Jun 9, 2023
Reaching full potential. Becoming independent. We want these things for our children. For kids with disabilities, providing the assistance they need while trying to achieve these goals is like walking a tightrope. Help from even the most well-intentioned people, often is not helpful. It’s not just educators, parents unintentionally hold their children back as well.
Dr. John McNaught has made it his life’s work to reshape how we teach students with disabilities. Early on, he realized parents need to be educated too. The lesson plan: SELF-DETERMINATION.
He has witnessed first hand the transformation that happens when you give children the tools to make decisions for themselves. He has watched students move from self-contained classrooms, to general education classrooms, and onto college campuses.
Take a listen and learn how powerful self-determination and meaningful inclusion can be when done right.
The Odyssey: Parenting. Caregiving. Disability.
The Center for Family Involvement provides informational and emotional support to people with disabilities and their families. All of our services are free. We just want to help. We know how hard this can be because we're in it with you.
You can learn more about I’m Determined here.
You can read the research article Dr. McNaught’s mentioned about struggles students face because they don’t understand their disability here.
TRANSCRIPT
Welcome to The Odyssey.
Parenting, Caregiving,
Disability.
I'm Erin Croyle, the creator and
host.
The Odyssey podcast explores the
turn our lives take when a loved one has a disability.
My first child was born with Down's
Syndrome in 2010.
His diagnosis hit me like a freight
train.
It's the most common chromosomal
condition diagnosed in the United States. Yet so little is
known.
I was a new parent with a newborn
son who was the first person I ever met with Down
syndrome.
I had so much to learn. So I
started right there next to him in the neonatal
ICU.
Now I'm here working with the Center
for Family Involvement at VCU's Partnership for People with
Disabilities.
This podcast digs deep into the joys
and hardships we face.
We're going to celebrate how amazing
the odyssey of parenting, caregiving and disability
is.
But we won't shy away from the tough
stuff either.
Something a lot of families struggle
with are the many roadblocks our children face throughout
their lives. These roadblocks are in our communities, our
workforce, our schools, even in ourselves.
Thankfully, more and more bridges to
independence are being built for our children.
One of those bridges is a program
called I'm Determined.
This state directed
project funded by the Virginia Department of
Education. Works with youth, especially those with
disabilities, to help them steer the course of their lives
rather than being the passenger.
It's all about
self-determination.
The program isn't just for youth,
though.
There's a family component that
helps parents learn how to better listen to and support their
children.
And there are resources for
educators as well.
Joining me today is Dr. John
McNaught.
he was one of the first people in
Virginia to implement student directed IEP meetings.
His focus has always been bringing
the student voice to the forefront.
He's also the founding member and
principal investigator of the I'm Determined
Project. so.
John, I'm so excited to talk to
you.
I've known about I'm determined for
years, but last year was the first time I was able to attend the
summit working with its communications team.
I have to be honest, while I've
known about I'm determined for ages, it's hard to fully grasp what
it's about without being there.
I would love to start with you as a
founding member. Summarizing, I'm determined in a
nutshell,
So in a nutshell, I'm
determined is all about opportunities to practice self-determined
behaviors in an environment that supports those behaviors. And so
it's that simple. I think a lot of times we where we fail with self
determination is we do a little bit of an instruction and we toss a
kid into an potentially unsupportive or scary
environment.
And what if we approached life that
way? What if the first time you drive a car, you know
there's no instruction or there you read the manual and then you
just get in the car and drive by yourself with nobody
there.
And so it's all about scaffolding
supports providing that environment, right? You
become competent in your ability to do things like advocate or
problem solve, and you do it around people who are, you know,
supportive.
And that gives you the ability and
the confidence then to go try that somewhere else like school. So
that's how you know, in a nutshell, that's how I would describe it.
There's a lot of probably 10,000 intertwining pieces that make that
happen. But that's the best case.
John, before we dive in deeper,
there's something that kind of always intrigues me reading
your full bio, right? I wonder what brought you to this place
professionally. And I ask this because until I had my son, I was
totally ignorant, to the struggles and marginalization that
people with disabilities face. And by the time my son was one, I
was then immersed in advocacy. my son, he's just opened up my
life in this spectacular, fair way.
So I now see all the room for growth
in our educational systems, our workforce, our community that I
wasn't aware of. So I'm really, really curious if there was an
event or a person or something that put you on this
path.
Yeah. So there are multiple things.
So I'll start with, know, I grew up in a small town. It
was a kindergarten through eighth grade school and everybody knew
everybody and it was an inclusive model.
our football coach, his son, was an
individual with Down's syndrome. He's the same age as us. Chris was
his name was in all of our classes he was the manager of the
football team. And, you know, he was just one of one of the
guys.
Right. and then we graduated
eighth grade and we went to regional high school.
And my mom was actually a teacher at
that high school. And I can remember, like after about two
weeks, you know, I probably wasn't even in two weeks
realizing, Hey, where the heck is Chris? I haven't seen him, you
know, in two weeks.
And I remember asking my mom and I'm
like, Hey, where's Chris? And she's like, What are you talking
about? I'm like, I haven't seen Chris, you know, since school
started. And she's like, Oh, well, you know, he's in the special ed
program. And I'm like, All right, well, where is that? And, you
know, I mean, you know the story, right down the hall, down the
stairs, around the corner, next to the boiler.
And that just kind of stuck with me
as just not being right, not feeling right. He was such a
part of our everyday life. And then it's like you don't even see
the kid.
that's how it was for four years,
you know? I mean, we you know, we tried to, you know, break him
out, but inclusive education was certainly not a
thing.
And social inclusion was definitely
not a thing. And so that that kind of stuck with me. And then
honestly, I did some volunteer work in college at a place
called the Virginia Home for Boys you know, it was just a lot
of kids would with different stories, but some of it was behavior
related. Almost all of it was disability intersectionality of
disability and and some other issues.
01:06:31:12 -
01:06:40:21
Unknown
And, you know, just kind of watching
them at such a young age like, you know, teenagers just in this
home, residential, no choice, no voice.
And it just kind of brought me back
to this idea of Chris and then I graduated college and I didn't
know what I wanted to do. And so I decided to hike the Appalachian
Trail from Maine down to Georgia.
And in the middle of that hike in
Virginia, I ran into this group of kids from this wilderness
school, and they fed me an and remarkably, one of the
kids from the Virginia home for boys that I had volunteered
with was a student in this wilderness school who recognized
me. And so we started having this conversation and it turned out
this was a school for, you know, kids with ADHD, emotional
disability, learning disability.
And they were there because they
also had some behavioral issues. So they were either there because
they had a problem in school, their parents sent them or the court
sent them. And I was like, this is this is interesting. And we just
kind of hung out all night. And so I got off, finished the trail
and
I was telling my dad how I didn't
want to my major, what my undergrad major was business.
