Monday, March 2, 2009

Film by developmentally disabled adults wins award at Canadian film festival

From BBC News in the UK. You can watch the film, "Germ Academy," here. As someone who is a bit germ-phobic, my one sentence review is, it's great! Wash your hands!

A film made in Somerset by adults with learning disabilities has won the Best Educational Film Award at a film festival in Canada.

The group of 20 people, who are all trainees with Somerset Work Preparation Service, put the film together after learning about food hygiene.

They all shared the acting, filming, sound recording as well as organising and setting up props. A county council disability service spokesman said it was a great film.

He said: "The film takes a very entertaining look at the effects that a lack of food hygiene has on our health,"

"Viewers tend to find it very engaging and are able to absorb the information about food safety."

After winning the Best Special Effects category at the Oska Bright Awards, Germ Academy was shown at venues throughout the UK.

It was also screened as part of the Prague film festival in October 2008.

Recently, it won the award for Best Educational Film at the Canada Film Festival.

Saudi mother tries to break silence about Down syndrome in Arab world

From The National in Saudi Arabia:

ABU DHABI -- When the doctor asked Sonia al Hashimi 22 years ago if she knew about Down’s syndrome, little did she realise that her search for its meaning would change her life forever.

“I vaguely remembered a photo of a child with distinct features labelled as suffering from Mongol disease on a school board, and didn’t understand what that had to do with me,” said Mrs al Hashimi, recalling the conversation with the doctor who helped deliver her afflicted son at the Abu Dhabi Corniche hospital.

In an incubator, suffering from heart and muscle complications after a premature birth, her four-day-old son Saif was fighting for his life. As the days went by one of the nurses advised Mrs al Hashimi to “just give up” as Down’s syndrome babies “rarely survive”.

“That statement just did something to me,” she said. “It stirred in me a feeling of defiance, where I wanted to prove to the world that my son is going to make it, and he will be something special.”

Saif (pictured) has since won five medals in swimming at Special Olympics, and today Mrs al Hashimi is the president of the UAE Down Syndrome Association.

Down’s syndrome, named after John L H Down, the English doctor who first described it in 1866, is a genetic disorder stemming from a chromosomal abnormality. Those with it are normally intellectually impaired, and may have stunted growth and other physical abnormalities.

“For the first five years of Saif’s life, I put everything on hold,” Mrs al Hashimi said. “I held off having more children and devoted myself completely to teaching him to become independent.”

She did everything to “stimulate” her child’s development, including regular doses of Sesame Street, muscle exercises and recreational outings. “I painted his bedroom with vibrant, loud colours, and brought him intellectual, stimulating toys,” she said, “and did everything I could to awaken in him all his senses.”

Mrs al Hashimi even learned English to be able to read books on Down’s syndrome. She eventually had five more children. Saif is now the attentive big brother.

Mrs al Hashimi recalled “too many” troubling social incidents – from parents demanding that her son be pulled from a mainstream public school when she tried to integrate him there, to acquaintances asking her to keep him at home when she attended social gatherings. “It used to hurt me so much,” she said, “but I refused to keep my son locked up. If something is not perfect on the outside, then people here just reject it.”

According to recent statistics by the Centre for Arab Genomic Studies, 21.4 babies per 100,000 are born with Down’s syndrome in the UAE, about double the global rate.With the launching of a nationwide awareness campaign by the Ministry of Education and the Emirates Foundation that is targeting 70 schools, Mrs al Hashimi believes the incidents of “ignorant” behaviour could decrease and that parents of children with the condition will “come out of their shell”.

“I have already witnessed such great change and awareness,” said Mrs al Hashimi, who has already participated in two lectures by the campaign as a representative from the association.

Saif also gave a presentation and told the students: “I am normal.” He talked about his father coaching him in sport and said that, because of his father’s unshakable support, he became a professional swimmer.“I love to swim; I am a champion,” he said as he held up his medals.

The Down Syndrome Association grew from a handful of mothers with afflicted children who were running a support group in Dubai to a 300-member association.

In 2006, the Ministry of Social Affairs launched the association as a public benefit group with the aim of “unlocking hidden potentials” in people with Down’s syndrome aged from a few months to 30. It is under the patronage of Sheikha Manal bint Mohammed bin Rashid Al Maktoum, the President of the Dubai Women Establishment and wife of Sheikh Mansour bin Zayed Al Nahyan, Minister of
Presidential Affairs.

The association has several committees, including cultural, family care and sport, as well as a medical committee, of which Dr Manal Jarour is a deputy head. Being a paediatrician, she had a big hand in connecting a lot of mothers with Down’s syndrome children.

“Whenever I saw a Down’s syndrome child on the street, I would grab the parents and tell them about our support group and how they can help their child lead a better life,” she said.

Dr Jarour’s last child, Mahmoud, 10, has Down’s syndrome and she too found it difficult to get a school to accept her child.

“None of the private schools would take him in. We had to pull so many strings before Mahmoud was accepted into one of the public schools.”

Dr Jarour stressed the importance of early intervention as well as regular schooling, because without that, it will be very difficult for them to lead normal lives. “We have to get everyone involved, the families, the societies, the officials, the schools, and force them all to accept people with Down’s syndrome,” she said.

The association runs a free clinic, with occupational and speech therapists, but is in need of an Arabic speech therapist. “There is still a lot that needs to be done,” she said. “I am a medical doctor, and still I didn’t know much about Down’s syndrome and had to research. I am still learning something new each day.”

Her son, Mahmoud, has a talent for taking photos, she said, and takes his camera everywhere. Often, he would charge a fee of “a smile and a hug” for one of his photos.
His mother is hopeful he can turn his passion into more than just a hobby. “They have hidden talents, you just have to dig deeper than usual to find them,” Dr Jarour said.

Mrs al Hashimi and Dr Jarour are among the few brave Emirati women willing to discuss Down’s syndrome and the great challenges of raising up their children in a society still unaccustomed to the disability. Now good friends, the two women run an aggressive rights campaign for people with Down’s syndrome.

