Subscribe to A'yani's Journey Subscribe to A'yani's Journey's comments

Take Action!

ASK YOUR MEMBER TO SIGN ONTO THE ABLE ACT OF 2011

National Down Syndrome Society

D.A.D.S. National

National Down Syndrome Congress

The Achieving a Better Life Experience Act (ABLE) of 2011 will be reintroduced in the U.S. Senate and House on November 15. The ABLE Act will give individuals with disabilities and their families the ability to save for their child’s future just like every other American family, and help people with disabilities live full, productive lives in their communities without losing benefits provided through private insurances, the Medicaid program, the supplemental security income program, the beneficiary’s employment, and other sources. 
The account could fund a variety of essential expenses for individuals, including medical and dental care, education, community based supports, employment training, assistive technology, housing, and transportation.
ACTION REQUIRED:
We need your help! We need you to call your two Senators and Representative (click here and input your zip code for your Members: http://capwiz.com/ndss/home/) and ask them to be an original cosponsor of the ABLE Act of 2011.
We’ve included a call script and all the information you need to make your phone calls. **Note: Double check to see if your two Senators and Representative signed onto the bill in the last Congress (see below)
Please click Take Action Now (right hand corner)!

 ***Should you have any questions or feedback you’d like to send us, please contact Sara Weir (sweir@ndss.org).

ABLE Senate sponsors:  S. 493
Sen Brown, Sherrod [OH] – 4/21/2010
Sen Brownback, Sam [KS] – 2/26/2009
Sen Burr, Richard [NC] – 2/26/2009
Sen Cochran, Thad [MS] – 5/26/2010
Sen Collins, Susan M. [ME] – 2/26/2010
Sen Dodd, Christopher J. [CT] – 2/26/2009
Sen Feingold, Russell D. [WI] – 3/15/2010
Sen Gillibrand, Kirsten E. [NY] – 7/30/2009
Sen Hatch, Orrin G. [UT] – 2/26/2009
Sen Isakson, Johnny [GA] – 3/16/2010
Sen Kennedy, Edward M. [MA] – 2/26/2009
Sen Kerry, John F. [MA] – 7/13/2010
Sen Klobuchar, Amy [MN] – 4/21/2010
Sen Landrieu, Mary L. [LA] – 2/24/2010
Sen Lautenberg, Frank R. [NJ] – 4/22/2009
Sen LeMieux, George S. [FL] – 2/24/2010
Sen Menendez, Robert [NJ] – 4/30/2010
Sen Mikulski, Barbara A. [MD] – 5/26/2010
Sen Risch, James E. [ID] – 4/30/2009
Sen Specter, Arlen [PA] – 3/25/2009
Sen Stabenow, Debbie [MI] – 7/22/2010
Sen Tester, Jon [MT] – 9/15/2010
Sen Whitehouse, Sheldon [RI] – 10/1/2009
Sen Wicker, Roger F. [MS] – 3/19/2009
ABLE House Sponsors:  HR 1205
Rep Ackerman, Gary L. [NY-5] – 6/12/2009
Rep Akin, W. Todd [MO-2] – 3/3/2009
Rep Andrews, Robert E. [NJ-1] – 3/17/2009
Rep Arcuri, Michael A. [NY-24] – 7/13/2010
Rep Bachmann, Michele [MN-6] – 4/22/2010
Rep Bachus, Spencer [AL-6] – 3/6/2009
Rep Baldwin, Tammy [WI-2] – 5/7/2009
Rep Barrett, J. Gresham [SC-3] – 5/13/2010
Rep Barrow, John [GA-12] – 4/21/2009
Rep Bean, Melissa L. [IL-8] – 3/18/2009
Rep Berkley, Shelley [NV-1] – 3/12/2009
Rep Bishop, Sanford D., Jr. [GA-2] – 5/7/2009
Rep Bishop, Timothy H. [NY-1] – 5/13/2009
Rep Blackburn, Marsha [TN-7] – 3/3/2009
Rep Blunt, Roy [MO-7] – 3/3/2009
Rep Boccieri, John A. [OH-16] – 5/21/2009
Rep Bonner, Jo [AL-1] – 3/4/2010
Rep Bono Mack, Mary [CA-45] – 6/19/2009
Rep Boozman, John [AR-3] – 3/30/2009
Rep Bordallo, Madeleine Z. [GU] – 3/12/2009
Rep Boucher, Rick [VA-9] – 1/27/2010
Rep Brady, Kevin [TX-8] – 3/6/2009
Rep Braley, Bruce L. [IA-1] – 7/8/2009
Rep Brown, Corrine [FL-3] – 3/12/2009
