Showing posts with label Inclusion. Show all posts
Showing posts with label Inclusion. Show all posts

Monday, September 21, 2020

Create a bill that ensures Personal Care Attendants earn a living wage #EndSubminimumWage

Create a bill that ensures Personal Care Attendants earn a living wage #EndSubminimumWage
 
Are you going to create a bill that ensures Personal Care Attendants earn a living wage?

Did you know Attendants are paid less than a fast food employee?

I can not find an attendant and without one I can not get out of bed or clock in for work at home.

Paying subminimum wage must end now. My care and contribution to society is worth paying an attendant a living wage.




Watch my #WhatWeNeed video:
https://youtu.be/Scd8PQjqe6k

Email me to join the movement to end subminimum wage. View email address HERE

#VirginiaCARESforDD
#WeAreEssential
#WhatWeNeed
#DoYourJob
#GetBackToWork

Friday, July 18, 2014

Ask Not What Your Country Can Do To Include You, Ask What You Can Do To Include Yourself In Your Country

I got nearly 100 likes on Facebook when I posted this, so I decided to Blog It!



I heard behind me at my local Recreation Center (pool) today,
“She can’t talk.” in a young sweet voice.

I turned my wheelchair around and in a kind cheerful tone said, 
Yes I can. How are you doing today?”

A few seconds went by, The four young girls started smiling. The staff person with them said they had went into the deep end of the pool.

“Was it fun?” I said with a smile.

They nodded and one of them said yes.
I love kids, they say what is on their mind. so simple and without malice.

All you have do is show up regularly. The general population will get used to you. 
it’s no big deal.
Relationships and even friendships might form. Wow, what a concept.


ALSO this makes me ponder and remember.
- This young girl couldn't have been more than 6 and already the "can't" stereotype had set in. I can't wait for a couple of more weeks until Youth Leadership Forum ... a whole 5 days of telling them "You Can".

- Today I’m reminded of the reverse lie I told myself in tough situations when I was young. 
I told myself, “Ivy, you do belong." 
I really did belong that's why I’m calling it reverse. Fake it until you make it. Shame on whatever people or situations that made me reassure / lie to myself.



In the Facebook comments I said:

I hope parents don't 'unteach' my example. lol! It's the adults you have to worry about you know.
&
As I think back on this moment today, it was so awesome the staff person helped the convo along. She KNEW what I was up to. Major kudos to her.
Either I got there a minute too late or I wasn't listening until I heard CAN'T but I’m curious why the young girl said that in the first place? So cute! I’m very tickled by this little moment in time.


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Tuesday, October 8, 2013

Vanguard Landing, a choice or same pattern of segregation in Virginia?

I spoke a city council meeting 10.8.13


As a person with a disability and was once employed Moms in Motion, a waiver facilitator that assist many Virginians with disabilities live in their community, I'm confused and angry over the the expense and the intent the City has shown for Vanguard Landing.

While I realize people deserve home care options, I believe seclusion and segregation is never the answer. Those two factors are dangerous. If you were to look at the history of people with disabilities, you will find, again and again, a pattern of segregation and abuse. I'm not only referring to physical abuse but corruption of the internal care system that will surely happen in the future.

Why are we continuing to make the same mistakes of the past? Why do the founders of Vanguard Landing think this is best option, when the US Department of Justice came into Virginia and said the (secluded) Training Centers had to be closed immediately? Isn't that a heads up that these type of places are dangerous?

The answer to caring for people with disabilities can be found by studying Disability History.
I invite everybody listening right now to my Disability History presentation on October 21st at 6:30 in Norfolk at Hope House hosted by The Arc of South Hampton Roads. If you study Disability History you will see segregation leads to abuse. Stop profiteering from caring of people with disabilities. There are current practices being used now to care for people with disabilities in their homes. It cost less to serve an individual in their home. Viruses such as COVID-19 kills at an increased rate in segregated settings such as Vanguard Landing.

