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How Important is Your Child’s Designation?

July 17, 2012 in Ask the Special Ed Lawyer, Community Wisdom, Featured by dianaglick

As discussed in previous articles, eligibility is found when a student has one or more qualifying disabilities and the IEP team determines that special education services are necessary for the child to access his or her education. When a student has a single and very obvious disability, this is a very straightforward process and if you are not wondering about the designation (disability category) that will be listed on your child’s IEP, you are probably in one of these straightforward situations.

This discussion is geared towards those families who are struggling to identify an appropriate designation and wondering how the choice of one or another might affect their child’s ability to obtain services.

A Ticket to the Game

From a legal perspective, a designation is simply a “ticket to get into the game” and does not necessarily result in any particular placement or services. Further, students and parents are not legally entitled to any particular designation; rather, the right is to a free appropriate public education (FAPE). This is because special education is “specially designed instruction” that is supposed to focus on the unique needs of the child. If your child needs a specialized reading intervention, he or she can access these things through any of the qualifying disabilities on the list. The law does not assign specific services to certain designations but requires that any condition impeding the child’s access to his or her education be addressed. In other words, a child could have a vision impairment, but have “autism” checked on his IEP. As long as that child receives services to address his vision impairment sufficient to be considered a FAPE, the fact that he has a totally random designation means nothing in the legal world.

Back to Reality…

However, setting aside the legal framework of the IDEA and coming back to the real world, it is highly unlikely that a student who is hard of hearing will automatically be considered for mental health services or any other service that may not necessarily jump to mind when thinking about the needs of students with hearing impairments. It also means that a student who is eligible with a designation of Speech/Language Impairment (SLI) may not be offered more intensive interventions that would be considered for a child with a designation of Autism, even if the student with an SLI requires these services in order to access his education. In reality, some families face an uphill battle in obtaining all the services their children need and in those cases it’s important to have the most accurate designation possible.

In addition, some states have categories of “low incidence” disabilities, which are tied to a certain level of funding based on the ability to access federal funds for these particular disabilities. While in an ideal world, a designation determination would never be driven by the funding or services available, this often ends up being a factor in the IEP team’s decision-making process.

One of the most important things to remember is that designation is an IEP team decision, which means that everyone’s input is important, including that of parents, assessors and teachers. There is also a difference between a medical diagnosis and an educational designation. A doctor’s diagnosis can inform the team, but a student’s designation is determined according to educational criteria.

While there is no set formula for determining the proper designation, there are some key questions that can be posed to the team that will help frame the discussion:

1. What, if any, medical diagnoses does the student have?

➢ While the designation is an educational decision, a medical diagnosis in some situations is an excellent “jumping off point” for the IEP team’s deliberations.

2. What are the key areas of need demonstrated by the student?

➢ You will want to consider needs observed during evaluations, in the classroom and by the parents in the home and school settings

3. Of the challenges and deficits experienced by the student, which is the biggest impediment to his ability to access his education?

As a special education attorney, I saw many families face the “ED or OHI?” conundrum. This occurs when a child has a diagnosis of ADHD, which would usually point towards the Other Health Impairment (OHI) category. However, sometimes students with ADHD also have moderate to severe mental health issues and could also be considered Emotionally Disturbed (ED). There are many factors that go into a decision to opt for one designation or another, including the predominant behavioral challenges experienced by the student, his or her age, and in some cases the student’s preference.

Just When You Thought it Couldn’t Get More Complicated

Some District IEP forms contain spaces for a “primary” and a “secondary” disability category. Just as there is no legal right to a particular designation or a correct designation, the law does not distinguish between primary and secondary designations. In some cases, being able to put down more than one category can help resolve a conundrum, such as determining whether a child should be considered ED or OHI. In other cases, it can lead to more confusion and conflict as IEP teams feel compelled to identify which of two disabilities is primary and which is secondary. If you find yourself being dragged into a conflict about designation, take a step back and look at the big picture: what are my child’s needs as determined by the assessments and parental input and what services are being offered to address these needs?

Despite the fact that eligibility categories do not drive litigation, they can have a significant effect on the way a child and his or her needs are viewed by school professionals. The determination and agreement on a child’s designation is a key part of the IEP team’s process of identifying needs and matching services to satisfy those needs, with the goal of offering the child a free appropriate public education.

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Disclaimer:

This column reflects the views of Diana B. Glick in her individual capacity. Diana represented parents and students as a special education attorney for four years and is now a legislative analyst with the California Assembly.

The purpose of this column is to assist in dissemination of information about federal special education law, but no representation is made about the accuracy of the information. The information contained in this column is provided only as general information for education purposes, and topics may or may not be updated subsequent to their initial posting.