Rep Brown-Waite, Ginny [FL-5] – 3/6/2009
Rep Burton, Dan [IN-5] – 3/3/2009
Rep Calvert, Ken [CA-44] – 4/21/2009
Rep Campbell, John [CA-48] – 4/2/2009
Rep Cantor, Eric [VA-7] – 4/2/2009
Rep Cao, Anh “Joseph” [LA-2] – 7/8/2009
Rep Capito, Shelley Moore [WV-2] – 3/25/2010
Rep Carnahan, Russ [MO-3] – 5/13/2009
Rep Carson, Andre [IN-7] – 3/18/2009
Rep Cassidy, Bill [LA-6] – 3/4/2010
Rep Chaffetz, Jason [UT-3] – 4/21/2009
Rep Chandler, Ben [KY-6] – 4/15/2010
Rep Childers, Travis [MS-1] – 5/21/2009
Rep Cleaver, Emanuel [MO-5] – 6/19/2009
Rep Cohen, Steve [TN-9] – 3/17/2009
Rep Cole, Tom [OK-4] – 3/19/2010
Rep Connolly, Gerald E. “Gerry” [VA-11] – 7/31/2009
Rep Courtney, Joe [CT-2] – 5/4/2009
Rep Culberson, John Abney [TX-7] – 6/12/2009
Rep Davis, Geoff [KY-4] – 3/30/2009
Rep Davis, Susan A. [CA-53] – 6/10/2010
Rep Delahunt, Bill [MA-10] – 4/21/2009
Rep DeLauro, Rosa L. [CT-3] – 3/2/2010
Rep Dent, Charles W. [PA-15] – 12/1/2010
Rep Deutch, Theodore E. [FL-19] – 6/24/2010
Rep Diaz-Balart, Lincoln [FL-21] – 3/6/2009
Rep Diaz-Balart, Mario [FL-25] – 3/4/2010
Rep Donnelly, Joe [IN-2] – 10/6/2009
Rep Doyle, Michael F. [PA-14] – 4/27/2009
Rep Dreier, David [CA-26] – 3/17/2009
Rep Driehaus, Steve [OH-1] – 4/30/2009
Rep Ehlers, Vernon J. [MI-3] – 3/17/2009
Rep Ellison, Keith [MN-5] – 9/10/2009
Rep Ellsworth, Brad [IN-8] – 3/18/2009
Rep Emerson, Jo Ann [MO-8] – 7/13/2010
Rep Eshoo, Anna G. [CA-14] – 5/5/2010
Rep Filner, Bob [CA-51] – 3/24/2009
Rep Fleming, John [LA-4] – 7/8/2009
Rep Fortenberry, Jeff [NE-1] – 11/19/2009
Rep Frank, Barney [MA-4] – 3/18/2009
Rep Fudge, Marcia L. [OH-11] – 4/30/2009
Rep Gerlach, Jim [PA-6] – 4/30/2009
Rep Gonzalez, Charles A. [TX-20] – 7/30/2010
Rep Goodlatte, Bob [VA-6] – 7/17/2009
Rep Gordon, Bart [TN-6] – 3/24/2009
Rep Graves, Sam [MO-6] – 3/3/2009
Rep Grijalva, Raul M. [AZ-7] – 6/12/2009
Rep Gutierrez, Luis V. [IL-4] – 3/2/2010
Rep Hare, Phil [IL-17] – 3/10/2009
Rep Harper, Gregg [MS-3] – 3/3/2009
Rep Hastings, Alcee L. [FL-23] – 5/26/2010
Rep Heller, Dean [NV-2] – 3/24/2009
Rep Herger, Wally [CA-2] – 6/26/2009
Rep Herseth Sandlin, Stephanie [SD] – 3/4/2010
Rep Himes, James A. [CT-4] – 1/27/2010
Rep Hinchey, Maurice D. [NY-22] – 5/21/2009
Rep Hoekstra, Peter [MI-2] – 5/5/2010
Rep Holden, Tim [PA-17] – 3/24/2009
Rep Holt, Rush D. [NJ-12] – 3/10/2009
Rep Inslee, Jay [WA-1] – 12/1/2010
Rep Jackson, Jesse L., Jr. [IL-2] – 6/12/2009
Rep Jackson-Lee, Sheila [TX-18] – 7/8/2009
Rep Jones, Walter B., Jr. [NC-3] – 7/30/2010
Rep Kennedy, Patrick J. [RI-1] – 2/26/2009
Rep Kildee, Dale E. [MI-5] – 5/4/2009
Rep King, Peter T. [NY-3] – 4/2/2009
Rep Kirk, Mark Steven [IL-10] – 3/6/2009
Rep Klein, Ron [FL-22] – 3/2/2010
Rep Kline, John [MN-2] – 5/13/2009
Rep Kosmas, Suzanne M. [FL-24] – 6/19/2009
Rep Lamborn, Doug [CO-5] – 5/13/2009
Rep Langevin, James R. [RI-2] – 4/21/2009
Rep Larsen, Rick [WA-2] – 5/13/2010
Rep Larson, John B. [CT-1] – 9/16/2010
Rep Latham, Tom [IA-4] – 5/4/2009
Rep Lewis, John [GA-5] – 5/13/2009
Rep Loebsack, David [IA-2] – 7/30/2010
Rep Lofgren, Zoe [CA-16] – 5/4/2009
Rep Lucas, Frank D. [OK-3] – 4/15/2010
Rep Luetkemeyer, Blaine [MO-9] – 4/27/2009
Rep Lynch, Stephen F. [MA-9] – 6/12/2009
Rep Mack, Connie [FL-14] – 3/18/2009
Rep Maloney, Carolyn B. [NY-14] – 7/27/2010
Rep Markey, Edward J. [MA-7] – 4/22/2010
Rep Marshall, Jim [GA-8] – 3/24/2009
Rep Massa, Eric J. J. [NY-29] – 5/4/2009
Rep Matsui, Doris O. [CA-5] – 4/27/2009
Rep McCarthy, Carolyn [NY-4] – 4/30/2009
Rep McCarthy, Kevin [CA-22] – 7/17/2009