I believe in small group homes sprinkled throughout our community.
I believe in strengthening home care support so anybody with a disability can live at home.
I believe everybody should live in their community, near or with their loved ones.
Segregation is not the answer. It never was and never will be.
 
Segregation is not the answer. It never was and never will be. Do not fund Vanguard Landing.

Please look at the Facebook page that I and another advocate made:
https://www.facebook.com/advocatesagainstvanguard



A conversation on my Facebook

__________________________


Released March 9, 2014
New York Times Documentary: The Men of Atalissa

Produced by Kassie Bracken, John Woo and Dan Barry, "The Men of Atalissa" is the evocative, haunting story of a few dozen men with intellectual disability who lived in an old schoolhouse on top of a hill. For more than three decades, they were an integral part of an Iowa farming community, worshipping at the local churches, dancing at the local bars, working at a nearby turkey-processing plant; they were affectionately known as "the boys." But none of their neighbors knew of the day-to-day abuse the men endured in that schoolhouse on the hill.

The Iowa community had no idea of the abuse going on inside the bunkhouse.
“I’ve been in the building back when it was nice.”
“Never heard them complain.”

Video  |   Article   |    A conversation on my Facebook


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Tuesday, June 4, 2013

To explain or not to explain: That is the question


When talking to the public don't explain your disability at great length and then turn around and ask them to treat you like everybody else.
It's a very contradicting message and I would love to see people with disabilities (and parents) stop using this way of introducing themselves.

Your disability is a part of you, but it does not define you. It's not the most important thing about you.

If you start a conversation off with your medical diagnosis and rattle off how or why a disability effects you, I feel strangers will just compile the information into a large pile of CAN'T. You are building your own mountain that you will have to scale. People with disabilities have enough barriers, why create them with words?

A person is much more than their disability. Choosing how you communicate with the public that will convey that. Stop explaining yourself away. Stop self-identifying as a label. 

When meeting a person for the first time, find common ground with them. Friends heighten quality of life. Friendship can form under any shared interest. If the first thing out of your mouth is 'disability', however honest and clear you describe it it will create divide between you and the potential new friend.

Do you hear people say, "Hello. My name is Bob. I have high blood pressure."? No, you don't. Leave the medical labels in the doctors office. Even then doctors can be wrong, or medical diagnoses are always changing, or medical discoveries are made, so why bother trying to stuff yourself into a pre-labeled box?

I used to tell anybody and everybody about disability, in hopes of if people understood then then they would accept. Explaining yourself into oblivion does no good. It takes and leaves you with nothing. It dehumanizes you. There is a time and place to explain your disability.

I do believe in teaching awareness in a careful all encompassing way. 
This disability month, that disability month…. It's starting to really get on my nerves. How much awareness does a person need to be beat over the head with? I'm sure by now, the bombardment of awareness has turned into a dull mind-numbing roar that the public has tuned out. 
Instead of a particular disability awareness plug/PSA, advocate how people with disabilities should be treated. BUT then when doing that, you'll see the disabled community run into this paradox:

"Just like you." 
OR 
"Different. It's ok to be different." 
If it's confusing to me, our children must be baffled!

I'm sure we all want to be accepted. We want a space at the family table, so to speak. In that aspect everybody on earth is the same. The truth is we  each have our differences and as humans we are intelligent enough to include everybody.

______________


"As we think so shall we speak, as we speak, so shall it be.”

People First Language is a way of speaking about people with disabilities in a positive manor that does not put disability in the spotlight. Too often the disability takes over conversations when the true focus should be on the person's likes, needs, wants and life goals. The way we choose to speak is so important, because it forms the world around us.
People First Language also changes how we describe assistive devices.
For example: She's in a wheelchair Changes to: She uses a wheelchair.
People First Language may seem like a small thing, but if more people used it attitudes towards disabilities will change for the better. So be sure to try and use it and maybe just by listening, somebody near you will start using it too.

Here's a fabulous webpage that gives more detail about People First Language:
http://www.gcdd.org/news-a-media/people-first-language.html


______________


When reaching out for support or advocating for your child, at what point can it be damaging to social perception of disability?

