Yahoo! Groups

My Groups | AutismFirstStepsAutismNewsletter Main Page




 
AUTISM FIRST STEPS
AUTISM DAILY NEWSLETTER     
Monday January 7, 2002  


INDEX:
*  Common Antibiotic May Be Potential Treatment For MS
*   
Arrested Teen Says He Sent Daschle Anthrax Letters, Boy Autistic
*  
Writer Emerges From Martian Past
*  
"How the Clip 'N Snip's Owner Changed Special Education"
*  
  "Camp Fear"

*
*****************************

Common Antibiotic May Be Potential Treatment For MS


A common antibiotic, long used to treat infections in humans, may have potential as a treatment for multiple sclerosis, a devastating disease of the central nervous system, according to a new study published Dec. 21 in the Annals of Neurology.The drug, minocycline, is a member of the tetracycline family of antibiotics and was tested in a condition that mimics MS. Study results portray a potential treatment for MS that could significantly decrease the severity of disease attacks or even block the onset of relapses, hence ameliorating many of the disease's debilitating symptoms.The drug was tested in rats with autoimmune encephalomyelitis. "Animals treated with minocycline did not develop neurologic dysfunction or had a less severe course than untreated rats," says Ian D. Duncan, a University of Wisconsin-Madison neurology professor in the Department of Medical Sciences in the School of Veterinary Medicine and the senior author of the study performed in collaboration with C. Linington of the Max Planck Institute of Neurobiology in Germany."This clinical difference was confirmed by the relative lack of pathologic change in the nervous system of treated animals," Duncan says. "We therefore think that a similar therapy could be used in MS patients with early relapsing-remitting disease."In many respects, MS remains an enigma to medical science. The majority of patients have a relapsing-remitting course of disease with later more chronic progression in many cases. While the trigger for relapses is often unclear, infectious disease such as a cold or flu are frequently associated with their onset.There is no known cause or cure, and treatments to date have proved to be only partially effective. The disease is especially common in far northern and southern latitudes; the farther from the equator, the greater the prevalence of the disease. The disease is characterized by inflammation and loss of the myelin sheaths that insulate nerve fibers of the central nervous system. Eventually there is scarring and nerve fiber loss. The location of the inflammation in the central nervous system -- the brain and spinal cord -- varies from patient to patient and from episode to episode."In the rat model, we show that you can treat the animal successfully either before or after the onset of the disease," Duncan says. In other words, in the context of the human disease the drug could be given when patients start to show signs of neurologic illness to forestall MS's progressive, nerve-damaging inflammatory episodes, or prior to a potential relapse."We believe," notes Duncan, "that the drug is acting at many levels. While it has effects on the peripheral immune response, its actions may be primarily as an anti-inflammatory compound. Indeed, the drug is widely used in another autoimmune disease, rheumatoid arthritis, where it is thought to play such a role."In the rat model Duncan and his colleagues used, they believe that minocycline primarily inhibits the inflammatory cascade in the central nervous system, particularly the activation of a cell known as a microglial cell, a step that may be critical to the loss of myelin and the myelin-producing cells. Duncan says evidence from other labs has shown that minocycline can protect the nerve cell or fiber itself from loss in other disorders; this may be additionally useful in MS."If we are correct that it is targeting microglial cells, then this raises the possibility that the drug or compounds with similar actions could be used in other neurologic diseases such as Alzheimer's or Parkinson's disease where microglial activation may be the common final pathway in neuron loss," says Duncan. "This will require further work, however."The drug will be tested in humans next year in a Phase I clinical trial in MS patients at the University of Calgary. "It is very important that a well-conducted clinical trial is carried out to test whether it is safe and has efficacy in MS," says Duncan. "As envisaged, minocycline could have advantages over other drugs presently used, notably the interferons or copolymer I, as it is less expensive, could be administered orally, and only for prescribed periods at the time of ongoing disease."Co-authors of the paper include Natalija Popovic, Brian Goetz, Su-Chun Zhang, all of the UW-Madison School of Veterinary Medicine; and Anna Schubart and Linington of the Max Planck Institute for Neurobiology, Martinsried, Germany.The results of the study are published online at this URL. - By Terry Devitt


