Lisa Blunt-Rochester: “To Be Able To Have The Luxury To Opt Out Is A Luxury”

Lisa Blunt-Rochester

At the Delaware Congressional education debate last evening, a question concerning state testing led to some very offensive comments from candidate Lisa Blunt-Rochester.  Senator Bryan Townsend was asked a question by a member of the audience concerning his fights with state testing at Legislative Hall and his endorsement by DSEA (the Delaware teachers union).  The question was confusing but it alleged that since civil rights groups stand by testing as an accurate way to measure the progress of African-American students, and he fought against the state testing, how would he respond to that? The question was read by one of the moderators, Nichole Dobo.  Townsend defended his stance on testing because the testing was being used for purposes it was not meant for.

By the time candidate Lisa Blunt-Rochester answered, the subject of opt out had already come up by candidate Scott Walker.  He indicated he does not support opt out, especially for students with disabilities and feels it is illegal.  I’m assuming Walker didn’t see the very atrocious scores students with disabilities had on the Smarter Balanced Assessment this year.  But I digress.  By the time the question came back to Rochester, this was her response, as I understood it, while I typed it as I was live blogging:

The original question was about civil rights.  She understands why some folks would opt out, but as a person coming from the Civil Rights movement, to not measure anything is a problem.  Opting out isn’t the issue.  We need to measure to know where we are discriminating.  We need to put our money where our mouth is.

This is what she actually said, thanks to videos shown on the DelaCore Leaders Facebook page:

So the original question was about civil rights organizations and their positions on state testing and the concern that you can’t have it, kind of, both ways.  I understand why some folks would want to opt out, but for myself, as a parent, also as a person who comes from a Civil Rights background, you have to measure growth.  Maybe that’s part of what the challenges folks were concerned about, what we were measuring.  To not measure anything is a problem, to be able to have the luxury to opt out is a luxury.  If we need to fix the test, let’s fix the testing.  But we do have to hold ourselves accountable.  In all the conversation about discrimination, we need to be able to measure, so that we know we are being discriminated against.  So, I think, you put your money where your mouth is.

This statement could be taken a lot of ways.  I see it as the same argument as other folks defending the civil rights groups statements as “it doesn’t matter how bad the test is, we still need that measurement.”  I’m sorry, but I can’t, won’t, and never will buy that logic.  First off, there is a cultural bias with the Smarter Balanced Assessment.  It wasn’t written for African-Americans, English Language learners, or students with disabilities.  It was written for white kids.  We see this with every single score release of standardized tests.  This isn’t new.  It has been going on for decades.

If Blunt-Rochester feels opting out is a “luxury”, an option that is truly open and is not illegal under any circumstances in Delaware, then by her logic we can all enjoy that luxury.  Parents don’t opt out because it is a luxury.  They opt their kids out of the state assessment, which in Delaware’s case is the Smarter Balanced Assessment.  They don’t opt out of MAPS, or SRI, or SMI, or final exams.  They opted out of the Smarter Balanced Assessment.  The test is long.  Parents and teachers don’t get the scores back on time.  Students aren’t even given the exact same test.  It is a test for accountability for schools.  This was said by Jon Cohen, who runs the American Institutes for Research (AIR), which just so happens to be the testing vendor for the Smarter Balanced Assessment:

When you use a test for accountability, you’re not really using it to measure the kid.  You’re using it to measure the school, or the teacher, or the district.  And you want that school or teacher or district to have an incentive to teach the full range of curriculum.

This statement was taken from a video that used to appear in an article about AIR on this very blog, but AIR changed the settings on it so it could not be embedded outside of their reach.  It is my contention they don’t want people seeing this video.  When talking about the computer adaptability of the assessment, Cohen very frighteningly tells viewers students are not receiving the same test.  The questions aren’t the same for every student.  I wrote in greater detail about this a few weeks ago.  For all the talk about resources and funding we need for schools in Delaware, the one question many candidates aren’t asking is where is the existing funding going?  In Delaware, we have given AIR well over $40 million dollars over a five year period.  That is $8 million a year.  For results that really haven’t changed much when looking at this measurement.  I don’t know about you, but I’m sure our schools would be more than happy to be able to use that money towards lower class-room sizes or more support for students who are at-risk.