And I was like, There's no way I'm
going to work in business. And he happened to see an ad for a
wilderness school. I go on the interview and it's that school and
those kids are still there.
so I started a week later. did
that for three years, living out in the woods and eventually
decided that, you know what I want to learn more about special
education, went back, got a master's degree, and then went into
teaching.
And my first kind of foray into
teaching was I was given a room. So I was working was I got hired
as a teacher of students with emotional disabilities, and they gave
me my first classroom and it was like, you know, I don't know, an
eight by eight closet with no windows. And an A caseload of
25, but I had seven who were seniors who were 100%
self-contained I was just like, wait a second, we're supposed
to hang out in this room for 6 hours together by
ourselves.
So I was like, This is crazy. I
don't think we're going to do this.
I will never forget this. I thought
this was such a great idea. I on the first day of school, I handed
them all their IEPs and they said, What's this? I was like,
Get your IEP. And they're like, What's an IEP?
Whoa. Now I can start getting a
little bit nervous. And then, you know, back in the day it was
called emotional disturbance. So they see their name, they see
the word emotional disturbance, and they're starting to get, you
know, what the heck's emotional disturbance? Well, then they start
reading the present level. And in hindsight, I probably should have
read those a little more closely through a different
lens.
So they were super negative, right?
It was basically summary of every bad thing that kid ever did and
every, you know, And so they're starting to get upset. And I'm
like, Who wrote this? And I said, This is my first day teaching. I
mean, look at the back page, see who signed it. Like, I didn't
write it. So, you know, we sat we started having a conversation and
these kids didn't know they were in special ed and they had been in
special ed since third grade.
They're now 18 or 17. It's fall
semester of senior year. And so I talked to the principal. I'm
like, Yeah, we're not going to do this self-contained thing. We're
going to these kids, This is crazy. And, you know, we moved to
an inclusive model with the idea that if there's behavior problems
that I'm going to have to deal with it and we're going to, go
back to the old model.
If we have to.
And, you know, I just watched trying
to give these kids some choice, and they were just so unwilling to
take the leap because they'd been told what to do forever. And now
they're 17 and some new young kids in their talent on that. They're
in charge and they're like, I don't think so, man. Like, I don't
you know, I don't trust you.
I don't know you. I don't even know
what to do and how to be in charge. it was a hard year. We
made a lot of strides. But you cannot in one year make up for six
years of, you know, self-contained education or lack of
education.
And so I was a little, you know,
like, all right, we got to change this whole model.
And then that that same year at
the time we had what was called IEP Day. And so it's April and I
had like 27 on my caseload, including and those kids were all
graduating. So they didn't they didn't need I didn't need to
rewrite their IEP, but 27 kids every IEP do on the same day. And
you know, for anyone my age or older, you'll remember pre
computers, we had the NCR paper.
So each sheet of the IEP was like
seven pages thick and you had to write really hard. That's right.
Right. So, you know, I wrote 27 IEPs, I'll do the same day. And so
then the kids would come to school until noon and then leave
because it was a half day. And then we were supposed to schedule 27
IEP meetings from 1 p.m. to 9 p.m. like in every
special.
The teacher in the school is doing
this. And so
I was like, This is crazy, but okay,
this is what we do. So we're going to do it. And I told the kids, I
said, Look, if you come to your IEP meetings, I know I knew from
asking them they hadn't done it before. You come to your IEP, meet
me, I'll buy you pizza the next day.
And they're like, Yeah, yeah, yeah,
we'll see you there. So I thought they were going to show up. And
so the day comes, they leave the meeting start. I've got
administrators just walking in and out of classrooms, just signing
their name and leaving.
I've got, you know, parents who, you
know, some want to sit down and have a meeting, but some just want
to sign it and walk out the door.
And out of 27 possible kids, I had
zero show up.
this is like a bad origin story. I
was so annoyed at those kids for not showing up. Right? And so I go
to school the next day. I'm like, I can't believe you didn't show
up. What is the deal? I was going to buy you pizza.
And they're like, they're like,
Look, dude, school ended at 12? So let me just get this
straight. You want me to come back to school? That which I hate?
You want me to sit in a meeting with a bunch of people? I don't
like so I can hear about all the things I can't do? They're like,
No, thanks.
And I'm like, WhatIf you had looked
at the IEP, I wrote, but they had no say in it, right? They didn't.
You hadn't even seen it. And so in hindsight, not a big shock. They
didn't show up. So I said to them, out of out of frustration, you
know what? Anyone who's not a senior, you're going to write your
own IEP next year. I'm just not going to do it. And I just
happened to go to a conference a month later and met one guy out of
Northern Virginia, and he had this grainy VHS tape of this kid
participating in his meeting. And I was like, Oh, this is a thing
like, we're doing it like this is a thing. And so the next year I
started what I called back then, student led IEPs. we went for
it and we did it it was awesome. It was a lot of work, but it
was a lot of relationship building and it totally
changed.
It changed the kids, it changed the
parents, it changed the administrator perspective of the kids.
It changed the general education perception of the students.
it was really just this magic thing that they just kind of took
off.
And my wife was also a special
education teacher at the time in the same district at a neighboring
high school. And she started doing it and it started taking
off. this is all kind of pre undetermined. Right. I'm a term
wasn't a thing yet. so that's a long way of around how I got
to coming up with this thing called undetermined
John I just have to say what really
strikes me in my heart as a mother of a kid with Down
syndrome and as a person who helps other families, you know, do
this, it is just like, wow, that was one student.
This all started because of
inclusion with one student back in elementary school. And I just
think, so often, parents still have to fight to have
their kids included. You know, they you have a certain code and
automatically you are put in a self-contained classroom, you're
segregated. And that argument that we still have to make constantly
as advocates, which is, inclusion is better for
everyone. students with disabilities do as well, if not
better, and students without do as well, if not better. And your
story is like this beautiful example of what a difference it can
make. Just seeing someone with a disability in the same room as
you. I mean, that changed your entire trajectory. It did. I'm
floored. I just to me, it speaks volumes
to inclusion and then to hear the
stories, about the IEPs, that does not shock me.
I mean, we're still at a place where
a lot of schools, you have to fight to have a student lead
their IEPs. I mean, you know, I've been doing this now for 25
years you know, I'm finally I'm finally the old guy in the
room who's like, we've been talking about this for 25 years. People
like, come on, You know, I mean, I can remember thinking, oh, I'm
never going to be able to say that, yet here I am. Like, we're
still talking about getting kids involved in their IEP
meeting,
what's happening now we're trying to
fight against, right, is that students participating in their IEP.
It's it's awesome. It's a feel good moment, but it is not
going to move the needle for the kid. Okay. It's a it's a once a
year thing.