A Facebook chat about two articles:
Paying For My Special-Needs Child
&
Why We Published A Photo Of A 16-Year-Old In A Diaper

_____________


“I stopped explaining myself when I realized people only understand from their level of perception.” 

_____________

Stop blaming the disability. Take it off your list as the #1 go to reason when there is a problem.
Facebook chat
 


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Thursday, November 8, 2012

People with Disabilities and the Republican Party – Election 2012


If you were only looking at the presidential debates in terms of people with disabilities, here's how it added up:

Obama mentioned either people with disabilities, or disability issues around four times. Each time he did so, it was in a positive light.

Romney only mentioned 'the disabled' once. (He couldn't even use People First Language as Obama did.) What added to the offensiveness was when he said something like, “The disabled will always be taken care of.”

Fuck that! I don't want to be taken care of, I want a job!
The party who preaches that the government and tax payers shouldn't help people can can help themselves, are such hypocrites and/or out of touch with people with disabilities!
I can help myself, I can be employed. In fact, I am employed with Moms in Motion. A Medicaid Waiver Facilitator.

I wouldn't be a so-called drain on society if more focus was given to education and employment for all. But inclusion of students with disabilities in school doesn't seem very important to this country. It's all about seclusion so we can provided services to 'help' them. Services that the Republicans distain and want to cut. If there was more inclusion, many of these services wouldn't be needed!

It's extremely offensive to me, a person with a disability when I hear I “need to be taken care of” and then to hear that I'm a “freeloader” that is dependent on the tax payers that work hard for their paycheck!

I'll give you a need....
The Republicans need to get with it on so many issues. They are so out of touch with so many Americans.


P.S. People with disabilities are the largest minority group in the US.

___________


A report by Youth Transitions Collaborative
Power in Numbers: A Profile of American Voters with Disabilities
July 12, 2013



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Thursday, October 6, 2011

Virginia Employment First Summit - Virginia Beach October 4-5 2011

First I'd like to say, I'm grateful to have gone. The ARC gave me a scholarship. It was good to hang out with friends I don't see often and awesome stay in an ocean front room. As a self advocate I was urged to attend even though I was reluctant to go. Turns out my icky feelings were justified.

The summit did not renew my faith in employment for people with disabilities. My same opinion was firmly held in place; All the agencies (the service system) finds jobs for people with disabilities. If all people with disabilities had jobs THEY wouldn't. So at the start it's flawed.

I had been out of that loop for over ten years and it makes me furious to see 'they' are still spewing the same bullshit! Though there were good concepts sprinkled in here and there. Even my personal aide who knows nothing of that field pointed out twisted policies she overheard. I'm grateful I was able to give a bit of my opinion but just know I had to bite my tongue a lot!

One example of a backwards policy they were talking about was the concept of paying a co-worker to help the person with a disability on the job.
Who wants a friend that's paid for?

Not enough self-advocates were at the summit. The people who were there were on the same side of 'the game' patting themselves on the back, blowing hot air, and painting pictures of happy unicorns flying over rainbows. Who was missing? EMPLOYERS.

Inclusion in the classroom and teaching awareness and rights (in school curriculum and at businesses) was mentioned a little but not enough, which DO effect employment so much I believe. No talk of changing people's perception of disability, which I think is the linch pin to everything. It also seemed backward to me, no talk of inclusion in school but then 'they' expect integrated employment to just happen? Good luck with that!

Another thing that bothered me was somebody said, "Go find a person with a disability who wants to work and then go back to your network and find them work."
NO! Your network is not my network. Swamping is not going to work. Every person alive needs their own social network to draw from. If you're being PAID to refer people it takes the creditability out of it. Right?
Inclusion in the classroom will build social network. Segregating kids with disabilities has to end for many reasons, but simply for the reason of employment. In the real world for anybody many jobs are found by social networking.