Rep McCotter, Thaddeus G. [MI-11] – 5/21/2009
Rep McDermott, Jim [WA-7] – 7/13/2010
Rep McGovern, James P. [MA-3] – 4/22/2010
Rep McHugh, John M. [NY-23] – 5/4/2009
Rep McIntyre, Mike [NC-7] – 4/21/2009
Rep McMorris Rodgers, Cathy [WA-5] – 2/26/2009
Rep Meek, Kendrick B. [FL-17] – 2/26/2009
Rep Meeks, Gregory W. [NY-6] – 11/6/2009
Rep Melancon, Charlie [LA-3] – 3/9/2010
Rep Mica, John L. [FL-7] – 3/3/2009
Rep Michaud, Michael H. [ME-2] – 3/9/2010
Rep Miller, Brad [NC-13] – 7/1/2010
Rep Miller, Jeff [FL-1] – 9/29/2009
Rep Moore, Dennis [KS-3] – 3/3/2009
Rep Moore, Gwen [WI-4] – 4/15/2010
Rep Moran, James P. [VA-8] – 3/3/2009
Rep Murphy, Christopher S. [CT-5] – 9/16/2010
Rep Murphy, Scott [NY-20] – 3/4/2010
Rep Murphy, Tim [PA-18] – 6/26/2009
Rep Myrick, Sue Wilkins [NC-9] – 4/30/2009
Rep Napolitano, Grace F. [CA-38] – 7/8/2009
Rep Neugebauer, Randy [TX-19] – 4/2/2009
Rep Norton, Eleanor Holmes [DC] – 3/10/2009
Rep Nunes, Devin [CA-21] – 4/2/2009
Rep Nye, Glenn C. [VA-2] – 6/10/2010
Rep Olson, Pete [TX-22] – 3/30/2009
Rep Olver, John W. [MA-1] – 3/4/2010
Rep Pascrell, Bill, Jr. [NJ-8] – 3/9/2010
Rep Paul, Ron [TX-14] – 3/3/2009
Rep Paulsen, Erik [MN-3] – 3/6/2009
Rep Payne, Donald M. [NJ-10] – 7/8/2009
Rep Pence, Mike [IN-6] – 3/24/2009
Rep Peterson, Collin C. [MN-7] – 4/30/2009
Rep Pingree, Chellie [ME-1] – 7/30/2010
Rep Platts, Todd Russell [PA-19] – 3/6/2009
Rep Poe, Ted [TX-2] – 5/5/2010
Rep Posey, Bill [FL-15] – 4/30/2009
Rep Price, David E. [NC-4] – 7/31/2009
Rep Putnam, Adam H. [FL-12] – 7/27/2010
Rep Reichert, David G. [WA-8] – 7/31/2009
Rep Richardson, Laura [CA-37] – 3/25/2010
Rep Roe, David P. [TN-1] – 4/2/2009
Rep Rogers, Harold [KY-5] – 12/16/2009
Rep Rogers, Mike D. [AL-3] – 12/8/2009
Rep Rooney, Thomas J. [FL-16] – 4/2/2009
Rep Ros-Lehtinen, Ileana [FL-18] – 3/6/2009
Rep Roskam, Peter J. [IL-6] – 3/3/2009
Rep Ross, Mike [AR-4] – 9/16/2010
Rep Rothman, Steven R. [NJ-9] – 3/10/2009
Rep Rush, Bobby L. [IL-1] – 3/4/2010
Rep Ryan, Tim [OH-17] – 3/3/2009
Rep Sablan, Gregorio Kilili Camacho [MP] – 4/30/2009
Rep Sanchez, Linda T. [CA-39] – 7/27/2010
Rep Schauer, Mark H. [MI-7] – 6/26/2009
Rep Schmidt, Jean [OH-2] – 3/30/2009
Rep Schock, Aaron [IL-18] – 5/7/2009
Rep Scott, Robert C. “Bobby” [VA-3] – 3/9/2010
Rep Sessions, Pete [TX-32] – 3/3/2009
Rep Sestak, Joe [PA-7] – 5/4/2009
Rep Shimkus, John [IL-19] – 4/22/2010
Rep Sires, Albio [NJ-13] – 6/26/2009
Rep Skelton, Ike [MO-4] – 12/1/2010
Rep Smith, Christopher H. [NJ-4] – 3/3/2009
Rep Souder, Mark E. [IN-3] – 5/13/2009
Rep Speier, Jackie [CA-12] – 7/13/2010
Rep Stark, Fortney Pete [CA-13] – 12/8/2009
Rep Tauscher, Ellen O. [CA-10] – 3/10/2009
Rep Terry, Lee [NE-2] – 4/21/2009
Rep Thompson, Glenn [PA-5] – 4/27/2009
Rep Thompson, Mike [CA-1] – 3/17/2009
Rep Tiberi, Patrick J. [OH-12] – 3/4/2010
Rep Titus, Dina [NV-3] – 7/13/2010
Rep Tonko, Paul [NY-21] – 6/12/2009
Rep Towns, Edolphus [NY-10] – 11/6/2009
Rep Tsongas, Niki [MA-5] – 7/17/2009
Rep Turner, Michael R. [OH-3] – 7/8/2009
Rep Upton, Fred [MI-6] – 12/11/2009
Rep Van Hollen, Chris [MD-8] – 3/9/2010
Rep Visclosky, Peter J. [IN-1] – 3/4/2010
Rep Walz, Timothy J. [MN-1] – 7/30/2010
Rep Wamp, Zach [TN-3] – 12/16/2009
Rep Welch, Peter [VT] – 4/30/2009
Rep Wexler, Robert [FL-19] – 4/21/2009
Rep Wilson, Joe [SC-2] – 5/4/2009
Rep Wittman, Robert J. [VA-1] – 3/4/2010
Rep Wolf, Frank R. [VA-10] – 3/3/2009
Rep Wu, David [OR-1] – 5/26/2010
Rep Yarmuth, John A. [KY-3] – 12/11/2009
Rep Young, C.W. Bill [FL-10] – 3/6/2009
Rep Young, Don [AK] – 5/4/2009