What moves the needle for the kid is
opportunities to practice being self-determined at home, in school
and in the community on a daily basis. Right. And so that's where,
you know, and you can still do still what? IEPs because it's fun
and it's cool. Just can't be the only thing you do.
And so it's all about those
opportunities to practice.
You know, I look at it now, you
know, my lens now, 25 years later is, you know, I'm a researcher,
I'm a teacher, but I'm also a parent of two high
school girls, one of which has a disability, has
ADHD, anxiety and OCD. And so I come at this through
those three lenses. Right. And if you're only working on this stuff
at school, it's not going to cut it, right?
You've got to have families and
teachers speaking in common language, working together, providing
those opportunities. And I watched it with my own kid because,
look, my my daughter is at the high school that my wife and I
taught at. Okay. I know almost every teacher. I know all of the
administrators. All right. She has a wonderful plan.
I have all the privilege in the
world. I mean, I am a white male with a terminal degree, and I have
all the connections at the school. Right. You know how my kid gets
accommodations? She advocates because when she wasn't advocating,
it wasn't happening. And if it's not happening for me, right, then
it's not happening for anybody, I can promise you.
Right. Because if there's anybody's
kid that should be getting it, they would be like, Oh, look, watch
out for this guy, right? Make sure his kids are getting what they
need, not the case. And so I'm like, all right, you know what? Then
you're going to go do it. And luckily, you know, we've been raising
her as a self-determining, self-determined child for so
long. She was like, okay. and what a change. Like, what a
change. Like, I haven't had to have one conversation in a year and
a half with anybody because she's taking care of it. And that
was my like, light bulb moment. Like, Wow, you got to put it in the
hands of the kids.
You do.
And that's this is perfect is I want
to talk about that more. I want to talk about I'm determined. And I
think also the beauty of I'm determined, right, is one, it's an
ongoing project. It's not just the summit, but also, you know, you
work with kids who have disabilities, but those disabilities vary
greatly. And I think a lot of times we talk about student LED IEP,
but what about those students who don't have, traditional
expressive language abilities, who have a very hard time
communicating in a way that, non-disabled people
understand?
You know, my son is a perfect
example. I have had him attend his IEP meetings
since preschool I'm still working to have that
participation be meaningful because that communication piece is
just not there yet. So I would love to hear more about I'm
determined and how you help kids of all levels and ages and
all of it.
so. Communication is like that's the heart of everything, right? And it's so hard being a parent. And I'm a parent with a degree in special ed and I still feel like I don't know, I don't know everything, but to I had to get out of this mindset of like, automatically looking at the teacher as the expert. Well, I'm not going to question right. Even myself and also understand you as a teacher.
They don't necessarily get exposed
to all of the resources that are out there, especially around
communication. Right. Technology's changing every minute. And so a
lot of the work we do is exposing teachers, kids and families to
assistive technology because there is so much out there.
Right. And not everything has to
cost $10,000. Right? There are all sorts of apps or
functional communication devices, speech generating devices. And
what is so one of the things we did that I really love is is
through I'm determined and a t tac in the College of Education at
James Madison University is we opened up what we call the
Accessibility and Inclusion lab where we've invested, you know, a
quarter of $1,000,000 in technology and accessibility and we open
it to free service teachers, in-service teachers, parents and
kids.
Let's say you have a kid who's
strong, who's who's got some communication needs and you can't
necessarily figure it out. You come to the lab and you can try
everything, right? Because if the kid isn't motivated to use a
device, it's not going to be a good fit. I've had kids weighing
iPads across the room because they don't want the iPad.
Right. And so it's a heck of a lot
easier to come to us and throw our iPad across the room than it is
for a parent to drop two grand on an iPad and then it's broken or a
school division, whatever. every kid is different. Every need
is different. And again, it's that opportunity to practice,
right?
So exposure and understanding
that, not everyone's got the budget or the ability to bring
all these pieces together for somebody to try. And, you know,
that's one of the goals of the lab. So like, come in, explore it.
And we've seen you know, we worked with a student, Chloe,
who's an amateur one youth leader.
She's actually about to graduate
from VCU as a journalism major.
She has cerebral palsy. She
absolutely hates to use a speech generating device. Now, I work
with Chloe all the time. I've known Chloe for almost a decade. I
don't have an issue understanding her.
But if you just met her, you're
potentially going to have an issue. for Chloe, it was like it
was all about speed, right?
If I asked you if someone asked the
question. Right. The fast processors can always answer first. If
she's got to always type it into a device. Right. Especially if
it's a kind of a antiquated device. They're already on six
questions down. She's still trying to get her device geared for
question one. There are question six, And so, hey,
understanding that
we got to find the right piece for
her, but her also understanding that there's going to be times
where, although it's not her preferred mode of communication, she's
going to have to use something to get her point across. And
that for her, that was a process that she really had to kind of
come to.
And then having her the ability to
try all this new technology and be like, Oh, so I can have
something preprogramed and boom, click and I'm right in
it. it's sad sometimes. You see kids are still walking around
with like, like a picture exchange communication system book,
right?
The thing weighs like 600 pounds.
You know, you got to flip 80 pages to get to hamburger. I mean, I
don't know how functional that is, right? I mean, are you going to
be walking around with that thing
in the community?
I just think this idea of embracing
technology and understanding that everyone has a desire to
communicate, right.
And if they can't do it verbally,
they'll do it through behavior.
we've got to find out where they
are. I've had students lead IEP meetings with every disability you
can imagine. one of my first years, I had a kindergartner with
Down's syndrome, run his own meeting, show his PowerPoint. You
know, I ran into the kid like two months ago.
It's got a full time job at
Costco.
And I was like, Oh my gosh, oh, my
gosh. She's I'm like, oh, he's got like a full beard. You know? I'm
like, I remember you from kindergarten. it's accessibility in
the ability to understand that these resources are available. We
got know how to source them.
And that's hard That's hard for
families.
That is I mean, you say JMU for
those listening, that's in Harrisonburg, which is kind of central
Virginia, beautiful town.
And you mentioned TTAC. So I want to
stop for clarity that one, if you can explain TTAC. But also the
question is, do you know of other places that do a lab like this
where where can people find something like this locally?
So Virginia has a model where as far
as technical assistance to schools for special education, we
have offices at seven different state universities and we cover the
entire state. We're free resource the schools. And so for
Virginia, you know, that's great, right?
There are some other universities in
Virginia, George Mason, Virginia Tech, that all have access to
these kind of resources.
But the reality is, no matter where
you are in the country, universities is where you need to
look. if you're in New York, I'm looking at, you know, maybe
Cornell, if that's the area of the state you're in, what is their
special ed? You know, who's our special ed department head? What do
they have to offer?