There was hardly no talk of college at the summit which made me mad but they talked about person centered planing and about setting goals early in middle school which will cover college for some students with disabilities. If person centered planning is done right it will bypass putting people with disabilities in convenient, over used job categories. These present categories are so limiting and demeaning. As some call these categories the three f's: filth, food and flowers. I realize some people with disabilities can only do these, but we all don't have to! Really if you're creative about it ANYBODY with a disability can do jobs way beyond the three f's. Rather in employment or education, the expectations need to be raised for people with disabilities.

Tax dollars are paying for this, a twisted broken service system! The employment summit meant well but the people there are not thinking straight. I felt very out of place. Wait, am I the crazy person here or are they? I had that same feeling years ago when I was wrapped up in employment services. It is NOT a good feeling.

UPDATE 10.18.11: Kathie Snow author of Disability is Natural featured this (stay out of job services) on her 'Your stories' webpage Here



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Tuesday, August 9, 2011

Inclusion: My experience as a student

Inclusion: My experience as a student
at
Regent University

speech video HERE OR HERE
slideshow video HERE


Hi, it's such a honor to be here today with you. My name is Ivy. I'm I disability rights advocate. I went to public school in the 80's and 90's in Williamsburg James City County. I went to Special Ed preschool but after that I went to regular classes with my non disabled peers. Back then it was called mainstreaming. Today the model is is a little different, it's called inclusion. I had an aide one on one to write for me and handle my books. She was there for me only. With inclusion I understand the Special Ed teacher is supposed to work together with the teacher to modify curriculum for students with disabilities.

I had an IEP and one of the things it stated that I was to have a computer with me at all times. Now this was the 80's. the computer was big and heavy and even though it was on a desk with wheels. Turned out that it didn't work for me to do my classwork on, because of time limits. Plus at that time Assistive Technology isn't what it is today. I didn't have the equipment to speed up my use of the computer. Truth be told I didn't the latest technology until I graduated high school at Woodrow Wilson Rehab.

IDEA is a United States federal law that governs how states and public agencies provide early intervention, special education, and related services to children with disabilities. There was no fighting over my IEP. I now see how lucky I was that there was no opposition to it. I'm not sure if it was because it was still early after the IDEA/Education for All Handicapped Children Act of 75, or if it was because I was surrounded by smart opened adults who saw my potential. I'm sure it helped that my disability was physical and not mental.

Inclusion is a collaboration to teach children, there is no set standard model. I suppose you can learn techniques, but what works best for one child may not and probably won't work for another child. You have to be open minded, patient and be very creative. In the inclusion process adults will be challenged to give their best and that effort will positively benefit every child in the school.

Teachers are molding tomorrows world, right? Think about the effects of inclusion in the long run. The disability employment rate is horrible and will remain horrible until students with disabilities are included with their peers in school. I believe teachers should think about these goals when educating children with disabilities: Preparation for employment, or college, or independent living. Sometimes all three, or a combination applies to a student. Parents need to be aware from the start if the path is going to lead to a regular or a modified high school diploma.

One thing that excites me about inclusion is when it's done well it will stop the need to pull some children out, for say reading or math help. Pulling a child out is not good. it singles them out from their peers, and disrupts attention spans. I was pulled out in elementary some. I hated it. Just think, how well does it benefit the child if the child doesn't even want to participate? A child shuts down when they're angry or embarrassed. It can be embarrassing to be pulled out of a class.

I had many creative minds in my education. from homemade splints to homemade worksheets that made it easier to trace my name. My teachers, therapists and my aide were always coming up with something so I could be included in class.

There were times where my peers helped me. At lunch my friend helped me eat. I used a special designed block. My aide and her husband designed it for me. I still use it to this day. My friends would set a sandwich or a piece of pizza on the block and I'd eat at my own pace. The block was eye level. It had a juice box holder on the side. Being alone with my peers was critical in my development. It allowed for bonds to be formed that never would have happened if there was an adult present. I remember in elementary school one of my aides kept following me around during recess. It took some courage for me to ask her to back off. She took it well thank goodness. Children act differently towards one another when there is adults around.

