The buzz in Special Ed is the new alternate assessment coming down the pike. Well, I worked on the project this summer. It is going to be wonderful! Imagine, a computer adaptive test for students with significant cognitive disabilities? It's in the works.
What's a Dynamic Learning Map?
What teachers say about the Dynamic Learning Maps?
DLM Project Updates
Self-directed Learning Modules for Teachers by DLM
Everything you need to know about the new alternate assessment in Kansas.
Wednesday, September 11, 2013
Sunday, April 14, 2013
Advantages to Autism
So one of my son's friends posts on Facebook, "in my opinion Autism is worse than cancer." His friend has PDD-NOS. This friend never had to deal with being non-verbal for his young life like my so did. As a teen, I am guessing this friend also has not watched their grandmother battling breast cancer as we have either.
I told my son, feel free to reply that that you strongly disagree if that is how you feel.
It is how I feel, my so stated in his pragmatic tone of voice.
Furiously he types on his iPhone into Facebook.
Why do you disagree, I ask.
Because there are advantages, he says.
Like what?
He says, I think in pictures. So I can build battle mechs or giant robots in Google sketch up from nothing in less than a week. He smiles to himself.
Plus I rather enjoy echolalia. It's a joy in my life and he laughs to himself. Then starts his internal repertoire that I am sure is his own ongoing comedy skit.
While I type this he finishes his post to Facebook.
He wrote: As a person with autism, while autism comes with disadvantages, it does come with advantages. People just have to find these advantages within themselves. For example, my autism lets me see in pictures and I have used this ability to build giant robots with 3-d modeling software in less than a week.
He had me grammar check it for him. I do so without changing any of his words.
Now he's onto funny posts on the interwebs, laughing to himself.
It is I, the mother, who can't let this go.
Autism is not like cancer. For a person with Autism does not know what their life would be like without autism. If you took it away from them they would not think it was a gift from God as many people with cancer would. A person can lead a normal life and then by struck with cancer. They may even heal. Carry around scars and be stronger for the cancer that came and went. They may have had lasting friendships with no trouble. May have achieved in school, had a career, marriage and family without any strife what so ever.
As a mother I look to the future for my son with uncertainty. My husband and I plan for our son to live with us as long as
His friend posts back: I'm probably the most higher functioning side, but so am I. And yes there are advantages, but you don't have a choice, you take the disadvantages and what advantages that come with it.
What do you want to post back, I say. Do you agree?
Hmm as he eats away part of a baguette: Well I do agree that we don't have a choice in the matter, but we have to work with what we got here.
I battle internally with giving him my thoughts on that matter or letting him tell me more of his.
So are you going post back, I ask.
Humph he says scratching at the gap between the leaf and the wooden table. He checks his Facebook again.
I wonder if I should unfriend his mother. It is difficult to be a child of autism. It is just as difficult to be a mother of a child with autism. I have heard this mother scream and yell at her son that is my son's friend. I have heard her curse his PDD-NOS. I wonder if this boy curses his neurological difference because of his mother or his own actuality.
My son posts: while we don't have a choice in being autistic, we have a choice in making the best with what we've got.
Someone else posted before me, he says. It's really long and he read it aloud to me.
He asks, can I like a strangers post.
Yes, you can even send them a Facebook email and tell them that you saw their post. You have autism too and they might turn out to be a good friend, says I.
I kind of have a rule of not being friends with people on Facebook unless I know them in the real world, he says.
I try to explain about making friends via the Internet and how it can be helpful even if you never meet them in real life. How having autism in a smallish town, he may not get a chance to meet someone who sees having a neurological difference as a good thing. He goes silent.
My mom-ness pops up and I think, he's a good boy. I've bounced onto one his hard and fast rules and there is no way he is going to change his mind. This is an absolute. Yet he loves me too much to argue. The Love and Logic I've used for years is evident in this. Yet, because of the autism, he can't quite voice it. So he moves onto his homework that is next to his breakfast plate. He asks me if the Planet Comicon flier should be recycled or if I want to keep it.
He moves on. This is done for him.
As a mother this is not done for me.
I struggle with whether I want him to be with more people such as himself. I struggle with how others view him. I struggle with when to push against an absolute in his mind and when to leave it alone. Should I have sent him to autism summer camps? More like, should I have forced him to leave home to go stay a week with strangers in a strange place and strange foods where he feels powerless? No, I say to myself. Let him be who he is.
I told my son, feel free to reply that that you strongly disagree if that is how you feel.
It is how I feel, my so stated in his pragmatic tone of voice.
Furiously he types on his iPhone into Facebook.
Why do you disagree, I ask.
Because there are advantages, he says.
Like what?
He says, I think in pictures. So I can build battle mechs or giant robots in Google sketch up from nothing in less than a week. He smiles to himself.
