroom, participate in community activities, be employed in a real job, live in the home of her choice, etc. It’s easy to see that our actions put people with disabilities in a no-win situation: because we presume they’re incompetent, we don’t give them opportunities to demonstrate their competence, and this, in turn, is taken as “proof” that they are, indeed, incompetent. The vicious cycle of the self-fulfilling prophecy is realized.

We would never, ever tolerate a change in our judicial system to a “presumed guilty” paradigm, in which the burden of proof was on the arrested person. And what kind of society would we have if everyone was routinely “presumed incompetent”? For example, what if your house was on fire, but you didn’t call 911 because you presumed the firefighters were incompetent? Ponder other scenarios and recognize that the social contract, as we know it, would come to a screeching halt.

So why do we continue to inflict this horrendous injustice on men and women and boys and girls who happen to have conditions we call disabilities? Is it because we devalue people with disabilities? Do we see them as “less than” or “not fully-human” (one of many relics of ancient history), and therefore not entitled to the presumption of competence the rest of us take for granted? Can we admit this, and then correct it? If we don’t acknowledge the problem, we cannot solve it!

The presumed-incompetent-mentality cannot be changed systemically in one fell swoop; the change has to come from each of us, individually. Then, the cohesion of our collective attitudes can and will influence the system and our society as a whole.

It’s not as hard as it might seem. We’ve allowed ourselves to be brainwashed into our current form of erroneous thinking; thus, we can “deprogram” ourselves by presuming people with disabilities are competent and ensuring they have the assistive technology, supports, and/or modifications they need in order to enjoy ordinary opportunities and experiences in inclusive environments.

Granted, it might be easy to look at someone who, for example, doesn’t walk or talk and exclaim, “He can’t [do whatever]; he’s more like a baby than a 20-year-old!” Instead, we can ask, “What will it take? What will he need? How do we need to change our thinking, or what do we need to change in his home/school/workplace/community?” For we don’t need to change people with disabilities, they’re fine just the way they are. (There have always been people with disabilities in the world and there always will be. And if we live long enough, any of us may become a person with a disability as a result of an accident, illness, or the aging process). We do need to change ourselves—how we think, talk, and behave—and when necessary, we need to change the environment (such as modifying a classroom, the curriculum, a job site, or home; and/or providing assistive technology, modifications, supports, etc.).

Within the presumed-incompetent-mentality are safety issues and the “get ready” paradigm. If a person isn’t considered ready for [fill-in-the-blank], he could be harmed. But think back to when you left your family’s home: were you ready? Were you competent to go out on your own? You most likely believed you were, but what about your parents? They were probably fearful for you, scared you’d fall flat on your face, get in trouble, and more. And maybe you did take two steps forward and one step back—and you also learned from your mistakes, found the help you needed from others, picked yourself up, and made it—one way or another! In the process, did you always listen to the wisdom of your parents or others? Probably not—you learned through experience, becoming more and more competent along the way!

Why can’t people with disabilities have those same opportunities? To learn from experience, to dig deep for strength and find resources when the going gets rough, to savor the pleasure of success and the awesome learning opportunities that are borne of failure, and perhaps most importantly, to belong.

We can continue to presume incompetence; ensure the dependence, helplessness, and isolation of people with disabilities; and maintain an “us/them” society. Or we can presume competence and create communities where all are valued and included. Which will it be?

New Bush Policies Limit Reach of Child Insurance Plan

By Christopher Lee
Washington Post Staff Writer
Tuesday, August 21, 2007; Page A04\

The Bush administration, engaged in a battle with Congress over whether a popular children's health insurance program should be expanded, has announced new policies that will make it harder for states to insure all but the lowest-income children.

New administrative hurdles, which state health officials were told about late last week, are aimed at preventing parents with private insurance for their children from availing of the government-subsidized State Children's Health Insurance Program. But Democrats and children's advocates said that the announcement will jeopardize coverage for children whose parents work at jobs that do not provide employer-paid insurance.

