Parents want to give their autistic children a voice in schools, but scientists call their technique ‘false hope’

From Washington Post:

By Michael Alison Chandler February 28 at 7:59 PM 

In a science class at Lakelands Park Middle School, 13-year-old Mike Keller sat between his professional aide and his science partner during a lesson about how force affects balance. The Montgomery County teen, who has autism, stood up a few times in a burst of energy and once walked out of the room. But with some redirection from his aide, he appeared to focus on a series of questions that his teacher posted on the whiteboard. 

His teacher asked him an easy yes-or-no question at one point, and as an aide held a keyboard in front of him, Mike typed the word “Yes” on the iPad, followed by a touch of sarcasm: “Duh.”

Mike is not able to speak. He points at letters on a laminated alphabet board or types on a keyboard that an aide holds. Nationally, most students who can’t talk are in self-contained classrooms or autism programs or, like Mike used to be, in a separate school for students with severe disabilities.

But five years ago, Mike and his mother traveled to Texas to explore a novel communication technique called Rapid Prompting Method that led to what his family describes as a breakthrough. About a year later, he joined a new pilot program in Montgomery County Public Schools for autistic students who rely on keyboards and communication partners.

Montgomery County is unusual, if not unique, in creating such a program. Many schools have denied similar requests for programs that allow rapid prompting, or a similar technique known as facilitated communication that was widely discredited by the scientific community in the 1990s.

A generation later, there is a resurgence of non­speaking students who type to communicate and rely on a communication partner through various techniques. Active communities of “typers” are growing in Southern California, Michigan, Boston, Atlanta and the D.C. region, areas where families have access to private training. As their numbers grow, more families are pushing for their children to be included in public schools.

In an autism world with few documented treatments and many high-cost promises, the use of these techniques has stirred strong emotions. Critics say they offer false hope to desperate families, while advocates argue that they help some people and that it is wrong to stop exploring the only means some may have of communicating.

In Arlington, Va., the Autistic Self Advocacy Network filed a discrimination complaint last spring with the Justice Department on behalf of five nonspeaking students — dubbed the “Arlington Five” — whose requests to use letter boards and trained communication supporters to access general education were denied by the school district.

By denying students their “preferred communication method,” the complaint stated, they are being “prevented from communicating their thoughts, ideas, and feelings,” and “being consigned to an inferior education with fewer opportunities and lower expectations.”

Brenda Wilks, an assistant superintendent overseeing special education for the Arlington County schools, said in a statement that the district “will continue to explore best prac­tices and educational research in this area as we evaluate the use and potential benefit of [Rapid Prompting Method] and other related methodologies to support our students.”

Critics point to research that indicates the techniques are not effective.

In response to an international resurgence in the use of facilitated communication, Ralf W. Schlosser, a professor of communication sciences and disorders at Northeastern University, led a systematic review in 2014 of more than 20 studies of the technique. It found overwhelming support that the facilitator was controlling the message.

“In the field of augmentative communication, we want to empower people with disabilities to speak their own minds, so if someone else is speaking, that is a big problem,” he said.

But advocates question some of the research methodologies and say better training and newer techniques, including rapid prompting, offer safeguards against facilitator influence.

Underlying the debate, some maintain, is a fundamental civil rights question.

“When Helen Keller first learned to communicate, no one believed her,” said Vikram Jaswal, a University of Virginia psychologist who has an elementary-aged daughter with autism who he said is learning to spell to communicate. “We routinely segregate people who can’t talk. Why do we assume they can’t learn?”

Different approaches

First developed in Australia, facilitated communication was introduced in the United States in 1990 when Douglas Biklen, a Syracuse University education professor, wrote about it for the Harvard Education Review.

It was embraced enthusiastically as a miracle technique that could unlock the potential of people who had been written off as very low functioning. There were media reports of people previously thought to be mentally retarded graduating from high school or writing lyrical poetry.

In facilitated communication, a trained facilitator helps the nonverbal person type by supporting their arm, wrist or hand. It is based on the theory that autism has a significant motor component, and many have difficulty with intentional movement and so need physical support to demonstrate what they know.

Syracuse established an Institute for Facilitated Communication and trained thousands of facilitators, many of them public school educators, from across the country.

Its downfall was swift and steep. A series of controlled studies in the 1990s found strong evidence that the communication was extremely susceptible to facilitator influence. In so-called message passing tests, when the subject was asked about something that the facilitator could not know, the responses were routinely inaccurate. Researchers found that facilitators were unaware they were influencing the response.

At the same time, in dozens of cases, nonverbal people made accusations of sexual assault through their facilitators. Some highly publicized allegations involved a parent or family member. Judges found these claims to be false, and the facilitated messages unreliable.

By 1994, the American Psychological Association adopted a position statement opposing the use of facilitated communication. Other professional organizations followed suit.