Share

Guest post from: Joe Castro

I recently logged onto www.satelliteinternetbroadband.com/ and got satellite internet at our house. The one person in my family who is not computer literate is my husband, but I think that he has liked the internet the most. The other day I came home and he had discovered a website that let your compare prices across websites. He was in the market for new ski gloves. We plan on doing a lot of skiing this winter and he picked some ski gloves that we couldn’t find in town. After comparing all of the prices, he ordered them on the internet and ended up getting them half off. I am glad that he got such a great deal on the gloves, but I am hoping that buying stuff on the internet doesn’t turn into a huge habit. Now we have access to some really great things that we wouldn’t have had access to before. Maybe I should start shopping on-line too! I’m sure that he wouldn’t be too happy with that because when I shop, I really shop!

Share

Down Syndrome Fact Sheet

• Down syndrome occurs when an individual has three, rather than two, copies of the 21st chromosome. This additional genetic material alters the course of development and causes the characteristics associated with Down syndrome.

• Down syndrome is the most commonly occurring chromosomal condition. One in every 691 babies is born with Down syndrome.

• There are more than 400,000 people living with Down syndrome in the United States.

• Down syndrome occurs in people of all races and economic levels.

• The incidence of births of children with Down syndrome increases with the age of the mother. But due to higher fertility rates in younger women, 80% of children with Down syndrome are born to women under 35 years of age.

• People with Down syndrome have an increased risk for certain medical conditions such as congenital heart defects, respiratory and hearing problems, Alzheimer’s disease, childhood leukemia, and thyroid conditions. Many of these conditions are now treatable, so most people with Down syndrome lead healthy lives.

• A few of the common physical traits of Down syndrome are low muscle tone, small stature, an upward slant to the eyes, and a single deep crease across the center of the palm. Every person with Down syndrome is a unique individual and may possess these characteristics to different degrees or not at all.

• Life expectancy for people with Down syndrome has increased dramatically in recent decades – from 25 in 1983 to 60 today.

• People with Down syndrome attend school, work, participate in decisions that affect them, and contribute to society in many wonderful ways.

• All people with Down syndrome experience cognitive delays, but the effect is usually mild to moderate and is not indicative of the many strengths and talents that each individual possesses.

• Quality educational programs, a stimulating home environment, good health care, and positive support from family, friends and the community enable people with Down syndrome to develop their full potential and lead fulfilling lives.

• Researchers are making great strides in identifying the genes on Chromosome 21 that cause the characteristics of Down syndrome. Many feel strongly that it will be possible to improve, correct or prevent many of the problems associated with Down syndrome in the future.

Share

Orthotics isn’t a medical field that is commonly known in families, but its importance in the lives of children is very important. Children need to be able to experience comfort when it comes to walking and running, and shoe inserts is the best way to give them this. Children with cerebral palsy, Down syndrome, and other conditions will certainly benefit from shoe inserts, as well as children who have difficulty in walking caused by injury or a serious illness and those who experience discomfort and pain in their shoes. When choosing your child’s shoes, make sure that the shoes are half a size bigger than the usual size for your child so that the shoe inserts will fit inside. A growing child’s feet should often be measured so that you can determine whether the shoes are still appropriate, as well as the shoe insert.

 

If your child is an athlete or a teenager who is fond of wearing high heels, then shoe inserts will provide them the right support and comfort that their feet need when it comes to their footwear. Serious injury can be prevented when you make use of the correct type of shoe inserts. Children with flat feet will certainly benefit greatly from orthotics. Children with low muscle tone or hypotonia will benefit from bracing.

 

There are a lot of devices and shoe inserts on the market that can help the child be able to walk and run well. Together with a good therapist or a professional, your child will have the proper support and guidance when it comes to the health of their feet and mobility. Helping your child’s walking and running abilities with shoe inserts can also affect their socialization skills, physical fitness and general health positively. There are many clinics that have orthotics and prosthetics programs as well as early intervention centers, podiatrists, and orthopedists that you can go to in order to give your child the help that they need. Shoe Inserts provides you a wide variety of information concerning footwear and orthotics Shoe Inserts, feet measuring methods and market. You can have lots of stuff to read about orthotics Shoe Inserts.