By using this column you understand that this information is not provided in the course of an attorney-client relationship and is not intended to constitute legal advice. This blog site should not be used as a substitute for competent legal advice from a licensed attorney in your state. This column is not intended to be advertising and Diana B. Glick does not seek to represent anyone desiring representation based upon viewing this blog site in a state where this blog site fails to comply with all laws and ethical rules of that state.

Getting Started in Special Education: First Steps

August 1, 2011 in Ask the Special Ed Lawyer, Featured, Insider Insight, Latest Articles by dianaglick

This first published in May 2010. It was Diana Glick’s 2nd article for us and it’s a terrific reminder right now – before regular session school starts – to start educating ourselves about the basics. If you get a chance read all of Diana’s articles from the start. Especially helpful is the one about what your legal team will need from you; should you ever have the need for one..

On a personal note, about Diana. She contacted me from my personal blog Kidneys and Eyes after I’d posted something about my son’s IEP. It was just a little advice; something to keep him mind. I wrote her back, thanked her and promptly asked her if she’d be willing to contribute to the site and she agreed without hesitation. Why? Why would a busy attorney want to write for a site like ours? Pure desire to educate parents navigating the maze of special education.

Thank you Diana!

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By Diana Glick

If you have decided to seek special education services for your child, you have likely traveled a long and often difficult journey already. Your child may have a longstanding medical diagnosis, or you may have been concerned about her performance in school and tried other interventions before getting to this point.

The Individuals with Disabilities Education Act (IDEA) that I discussed in my introductory column has two major categories of services for disabled children: Part B and Part C. Part B will encompass the majority of our discussion of the legal perspective as it applies to school-age children; however, if you are the parent of a very young child with an already diagnosed disability, you should know that services are available to children aged 0-3 under Part C.

Early Intervention

Part C, also referred to as Early Intervention, is available to children with developmental and other disabilities from 0-36 months of age, and includes assessments and services. The services under Part C are provided in accordance with an Individualized Family Service Plan. Part C programs are available in all 50 states, but eligibility criteria vary significantly. If you are interested in seeking out programs for a child under three, the best place to start is at the website for the National Dissemination Center for Children with Disabilities. This website contains information about what is available under Part C and provides Early Intervention contact information for each state.

After Early Intervention

Part B of the IDEA encompasses special education services for children ages 3 through 21, which are administered by local school districts. If you suspect that your child needs special education services, the first step is to request an assessment. It is best to make this request of the school principal and to do so in writing. Each state has different timelines for assessment. For example, in California, once the school receives a request for assessment, they have 15 days to provide parents with a written assessment plan. This is not the case in Ohio, where the school has up to 30 days to respond to a request for assessment. Federal law provides that the District must obtain your written consent to proceed with testing, which is typically done with an “assessment plan.” Once you have signed and returned the assessment plan, the District has 60 calendar days to conduct the assessments and convene and IEP meeting to discuss their findings, unless state law provides a different timeline.

Getting a response

What should you do if you make a written request and get no response? As an attorney, I often hear stories of difficult communication with schools and school district personnel. The last thing you want to do is get off on a bad foot with people who are there to help your child. On the other hand, it is frustrating to be ignored. If you are not getting a response from your child’s teachers or the school principal, the next step is to contact the school district’s special education director. This person is sometimes housed in the Student Services or the Special Services department. It is also important to conduct communication in writing and to start a binder with your child’s special education documentation. A well-organized binder helps you track your child’s course through special education and safeguard important documents. If you are having difficulty getting a response from the District to requests for an assessment, I recommend keeping a copy of all of your communications and having a school secretary or administrative assistant initial and date your copy to confirm the date of receipt.

In my next column, I will discuss the various eligibility categories and what parents can do when there is a disagreement about eligibility among the members of the IEP team. In future columns, I will also discuss alternatives to an IEP, such as 504 plans.

We are also interested in hearing from you! Feel free to suggest topics for further discussion; just keep in mind that I cannot provide legal advice for your specific situation.

Disclaimer:
This column reflects the views of Diana B. Glick in her individual capacity. It does not necessarily represent the views of her law firm or her clients, and is not sponsored or endorsed by them. The purpose of this column is to assist in dissemination of information about federal special education law, but no representation is made about the accuracy of the information. The information contained in this column is provided only as general information for education purposes, and topics may or may not be updated subsequent to their initial posting.
By using this column you understand that this information is not provided in the course of an attorney-client relationship and is not intended to constitute legal advice. This blog site should not be used as a substitute for competent legal advice from a licensed attorney in your state. This column is not intended to be advertising and Diana B. Glick does not seek to represent anyone desiring representation based upon viewing this blog site in a state where this blog site fails to comply with all laws and ethical rules of that state.

