The Dragon’s Nest

For now, I’m going to skip ahead a little of Jared’s infancy.

It will be necessary to include that portion in my book, but it is safe to say that over the next few years, our world revolved around the quirks and needs of Jared’s schedule.

The needs were excessive; what he ate, the afternoon nap involved changing him into pajamas, his favorite books, and Teddy Ruxpin (a mouth-moving mechanical bear – SO CREEPY!!); afternoons watching Sesame Street, and an every-increasing library of tapes from Disney’s complete set – to the National Geographic 4 video-tape set on dinosaurs.  From all this, cross-legged, rocking to and fro, came his form of language.  He memorized names for all known dinosaurs, as well as the full dialogue (sound effects included) of every Disney movie.  If any of his Disney recitations were interrupted, he would look past you – and start again at the beginning.  He was capable of speech, but lacked the desire or ability for pre-verbal or interactive speech.

I had been exposed to children and infants all my life.  My fear for my beautiful son lay curled and sleeping deep in my gut.  Like the dragons in Jared’s fantasies, it would stay until a behavior or someone would comment on his lack of communication and I could feel the dragon shift and flare, making it hard to swallow or breathe; or I would mumble “he’s just shy.”

In Howard County, in Maryland there is a well established screening process called “Child Find.”  However, the child in question needed to be referred by the child’s Pediatrician.  With this in mind, Mayer and I made an appointment with Jared’s doctor.  Dr. S was, and still is a decent man and a very good doctor – but diagnosing Autism was like “hunting for Sasquatch” back in 1987. ; no one believed in it, and those who did – feared it!

The appointment went fairly well.  We verbalized our concerns.  In response, to check Jared’s knowledge base, Dr. S. Pulled out a book of dinosaurs.  Every neuron in  my brain was screaming “Oh Sh*t!!”  He pointed at one and Jared replied “Pachycepahalosaurus;” next “Parasauralophus” – “SUPER,” I thought!  Next, came “Styracosaurus.”   Dr. S. corrected him, “no, that’s a Triceratops.”  Jared looked puzzled, repeated his answer so Dr. S. looked at the book, chuckled and conceded that Jared was right, and he concluded, and shared – that I was an anxious first time mother. To add insult to injury, he said Jared was “very intellingent” and thought maybe I should “speak to someone.”

To Mayer’s credit, he was just trying to keep me calm while we considered other options.  Also, Jared always held it together long enough for a “well child checkup.”  I felt lost and confused.  Mayer could tell I was on the edge and tried to calm me, saying we would go to see someone else.  At that moment in time, I decided I didn’t want to wait.  I wanted someone to feel the same fear that I was feeling. As I strapped Jared into his car seat, his fingers came up before his eyes, playing a symphony accompanied by his atonal “Ahwebegabeyo” song.

In simple terms, I “lost my NUT!!”

I pulled Jared out of his car seat, and headed for the third floor of the Medical Building, with Mayer close behind, trying to get me to slow down.  But there was no “slowing me down” at that point.  With Jared on my hip, I put him on the counter and demanded to see Dr. S. – now! I think by that point, the entire 3rd floor could hear me.

The secretary said the doctor was in another Exam Room, and I replied he had one minute and then I was going to start opening every door until I (found) him.”  By this time the Dragon was in full “hunt mode” and I had no desire to pacify it.  Actually, I wanted to feed it and let it take flight.

To quote my grandmother, I “had my FULL IRISH UP!”  Finally, Dr. S. appeared.  I pointed to Jared, and asked Dr. S. whether he considered a child who stared off into space, and recited the same skits (over and over) to be “normal.”  He tried to speak to Jared, and he asked him to stop  without success.  He brought back the dinosaur book, but Jared ignored it, as well.  For the first time, Dr. S. looked confused and he was genuinely concerned. At this point, I told him all we wanted was a  referral to Child Find.  I also told him that if Jared’s results showed that he was “normal,” that I would get professional help for my problems. I had to reassure myself that we Moms and Dads are with our children 24/7; while doctor only sees him for 15 minutes, once every 2 months.