Plus I rather enjoy echolalia. It's a joy in my life and he laughs to himself. Then starts his internal repertoire that I am sure is his own ongoing comedy skit.
While I type this he finishes his post to Facebook.
He wrote: As a person with autism, while autism comes with disadvantages, it does come with advantages. People just have to find these advantages within themselves. For example, my autism lets me see in pictures and I have used this ability to build giant robots with 3-d modeling software in less than a week.
He had me grammar check it for him. I do so without changing any of his words.
Now he's onto funny posts on the interwebs, laughing to himself.
It is I, the mother, who can't let this go.
Autism is not like cancer. For a person with Autism does not know what their life would be like without autism. If you took it away from them they would not think it was a gift from God as many people with cancer would. A person can lead a normal life and then by struck with cancer. They may even heal. Carry around scars and be stronger for the cancer that came and went. They may have had lasting friendships with no trouble. May have achieved in school, had a career, marriage and family without any strife what so ever.
As a mother I look to the future for my son with uncertainty. My husband and I plan for our son to live with us as long as
His friend posts back: I'm probably the most higher functioning side, but so am I. And yes there are advantages, but you don't have a choice, you take the disadvantages and what advantages that come with it.
What do you want to post back, I say. Do you agree?
Hmm as he eats away part of a baguette: Well I do agree that we don't have a choice in the matter, but we have to work with what we got here.
I battle internally with giving him my thoughts on that matter or letting him tell me more of his.
So are you going post back, I ask.
Humph he says scratching at the gap between the leaf and the wooden table. He checks his Facebook again.
I wonder if I should unfriend his mother. It is difficult to be a child of autism. It is just as difficult to be a mother of a child with autism. I have heard this mother scream and yell at her son that is my son's friend. I have heard her curse his PDD-NOS. I wonder if this boy curses his neurological difference because of his mother or his own actuality.
My son posts: while we don't have a choice in being autistic, we have a choice in making the best with what we've got.
Someone else posted before me, he says. It's really long and he read it aloud to me.
He asks, can I like a strangers post.
Yes, you can even send them a Facebook email and tell them that you saw their post. You have autism too and they might turn out to be a good friend, says I.
I kind of have a rule of not being friends with people on Facebook unless I know them in the real world, he says.
I try to explain about making friends via the Internet and how it can be helpful even if you never meet them in real life. How having autism in a smallish town, he may not get a chance to meet someone who sees having a neurological difference as a good thing. He goes silent.
My mom-ness pops up and I think, he's a good boy. I've bounced onto one his hard and fast rules and there is no way he is going to change his mind. This is an absolute. Yet he loves me too much to argue. The Love and Logic I've used for years is evident in this. Yet, because of the autism, he can't quite voice it. So he moves onto his homework that is next to his breakfast plate. He asks me if the Planet Comicon flier should be recycled or if I want to keep it.
He moves on. This is done for him.
As a mother this is not done for me.
I struggle with whether I want him to be with more people such as himself. I struggle with how others view him. I struggle with when to push against an absolute in his mind and when to leave it alone. Should I have sent him to autism summer camps? More like, should I have forced him to leave home to go stay a week with strangers in a strange place and strange foods where he feels powerless? No, I say to myself. Let him be who he is.
Sunday, February 10, 2013
Parenthood: Rights & Advocy
As a teacher, I work for the school district that employs me. I must follow their guidelines and their rules for writing and implementing IEPs (individual education plans). Having worked in 3 districts now, I know that each district does things differently. These 3 districts do things even more differently than my home district does ( where my own children who have IEPs go to school).
That being said, you are the parent. There is no greater voice or resource than you on your child. The special Ed teacher is the expert on finding ways to adapt the curriculum to meet your child's needs. The regular Ed teacher is the expert on the curriculum and the regular peers. The LEA (local education agency) -- usually the principal-- is the expert on what the district has to offer your child.
YOU are the expert on your child.
NEVER let anyone convince you that the other 16 hours you spend during the week, 48 hours on the weekend (not counting breaks, illnesses, and holidays) are not valid. You gave birth to your child. You carried your child. You raised your child. You will be there for your child when this set of teachers transitions your child to the next set of teachers. You are the constant!
In mathematical terms you are the x variable in the equation: y=mx+b
Y being your child's potential, m being your child's personality, disability,and abilities, b is their education. We teachers are merely and additional part of the equation. Parents multiply their child's potential! Parents make the difference!
As a special Ed teacher, I love active parents. I love having a parent come in and observe my work. I love their feedback! I work to please the student first and the parent second. Usually when I work to get growth out of the student, the parents are happy! Unfortunately, districts can mess that all up with their own rules, regulations, and finances. School budgets are a mess now, especially with no one wanting to pay the taxes necessary to educate the regular student, not counting the exceptional students!
