Wednesday, April 16, 2014
Sluggish cognitive tempo: the ADHD-like disorder that explains daydreaming?
http://www.theguardian.com/society/shortcuts/2014/apr/15/sluggish-cognitive-tempo-new-disorder-rival-adhd
Tuesday, February 11, 2014
Dr. Rosa A. Hagin
I am sorry to report that Dr. Rosa A. Hagin, died on Friday, Feb. 7, 2014, at the age of 92. She was an educational psychologist and had worked as aresearch professor of psychology at New York University School of Medicine. Her area of expertise was in the neuropsychological core of reading. She had also taught at Trenton State College and Fordham University. She did research and taught educators about effective tools for early child intervention, how to identify young students with LD (learning disabilities), and how to treat them early in their academic careers.
I knew her as a mentor, teacher and advocate for children and adults with learning disabilities.
When I was diagnosed with learning disabilities & ADHD as an adult, I was told I would have a difficult road ahead of me to earn my graduate degree. Some professors actually tried to discourage me from getting an advanced degree. I found out about Dr Hagin and that she was an expert in adult learning disabilities. She lived in Manhattan at the time, and I called her to set up an appointment. To my surprise she answered the phone herself. I visited her home office the same week. She gave me a lot of encouragement and became my mentor for a short while. Her effect on me has lasted until today. She encouraged me to be a tenacious learning disabled student. When I told her I wanted to co-found a non-profit organization to helps others with learning disabilities, she told me it would be hard but I could do it. And I did! In 2001, LD Resources Foundation was founded.
You might have heard about the Bartlett case, a landmark case decided in New York City in 2001 by then Federal Judge Sonia Sotomayor . Jo Anne Simon (a member of the LD Resources Board) was the attorney representing a law school graduate with dyslexia, who was eventually allowed special accommodation to take the bar exam in New York State. Dr. Rosa Hagin was an expert witness in that case.
Dr. Isabella Reichel, Ed.D., SPL-A, CCC a Speech-Language Pathologist and Audiologist, is also a board member and advisor to LDRF, and acknowledges Dr. Hagin’s influence in mentoring and guiding her in her career.
It’s no coincidence that Dr. Hagin was a mentor to three of us who have made it a priority to help people with learning disabilities, through our own careers as well as through our work with LD Resources Foundation.
Dr Hagin published many scholarly articles, as well as what I consider the most important textbook on learning disability: "Disorders of Learning in Childhood ".
She will be missed dearly by all of us.
Monday, July 22, 2013
State Action Round-Up on Affordable Care Act Implementation
In less than six months, the major health insurance provisions of the
Affordable Care Act will go into effect. This is the second post in a
series that offers an overview of action on the new state health
insurance marketplaces, or exchanges, and expansion in eligibility for
the Medicaid program.
Insurance Marketplace Updates
Beginning on October 1, 2013, Americans who do not have affordable health benefits through a job will be able to go to a new health insurance marketplace in their state and enroll in a private health plan. Adults with annual incomes up to 400 percent of poverty ($45,960 for an individual and $94,200 for a family of four) will be eligible for premium tax credits to help reduce the cost of coverage. In most states, companies with 50 or fewer employees will also be able to select plans through their state’s small-business marketplaces.
Currently, 16 states and the District of Columbia intend to operate a state-based marketplace, while the remaining 34 states will have a federally facilitated marketplace. Seven of these 34 states will conduct plan management activities and/or consumer assistance and outreach functions in a state–federal partnership model. Another seven of the 34 will conduct plan management activities only, and one, Utah, will operate the small-business marketplace while the federal government operates the individual marketplace.
Here is a list of recent state and federal activity.
Action on state-based marketplaces:
Insurance Marketplace Updates
Beginning on October 1, 2013, Americans who do not have affordable health benefits through a job will be able to go to a new health insurance marketplace in their state and enroll in a private health plan. Adults with annual incomes up to 400 percent of poverty ($45,960 for an individual and $94,200 for a family of four) will be eligible for premium tax credits to help reduce the cost of coverage. In most states, companies with 50 or fewer employees will also be able to select plans through their state’s small-business marketplaces.
Currently, 16 states and the District of Columbia intend to operate a state-based marketplace, while the remaining 34 states will have a federally facilitated marketplace. Seven of these 34 states will conduct plan management activities and/or consumer assistance and outreach functions in a state–federal partnership model. Another seven of the 34 will conduct plan management activities only, and one, Utah, will operate the small-business marketplace while the federal government operates the individual marketplace.
Here is a list of recent state and federal activity.
Action on state-based marketplaces:
- New York state regulators announced that insurance rates for plans sold through the exchange in 2014 are as much as 50 percent lower than what individuals currently pay to purchase a plan on their own.
- Approved 2014 rates.