SB 10-Georgia’s Special Needs Scholarship Program: Win Some, Lose Some

May 16, 2011 in Ask the Special Ed Lawyer, Featured by dianaglick

[In addition to the usual disclaimer that accompanies these columns, I’m going to start this one out with an extra special one: I am a California attorney.  I was raised in the Midwest, but have lived in California for the last 15 years and have practiced law exclusively in this state.  When I was asked to write about an issue particular to special education in the state of Georgia, I had some reservations.  However, as someone who works closely with parents who have become professionals at advocating for their kids, I know how hard it is to say “no” to the mom of a special needs child.  When I tell you that it was a special mom/advocate who asked me, our own Julia Roberts, you’ll understand why I immediately got to work on it!  Through my research, I found that several other states, including Arizona, Florida and Ohio also have scholarship and school choice programs for special needs students.  The issues to be aware of will be similar from state to state and I will be analyzing them from the perspective of federal law.]

 

The Georgia Special Needs Scholarship (GSNS) program, originally proposed as Senate Bill 10, was enacted in 2007 to provide additional school choice for students with IEPs in the state of Georgia. The eligibility requirements are simple, but appear to be strictly enforced.  I recommend that you consult http://www.doe.k12.ga.us/sb10.aspx to determine whether your family qualifies.

There are three major elements of the program for those students who meet the criteria to participate:

1.      Eligible students may transfer to other schools in or outside of their school district of residence.

2.      Eligible students may be placed at a state school for those with visual or auditory impairments.

3.      Eligible students may obtain a scholarship to cover some or all of the costs of private school.

Of course, each of these options comes with its own set of caveats and exceptions.  Principally, for options one and two, the receiving district or school must have room for your child and must be considered an appropriate placement given your child’s needs.

Option three, which is the scholarship money that is applied to private school tuition, is the trickiest of them all.  First, the private school that you choose must participate in the GSNS program.  Second, the amount you receive depends upon a formula that takes into account the severity of your child’s disability and how much money the state has allocated for your child in the past.  It has nothing to do with the cost of the private program.  Without knowing what private school costs in Georgia, my guess is that the scholarship funds will not fully cover the cost of many private schools, particularly those geared towards students with special needs.

Finally (and here’s the big “but”), if you accept the scholarship funds, you must give up your child’s right to receive special education services.  Your child will be treated like any other private school student with special needs—there may be services available in your district of residence, but it is entirely at the discretion of the school district whether your child receives them, and there is no individual entitlement to any service at all, which means there is no recourse to due process.  Private schools (with few exceptions) are not required to adhere to the Individuals with Disabilities Education Act, so there is no recourse against the private school if your child’s special education needs are not met.

This all sounds a little abstract, so let’s consider a couple of potential examples:

Example 1: Sarah, who is seven years old, qualifies for special education as a student with autism.  Since becoming eligible for special education at an early age, she has received speech and language therapy, occupational therapy and specialized instruction at her public school.  Sarah meets the eligibility criteria for GSNS and her parents would like to send her to a private school that is designed for students with autism.  The school is a participating school in GSNS.  Tuition costs $10,000 per year.  Assuming that Sarah is awarded approximately $6000, which was the average scholarship amount last year, her parents will be responsible for the balance of $4000.  Because this is a specialized school, therapies are built into the daily program, including speech and language and occupational therapy, so Sarah’s parents are confident that she will continue to receive these services at appropriate levels to help her access the curriculum and make progress.  In addition, because the private school is geared towards students with autism, they make use of the latest research-based interventions for curriculum delivery, such as Applied Behavior Analysis and Discrete Trial Training.  Fortunately for Sarah, her parents are financially able to pay the difference between the scholarship amount and the total cost of tuition, so this is truly an option for them.

Would I recommend that Sarah’s parents take advantage of the GSNS program and place Sarah privately?  The answer to that question would depend on a few things.  How do they feel about Sarah’s current public school placement?  If they are satisfied, there is no reason to look elsewhere. How would Sarah handle it if things didn’t work out and she needed to return to her public school placement in order to obtain appropriate services?  Is this a child who struggles with change and upheaval?  Do they fully understand the rights they are giving up?  If they do understand the trade-offs, and if the answers to the other questions make sense, I believe that GSNS and private school could be a very positive option for Sarah.