“You would be surprised what they can do if given a chance and the right environment,” said Mrs al Hashimi, who recently placed one of the children from the association in ballet classes.

“People said, including the instructor, it couldn’t be done, but the six-year-old girl is dancing on her toes, and she is doing it gracefully.”

Washington state dropping MR language from state's laws

From The AP:

OLYMPIA, Wash. -- The term "mental retardation" would no longer be used in new state laws, under a bill that has passed the state House.

The bill sailed through the Legislature's lower chamber by a unanimous vote on Friday. It now goes to the Senate.

Under the measure, the phrase "intellectual disability" will be used in place of "mental retardation" in all future state laws.

Officials will also have to scrub "mental retardation" from old laws, when those statutes are revised.

Supporters say the term "mental retardation" is an outdated and insulting way of referring to people with intellectual disabilities.

The bill is House Bill 1835.

Ghana disability organization pushes for a person with a disability to be name a government minister

From AllAfrica.com:

The Disability Network is urging President John E. Atta-Mills to fulfill his promise of forming an all-inclusive government by giving at least one deputy ministerial position to a person with disability (PWD).

Members of the network are of the view that such an appointment is overdue. A few weeks ago, a delegation of the disability movement, called on the President at the castle and tabled a number of requests including the appointment of PWDs as ministers.

With the President already naming substantive ministers, the disability movement has turned its attention to the few deputy ministerial nominations yet to be made; bearing in mind that a list of 23 deputy minister designates was released over the weekend.

At its first meeting for 2009 held in Accra on Tuesday, members of the Disability Network felt the need to rehash their call. Mr. Emmanuel Sackey, Communications Officer of the Ghana Federation of the Disabled (GFD), noted that it was regrettable that no PWD was named among the ministers or their designated deputies.

Mr. Alexander Kojo Tetteh, Executive Director of the Centre for Employment of Persons with Disabilities, agrees with Mr. Sackey but adds that the appointment is even more warranted by the President's own acclaimed commitment towards all-inclusiveness.

"I think the time has come because we are talking about all-inclusive government," he told Public Agenda.

He indicated that such an appointment will ensure that the marginalized forms part of the decision making process. "That individual will bring more support to disability issues."

The opinion of Mr Charles Appiagyei, acting Executive Director of Action on Disability and Development (ADD) was that the governing National Democratic Congress (NDC) "has long expressed interest in persons with disabilities once expressed, they must live it."

If appointed as minister, a PWD will give better representation to issues raised by the GFD and its member organizations, as well as their affiliates, he pointed out. Mr. Appiagyei added that a minister who is disabled "will serve as a role model and bring inclusion."

He said PWDs are a set of heterogeneous people and cut across various facets of the society - they are women, men, children, employed, unemployed, educated, uneducated, etc. - therefore, such an appointment can positively affect many lives.

"PWDs have a constituency that can be leveraged," he stated.

Miss Rita Kyeremaa Kusi, Executive Director of GFD, also shared the view that disability was a cross-cutting issue. She said the disability movement was still hopeful that a PWD would be appointed among deputy ministers.

On his part, Mr. Joseph Adu-Boampong, the First Vice President of the GFD, said PWDs could better present their issues through a minister who is disabled because he would have fellow-feeling.

"I believe that PWDs will be able to speak better for PWDs," according to Mr. Humphrey Kofie, Conmmunity Programmes Coordinator of BasicNeeds-Ghana.

In his view also, "It is time that they (PWDs) took the mantle themselves." He adds that PWDs will feel more comfortable channeling their concerns through one of their own.

Economy leaves donated house for family with kids who have MD unfinished

From KIDK-TV:

REXBURG, Idaho - This house is supposed to be finished, but it's not, pretty disappointing for a family with four kids with muscular dystrophy. They were expecting donations from local businesses but due to the economy, they've been backing out.

So to help, The Rexburg Fire Department has been donating their time this week in a drive to get the home finished.

"With the economic down turn, one, a lot of people like the trim carpenter, he's just gone, he's out of business. We're happy we have some skills on the side. We can help finish the home," said Fire Marshal Chuck Mickelsen.

"It would just be awesome to have a big room that we can all be in at one time, so we don't have to take shifts eating. When you are in the living some of you don't have to be in the hallway or part way into the dining room," cried mother Ruth Clark.

"Having all the wheel chairs in one room, if I want to go to the kitchen I can't go any where... Everybody has to go move - backup - so I can move," explained Russell Clark, who has muscular dystrophy.

Muscular dystrophy is a genetic disease that deteriorates muscles. Despite that, the Clark family has still managed to go hunting. The new home will have a lot more space for their trophies. And to fight off germs it has a radiant heater, which will warm the home from the ground up.

The family is especially looking for manpower so they don't have to dip into the donation fund that was setup for them last April. They would also like to point out that they have full control over funds that were set aside to help the build the house, but only have funds set apart for materials in the home.

Visually impaired teacher plans book about service dogs

From WLFI-TV:

LAFAYETTE, Ind. - Kathy Nimmer, a Harrison High School English teacher who is legally blind, just received a $25,000 Lilly Endowment Grant. She plans to use the money to set up a web site to gather information and stories from people with service dogs, and use these stories to write a book.

The project is called Two Plus Four Equals One, which Nimmer says describes the partnership between the disabled and their service dogs.

Nimmer hopes her book makes others more aware of people living with disabilities.

"If my students can see their stories come alive through this book and see me as a disabled person succeeding in a very challenging publishing world, then I hope that the book will make a difference," said Nimmer.

Nimmer hopes to finish her book and get a deal by the summer of 2010.

Oklahoma hosts event for disabled farmers, ranchers

From The Oklahoman. In the picture, State Rep. John Enns uses a chair lift to get to his tractor in Waukomis in a 2007 photo. Enns, who was paralyzed in a farming accident, sponsored a bill that formed the Oklahoma AgrAbility Project.


Oklahoma’s farmers and ranchers know their occupation is a risky business.

A 2000 study by Oklahoma ABLE Tech, which serves Oklahomans of all ages and all disabilities with assistive technology, reports 26 percent of farmers and ranchers, or about 17,000, in the state have had some type of disability that affects their livelihood or quality of life.