As we left, Mayer picked Jared up to hold and to carry him.  The sound of “Ahwebegabeyo” began to follow me to the car.  We both knew I couldn’t touch him without him feeling my feelings and at times like this, Jared was more comfortable in Mayer’s arms. As Dragons would become a beautiful part of his special world, he couldn’t handle the one inhabiting me.  Mayer carried him to his car seat, where he could resume his finger play and humming.  I was very concerned how the interchange may have affected him; but he was humming at his fingers and smiling at “the world beyond.”

I sat in the car rocking and crying with my Dragon, both of us knowing that the steps to come would be brutal, but every day was more important than the last.

There would never be a day without Jared’ challenges being and ongoing fight.

There would never be a day of “completely letting go.”

(C) 2016, Sheila P. Max

Holding your World in Orbit – Jared’s View on Autism

Displayed here is a triad of pictures portraying a Person on the Autism Spectrum and how well they function in certain situations, in the form of a solar system.  The Sun represents the Autistic Person themselves.  The planets symbolize the aspects of their everyday life which make them whole.  Finally, their orbits signify how things go, in accordance to the person and their rituals, and such.

Serenity - all Autism Planets are aligned in Orbit
Serenity: All the planets are moving around the glowing sun; all is in order

Serenity:  The planets are moving about in their orbits the way they’re supposed to be, and the sun is glowing bright with contentment.  All is in order.

Disturbance: A mysterious giant hand appears, touches the sun, making it dim, and planets cease orbital motion in unfavorable halt
Disturbance: A mysterious hand touches the Sun, making it dim and bringing the planets to an unfavorable halt

Disturbance:  A mysterious hand appears and touches the sun, making it dim from perturbation, and causing the planets to cease their orbital motion.  All has been brought to an unfavorable halt.

Destruction: The hand plucks Sun from its seat; it is extinguished; precious planets are ruined; all is ruined
Destruction: The hand plucks out the Sun, extinguishing it and destroying the planets; all is ruined

Destruction:  The hand plucks the Sun from its seat in the center of its system.  It is now extinguished from utter tumult and its precious planets have all exploded.  All is ruined.

We autistic people need to remain in our spaces of comfort, order and safety, with all our personal rituals therein, if we are to function properly.

Any imposition, and everything falls apart with us.   Our soundness of mind becomes so deficient that we are drained of whatever manner of productivity that makes us grand.

But, if we’re allowed to be where we need to be, do what we need to do (and how we need to do it), then one may find it rewarding and worth the effort.

(c) 2016 Jared Stephen Max

Down the Rabbit Hole

Photos of Jared and Family - for Down the Rabbit Hole
Down the Rabbit Hole Photos

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IN THE BEGINNING…some of the world’s greatest stories in history have begun with these evocative words.  I’m not comparing this story to the greatness of the Bible, but showing the importance of understanding that a journey into the world of Autism must have a beginning to fully grasp the enormity it will bring to all your days, and all your years of constant involvement.

Often it may begin even before your child is born. As humans we possess the blessing and curse of imagination.  Every woman will tell you that as soon as she receives the news that she is pregnant, that tiny little speck will be dreamt of, and prayed for. It becomes fully realized person with an imagined eye color, hair color, talents in music, science, art and undoubtedly, a genius.  This is one of the reasons that a miscarriage is so gut wrenching for women; because in their minds, the child is real.

In understanding this, you can take your first step into the adventure in Autism.  Let’s begin with my quest to understanding at a time when Autism was completely misunderstood.  At that time, the medical community had only jut recently moved away from the “Frigid Mother” theory.

When introducing Jared to people, with the caveat that he is Autistic, I often hear the comment that he must be “highly functional” or “just Asperger’s!”  I’d be lying if I said I don’t get a bit irritated.  It seems now that everyone has someone in their family or in their social circle that has been diagnosed on the Autism Spectrum and, ergo, everyone is an expert.

The adult you see now is the product, for lack of a better word, of 31 years of hard emotionally exhausting work. When Jared was finally diagnosed, he was given the label of “Autistic,” pure and simple.  But maybe that is easier to understand if I take this explanation back to the beginning.