A’yani’s Shoe Insert Fitting

Share

Pamela Wilson
BellaOnline’s Children with Special Needs Editor

Families of children in early intervention programs and those who participate in physical therapy centers often have questions about the use of shoe inserts known as orthotics for their children. Although orthotics are mentioned in many books available to families and professionals, there are few magazine articles or newspaper stories that mention these commonly used shoe inserts that do make a difference to children with cerebral palsy, Down syndrome or other disorders; those who have challenges related to injury or serious illness; and teens who have pain or discomfort due to walking differently during early childhood and beyond.

It is important to find shoes half a size larger than usual so that orthotics fit inside, and to have children’s feet measured regularly so that the orthotic and the shoe is the proper fit.

Mainstream children who do not develop a normal arch by the age of six are often referred for orthotics. Bracing may be recommended for children with low muscle tone (hypotonia). Too often, foot problems are not noticed or addressed in children with disabilities or their mainstream peers as early as should be done.

There are a variety of devices available, including orthotic braces, that require the expertise of a compassionate therapist or licensed professional to adjust and monitor over time. Custom orthotics or braces are available from many reputable sources, including hospital and university clinics, orthotics and prosthetics programs, physical therapists at early intervention centers, orthopedists and podiatrists.

Children and teens with disabilities are not the sole users of orthotics – they are also recommended for athletes in various sports to avoid injuries or help them heal afterward.

While orthotics improve mobility skills, help in healing after injury, and have other benefits, there are other simple accommodations and supports that can be applied according to the individual’s situation so they can participate in sports and recreation opportunities throughout their lifetimes. Socialization skills, physical fitness, and general health benefits from these activities are too important to set aside when physical challenges are used as an excuse for exclusion or restrictions not related to a child’s health or safety.

Share

Fri, 2011-09-30

PLEASE CLICK HERE TO SIGN THE PETITION BEFORE 16 OCTOBER 2011

START DATE 30.09.2011
END DATE 16.10.2011

Since 2006, Down Syndrome International (DSi) has coordinated an annual observance known as World Down Syndrome Day (WDSD), held on 21 March (21/3) to signify the uniqueness of the triplication (trisomy) of chromosome 21 which causes the genetic condition Down syndrome.

The aim of this day is to raise awareness and understanding of a condition which affects approximately 1 in 800 births worldwide, and to promote the inherent rights of persons with Down syndrome to enjoy full and dignified lives and be active participants in their communities and society. Activities and events which take place on this day typically showcase the abilities and accomplishments of persons with Down syndrome and encourage independence, self-advocacy and freedom for persons with Down syndrome to make their own choices.

WDSD is observed by persons with Down syndrome and those who live and work with them in over 60 countries around the world in a variety of different ways, but with a common purpose, and the website www.worlddownsyndromeday.org provides an international forum for sharing experiences. Further information on WDSD is available on the DSi website here.

A draft resolution will be presented to the 66th Session of the United Nations General Assembly in October 2011, proposing that WDSD become a United Nations Observance Day with effect from 2012. If successful, this will greatly assist to raise the international profile of WDSD and awareness of the condition.

We request that you CLICK HERE to sign the petition, which we will then send to the United Nations so that its Member States are made aware of the global public support for this important initiative.

For further information please contact Andrew Boys at DSi.

Share


HELP PROTECT SPECIAL EDUCATION FUNDING
ISSUE

On June 16, 2011, the U.S. Department of Education’s Office of Special Education Programs (OSEP) issued new “informal guidance” that would allow local education agencies (usually known as school districts) that lower special education funding in violation of the law one year to continue to provide funding at this lower level in future years without consequences, even when they don’t meet the legal criteria for reduced funding. The lower funding level would be permitted regardless of whether the district has failed to meet the needs of students with disabilities.

Imagine applying this same result to your own life. What would happen if you violated your lease by paying only half of your rent this month and then the next month you expected the rent to be changed to the lower amount indefinitely? The landlord would never let you be enriched by a violation in this way. You would have to go back to paying the rent you owed before you violated the lease.

ACTION

Contact your Representative and Senators by calling the U.S. Capitol switchboard at (202) 224-3121 and asking for his/her office. When you get through to the office, ask to speak to the education legislative assistant. You can also email your elected officials by clicking on the Take Action button on this alert. A sample email is provided.

MESSAGE

Maintaining the local special education funding level (called “maintenance of effort” in IDEA) is essential in order to protect the right to a free, appropriate, public education for student with disabilities. This is a civil rights issue.

Parents shouldn’t be put in the position of having to go to due process to protect their child’s services, as a result of insufficient local special education funding condoned by OSEP.

States and districts that agree to take federal IDEA funds have an obligation not to cut local special education funding even when other budget cuts are made, unless they meet certain criteria in the law.

We need our Members of Congress to call on the Secretary of Education to rescind this informal guidance and reinforce to states and local districts the standards they must follow to be eligible for federal funds under IDEA

*It would be helpful to add a personal comment about how a student with disabilities in your life relies on special education funding or how services are hard to get even with the current funding levels.

BACKGROUND

The “informal guidance” issued by OSEP involves the “maintenance of effort” (MOE) requirement of the Individuals with Disabilities Education Act (IDEA). MOE, as it applies to local education agencies (LEAs-also known as school districts) means that districts have to provide at least the same level of local special education funding this year as they provided last year, as a condition of receiving federal IDEA funding. This new OSEP guidance would permit districts that lower special education funding this year below the amount from last year, in violation of the MOE requirement, to base next year’s education funding (and funding for future years) on the lower funding level that violated the law.