I did get teased some, but nothing like the bullying I hear about today. I'm sure it helped that there was my aide around for a lot of the time. I can't imagine being bullied by todays kids. The teasing I received didn't bother me much. Maybe because it never lasted long or my personality handled it well. I believe if inclusion is started young children with disabilities in the classroom will be the 'norm' as they should be. Bulling often exist because of perceived differences. Friends will stick up for friends when they are being bullied. Bullying can not be the sole reason not to include students with disabilities in the classroom. Bullies will do what they do regardless if there's a child with a disability present or not. The disability itself should not turn into the scapegoat to reason of bullying. Address the root of the problem, which is the bullying not the disability.

Some of my accommodations I can remember were, my one on one aide, PT and OT during PE, a homemade splint to keep my finger straight for computer typing in kindergarten also a board with cutout holes for the keyboard. Later on a head stick which I just LOVED wearing around teenaged boys in high school computer class. Now I have a Jouse that's 100% faster that mounts to the desk and not me. Book holders never worked. Either they were too bulky to carry or paperback books wouldn't stay open. The point is we tried them though. In high school I left classes 5 minutes early because the school was overcrowded and hallways became a nightmare. On some occasions I did have to maneuver through the crowd kids would line up and walk behind me because I happened to part the sea of people with my power chair which was funny. I gave answers verbally, so I whispered a lot. I took my test in the hallway. It wasn't until the new middle school opened until I had a room to go to take tests. In high school it was back to the hallway. My first power chair came from my IEP. I got it in kindergarten. Of course it belong to the school and I couldn't take it home. I didn't get my own power chair until third grade.

Inclusion needs the cooperation of teachers, student and parents. There was a time in my education where choices were made that had a negative outcome for me. Early in school when it was still simple enough I was teamed up with a friend of mine to complete classwork. In 8th grade science it was my friend Stephanie. She was so smart it was incredible. I did contribute to the class work, but the trouble happened when we moved to 9th grade. It was clear Stephanie needed to be placed in advance science, but did I? But that's what happened and it turned out to be a big mistake. I had failing grades for 3/4 of the year, before switching to regular science. I tried my best. I loved the teacher, but I did not belong in advance science. After the switch I made B's instead of F's.

Another thing that is positive about inclusion is children from the same family can go to the same school. No more segregating children into separate schools. Special Education is a service not a place. My younger brother is three and a half years younger than me. There weren't a lot of times we went to the same school. I did looked forward to riding the bus home with him and the neighborhood kids. There was a few years here and there when I rode the special ed bus. I hated it! I was alone by myself on a long ride because I lived in the country. I've heard bad stories about children with disabilities riding a special bus because they had to go to a special school. When there is no other eyes around to witness bad things can happen. Nothing bad happened to me but I do remember the bus aide and driver talking about unappropriated things and it gave me nightmares. Also I remember nightmares about being on a run away bus all by myself. Siblings should go to the same school and ride the same bus.

I graduated high school with a regular diploma. My IEP team knew from when I was young a regular diploma was my goal. We used the IEP once to allow for no foreign language for me and I still would earn a regular diploma. I took a year and a half of latin in high school. It was not good. Do I feel I sometimes 'cheated'? Yes. But my aide was very adamant that no shortcuts were to be taken if it could be helped. I owe her a lot. She kept my education fair as possible. In high school assignments were more heavy. Later on she told me some of my teachers came to her because they had a hard time grading me. They weren't sure how to take into account my disability and my school work. My technology wasn't that great and it cause me to be slow. So in classes like computer often the teacher had to grade me on what I had done. It was tough and I feel the same problems when it comes to employment. A boss needs things done in time to meet the bottom line. It's just a fact. Some employees with disabilities need extra time. So how does that fit in?