Under the new policy, a state seeking to enroll a child whose family earns more than 250 percent of the poverty level -- or $51,625 for a family of four -- must first ensure that the child is uninsured for at least one year. The state must also demonstrate that at least 95 percent of children from families making less than 200 percent of the poverty level have been enrolled in the children's health insurance program or Medicaid -- a sign-up rate that no state has yet managed.

To read the complete article, click here:
Washington Post Article, August 21, 2007

Monday, August 20, 2007

Community Service: A Family's Guide to Getting Involved

It's easy to feel disconnected, as many parents juggle work, family, and activity after activity. But there are a number of things that can help bring us back together - playing a game, going for a hike, or cooking a meal as a family.

One of the most satisfying, fun, and productive ways to unite as a family is volunteering for community service projects. Not only does volunteerism set a good example for your kids, it's helpful to the community as well.

Here Are Some Reasons to Get Involved.

From: Kids Health

Postsecondary Resources for Students with Intellectual Disabilities

COLLEGE OPTIONS FOR STUDENTS WITH INTELLECTUAL DISABILITIES
The Postsecondary Education Research Center Project, coordinated by TransCen, has launched a web site that provides information and resources on college options for students with intellectual disabilities. The site provides answers to frequently asked questions related to developing or expanding services for students with intellectual disabilities in college settings. It also provides access to a free online evaluation tool, the PERC Self-Assessment Tool, that allows users to evaluate aspects of programs or services for students with intellectual disabilities on college campuses. This self-assessment tool provides a snapshot of the quality of existing services and provides users with a concise evaluation report. It also provides users with the opportunity to create an itemized action plan that can be used to address areas in need of improvement. The website can be found at http://www.transitiontocollege.net

INDIVIDUAL SUPPORTS TO INCREASE ACCESS TO AN INCLUSIVE COLLEGE EXPERIENCE FOR STUDENTS WITH INTELLECTUAL DISABILITIES
The purpose of this online training module is to provide guidance on developing an Individual Support Model (ISM) to increase access to inclusive college experiences and to improve chances for the success of students with intellectual disabilities. An ISM approach provides students with individualized services and supports (e.g., educational coach, tutor, technology, natural supports) in college courses, certificate programs, internships, and/or degree programs. Offered by the On-Campus Outreach project at the University of Maryland; funded by the U.S. Office of Special Education Programs.


TRANSITION SERVICES FOR STUDENTS WITH SIGNIFICANT DISABILITIES IN COLLEGE AND COMMUNITY SETTINGS: STRATEGIES FOR PLANNING, IMPLEMENTATION, AND EVALUATION
This resource is recommended for professionals responsible for designing or implementing transition services for students with autism, developmental, multiple, or other significant disabilities. The book, guides readers through each phase of developing, implementing, and evaluating effective and appropriate transitions services for students with significant disabilities. Click for purchasing information.

REFERENCE POINTS, transition updates from the TATRA Project, features resources and information to help parent organizations, advocates and professionals better serve adolescents and young adults with disabilities, and their families. Administered by the TATRA Project at PACER Center, REFERENCE POINTS was launched with the initial support from the National Center on Secondary Education and Transition. TATRA is funded by the U.S. Department of Education, Rehabilitation Services Administration.

Thursday, August 16, 2007

I-Matter Conference

Community Options, Inc. is a non-profit corporation that provides community based support for people with disabilities in eight states. Each year we host a single topic conference to disseminate information that is important to our stakeholders. This year the topic is new Medicaid initiatives for funding flexible and consumer directed community support.

The conference, entitled I-Matter, will be held at the Inn and Spa at Loretto in Santa Fe, New Mexico, October 1st and 2nd 2007.

We have commitments from nationally recognized speakers such as Colleen Wieck and our keynote address will be given by Governor Bill Richardson.