Mayer and I were married in November of 1984.  When I found out was pregnant, I was overjoyed.  Early on, it was an uneventful pregnancy.  Jared was due in mid-August.  It was a horrendously hot summer, so I attributed my overall swelling to the heat.  My doctors had me go 3 weeks late- even though my blood pressure was dangerously high.  To spare our audience the gruesome details, I will say only that Jared was in distress, lacking oxygen and damaging his forehead for 3 days before being delivered by Caesarean Section (C Section).  His forehead was bruised from his nose to the top of his head. Knowing now of the presence of some peri-autistic traits in members of our family, yes I think he would be quirky to a degree.  I think, however, that the insults to his brain increased the severity of his Autism.

Jared was a difficult baby. He did not cry; he screamed.  In retrospect, I can only imagine how horrible his headache must have been. He could not be comforted by being held or nursed; any physical contact caused him to arch his body away and cry harder.  He preferred to be in his infant seat, swaddled tightly in a dimly-lit room. Ultimately, he came to tolerate being held long enough to be fed from a bottle with pumped breast milk.  As a nurse, i felt helpless and that I should be able to “fix” whatever was going on.  I was lost.

Jared cried incessantly. Nothing helped.  There were times when I would put him safely in his bassinet, go to the next room, set a timer for 15 minutes, and then go into the shower to cry.

At about 3-4 months of age, some of the screaming stopped. I prayed we had turned some kind of a corner and that we would have the happy situation we had hoped for.  I have some beautiful pictures of Jared, with his beautiful green eyes and a quizzical smile.  I realize, now, that he was never focused on me, but on some spot past me that only he could see.

As when he was an infant, he was happiest lying on his back – watching a mobile, lying in his stroller – watching leaves move, but if a face intruded he would look puzzled and he would begin to cry.

In finishing this chapter, I would say simply that i spent lot of time puzzled and crying myself to sleep.  I knew that something was wrong, but I didn’t have the first clue as to what it might be.

Autism wasn’t a term we had ever heard.  That would change very soon and then nothing would ever be the same.

Sheila Max, Mom, RN,

(c) Ais4Autism 2016

Jared’s Journey: A Series of Fits and Starts – and Fits Again

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Japan Tsunami Disaster Preparedness Summit and Research Travels throughout Japan ;

Image of hand cupping "perfect flower" , representing perfection of family and mind
Autism for Families / Ohana

Jared develops the logo of Ohana (to be supported by family, medical, and communities); he speaks to Autism and Traumatic Brain Injury / PTSD at US-Japan Exchanges and Medical Conferences in Washington, DC, and Hawai’i ;

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Jared’s induction into Omicron Delta Kappa, a University Service and Leadership Honor Society, for his efforts for Persons with Autism, Traumatic Brain Injury (TBI) / Post Traumatic Stress (PTSD); and Tsunami and Disaster Risk Reduction in Japan, the US, and worldwide  ;

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Jared captures his journey through Autism, and his attempts to help others;

(  www.maxfantasy.weebly.com/about )

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Jared reaches out to Sammie – the next Generation on the Autism Spectrum; Jared  sensed Sammie’s need to be cuddled; this contact is very difficult for Jared’s Sensory Defensiveness. For Jared, a handshake is often a “bridge to far!  ” Sammie reaches out- and Jared connects and comforts.”  These guys make the day for 2 Happy Dads!

Jared’s 31st Birthday: An Update
Jared has taken on challenges – and used his gifts, his journey, and insights from the worlds of challenges – to help provide hope to so many others.

Jared’s Journey: “A Series of Fits and Starts – and Fits Again! “

Until the age of 5, Jared’s world was self-contained; He lived through the movies, images, dinosaurs, Disney, and the unique visions and animations created by his “Mind”s Eye.”.

Mom ( Sheila ) said “..we need to find a way to ‘connect’!”

His first words – to us – were directed to his Baby Brother, Ryan.
*** His Mom, Sheila and I were thrilled beyond words; no guarantees, but we have embarked with Jared, and his brothers Ryan and Nathan, to connect with the world – and with each other – as a Family.