[Contact: Ian Duncan, Terry Devitt]

http://unisci.com/stories/20021/0103024.htm
*
*****************************

Arrested Teen Says He Sent Daschle Anthrax Letters, Boy Autistic


Brentwood N.H. (AP) - A teenager who told police he sent ananthrax-laced letter to U.S. Senate Majority Leader Tom Daschle is acompulsive liar who has been treated in a state psychiatric hospital, hisfather said Saturday.Elijah Wallace, 18, made the claim when he was arrested for breakinginto a vacant home Friday. Police found him hiding in a closet with a gunand two knives. Investigators also found five letters addressed to localbusinesses and a bag of white powder in the house with Wallace.Preliminary tests on one of five letters found with the teen wasnegative for anthrax.Wallace told police he was preparing to send anthrax-laced letters andhad already had sent four others, including one mailed last week to Daschle,Fremont Police Chief Neal Janvrin said.But officials said they do not believe Wallace sent the Daschle letterbecause, with heightened security measures, it would have taken up to threeweeks for a letter to reach the congressman.The Daschle letter contained a white powdery substance and threateningletter. U.S. army scientists and the FBI said Friday the substance was talcand contained no trace of the deadly bacteria."He's telling a story that is a sensational story to, I think, feelimportant," the teen's father, Eric Wallace, said Saturday."I don't think there's any chance any anthrax was involved."Wallace said his son was diagnosed with Asperger's Syndrome, ahigh-functioning form of autism, when he was a child."We've been trying since the third grade to get him help but it's beenvery difficult," the elder Wallace said."He gravitated to the worst of the worst."Wallace, 45, a software engineer, said his son was expelled fromjunior high for making a threatening comment about wanting to kill Jews. Hegraduated from a high school for troubled youths and in recent years hadbeen in and out of jail, mostly on minor theft charges.Wallace began assaulting his family members last winter when hecouldn't have his way, his father said.His parents had him committed to the state psychiatric hospital lastFebruary and he was released in April.Wallace entered no plea when he was arraigned on a burglary charge.

