Wednesday, September 26, 2018

Dear David Coon, Brian Gallant, Blaine Higgs, and Kris Austin. Please Work Together to Build NB Adult Autism Residential Care and Treatment





Dear David Coon, Brian Gallant, Blaine Higgs, and Kris Austin.

Please embrace the NB Autism Spectrum Village Proposal (McDonnell 2015) together and work as a united NB government to begin putting in place the adult residential care network so badly needed. In the attached picture my younger son Conor is happily washing windows at the Willie O'Ree Centre in Fredericton as he loves to do with the assistance of Jobs Unlimited. As I grow older & pass on, residential care & treatment as described in the NB Autism Village Proposal Satellite Model (McDonnell, 2015) will be required for Conor and autistic adults like him who suffer from severe autism, intellectual disability and seizures. Current US CDC figures estimate 1 in 59 persons on the autism spectrum. That would include approximately 44% who suffer from ID. I have forwarded to you, in some cases several times now, the McDonnell 2015 proposal. It is not intended as a final model. It is an excellent model to start working on now to address the needs of those adults with autism who will need permanent care and can not live alone, either completely independently or with assisted. Again please work as a united NB government to begin putting in place the adult residential care network so badly needed.

Respectfully, Conor's Dad

Monday, September 24, 2018

To NB Government September 25, 2018: Adult Autism Centre in Fredericton vs Psychiatric Hospital in Campbellton?



To NB Government September 25, 2018.

Congratulations on your victory.

Will your government start working TODAY to end the inhumane practice of banishing autistic adults to live their lives far from the vast majority of families and without expert autism supervision and care?

Adult Autism Centre in Fredericton vs Psychiatric Hospital in Campbellton

As the father of an adult son with severe autism, intellectual disability and seizures living in Fredericton I am not afraid of an autism centre as part of the Autism Village Network proposed to the Liberal government by Paul McDonnell in July, 2015. I am afraid your government will continue the inhumane practice of sending people with severe autism disorders like my son to the Regional Psychiatric Hospital in Campbellton on our Northern Border far from the vast majority of families and far from the autism expertise already developed in Fredericton (UNB-CEL) to provide services to persons with autism aged 2-5, autism trained school aides and consultations to age 19 (Stan Cassidy).
Why abandon our severely autistic adults to life far from home and community instead of building the Autism Spectrum Village Network proposed by Paul McDonnell in 2015 with autism specific group homes in facilities (in addition to assisted individual living already existing) and a centre of autism expertise in Fredericton to provide training and oversight for the homes and permanent residence and care for those most severely impacted by autism and related comorbid conditions of depression and epilepsy made more difficult by their autism disorders? See The New Brunswick Autism Spectrum Village - Satellite Model (Paul McDonnell, 2015)


Saturday, September 22, 2018



Dear NB Government September 25, 2018:

Please don't forget to invest in the 1 in 59 NBers with autism spectrum disorders. Please invest in the health and well being of persons with autism including those who die 9 years earlier than persons in the general population at the higher functioning end and 30 years earlier on the severe end of the spectrum.(Personal Tragedies, Public Crisis, Autistica UK). NB has chosen to send severely autistic NBers to a Psychiatric Hospital on our Northern Border far from the vast majority of families and far from the World Recognized autism expertise developed in Fredericton. The Autism Village Model Proposal was submitted to Government in 2015 and ignored. Please at least read these 2 paragraphs from the introduction: 

""It is therefore imperative that New Brunswick establishes an Autism Treatment and Residential Centre. The centre should be situated in Fredericton so that it is physically close to regional autism expertise at the UNB-CEL autism program and the Stan Cassidy Centre. The Centre would provide treatment for all autistic adults who are too old for treatment at the Stan Cassidy program and permanent residential care for the most severely autistic some of whom have been sent to the Spurwink Facility in the State of Maine and to the Restigouche Regional Psychiatric Hospital in Campbellton. Autism specific group homes around the province are required with autism trained staff and oversight from the Centre.
In this sense, the model proposed could be characterized as a “satellite” model in which the centre in Fredericton would be linked directly to a number of satellite homes around the province. Medical issues commonly associated with autism disorders including epilepsy and depression would also be treated in the context of persons suffering from autism and the extra challenges it presents to treating those common co-morbid conditions.""

