Sunday, August 30, 2020
Thursday, August 27, 2020
A man with autism lost his right to vote or buy a home. He’s fighting to reclaim them
A man with autism lost his right to vote or buy a home. He’s fighting to reclaim them
Miami-Dade County
At 22, Tyler Borjas had a job, a bank account and got around using Uber and Metrorail.
But he couldn’t legally vote, buy a house or make travel plans. That’s because a Miami-Dade court deemed Borjas, who has autism, “incapacitated,” and placed him under guardianship.
”I want to make my own decisions,” Borjas, who is now 25, said. “I want my rights back.”
Guardianship essentially stripped Borjas of his rights, meaning he couldn’t legally make decisions for himself, said Viviana Bonilla López, an attorney working with Disability Rights Florida, an advocacy group.
Bonilla López has set out to change that for Borjas and other adults by promoting a mechanism known as Supported Decision Making instead of guardianship. If Borjas succeeds, it’s believed he’ll be only the second person in the state to reclaim his rights back in this manner.
Supported Decision Making allows adults with disabilities a “less restrictive alternative” while ensuring that they have oversight and help in making important decisions. Bonilla López filed a “suggestion of capacity,” (similar to a motion) in court on Thursday asking a judge to give Borjas his rights back and name his mother, Kelly Bain-Borjas, and two sisters, Hayley and Jade, as his supporters.
“Supported Decision Making better enables people with disabilities to protect themselves from abuse and neglect,” Bonilla López said. “Guardians and guardian advocates have sole control over the person in their care’s life with little oversight.”
So if Borjas wants to go on a trip or buy a car he would run the idea by his supporters and together they would make a decision. Borjas would be able to play a more active role in controlling his own life.
Tyler as a child
Borjas was a toddler when his mother started to notice her son wasn’t hitting certain milestones, including talking. Her brother told her not to worry, because boys tend to develop a little slower.
She ended up taking him to a neurologist and learned her son had autism.
She enrolled him in a Miami preschool that offered a program for children with autism. He was placed in an ESE class in elementary school and “he excelled,” his mom said.
Bain-Borjas said she didn’t want to hold her son back from doing anything he wanted to do. He wanted to learn martial arts. She obliged. He wanted to volunteer. So she signed him up. He wanted to work. She helped him get a job.
At 16, Borjas was already learning the importance of helping others and working. His first volunteer job was at a bird sanctuary. While in high school, Borjas was placed in a job-training program at the University of Central Florida, where he got experience by working at places including Publix and an assisted living facility.
“One thing about Tyler, is he is very self-motivated,” she said.
A life for himself
Borjas completed an internship at Nicklaus Children’s Hospital, and in 2016 he got a job at AmericanAirlines Arena working in the Papa John’s. He is currently not working because the pandemic has shut down major events.
Borjas does it all. He uses the dough machine, makes the pizza and delivers throughout the arena.
He was living at home, but building the life he wanted.
How they fell under guardianship
When Borjas was 22, his mother filed a personal injury lawsuit on her son’s behalf. She said a lawyer told her the only option was guardianship.
She had heard about guardianship while her son was in school, but never went that route because she didn’t think her son needed it.
She said before she knew it, the judge deemed Tyler incapacitated.
“I was thrown off,” she said. “I didn’t want to take his rights away. I was very distraught.”
What led them to Supported Decision Making
Bonilla López is an Equal Justice Works Fellow working with Disability Rights Florida.
Her project, which is sponsored by the Florida Bar Foundation, is focused on expanding the use of Supported Decision Making.
She said she met Tyler and his mom at an event in October where she presented on the topic.
That’s when Bonilla López decided to take on Tyler’s cause.
“Tyler’s case is a perfect example that a guardianship should never have happened,” she said. “He was already independent and he was being found incapacitated.”
The first Florida case
Michael Lincoln-McCreight became the first person in Florida to terminate his guardianship in favor of Supported Decision Making.
In 2014, Lincoln-McCreight, who has a developmental disability and was in foster care, was deemed incapacitated after an advisor decided guardianship was the best route for him.
Now 25, he was around 20 at the time and participated in the Sheriff’s Explorers, volunteered at hospitals, went to church, and loved movies.