While I respect your right to choose whether or not your child takes the Smarter Balanced Assessment, what I don’t respect is you’re telling me that my choice is a luxury.  I actually found this extremely offensive.  I have a child with disabilities.  For these students, who score much lower than African-Americans, it frequently takes them two to three times longer to take this test with accommodations than their peers.  And yes, non-disabled African-Americans are their peers.  They are easily frustrated being forced to take a test for this long.  Because at the same time, their neurological disabilities are manifesting.  Whether it is high-functioning Autism, or Tourette Syndrome, or ADHD, or OCD, or in some cases (as it is with my child) a combination of co-morbidities.

I would like anyone reading this to try something.  Grab a piece of paper and start writing the Pledge of Allegiance.  While you are writing with your hand of choice, take your other hand and start swinging it out.  Keep writing.  At the same time you are doing both of these, start making humming noises.  Do all three at once.  How far did you get on the Pledge of Allegiance?  Now put that in a scenario where you are taking the state assessment on a computer.

Now, imagine you are a low-income African-American student with disabilities taking this test.

I’m sorry Lisa Blunt-Rochester, but you don’t get the luxury of telling me it is a luxury for me to opt my son out.  I respect your choice, but if you want to talk about discrimination, we can do that.  I can talk about how my son was denied an IEP at a charter school in Delaware because of a poorly-trained special education staff who were not even aware of the classification for disabilities of “other-health impaired” until my wife told them.  I can talk about how they treated his disability as behavior issues and wanted to punish him when they wouldn’t give him the accommodations he deserved under federal law.  And when things got so bad there, over a dropped cookie in the lunchroom, he ran to a confined space because he was so scared of their behavior interventionist who told him he would be suspended if he didn’t pick it up.  When they found him, he wanted to get out of that confined space.  And as my son sat there screaming to be let out of that confined space for half an hour, while I was in the school substituting that day and they never bothered to come get me knowing I was there, I found my son in a state I had never seen him in before.  I also found the behavior interventionist sitting in the hallway eating a sandwich and the head of school sitting there as well.  His face was the only face my son could see as they ignored his cries for help.  As I managed to coax my son out, who was crying, embarrassed, and afraid, the head of school and I took him to a conference room.  He explained I should take him home and talk about this the following Monday.  My son, who was in a very distraught state, said to the Head of School, “I’m going to get revenge on you.”  He didn’t specify what kind of revenge or anything he would do.  He just blurted it out.  The Head of School yelled, “That is duly noted”.

As I drove home with my son, my wife called the school.  She was unaware of what had just gone down.  She spoke with the Head of School.  When my wife asked him what he knew about Tourette Syndrome, he started making a tapping noise and said “I know there is a meeting on Concord Pike next week about it.”  He wound up yelling at my wife and hanging up on her.  When we brought my son back into school the next Monday, we were told my son was suspended for three days and when he came back he had to meet with a police officer to discuss “terroristic threats”.  That was the last time my son was in that school.  He was nine years old.

We pulled him out and took him to the local school district.  He got an IEP… after five long months.  It was the end of the school year.  The way my district is set up, he went to 5th grade in a middle school.  We were told by the new IEP team that his IEP was too complicated and we should rework it.  Over the next four months, my son was physically assaulted nine times.  The last of which gave him a severe concussion two days before Christmas.  That was the last time my son was in that school.  He was on homebound instruction for the rest of the year, along with months of physical therapy, headaches, and a very real fear that if he stepped out of the house he would get beat up.  He was ten years old.

We tried a local private school who would only take him on a probationary status because of his disabilities.  He received hours upon hours of homework each day which he had not received in the other two schools.  It was too much for him, so we pulled him out.  He was eleven years old.

We found a good school for him now, far away from Common Core and the Smarter Balanced Assessment.  He is receiving the best instruction he ever has.  He is twelve years old.