Tuesday, September 18, 2018

The New Brunswick Autism Spectrum Village - Satellite Model (Paul McDonnell, 2015)







In September, 2010 Paul McDonnell, Professor Emeritus, Psychology, UNB) and a Clinical Psychologist who was actively involved with establishing NB's internationally recognized, evidence based, early autism intervention program was interviewed by CBC (Dan McHardie) and drew attention to autism needs in NB:


"Our greatest need at present is to develop services for adolescents and adults. What is needed is a range of residential and non-residential services and these services need to be staffed with behaviourally trained supervisors and therapists. In the past we have had the sad spectacle of individuals with autism being sent off to institutional settings such as the Campbellton psychiatric hospital, hospital wards, prisons, and even out of the country at enormous expense and without any gains to the individual, the family or the community.
We need an enhanced group home system throughout the province in which homes would be linked directly to a major centre that could provide ongoing training, leadership and supervision. That major centre could also provide services for those who are mildly affected as well as permanent residential care and treatment for the most severely affected. Such a secure centre would not be based on a traditional "hospital" model but should, itself, be integrated into the community in a dynamic manner, possibly as part of a private residential development.The focus must be on education, positive living experiences, and individualized curricula. The key to success is properly trained professionals and staff."

McDonnell elaborated on the needs identified in his 2010 statement in the 2015 NB Autism Spectrum Village - Satellite Model proposal which was presented to then Social Development Minister Cathy Rogers in July 2015.  Unfortunately, the proposal was not responded to or developed by the Gallant government but it remains the most cogent public discussion of adult autism needs in NB:


The New Brunswick Autism Spectrum Village     

It Takes a Village to Support Adults with Autism Spectrum Disorder

NEW BRUNSWICK SATELLITE MODEL FOR
ASD SERVICES FOR ADULTS

New Brunswick has made great gains in providing early intervention programmes for children with
autism spectrum disorder (ASD), a neurological disorder, and is currently developing a
comprehensive programme to train teachers and teacher assistants within the province to work in an effective manner with our students.  To date, no initiatives have addressed the needs of adults.
Once a student reaches the age of 21 years, there are no services, no supports, and the entire
burden of support and care falls upon parents and family.

It is therefore imperative that New Brunswick establishes an Autism Treatment and Residential
Centre.  The centre should be situated in Fredericton so that it is physically close to regional
autism expertise at the UNB-CEL autism program and the Stan Cassidy Centre.  The Centre would
provide treatment for all autistic adults who are too old for treatment at the Stan Cassidy program
and permanent residential care for the most severely autistic some of whom have been sent to the
Spurwink Facility in the State of Maine and to the Restigouche Regional Psychiatric Hospital in
Campbellton.  Autism specific group homes around the province are required with autism trained
staff and oversight from the Centre.  In this sense, the model proposed could be characterized as a
“satellite” model in which the centre in Fredericton would be linked directly to a number of
satellite homes around the province.  Medical issues commonly associated with autism disorders
including epilepsy and depression would also be treated in the context of persons suffering from
autism and the extra challenges it presents to treating those common co-morbid conditions.

The scope of the problem can be appreciated when one considers the fact that autism spectrum
disorder is the single largest disability across Canada. Current estimates of the number of
individuals diagnosed with autism spectrum disorder range from the recent estimate by the Center
for Disease Control in the USA of 1 per 68 persons1  to slightly more conservative estimates around 1/1602. This means that the incidence of autism spectrum disorders ranges from 4700 to 11,100 individuals in New Brunswick.  It also means that services are needed for roughly 3,300 to 7900 are in the age range between 22 years and 75 years.

1CDC, Prevalence of Autism Spectrum Disorder Among Children Aged 8 Years — United States, 2010,
March 28, 2014 / 63;1-21
2Elsabbagh M, Divan G, Yun-Joo Koh YJ et al.. Global prevalence of autism and other pervasive
developmental
tism Res. 2012;5(3):160–79

One can also understand the scope of this problem by looking at the following list of challenges
that are faced by parents of an adult son or daughter with autism spectrum disorder. Because the
range of disability within ASD is so broad, we present a wide range of very typical challenges that
families face.

• Cessation of Educational Opportunities – Once a student leaves the school environment in which they have supported learning opportunities, there are few if any places a student can go to advance their learning. Most of these students could not avail themselves of post secondary learning opportunities, as they require a significant amount of scaffolding to enable them to succeed.  At age 21 most typical students have a variety of skills and are reasonably literate.  Even they needongoing training and many even most do some form of additional education or job training.  This is not possible for the majority of the young people with ASD.