The second AgrAbility Day, scheduled for March 9 at the state Capitol, is intended to increase legislators’ awareness of those numbers and of the importance of the Oklahoma AgrAbility Project, which helps Oklahoma agricultural producers who have disabilities. Exhibits and large-equipment demonstrations are planned.

The project began in 2002 and has helped people with things as simple as high-illumination lighting in a barn and painted fences, which help people with deteriorating eyesight. More complex items include a modified cattle guard that prevent a rancher’s power wheelchair from tipping and a lift and hand controls on a tractor and pickup that help a person in a wheelchair continue farming.

In 2008, AgrAbility helped 31 families and gave information to about 35 more, said project co-director Linda Jaco.

"They could have got into that situation on the farm or away from it. Now it creates a barrier to do successful farming,” Jaco said.

An assistive technology specialist with the program visits farms and ranches to assess a person’s needs. Those applying for help are encouraged to request money from the state Rehabilitation Services Department.

The department is responsible for determining who is eligible to receive aid. Farmers and ranchers must share some of the costs.

The Rehabilitation Services Department last year provided $28,000 — and $200,000 since 2003 — to pay for technology needs of disabled agricultural producers, Jaco said.

Deaf model fights discrimination in fashion industry

From The Independent in the UK:

Dressed in denim hotpants, knee-high leather boots and a chequered shirt, Kellie Moody looks every bit the model as she poses for a photographer in a west London hotel.

Draped over a leather armchair, the 24-year-old effortlessly switches her poses, from sultry or innocent, to timid and then empowered, laughing and chatting animatedly in between takes with the photographer.

For more than three years the Leicester-born make-up artist has tried to make it as a model but most agencies will not go anywhere near her for the simple reason that Ms Moody is completely deaf.

The modelling agencies would never admit that, of course, but the fact remains that disabled people are still as noticeably absent from the fashion and media industries as black faces once were from the catwalk and magazines.

Only this week a furore was caused when a small number of parents complained to the BBC about a new CBeebies presenter who has only one arm. Cerrie Burnell was born without a right forearm and has always refused to wear a prosthetic. She beat more than 1,500 applicants to land a presenter role on the popular children's television channel but when her shows were broadcast the BBC received nine complaints from parents who were concerned that her disability would frighten their children.

A Facebook group set up by a disabled rights activist in support of Burnell has already attracted nearly 30,000 supporters. But the very fact that some people – albeit a small minority – felt a one-armed presenter was something to be scared of shows just how difficult it remains for disabled people to find acceptance within industries where a staunchly traditional view of aesthetics so often excludes them.

Speaking in the thickly accented tones of a profoundly deaf person who proudly tries not to use sign language, Ms Moody explains why she believes it is time for the fashion world to embrace disabilities.

"The fashion industry really should be much more open-minded and willing to take on models that are perhaps a little different to what they are used to," she says. "They really do have a responsibility to give disabled models the chance to show that they can be just as good as anyone else. If a woman is beautiful, has the right body build and height, then why shouldn't she be able to become a model? The fact of the matter is that the only difference between me and a model on the runway is that I am deaf."

Ms Moody's experience of trying to break into the world of modelling is a story of constantly battling against the prevailing perception that the fashion world, with its strict criteria on what constitutes beauty, is not a place for those with disabilities – even though her particular disability does not manifest itself physically.

When she was 19, a talent scout at the London Fashion Week spotted Ms Moody in a crowd and gave her a card. "She had no idea that I was deaf but she clearly thought I was a potentially suitable model," she recalls. In 2007 she became the first winner of the now annual Miss Deaf UK and won a photoshoot with a renowned photographer. But the photographer didn't return her calls and the shoot never happened.

Then six months ago Ms Moody and seven other women, all with varying degrees of disability, appeared on Britain's Missing Top Model, a televised competition which pitted the wannabe models against each other for a chance to win a shoot with Rankin, the photographer, and a contract with the mainstream agency Take 2 Models.

The show, which was broadcast on BBC Three last year, billed itself as the first serious attempt to launch a disabled model's career within mainstream fashion but its critics described it as an insensitive reality show that makes entertainment out of disability.

"When they first showed Britain's Missing Top Model it opened up a debate in a positive way about the role of disabled models within the fashion industry but I haven't seen that debate maintained since then," says Ruth Deane, editor of Every Model magazine.

Deane believes the fashion industry needs to open its studios to disabled people but says all models should be aware that virtually every photo shoot, catwalk run and fashion show is, by its very nature, discriminatory.

"It's worth remembering that within the industry itself people are discriminated against for all sorts of reasons," she says. "Models may be rejected by a client because they want dark hair, or light eyes, black skin or height. You could argue that even these decisions are a form of discrimination. But what the clients want, modelling agencies have to provide."

Even with the added publicity from Britain's Missing Top Model, many of the women who went on the show have still found it difficult to find modelling work. Friends of Kelly Knox, the 23-year-old one-armed former credit controller who won the competition, say even she has difficulties finding clients who want to commission her. Take 2 Models, the agency that signed her after the show, failed to respond to The Independent's requests to speak to her about her experiences in finding work over the past six months.

One of the contestants who appeared to be the most uncomfortable with the format of the show was Sophie Morgan, a wheelchair-using artist living in central London who broke her back in a car accident the day after she received her A-level results. She still models but is remarkably frank about the problems she faces as a model in a wheelchair.

"I genuinely don't think the industry is going to change," she admits. "The fashion industry has always struggled with these sorts of topics. The type of women it chooses to model their clothes are never the women who end up buying them."

Often the only work disabled models can rely on is with the various charities or companies that represent their own individual disabilities. But while work may be hard to come by it is still out there. Fifteen years ago Louise Dyson sold off her successful mainstream modelling agency to create VisABLE People, the first company in Britain to exclusively represent disabled models and the agency that also represents Cerrie Burnell. She believes that too many prospective disabled models believe that high fashion and editorial modelling is what they should aim for.