But that didn’t matter. In September 2014, the Circuit Court of St. Lucie County declared Michael incapacitated and he lost his rights.
“My dad always taught me to be independent,” he said. “I was shocked that it happened.”
Working with Disability Rights Florida, Lincoln-McCreight, who is a security guard, got his rights back in 2016.
He now works to help others like Tyler.
“People with disabilities can do anything if they set to their mind to it,” he said.
On a mission
Bonilla López’s main goal is to spread the word that Supportive Decision Making should be used as an alternative to guardianship when it is appropriate.
“Guardianships are overused when really the person could be making their own decision with support,” she said. “A lot of times people confuse needing help with not being able to do something. But all of us need help, all of us need advice and people with disabilities are no different.
Bonilla López said they are also working on legislation that would require Supportive Decision Making to be considered before a disability guardianship is activated.
For Tyler, getting his rights back would mean he is in control.
For his mom: “I am just so happy that there is something in place that can help Tyler.”
Wednesday, August 26, 2020
Autism and Anxiety
Autism and Anxiety from the Autism Research Institute (For Educations Purposes Only):
Anxiety disorders are among the common comorbidities of autism spectrum disorder. The reason for this overlap is still under investigation. However, several treatments for anxiety may deliver positive results for people with both anxiety and autism spectrum disorder.
What is anxiety?
Anxiety is an emotion marked by heightened alertness. This emotion is a natural response to a threat or stressor. When the symptoms persist after the stressor is removed, or when the anxiety response becomes chronic, this may indicate an anxiety disorder.
Common symptoms of anxiety disorders include:
- feelings of fear or doom
- restlessness
- increased heart rate
- difficulty concentrating
- muscle tension
- Irritability
- changes in appetite
- sleep disturbance
Several of these symptoms overlap with common symptoms of autism. These include repetitive behavior, the rigidity of routine, rituals, flat affect, or limited social interactions. The overlap can make it more difficult to identify anxiety disorders in people who already have an autism diagnosis.
How common is anxiety?
Anxiety disorders are the most common mental disorder in the United States, affecting about 18% of the general population. Research has shown that the incidence of anxiety in people with autism may be significantly higher than in the general population. One systematic review of the published research on anxiety and autism found that almost 40% of children with autism and 50% of adults with autism experience some sort of anxiety disorder (Van Steensel, 2011). Adolescents and school-age children with autism have the highest prevalence of clinical (40%) and subclinical anxiety (26%) compared to other age groups with autism. This mirrors patterns found in the general population.
Specific phobias are the most common form of anxiety disorder among people with autism. A person with a phobia experiences extreme distress when exposed to a specific stimulus or situation. Obsessive-Compulsive disorder and social anxiety disorder also occur frequently.
Anxiety and autism can interact in ways that intensify the challenges for a person living with these disorders. The symptoms of autism may make anxiety more challenging to manage. At the same time, the symptoms of anxiety may create barriers for a person with autism as they work with clinicians and therapists, interact with friends and family, and pursue personal or professional goals.
Why are rates of anxiety higher in people with autism?
Although the research above has shown that anxiety is more common in people with autism, researchers are still exploring why this is the case. Each individual may experience the overlap between anxiety and autism differently depending on their personal combination of symptoms and skills.
In the webinar Anxiety, Autism: Five Prime Suspects, Christopher Lynch, Ph.D. explores five ways that anxiety and autism may interact.
- Attention to detail. People with autism tend to be more detail-focused. While this can be a valuable skill, it can also make transitions and changes in routine more challenging. When a person with autism, especially a child, is forced to shift their attention before they are ready, anxiety may result.
- Sensory sensitivities. Some individuals with autism experience noise, touch, sight, smell, taste, temperature, pain and other sensory factors more intensely. Overwhelming sensory sensations can lead to sensory overload which can trigger anxiety.
- Social situations. Increased sensory load and pressure to work within often unspoken social rules can increase anxiety in people with autism. A twin study reported by Spectrum News identified a link between high intelligence and social anxiety in autism. “It’s likely that some of these children’s worries stem from their acute awareness of their difficulties,” the article stated.
- Language. Some individuals with autism process language differently. Anxiety may increase when they find it difficult to express their wants or needs or when others fail to understand them.
- Task frustration. People whose autism symptoms include differences in motor skills, executive function, or abstract thinking may feel anxiety when working on a challenging task.