• Unemployment – The rate of unemployment among all levels of persons on the spectrum is close to 100%.  Some do manage to find limited employment opportunities through the services of centres such as Fredericton’s Jobs Unlimited.  However, the majority of persons on the spectrum are not successful.  It is believed that people with Asperger’s (the most functional of persons on the
spectrum) have a 75-85 percent unemployment rate.  Autism Speaks estimated that 85 percent of
adults with autism in the United States are currently unemployed or underemployed. Among young
adults between 21 and 26 years old, only 50 percent have ever had a paid job outside of their
households. This means that parents may have to support their son or daughter for most of their
lives.   There are some government supports such as the disability tax credit and the disability
retirement savings plan but we know that not all persons with a diagnosed condition will qualify
for support and even if they did, the support is minimal in comparison to a living wage.  The 40%
to 50% of persons with ASD who also have intellectual limitations are most likely to remain totally
unemployed although a few may find very limited opportunities through non profit community
agencies.  The half of the ASD population with relatively higher intellectual skills will also have
very limited employment usually because of social challenges.

 Regression of skills – All professionals who work with persons with ASD have seen the loss of
skills that results from a lack of stimulation that comes from learning in functional social
contexts.   In fact, several years ago, UCLA Psychologist, Ivar Lovaas, did a study in which
individuals who had increased their IQ scores in a three-year treatment programme, lost almost all
of the   3 functional skills (e.g., language skills, self-help skills, and cognitive skills) they had learned after three more years of no educational programming. We experience these kinds of regression frequently when an individual passes from a relatively stimulating learning environment to living at the family home without a planned curriculum.  Early intervention is the best way to provide long lasting learning but not all individuals will succeed sufficiently to be immune to regression of skills once formal training stops.

• Lack of respite Care – There are very few services available to provide respite to parents or
guardians of individuals on the spectrum.  In addition, even fewer services exist (if any) that
have staff that re appropriately trained.  This is a crucial service needed by almost all families
affected. Parents with adults on the spectrum can be in very desperate need for respite care. In
some cases, the individual with ASD will require care 24 hours a day and 7 days a week. Depending on a family ‘s circumstances, this may mean that either a father or a mother will need to be at home with the child at all times. In other circumstances, the needs may be different. An individual may not require as intense care but may present with many challenging behaviours and the parents may need short-term breaks.

• Lack of opportunity for recreation – Recreation has been shown to be an effective treatment for
many of the challenging behaviors we encounter with individuals on the spectrum.  In addition,
there is research to show that individuals with developmental disabilities tend to be less fit in
general and tend to have more illnesses.  In large measure this situation arises from lack of
suitable recreational and vocational services and far too much unstructured, idle, time.

• Restricted Social Lives – Individuals with a diagnosis are by definition less interested in
social interactions and more likely to seek solitary pursuits. The major disability in autism
spectrum disorder is a social disability.  Left on their own this pattern of behaviour intensifies
and we know that increasing isolation from healthy social interactions can lead to major
challenges.  With supports in employment and in other kinds of social interactions, persons with
ASD can enjoy and benefit from social contacts.

• Mental Illness – The research is clear.  Individuals with ASD are more likely to be affected with
co-morbid forms of mental illness such as depression.  The factors that contribute to the high
percentage of mental illness are social isolation, lack of social supports in meaningful
activities, lack of education, and lack of meaningful work and recreational activity.

• Behavioural Challenges – We need to point out that access to regular society (employment,
residential living, recreation, etc) requires a minimum of compliance and an absence of aggressive
behaviours.  Many individuals with more severe forms of ASD have some level of behavioural
challenge.   These behaviours are almost always caused by poor communication skills and inadvertent reinforcement of problem behaviours by caretakers who do not have sufficient training to handle these kinds of behaviours.

Summary of the Problem:  It is clear from the description above that families with an adult child
can be faced with overwhelming challenges and stress related to providing the very best services
they can to their son or daughter.

Solutions:  The needs of individuals and families and the scope of the problem described above canbe mitigated or overcome by our proposed centre.

Our proposed centre would not be a single building as such but rather a satellite network of homes, apartment-styled buildings and other facilities integrated as much as possible within residential neighborhoods. The design is explained in more detail below.  Our approach will be innovative and uniquely designed to suit families in the New Brunswick situation.  The key principles for this proposed village are that all programmes and services are as much as possible evidenced-based, that the centre be dynamic in the sense ofbeing flexible enough to meet diverse needs.  It also needs to have a meaningful connection to the NB community and that includes accessibility of services and easy accessibility for families to maintain a connection to the clients in the centre (or centres).