Example 2:  Jack is a ten-year-old child who is similar to Sarah in terms of disabilities and needs, but his parents are considering placement in a parochial school that is not necessarily geared towards students with disabilities.  In that case, I would be much more careful about advising his parents on what they are giving up.  I would want to know whether any related services (speech and language, occupational therapy, social skills training, etc.) will be available to him in his private school placement and if not, whether his parents are financially able to pay not only any difference in tuition, but the cost of private therapies as well.

Determining whether to seek out a private school placement could be extremely difficult if your child’s disabilities are more subtle, such as in the case of a specific learning disability.  Sometimes, children with mild learning disabilities are able to function quite well with simple alterations to their programs, such as smaller classes, more one-on-one attention from the teacher and extra time to complete their work, all of which are often available in a private school setting.  However, the private school is not obligated to provide any of these things and typically does not develop an IEP for your child with all of the necessary services and accommodations spelled out.

It is also difficult to predict how students with emotional disturbances will handle different placements.  If the private school option is a therapeutic school designed for students who can do the work, but sometimes need a time out, need to be able to readily access a counselor or who get easily overwhelmed when the work piles up, then GSNS could be a great way for a family to be able to afford the right school for their child.  On the other hand, if parents are considering a more traditional private school with smaller classes in the hopes that this will be sufficient structure to help an emotionally disturbed child, they may be giving up a host of therapies and services that would be available through the public school system.

Another wrinkle is that children are constantly changing and so are their needs.  A placement that works right now, may not work in the future.  In Georgia, a move from public to private school with the help of GSNS must happen at the beginning of the school year.  However, if your child is not successful at his or her private school, you can return to the public school system at any time.  If you do return to public school, it is likely that you will have to make a request for your child to be evaluated for special education and start the process from scratch.

If I were the parent of a special needs child in Georgia, or in another state that has a special needs scholarship program, I would first read everything I could about the program in order to fully understand its risks and benefits. It’s clear that this option is not for all, especially those who cannot afford the difference between the scholarship amount and private school tuition and/or those who cannot afford to bear the cost of the multitude of therapies that their children may need.  However, it does appear that in certain circumstances, GSNS can increase the likelihood that a child will have his or her special education needs met.

As an attorney, I can only caution parents that under the Georgia model, by accepting the private school scholarship money, they would be giving up a federal entitlement that their child currently has.  That’s not to say that it wouldn’t work or be a good option for your child.  However, it is important to consider the risks involved and understand what you are giving up in exchange for the tuition money.

 

 

Wading Through the Alphabet Soup: An Introduction to Federal Special Education Law

December 11, 2010 in Ask the Special Ed Lawyer by dianaglick

One of the first things I explain to clients during an initial intake appointment is the basic federal standard for educating students with disabilities. This is frequently referred to as the “alphabet soup” of special education: the IDEA mandates that schools provide FAPE in the LRE according to the child’s IEP. Keeping in mind that talking in acronyms is just job security for attorneys, let’s break it down:

IDEA = Individuals with Disabilities Education Act

This is the federal law ensuring that special education services are provided to children with one or more qualifying disabilities, whose disability interferes with their ability to receive an education. The IDEA originated in 1975 under President Ford and has been reauthorized and changed several times, most recently in 2004. While the IDEA is federal law and applies to all public school children in the country, each state also has its own education laws that may be slightly different than the federal requirements; states may provide more protections than those available under federal law, but may not provide fewer or less than the federal standard.

FAPE = Free Appropriate Public Education

The IDEA defines a free appropriate public education as special education and related services that are provided at no cost to parents and are in accordance with the child’s Individualized Education Plan (IEP), among other requirements. 20 U.S.C. 1401(9) (2009). The majority of legal disputes are about the meaning of “appropriate” for a child’s particular circumstances. In 1982, the Supreme Court issued a decision in Board of Education v. Rowley, which provides a working definition of FAPE as “a basic floor of opportunity” providing “some educational benefit.” Bd. of Education v. Rowley, 458 U.S. 176, 200 (1982).

What does “a basic floor of opportunity” mean in real terms? Because children who are eligible for special education have such a wide range of disabilities and needs, it cannot be defined as a specific set of services. However, most children who have passing grades or are making progress towards their IEP goals will be found to have received a basic floor of opportunity.

LRE = Least Restrictive Environment

This is one of the major improvements that the IDEA has made for students with disabilities. No longer does the law allow disabled children to be warehoused or educated exclusively in a special education setting, as long as their IEPs indicate some mainstream time during the school day. The LRE requirement has led to better outcomes, both academically and socially, for disabled students. It can also be a double-edged sword in some instances when parents are seeking a more restrictive environment for their child.