Other possible explanations for the overlap between autism and anxiety include:
- Genetic factors. Anxiety and autism may have a shared genetic origin that researchers have yet to identify.
- Insufficient support. People with ASD may face challenges and have comorbidities that require additional support and resources. Worrying about, or being unable to access these resources, can increase anxiety.
- Social pressures. The stress of living in a world that expects individuals to act or interact in ways that don’t feel natural to them may intensify anxiety.
How to spot signs of anxiety
Both caregivers and people with autism should look out for signs of anxiety. Some symptoms of anxiety overlap with symptoms of autism. This can make anxiety more difficult to identify in a person with autism.
A person experiencing anxiety may lose their appetite or eat more than normal. They may struggle to fall asleep or stay asleep. Sometimes, anxiety can look a lot like anger or fear. Stay alert to changes over time to help you decide whether this is a passing mood or a long-term condition.
You may notice an increase in repetitive or compulsive behaviors or an increase in sensory sensation-seeking behaviors. These behaviors may represent an attempt to decrease or manage anxiety.
It can be helpful to keep a journal to track behaviors and moods. A written record is more reliable than casual observations and memory. Notice changes in sleep, appetite, excitement over special interests, and overall daily mood.
If you or someone you care for is experiencing anxieties, talk to your clinician. They may be able to recommend strategies or treatments to help manage anxiety. Your clinician may also refer you to a specialist or provide access to supportive resources.
Strategies to address anxiety
Work with your clinician to identify strategies and treatment options to address anxiety. Here are a few of the treatments and strategies your clinician may suggest:
- Remove the stressor or address the situation. For example, if a child is being bullied at school, this can lead to symptoms of anxiety. Addressing the bullying issue may help alleviate symptoms.
- Build new skills. Problem-solving strategies and coping skills can help people with anxiety to feel more in control and minimize anxiety, whether they have autism or not.
- Seek out accommodations. School and work accommodations can help people with autism manage symptoms of anxiety. Reducing sensory input and creating clear schedules or routines have both been shown to minimize anxiety.
- Psychological intervention. Modified Cognitive behavior therapy and Mindfulness-based strategies may a person with autism become more aware of thoughts and emotional responses, which can help them to address anxiety including situations before they become overwhelming.
- Medication. In some cases, medication provided under close medical supervision can help control anxiety while the individual builds skills, sets up accommodations, or begins therapy. There is limited data on the use of anxiety medication for individuals with ASD.
Anxiety, much like depression, is a common comorbidity of autism. It is also treatable. If you notice changes in mood or behavior, you can talk to your doctor about possible interventions or treatments.
SEE VIDEO HERE:
Tuesday, August 25, 2020
Spotting the problems with ‘camouflaging’ in autism research
Spotting the problems with ‘camouflaging’ in autism research
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Autistic people may feel pressure to fit in at work or at school, or they may pick up mannerisms to help them get by in a society that is not set up to accommodate them. Scientists and autistic people describe such thoughts and behaviors as ‘camouflaging.’
Over the past few years, research on camouflaging has expanded rapidly. Some autistic women, for example, have reported that they camouflage their autism so well that they did not receive a diagnosis until adulthood. And studies show these women have brain activity in regions associated with social interactions that more closely resembles that of their typical peers than that of other autistic women. Researchers have sought to quantify camouflaging as the mismatch between an autistic person’s self-reported autism traits and their traits as measured by the Autism Diagnostic Observation Schedule (ADOS). They have also suggested that more women camouflage than men do.
But some of this work is misguided, argues Eric Fombonne, director of autism research at the Institute on Development and Disability at Oregon Health and Science University in Portland. In an editorial last month in the Journal of Child Psychology and Psychiatry, he laid out the problems he sees with this burgeoning field of study1. He spoke with Spectrum about the catches with quantifying camouflaging, the potential overdiagnosis of autism in adults and the possibility that camouflaging is not unique to autism.
Spectrum: What is camouflaging?
Eric Fombonne: ‘Camouflaging’ is not very well defined in the literature. When you read the papers, it is sometimes defined as the feelings or subjective experiences that people who have autism have when they are in social situations. They feel that they want to hide their autism features to not be stigmatized or detected. Then researchers sometimes use ‘camouflaging’ to describe what these people do to actually improve their fit into a social situation and decrease their visibility as a distinct individual. This is where you have camouflaging become a repertoire of cognitive strategies or behaviors, which include ‘masking’ in particular.