Based on OSEP’s interpretation of the MOE requirement in the guidance, if a district is supposed to provide $1 million for special education funding in Year X (because that is what they provided the previous year) and the district violates this rule by only providing $500,000, then the new special education funding level for the year following Year X (and every year thereafter) would be $500,000, unless the district decides to raise it or violates the law again by lowering it further. In this example, OSEP would only consider the district to be in violation of IDEA in Year X even though funding will continue at the lower level for every year thereafter.

The purpose of the MOE requirement (demonstrating maintenance of effort by maintaining the prior year’s funding level) is to ensure that all students with disabilities receive the special education services and supports they need for a free appropriate public education (FAPE). For that reason there are only two limited exceptions to the MOE requirement: (1) if the district’s expenses for that year have been legitimately reduced (e.g. by the natural turnover of senior highly paid staff for younger, but still qualified, lower paid staff) or (2) if the district receives additional federal funding.

Special education funding for each year is supposed to be based on the amount of funding from the prior year to protect the students. Therefore, Congress could not have intended this to be the case when the funding level from the prior year violated the law. In addition this interpretation undermines the district monitoring provisions in IDEA because even districts with a poor record of meeting student’s needs would be permitted to maintain a lower spending level in the years following the MOE violation.

ADDITIONAL RESOURCES

The informal guidance by OSEP is at

http://www.ideamoneywatch.com/docs/OSEP.Ltr.LEA.MOE.06.16.11.pdf 

A letter to OSEP and legal analysis regarding this issue by the Center on Law and Education is at

http://www.ideamoneywatch.com/docs/CLE_MOE_OSEP_LTR_08.17.11.pdf 

Share

The use of highly potent multivitamin and mineral supplements during a double-blind study brought about significant improvements in the intellectual capacities of five children affected by Down’s syndrome; thus the study concludes that such supplements may bring some improvement in the condition of children affected by Down’s syndrome. However, no noticeable improvements were observed in following researches carried out to probe these results further, for example a larger double-blind trial done a similar group of children brought out no noticeable benefits from such a supplementation. Children with Down’s syndrome also showed no great difference in intellectual abilities when a multivitamin and mineral supplementation was used along with placebo’s in a controlled group, the placebo group gained as much as the group using multivitamins and minerals. And last of all, a through review of all the research done on these particular supplementation gives no compelling reason for the use of multivitamins or B vitamin supplements in people with Down’s syndrome especially where improving intellectual function is concerned and most of all it established no potential benefits existed from such supplementation.

On careful examination of the blood profile of people with Down’s syndrome and specifically the red blood cells, certain traits become apparent in these cells; in that such cells tend to show a tendency for deficient levels of the vitamin B12 or folic acid in the tissues. Other thorough examinations of the cells in Down’s syndrome patients however, indicate normal or average levels of folic acid. Moreover one a single study done with comparison groups of Down’s syndrome patients and normal individuals indicates a reduced level of vitamin B12 in the patients with Down’s syndrome. And these results have yet to be analyzed and proved conclusively as intervention trials using either vitamin B12 or folic acid and their possible role in the condition have not been investigated until now.

Down’s syndrome patients also have a greater tendency on the whole to develop other conditions such as Alzheimer’s disease, cataracts and other autoimmune diseases, along with a general increase in the pace of aging when compared with normal people on average. Free radical action leading to the damage of vital tissues in the body characterizes these diseases in general; that is free radical action is what impacts the body during the various stages of these diseases. According to the anecdotal evidence, it is deduced that the particular genetic characteristic that Down’s syndrome induces in a person leads to an increased demand for antioxidants and other nutrients necessary for the body to successfully ward off damage caused by free radicals-this deduction is further supported by blood and urine biochemistry tests that have borne out these genetic predisposition. The oxidative damage suffered by individuals afflicted with Down’s syndrome was found to be preventable by supplementation with the vitamin E, in a preliminary study carried out on a group of patients afflicted with Down’s syndrome and hence susceptible to this form of cellular damage from radical oxygen species. The situation becomes complex because when a comparison between healthy individuals and patients with Down’s syndrome was carried out it was observed that the blood levels of the vitamin C and the vitamin E, which are two important antioxidant nutrients, did not considerably differ to a great extent. Therefore further research and investigations still have to be carried out on the role if any of vitamin E and other antioxidants in treating some of the oxidative damage associated with Down’s syndrome.

While many researchers have found the levels of essential minerals like zinc and selenium to be low in the blood of patients afflicted with Down’s syndrome-other researchers have found these antioxidant minerals selenium and zinc were present in normal levels in at least one study of people with Down’s syndrome. This situation is further complicated by the fact, that still other studies show low levels of zinc in more than 60% of patients with Down’s syndrome. Hence, the possible implications of supplementation with these minerals is still haze and requires further investigation, for example during a preliminary study where selenium supplementation was carried out on children with Down’s syndrome, a marked improvement in the antioxidant activity within the body was discovered. Low levels of zinc along with very poor immune system function was found in a preliminary study conducted on a group of patients with Down’s syndrome, this can perhaps be related to the fact that sufficient quantities of Zinc is critical for proper immune function and for the proper functioning of the immune system and the immune cell activity. Therefore it an improved immune cell activity and immune system functioning can be achieved through regular supplementation using zinc. Down’s syndrome patients who were given zinc supplements during preliminary intervention trials, showed appreciable improvement in the immune cell activity along with reduced rates of infection, the dosage regimen was in amounts of 1 mg per 2.2 pounds of body weight a day during the trial period. However, these beneficial effects were not observed in children with Down’s syndrome during supplementation in a controlled trial, these children were given zinc at 25 mg per day for the younger children under the age of 10 years and the dosage was 50 mg for older children; thus this study shows that this form of supplementation may not be suitable for the treatment of children. However, this is not to say that zinc supplementation must not be carried out at all in all cases. It is known that zinc performs other important roles within the human body. Indeed the preliminary data gathered from various sources shows that zinc supplementation, at the rate of 1 mg per 2.2 pounds of body weight a day during the treatment period, effected an improvement in the functioning of the thyroid gland in all patients with the Down’s syndrome and in addition it also caused an increased growth rate in children suffering from the various symptoms associated with Down’s syndrome.