Because, you know, in my
experience, you're going to have a better chance finding it at
a university than you are at a local school system. Right? I mean,
local school systems are just not equipped for funding wise to
create this kind of they can do it for individual kids potentially,
but they're not going to have a room where you can try all these
different devices out. as a teacher prior to coming to the
university, that was not on my radar. Mike. I had no idea that
that's where I should look.
And so that's where I would
start as a parent.
That's good to know.
So I want to move towards we've kind
of gone everywhere, so let's go backward so we can go
forward.
So you start the student letter IEP
process and then how does that kind of evolve into I'm
determined, there was an opportunity for a job at James
Madison at TTAC.
I decided to interview for and I got
it. about a year later I was 25. And then in 2006, we
were tasked the Department of Ed, through the Tea Tax, were tasked
with coming up with a solution to or post-school outcomes for
individuals with disabilities. we did a bunch of research and
some things we found out were that at the time in
Virginia, kids were not attending IEP meetings. Kids did not
know what their disability was. They couldn't tell you any of their
strengths. They couldn't tell you any of their accommodations. They
couldn't tell you any of their rights under idea.
you know, we had poor for
post-school employment outcomes, for post-school secondary
education outcomes.
based on that and in our research,
we said, well, self-determination sounds like an area we need to
dig deeper into. And at the time, Mike Meyer out of Kansas was
doing a lot of research that we would kind of grasp on
to.
And then the second piece was we
knew it had to be in the very beginning teacher friendly, and so it
had to be something we had to create something that teachers could
use quickly that didn't feel like a curriculum because they weren't
going to do it.
And so we brought in some teachers
from across Virginia, we came up with what we call the three
core tools of I'm Determined. So you got the one pager, which
honestly is just a simple way to come up with strengths,
preference, interests, needs. We created the goal plan because
another piece of that data was that kids had they didn't have short
term goals.
They didn't have long term goals.
There was no real goal setting going on. So the goal plan and then
the Good Day plan, which was just simply like, what's going on
now?
You know, or what happens on it?
What on your perfect day, what happens? Is it happening now? What
needs to happen to fix it and who can help you?
And those were three easy tools and
everyone loved them and they jumped on board. And then I got
to focus on, okay, as a result of these three tools, let's
keep this student let IEP train. And I started moving, right? And
so we brought in some professional film crew and just
started making movies of kids leading IEP meetings, kids talking
about their disability, understanding what their strengths
were general education, teacher, special education, teachers,
administrators, parents.
Right. And honestly took I'm
determined from from the nine pilot schools we started with in 2006
to, all the school divisions in Virginia, plus over 40 states
that I've worked with over the past. You know, however many
years has been the video storytelling. Right.
Because people can see themselves in the stories.
And that's powerful. And they want
it.
They want to see it, to believe it
kind of thing. focused a lot in the beginning on driving
around the schools in Virginia and shooting video, that was
probably, you know, I don't know, maybe the first ten years of
work. And then with that, this idea started in the year two. Okay,
Well, that's the teachers now.
We got to hit the kids directly. And
so we came up with this idea of a summit.
And so the very first summit, it was
just a youth summit. And we had 15 kids with disabilities from
across the state. And had kids with L.D., kids with autism, kids
with Ida. And, you know, we had one kid who was the leader she
ran this this two and one half day summit.
And the whole time I couldn't get
rid of the parents. So the parents are sitting outside our doors
trying to, like, poke their head in, see their kids, okay. And
they're driving me crazy. And and I wasn't a parent at the time.
Okay? My wife was pregnant with our first kid, I couldn't
really know why these parents are killing me and my
colleagues.
Like, we need to do an event at the
same time for the parents, I was like, Man, I don't want to do
that. That's going to be a pain in the butt. And she's like, It's
going to be easier than this. And I'm like, All right, let's do it.
And so the next year, five of those kids from the original summit
came back as the leaders, we we said, All right, parents, we got
something for you, too.
And we went from like, you know, a
summit of 15 to 20 to 50.
and we found that and the parents
had so many questions, right? So many questions around
disability, around opportunity, around just navigating school and
life and these these parents formed this like, support group
outside of us back in the times everyone's using
Facebook.
The youth formed their own support
group on Facebook and left us out of it.
you know, we did another year of 50
and then next year we're at 100 and 150 you know what I found
with parents? And this kind of speaks to why we really try to get a
wide array of individuals with disabilities as if my kid has
ADHD.
I want to hear from another parent
whose kid has ADHD. And if my kid has Down syndrome, I want to hear
from another parent whose kid has Down syndrome.
And at first I didn't totally
understand it, but I kind of get it more now because it's just
that like they can totally relate, And so we made sure that we had
a wide range so that everyone had. if I'm if my kid
is, 13 and just kind of going through it and I can run into a
parent whose kid is now 19 or 20 and they can kind of tell me all
the hoops they jump through and all the barriers they
broke.
For the parents, they can see the
light and they learn some tricks for the kids, This is the
crazy part. Every time a kid came to the summit and I wrote a whole
article on this, they they'd say, I thought I was the only kid with
L.D.. I thought I was the only kid with dyslexia in the world. I
thought I was the only kid with intellectual disability in the
world or autism. And then I come and I meet all of these other and
this kid's got the same disability as me, and they're in
college. Like, I can do that. That's a thing. And it just
started right. The ceiling, just their own ceiling started raising.
And so then we knew at that point, okay, we got the kids, we got
the parents, we've got the special ed teachers. Now we got to raise
the general led ceiling.
you know, if I could do the whole
thing over again, I would have never build this as a special
ed initiatives.
honestly, after about year five with
my work with schools, I build it as an all kid initiative. And if
you want to make inclusion happen, that's how you do it, right? All
kids need these skills. All kids need to tell you what their
strengths are, what their needs are, and by doing that right, I've
got schools that every single kid's got a one pager, every single
kid's got a good day plan, and it just changes.
It's just more of an inclusive
mindset. So I wish that I had that kind of foresight way back when
we first started it, because the places where I started as a
special ed initiative, it was really hard to kind of remarket it as
something for all kids. And that's still kind of drives me
crazy. Yeah, I can see that.
Although I think, it may not
belong to you because it's your baby and you've been doing it a
while, but it is still young and there's so much room for growth.
And I love that you've brought this up because I'm quite curious,
you know, when you were talking earlier about special education in
that first room you started in and that mantra that we learn as
advocates, special education is a service, not a place is so
important. And hearing what you're saying now, when I
speak to university students and I talk about inclusion with them,
and one of the things they mention is, is the failure of higher
education to teach special education to all teachers, including
general ed teachers, because these practices, these practices
benefit every single student and co teaching models are
beneficial, all students. And we just see in our structures that
lack of funding of public schools, the lack of education in higher
education to make this happen.