Public schools, for the most part, closed their doors tight to the practice.

The center at Syracuse never closed, although it changed its name to the Institute on Communication and Inclusion. And Christine Ashby, its director, said that interest in facilitated communication did not go away and has increased in recent years.

A handful of school districts — including those in Syracuse, N.Y., Barre, Vt., and Whittier, Calif. — have trained teachers and supported students over time, Ashby said. But most considered each case individually and provided services quietly.

The institute promotes standards of practice designed to reduce the chance for facilitator influence, including providing the least amount of physical support possible, and training typers to work with multiple facilitators, Ashby said.

“It grew too fast, without the right procedures in place, and a lot of poorly trained facilitators,” she said.

At the same time, rapid prompting, which is not taught at the Syracuse institute, has gained traction among nonspeaking people with autism.

The approach was popularized in the United States by Soma Mukhopadhyay, a chemist by training from India who dedicated her life to educating her autistic son.

Practitioners say the approach is fundamentally different from facilitated communication because, in rapid prompting, an aide typically holds a keyboard but does not touch the person typing.

The process involves using verbal encouragement and tactile stimulation derived from having someone hold the board. Such prompts are supposed to help the person initiate movement and stay focused on typing despite sensory distractions.

There is very little research on rapid prompting, in part because Mukhopadhyay has resisted participating in studies.

Critics say this method is also highly susceptible to facilitator influence. They describe it as a process of learning to respond to increasingly subtle cues.

Howard Shane, director of the Center for Communication Enhancement and the Autism Language Program at Boston Children’s Hospital, questioned the validity of any communication method that requires the physical help of someone else.

“We have five different ways of controlling a computer with your eyes,” he said. “We can most of the time find some way for them to communicate independently.”

Shane said he has seen nonverbal autistic people create full sentences independently but has never seen high levels of intellect suddenly unlocked.

Matthew Belmonte, a neuroscientist at Nottingham Trent University in Britain and a visiting researcher at a Bangalore clinic that teaches communication techniques similar to rapid prompting, said the method’s theoretical underpinnings are sound and some nonspeaking people with motor impairments can potentially benefit.

Research is needed, he said, to ascertain whether, for whom and in what contexts the technique works, and to improve and automate the process.

“We have to be very careful if we are denying the veracity of potentially the only means of communication that some people have,” he said.

‘He had been there all along’

In the decade after her son’s autism diagnosis, Lori Mitchell-Keller spent untold hours pursuing treatments.

“I can count on one hand the things that worked,” she said.

Then in 2012, she learned about Mukhopadhyay, who ­teaches her method to a growing list of families from an office in Austin.

Mitchell-Keller arranged for Mike to take lessons from her over the course of a week.

The results astonished her, she said. It appeared to her that Mike not only knew how to read and spell but that he also had been comprehending far more than they had imagined.

“I realized he had been paying attention, he had been there all along,” she said. Back at home, their family transformed as they got to know a boy who, his mother said, is bright, spiritual and affectionate.

Mike joined the Montgomery pilot program and enrolled in typical fifth-grade classes. The program started in fall 2013 with five boys, some using facilitated communication and some using rapid prompting.

A few more students have been added since, but the program will remain small without further evidence of the effectiveness of the techniques, said special education director Philip Lynch.

Officials are monitoring the students for progress toward independent communication, as well as social and emotional progress, Lynch said. He noted that Mike had made friends at his school and said: “How do you measure the impact of being included in your public school?”

After four years of practice, Mitchell-Keller said her son is making progress toward fully independent communication. He is now able to type without someone holding the keyboard, although the process tires him much more quickly, she said.

On a late November afternoon, Mike sat with the keyboard on the kitchen table in front of him and answered a few questions from a reporter about his Thanksgiving.

“My thanksngi mm. was golden,” he typed.

“my cousin Theo” visited and “really had great trimester here,” he wrote, with auto correct filling in the word “trimester.” “HE IS FROM. MINNESOTAN,” he wrote.

He yawned widely while he slowly typed the letters and hit the backspace key and typed again.

Mitchell-Keller, who travels extensively for work, said her son has worked with dozens of communication partners. When she is with him, she usually holds the keyboard, but this time she sat next to him without touching it. She reminded him to sit up straight, and she read the letters he typed aloud and encouraged him to keep going. She kept one hand on the edge of the table or underneath it. With the other, she held the tip of his collar between her forefinger and thumb.

“I am not even sure he feels it. I am not touching his skin, but I think it gives him a level of reassurance,” she said. “He’s not all on his own. There’s a lifeline there.”

Say NO to House Bill 610

If you care about public education -- please take action!

House Bill 610 makes some large changes.

Inform yourselves.

This bill will effectively start the school voucher system to be used by children ages 5-17, and starts the defunding process of public schools.