Community Options, Inc. will again be awarding scholarships to participants of Partners in Policy Making. However, we will not be able to offer as many scholarships as last year due to funding.

We are also offering opportunities to sponsor participants of Partners in
Policy Making. ** Sponsorship provides opportunities for individuals with disabilities and/or their families to attend the iMatter conference** Please click here for sponsorship levels and conference information. Contact Lisa Smith if you would like to be included in this important event.

Thank you for your consideration,

Lisa Smith
Director of Training & Quality Assurance
Community Options, Inc.

"Caregiver Syndrome"

Do you take care of someone in your family with a chronic medical illness or dementia? Have you felt depression, anger or guilt? Has your health deteriorated since taking on the responsibility of caregiving? If your answer is yes to any one of these, you may be suffering from caregiver stress.

This condition is increasingly being referred to as "caregiver syndrome" by the medical community because of its numerous consistent signs and symptoms. In the pamphlet, "Caring for Persons with Dementia," Dr. Jean Posner, a neuropsychiatrist in Baltimore, Maryland, referred to caregiver syndrome as, "a debilitating condition brought on by unrelieved, constant caring for a person with a chronic illness or dementia."

An increasing number of Americans are finding themselves taking care of someone who's aging or ill or both. According to the American Academy of Geriatric Psychiatrists, one out of every four American families cares for someone over the age of 50. As America's population ages, that number is expected to skyrocket. In 2000, the Census Bureau reported, just under 35 million Americans were 65 or over; by 2030, the number is projected to more than double, to more than 71 million...

To read the complete article, click:
Exhaustion, anger of caregiving get a name
By Andree LeRoy, M.D.
CNN.com/health

How A Party Can Save Your Life

Did you know that just being a woman makes you at risk for Breast cancer?

Did you know that after treatment for early breast cancer, the death rate of women with disabilities is higher than that of other women?

Did you know that there are wheelchair accessible mammogram locations in the Atlanta-Metro area?

Did you know that Medicare and Medicaid can pay for a mammogram screening?

The Disability Resource Group and the Susan G. Koman Foundation of Atlanta are doing educational outreach to women with disabilities on breast cancer. This effort will include informational sessions that are fun and interactive to help educate women with disabilities about the importance of breast cancer awareness. This 2-hour session will include exciting door prizes and gifts, refreshments and information packets on breast cancer information.
Date: Saturday, August 18, 2007

Time: 10:30 a.m. to 12:30 p.m.

Location: Disability Link, 755 Commerce Drive, Suite 105, Decatur, GA 30030

Please RSVP to ensure available space and refreshments. For sign language interpretation please contact by August 13th. Email Ms. Empish Thomas

COMMITTEE MEETINGS - AUGUST 28 & 29, 2007

MEMORANDUM

TO: HOUSE AND SENATE APPROPRIATIONS HEALTH SUBCOMMITTEES
FROM: SENATOR GREG GOGGANS
REPRESENTATIVE MICKEY CHANNELL

SUBJECT: COMMITTEE MEETINGS - AUGUST 28 & 29, 2007
PURPOSE: CMO UPDATE

The House and Senate Appropriations Health Subcommittees will hold meetings on Tuesday, August 28 and Wednesday, August 29, 2007 in Room 341 of the State Capitol. Details for the meetings are as follows:

TUESDAY, AUGUST 28, 2007
10:00 AM – 4:00 PM
ROOM 341 CAP
AGENDA:
● Update from DCH
● Public Hearing

Sign-up sheet located in 245 State Capitol or call Tammy at 404-463-2247)
WEDNESDAY, AUGUST 29, 2007
9:00 AM – 12:00 PM
ROOM 341 CAP
AGENDA:
● Update from CMO’s

Monday, August 13, 2007

Dear Friends and Colleagues:
The Institute for the Study of Disadvantage and Disability's Adult Down Syndrome Program is offering a Caregiver Support Group. This has been suggested by many parents and adult siblings. We encourage and invite you to spread the word to your families. Please do so as soon as possible as the spaces are filling up. This is designated for families who have teens and adults with Down syndrome.