John, if you could change
something what do you think the the thing is that could have
the most impact?
Yeah, honestly, you hit the nail on
the head and I'm I'm involved in a project and that's what we're
doing right now in it is re-envisioning educator prep programs
because we can't keep churning out teachers who are not
prepared.
And so like you said, especially
with the teacher shortage right there, kids, students with
disabilities are going to be in general education. And that's just
a fact. End of story. A lot of our educator prep programs, right.
You can you can say I want to be a high school math teacher. And
outside of your intro to Ed class, never hear the word
disability. Ever. And then you come out and you're teaching
algebra one in 15 to 20% in the kids in the room have an IEP and
you even know what it stands for. Now, what kind of that model
makes no sense right, Right. And so we're working on both at, you
know, with the Department of Education and a select number of
universities in Virginia is just, hey, that model makes no
sense.
We need to do better than that. The
other side of that coin is this. You're going to want you're going
to college because you want to be a special ed teacher, okay? At
some colleges, you can go through four years and never interact
with a general education undergrad, and then then they get a job
and it's like, Oh, cool, I want you to go co teach math.
And they're like, Whoa, what? I
that's not what I do. I'm not. I'm not that. And so we're failing
and on both sides, And so we're teaching this model that is
like honestly, like a pre 1975 model. Yeah. And we're still doing
it.
I came to that realization like
maybe two years ago in this, this grant opportunity showed up a
year ago.
So I was all over it because I'm
like, I'm tired of constantly going into in-service classrooms and
trying to fix things that need that could be addressed in re
service universities. And so to me, like that's what we need to
do and that's what I'm excited about kind of moving forward.
And I'm a little I'm a little worried about with the teacher
shortage, with all these people going coming in my kind of
alternate route who aren't necessarily having those classes like
that scares me a little bit.
But I'm putting my eggs in that basket. We need to we need to fix those educator prep programs. We need to get them aligned. They got to work together they got to understand, like all kids means all kids both and need to understand that. you know, I have hope for the future because I think we're getting there.
I think we're we're looking at that
model. And I know some universities already have like what I'm
talking about, like, I know Radford University in Southwest
Virginia has been doing a model like that for years. And guess
what? Those teachers come out better prepared because I've seen
them.
So we can do it.
Yeah. And Radford has a great
reputation.
It's unfortunate. I mean, we have
the teacher shortage and then we also are seeing some colleges and
universities are losing money and they're having to get rid of
programs that were actually hugely beneficial. And I guess we can
just I mean, hope is great. So let's hope that it starts to see the
pendulum start swinging back. But I think advocacy is also
necessary speaking about these things and spreading it.
I know so many teachers who care
deeply about teaching, but it's a struggle because they have to
relearn so much.
After going through school and
getting a master's here, they are relearning through professional
development. And you know that same question like from a
parent lens. Yeah, I think what I've learned is that you've got to
put 100% of your effort into creating the most self-determined son
or daughter that you can because even though I know better, I
wanted to solve my kids problems.
I wanted to call those teachers out
and be like, what are you doing right? And I did that sometimes
like, I would. I did it sometimes. And it didn't have a it didn't
have any effect. Right? And so watching my own kid learn to
navigate the system and just be fearless about it because they
they've been practicing it for so long that, you know, as a
parent lens, that's what I'm going for.
And I'm going to make, you know, my
kid has more significant support needs. I'm going to make sure 100%
they have some kind of communication device. So when I'm not there,
they can communicate those needs and we're going to practice that
all the time.
that's just as a parent, that's
where I am. And, you know, I'm going to feel like, okay, my kids
prepared.
Well, let's touch on that more,
because I think and I bet you've run into this a lot and I bet the
parent summit helps. But,
as parents, you know, that parental
instinct to protect your child is so ingrained in us. Yeah. And
then when you combine that and having a child with an intellectual
or developmental disability, that protection radar is just up a
notch.
And I think as parents, we can
sometimes do a huge disservice to our children in just thinking
that we're protecting them and thinking that we're helping them and
thinking that they need these things. We kind of hold them back a
little bit.
So I'm curious, you know, how often
you see that and also how you help parents kind of understand how
detrimental it can be, though.
I see it all the time and I've been
guilty of it myself. But so I think with self determination
right at home you start small.
I'll give you this example. So my
kids who are now about to be 16 and 17 when they are around
five, one night a week, they pick, they pick a meal, they make
the grocery list, we go shopping and they help cook the meal
cook.
And so, you know, here we are at 17
and 16. They're both extremely competent and confident in the
kitchen. I've got one who's like a master dessert maker and one who
can cook any kind of pasta and loves to grill cook. And so taking
the time to give that opportunity to think about when
they're in an argument, right, they're only a year
apart.
Like there were times as a parent
where I'm like, You be quiet and sit over here. You be quiet and
sit over here. But then 5 seconds later, they're in that same
problem, right? So and not every moment, a teachable moment. Right.
But your default all needs to be teachable moments. Okay? And
that's how you're going to start building that up.
Think of choices. Our kids can go
through school, Think of elementary school. There's like zero
choice built in, Right? I think my kids couldn't even pick where
they ate lunch by until fifth grade. You imagine that?
And so how can we build some choices
and build in some autonomy, as they get older? And this is the
hard part.
Okay. They've got a decision to
make.
And I say, look, if you choose
this path, these are the consequences, meaning this is what's going
to happen potentially you choose this path. These are the
consequences.
Hard part is stepping that stepping
back as the parent and letting them choose the path,
especially when it's not the one you would choose.
I've watched my kids make mistakes
and, you know, cringe. And the key pieces, which we don't do
well in school. Okay. Failure Is the middle, not the end. We chose
the wrong path. We have some consequences. Let's reassess what went
wrong. What should I maybe done, what didn't I think about? And
then let's try something again.
Think about how they go through
school. They fail a test. The next day you're on to New material,
right? In their mind, failures. In the end, you can't go through
life that way, You've got to learn to look at failure as the
middle. And so the more that we can kind of instill that in our
kids, you know, my my teaching, my oldest attire, shoes, she's a
lefty.
You know, at one point I was like,
you know what? We're just going to buy Velcro because I can I am
not a fine motor skill visual. Like, I just can't do it. And so,
you know, also knowing when we're just going to need Velcro and
we'll figure this out later, giving yourself some grace, but really
looking at how you your family system, how much choice is
built in, how much opportunity to try things are built in, how much
are you connecting, what they're interested in.
You know, when my kids were in high
school, they always had a chore list. But this is more recent. The
rule was chores had to be done at 3 p.m. on Sunday. Right? And they
were just blowing it off. They just weren't doing and it was
annoying. And my wife was annoyed and I was annoyed and were
nagging them nonstop and it was just unenjoyable and I was like,
What do we do?