So we can sit here and talk about equity and discrimination.  But I can tell you I have lived it through my son.  So I’m sorry you see it as a luxury that I opted him out at the school where he got his concussion.  The ironic truth is that even though I opted him out, he didn’t have to take the test because he was released from the obligation by the school due to his medical issues, received at the school.  While all this was going on that year, I spent a considerable amount of time at Legislative Hall fighting for the rights of other parents to opt their child out.  In all the conversations about opt out, I never heard it referred to as a luxury.  Until last night.

The odds of your child having greater success at life are greater than mine.  This is a fact for persons with disabilities.  So if I make a choice to opt my son out of a test, that has nothing to do with your child, or someone else’s child.  It has nothing to do with civil rights.  I chose not to have my son be used as a guinea pig for results that have stated the same measurements you so vigorously defended last night.  A person can defend civil rights and be against state assessments.  They can have it both ways.  Many civil rights groups do this already, without financial backing from the Gates Foundation.  I am a staunch supporter of civil rights.  But I refuse to let my child be a part of your measuring stick for a test that is horrible to begin with so we can endlessly compare where your child is against mine.  You are a pawn to a money-making scheme that has been going on far longer than you realize.  All our children are being used.  It has nothing to do with proficiency.  The tests are rigged so there will always be winners and losers.  I don’t need my son to take a test to know he has been a victim of disability discrimination.  He didn’t even have to log onto a computer for me to realize that.

I have a very strong suspicion why Senator Townsend was asked such a specific question about state testing, civil rights, and DSEA.  It was meant to trip him up.  It was very carefully worded.  There was only one person in that audience who would have asked him a question like that.  You may or may not know who it is.  I doubt he would ever own up to it.  But he now knows I know.  I’ve seen his manipulation at play before.  But it backfired and most likely forced you to address something that may end up hurting your campaign.

As a candidate for Congress, you need to be aware of how you can be used and how other people’s agendas can backfire on you.  There were hundreds of people in that audience last night.  How is that was the only question asked by a member of the audience at an education debate?  I invite you to think about that.  But in the meantime, let’s stop talking about measurements.  When I cast my vote in the primary, I will be choosing a candidate who looks at all sides of the issues, for all Delawareans, and what is best for us as a state.  I support civil rights and equity.  But I don’t think constantly measuring students so we can hold schools, teachers, and districts accountable is moving forward.  As long as some support this mistaken belief about measuring students against each other while ignoring the individual student and their individual needs, we will continue to have this conversation while testing companies and hedge fund managers make tons of money that isn’t going into our schools.  I am unable to support you as a candidate based on what I heard tonight.  And yes, one word left a very big impression on me.  I respect your choice to put your money where your mouth is.  Please respect my choice to put my voting finger where my beliefs are.  Because the only gap I saw tonight was how far away you and a couple of other candidates are to the reality of what is truly happening with Delaware education.

Federal representatives voted for the No Child Left Behind Act.  Federal representatives stood back while Race To The Top bribed and coerced our states into accepting dubious state standards, tied to a state assessment, and put our highest needs schools into a deplorable cycle of test, label, punish and shame.  Federal representatives (from Delaware) voted no for a clause that would have honored a parent’s right to opt their children out of the state assessment.  Federal representatives (from Delaware) voted yes for the Every Student Succeeds Act which reversed the other two but essentially kept the very worst from what came before but promises vast amounts of money for other things.  We have once again, been duped.  Many of you won’t know it until it is too late.  So yes, opt out is just as much a federal issue as it is a state issue.  But one thing will not change: my unwavering belief that all parents have the constitutional, God-given, and fundamental right to decide what is best for their child.  Education is only one part of what an elected U.S. representative faces.  But education, which is the foundation for our children, is also the foundation for our democracy.  It is our way of instilling hope for the future.  It isn’t a measurement, or accountability.  It is about what is best for each child based on their own unique and beautiful mind.  When we constantly compare, there are always going to be winners and losers.  This creates an environment of discrimination.  I don’t care what any candidate looks like, the color of their skin, or their gender.  I don’t care where they come from.  I care about what they are going to do.