The Caregiver Support Group (CSG) of the Adult Down Syndrome Program provides support, information and resources to family members care for teens and adults with disabilities.

CSG provides an environment of support to family members so they may
• Connect with other families undergoing similar life situations
• Learn about the medical aspects of adulthood and aging for persons with Down syndrome
• Learn nutritional interventions to help prevent onset of chronic health conditions, such as diabetes, obesity, high blood pressure, high cholesterol, heart disease and common gastrointestinal difficulties
• Learn about planning for options of living and aging in a community setting
• Become familiar with appropriate community resources
• Plan for the future


Dates: Three Sessions, Saturday afternoons
September 15, 2007
October 20, 2007
November 10, 2007

Time: 1:30 – 3:30 pm

Cost: $30 (per person for the series)
$50 (families for the series)

Place: Decatur Family YMCA
1100 Clairemont Avenue
Decatur, Georgia 30030
phone (404)377-9622

RSVP: Reserve your spot. Space is limited.
Email Janice Nodvin to reserve.

Support group is led by a licensed social worker and a licensed dietician/nutritionist.
Group will also have guest speakers.

2007-2008 Citizen's Handbook from the Georgia League of Women Voters

Click to view the 2007-2008 Citizen's Handbook from the Georgia League of Women Voters. It includes contact information (addresses, e-mail, phone) for all statewide elected officials, members of the U.S. House (except Paul Broun), 20 state agencies, and the Supreme Court, as well as dates of elections, deadlines to register to vote for those elections, and information on how to register to vote.
It's from their web site's Citizen's Empower Tool Kit which also includes the following:
How Does a Bill Become Law?
How Do I File an Open Records Request?
Tips on Contacting Elected Officials
Guide to Georgia's Judiciary
How Do I Write an Op-Ed?
State Constitution of Georgia
How Is Education Funded in Georgia?

Monday Blog

CALL FOR APPLICATIONS: THE 2008 PAUL G. HEARNE/AAPD LEADERSHIP AWARDS (due: Sept. 21, 2007)
The Paul G. Hearne/AAPD Leadership Awards program was established to identify and support emerging leaders with disabilities who will carry on the disability rights movement. Administered by AAPD and sponsored by the Mitsubishi Electric America Foundation, the 2008 Paul G. Hearne/AAPD Leadership Awards identifies up to two emerging leaders with disabilities to each receive $10,000 to help them continue their progress as leaders. These individuals will also have an opportunity to meet and network with national disability leaders at the annual AAPD Leadership Gala in Washington, DC in the spring. Applications are available from www.AAPD.com.

Apply by: Friday, September 21, 2007.

Questions and submissions for the Paul G. Hearne/AAPD Leadership
Awards program to: aapdhearne@aol.com

Primer Examines Health Care Costs

Kaiser released a new primer on health care costs that examines the rapid growth in the nation's health care costs since 1970 and the factors that influence health care spending, including new medical technologies, population changes and changes in disease prevalence. The primer also looks at the impact of health care costs on families, with insurance premiums rising 87 percent between 2000 and 2006, More than four times the growth in wages. Click for more information: "Health Care Costs: A Primer"

ADCR-TAE Fact Sheet: How to Secure Medicaid Federal Financial Participation (FFP) for ADRC Functions: The Basics
Summary: The federal government will match expenditures that it deems necessary to support the "efficient and effective" administration of the Medicaid program. This administrative federal financial participation (FFP) is typically 50% of the costs, but in certain cases, enhanced match of up to 90% is available. Medicaid administrative activities can include many of the ADRC functions.