http://www.washingtonpost.com/wp-dyn/articles/A2435-2002Jan5.html

******************************

Writer Emerges From Martian Past


By Valerie Grove


The title of Clare Sainsbury’s book about Asperger’s syndrome, Martianin the Playground, sums up exactly what she felt like at primary school: shelooked perfectly normal but she felt like an alien.“Half the time my parents were told I was a gifted child, and half thetime that I should be in a school for kids with special needs,” she says.Clare was hyperlexic — an unusually early and fast reader — and wouldpace around the classroom talking, reading Gerald Durrell when the otherswere on Roger Red-hat. Before starting school she evolved her own privatelanguage. She hated disruptive excitement such as children’s parties.School brought new horrors: playtime, noisy corridors, the lunchqueue, fluorescent lights, physical closeness to others. April Fool’s Day,with its pointless and cruel jokes, was an incomprehensible torment. AllAsperger’s children know the pervasive isolation of the child who cowers atthe edge of the playground, makes no friends, plays no games, is unable tofit in.“Asperger’s children make perfect victims, as bullies are quick todiscover. We have no tactics for physical or verbal self-defence,” Clarewrites.Clare never even thought of telling her parents about all this. “Ijust assumed that school was supposed to be like that,” she says.School life is designed for team players, conformists and good mixers.Teachers can handle physical disability, learning difficulties, behaviourproblems. But what to do with an intelligent kid who is simply weird?Francesca Happe, an autism expert, says that whenever she lectures, there isa moment when her audience goes quiet, and she knows that they areremembering someone in their class at school who was always left out ofeverything. There must be at least one Asperger’s child in every school,since the ratio is one in 200.They may baffle teachers by being unable to learn times tables, yethaving an eidetic (extraordinarily accurate and vivid) memory for facts onwhatever topic obsesses them: whales or coins or Mesopotamia or the Book ofGenesis. Their interests become surrogate companions.David Sainsbury, now Lord Sainsbury, and his wife Susie staunchlydefended their daughter when teachers suggested that she was emotionallydisturbed, “or just bloody minded, incredibly irritating, bright but lazyand perverse”.When it was hinted that they were the lax parents of a rude child,they retorted that Clare was clearly just different: she was happy at homeand they were delighted by her academic prowess.One teacher told them that Clare acted “like an autistic child” whenshe was six, yet she could speak fluently. But the only friend Clare made inchildhood was an autistic girl who was totally mute.In her school reports — “not very communicative and somewhat taciturn”was typical — she can see retrospective clues to her condition. But no labelseemed to fit. She is grateful not to have been wrongly classified, sinceshe knows other people who were misdiagnosed as schizophrenic, or put intointensive psychotherapy.At St Paul’s Girls’ School she felt disliked. “Schoolchildren seem tohave a very limited tolerance for social deviance of any sort,” she says.Teenage years can be excruciating for people with Asperger’s, who often donot see finding boy and girlfriends and going to parties as a priority.Theyappear stuck up, rude, painfully shy. In her younger sisters Clare couldobserve normal teenage behaviour.“My sister Lucy is the exact opposite of me: socially gifted,particularly good with children. She now wants to teach special needs. Shesays that growing up with me was excellent training.”At 27 Clare is lovely, a taller Helena Bonham Carter. “Did peopleoften say this?” I asked by e-mail. “Nope. Never,” she replied. In her teensClare sought help for depression, but psychotherapy put her into a Catch-22situation.“I was pretty self-aware and gave a textbook description. I said, ‘Ican’t fit in, I can’t make friends with people, there is something wrongwith me, please tell me what it is.’ But since they’d never heard ofAsperger’s, they only saw how articulate I can be in a one-to-one situation,and said, ‘There’s nothing wrong with you, you only think there is becauseyou are so depressed’. So I said, ‘No, I am depressed because I am isolatedand don’t fit in’. And so it went on.” Like fellow sufferers she was told:“Everybody feels like that sometimes” ; “You can do it if you just try” ; “I’m sure they like you really.”It was not until Clare went to read philosophy and politics at NewCollege, Oxford, and found herself encouraged to challenge other people’sarguments, that she felt more at home. “I gained more confidence and stoppedbeing so horribly depressed — but I also realised that, although no longerdepressed, I stayed weird.”Oxford is tolerant of quirky individualism, but imposes an obligationto socialise. In Clare’s first term, her behaviour convinced fellow studentsthat she was having a nervous breakdown.“I would stay in my room, and never went into the noisy, crowdedcollege bar. I can’t hear properly when there’s background noise. And Iwould walk around the college gardens talking to myself and gesticulating. Iknew that talking aloud is socially forbidden but the only way I can managesocial occasions is by rehearsing things to say, over and over, whilewalking alone.”One day she went into a bookshop and in the psychology section shefound Uta Frith’s Autism and Asperger Syndrome, in which she read an exactdescription of herself.“It was uncanny. I realised that there were other people just like me.It was too good to be true, I was afraid to believe it. I showed it to mymother. She said, ‘It does sound rather familiar. This is a description ofyou, isn’t it?” Later Frith gave her the Wechsler IQ test: Clare has an IQof more than 130. “I just wished I’d known years earlier. Just knowing couldhave made a difference,” she says.She found herself joining in student drama. “Stage managing is aperfect job if you like lurking in corners and checking through listsseveral hundred times,” she says. She was assistant director on TwelfthNight.“Having an obsession with Shakespeare and the meaning of words, Icould be a walking Arden Shakespeare footnotes, and explain Elizabethanjokes.” Clare also got a first-class degree.She reported her Asperger’s diagnosis to Janet Gough, a teacher, laterHigh Mistress,at St Paul’s, who had been particularly understanding. Shetold Clare that they now had another girl just like her, who wassubsequently diagnosed.Clare is passionate about raising awareness, and supporting theNational Autistic Society’s Prospect scheme, which finds companies willingto employ people with Asperger’s, such as computer companies. “Asperger’speople naturally understand the rigid, binary, literal way a computerthinks,” says Clare.When Martian in the Playground won an award, Clare gave the £500cheque to the NAS, in addition to all her royalties. She runs a website andsupport group for university students with Asperger’s, and works part-timewith autistic children, who sometimes remind her of the way she was as achild.“It is such a subtle disability, but just being socially out of synchresults in devastating isolation. There are so many bright able people withAsperger’s in their 30s and 40s, living alone or with their parents withenormous collections of information on Star Trek or trains or medievalmusical instruments or maps of the world. They can’t get jobs, can’t usetheir qualifications. They are regarded at best as loony but harmless, atworst loony and dangerous.”She says that she and others are often followed in shops by securityguards. Their awkward movements and indecisive loitering excite suspicion;their failure to make eye contact looks shifty. “It’s ironic, since we tendto be painstakingly law-abiding. It always makes me wince when newspapersreport that an accused murderer was a loner, a weirdo, had no friends, as ifall such people are dangerous.”Last summer she wrote to The Times when Professor David Canterdismissed Asperger’s as a fashionable term. Clare says this is a commonmisconception. “People think, ‘You look normal, you talk fluently, youshould just pull your socks up and stop acting weird’. It works against usthat we are so competent in some areas. People see you as being wilfullydifficult.”But small amounts of support — such as arranging socialopportunities — can make an enormous difference. “Since my book came out,one boy I quoted has committed suicide. He was only 20, very articulate, butfelt so isolated and depressed he took the only way out. That is notatypical.” Copyright 2002 Times Newspapers Ltd.