I’ve been hearing a lot of people say, even before it came out, that we need to fix the test.  And yet, Smarter Balanced is still here.  With no indication of it disappearing anytime soon.  Our United States Secretary of Education just okayed illegal flexibility waivers for Delaware under the condition we use the Smarter Balanced Assessment until June 30th, 2019.  We can talk about the importance of “growth”, but for students with disabilities, their “growth” requires two to three times more “growth” than their peers according to the Delaware Department of Education.  But yeah, let’s keep using a flawed test to measure students.  But you don’t have to be an elected federal Congresswoman to speak up against the Smarter Balanced Assessment and “fix the testing”.  Please put your money where your mouth is.

So How’s My Kid Doing?

Bullying Against Students With Disabilities

Thank you to all who have sent their concerns and well wishes for my son.  I just wanted to give an update.  He is currently on homebound instruction for the foreseeable future due to the concussion he received from another child at his school the last day before Christmas break.

His MRI came back clean, but we are awaiting the results of a second impact test which shows if there is any problems arising from the concussion.  He is under a lot of physical limitations.  He wanted to ride his bike today, but he can’t.  He can’t be in a travelling car for more than half an hour.  Screen time is vastly reduced.  He’s not as tired as he was a couple weeks ago, but he has not gotten back to his normal sleep pattern.  His doctor recommended some physical therapy for the concussion, so we have that coming up as well.  He misses some of the kids at his school, and some of his teachers.

One punch.

That’s all it took to wreck his life.  One punch.

There is a lot about this situation I am unable to write about at this time.  But I did commit to making bullying a top priority for this year.  For those who have been following this blog from the beginning, you know when I start on a big topic, I tend to write a big article about it.  It’s coming.

In the meantime, I pray he gets better soon.  Many parents have said “Why doesn’t he fight back?”  Cause we’ve told him not to.  This is a child with disabilities.  Sure, there’s a part of me that wants to say go to town if he is assaulted, but the reasonable part of me knows what could happen.  Kids with disabilities that fight back don’t always have the best future.  Some of them wind up in residential treatment centers.  Possibly out of state.  And it’s not like our schools are always fair when a kid defends himself.  I wish he didn’t have to defend himself.  I wish kids would see him the way I do.  But you can’t always get what you want and all that.

I will defend him though.  Against the forces that are bigger than him, bigger than most of us.  I will fight the future.  I will fight those who say they want the best for our children while they fill their wallets with our  money.  I will fight those who sit behind the protection of the state but take advantage.  I won’t be a bully for my son, I will be a warrior for him.

Office For Civil Rights Gives Stern Warning To Schools About Bullying Against Students With Disabilities @KilroysDelaware @ed_in_de @dwablog @TNJ_malbright @DeDeptofEd #netde #eduDE

Bullying Against Students With Disabilities

The Office For Civil Rights division of the United States Department of Education wrote a colleague letter today about the rapid increase of bullying against students with disabilities.  The department has seen a huge rise in bullying reports since 2009 according to a report by Disability Scoop.  Even though they have written letters about this issue to US schools in the past, this new one gives more detail about what constitutes bullying against students with disabilities.

One part even suggests that even if a report rules that bullying did “not create a hostile environment” the school is still obligated to determine if a free and public education (FAPE) was violated under Section 504 and IDEA guidelines.

“When a student who receives IDEA FAPE services of Section 504 FAPE services has experienced bullying resulting in a disability-based harassment violation, however, there is a strong likelihood that the student was denied FAPE.  This is because when bullying is sufficiently serious to create a hostile environment and the school fails to respond appropriately, there is a strong likelihood both that the effects of the bullying included an impact on the student’s receipt of FAPE and that the school’s failure to remedy the effects of the bullying included it’s failure to address those FAPE-related concerns.

This ruling by the OCR also indicates a significant shift in how IEP or 504 teams must handle bullying issues.

“If the school suspects the student’s needs have changed, the IEP team or the Section 504 team must determine the extent to which additional or different services are provided, ensure that any needed changes are made promptly, and safeguard against putting the onus on the student with the disability to avoid or handle the bullying.”

This means that a response to bullying on a school’s part cannot be isolating a student away from situations or peers where bullying can occur. The letter reminds schools they need to be vigilant in regards to preventing any type of bullying, whether it is disability discrimination or not.