- Governor’s press release.
- $7,243,004 of $150 million in grants to community health centers went to 57 centers in New York
- More.......
http://www.commonwealthfund.org/Blog/2013/Jul/State-Action-Roundup-July-19.aspx
Tuesday, July 16, 2013
http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm360811.htm
FDA permits marketing of first brain wave test to help assess children and teens for ADHD
The U.S. Food and Drug Administration today allowed marketing of the first medical device based on brain function to help assess attention-deficit/hyperactivity disorder (ADHD) in children and adolescents 6 to 17 years old. When used as part of a complete medical and psychological examination, the device can help confirm an ADHD diagnosis or a clinician’s decision that further diagnostic testing should focus on ADHD or other medical or behavioral conditions that produce symptoms similar to ADHD.
http://www.nytimes.com/2013/07/16/health/brain-test-to-diagnose-adhd-is-approved.html
The test uses an electroencephalogram, or EEG, with sensors attached to a child’s head and hooked by wires to a computer to measure brain waves. It traces different types of electrical impulses given off by nerve cells in the brain and records how many times those impulses are given off each second.
The test takes 15 to 20 minutes, and measures two kinds of brain waves — theta and beta. Certain combinations of those waves tend to be more prevalent in children with A.D.H.D., the Food and Drug Administration said in a news release.
Tuesday, July 9, 2013
Dancing and tears greet book treaty for blind
http://www.groundup.org.za/content/dancing-and-tears-greet-book-treaty-blind
Marrakesh Treaty to Facilitate Access to Published Works for Persons who are Blind, Visually Impaired, or otherwise Print Disabled,
http://www.internationaldisabilityalliance.org/en/article/ida-press-release-new-wipo-treaty-27-june-2013Geneva 1 July 2013 – Last week (27 June 2013), a new historic treaty was adopted in Marrakesh under the auspices of the World Intellectual Property Organization (WIPO) to boost access to books for the benefit of hundreds of millions of people who are blind, visually impaired and print-disabled.
The treaty, called the Marrakesh Treaty to Facilitate Access to Published Works for Persons who are Blind, Visually Impaired, or otherwise Print Disabled, requires the contracting parties to adopt national law provisions that permit the reproduction, distribution and making available of published works in accessible formats through limitations and exceptions to the rights of copyright right holders. It also provides for the exchange of these accessible format works across borders by organizations that serve the people who are blind, visually impaired, and print disabled. In this regards, it will harmonize limitations and exceptions so that these organizations can operate across borders. The Treaty, which calls for cooperation among its contracting parties in order to foster cross-border exchanges, has been also designed to provide assurances to authors and publishers that that system will not expose their published works to misuse or distribution to anyone other than the intended beneficiaries.
This Treaty will benefit more than 314 million blind and visually impaired persons worldwide. Currently only 5% of all published books in the developed countries and less than 1% in the developing countries have been produced in accessible formats.
The World Blind Union (WBU) has been instrumental in the negotiations of this Treaty, which has been the culmination of many years of work on improving access to published works in formats such as Braille, large print text and audio books.
The treaty will enter into force after it has been ratified by 20 WIPO members.
Stevie Wonder Speaks at Close of Marrakesh Treaty Negotiations
http://www.youtube.com/watch?v=oPG11HGCZNQ&list=PLsm_LOEppJazVkT-dgHlHRI9jGqlqJLBF
Tuesday, July 2, 2013
Connect with us
The foundation in 2001
with the goal of giving financially needy college students with LD/ADHD the
tools to successfully complete their college education. We provide AT
scholarships to those who cannot afford to purchase these technologies on their
own.
You know, as a professional working with this population, more and more
students with learning disabilities are graduating from high school and going
to college to continue their education. However this population faces many
challenges to achieve their dreams of obtaining a diploma.
The LD Resources Foundation, Inc. is the only grassroots, donor based
foundation in the United States to give Assistive Technology tools DIRECTLY to
students not only to use for their college studies, but to use in their
careers.
This fiscal year was our main focus was to award
assistive technology to the 24 students who financially limited.
In the fall we completed our pilot program at
Churchill School and awarded technology tools to several of their graduating
seniors. Those students are now using their awards in their first year in
college. I continue to provide consulting and technical assistance to the
school.
We have expanded outreached to colleges and
universities in New York City and around the country and we hope to keep expand
our outreach with collaboration with The National Center for Learning
Disability.
Please visit http://www.ldrfa.org/assistive-list.html for our latest list of assistive technology
review
The LDRFA.org Resource Center has assembled
several sources of information to educate people on the pros and cons of
different assistive technology tools. These tools are invaluable, because they
assist people with learning disabilities master such important tasks in college
as studying for exams, completing reading assignments, taking notes in classes
and writing research papers. People with various disabilities are using
assistive technology tools at work, college, and at home.