Some individuals have repetitive movements, and they learn how to control them. They learn how to reduce behaviors which might signal that they have autism, and they also employ some compensation strategies. If someone doesn’t make eye contact easily, there are ways to give the impression to your interlocutor that you have better eye contact by looking in between their eyes, or at their nose. So it’s masking, compensating for that.
And then it’s also used to describe the situation of people who are so well adjusted in the work or social environment that you actually do not detect a difference between them and the group. That’s ‘camouflage’ defined not as a behavior, not as a subjective experience, but more as an endpoint. It’s also used sometimes to describe the cognitive processes by which people have engaged in camouflaging behavior.
S: What do you think is unclear about how people use the term ‘camouflaging’?
EF: One wish I have is that when I’m reading a paper, the authors define ‘camouflaging’ and the construct that they study in a clear way, up front. Tell me what you want to study, and tell me what you are not studying, when you say ‘camouflaging.’ Unless it is defined narrowly and specifically, it’s confusing. And once it is defined, the next critical issue is how it is measured and operationalized in a given study.
S: What are the problems with how researchers have attempted to study camouflaging?
EF: It’s an area where there have been essentially two approaches. One is what is called the discrepancy approach. They ask an autistic individual to complete a checklist, let’s say the Social Responsiveness Scale, giving a score of self-reported autism symptoms. Then they take the ADOS score that has been given by a professional, and that’s considered the ‘true’ autism score of this person — not self-reported but observed. They take the difference between the self-report and the external display, and they say this difference is a measure of camouflage.
Maybe it’s an okay approach, but this discrepancy between the high score here and the low score there does not necessarily mean that this person taking the ADOS was hiding or masking or compensating. You simply don’t know. You just cannot take that difference as an index of camouflage, unless you take specific steps to demonstrate that this difference of score is actually a measure of camouflaging — and this has never been done. They don’t do it. They just assume that the difference of score is a measure of camouflaging.
They say, well, it must be a meaningful index because it has correlations with other variables, sometimes external to the camouflaging context. But this is not the way science works. They should demonstrate that the difference in score has construct validity, that it is really a measure of camouflaging, and no study has ever done that.
Some people have used another approach to measure camouflage: They devised a questionnaire, called the CATQ, the Camouflaging Autistic Traits Questionnaire. I like this step. But the questionnaire was devised in a very unusual fashion. They interviewed people on the internet who volunteered for the study, and really they don’t know if they have autism or not. It is based on a poorly defined sample to start with.
And then, you look at the questions, I quote one in my editorial that says, “I am always concerned when I go in a public place, people are going to look at me and judge me.” This is typical of social anxiety. It has nothing to do with autism. The questionnaire is full of questions like this. Why do they not pick that up? It’s really concerning.
And then, guess what? When they analyzed the camouflage questionnaire study, it correlated with social anxiety scores more than with autism. So, it seems that their questionnaire is actually a better measure of social anxiety than a measure of autism, and yet again, they have that in their paper, and they just ignore it.
In none of these studies did they confirm that these people who answer the questionnaire really have autism. Many of them have a self-reported diagnosis.
S: Why does the term ‘camouflaging’ not necessarily apply to autistic adults in the way that people often use it?
EF: I see a number of adults who are diagnosed with autism, even though when you look at their developmental history, they didn’t have signs of autism.
A number of people have mental health difficulties in adulthood. And now some providers, family doctors or adult psychiatrists, have embraced the spectrum idea of autism, and it becomes very easy to say, “Well, yes, this person has always had relationship difficulties. She’s isolated, she doesn’t have many friends, she has social problems. She never really shows empathy for others. Okay, so that’s another flag. And then she’s obsessed with a number of things.” And bing, bing, bing, you can suddenly score the three domains of autism. They can be even more loosely scored on a self-completed diagnostic checklist sheet, and people overuse this diagnosis now.
Sometimes, a positive ADOS is used as ‘proof’ of autism. The diagnosis of autism is helped by ADOS testing, but it relies on the clinician to integrate all the information. Having a high ADOS score is in no way sufficient.