It gives three examples of the following classifications: 1) Disability-Based Harassment Violation and FAPE Violation, 2) FAPE Violation, No Disability-Based Violation, and 3) No Disability-Based Violation, No FAPE Violation.

To read the full letter, please go to http://www2.ed.gov/about/offices/list/ocr/letters/colleague-bullying-201410.pdf

The US DOE has also issued a fact sheet for parents: http://www2.ed.gov/about/offices/list/ocr/docs/dcl-factsheet-bullying-201410.pdf

Bullying Against Students With Disabilities in Delaware #netde #eduDE @KilroysDelaware @ed_in_de @DEStateBoardEd

Bullying Against Students With Disabilities

In a study done in 2011 by the Delaware Developmental Disabilities Council on bullying, the council found that 3.2 million students are bullied every year on a national level, and 3.7 million students engage in bullying behavior. As well, each school day it is estimated that 160,000 students miss school because of bullying. These are alarming statistics, and unfortunately students with disabilities are often the victims of bullying. The report states “The Individuals with Disabilities Education Act (IDEA) guarantees all students and adults have access to a “free and appropriate” public education. If “peer-on-peer” harassment infringes on this right, then schools, parents and state entities must be prepared to advocate and intercede on behalf of bullying victims. This position statement outlines the DDC’s stance on bullying students with developmental disabilities and possible courses of action to limit further bullying.”

In the 2011-2012 school year, there were 549 substantiated (determined to be bullying by administration) incidents of bullying and 662 “substantiated” incidents. This report was made available to the public on 9/18/12. For the 2012-2013 school year, there were 713 substantiated incidents. That school year was the first where schools were obligated to report the number of alleged incidents, which was 2,446. While I’m sure there are some reports that may either be false accusations or not actual bullying, that still seems like a very huge amount of alleged bullying incidents not counting as substantiated bullying. The percentage rate between alleged reports and substantiated reports is a little over 29%. The 2013 report does show a breakdown, and out of the 713 incidents, it showed 32 were due to disability bullying.

But on February 19th, 2014, Lieutenant Governor Matt Denn and Attorney General Joseph Biden, III issued a report entitled Unfinished Business: Implementation by Delaware Public Schools of the State’s 2012 Anti-Bullying Laws. The report indicated most public schools were in compliance in regards to listing information about the state ombudsman of bullying, through the Attorney General office, on their websites. Most charter schools were not in compliance. The report stated “The most prevalent reported causes of bullying in Delaware public schools are students’ physical appearance, student disability, and student gender identity.”

The report cited a study done by the National Center for Education Statitistics which estimated 28% of middle school students are bullied. It went into more detail about the disability status, which showed 10% of the 713 reported bullying incidents in Delaware during the 2012-2013 school year were against a student with a disability which starkly contradicts the 4.48% reported by the DOE.

What none of these reports cover is the unspoken bullying. The students who are too afraid of retailiation and say nothing. This goes on every single day in schools. Students who would rather be mocked and ridiculed at a lower level than “snitch” and be retailiated against. Pacer’s National Bullying Prevention Centers cited on their website that 64% of bullying goes unreported.

For students with disabilities, this is immensely cruel. These students have a hard enough time with their disabilities, and then to have students tease them because of it? And to be so afraid to speak up about it? Unacceptable. They already know they are different, and then they feel like they are being punished for it. Pacer had some very shocking statistics in their reports. Among them were the following:

Statistics about bullying of students with disabilities

Only 10 U.S. studies have been conducted on the connection between bullying and developmental disabilities, but all of these studies found that children with disabilities were two to three times more likely to be bullied than their nondisabled peers. (Marshall, Kendall, Banks & Gover (Eds.), 2009).

Researchers discovered that students with disabilities were more worried about school safety and being injured or harassed by other peers compared to students without a disability (Saylor & Leach, 2009).

The National Autistic Society reports that 40 percent of children with autism and 60 percent of children with Asperger’s syndrome have experienced bullying.