http://www.thetimes.co.uk/article/0,,2-2002004296,00.html

******************************

"How the Clip 'N Snip's Owner Changed Special Education"


by Brent Stapes, New York Times, January 5, 2002

The people of Florence, S.C., know Shannon Carter as the owner of Shannon's Clip 'N Snip, a barber shop where the locals get haircuts and conversation. The Clip 'N Snip has room for seven barber chairs, but Shannon is limiting the business to two for the moment and renting out space until the economy improves enough for the barbering business to expand.Shannon's public school teachers are no doubt surprised to see her running a business and working out a financial plan. During the 1980's she finished ninth grade failing virtually every subject, and was nearly illiterate. The schools told Emory and Elaine Carter that their daughter was terminally lazy and would "never see a day of college." In truth, Shannon was suffering from a common but undiagnosed learning disability that made it difficult for her to comprehend the little that she could read. Alienated and depressed, Shannon became suicidal. In desperation her parents placed her in a private school for disabled children, where she jumped several grade levels within a few years and graduated actually reading on grade level.The Carters then sued the school system for private-school tuition and were upheld in the landmark Supreme Court case known as Florence County School District Four v. Shannon Carter. The law before this case limited parents of disabled children to schools approved by the state. But the court ruled in Shannon's case that the school system lost its right to plan a disabled child's education if it failed to provide an "appropriate public education" as required by the federal Individuals With Disabilities Education Act, known as the IDEA.Ask about Shannon Carter in New York or Los Angeles, and you see school board lawyers snarling or hanging their heads in dismay. The school boards see Carter cases as "a voucher program for the rich," in which affluent parents reserve spaces in private schools and then badger the school systems into paying burdensome tuition costs. Critics have a point when they note that small districts can be destabilized by the cost of one student's stay at an expensive residential school, and that urban districts with too few textbooks are sometimes forced to underwrite lavish private school tuition. But as Congress prepares to reauthorize the federal special education program, it should bear in mind that the Carters went to court only after the public schools failed at their most basic mission: teaching Shannon to read.The task of teaching reading is undermined by the common but mistaken belief that children are somehow neurologically "wired" to read. This view led to the "whole language" fad of the 1970's, in which children were allowed to wander through books, improvising individual approaches to reading. The whole language technique works well with some children. But data from four decades of studies by the National Institutes of Health show that it is disastrous for the 4 in 10 children who have trouble learning to read. Nearly half these youngsters fall behind in the early grades, never catch up and eventually drop out.In the most extreme cases, children seem to have abnormal activity in the parts of the brain that process phonemes — the basic sounds that correspond to the letters of the alphabet. The simplest rules of language make no sense to them. Asked for a word that rhymes with "cat," for example, they simply draw a blank. The disorder strikes children of all backgrounds. It afflicts those who are read to as infants as well as those who grow up without a book in the house.The fortunate children are diagnosed early and assigned to smaller classes where teachers take special care to teach them the fundamentals of written language that others take for granted. The children are walked through the alphabet again and again, learning to connect the letters to the sounds, the sounds to the syllables, the syllables to words and so on. The good news from the N.I.H. findings is that 95 percent of learning- impaired children can become effective readers if taught by scientifically proven methods. The bad news is that less than a quarter of American teachers know how to teach reading to children who do not get it automatically. At the moment, nearly half of all children placed in special education are there for reading difficulties. Federal scientists commonly describe them as "casualties of bad instruction."Part of the blame lies with colleges that have resisted federal attempts to improve teacher education programs. Part of the blame lies with Congress, which has clung to the view that curriculum is a state and local matter in which the federal government should not meddle. Congress failed to even notice the reading research until just recently, when the Bush administration made reading a priority.Congress has focused almost solely on the fact that special education is expensive — and that it takes away money from regular education. The debate will go nowhere until lawmakers begin to view special and regular education as part of a single system that is being hampered by an all too pervasive problem — that schools are teaching reading in a way that fails to effectively reach millions of children. The basic lesson of the Carter case and the tens of thousands that have followed is that the country needs a national reading campaign, based on science. The longer we delay, the more families like Shannon Carter's will bolt the system, taking public dollars with them.