In high school there was no such push for me towards college. I do believe in options and choices BUT WHAT SCARES ME and what happened to me was I got placed the easiest, safest, most exercised option. I was not challenged to go to college. I was placed in a vocational training with all the other kids with a disability. The vocational rehab gave out certificates, not degrees which is what I needed to be taken seriously in job interviews. It always puzzled me as to why all this effort and resources had been put into including me in public school just to be dropped after graduation? What a colossal waste! After high school I was too busy learning the ropes of organizing my independent living and my home care to worry about college. Years later I'm still learning how to manage my home care. Why is this not taught at Woodrow Wilson Rehab (Vocational Training) or better yet in high school? Why wasn't there somebody at my high school to help me plan for managing aides for college?

I believe children eyes are opened up to knew ways of thinking when students with disabilities are included in the classroom. In 8th grade computer class I used a stick that was attached to head gear to type. I used sticky keys and mouse keys to operate the computer. The numeric pad was used as a type of compass to move the cursor and to act as a mouse. One day the boy beside me said to me, “The way you're doing it is better. You can be more precise with the drawing because with my mouse it moves all over the place.” That made me feel better, because as I said before I was slow in computer class. It never occurred to me I may have had an advantage over my non-disabled classmates. We both taught each other something that day.

To this day it's not kids attitudes that are a barrier to me, it's adult's. Society has to change its perception of disability and a big part of that is how society chooses to educate children with disabilities. The first time I was made aware of perception barriers was in 6th grade. The teachers had to choose who they thought would do the best job showing the upcoming 5th graders around the school. I was chosen from my class. Apparently one of the Guidance Counselors thought otherwise. It hurt me very much. It was my first time I was aware of a person discriminating towards me. My teacher thought I'd be the best to show them around. I was chosen for a reason. Clearly this meant nothing to the Guide Counselor. On a side note, the Guidance Counselor was African American. I never understand why a group that was once discriminated against... and still is would practice discrimination towards another group? Long story short my aide strongly advocated for me and I got to show the 5th graders around school.

I've noticed the Principals that practice inclusion don't see it have anything to do with special education. They see as a way of educating their students on a whole. No one is singled out as getting a 'modified' education. To achieve to best education for a child the teacher, special ed teacher, the parent, and student should give their all. At times it can be hard working together. People must keep a level head.

Of course every child with a disability is not going to be able to earn a regular diplomas but teachers need to push every child to their maximum. The expectations for students with disabilities need to be higher. Some of us CAN go to college. Teachers need to recognize the potential in kids with disabilities. Teachers can open up the world to an amazing future if they push and expect more from students with disabilities.

Each child with a disability's education should be individualized. What works for one child may not work for another and that's ok. I hope you realize that's the case for children without disabilities too. Long term goals should be set early on. Does the future hold college, or are learning basic independent living skills more practical? At each IEP meeting the parent should be making sure if their child is being challenged. An IEP is a work in process and should be edited regularly. Inclusion a collaboration between, student, teacher, and parent at every IEP meeting. Don't have an IEP without the student present.

T/TAC online ttaconline.org is Virginia Department of Education's Training and Technical Assistance Centers serving children and youth with disabilities. Every principal, assistant principal and teacher should know about T/TAC. They provide services to increase the abilities of schools, school personnel, service providers, and families to meet the needs of children and youth.

I believe the end of segregating people with disables in society starts with inclusion in school. When children grow up together perceptions about disability change. I'm proof inclusion can work. I still keep in touch with a lot of my classmates. Recently I gave public comment on inclusion to my local school board. I had the opportunity to ask my classmates what it was like being in the classroom with me. They were kind enough to allow me to read their comments to the school board.

Inclusion has provided me with lifetime friends. That's a huge gift that has made my quality of life more meaningful. Friendship and health are the two most important things many different cultures say. Average friends of "typical" adults: 150. Average number of friends for adults with disabilities: 20 (and half are family, other half are service providers) By segregating children with disabilities from their peers it's depriving them the gift of friendship.

I've seen teachers and administrators get caught up on the logistics of inclusion such as having never ending conversations about the cost. That is important but meanwhile guess who is loosing out? …. the student waiting to be educated. There is no one size fits all to inclusion. You have to jump in, be open-minded, work together, be creative to reach success.