I talk about this stuff all the time
and I'm doing everything I said not to do, right? And so I was
like, okay, new plan, Here's your chore list, Here's your chore
list. This is the this is the plan. I don't care when you do them,
but they need to be done by 3 p.m. on Sunday. If they're not, then
you turn in your cell phone until they're done. Well, my youngest
looks at me and she's like, Yeah, right. You always say this
kind of stuff. You're not going to follow through. I don't really
care. Mike Okay, let's see, right? First Sunday rolls around, my
oldest Saturday, all the chores are done. She's not feeling any
pressure. My youngest, Sunday, real five. Still not done. Mike,
give me the phone.
She's like, now to get the phone
back. Do I have to do them or is this just like a time thing? I'm
like, No, you got to do it. You get the phone back, right? So she
learns. So now, you know, three years later, my oldest still does a
on Saturday in my youngest, although she's never missed another
deadline, is still sprinting through the house at 259 on
Sunday.
The difference is I'm not annoyed.
My wife's not annoyed.
And it's her conscious choice to do
it that way. And little things like that. build up our
kids.
You know, I set this up thinking
we're just going to talk. I'm determined. And here I think you
might have problem solved. One of my biggest frustrations, I'm
going to give this I mean, they don't have phones, but I can think
of something.
I'm going to give this a shot. So
thank you.
I think so often, looking at
this as a parent, we put people like you, John, and my
colleague Dana Yarbrough, who I just think is the best thing
since sliced bread. we put professionals on a pedestal because
we see what you say.
But to hear you talk about
implementing it at home being difficult, it just makes it
easier for us to not feel so bad about our failures because you can
try so many different things and it depends on the kid, you know?
Absolutely.
I've done so many things wrong.
Yeah, yeah. I mean, and yeah. And then you have a self determined
kid who doesn't want to listen to you because they're self
determined.
And so it's like that. That's what I
have now. I've got two teenagers are like, I got this, I got this
like, hey, I just scheduled myself for junior and senior
year, and oh, my youngest says, and I signed your name. So I'm
like, Whoa, dude, there's a line between self-determined and
forgery. Like, I need to at least see what you're
planning.
But they're just taking control. And
so, I mean, it's cool, but there's definitely, like, as a parent,
there's like, Oh, remember the good old days when I could just
control you? Yeah, that's, you know, it's a whole it's a
thing.
Well, and I, you know, I have an
eight year old who? My daughter, they were born
self-determined I just got to hold on to the seat tightly
until they're mature enough to make decisions that are not
harmful.
But I think that's the beauty of I'm
determined. Right? So you have this perennial project that is year
round where you're constantly working with schools and then this
summit and I have to tell you, after finally being able to go to
the summit last year and watching these young people just grow so
much in three days, it is inspiring.
And frankly, it's just
electric.
So can you kind of walk us through
the thought process? Because not every person is born like my
daughter who comes out just ready to take on the world. So how do
you work on like building confidence and teaching these young
people self-determined Nation?
what makes the summit special is
that it's kids leading kids, kids to disabilities, leading kids to
disabilities and the adults really take a back seat and we are
there, but we're there if there's a problem, if there's a
question, you know, if a student's got a, you know, significant
support need and whatever, we can do that.
And look, that can be it's two
things. It's very scary for parents because I purposely put parents
on the other side of campus and I set up, face time stations
in case there's, an issue. But it's almost always the parent
wanting to talk to the kid and not the kid wanting to talk to the
parent.
Kids just inherently take care of
kids. Right? And so I had a mom who's like, well, who's going to
who's going to cut my daughter's food at the dining hall if I'm not
there? I'm like, it's not going to be an issue. in a what? And I
didn't even set it up right a kid, they all walk
together.
It's like, Oh, what do you need help
with? And I just took a little video and texted it to her of like,
Here, here's your kid with another kid and everything's
cool, that's not something you teach or train. That's just
kids accepting kids and feeling like they're not getting
judged.
There's no hierarchy.
And that's what the kids of the kids
talk about all the time.
I don't think it's anything we do
other than consciously we're not in charge. Right? And so in the
leaders, we do a lot of training with our leaders who are anywhere
age 13 through 21, and they're trained to, you know, make sure
everybody's involved.
They're trained to certainly
when to ask for help from an adult.
But it's just like
this, natural kind of we're just going to take care of each
other.
And for parents, where I get a
lot of heat is this is the first time mom or dad has ever
like given this level of independence to their kid.
I have a better appreciation now for
how scary that can be. My younger self found it mildly annoying but
I get it because they are away and they're not.
they say goodbye in the morning and
they're not going to see them again to like 6 p.m..
And there's there's some
unstructured time built in there.
I still remember this mom. She came
back and she couldn't find her son. I said, all right, well,
what's what's his name? Because I take pictures of everybody and I
look and she's frantic. I mean, tears. And I walked downstairs and
her son made a friend and they're in the room shooting
pool.
And so I just take a picture of them
and walk back upstairs.
she was just like, there was relief. But there was also just like, shock, right? Like, my kid doesn't have friends. I'm like, well, he does now. I mean, like, I can go get him if, you know. No, no, no.
So, you know, it's just it's a
big step for parents.
And a lot of the Parents Summit
focuses on how to take that step. And it's the first steps, the
hardest. And then it gets easier and easier and easier.
and I think once the parents start
hearing from other parents who have been through exactly what
they're going through currently, that's really powerful for
them.
I know for myself and my kid was
first diagnosed we got done with the initial eligibility and
the special ed teacher was like, you know, it was like, hey, you
know, I have a daughter a little bit older who who is literally a
carbon copy of your kid. and just was like, if you ever want to
talk secure in And so that's huge, right parents I mean if you
think back to like initial eligibility especially if your kid got
identified at a young age.
Right. You're sitting in this
meeting, you hear the word disability and you hear all these other
words and you've got 10,000 things going through your
head,
And you're not even half listening
to what everybody's saying. When's the next opportunity as a parent
that you have to get all those people together again in the same
room? For a lot of our families, that could be years and years are
never that feeling of aloneness is a real thing. That's real,
right?
And so the summit for them just kind
of like makes them feel less alone. that's huge. And then
immediately when they reconvene that first night, we have a dinner
together and the kids don't want to eat with their parents because
they've made friends.