******************************

"Camp Fear"


Gina Score was the latest teenager to die at a juvenile boot camp. Why do so many states still insist that humiliation and abuse will straighten out troubled kids?
by Bruce Selcraig , MotherJones.com, November/December 2000

For more stories like this one, visit www.EducationNews.org.  In a town the size of Canton, South Dakota, population 3,195, plenty of people knew that 14-year-old Gina Score liked to steal things. She stole Press-N-Go fingernails worth $2.99 from the ShopKo in Sioux Falls, stole four Beanie Babies from Brower's Gifts and Collectibles in Canton, stole $60 from a sleepover girlfriend, even stole candles from her Lutheran church. Outwardly, Gina didn't seem troubled -- she babysat for neighbors, wrote cute poems, and smiled radiantly for pictures. But she confided to social workers what they surely guessed: Kids can be cruel to eighth grade girls who weigh 224 pounds. Sometimes Gina cried herself to sleep. Supported by her parents, Gina endured years of programs and punishments intended to change her behavior: community service, individual and family counseling, group care, house arrest, fines, restitution, probation, juvenile detention. Nothing really worked. Finally, in June of last year, after yet another parole violation, a judge placed Gina in state custody until age 21 and sent her to a military-style boot camp for teenage girls located at the State Training School in Plankinton. Like boot camps in two dozen other states, the Plankinton boot camp and a counterpart for boys in the town of Custer were set up to treat children like military recruits. Kids were forced to rise before dawn, perform rigorous exercises, and march like soldiers. Phone calls and visits from parents were prohibited for the first month, and the slightest rules violations were met with swift punishment. As in many other states, the South Dakota boot camps were part of a political campaign by a tough-on-crime governor; Bill Janklow, a popular Republican and ex-Marine now in his fourth term, promoted them as a commonsense solution to juvenile crime. Despite widespread abuses at boot camps from Florida to California, many politicians and frustrated parents have found salvation in the camps' simple goal: to reduce troubled teenagers to their emotional core, back to frightened children, so that their minds will open long enough to imagine a life without drugs, crime, and self-hatred. As a boot camp warden from Texas explains, "We want to turn their lives upside down." Five days after Gina Score arrived in Plankinton, she and 15 other girls from Cottage B began a mandatory 2.6-mile jog at about 6:30 a.m. on the gravel roads outside Plankinton's razor-wire fences. What happened that morning is detailed in medical reports and eyewitness accounts by inmates and staff members at the boot camp. The girls trotted past sprawling farms of corn and soybeans and a small community cemetery; but it's doubtful that Gina appreciated the pastoral scenery. She must have been panicked. Gina was severely overweight and "hated to run," as her mother later recalled. The temperature and humidity were both around 70 and climbing. Within a block or two, Gina started lagging behind. As the girls reached each corner of the rectangular route, where they were allowed to rest briefly and drink water, they waited for Gina to catch up. Two youth counselors repeatedly shouted for Gina to keep moving, sometimes interlocking their armIn a town the size of Canton, South Dakota, population 3,195, plenty of people knew that 14-year-old Gina Score liked to steal things. She stole Press-N-Go fingernails worth $2.99 from the ShopKo in Sioux Falls, stole four Beanie Babies from Brower's Gifts and Collectibles in Canton, stole $60 from a sleepover girlfriend, even stole candles from her Lutheran church. Outwardly, Gina didn't seem troubled -- she babysat for neighbors, wrote cute poems, and smiled radiantly for pictures. But sheIn a town the size of Canton, South Dakota, population 3,195, plenty of people knew that 14-year-old Gina Score liked to steal things. She stole Press-N-Go fingernails worth $2.99 from the ShopKo in Sioux Falls, stole four Beanie Babies from Brower's Gifts and Collectibles in Canton, stole $60 from a sleepover girlfriend, even stole candles from her Lutheran church. Outwardly, Gina didn't seem troubled -- she babysat for neighbors, wrote cute poems, and smiled radiantly for pictures. But she confided to social workers what they surely guessed: Kids can be cruel to eighth grade girls who weigh 224 pounds. Sometimes Gina cried herself to sleep. Supported by her parents, Gina endured years of programs and punishments intended to change her behavior: community service, individual and family counseling, group care, house arrest, fines, restitution, probation, juvenile detention. Nothing really worked. Finally, in June of last year, after yet another parole violation, a judge placed Gina in state custody until age 21 and sent her to a military-style boot camp for teenage girls located at the State Training School in Plankinton.