For years, we’ve connected to Jared through (his) Animations, movies, dialogue.

As an adult he still communicates visions through his Art and imagination.

Jared has also reached out to connect the worlds of Autism; Veterans and Persons with Traumatic Brain Injury (TBI) and PTSD; and Cognitive and Physical Disabilities to medical experts, technology and reading Consortia, and advocates – to develop shared abilities, shared Family dreams and our common humanity.

At a U.S., Japan, VA Veterans Health medical Best Practices Conference, Jared spoke to the Medical and Research and Government and Non-Profit Panelists.

** Jared stated: “All of us bear our own flaws; each of us also bear our own gifts; all we ask is is that you allow us to join you and to share our gifts; That’s all I have to say.”
**

Jared spoke of inclusion and dignity for: Persons with Autism; Veterans with TBI/PTSD; and for all Disabilities.
The physicians, Neurologists, and scientists said – that Jared’s words impacted them more than all other lessons shared.

He has spoken with gentle (but strong) words of hope; of the need for: Gaman shi Maisho (Japanese: “to Soldier on..despite trials and tribulations”).

Jared has braved Sensory Overload and overwhelming Conferences – to share these gifts of insight and dreams for many Families.

These included National and International Conferences for:
Persons with Autism;
Veterans with Traumatic Brain Injury and Post Traumatic Stress (PTSD );
Persons with Disabilities for Survival of Tsunami and Disasters – both across the U.S. And Japan.

Jared has spoken at, and contributed to, Medical and Disaster Preparedness Conferences with magnificent physicians, researchers, and worldwide champions from :
– The Defense Veterans Brain Injury Center;
– The Japan Autism Society;
– The U.S. VA/Veterans Health Affairs;
– The Japan National Rehabilitation Center for Disabilities ( NRCD), Tokyo ;
– The University of Louisville Kentucky Autism Training Center;
– The DAISY Worldwide Consortium for Disabilities Libraries and Reading;
and
The MindKnit Research Center, Non-Profit.

** It has been my responsibility, my purpose – and my honor and privilege to help fight for Jared’s “Right to Rise Up” – through 50-54 adversarial Education Department hearings. Mom and I have fought to design and build a continuously planned, and fine-tuned education, with a critical connection to the world and to the supportive people embracing him.

I’ve been privileged to use my Neuro-Sensory mapping research background and Autism to strive shoulder-to-shoulder – alongside his Mom (Sheila) who brought her: RN in nursing, her empathic link with Jared, and her( vital ) human connection and communications, and social skills insights and training gifts. We have also worked “hand-in-glove” with supportive members of his School Disabilities Teams.

We have stood up against Administrators who said “…a “C Level Education is all we owe him!” This devaluation and depreciation of Jared was narrow and small; and it came from (a very few) small minds – who would (settle) to see him “sit on the sidelines of school, work, Family and Life!”

Jared, and his brothers Ryan, and Nathan, have always supported each other as “…one mind, one heart, and one pulse!”

This Brother’s Ryan and Nathan; and Mom and Dad Mentor Team stood behind him, when needed for advice.
Jared evinced the grit and determination to balance the sensory overload; and the indecipherable fog of interpretation and innuendo of Spanish and Art Appreciation; as he devoured computer animation, graphics, and Art expression classes – which “fit his world.”
Jared persevered in his 7 1/2 year drive to earn his Associates and his Bachelors Degree in Visual Arts and Computer Animation. He was also inducted into the Omicron Delta Kappa Leadership and Service Honor Society – for his contributions to Persons with Autism; Veterans and Persons with TBI and PTSD; and to Tsunami and Disaster Warning for Disabilities, and for all Persons.

**Not bad for the Kid…who was treated as the “Odd Man Out” – in Elementary School.
He has endeavored to help “heal the world” ( Tikkun Olam ) – for Persons with Disabilities and for us all.

Our hearts stay warm, knowing that these Brothers will be there for one another – for Life.

**They are. One and All, our most precious gifts and Treasure.

Jared, 31 years ago you came into our Lives.
You have enriched our Family, and we Love you Forever!