A good example of successful inclusion is in Montgomery County Virginia's public schools.
For your homework, rent and watch the documentary “Including Samuel”. Also go to youtube and watch the clip from that documentary about Keith Jones. Kathie Snow has excellent chapter on education in her book, “Disability is Natural”

Tuesday, June 7, 2011

Inclusion speech at local school board meeting

Hello. It's a pleasure to be here tonight. My name's Ivy Kennedy. I live here now but grew up in Williamsburg James-City County. I was included in class with my non-disabled peers Kindergarten through 12th grade. I had an assistant write for me and handle my books in class. I graduated with a regular diploma.

I believe if you're included in school, you will stay included throughout life. Inclusion is not impossible. I am proof.

Many of my friends with disabilities have told me they were not challenged in Special Ed. To quote they were given, “Busy work”. The bar of expectation needs to be raised for students with disabilities. All children in public schools deserve a quality education. I believe by including kids with disabilities it will benefit all kids.

Schools are mirrors of our community. By not including students with disabilities you are saying it's ok to segregate. This has to end. We as a society can do better.

The disability employment rate is horrible and will remain horrible until students with disabilities are included with their peers in school.

I had lots friends in school. I'm sure that I would not have had as nearly as many of them if I had been kept in a Special Ed classroom. Friends are the most important in life if you ask me and by keeping children in Special Ed you are depriving them of that gift. Young kids are so opened minded. If you start inclusion young bonds will develop. These bonds will protect kids from bullying and build a strong community.

I realize every child is different. I believe we have the brain power to be creative so every child can be included in the classroom. In the inclusion process adults will be challenged to give their best and that effort will positively benefit every child in the school.

People with disabilities have been around since the beginning of man. It's way pass time to stop segregating them. …..and it starts with our children.


________________

on 6/21/11 I went back to the school board.

I spoke at the last meeting on my experience with inclusion. I'll read a condensed version of what a few of my peers had to say about sharing the classroom with me. I have left their comments in their entirety with the clerk.

Joseph - If it wasn't for "Inclusion", I would not have had the chance to meet and work with such a wonderful person. Ivy was not the only person that had a disability or mental challenge that I attended classes with. It is amazing how well she got along with her fellow students, what she had learned and with her disability.

Joshua - I know having you in my life has affected the way I've treated disabled folks up to this point in life, and will for the rest of my life.

Danita - You showed and continue to show me a life full of friends, activities, education! Now as a parent of a child with a disability I look at (Ivy) as an example of how full my own disabled daughter's life can be.

Katie - Having you in class was beneficial to me, in that I did not look at you as being different from my other peers, which in turn, helped to mold my opinion of disabled people that I would meet later in life. You were part of the class, while you might have had different learning obstacles than I did, so did a lot of people in class.

Shannon - As I was growing up, I've always let what people say about my differences shadow my confidence. I am so glad that Ivy and I shared a couple of classes, lunch tables and graduated together. She has shown me that no matter what our differences, we can take the opportunities we've had and make them blossom in our own way.

Brandie – Others.... mainly adults viewed her as having a disability but not us! Being friends taught me life skills that not even the best college could have taught me … to have compassion and not turn a blind eye to those with a disability.

Stephanie - Just because people are in a wheelchair or are different doesn't mean they aren't awesome people. In fact most of these folks just as Ivy taught me are way cooler and more awesome than most other folks!

Christopher - No mater how bad of a day I had, seeing Ivy smile and the way she tackled life. Always made my day better.

Bertelle - (because of Ivy) I was inspired me to go into the career field of Rec. Therapy. My favorite part of that job is showing others with disabilities that they can do anything they want if they put their mind to it, just like (Ivy) showed me.

Billy - (Her disability) was no big deal to her...always positive. That positivity transcended through me and the rest of my classmates in ways immeasurable. She essentially provided me with the social gift of equality that I now use on a daily basis as an adult.

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