Comparative Analysis: There are some existing facilities that serve adolescents and adults across
Canada, in the USA and in Europe.  For example, in the Toronto region there is a group called
Kerry’s Place that offers evidenced based services for adults.  New Jersey has some outstanding
private facilities and in particular the model developed at Princeton Child Development Centre is
called Mountain View.  There are no services in New Brunswick that are remotely comparable to these  services.  Currently, when we have an adult with ASD that is unmanageable in a home or in existing special care homes, they are sent to a facility in Maine called Spurwink . The facility in Maine is a fine service but it costs the taxpayers thousands of dollars and is far away for the client’s family.

THE NEW BRUNSWICK “SATELLITE” MODEL: We have proposed a
"satellite" model that would provide residential and other adult services in several regions around
NB but also would have a home base located in Fredericton.  In general, the best way to provide
the physical spaces and to find appropriate staff is to make use of existing facilities but offer
upgrading and training.  There are a number of options available such as providing training and
other upgrades to selected group homes in the province. In addition, one can look at working with
selected developers to create some residential complexes for both typical individuals and persons
with special needs of various kinds.

Possibly, an autism centre can be created at UNB or in association with the Stan Cassidy Centre.  

The details of the physical spaces need to be planned carefully but the guiding principal is to  provide dynamic services for all adults involved either as residents or as day users of the facilities.  As well, we want facilities that serve the diverse needs of the adult population.

SERVICES OFFERED BY THE NEW BRUNSWICK MODEL:

In a future draft of this proposal we will provide a detailed description of the kinds of services
that we envisage.  These will include at a minimum residential services, sheltered work and
vocational services, ongoing training in life skills and personal care, treatment of behavior
problems, recreational skill development, respite care for families, training of families in skills
needed to maintain their son or daughter in a home setting, and social skill development. There are
clearly levels of support needed and the following is a list of some of the more obvious levels.
Over the course of their lives, individuals may move from level to another.

•                         Independent living with assistance. Some adults with ASD are able to live
on their own. Others can live in their own home or apartment if they get help dealing with major
issues, such as managing personal finances, obtaining necessary health care, and interacting with
government or social service agencies. Family members, professional agencies, or other types of
providers can offer this assistance.
•                         Living at home. Government funds are needed for families who choose to
have their adult child with ASD live at home. These programs include some form of pension,
disability tax credits, and support for extra services. However, we know that there is a point at
which family may no longer be able to provide support at home and other options need to be
available. Training for parents needs to be available.
•                         Other home alternatives. Some families open their homes to provide
long-term care to adults with disabilities who are not related to them. A home setting such as this
type needs to provide some form of skill development such as teaching self-care and housekeeping
skills and arranging and getting involved in leisure activities.


The New Brunswick Autism Spectrum Village    

•                         Supervised group living. People with disabilities often live in group
homes or apartments staffed by professionals who help with basic needs. These needs often include meal preparation, housekeeping, and personal care. People who are more independent may be able to live in a home or apartment where the staff only visits a few times a week. Such residents generally prepare their own meals, go to work, and conduct other daily activities on their own.Once again however, training of staff is a key to success.

Long-term care facilities. This alternative must be available for those with ASD who need
intensive, one-on-one constant treatment and supervision. While this group is a minority, they present the biggest challenge for their families who, at present, have no means to provide the services required.

THE SATELLITE MODEL: There are good reasons to have the base for our satellite model located in Fredericton.  There are already a number of sources of autism expertise in this location.  For
example, a satellite model based in Fredericton would have would have a permanent connection to the University (Psychology, Education, Nursing) and the autism team at the Stan Cassidy Centre as well as other local health professionals.  The base would also be the home for one of the most
 important functions of our model and that is the training of staff and setting forward operational procedures and protocols.  Since 2003, the University of New Brunswick (especially the College of Extended Learning) has been a key in the development of training for staff for preschool and school-aged children to date. It has also been involved in building capacity for Applied Behavior Analysis in other jurisdictions such as Saskatchewan and has developed new programs for undergraduates at UNB as well as an open access programme.   Thus, we envisage a Fredericton-based centre that offers training and support and then a series of satellite facilities around the province that follow service protocols developed by team at the main centre.

THE IMPORTANCE OF EVIDENCE-BASED SERVICES:  The key to success
in providing excellent services to adults and adolescents is that the methods employed are groundedin a body of research evidence.  The philosophy of the proposed model is one that embraces growthfor all of its clients at all times.  In no way are the centres to be construed as facilities forwarehousing clients – quite the opposite. The philosophy is to keep residents and other clientsengaged in meaningful social, work, and recreational activities.   Keeping all clients learning andactively involved in a range of activities is crucial.  All services delivered need to be held up
to the rigorous standards of evidence.