I’m pretty certain that a number of adults with an autism diagnosis, especially if it was given later in life, if it were reviewed with scrutiny, many of the diagnoses would not be confirmed. I found the same issue to apply to diagnosis in older children or teenagers with a mixed bag of problems referred late to our clinics.
S: How do other conditions confound the notion that camouflaging leads to delayed autism diagnoses?
EF: In a lot of these studies, they sent research assistants, young people just out of college, or in college, who have been doing like three days of training on the ADOS, and they’re administering the ADOS. They’re going to adults who are complicated people, and these adults score high, but that doesn’t mean that they have autism. There are studies showing that if you have schizophrenia or social anxiety or other things — conditions that emerge during teenage years or young adulthood — the likelihood that you will score high on the ADOS is very, very high, even in the absence of autism.
So what I mean is that adult diagnosis needs to be really taken seriously. When we meet an adult who may have autism, we need to have a lot of autism expertise, as well as psychopathology expertise, involved in the process of evaluation.
The other aspect is that we need to bring development into this adult assessment. You cannot diagnose autism without evidence that there has been a trajectory of developmental difficulties early on. It is necessary to bring in an evaluation of the early developmental trajectories and social interactions, communication and other peculiar behaviors, to solidify the diagnosis of autism in adults at later ages. That needs to be taken much more seriously than it is.
The way these studies are done is muddling the whole situation. They say that these women have not been diagnosed, and then they say, ‘Therefore, there must be many more women who have not been diagnosed and are camouflaging, and their camouflaging has been successful in hiding them and deferring the diagnosis.’ This is a good example of circular reasoning.
S: You argue that camouflaging behaviors are not specific to autism. What does this mean for our understanding of camouflaging among autistic people?
EF: I’m a psychiatrist, so I have treated adults and I know a number of adults who have chronic mental health conditions. When they feel better or they want to re-insert themselves into a more normal role when they are doing well, they want to not be seen as having mental health issues. A schizophrenic person who is looking for employment will be aware that when they have a little tremor due to medication, they must hide it. If they have a tendency to have facial expressions which are a bit fixated because it is a secondary effect of the neuroleptic, they will be conscious of that and try to accentuate their facial expressions to cover for that.
I’m short, so if I have the choice between two equivalent shoes, I tend to pick the one that has the highest heel. Likewise, overweight people may prefer black or dark clothing that ‘masks’ their body shape. It’s part of life. When I’m reading these camouflage studies, I think, ‘Well, yes, of course that may happen.’ It’s not specific to autism, I don’t think. I can see that in chronic psychiatric conditions and chronic medical conditions.
It’s maybe interesting to study, but I don’t see that as giving us some breakout understanding of mechanisms underlying the neuropsychology of autism. It’s more, for me, what’s happening down the road — the long-term consequences of autism and how people manage their autism in social adult life. If that is what it is, then let’s say it is that. And don’t say that camouflaging is a super-important domain of investigation, which it is not, unless you can define what about camouflaging is so unique to autism that it would be shedding a light or giving me a particular leverage to studying autism that I wouldn’t have otherwise. I don’t think there is any evidence that all this camouflaging investigation is novel in any conceptually substantive way.
No mask, no bus on first day of school for Layton boy with autism (KUTV article)
No mask, no bus on first day of school for Layton boy with autism
by Kyle Harvey
LAYTON, Utah (KUTV) — The Neil family in Layton was eager to go back to school — perhaps none more than second grader, Easton.
“He was excited for school, we took first day of school pictures on the porch,” said father, Scott.
But when the bus pulled up for Easton, there was a hard rule — no one boards without a mask.
“Easton’s never been able to wear a mask; he’s autistic and has some sensory issues,” Scott Neil said.
We’re not upset or angry at anybody. We just think that for kids like Easton there needs to be a little latitude and little bit of understanding.”
Mom, Rachelle, tried to negotiate. Easton can pull his shirt over his face — and it was a large bus with just a small number of special needs kids.
“They could’ve social distanced,” she said.
Eventually, the Neils relented and put Easton in the car to go to school — his spirit crushed.
“He was really disappointed, you could see a change as we made the decision,” Scott Neil said.