When reporting bullying youth in special education were told not to tattle almost twice as often as youth not in special education (Davis and Nixon, 2010)

I went through many of the school district and charter school websites, and I found that the vast majority of them do have a list of potential reasons for the bullying, but many don’t show a section for disabilities.   So Delaware’s reporting of 10% of the bullying being against students with disabilities is most likely a much lower percentage than reality.  So it can be very difficult to understand why there are the two major discrepancies between the two reports.  I question the validity of any report of bullying against children with disabilities within the state of Delaware because of these factors.

Something needs to change. I have heard from many parents who report that schools are very resistant for education of a class in regards to a physical manifestation of a child’s disabilities. As a father of a son who has been bullied, it breaks my heart. Schools need to be aware that repeated offenses against children with disabilities can lead to civil rights investigations.

My advice to special needs parents of students with disabilities, do not wait one second when your child reports a bullying incident. Report it right away, in writing, and if the school’s form doesn’t include a “disability” section or any suspected reason checklist, write it down, apart from everything else so it stands out. If you don’t hear back from the school within 48 hours, go to the school with a pen and paper and ask to see the principal.  Write everything down!  The Delaware DOE is required to receive any bullying report from local school districts or charter schools within 5 business days (not school days) of any bullying incident (alleged or substantiated) so parents can certainly check with them to see if the school has been in compliance.

This is just one more thing children with special needs have to deal with on any given school day. The bullying needs to stop and teachers and school staff need to be watching and paying attention much more than they have been.

 

Eagles Wings Ministries: Last Warning- No member of your flock is to go near my son, adults and children included! #netde #eduDE @DoverPost

Disability Discrimination

This is your absolute last warning. I don’t know what kind of church you run, and I don’t really care. What I do know is your youth group leader ABUSED my son physically, and your church turned a blind eye and then denied it with the only true witnesses being the youth group leader and her son. You then used children to cover your asses and deny it to the police. Yes, my wife yelled at you and swore at you, but any parent would after your cover-up. No more. Tell your youth group leader that her daughter can not and will not bully my son at school. We will be filing a report tomorrow, so you may want to get some intervention for a certain family in your flock. I will not be having this conversation again. Once again, this is your last warning. If you don’t like my stories about you, then leave my son the hell alone. You don’t get to play the victim here. Do you understand me? If not, I would be more than happy to talk about it in front of a police officer.  Again…

UPDATED: For any new readers, this is an ongoing thing with a whacked-out church in my area.  I know they are reading this, so I just needed to make things very crystal clear for them.  And Stacie Bohannon, I would tell your daughter to stay away from my son.  I don’t want her looking at him, laughing at him, sticking her tongue out at him, and certainly not spreading rumors about him.

You’ll Never Guess What My Son Got In The Mail Yesterday!!! Will He Go? Hell No!!!

Disability Discrimination

So I get home from work yesterday, go to the mailbox, and I see this in there:

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For those unfamiliar with this story, please read this: https://exceptionaldelaware.wordpress.com/2014/06/21/disability-discrimination-local-church-youth-leader-assaults-my-son/

and this: https://exceptionaldelaware.wordpress.com/2014/06/23/eagles-wings-ministries-started-their-bible-school-this-week-parents-beware/

and this: https://exceptionaldelaware.wordpress.com/2014/06/24/the-eagles-wings-ministries-and-pizza-google-search/

Okay, now that you know the lowdown, I will address the rest of this post to Eagles Wings Ministries. before you go, please don’t go to this bizarre Lion King Pride Rock thing. A guy named Jim Jones had some church thing with Kool-Aid once. Stay home, watch Shark Week. It’s free, and your children won’t be emotionally scarred. But if you do go, watch your kids, especially if they don’t go on the slip and slide! Back to the church that may have named themselves after a Bette Midler song.