"The mistake a lot of potential disabled models make is that they look at the catwalk and think that's where they should be," she says. "But runway modelling is such a tiny part of the fashion industry it is almost not relevant. It's an incredibly specialised area that has strict demands on what a model should look like, whether you are able-bodied or not."

Since leaving Britain's Missing Top Model, Ms Moody has been able to land a permanent modelling contract with Siemens Hearing Instruments, but even she admits it would be a major triumph to model clothes rather than hearing aids.

"I love the modelling work I do at the moment with Siemens but of course I'd like to do more mainstream fashion modelling," she says. "Whether it's Primark or Prada I wouldn't care, for me it would be an amazing victory for a deaf woman to model for a high street brand."

Armory Show will feature 16 artists with disabilities

From VSA Arts:

VSA arts will introduce the work of sixteen artists with disabilities in Booth #1601 on Pier 94, from March 5-8 in New York City. The Armory Show has been the world's leading art fair devoted exclusively to contemporary art since its introduction in 1999. By showcasing work that is heavily influenced by the disability experience, as well as artists who are included in established movements such as Outsider Art, VSA arts endeavors to position the work of artists with disabilities within a greater context.

Highlights include: Emily Eifler's whimsical fabric sculptures are reminiscent of costuming, exploring boundaries in objects that are derived from the body (pictured). Eifler, who has a progressive neurological disorder resulting in limited mobility, uses her work to examine biological forms in an effort to exert control. She uses soft, easily manipulated forms that conjure childlike, Seussian daydreams.

Ken Morgan's exhibition history spans three decades, with solo and group shows all over the country. His minimalistic drawings are indicative of larger art world trends. In 2007, Morgan had to reclaim art and embrace technology after a stroke. Morgan's work creates safe havens, mindscapes, places to play, and momentary impossible realities.

Linda Carmella Sibio concentrates on painting and drawing, creating both large-scale works and intimate pieces. In the mid-'80s, Sibio began to practice interdisciplinary work, combining her visual imagery with performance. The themes of her work originate from difficult issues such as homelessness, mental illness, suicide, and mass murder.

Additional exhibiting artists:Lanham Bundy of Providence, Rhode Island; Caleb Charland of Brewer, Maine; Busser Howell of New York City; Sophie Kahn of Brooklyn; Lihua Lei of Solon, Maine; Ryan McDonnell of Northampton, Massachusetts; Eric McGehearty of Lewisville, Texas; Coralina Meyer of Brooklyn; Katie Miller of Parkton, Maryland; Mark C. Parsons of Brooklyn; Gordon Sasaki of New York; Ricky Subritzky of Australia; and Mare Vaccaro of Brooklyn.

The Armory Show - The International Fair of New Art takes place from March 5-8, 2008, at Pier 94 on the Hudson River (Twelfth Avenue at 55th Street), New York. For ticketing and additional information visit: www.thearmoryshow.com.

Transportation cuts will leave disabled people in St. Louis area stranded

From the St. Louis Post-Dispatch:

BALLWIN, Mo. — Stuart and Dianne Falk love the local theater. The production. The writing. The performing.

Though both have multiple sclerosis and use wheelchairs to get around, the couple still eagerly take the stage whenever they get the chance.

"There is such a sense of family and community and mutual support, it makes the disability go away," Stuart Falk says. "It's a wonderful release."

The Falks work with the DisAbility Project, a theatrical ensemble that performs sketches to bring awareness about living with a disability: What it's like to get a wheelchair through the door of a coffeehouse, or find a job, or find a parking space.

Now, they have a new topic — how to find an affordable ride.The financially ailing Metro transit agency will slash its Call-A-Ride service on March 30, shrinking the area where it can serve those with special needs at subsidized rates.

The Falks live in a nursing home in St. Louis County that won't be near a transit stop after the service cuts, so their only option would be to pay at least five times the current round-trip fare of $8. That leaves them with a choice that is really no choice at all — pay the dramatically higher price for a ride or stay home.

"I can't wrap my brain around what it's going to be like to be frozen in here," says Stuart Falk, 46.

The Falks are among many with disabilities who are the most vulnerable to cuts in public transportation that are sweeping the country. Advocates for the disabled say there's a growing sense of fear about the looming cuts in St. Louis.

"By cutting back public transportation, you are limiting their ability to be independent," said Elizabeth Leef, policy analyst with the National Council on Independent Living.

Medicaid covers trips to the doctor, but for most everything else, the Falks are on their own. The couple rely on Call-A-Ride to get to Paraquad offices, where they take part in weekly theater rehearsals and work out on accessible exercise equipment.

They also use Call-A-Ride to whisk them to religious services, too. Dianne attends the Church of Jesus Christ of Latter-day Saints in Chesterfield. Twice a month, Stuart tries to attend services with the Shir Hadash Reconstructionist Community in St. Louis.

The couple share a room at West County Care Center. Their modest quarters is filled with pictures. Some are from the couple's wedding at the nursing home. There's one from Fenway Park in Boston. Another shows a much younger Stuart Falk running through the streets of Boston. Raised in New York, he ran a number of races, mostly 10Ks.

He earned a philosophy degree in 1985 from Northeastern University in Boston, and aspired to become a chiropractor. He and his first wife moved to St. Louis, where he attended Logan College of Chiropractic, but he had to quit because of the toll multiple sclerosis had taken on his body. The marriage fizzled.

Dianne grew up in Ballwin and graduated from Webster University in 1991 with a communications degree. Dianne was in her mid-20s when she learned she had multiple sclerosis.

She lived with her parents for a few months after her first marriage ended, then moved into the nursing home about eight years ago. When Stuart moved into the home in 2005, he was soon introduced to Dianne by a mutual acquaintance who arranged for Stuart to perform a comedy routine.

The laughs led to love, and it was Dianne, now 40, who took the initiative and asked Stuart to marry her. Stuart recalls the April 2006 wedding as a beautiful party.

"The place just sparkled," he recalls. Today, the couple live in a place where they are youngsters compared to the other residents.