In addition the bill will eliminate the Elementary and Education Act of 1965, which is the nation's educational law and provides equal opportunity in education.

It would repeal ESSA (Every Students Succeeds Act):
ESSA is a big comprehensive program that covers programs for struggling learners, AP classes, ESL classes, classes for minorities such as Native Americans, Rural Education, Education for the Homeless, School Safety (Gun-Free schools), Monitoring and Compliance and Federal Accountability Programs.

The Bill also abolishes the Nutritional Act of 2012 (No Hungry Kids Act) which provides nutritional standards in school breakfast and lunch.

The bill has no wording whatsoever protecting SN kids, no mention of IDEA and FAPE.
Some things ESSA does for Children with Disabilities
-Ensures access to the general education curriculum.
-Ensures access to accommodations on assessments.
-Ensures concepts of Universal Design for Learning
-Includes provisions that require local education agencies to provide evidence-based
interventions in schools with consistently underperforming subgroups.
-Requires states in Title I plans to address how they will improve conditions for learning including reducing incidents of bullying and harassment in schools, overuse of discipline practices and reduce the use of aversive behavioral interventions (such as restraints and seclusion).

Please call your representative and ask him/her to vote NO on House Bill 610 (HR 610) introduced by three Republican reps.

MRI of the Brain

As part of the standard of care for anyone that's diagnosed with Phelan McDermid Syndrome, Darus had his first brain MRI, under anesthesia, today at UCLA. I was anxious the entire time, but Darus was a real trooper and did great! The MRI was scheduled (not an emergency). We're hoping it will give us a baseline picture of his brain, if nothing else. His neurologist believes we will see methylation (due to his hypotonia) and there is a possibility of other abnormalities, including arachnoid cysts, which are typically benign, but common in the PMS community. Thanks to everyone for sharing this journey with us, your support is invaluable and much appreciated. #phelanmcdermidsyndrome #strongertogether

 

 

 

Research Study at UT-Southwestern

Attending the Global Genes conference really inspired me to do more for Darus, and all others affected by PMS (and rare genetic conditions).  Upon my return from the conference, I scoured the internet in hopes of finding another research study in which we could participate, and guess what?  I found it!

From the website ::  The purpose of this study is to further characterize Phelan-McDermid Syndrome (PMS) by identifying objective electrophysiological biomarkers (measurable/identifiable EEG patterns) that can be used to understand underlying neural functioning in this study population. Utilizing measures of neurophysiological (related to the functioning of the nervous system) visual and auditory reactivity, we hope to identify electrophysiological biomarkers which (1) can be used as outcome measures in future pharmacological (drug studies) and behavioral intervention studies and (2) aid in predicting treatment response.

Traveling with Darus in the past has been a bit of a challenge.  Airports, airplanes, rental cars, hotels, etc.  However, we really tried our best to prepare Darus for what was coming and we think we did a pretty darn good job, because he travelled – and participated – really well! 

Day 1 - We started at UT-Southwestern by meeting Dr. Craig Powell and his associate Adrian Avila.  Everyone was very kind and hospitable.  Darus took to all of the new places and faces right away and even gave kisses and said good bye when appropriate.  We spent most of the morning doing an EEG.  It was a bit of a challenge getting the specialized cap properly positioned - as there were dozens of leads that needed to be glued and set (many more than what we're accustomed to with our overnight EEGs).  We then spent the afternoon undergoing a complete physical and going over all of Darus’ history.  Lastly, we went to Dallas Children's Hospital for a blood draw, which Darus handled like a boss.

Specialized EEG with over 100 leads! 

Day 2 – The morning started with psychological exams, which are never fun.  The exams are standardized and really do a poor job at gauging Darus’ cognition and abilities.  They are frustrating for us, as parents, and undoubtedly frustrating for the test subjects, too, that have to endure them.  I didn’t let that stop me from encouraging Darus to show off his skills in his own way – I had him spell out answers to my questions using letterboards.  Understandably, they cannot use the data he demonstrated- as it isn’t standard – but it’s my hope that eventually these tests will evolve to be more practical and functional for accurately assessing people like Darus.  We then moved on to the physical movement portion of the study, which was held at Dallas Children’s.  This was my favorite part.  It was very interactive and really hi-tech.  We were in a room similar to a room that they'd use for animating video games.  Darus had small plastic pieces attached to most of the joints in his body - and then was recorded/analysed while prompted to complete different motions.  There was also a weighted platform that was used as well to measure his biometrics while he sat, stood up and walked.   

IMG_0401.JPG

Overall, Darus was a great travel buddy and tolerated all of the new places and new people really well. His iPad was definitely a crutch, but we'll take it, compared to the alternative.  Jonas and I are very proud of him and his participation!  