Happy Birthday Jared,
Love, Dad, Mom, Ryan, and Nathan

Jared’s Journey through Autism, Japan, and Tsunami

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( Photo/Woodblock Credit: Geat Wave of Kanagawa, Hokusai )

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( Image/Narrative Credit: Jared Max, 2016  (c) )

Jared overcame difficult travel to Japan – to aid efforts with our magnificent hosts and partners in Japan, including:

  • the  Japan National Rehabilitation Center for Disabilities (NRCD), World Health Organization Cooperating Center;
  • the Japan Autism Society;
  • many other Japan (and US) Universities Partners and Hosts in Kobe, Yokohama, and Tokyo.

These researchers and Societies, and persons from Japan, the US, the World Wide Web Consortium among others – came together to help Persons with Autism, Schizophrenia, and Cognitive Disabilities – to understand, train, and preserve lives during Tsunami and Disasters (Bosai Keikaku ) ]

For the view on this Tsunami and Disaster Preparedness and Resilience work from Jared’s vantage point:

[  See:  www.maxfantasy.weebly.com/about ]

Our magnificent hosts, partners, and worldwide organizers included:  Mr. Hiroshi Kawamura, Dr. Yayoi Kitamura, Dr. Reiko Fukatsu, Director, Research NRCD; Dr. Yasoichi Nakajima, Director-General, Japan NRCD; and the Japan National Rehabilitation Center for Disabilities, World Health Organization Cooperating Center; the Japan Autism Society

** Please take a moment to view the “World of Autism’s Wonderment” –  from Jared’s: Mind, imagination, heart, and hands – into his Art and Animation.

[ www.Maxfantasy.weebly.com ]

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Happy 31st Birthday Jared,
Love, Dad, Mom, Ryan, and Nathan

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It occurred to me recently that our recurring picture of the hand and flower may not be self explanatory as it is to our family, so I will try to convey its importance as best I can. Much of its importance has evolved in retrospect, so that is where I’ll begin.

My husband ,Mayer spent the first 17 years of his life on Okinawa, Japan and although he is not Asian by decent, he has a deep connectedness formed by those early years. To the Japanese, the blossom of a cherry tree or Sakura is the Very personification of perfection.

My home in Massachusetts was where my love of autumn and apples began. To this day, as I make my own applesauce, it always takes me back to my Aunt Edna’s kitchen in harvest season.

Fast forward to when my sons were 9,6 and 3. They had each gotten a tiny little apple tree sapling, no bigger than a stick with a few roots attached. All three were planted. But early on it became apparent that the two trees assigned to my younger two sons were too close to the house and not doing so well. Jared made it very clear that no one was going to touch his tree. Over the following years the Jared tree was deluged by snow,and knocked over in a severe storm which required supports and careful replanting. But like Jared, it continued to grow, two steps forward and one step back.

Although, to be fair, it is a little catty wampum, it began to bloom and bloom furiously when Jared was about 14 years old. Each year, Jared would watch his tree grow and bloom as we watched him grow and bloom as well.

As as a family we have had the opportunity to share our family’s various talents with Japanese centers for children and adults with learning disabilities including autism. We needed a logo, a touchstone for our endeavors. By this time, the little tree that could had come to dominate our front yard, shading Jared’s room in the summer, delighting him with blossoms in the spring and dropping apples all summer and autumn long. One spring evening Jared was showing us how beautiful the tree was. He cupped a blossom in his beautiful artist’s hand and a star was born. It was the perfect blend. Apple rather than cherry blossom. Similar but unique, held by the loving hand that had believed in it for so long. An image that touches my heart, our hearts whenever we see it. Embodying so much of our family’s journey.

Sheila Max R.N. (Mom)

In the Beginning

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(8/26/2016)

This is an introduction; I hope you will follow along as we expand our blog, and our story.  We will also begin to offer classes as time goes on; perhaps this may offer a lesson or idea which will resonate with your child, your Family, your friends, or with you – as a Person on the Autism Spectrum

It’s never as easy as one might think to remember when the whirling dervish that is Autism wasn’t a part of our lives; but I guess there was a time when it wasn’t.  I’m aware that this blog will require me to look down the long corridors of my memory for all those chapters, both good and bad.  Hopefully, these memories will resonate with other families and friends dealing with Autism in it’s many incarnations. At the very least, I hope they will help others to know that they aren’t alone or misunderstood.