Eventually, the Neils relented and put Easton in the car to go to school — his spirit crushed. “He was really disappointed, you could see a change as we made the decision,” Scott Neil said. (Photo: KUTV)
Davis School District spokesperson Chris Williams said the governor’s mandate about masks in the classroom extends to bus rides.
The district has created a process for those seeking exemptions that they tried to promote in advance of the first day — communication the Neils say they did not receive.
Williams said the district is making careful documentation of those who cannot wear masks, as well as those considered to be at higher risk for the disease, for their own safety.
“In case someone in a school gets COVID-19, those are the first people we need to contact,” he said.
Even those like Easton in a special education classroom must fill out a form with a doctor’s note, which gets reviewed by a committee comprised of the district’s risk management director and school nurses.
The committee has received 58 requests as of Tuesday. Williams wasn’t aware how many requests have been approved.
The Neils’ request is in now and they will drive Easton to school until they receive a verdict.
The first day did end better than it began for the second grader. He managed a mask for at least some of the day and was all smiles leaving campus.
“He did great today,” Rachelle Neil said. “It just got started — it was a rough start.”
Human Gut Microbiota from Autism Spectrum Disorder Promote Behavioral Symptoms in Mice
Human Gut Microbiota from Autism Spectrum Disorder Promote Behavioral Symptoms in Mice
SUMMARY
Autism spectrum disorder (ASD) manifests as alterations in complex human behaviors including social
communication and stereotypies. In addition to genetic risks, the gut microbiome differs between typically developing (TD) and ASD individuals, though it remains unclear whether the microbiome contributes to symptoms. We transplanted gut microbiota from human donors with ASD or TD controls into germfree mice and reveal that colonization with ASD microbiota is sufficient to induce hallmark autistic behaviors. The brains of mice colonized with ASD microbiota display alternative splicing of ASD-relevant genes. Microbiome and metabolome profiles of mice harboring human microbiota predict that specific bacterial taxa and their metabolites modulate ASD behaviors. Indeed, treatment of an ASD mouse model with candidate microbial metabolites improves behavioral abnormalities and modulates neuronal excitability in the brain. We propose that the gut microbiota regulates behaviors in mice via production of neuroactive metabolites, suggesting that gut-brain connections contribute to the pathophysiology of ASD.
Monday, August 24, 2020
'We are failing our children:' Durham mother says her child with autism struggles with virtual learning amid COVID-19
'We are failing our children:' Durham mother says her child with autism struggles with virtual learning amid COVID-19
ABC11 spoke with Princess Pedew, a Durham mother with a child who has autism. Pedew said a week into the new school year, she is feeling stressed out, anxious and frustrated.
"We are failing our children. We're not helping them," Pedew said.
Pedew works from home and is a single mom to 12-year-old QJ.
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Between 8 a.m. and 3 p.m., QJ sits on Zoom calls with three special education teachers. But Pedew said she is struggling to do her own work because QJ won't stay focused.
"He's waving, 'Hi mommy. Come scratch my back. Oh, it's lunchtime. Can QJ ride bike? Or I want my iPad,'" Pedew said. "I'm not a special needs teacher. I have to run this household. I have to work. Technology issues, log-in issues, sites down. That triggers more anxiety or meltdowns for QJ."
Princess worries that QJ's social and academic development will regress under remote learning.
It's a common concern for parents with children who have autism to feel that in-person learning is preferred.
FULL CORONAVIRUS COVERAGE
According to the Autism Society of North Carolina, 1 in 57 children in the state has autism.
The group said it is important for parents to document their challenges and communicate those concerns to the school system.
"You have to take care of yourself and be calm so you can project that calm feeling for your child," said David Laxton, a spokesman for the Autism Society of NC.
Laxton said the organization is offering free webinars to help families who need help calming their child, or tips and guides on providing structure.
"Social narratives are basically stories that have words and pictures and for an individual with autism, it helps make things more understandable, makes it more concrete and relatable to them," Laxton said.
Durham Public Schools responded to Pedew and other parents with similar plights.
"We are working closely with our staff to ensure they have the supports and resources they need and encouraging Individualized Education Program teams to meet to plan and problem solve around individual student needs."
Pedew said she has communicated her concerns to her son's teachers.
She's considered hiring a tutor but learned that would cost her $1,400 a month.