Topic(s): Aging Issues, Developmental/Psychiatric Disabilities, Physical Disabilities, Resource Center, Single Point of Entry/No Wrong Door
Source: The Lewin Group
Click for More Information

Redesigning Case Management Services for People with Disabilities in MinnesotaSummary: Minnesota, like many states, faces the challenge of limited resources in the face of increasing consumer demand for more consumer control of services. This report includes recommendations for providing choice of case manager, streamlining administration, funding options, standardizing caseload size, regionalizing some county functions, standardizing performance measures across disability groups, and maximizing individualization. Innovations in case management in other states are also presented.

Topic(s): Consumer Direction, Developmental/Psychiatric Disabilities, Physical Disabilities
Source: Institute on Community Integration, University of Minnesota
Click for More Information

Wednesday, August 08, 2007

PRESS RELEASE: Governor Perdue Announces Major Initiative to Aid Georgia’s Working Uninsured


Tuesday, August 07, 2007
Health Insurance Partnership to focus on employees of Georgia’s small businesses

Governor Sonny Perdue announced preliminary details on a major new health care initiative for working uninsured Georgians called the Health Insurance Partnership for Georgia...

Under Governor Perdue’s proposal, small businesses will be able to voluntarily join the program and offer private health insurance to employees. The cost of the insurance plan will be shared by the employee, employer and a combination of state and federal funds. Because of Medicaid initiatives that have realized savings in both state and federal funds, the state anticipates federal approval of using saved federal dollars to help cover its share of the cost.

More than 1.7 million Georgians lack health insurance. Approximately 380,000 of Georgia’s uninsured work for employers with less than 50 employees, and earn less than 300 percent of the FPL. The Health Insurance Partnership will enable sole proprietors and small businesses that have not been able to offer health insurance in the past the opportunity to offer a menu of private benefits options to employees.

The goal is to offer this segment of Georgia’s uninsured a variety of options for private health care coverage. The options vary based mostly on the level of premium the employee chooses to pay, such as:

Benchmark benefit plan comparable to the plan offered to state employees
Basic benefit package meeting the requirements of the Small Business Employee Choice of Benefits Health Insurance Plan Act: a basic employee health option authorized through SB 174 which went into effect July 1, 2005.
High Deductible Health Plan with a Health Savings Account (HSA).

Health Insurance Partnership FACT SHEET

Small Business Challenge:
Georgia is home to more than 800,000 small businesses, many of whom have been priced out of the health insurance market because of their small number of employees or pre-existing conditions within their group
An estimated 62,000 small businesses have less than 50 employees and do not currently offer health insurance coverage for employees, which accounts for approximately 380,000 uninsured Georgians earning less than 300 percent of the federal poverty level (FPL)


Georgia’s Solution:
Allows small business to join together in a larger group plan and offer private insurance to their employees through the free market
Insurance cost shared by Employee, Employer and State and Federal Funds
Implement by July 1, 2008 and administered by DCH


Financing the program:
State to apply for an 1115 Medicaid Waiver:
Waiver period of 5 years, but can be renewed if meeting objectives
o Allows changes to benefits, reimbursement and coverage of expansion groups
o State commits to a policy pilot that can be formally evaluated
o Anticipate federal approval of waiver because of savings from Medicaid program efficiencies
o Obtain federal match from the Centers for Medicare and Medicaid Services (CMS)


Eligibility for the plan:
Income less than or equal to 300 percent of FPL
Employed by a small business with less than 50 employees or a sole proprietor.
Works a minimum of 20 hours a week
Resident of Georgia for at least six months
Citizen or qualified legal alien


Who is NOT eligible for the plan:
Employees who have had health insurance during the past 6 months
Spouses with access to health insurance coverage through their employer even if he/she chooses not to enroll
Individuals covered by Medicare or TRICARE, or another insurance plan


Businesses are eligible to offer the plan if:
Business is located in Georgia
Employs fewer than 50 employees or a sole proprietor
Insurance must be offered to all eligible employees
Have not offered coverage within the last six months, or agrees to maintain existing contribution levels for the first 12 months of being on the program


Health Plans may participate in the plan if:
Agree to not impose a pre-existing exclusion clause
Agree to offer a premium consistent with State requirements
Agree to other participation criteria established by the State

To access the entire article, please click here.