From a young age, I grew up in a small New England town, and I was babysitting children of all ages, infants included.  I was exposed to the medical profession from a very young age, due to my father’s sever heart condition, so it made sense to go into nursing school back when nurses were required to carefully observe their patients. From there, I headed into my adulthood, to start my life.

I am grateful that my early life prepared me for what was to come.

I’m sort of glad that i began my journey when i was young and adaptable. I’m grateful my husband was an equal participant in the many battles for our son, Jared’s, well-being.

I believe this kind of trauma or challenge can make or break a marriage.  Luckily, our challenge made us stronger and taught us lessons that we never knew we needed to learn.

We look forward as we embark on this journey to reach out and help other Families, friends, and Persons on the Autism Spectrum

Respectfully, Sheila Max, RN, Ais4Autism.com

(c) Ais4Autism 2016

Sheila_Autism is Elephant in Room_Updated

( 8/15/2016) ( Sheila Max; Co-Founder Ais4 Autism; RN; 31 Year Autism Veteran ) Autism….there is the elephant in the room. A word that strikes fear in the heart of any parent. We first heard that word in 1987 when our eldest son was diagnosed. A year when autism was considered a rare occurrence. There was no information available, no support groups, just a yawning chasm of grief and confusion. We were alone and scared. All we had was burning drive to find help and answers.

For almost 30 years we have forged our own path and this site is our way to share the many lessons we have learned on the way. We hope some of our experiences will be useful to others at any stage of their journey as well.

Hope is a wonderful thing’ and there is always hope for improvement in your child’s potential regardless of their challenges.

We don’t pretend to have all the answers. But living with autism for 365 days of the year for almost 31 years now, we most definitely have some of them.

This site is just beginning and we hope you will follow as we begin to share our story and look forward to engaging with others as well.

(C) 2016 Ais4Autism

Mayer Motorcycle Crash_Renewal Recovery and Return to Autism Priorities

Mayer motorcycle trip to New York, standing with motorcycle
Mayer Motorcycle Trip to NY – standing with motorcycle
Motorcycle traveling through mountains of New York to Albany VA Medical Center
Motorcycle traveling through mountains of New York to Albany VA Medical Center

( 8/16/2016) An Autism Dad celebrates “Life Plus 3” with Family:

* Today I celebrate “Life Plus 3”:
3 years ago I was thrown head-onto-the-highway at 70mph,  with a 40,000 ft lb force.
“I died on the highway…only to come back and ‘try again’.”
This is my gift from a much greater power!

in an “Autism Family”, When you get “knocked down” – you get back up and “put your shoulder back into it,” sustaining and growing your family, once again.
====
An Autism View of Life “Re-gifted”:

If you could “Live Again” what would you treasure in your life?
* My answer is: Live every moment connected to your Family and friends, and treasure every new memory, as seen through the eyes of your children, Wife/Spouse/Partner, and loved ones.
—-
My Story:
3 years ago, my motorcycle was floating through the mountains of New York, as I rode 400 miles to work on joint Traumatic Brain Injury/ PTSD Research with the Albany New York VA Medical Center.
Suddenly, my rear tire was slashed and came off of the motorcycle rim; it threw me headfirst over the windshield at 70mph, into the middle of a thundering herd of Semi-trucks, as they raced for the Canadian border. I landed headfirst on the highway with 40,000 foot pounds – strong enough to break one’s neck 50 times (over). A lifetime in Judo, from my early years in Okinawa – until today, taught my body to roll in a diagonal “hoop” – call Zenpo Kaiten.
Judo allowed me to (avoid) landing headfirst and breaking my neck…and every bone from the crown of my head to my feet.
The New York State Trooper who responded to my accident said ” yeah…that Judo stuff was pretty good; we were amazed that you were not ‘taken out’ by the crush of Semi-trucks, racing up the New York Thruway at ‘rush hour.'”
===
Enter “My Second Life:”
* As I woke up to see semi-truck tires whizzing by my eyes, I thought “…I was gone and, now, I’m back. I get to watch Jared – my Eldest Son/our Computer Animator on the Autism Spectrum – graduate from college 6 months from now, after an 8 year campaign to earn his Bachelors Degree!”