We look forward to hearing from you.
Have a Happy 4th of July,
Have a Happy 4th of July,
Board of LD Resources Foundation, Inc.
1-646-701-0000
Sunday, December 4, 2011
Matthew P. Sapolin, Commissioner of the Mayor’s Office for People with Disabilities, died of cancer on Tuesday 11/29/11 at the age of 41.
Matthew P. Sapolin, Commissioner of the Mayor’s Office for People with Disabilities, died of cancer on Tuesday 11/29/11 at the age of 41. Commissioner Sapolin was an inspiration for all people with disabilities. He refused to accept that his blindness caused him any limitations. In fact, he accomplished in his too- short lifetime more than many people I know, including being a drummer in the band he formed, serving as co-captain of the wrestling team at NYU, playing chess and becoming a marathon runner. He had a great sense of humor and was a big sports fan; he particularly loved baseball.
After losing his sight at a very young age, he attended regular classes in the Islip, NY school system, through the advocacy of his mother, so that he had the opportunity to interact with students without disabilities. I think that such an educational experience gave him the strength to realize that he had no limitations to achieve success in whatever he wanted to pursue.
I believe Matthew was the best advocate we have had in New York City for people with disabilities. He was a great negotiator, and was able to achieve significant victories for people with disabilities. Among his achievements were working to make the city’s building code more accommodating, initiating a rent freeze for some people with disabilities in New York city (Disability Rent Increase Exemption - DRIE) and initiating Disability Mentoring Day in New York City, which was held this year on October 19.
Matthew’s spirit was felt at his funeral, which had an overwhelming turnout of family, friends and colleagues on Friday, December 2 at St Patrick’s Cathedral. Mayor Bloomberg gave a most heartfelt eulogy; his words showed his admiration for Commissioner Sapolin when he said “nothing could stop Matthew” (view the original article here).
Personally, the Commissioner was an inspiration to me and the organization that I helped co-found, LD Resources Foundation. In 2009, he was my professor at CUNY’s graduate program in Disabilities Studies. He asked me if I had been able to read the books he had assigned for the class. I answered I had not read them, as they were not available in readable format with assistive technology. Matthew dismissed all the books that were not accessible and taught our class based on his experiences in life. It was the most amazing class I have ever taken.
Matthew became a mentor to me in my non-profit work, and an inspiration to many people in New York City. He taught me that disabilities are not a barrier for achieving success. I learned from Matthew how to negotiate successfully for resources for people with learning disabilities. As Disabilities Commissioner, Matthew was easily reachable at his office, and always had time to discuss an issue or question that was important to me. He was a supporter of LD Resources Foundation. His concern about helping people with learning disabilities helped me learn how to advocate with colleges and libraries to provide adaptive technology for people with LD.
Matthew, your spirit will be with us forever…
After losing his sight at a very young age, he attended regular classes in the Islip, NY school system, through the advocacy of his mother, so that he had the opportunity to interact with students without disabilities. I think that such an educational experience gave him the strength to realize that he had no limitations to achieve success in whatever he wanted to pursue.
I believe Matthew was the best advocate we have had in New York City for people with disabilities. He was a great negotiator, and was able to achieve significant victories for people with disabilities. Among his achievements were working to make the city’s building code more accommodating, initiating a rent freeze for some people with disabilities in New York city (Disability Rent Increase Exemption - DRIE) and initiating Disability Mentoring Day in New York City, which was held this year on October 19.
Matthew’s spirit was felt at his funeral, which had an overwhelming turnout of family, friends and colleagues on Friday, December 2 at St Patrick’s Cathedral. Mayor Bloomberg gave a most heartfelt eulogy; his words showed his admiration for Commissioner Sapolin when he said “nothing could stop Matthew” (view the original article here).
Personally, the Commissioner was an inspiration to me and the organization that I helped co-found, LD Resources Foundation. In 2009, he was my professor at CUNY’s graduate program in Disabilities Studies. He asked me if I had been able to read the books he had assigned for the class. I answered I had not read them, as they were not available in readable format with assistive technology. Matthew dismissed all the books that were not accessible and taught our class based on his experiences in life. It was the most amazing class I have ever taken.
Matthew became a mentor to me in my non-profit work, and an inspiration to many people in New York City. He taught me that disabilities are not a barrier for achieving success. I learned from Matthew how to negotiate successfully for resources for people with learning disabilities. As Disabilities Commissioner, Matthew was easily reachable at his office, and always had time to discuss an issue or question that was important to me. He was a supporter of LD Resources Foundation. His concern about helping people with learning disabilities helped me learn how to advocate with colleges and libraries to provide adaptive technology for people with LD.
Matthew, your spirit will be with us forever…
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