Are you out of your friggin’ mind? You knew my son lived in this neighborhood. You couldn’t have done just a tiny bit of research to know which mailbox NOT to put your Lion King Thing inside of? Really? Do you honestly think for one second I would bring my child back to your Child Abuse-Denial Church? The odds of me ever bringing him back to your little safari adventure are about as great as me bringing him to special education night at Campus Community School with Janet Asay Miller and Chuck Taylor. My bad, Chuck isn’t there anymore. He’s too busy blowing the Charter School Network trumpet. Or is that Kendall? You can never tell these days. Hey Readers, did you check this out: https://exceptionaldelaware.wordpress.com/2014/07/18/the-charter-school-network-wants-you-to-comment-cmon-special-needs-parents-lets-comment-netde-edude-delaware_gov/ or this: https://exceptionaldelaware.wordpress.com/2014/08/01/googling-delaware-charter-schools-network-special-education-netde-edude-delawarebats/

Whoa, got off track there. Too busy shameless plugging when I was talking about your cult, er, uhm, AHEM, Church! You see, this almost went away. Right after (and I mean literally, right after, I posted the Eagles Wings and Pizza Google thing, I saw an article from the News Journal which prompted this: https://exceptionaldelaware.wordpress.com/2014/06/24/breaking-news-feds-want-to-intervene-in-delaware-special-education/ and I that got me upset too. But that was a good thing, cause I’ve done a bit of investigating to find out what was up with that: https://exceptionaldelaware.wordpress.com/2014/07/09/delaware-doe-the-eye-of-the-hurricane-in-special-education-netde-edude-del_gov-destateboarded-usedgov/ and https://exceptionaldelaware.wordpress.com/2014/07/16/delaware-doe-the-eye-of-the-hurricane-in-special-education-part-2-netde-edude-usedgov-delaware_gov/ and https://exceptionaldelaware.wordpress.com/2014/07/23/part-3-of-the-delaware-doe-the-eye-of-the-hurricane-in-special-education-netde-edude-usedgov-delaware_gov/ All those stories totally kicked your ass in terms of readers. But up until my last story about your bird church, the story of how your Youth Group Leader assaulted my son got the most readers. And people still read it, just about every day since.

But I’m sure you don’t want to hear about blog statistics. Let’s get back to disability discrimination! I never heard back from you guys at all. We left a message with your “district” headquarters, but they never called. Maybe they were feeding kids at summer camp like it’s ration night in London during the Blitz in World War II. Just because I got distracted on my special education blog with, you know, special education, doesn’t mean I forgot about you. I drive past your church all the time. And instead of what I used to think before my son went to your famine dinner youth group, “Wow, that church is empty all the time”, I now think “That’s where Stacie Bohannon told my son to consider his ways before and after she kicked, tripped, and pushed him to the ground.”

In any event, just between us, you may want to keep the kids away from Miss You-Know-Who. I understand this event will have trips through the Amazon Rainforest, the African Savannah and The Australian Plains (which most people call “The Outback” by the way, they even named a steak house after it. Oh wait, don’t want families to think they are getting steak. Gotcha!). Kids might get pushed into quicksand, thrown off a cliff, or kicked by a kangaroo if Miss You-Know-Who has her way. Just sayin’. Since your going with The Lion King theme, you might want to have parents stay away from Miss Scar.

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I have to ask. Why the whole Lion King theme? That would have been cool if it was, I don’t know, 1994! Kids these days aren’t into Lion King that much. Their more into The Lego Movie and the other 50 movies Disney has released since the Simba Death movie. Whatever floats your boat. Speaking of boats, did you check this out dear readers: https://exceptionaldelaware.wordpress.com/2014/08/09/indian-river-student-injured-in-classroom-titanic-experiment/ Dammit, I strayed again. Sorry Eagles Wings. I keep doing that, don’t I? What was I saying? Oh yeah, your theme. If your going to go for an older movie theme, might I suggest this:

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But I do see you have more food bait for families to attend your event. More pizza slices cut into four pieces for kids? Or are you going to try new stuff, like rotisserie chicken and the kids get to eat the skin? Or maybe it will be spaghetti night, and each child will get three strands of spaghetti with ketchup! Will drinks be provided or will they have to drink from that nasty water fountain again?

Good luck with the rumble through the jungle Eagles Wings. If I hear any police sirens this week, Monday to Friday, August 11th to the 15th, from 6pm to 9pm, it won’t be hard to guess where they are going! Hakuna Matata!