And for some it's like, oh, it's
it's hard, you know, they let it happen. And I am like, Look,
Jimmy's not going to eat dinner with you. I know you think Jimmy's
going to eat dinner with you, but I promise you, it's not going to
happen right? And they're like, Yeah, whatever. That's
not. and purposely I do. I stagger it. So the kids go to
dinner or 15 minutes early so I can kind of get them through the
food line and get them all settled so that the parents can walk in
and be like, Well, how'd you get a cheeseburger? You're eating a
cheeseburger. I'm just like, you know, so don't hover
parents.
it can be an intense experience for
parents, seriously, because it's a lot of independence.
you know, I think they leave and
they're just like they kind of see the light like, okay, I get
it.
I know. there's light
potentially at the end of the tunnel. I've met some people who have
gone through what I'm going through.
My kid has made some friends. I
mean, we do a a social the last night for the kids. And
we get a DJ, we get karaoke for years parents would beg me to come
to it. I'm like, No, you can't. This is a kid social. finally one
year I was like, All right, this is the deal. You can go up on the
balcony for 5 minutes at a time.
You cannot call your kid's
name, but you can watch for 5 minutes.
And I mean, their kids are dancing.
Their kids are singing karaoke and they're the parents are just
bawling. They're like, we don't ever have this opportunity. And I
can't believe our kids on the dance floor, you know, or singing
karaoke. And,
It's cool to let them see
that, sometimes, you know, you're just not going to believe it
without seeing it.
it's quite an experience for
sure.
It's interesting to everything
you're saying. I'm soaking in and I'm just thinking about the
constructs we set up for our young people with disabilities. You
know, you need the support in school.
So a lot of times you have a
teaching assistant or a 1 to 1 support, makes them dependent
on someone else. Instead of building independence. And I think
parents do that accidentally.
And I think that parents
forget from basically from 11 on, if your kid wants to hang
out with you, you're lucky and a group. And it doesn't matter if
you have a disability or not. It's beautiful that they are finally
having an opportunity to make friends without an adult hovering
over them.
And I hope I mean, do you see when
you see that experience there, do you see those parents taking that
as a learning experience and hopefully trying to foster that when
they get back home?
Yeah, I think so. First learned
helplessness is a real thing for everybody, right? So like, if
someone's going to do something for me, especially if I don't
really want to do it, I'm not going to change my behavior, right? I
don't like making myself a sandwich. If my wife was going to make
me a sandwich every day, I'd be like, Heck yeah, do
it now.
That's not a disability thing.
That's just a human nature thing,
Yeah, I think for parents, I think
what I've learned is so I had a mom call me one time and they came
to their first summit and the mom called me and she's like, you
know, I just want to I just wanted to say we had a great time at
the summit.
But, Emily just not being
self-determined. and I kind of in my head laughs. I'm like, Look,
this isn't a magic pill. You don't come here for three days and
boom, you're going to start being self-determined, right? You're
you're getting exposed it. And I think for most kids and parents,
like three years in a row is like the sweet spot.
I think it's the first year it's so
overwhelming, especially for parents that you've got so much
in your head. And I try to tell them, leave here and try one
thing,
Don't go home and give your kid a
chore list and make them cook dinner and you know, and like. Right,
because their heads are going to spin, Try one thing and then
come back. think that after at least two years, especially if they
stay involved with the parent group, the idea of learned
helplessness. They grasp it. But I will tell you this, if your kid
is 15 understands learned helplessness and has not done a
certain task for 15 years that's non-preferred, and all of a
sudden you're trying to make them do it, or her do, it's going to
take a while and it's not going to be fun, right?
I mean, that's a real saying that,
but doesn't mean you shouldn't try it.
And I think sometimes we get like
the whole, paraprofessional one on one support thing. I think
we just need to be really careful. And I talk to parents a lot
about and teachers. What does scaffolded support look
like, how do we promote independence and failures?
Not a bad word. I would rather give
a kid too much independence, fail at something, reassess, try again
with a little more support than give too much support in the
beginning to where we never take it away because we're getting the
expected outcome
I mean, I struggle with that today
with my own kids.
You know, one just got our license
and one is currently I'm teaching her how to drive.
And so it's a constant battle.
You're not just I've been talking self-determination for 25 years.
I still have to think about it sometimes in the context of my own
children and what this is going to look like today.
It's just a journey.
And it doesn't end when school's
out,
I've been around long enough that
some of my original youth leaders are married. They're almost 40.
They have jobs. they say, like self-determination is a thing I
practice every day.
And disability doesn't disappear
just because you graduate high school or college it's still
there.
You might have learned how
to use accommodations, focus on your strengths, but it's still
a struggle.
And I've got tools to overcome
barriers. But, at the end of the day, I still have autism and
I've got to work on certain things and for whatever reason, a lot
of our kids came to us with This idea of disability is only a
school thing, and when I get done with school, I'm not going to
have it anymore.
And it was kind of like, Huh, where
does that come from? We got to figure that out a little bit. That's
how.
Have you ever tapped into figuring
out why they feel that way?
I think that because it's often
associated with where they're experiencing the most
failure.
if you constantly go to the place
and fail, you're going to think that when I get out of that
place, I'm not going to experience all that failure.
I've had a difficult time really
pinpointing outside of they all experience a lot of fear of failure
at an early age in school really think that's it.
but yeah, it's interesting. It's
been an interesting phenomenon.
The other interesting thing, I just
I just want to touch back on that you talked about briefly is
those supports in the scaffolding of support. I think that
when doing the IEPs have to be very intentional to say that it's
okay if something happens. I want this independence, especially the
1 to 1 support, they don't make a lot of money.
They're not trained properly. They
feel like their job is just to keep the students safe.
And so they they hover. And this
poor kid is is stripped of any chance of not just
independence, but of making friends because. No, you know, middle
schooler or high schooler wants to hang out with the grown up. But
the kid who's hanging out with the grown up all the
time.
I mean, how do you help students and
parents with an IEP to make that sort of thing clear?
Honestly, with parents, I haven't
talked to other parents that are I mean, the whole idea of a one on
one support outside of a kid with some significant medical
needs.
I mean, there's just a lot of
research in this does more harm than good.
And so I direct them to and they can
hear me say it, but I don't have a kid who had one on one supports
right now. I have, you know, parents who have gone through that and
and kind of talk them through it. And, you know, for the most part,
they get their and then we also train paraprofessionals we
just trained 300 paraprofessionals for our school
division.
Right. Because you're exactly right.
They think their job is to protect the kid or prevent failure.
Right. And when you do that,
what are we actually doing that
that's not that's not really your job.
special ed teachers sometimes. And I
as a former or current special ed teacher, former high school
special education teacher, sometimes we're worst.
Sometimes we're trying to prevent
failure so much. My first couple of years teaching, all I was
trying to do was prevent any failure because. They've experienced
so much already.
problem is I'm putting this
bubble around them and then they leave and then the bubbles gone
right and they fail and they don't know what to do.
sometimes special ed teachers are the worst. And honestly, sometimes that starts in pre-K in elementary school.