The normal functioning of the nervous system is assured by the presence of acetyl-L-carnitine, a vital compound that occurs naturally in the brain and the nervous system. Visual memory and attention showed marked improvements in all Down’s syndrome patients during a preliminary trial, where the test subjects were given 500 mg of L-acetyl-carnitine thrice a day during a testing regimen lasting a total of 90 days; clearly this substance has important functions in eliciting normalization of visual memory and in inducing marked improvements in nervous functioning. On carrying out the same treatment regimen in patients with obvious deficient mental faculties unrelated to Down’s syndrome and in untreated subjects on a placebo, significant results were not obtained. As far as people afflicted with Down’s syndrome are concerned a lot of careful research into the effects of L- acetyl-carnitine is necessary and will prove itself beneficial in the long term.

Mood and sleep timings are affected in the human body through a substance called 5-hydroxytryptophan (5-HTP); this substance is an amino acid that the body uses to manufacture the neurotransmitter serotonin. The body manufactures this 5-HTP from the amino acid tryptophan; this amino acid precursor is found in the food proteins consumed in the daily diet. Children suffering from Down’s syndrome have been shown to have low levels of serotonin as far as the early data on this aspect of their physiology is concerned, in addition to this factor the supplementation of 5-HTP in young children showed observable improvements in the muscle tone and a reduction in the protrusion of the tongue as a direct result of the supplementation. Moreover further symptoms such as restlessness, diarrhea and vomiting, and muscle spasms, including the elevation of blood pressure were observed during supplementation with 5-HTP in patients afflicted with Down’s syndrome. Infants who underwent 5-HTP supplementation during one study showed seizures as a further side effect of the supplementation as a further complication. The beneficial effects of supplementation using 5-HTP have been shown by other studies to be mostly non-existent. Taking all these studies into account and because of the high incidence of other complications including adverse side effects the use of 5-HTP in infants and children with Down’s syndrome is not recommended at this time- this substance also has no proven beneficial effects.

Share

About Buddy Walk

The Buddy Walk® was established in 1995 by the National Down Syndrome Society to celebrate Down Syndrome Awareness Month in October and to promote acceptance and inclusion of people with Down syndrome. Today, the Buddy Walk program is supported nationally by NDSS and organized at the local level by parent support groups, schools and other organizations and individuals.

Over the past sixteen years, the Buddy Walk program has grown from 17 walks to nearly 300 expected in 2011 across the country and around the world. Last year alone, 285,000 people participated in a Buddy Walk! They raised more than $11.2 million to benefit local programs and services as well as the national advocacy initiatives that benefit all individuals with Down syndrome.

The Buddy Walk is a one-mile walk in which anyone can participate without special training. It is an inspirational and educational event that celebrates the many abilities and accomplishments of people with Down syndrome. Whether you have Down syndrome, know someone who does, or just want to show your support, come and join a Buddy Walk in your local community!

History

Over the last sixteen years, the Buddy Walk® has not only become the premier advocacy event for Down syndrome, but also the world’s most widely recognized public awareness program for the Down syndrome community.

Here are some milestones to show how the program has grown:

1995

  • The Buddy Walk program was established in 1995 by the National Down Syndrome Society (NDSS) to promote acceptance and inclusion of people with Down syndrome and to celebrate Down Syndrome Awareness Month in October.
  • 17 events take place across the country during the inaugural year of the Buddy Walk.
  • Chris Burke leads the flagship New York City Buddy Walk.

The premiere advocacy event for Down syndrome is off to a great start!

1999

  • NDSS introduces the Times Square Video to bring attention to the Buddy Walk program and raise acceptance of individuals with Down syndrome.
  • The Buddy Walk adds a fundraising component to raise money for local and national programs and services.

2001

  • NDSS introduces a new Buddy Walk logo‚Äîthe now familiar blue and yellow graphic with a family holding hands.
  • A Wal-Mart commercial featuring footage of the Buddy Walk in Colorado Springs, CO airs and is instrumental in the growth of the Buddy Walk program.
  • Over 100 Buddy Walk events take place this year.

2002

  • John C. McGinley joined NDSS as National Buddy Walk® Spokesman and since then has continued to generate national visibility for NDSS. Since then he has participated in countless PSA’s to promote positive public awareness for people with Down syndrome and most recently became the NDSS Ambassador in the My Great Story campaign.
  • The first BuddyWalk.org site is launched.
  • The first comprehensive Buddy Walk Manual for walk organizers is distributed.