And money is tight. After the nursing home gets its share of the couple's Social Security disability benefits, the Falks are left with about $30 apiece each month, Stuart says. Their families help out, but it's not enough to cover the cost of paratransit once Call-A-Ride's subsidized service goes away. The Falks have looked for nursing homes inside the Interstate 270 loop. So far, they haven't found one.

Stuart and Dianne say they need their time away from their nursing home. It's an environment for retirees, Stuart says — and that's not them.

"I need more than this place offers," he says. "I need to get out. I need fresh air. I need other people. I need other places."

Dianne says the DisAbility troupe is like extended family.

"My heart is just totally aching because I realized that the theater group is gone for Stuart," she says. "I am just disheartened."

They have written letters to local politicians. Dianne spoke up at a recent meeting with Metro officials at Paraquad, a nonprofit center for independent living.Metro officials say they wish more could be done, but the funds aren't available.

The agency's financial problems were worsening even before the banking collapse last year. Metro was struck by a combination of sagging subsidies and rising operational costs. The recession has only magnified the agency's problems by eroding sales tax collections and dimming the prospects of restoring services that are being cut.

"It's going to be lousy," said Patricia Hall, Metro's director of ADA services. "It's not going to get us to all the places where we want to go."

The Falks know all about that. While making dinner plans last week, Stuart and Dianne discussed what life will be like without Call-A-Ride. Without their theater troupe. Without the gym. Without church.

"So much to give up at once," Stuart says. "It's like going to prison, and I didn't commit any crime."

Sunday, March 1, 2009

N. Virginia magazine profiles people with Asperger's, autistic self-advocacy movement

From Northern Virginia Magazine:

Lively 6-year-old Joey’s an expert in dinosaurs and loves to talk about them, but play dates are a challenge, as his passion prevents other children from sharing their interests. Patrick could read when he was 4 and loves books, but becomes agitated by non-literal idioms, like “raining cats and dogs.” Second-grader Alice cries when the sound of rustling papers and background chatter in the classroom derails her concentration.

Each of these children has been diagnosed with Asperger’s Syndrome (AS). AS belongs to a group of disorders known as pervasive developmental disorders (PDDs), or autistic spectrum disorders. Experts agree that, if you meet one child with Asperger’s, you have met … one child. Each is individual, unique.

Patricia Velkoff of Vienna is a clinical psychologist specializing in lifespan development and family therapy. She describes the differences between Asperger’s and the layman’s view of autism:

“Children with both AS and autism have some degree of difficulty with social attunement and emotional self-regulation. The AS child’s challenges, however, are much less severe. They may isolate themselves when social contact becomes exhausting. They may repeat an idea that excites them even when others are bored. They may insist on their own way and not understand the needs of others. Each of the diagnoses applies to children who do not all look alike; a child’s individual profile must be understood before interventions are designed and implemented.”

According to Velkoff, each child’s diagnosis varies in strengths, challenges and “areas of average skill.” “An AS child, for example, may have highly developed, expressive language and memorization skills.”

Alex Plank (pictured) took the matter of limited information on the condition into his own hands. At age 17, he launched WrongPlanet.net, which now has registered users from Austrailia to Germany. “At the time, there were no resources that met my needs with a positive message of where people like me fit in the world. I wanted there to be a positive environment to help [those with AS] better understand themselves.”

Diagnosed at age 9, Plank is now a film major at George Mason University, and is producing a project interviewing autistic individuals about their experiences. His advice to those newly diagnosed with AS? “Get online, and read other people’s stories. It’s also a good place to make friends.”

Lucia Claster, who coordinates the Asperger Syndrome Information and Support group in Arlington, points out that students with high-functioning autism, Asperger’s syndrome and other related issues often fall through the cracks in school. Each demonstrates the isolating difficulties of being in one’s own world.

“These kids can ‘pass’ as normal in many ways, but not in theirs. Most are of normal intelligence, and some are of superior intelligence in certain subjects, so it seems to outsiders that they should be able to ‘access the curriculum.’ Yet because of
their processing difficulties and social communication skill deficits, they aren’t able to take in information or express what they know in the same way that typical learners do.”

Easily overwhelmed by sensory stimuli that wouldn’t bother the average student, “they cannot focus on their learning.” Classroom behavior deteriorates because they are stressed and anxious, “and teachers see the change as a ‘behavior problem.’”

Claster adds that, instead of giving AS students more support, “teachers sometimes feel the students are willfully acting out and will isolate them, give them a time out, send them to the principal’s office, take away their recess time, which makes these kids even more overwhelmed.”

She says AS students need a structured program geared to individual abilities as they progress through “the broadening of academic expectations, and the shift from [fact-based] task-learning in the early grades to more complex education [abstract concepts].”

Philadelphia-based certified relationship development intervention specialist Lisa Kowalski attempts to address the other-world difficulties with social interactions faced by her high-functioning Asperger’s children. “They don’t process much of the non-verbal information that is communicated within social interactions. Frequently they can tell you exactly how they are supposed to respond, but in the moment it’s so hard for them to actually do it.”

Professionals and families agree that people without AS rely on body language to regulate social communication and interpret unspoken implications. Those with AS have problems reading body language and thus become more isolated and misunderstood. “Many of the weaknesses can be remediated with specific types
of therapy aimed at teaching social and pragmatic skills,” Kowalski says.

Autistic Self Advocacy network coordinator Durbin-Westby read at a third-grade level at age 4. Those who grew up before AS could be properly diagnosed tell heroic tales of lonely discovery. Like Plank, many felt they were living on the “wrong planet,” and many have turned adversity into success.

Paula C. Durbin-Westby is Virginia coordinator for the Autistic Self Advocacy Network (ASAN) and board member in charge of the East Coast region. She learned about Asperger’s syndrome some two years ago while at work indexing a scholarly monograph. “I saw the acronym PDD-NOS in a book I was indexing. I looked it up, saw a link to high-functioning autism … I clicked and read my life story.”

Durbin-Westby printed out the description, deleted the word “autism,” and showed it to her husband. “He read it and exclaimed, ‘Wow! What is it?’ in a voice that told me he was discovering the same thing I was.”