Oh, this kid's really cute. I'm
going to do all this stuff for them because. And they think they're
being helpful, but they're not. And then you got learned
helplessness, right? And that that creeps in so early.
So a lot of what I like to do is
talk to parents of young children because it is so much easier, you
know, so much easier.
You know, when I started this
project, my personal focus was high school and you can get there,
but it is a lot of work. But if you can start this young and
get parents on board young and teachers on board young man, it is
just so much easier.
So, John, with that, I'm
curious, what's your vision? take, all the roadblocks out
of it?
Like, what would your vision be for?
I'm determined. Would it start in pre-K? would it expand
nationally? Like, what is your lottery winning vision for what I'm
determined could be?
Yeah. So the two things, one, we
just we just expanded into early childhood a year ago because
it just it just makes sense.
you can build choices into early
childhood, just like you can build it into third grade, eighth
grade and grade.
The second side of that is I'm
determined is great and it's cool. And we got a cool logo. But the
core of our work,
Honestly, we were we're not a
curriculum for a reason. And the core of our work is changing
teacher practices, changing parent practices.
And if I could get people to
understand that it is the every day opportunities it is if
you're a teacher, it is how you engage your class. So if
you
if you asked a question to the class
and you're only your your procedure is whoever raises their hand,
that's who you call on the fastest processors raise their
hands.
They always get called
on.
You're not going to build confidence
or competence in a kid who never gets asked a question and gets a
chance to answer it correctly. Right. So change your everyday
practices. Give kids a piece of paper, say write down your answer.
Nobody talk, give wait time. When you say go, everyone holds their
whiteboard or piece of paper.
You see what everyone answered. You
can give specific feedback to every many kids you
want,
It doesn't have to be this epic
thing of of leading an IEP meeting of bringing 500 kids to
campus for three days and running a summit. Those are all awesome.
They work.
But what really works are those
everyday opportunities that we're not always doing in the
classroom.
And so if I could get people to just
understand that and have an inclusive school, I don't I
don't care if it's co teaching Pinocchio teaching, right. But if we
look at post-school outcomes, if you grew up in a small town and
you went to high school and you never saw kid with a disability and
you went to college and you come back home and you open a business,
When I walk in trying to get my friend with Down syndrome a job,
what's chances you're going to hire them?
The chance is zero, right? Because
you have no exposure, you have no history. Now go back to you have
an inclusive high school. You've got kids with autism walking
around in classes with you, kids with Down's syndrome, whatever.
Right. You've experienced that. You've grown up with it. They're a
part of the community.
Then you come back home, you open a
business.
What are the chances that you're
going to hire that kid? I've done it. It goes up exponentially.
Okay. But we can't you can't keep doing this isolated model and
expecting that the data is going to change,
Because it's not. I mean, we've got
30 years of that data, right? And so one community, one school at a
time, understanding that that's what moves the needle for
kids.
And, you know, I've seen I've seen
it happen and I've seen it happen.
you know, that's how we do it.
There'll be companies out there who
are going to try to sell you a self-determination curriculum, and
you're going to go to this workbook and there might be a good
activity in there, but it's not what it's about, sometimes we
overcomplicate it, and it doesn't have to cost any money. I
mean, it's really just opportunities and opportunities and
inclusive mindset cohesion between families and schools and
community. if you do enough digging and you look for positive
post-school outcomes, that's the equation right there.
Think I have to stop myself from
like standing up and giving you a standing ovation because that is
just a it's so spot on and it's just baffling how we don't realize
that yet in our society and that we're still kind of stuck in this
cycle of what we're doing.
We're almost out of time. I want to
hear before we go, just one success story, or two or,
whatever, sum up something that just makes you happy when you look
back at all the work you've done.
Yeah. So I'll tell you story of
Daniela.
She was at an elementary age.
She was diagnosed with a learning disability.
They stuck her in self-contained
classes.
She got to high school. She was
still in that self-contained model and got exposed and determined
and said, Well, want to go to college? Like I've seen kids with a
learning disability who are in college. And she was
significantly behind academically because been in self-contained
K-8.
She fights the counselor, she fights
the school, she gets into the classes, she graduates, she gets
accepted into a college, she makes it through college, she gets her
master's degree, and she's now a lead teacher teaching in an
elementary school in an inclusive model, working with students with
autism.
I mean, that's that's it, right? The
sad part is that she's got to fight counselors and fight
educators,
To get access to it. Look, I can
tell you ten of those exact same stories. We've got another
student, Ben, on the autism spectrum. His parents tell the story of
he woke up one day and he's 16 and going to be out of the house in
two years.
And they're like, this kid
can't cook, this kid can't do laundry. We've been so focused on the
every day survival that we have on any future planning. And Ben
starts participating in on determined, learns how to advocate,
learns how to kind of take charge, learns how to set goals, decides
he wants to his special interests. His military history, gets into
college majors in history
currently in grad school about to
graduate.
opportunities support along the way
a group to pick them up when when he I you know for Ben in
particular he had some significant social deficits like a roommate
in college like there is a lot of work put into that and it still
didn't go well.
But we figured it out.
And so this idea that you know,
exposure, support setting the bar high, in life comes at you quick,
You blink and your kids are 18.
I mean, people told me that and I
didn't believe them. And here I am with a 16 year old and a 17 year
old.
so life comes at you fast.
Ain't that the truth? Yeah, my my
baby is eight. Just baffles me. My baby where I can. I'll put
all the stuff in the description so people can go to
links.
But just before we go, where can
people find you in? But then also say someone's listening
in
Oregon and they want to know more.
Where can they find out more about implementing this in their
state?
Yeah. So the easiest is just go to
the on the Sherman website and then we have a contact page on
there. You can find me directly or you can, email the project
directly the Gmail is on the website.
But again, you know, I've worked
with close to 40 states. What we kind of do is we look at where
whether your school, a school district or a State Department, where
are you currently, where do you want to be? And then we kind of
craft an individualized plan to make that happen, right? Because
there's a lot of different routes to go for
self-determination.
And so what what specifically what
does your data look like? What are you trying to do? And so we have
those conversations and we go from there.
you know, besides just the website alone, everything's free, everything's downloadable. look at it and you're good to go, just take our stuff and go and we just ask that, hey, tell us your story so we can highlight you.
Amazing. John, thank you so much. I
already have ideas for having you on again and talking about more
things. I it's been just fantastic having you.
I appreciate the opportunity. Thank
you.
and thank you listeners for joining
us. We're just getting started with this podcast and can't wait to
bring you more.
Please rate review and
share and tell us what you want to hear.
We've got tons of topics in the pipeline and are always welcome to ideas. This is the Odyssey Parenting, Caregiving, Disability. I'm Erin Croyle. We'll talk soon.