To See the whole story:
http://www.causeonline.org/Jan02/MoJo1-02.htm
******************************

Autism Awakening, Autism FIrst Steps Newsletter, or any staff do not endorse any individuals, groups or programs.  References regarding programs, meetings, resources, research, opinions, treatment, etc., should not be interpreted as an indication of endorsement.  They are provided for informational purposes only. This is an attempt to keep the nation advised to all diagnostic, treatment, therapy, educational,
options available as well as legislative autism updates and more.


To View Newsletter Policies they are located at the Newsletter Website:    
Direct Link::   Autism First Steps Newsletter
  
http://autismawakeninginia.bizland.com/autismfirststepsnewsletter/


To have friends, Family, or professionals join:
1.  they can go to the above link
2. They can go to the Newsletter Group page located at:
Direct Link:
: Yahoo! Groups : AutismFirstStepsAutismNewsletter    
http://groups.yahoo.com/group/AutismFirstStepsAutismNewsletter
3  Send a e-mail to AutismAwakening@aol.com and ask to be subscribed to the free online daily newsletter


Visit one of the largest websites Commited to bringing you the latest in news, options, and techniques, and more on Autism located at:
Direct Link:: Autism Awakening 4 Kids

www.AutismAwakening.com

To Submit a story, alert, readers post, or advertisement please e-mail AutismAwakening@aol.com

To be removed reply to this e-mail and requested to be removed from the list.

 


To unsubscribe from this group, send an email to:
AutismFirstStepsAutismNewsletter-unsubscribe@yahoogroups.com



Your use of Yahoo! Groups is subject to the Yahoo! Terms of Service.

 

ALL INFORMATION, DATA, AND MATERIAL CONTAINED, PRESENTED, OR PROVIDED HERE IS FOR GENERAL INFORMATION PURPOSES ONLY AND IS NOT TO BE CONSTRUED AS REFLECTING THE KNOWLEDGE OR OPINIONS OF THE PUBLISHER, AND IS NOT TO BE CONSTRUED OR INTENDED AS PROVIDING MEDICAL OR LEGAL ADVICE.  THE DECISION WHETHER OR NOT TO VACCINATE IS AN IMPORTANT AND COMPLEX ISSUE AND SHOULD BE MADE BY YOU, AND YOU ALONE, IN CONSULTATION WITH YOUR HEALTH CARE PROVIDER.