By the next day she had read enough about the criteria for AS and associated conditions to know that “I was on the autism spectrum.” And she discovered that “literature by experts … pathologizes qualities that are seen to be different, regardless of whether or not those qualities could also be positive.” Durbin-Westby, born in 1959, knows that a diagnosis today can cause feelings of devastation in parents. Her own parents had “no feelings of devastation at all.”

She joined her first online group for autistic adults and asked, “Would you tell people other than your family and maybe a close friend that you are on the autism spectrum?”

Ari Ne’eman, the founder and president of ASAN, provided her first reply. Then, ASAN was in its early stages of formation, so Durbin-Westby’s journey has always been intertwined with that of the organization.

Ne’eman’s reply: “It depends what your particular situation is. It’s not something to be ashamed of, though, and recognizing who you are may help you. Do what you feel comfortable with, but you shouldn’t be afraid to be openly autistic. I think it’s my right to be open in my neurology and to let my abilities speak for themselves.”

Ne’eman’s assertion reminded Durbin-Westby of the way she had lived her life: “I have never wanted to hide who I am … Every week I read posts by people on the autism spectrum who are trying to fake it, living in fear of making a social mistake that will cause them to lose their livelihood.” She hears from people who are “exhausted both from trying to do the things they need to do to survive and pretend they are something they are not.”

Durbin-Westby’s work with ASAN began seven months after her initial discovery. The organization has a broad agenda, including policymaking, education and outreach, a speaker’s bureau, social and support groups for people on the autism spectrum, as well as non-autistic parents, friends and other family members and allies. Through ASAN, Durbin-Westby made the happy discovery that, “I am good at networking.”

Consequently, she is interested in the proceedings of the National Institute of Mental Health’s Interagency Autism Coordinating Committee. “Advocacy is such a large part of my life.” She also is an organist and choir director, wife and mother.

Durbin-Westby demonstrates the intense interests displayed by those on the autism spectrum. “I was reading at an advanced third-grade level when I was 4.” The ability to read at an early age is common in children on the autism spectrum. Durbin-Westby also began studying piano at age 4.

Charles Bowen, 41, lives in Fairfax with his wife and two daughters. The son of an ordained Baptist minister in Danville, he remembers what he calls his first obsession.

“I have always obsessed on things. A week before my fourth birthday, lightning struck [our] church, and the sanctuary burned to a shell. Well into second grade I would obsessively talk about the church fire.”

Bowen says he was a loner in school, although he did have a few close friends. Puppetry, another of his obsessions, had a positive link: “I met my wife while doing puppet shows at her church in 1989.”

Another special interest triumphed when Bowen’s brother married a woman from Brazil. “I began to study Portuguese,” and found out that he was “an aspiring polyglot,” with a knack for languages. Bowen overcame social-skill challenges by reaching out to those of different languages and cultures. Since 2002, he also has taught English as a second language on a volunteer basis.

Charles attributes a work-related plus to his AS: “Office politics go right over my head.”

Martin , 50, who does not wish to disclose his last name, came from a family that emphasized the importance of learning. “My social skills were immature, and emotionally I was detached, more of an observer than a participant,” he says. “I wasn’t used to running with a group. I did well academically until college, when my poor study skills, emotional problems and lack of social graces led to near-failure.” He explains that he engaged in risky behaviors, defying authority. “I was fired from jobs repeatedly. The worst part of it all was the loneliness.”

Today Martin is a computer programmer for a government agency. “AS hasn’t been as much of a problem here as it was in my prior jobs. Much of computer work is solitary. I have a general feeling of acceptance among my peers. I’ve benefited greatly from the stability and independence of this job.”

Psychologist Patricia Velkoff warns of the stress associated with Asperger’s evaluation.

As Velkoff points out, “After diagnosis, some parents know what services are needed; for example, help with pragmatic speech.” When parents are not clear about what help to pursue, she recommends asking the evaluator if services are needed with several aspects of care.

Perhaps most importantly, Velkoff stresses that “children with AS benefit from an aggressive program of interventions in all necessary areas at the youngest possible age. This improves outcomes and reduces the gap with their same-aged peers.”

When multiple caregivers are involved regularly with a child (e.g.; parents, extended family and other care providers), Velkoff believes it is “most helpful if each caregiver is included in the treatment process. This helps all become skilled in working with the AS chi.”

Before diagnosis, however, comes the evaluation, a step involving preparation for both child and parent.

“If your AS child may be stressed by the evaluation, you may wish to visit the building with them, and even arrange to greet the examiner briefly, a day or two before the evaluation,” Velkoff advises. “Parents want to find out details such as: whether a parent will be with the child throughout the evaluation, whether snacks are allowed, what kinds of tasks will be presented.”

With the help of the ever-expanding number of online resources, information and support, today those with Asperger’s are in touch with themselves and know they are, indeed, on the “right planet.”

Velkoff cautions that “Asperger’s is a new specialty for professionals, with AS included in IDEIA [Individuals with Disabilities Education Improvement Act] only since 1990. Training, experiences and services across professionals vary widely. Think of these as long-term relationships.

“Do your homework about each person in advance so that your time, effort and money are well invested. Keep communication open about what you need and what they can provide.”

The needs of children with Asperger’s change over time as well, so services and providers may need to be flexible as progress is made and new stages are reached.

Amazon caves on text-to-speech issue for Kindle 2

From CNET News by Greg Sandoval. The National Federation of the Blind was fighting this issue, and blogger Penny for your thoughts, who is visually impaired, explains how misguided the decision is.

Apparently, Amazon won't fight the publishing industry on the issue of whether the Kindle 2's text-to-speech function violates copyright.

The retailer, which makes the popular Kindle electronic-book reader, announced late Friday that the company is modifying systems to allow authors and publishers to decide whether to enable Kindle's text-to-speech function on a per-title basis.

Amazon began its press release with tough talk. "Kindle 2's experimental text-to-speech feature is legal," Amazon wrote. "No copy is made, no derivative work is created, and no performance is being given."

But then the company says: "We strongly believe many rights holders will be more comfortable with the text-to-speech feature if they are in the driver's seat."