From birth until 5 were told that “..Jared is Autistic; he will (likely) never know you exist., even when you stand right in front of him!” Jared earned his Bachelors Degree – and he was inducted into the Omicron Delta Kappa Service Leadership Society – for work (while in Japan) to safeguard Persons with Autism and Disabilities during Tsunami and disasters; and to help returning Veterans with Traumatic Brain Injury/ PTSD – at national medical conferences.

Ryan, our middle son and Middle Elder:
Laying on the New York Thruway, I thought; “…I get to watch Ryan come back from teaching at the National University of Laos (as one of the first Fulbright Scholars to help in Laos, since 1946)…and I get to watch him earn a Global Health Scholarship and to graduate in the top of his class in: “Global Disease and Epidemiology Control” at the Johns Hopkins Bloomberg School of Public Health. He will go on to help save hundreds of thousands of lives and help girls and boys; women and men; Moms, Dads and families; farmers and city dwellers – from debilitating diseases, such as Dengue Fever and, now – Zika Virus.

Nathan, our Youngest Son who overcame Health and Life Challenges – to help “Heal the World”:
Nathan overcame life threatening health challenges, and an Education System which said “…that kid is always sick; if you educate him (outside) of the school – he will not ‘count against us’ on the State Assessments of the High School!”
* Nathan was awarded the American Chemical Society “Outstanding Chemistry Student Award” from his research university, as he contributed to “Gold Nanoparticle Research for Delivery of Cancer Diagnostics and Therapy.”
Nathan graduated with a ‘perfect 4.0 / A Grade Point Average’ and he outscored the Valedictorian of his class, earning a Bachelors of Science in “Biochemistry/Molecular Biology with studies in Mandarin Chinese, and Philosophy.”
** Nathan is now. Research Fellow at the National Institutes of Health, Laboratory for Immunogenetics and Structural Immunology.
* Nathan will help to “Heal the World” (Tikkun Olam) as he contributes to research on: HIV, Tumors, Alzheimer’s and basic immunology research – to help future diagnosis and treatment of life-devastating illnesses.
===
My “Life Plus 3” – is a gift from on-high. Now is the time to continue to share with Family, friends, and the world – as best I am able.
With Respect and Affection to Family and to Friends,
both those of Today, and those Yet to be Discovered,
Mayer Max, ( Okinawa / Maryland )
Ais4Autism , www.Ais4Autism.com
Mindknit Research Center , www.MindKnit.org

Motorcycle slashed tire leaves rim
Motorcycle slashed tire leaves rim
Hospital photo with destroyed head-to-toe armored jacket and pants
In-Hospital with destroyed head-to-toe armored jacket and pants
Hand cupping blossom on branch - sign of perfection for Autism Mind
Life with Autism continues – Nurturing Family, the world, and the “Persfect Mind”

(C) 2016 Ais4Autism

Sheila Elephant in Room

( 8/15/2016) ( Sheila Max; Co-Founder Ais4 Autism; RN; 31 Year Autism Veteran ) Autism….there is the elephant in the room. A word that strikes fear in the heart of any parent. We first heard that word in 1987 when our eldest son was diagnosed. A year when autism was considered a rare occurrence. There was no information available, no support groups, just a yawning chasm of grief and confusion. We were alone and scared. All we had was burning drive to find help and answers.

For almost 30 years we have forged our own path and this site is our way to share the many lessons we have learned on the way. We hope some of our experiences will be useful to others at any stage of their journey as well.

Hope is a wonderful thing’ and there is always hope for improvement in your child’s potential regardless of their challenges.

We don’t pretend to have all the answers. But living with autism for 365 days of the year for almost 31 years now, we most definitely have some of them.

This site is just beginning and we hope you will follow as we begin to share our story and look forward to engaging with others as well.

(C) 2016 Ais4Autism