Know as a parent that your view points are valid. Insist that your child get the appropriate education to help your child reach the regular curriculum. Every child can be taught. Every child can learn. The special Ed teacher's job is to assess and ascertain how to get your child there. Not every child can learn at the same rate as their peers, but that is what the IEP is about! The IEP is the plan to get your child on grade level. It is not simply enough for an IEP to be functional (life skills, daily activities, peer integration)! But an IEP must address the academic needs as well! How will this child be able to do mathematics? How will this child be able to read?
YOU, the parent have a right to ask these questions.
For further references who validate the importance of the parent check out:
The U.S. Department of Education, Office of Special Education Programs’ (OSEP’s) IDEA website: http://idea.ed.gov/explore/home
Parents' Guide to the Family Educational Rights and Privacy Act: Rights Regarding Children’s Education Records: http://www2.ed.gov/policy/gen/guid/fpco/brochures/parents.html
This is where you can find your official copy of parents rights in the state of Missouri:
http://dese.mo.gov/se/parentresources.html
This is where you can find your official copy of parents rights in the state of Colorado:
http://www.cde.state.co.us/spedlaw/download/2011ProceduralSafeguards.pdf
This is where's you can find your official copy of parents rights in the state of Kansas:
http://www.ksde.org/Default.aspx?tabid=2832
This is where's you can find your official copy of parents rights in the state of Arkansas:
https://arksped.k12.ar.us/sections/dss.html
This is where you can find your official copy of parents rights in the state of Nebraska:
http://www.education.ne.gov/sped/parentinfo.html
This is where you can find your official copy of parents rights in the state of Iowa:
http://www.educateiowa.gov/index.php?option=com_content&view=article&id=574&Itemid=510
Wright's Law is a disability advocacy law firm. They have a lot of plain English information about parents rights in the form of webpages, pamphlets, and workshops.
http://www.wrightslaw.com/
That being said, you are the parent. There is no greater voice or resource than you on your child. The special Ed teacher is the expert on finding ways to adapt the curriculum to meet your child's needs. The regular Ed teacher is the expert on the curriculum and the regular peers. The LEA (local education agency) -- usually the principal-- is the expert on what the district has to offer your child.
YOU are the expert on your child.
NEVER let anyone convince you that the other 16 hours you spend during the week, 48 hours on the weekend (not counting breaks, illnesses, and holidays) are not valid. You gave birth to your child. You carried your child. You raised your child. You will be there for your child when this set of teachers transitions your child to the next set of teachers. You are the constant!
In mathematical terms you are the x variable in the equation: y=mx+b
Y being your child's potential, m being your child's personality, disability,and abilities, b is their education. We teachers are merely and additional part of the equation. Parents multiply their child's potential! Parents make the difference!
As a special Ed teacher, I love active parents. I love having a parent come in and observe my work. I love their feedback! I work to please the student first and the parent second. Usually when I work to get growth out of the student, the parents are happy! Unfortunately, districts can mess that all up with their own rules, regulations, and finances. School budgets are a mess now, especially with no one wanting to pay the taxes necessary to educate the regular student, not counting the exceptional students!
Know as a parent that your view points are valid. Insist that your child get the appropriate education to help your child reach the regular curriculum. Every child can be taught. Every child can learn. The special Ed teacher's job is to assess and ascertain how to get your child there. Not every child can learn at the same rate as their peers, but that is what the IEP is about! The IEP is the plan to get your child on grade level. It is not simply enough for an IEP to be functional (life skills, daily activities, peer integration)! But an IEP must address the academic needs as well! How will this child be able to do mathematics? How will this child be able to read?
YOU, the parent have a right to ask these questions.
For further references who validate the importance of the parent check out:
The U.S. Department of Education, Office of Special Education Programs’ (OSEP’s) IDEA website: http://idea.ed.gov/explore/home
Parents' Guide to the Family Educational Rights and Privacy Act: Rights Regarding Children’s Education Records: http://www2.ed.gov/policy/gen/guid/fpco/brochures/parents.html
This is where you can find your official copy of parents rights in the state of Missouri:
http://dese.mo.gov/se/parentresources.html
This is where you can find your official copy of parents rights in the state of Colorado:
http://www.cde.state.co.us/spedlaw/download/2011ProceduralSafeguards.pdf
This is where's you can find your official copy of parents rights in the state of Kansas:
http://www.ksde.org/Default.aspx?tabid=2832
This is where's you can find your official copy of parents rights in the state of Arkansas:
https://arksped.k12.ar.us/sections/dss.html
This is where you can find your official copy of parents rights in the state of Nebraska:
http://www.education.ne.gov/sped/parentinfo.html
This is where you can find your official copy of parents rights in the state of Iowa:
http://www.educateiowa.gov/index.php?option=com_content&view=article&id=574&Itemid=510
Wright's Law is a disability advocacy law firm. They have a lot of plain English information about parents rights in the form of webpages, pamphlets, and workshops.
http://www.wrightslaw.com/
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