There is no mistaking what happened here. Amazon caved. For Kindle owners interested in the text-to-speech feature, the device just lost value.

The Authors Guild, a trade group representing 9,000 authors, began criticizing Amazon shortly after the Kindle 2 debuted earlier this month. The guild's president, Paul Aiken, told CNET this week that Amazon was taking a hard-line position in discussions between the guild and the company. He also said there was a possibility that the guild could sue over the issue.

"Anytime you have a new means of accessing content," Aiken said, "there's always some sort of aggregator that wants to control it and keep the value for themselves."

Fred von Lohmann, senior attorney at the Electronic Frontier Foundation, an advocate group for the rights of Web users and technology companies, said he was grateful that Amazon went out of its way to make the point that the company didn't
believe text-to-speech technology violated copyright.

"Nevertheless, Amazon decided to allow copyright owners to make the decisions themselves whether to use the feature," von Lohmann said. "They are entitled to do that. The issue of text-to-speech will have to wait for another innovator."

One point that von Lohmann noted was that there are plenty of PCs that offer text-to-speech, and the Authors Guild hasn't objected to those. "Maybe Apple should be looking over their shoulder," he said.

It's easy to understand why Amazon may have back-pedaled. Even the staunchest supporters of text-to-speech say that it won't replace audio books any time soon. Computers can sound like humans but they can't insert emphasis or offer much of a dramatic rendering because they don't yet understand what they're reading--and likely won't for a very long time, say the experts.

Golfer Ernie Els joins other celebrities focused on curing autism

From The AP:

PALM BEACH GARDENS, Fla. — For Ernie Els, (pictured) last year’s Honda Classic was filled with significance. It was not a major tournament; it did not come after some epic duel with Tiger Woods, and it lacked that dramatic moment on the 18th green. In fact, Els learned he won while standing on the driving range, prepping for a playoff that never happened.

But prevailing at the Honda gave Els more than a $990,000 winner’s check and his first PGA Tour victory since 2004. It provided the platform he had long sought to finally reveal that his family is one of many touched by autism, a brain disorder that hinders the ability to communicate and interact socially and is found in about one of every 150 children. Els’s son, Ben, is a healthy 6-year-old who is autistic.

So his father’s bag bore an Autism Speaks logo that week, and days after winning at PGA National, Els started speaking about it as well.

“It was good timing,” Els said. “It also had gotten to the stage where you’ve either got to talk about what’s happened to Ben or you’re just not. He was so in the public eye, especially not just in the U.S., but also worldwide. When you travel with Ben, you can really start seeing there’s something going on. I didn’t want to feel like we’re hiding anything.”

If that ever was the case, it is not anymore.

Els, who will defend his title at the Honda Classic next weekend, and his family are now at the front of fund-raising and awareness efforts.

Els’s wine label helped sponsor a golf outing that raised more than $300,000 last summer for autism research, and on March 23 at PGA National, he will host a pro-am featuring Jack Nicklaus, Greg Norman, Justin Rose, Raymond Floyd, Ian Poulter, Luke Donald and Tim Clark — who ousted Woods from the Accenture Match Play Championship on Thursday.

In the beginning, Els was hoping to lure 18 teams and wondered if he would draw that many. He wound up having to stop taking entries when the field reached 22 foursomes, even turning some pros down.

“We’ve got our foundation up and running now, and we can really start getting involved with finding a cure,” Els said. “Basically, that’s what we want to do.”

Keeping Ben’s condition silent pained Els for years.

At times, he was not the same Big Easy on the golf course, letting emotions get the better of him in certain situations, a far cry from his typical demeanor.

It was a strain at home, too, as it is for most families dealing with autism.

But Els counts himself lucky: His family is moving forward, not letting anger and frustration override everyday life.

“You can’t help but feel for this kid, Ben,” Els said. “He’s a healthy kid and everything about him is perfect. He’s just not going to be a, call it normal, kid one day. You’re not going to play the same sport and he’s not going to do the same things as you envisioned. That’s the hard part.”

In many ways, 2008 was a year of major changes for Els’s family.

After seeing one too many snowflakes in London, where he made his year-round base for some time, Els packed the family up and moved to South Florida, buying a home in Palm Beach County. Off-season training there is easier, many of Els’s friends live nearby and there is no shortage of places to play golf.

His son’s condition weighed heavily on the decision to move, with Els saying he finds United States facilities involved in autism research “so far more advanced in treating the condition or finding a cure for the condition.”

That helped make the decision to uproot the family seem rather easy.

“I don’t want to say the biggest factor, but he was the most influential factor for us to come here,” Els said.

He also wanted to make sure his daughter, Samantha, 9, would be comfortable. She has adjusted perfectly, Els said, after finding a soccer team, new friends and a good school and going horseback riding in her spare time.

His wife, Liezl, was also fine with the move — and with his choice to reveal Ben’s story. She has immersed herself in research about autism, even more so than when it was diagnosed.

“What we learned was startling,” she said in a public-service announcement taped after the family revealed their situation.

Starting a new philanthropic quest in these difficult economic times across the globe is not easy. But Els is seeing good things happen, and with the help of some power brokers, his quest is off to a flying start.

“Most of the people we’ve asked are guys who run major corporations or are friends of mine or guys I play golf with,” said Marvin Shanken, who is organizing Els’s March 23 event. “I want to say 90 percent of the people I went to said yes on the phone.”

Shanken, the publisher of Cigar Aficionado and Wine Spectator magazines, and a rabid golfer, said he was thrilled to see Els bring light to the autism fight.

“I was so proud,” Shanken said. “I wanted to help. I just want to be there for him and for all the other parents who face the same challenges.”

Golf is still Els’s passion.

He’s just made room to add another one.

Disabled, poor Floridians seeing many cuts to programs that serve them

From the Tallahassee Democrat:

Mary Ann Sanderford has a creative eye that she uses when she goes to the Pyramid adult day training site on Tennessee Street.