THE IMPORTANCE OF ETHICALLY-BASED SERVICES:  The second key
ingredient is that the services must have the highest level of ethics and as a

The New Brunswick Autism Spectrum Village   result we may base our model's ethical treatment on
a modification of other relevant ethics codes such as the BACB Guidelines for ResponsibleConduct
or the Canadian Psychologist Association.  In the CPA code there are four basic tenets or major principles that are fairly typical of most codes.  These include:

1) Respect for the Dignity of Persons  
2) Responsible Caring
3) Integrity on Relationships  
4) Responsibility to Society

Ethically–based services will not only meet with public approval, they will be more effective.
Clearly, one of the ethical principles is that we offer clients only those interventions that are
scientifically demonstrated to work. Thus, interventions are less likely to cause problems and
clients are more likely tothrive and develop more skills and adapt more to typical life.

Sunday, September 2, 2018

One Year Since Conor's Last Grand Mal Seizure (As Far As We Know)

It is now, as far as we know,  1 year since Conor suffered his last grand mal (tonic-clonic) seizure;  loss of consciousness, falling, violent convulsions.  It is possible he could have had a grand mal seizure while sleeping and we did not know.  I sleep on a living room couch near Conor's room so I can hear any noises but it is not a full proof system. It is also possible, although I am just a layperson, that he has had seizure related headaches of the sudden onset types resulting in Conor banging his head that led me to seek medical advice over whether he was having seizures. Our family doctor and the neurologist to whom he referred Conor agreed based on the pictures I was taking at the time with a fast, athletic setting on my camera, that it could have been epilepsy related. Testing and full grand mal seizures later left any doubt. It has though been a grand mal free year as far as we know and I will that that! ... For families with autistic children particularly those with autism and intellectual disability I have re-posted my last years commentary on autism and epilepsy.  


A dad's suggestion: Families should be aware that their autistic children could have a significant chance of seizure activities at some point and ask their doctors about that possibility.  


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Conor Suffers Another Seizure 6:05 a.m. September 2, 2017



Conor's latest tonic clonic (grand mal) seizure  took place at 6:05 a.m. this morning just after I placed his breakfast in front of him. .  I was expecting a grand mal seizure soon as it had been roughly 3 1/2 months since his last seizure in mid May and they have tended to happen 3 to 4 months apart.  This seizure happened while Conor was sitting on the couch, watching a movie and starting to eat his breakfast.  He started shaking violently and slid down off the couch.  I held him to keep his head from striking the floor and slid some soft blankets under his head.  He lay on his side and some of the food he had started to eat came out of his mouth.  Eventually the violent shaking subsided and he was able to speak and, with some help, move.  We went to the market for 2 of Dan's sausages and everything seems pretty noramal. 

Anyone with a  child with autism, especially if their child is developmentally delayed,  (persons with autism AND intellectual disability are much more likely to suffer from epilepsy/seizures) would be wise to consult their medical advisers.  Epileptic seizures are very common among persons with autism and they can have serious, dangerous, even deadly consequences.  The UK Autistica report, Personal tragedies, public crisis, based on a large high quality Swedish study found that persons with autism tend to die between 16 to 30 years prematurely with the high numbers found among those with autism, intellectual disability and autism.  It is also worthwhile to note that the Autistic report indicates that in cases of people with autism seizures do not appear until their teenage years unlike in the general population when it is likely to show up in the child's first years.  In Conor's case his seizures appeared in his teenage years.

Each grand mal seizure is a reminder of my son's scary future prospects. With autism, intellectual disability and epilepsy he is at serious risk of decades early premature mortality.  For now though he is with us and I am relieved and happy that it happened again while I was just feet away.

Premature Mortality In Autism and Intellectual Disability - Epilepsy



"Between 20% and 40% of autistic people also have epilepsy and this rate increases steadily with age – in contrast to a one percent prevalence rate in the general  population.1 0 In the typical population, the risk of epilepsy is greatest in a child’s first year, decreasing in risk through childhood, then remaining stable and not increasing again until old age. 11,12,13 In the majority of autistic people who develop epilepsy, their seizures do not appear until their teenage years, much later than average.5,14 This suggests that the underlying triggers of epilepsy may be different in autism. Autistic adults who also have a learning disability have been found to be almost 40 times more likely to die from a neurological disorder relative to the general population –with the leading cause being epilepsy.3"

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Ground-breaking new research now confirms the true scale of the mortality crisis in autism: autistic people die on average 16 years earlier than the general population. For those with autism and learning disabilities, the outlook is even more appalling, with this group dying more than 30 years before their time.