Children's Resources: Early and Periodic Screening, Diagnosis and Treatment (EPSDT)

What is EPSDT?
Federal and State law require that children (up to age 21) who receive Medical Assistance – including Medicaid, PeachCare for Kids, and children in Medicaid Waivers – receive early and periodic screening, diagnosis and treatment (EPSDT).

This means that all children on Medical Assistance under age 21 get both well child visits AND all treatment and services that a professional says are necessary.

Rights of Children who Receive Medicaid
• The State should not put children on waitlists for services.
• Services should be available throughout the State.
• Services should be approved and provided or denied with “reasonable promptness.”
• The State should ensure that providers are available.
• Families should have the freedom to choose their provider.
• There should NOT be caps on the length or amount of services provided.

What Types of Services are Covered?
ANY SERVICE that a medical professional says is
MEDICALLY NECESSARY for a child
.

The following services have been provided through EPSDT. There may be other services available:
• Healthy kid check-ups
• Case Management
• Physical, Occupational, and Speech Therapy
• Home Health Care
• Personal Care (in-home help with physical care)
• Private Duty Nursing (at home or in the community)
• Medical Equipment and Supplies
• Assistive Technology
• Therapeutic Behavioral Services (in-home aides)
• Mental Health Services
• Dental and Vision Care
• Therapeutic Nursery
• Medical Day Care
• Transportation to Appointments
• In-patient Hospital Care
• Limited Residential Services

You have an EPSDT issue if:
 You know a child who receives Medical Assistance (Medicaid, PeachCare for Kids, or Medicaid Waiver) AND
 The child has a need for services that has been identified or could be identified by a medical professional AND
 The child is not receiving the services, has been denied, placed on a waiting list, not received a response to an application for services in a reasonable time, been told the services are not available in that area, that there is a cap on the number of hours the service can be provided or the length of time it can be provided, or that there is no provider available

Please contact the Atlanta Legal Aid Society at 404-377-0705 x 275 (Mondays and Tuesdays) or 278 (Wednesdays and Thursdays). We may be able to advise you on the process to get EPSDT services and possibly provide you or refer you to free legal representation.

Click here for further information.

Money Follows the Person Toolbox:

Services for Individuals with Developmental Disabilities
This targeted Tools Update/Addendum is intended to compile information about states' efforts to transition individuals with Mental Retardation or Developmental Disabilities (MR/DD) from Medicaid funded facilities into the community and to provide support services to these individuals using techniques compatible with the Money Follows the Person (MFP) Demonstration program that has been created by the Deficit Reduction Act.

Click here for more information.

Wednesday, August 01, 2007

Tax Reform: A Reality Check


Georgia Budget & Policy Institute (GBPI) to Tour Georgia to Help Citizens Learn About Tax Reform and Modernization
This fall, GBPI will host a series of meetings throughout Georgia to educate the public about proposals being discussed by state legislators that would make major changes to the state’s tax system. The tour will be a collaboration of GBPI, AARP Georgia, Georgia Association of Educators, and Georgia Coalition United for a Responsible Budget.

Locations:
September 4, 2007 - Columbus State University
September 11, 2007 - Valdosta State University
September 25, 2007 - Macon State College
October 2, 2007 - Rome, Location TBA
October 9, 2007 - The University of Georgia, Athens
October 16, 2007 - Albany State University
October 23, 2007 - Augusta Technical College
October 30, 2007 - Savannah State University
November 6, 2007 - Gainesville State College

Each meeting will begin at 4:00pm and end by 6:00pm. Refreshments will be served.

The meetings are free and open to the public, but registration is required. To register for any of the meetings, please click here.