2003

  • NDSS further demonstrates its support for the growing Buddy Walk program by designating it as one of the Society’s five key strategic initiatives for the coming years and hiring a National Buddy Walk Coordinator to oversee the direction of the program and assist local organizers.
  • The Buddy Walk logo is trademarked by NDSS.
  • More than 190 Buddy Walk events take place in 49 states and 5 countries with over 180,000 participants raising more than $2.5 million.

2004

  • BuddyWalk.org is re-launched with new tools and features for Walkers and organizers.
  • More than 210 Buddy Walk events take place with over 200,000 participants raising more than $4.5 million.

2005

NDSS celebrates 10 years of the Buddy Walk!

  • More than 260 Buddy Walk events take place with over 200,000 participants raising more than $5.5 million.
  • Since the Buddy Walk was established in 1995, over 1,500,000 people have participated in a Buddy Walk worldwide.

2007

  • More than 270 Buddy Walk events take place with approximately 250,000 participants raising more than $9.5 million dollars, a 46.2% increase from 2006.
  • Since the Buddy Walk was created in 1995, over 2,000,000 people have participated in a Buddy Walk worldwide.

2008

  • The Buddy Walk program welcomed its first regional and national partners: Regal Entertainment Group, Knology and the American Physical Therapy Association, Section on Pediatrics.
  • The Buddy Walk Public Service Announcement was played nationwide at all Regal Cinemas before every movie for two weeks to celebrate Down Syndrome Awareness Month and the National Buddy Walk program.
  • More than 275 Buddy Walk events take place with over 250,000 participants raising more than $10.5 million.
  • The Buddy Walk was ranked in the top 30 fundraising events nationwide for: money raised, revenue increase, and best series event.

Source: 2008 Run Walk Ride Fundraising Council Survey Results

2009

  • NDSS held the first National Buddy Walk conference in Columbus, Ohio where Buddy Walk organizers were able to learn from NDSS leadership and share best practices with one another.
  • NDSS introduced a new licensing agreement that commits Buddy Walk groups to a 7% contribution that supports the NDSS National Policy Center in Washington D.C.
  • The first Buddy Walk held on a military base in a combat zone took place at Camp Phoenix in Kabul, Afghanistan.

Walk FAQ’s

Do I need to know someone with Down syndrome to participate in a Buddy Walk®?
Not at all. The goal of the Buddy Walk is to promote understanding and acceptance of people with Down syndrome. Whether you have Down syndrome, know someone who does or just want to show your support, come and join the Buddy Walk.

How can I find out if there is a Walk in my community?
To find out if there is a Walk in your community, you can enter your zip code in the Find A Walk box located at the top of the home page or you can click on the “Find A Walk” link. Either way, you will find the closest Walk to you. If you do not see a Walk in your area, you can e-mail the Buddy Walk staff at buddywalk@ndss.org to find out if a local support group has registered a Walk that is not yet posted.

Not everyone in my family is able to walk a mile. Are they still able to participate?

Yes. Buddy Walk events are open to participants of all ages and abilities. Each Walk location has places where you can sit down, relax, and watch the excitement if you choose not to walk. You can also become a member of the cheering section and cheer on the walkers.

Is there an age requirement for the Buddy Walk?

All participants are welcome! From strollers to seniors, all supporters of individuals with Down syndrome are invited to participate. Buddy Walk events are great places to network with families and learn more about support services available.

I’d like to volunteer at the Walk in my area. How do I get involved?

For information on volunteering at a Buddy Walk in your community, please click on “Find A Walk”. Review the events taking place in your area by clicking on your state or other states in the vicinity of your home. Click to select a Walk and contact the event organizer that is listed.

There isn’t a Walk in my area. How do I go about starting a Walk?

NDSS has all the tools to help you plan a successful event, from a planning timeline to posters and incentive ideas. Buddy Walks range in size from 50 people to more than 5,000 — so whatever your time and resources, you can plan a successful Walk for your community! NDSS has developed a user-friendly Buddy Walk Manual that provides valuable information about the Buddy Walk program and how to create the best walk you can.

Download and read the 2011 Buddy Walk Information Packet to learn more about the Buddy Walk program and how to organize a Walk. You can register a walk online by clicking on one of the “Organize a Walk” links.

Who designs the National Buddy Walk T-Shirts?

NDSS and the National Buddy Walk® Committee hold a nationwide contest for a new t-shirt design for the upcoming Buddy Walk season. The selected design will be featured on the t-shirt at the National Buddy Walk in New York City and will be available to all other Buddy Walks in the coming year.

Designers submitting their artwork can be individuals with Down syndrome, parents, siblings or friends. This artist will receive recognition on the Buddy Walk website for the entire year!

Click here for details regarding the contest.

Click here for guidelines and the entry form. An entry form must be included with each submission.

Can I bring my dog to the Buddy Walk?

While most walk venues will allow dogs, not all do. Please speak with the organizer in advance of your local Walk to find out if you can bring your four-legged friend with you.

Do I have to raise money to participate in the Buddy Walk?

There are no mandatory fundraising requirements for participants of a Buddy Walk. While most Walks choose to include a fundraising component to raise money for local and national programs, there is no individual requirement beyond the registration fee (if applicable).

 For More information visit: www.BuddyWalk.org

Share

Share

Theme Tweaker by Unreal