Camp Josepho Hike

I've had the honor of carrying both my babies in my stomach up this very same hike.  It's a favorite of mine.  It's a fireroad through the Santa Monica Mountains.  It's known to the locals as 'Top of Capri' or 'Camp Josepho'.  Below the hiking trail is a place FKA Murphy Ranch, which has a history all of its own.  All in all, I've spent a lot of time up here and today was the first day I took Darus, all by myself, with no stroller.  He loved it!  He stayed on the trail and just kept truckin'!  I look forward to many more adventures with him up here and hiking in general.  (By the way, we did a total of 3.5 miles in just over an hour - with a fair amount of elevation!)

 

  

Apple Boy

Darus' skills seem to come and go.  Once upon a time, apples were about the only food that he didn't like.  Now, he really enjoys them!  So much so that when he sees one sitting in the fruit bowl, he'll oftentimes help himself!  

Unlocking Knowledge

A friend of mine recently shared with me information about a type of 'speech' therapy know as RPM (Rapid Prompting Method) founded by Soma Mukhopadhyay.  The same friend shared that she had a local therapist that offers a similar type service and we started working with this therapist a few weeks ago.  Darus showed us that he knows how to spell words!  He also showed us that he knows how to do math!  He's shown us this by using his finger to point at different letters/numbers!  It's really been incredible to see how much Darus knows!  We are very thankful to Soma and Tracy for making this possible!

Below, Ms. Tracy read Darus a short story about lions in the jungle.  She explained to Darus that lions eat meat.  She then asked Darus, "what do lions eat?":

Teaching Acceptance

We are fortunate to have found a lovely local public school that Darus started earlier this year.  That said, as with any community that we find ourselves new to, we are vulnerable and it's a whole new opportunity to teach acceptance.  Earlier this week, I missed the opportunity and I posted the below on our school's FB page.

This morning as I was walking my 6 year old son to his classroom, there were two boys that saw my boy from afar. One of them pointed and said, “Look, there’s Darus”, in a way that was less than friendly. They both looked away after I made eye contact with them. It was apparent to me that they were pointing at my child because he is different from them. Darus is different. He has Phelan McDermid Syndrome in addition to autism. His condition impairs his ability to speak, process information and interact with others. It does not, however, stop him from being a very happy, loving & playful boy.

I somewhat froze in the situation because I really didn’t know how to respond. On one hand, I was grateful that they didn’t mock him – but on the other hand, they had no intentions of approaching us to say hi. I do not fault the kids. They are young – I’m guessing 2nd-ish grade. I am more upset with myself that I didn’t walk over to the kids and introduce myself to them as Darus’ mom. I then could have used the moment as a teaching opportunity to prompt Darus to say hi and the kids to say hi back to him. I could have possibly kindled an understanding of acceptance for these two boys.

I hope that if any of your children talk to you about a boy named Darus at school that you let me know. We’d love to invite you over for a playdate. We’d love to help bridge the gap between neurotypical and special needs. We’d love to share our world with you and yours.

My post quickly generated many "likes" and "loves" and my phone started buzzing as well with private text messages from a handful of parents that I've met since the beginning of the school year.  I definitely felt the love.  I also felt and realized that I'm not alone with my feelings.  There are other parents, that have children, that have differences, that have also felt that their kids have been picked on - for lack of better words.  One of the parents, Heather, kindly and courageously asked for my advice/input as to how to address this with her children.  Below is my response.

Thank you all, very much for your kindness. I really appreciate it. I have given a lot of thought to Heather’s question, and then found myself on Amazon. I was able to find 5 children’s books that I believe could be helpful in better explaining acceptance. I’ve purchased them, and after reading them myself, I am happy to pass them around to any parent that is interested and perhaps ultimately donate them to the school library? I think they could be really helpful in opening the door and facilitating conversations within our school community. 

Unfortunately, I don’t believe there to be a steadfast answer to Heather’s question, I really wish there was. I believe that each parent has a different way of wanting their child identified, and I, frankly, get confused with identifying my own, much less others. I currently refer to my child as having special needs (not sure if that’s right or wrong?) – however, I think that label can be confusing for children – because they then wonder why they aren’t special (when, of course, they are!). 

That said, I am hopeful the books can help open a dialogue. I want all of our children to know they are special. We have differences and similarities – but focusing on acceptance of differences, I guess, is what I’m trying to accomplish. Again, I appreciate all of your kindness and posts here and privately. Xo


A dialogue was started.  Now, as a community, we need to keep it going.  I hope these books help nurture the process.

   

Clinical Trial at UT Southwestern - Biomarkers associated with Phelan-McDermid (22q13) Syndrome

Attending the Global Genes Summit has really inspired me to dig deeper to find some answers and cures for my son, and all others affected by Phelan McDermid Syndrome.  I learned a lot at the conference and the fruits are hopefully to follow!  I've been in touch with a researcher at UT Southwestern and I'm hopeful that Darus will be able to participate in this biomarker study this Winter.