She has made a toy ambulance out of lumber, a toy bus out of Vienna sausage cans and colorful jewelry. Though she has sold her wares and gained confidence through the art program, her time there has become a victim of state budget cuts. Sanderford, 46, who suffers from Muscular Dystrophy, has had to shave her days from five to three a week at Pyramid, an art-based adult day training program, because of less funding.

“It just doesn’t seem fair,” said Sanderford, who is bound to a wheelchair. “It was like having candy snatched from you.”

Sanderford is one of many who are either disabled, poor or laid off that depends on the state for assistance, but receives less funding because of a tanking economy and the resulting budget cuts. When the legislative session begins March 3, lawmakers will have to decide where to further cut an already bare-bones budget. Many who work in health care and social services say cuts have already been deep, and more could be devastating.As more state departments receive cuts, so do the people they serve.

At the Agency for Persons with Disabilities, which assists Sanderford, there is a list with 18,000 people waiting for services.

“We will not be able to get anyone off that list until the economy picks up,” said APD spokesman Melanie Mowry Etters.

During the recent special session that legislators used as a midyear budget fix, the agency lost 175 positions, vacant but now never to be filled.

“We are hopeful our customers don’t experience any more reductions,” Etters said. “Most legislators know our customers have felt the impact of the cuts.”

Those cuts are also affecting Florida hospitals, who are receiving lower reimbursement rates for serving Medicaid patients. Consequently, those costs are passed to those with health insurance.

“Businesses are either dropping insurance or reducing the amount of coverage and shifting the costs to workers,” said Bruce Rueben, president of the Florida Hospital Association.

He said Florida hospitals receive 53 cents to 89 cents for every dollar of cost for a Medicaid patient. The Legislature cut Medicaid reimbursement rates by 4 percent in the last special session and 6 percent in 2008.

“That’s a quarter billion dollars in cuts,” Reuben said.

By most accounts, the lines for those who need help are getting longer.

In the Big Bend, officials with the Capital Area Community Action Agency, which offers emergency assistance, homeless services, utility assistance, food vouchers and bus passes, say the need for help is increasing.

“A lot of people are finding themselves in dire circumstances,” said Dorothy Inman-Johnson, executive director of the CACAA. “When we open our doors, we usually have people in lines waiting. . . . People with higher education, people who have worked all their lives, it’s a very diverse crowd.”

The Head Start program the agency offers, which gives free care to 3- and 4-year-olds who come from low-income households, is full but last year had trouble filling spots, Inman-Johnson said.

“The state has to do its fair share,” Inman-Johnson said. “The Legislature can’t depend on the federal government to bail it out.”

Sylvie Kramer, president of the Florida Association of Healthy Start Coalitions, will keep a sharp eye on this legislative session, also. Her non-profit group, which works to improve the health of pregnant woman and their babies, receives funding from the state and local communities.

“The funding is decreasing and it’s decreasing on all sides,” said Kramer. “I’m concerned we will have to turn women away (with more cuts). My case manages can only do so much.”

In the recent special session, the Legislature voted to reduce the coalition’s cut from 4 percent to 1.6 percent.

“It shows the legislators care,” Kramer said, of the partially restored funding. “But the year is not over.”

Meanwhile, others like Sanderford, will have to learn to do with less.

Sanderford, who lives in a group home managed through the Leon Advocacy and Resource Center, now spends her off days watching television.

Marilyn Yon, chief operating officer at Pyramid, said, “For Mary Ann, this has limited her income.”

“Businesses are either dropping insurance or reducing the amount of coverage and shifting the costs to workers,” said Bruce Rueben, president of the Florida Hospital Association.

He said Florida hospitals receive 53 cents to 89 cents for every dollar of cost for a Medicaid patient. The Legislature cut Medicaid reimbursement rates by 4 percent in the last special session and 6 percent in 2008.

“That’s a quarter billion dollars in cuts,” Reuben said.

By most accounts, the lines for those who need help are getting longer.

In the Big Bend, officials with the Capital Area Community Action Agency, which offers emergency assistance, homeless services, utility assistance, food vouchers and bus passes, say the need for help is increasing.

“A lot of people are finding themselves in dire circumstances,” said Dorothy Inman-Johnson, executive director of the CACAA. “When we open our doors, we usually have people in lines waiting. . . . People with higher education, people who have worked all their lives, it’s a very diverse crowd.”

The Head Start program the agency offers, which gives free care to 3- and 4-year-olds who come from low-income households, is full but last year had trouble filling spots, Inman-Johnson said.

“The state has to do its fair share,” Inman-Johnson said. “The Legislature can’t depend on the federal government to bail it out.”

Sylvie Kramer, president of the Florida Association of Healthy Start Coalitions, will keep a sharp eye on this legislative session, also. Her non-profit group, which works to improve the health of pregnant woman and their babies, receives funding from the state and local communities.

“The funding is decreasing and it’s decreasing on all sides,” said Kramer. “I’m concerned we will have to turn women away (with more cuts). My case manages can only do so much.”

In the recent special session, the Legislature voted to reduce the coalition’s cut from 4 percent to 1.6 percent.

“It shows the legislators care,” Kramer said, of the partially restored funding. “But the year is not over.”

Meanwhile, others like Sanderford, will have to learn to do with less.

Sanderford, who lives in a group home managed through the Leon Advocacy and Resource Center, now spends her off days watching television.

Marilyn Yon, chief operating officer at Pyramid, said, “For Mary Ann, this has limited her income.”

Blind woman finds her inner Ethel Merman

From a NY Times story:

They have gathered together from the five boroughs and paid $485 for a workshop to become the stars they always dreamed of being and to discover the Ethel Merman within.

After four nighttime rehearsals, 15 stars were born. Well, that’s a stretch, but nevertheless, some of them had never sung a note outside a shower curtain, and now they found themselves performing the other night at the Triad on West 72nd Street. They entered the stage and warmed to the spotlight, easing into their numbers with breezy patter. . . .

Peggy Eason, 62, (pictured) is blind and learns lyrics from a tape. She works for the New York State Parole Division.

“I always wanted to be a star and to make it on the Great White Way,” she said before performing a song a longtime friend had written for her, blasting out from behind dark shades. “Broadway, here I come!”