IEP = Individualized Education Plan

All students who are eligible for special education are to receive services in accordance with an IEP, which must be developed to meet the child’s individual needs. Those of you who already have some experience with special education have probably spent many hours at IEP meetings and have a sense of what they entail. We will talk more about IEPs in future columns.

I am excited to be included in this new community of families supporting children with special needs and look forward to sharing more of the legal perspective with you all. In future columns, I will address such topics as the difference between IEPs and 504 plans, discipline issues, assessments, the fair hearing process, private placements and knowing when to seek out legal help, among others.

We are also interested in hearing from you! Feel free to suggest topics for further discussion; just keep in mind that I cannot provide legal advice for your specific situation.

Author Diana B. Glick

Disclaimer:

This column reflects the views of Diana B. Glick in her individual capacity. It does not necessarily represent the views of her law firm or her clients, and is not sponsored or endorsed by them. The purpose of this column is to assist in dissemination of information about federal special education law, but no representation is made about the accuracy of the information. The information contained in this column is provided only as general information for education purposes, and topics may or may not be updated subsequent to their initial posting.

By using this column you understand that this information is not provided in the course of an attorney-client relationship and is not intended to constitute legal advice. This blog site should not be used as a substitute for competent legal advice from a licensed attorney in your state. This column is not intended to be advertising and Diana B. Glick does not seek to represent anyone desiring representation based upon viewing this blog site in a state where this blog site fails to comply with all laws and ethical rules of that state.

Assessments In the Driver’s Seat

November 3, 2010 in Ask the Special Ed Lawyer, Insider Insight by dianaglick

The most important thing to remember about assessments is that they not only determine eligibility — they also drive placement and services.

A good and appropriate initial assessment can be used by the IEP team to determine whether a child is eligible for special education. My prior articles have described the requirements for eligibility, in short: a qualifying disability and a showing that the disability interferes with a student’s ability to access his or her education. However, that initial assessment will also set the stage for the placement and services offered by the district. While the eligibility category (such as autism, specific learning disability, or a speech/language impairment) will signal the main interventions to be provided, an IEP should include services necessary to address all of your child’s areas of need.

For example, if a child is eligible for special education as a student with Other Health Impairment because of a diagnosis of ADHD, he should receive services designed specifically to address the challenges arising from attention deficit. However, it is possible that in the scope of the assessment, the evaluator also identifies some problems with social/emotional functioning, such as withdrawal, anxiety or depression. These issues should be addressed as well, usually by an initial offer of school-based counseling, or a social skills groups for students.

When Assessments Steer You Wrong

Clearly, when an assessment is used to conclude that a child is not eligible for special education or not eligible under a certain category that you may be seeking, this can be a frustrating setback in your advocacy efforts. However, the worst assessments are the ones that provide absolutely no useful information about a child. Even if you disagree with a particular recommendation or conclusion that the district may have drawn from an assessment, the data itself can still be very helpful in understanding your child’s educational strengths and deficits.

Some of the more common issues that that arise with assessments are when the district fails to use an appropriate testing instrument, fails to properly score a test, or fails to administer or conduct any testing in an area that is a known issue with the child. To expand upon the example above with the child who suffers from ADHD, if that child’s teachers have noted troubling behaviors in the classroom that they believe could be emotionally-based, or if his parents are raising concerns about his mental health status, this would be considered an additional area of suspected disability. When his triennial re-evaluation rolls around, the district should absolutely include some kind of assessment to address these concerns.

Federal law sets forth several requirements for evaluations, including that they be conducted at least every three years, but not more than once per year unless agreed upon by the IEP team. A full assessment should include a variety of testing instruments and tools, so as not to rely on a single measurement of a child’s ability. In addition, standardized tests should be administered in accordance with the publisher’s instructions by knowledgeable and qualified personnel, should be given in the language of the student and should not be racially or culturally discriminatory. One key requirement is that the child must be assessed in all areas of suspected disability.

Getting Back on Track

A major part of my practice involves helping parents navigate a situation in which their child has not been appropriately assessed. The law allows parents to obtain an independent educational evaluation (IEE) at public expense when they disagree with a district assessment. A key point to note: there generally must be an assessment with which to disagree. While there are exceptions to every rule, if the district simply fails to assess and you take them to court, they will likely be given an opportunity to conduct an evaluation before having to pay for a private one.

If you request an independent educational evaluation, federal regulations provide the district with two choices: they can either agree to your request or they can file for due process to establish that their assessment was appropriate. In most cases, the district will determine that it is more cost-effective to pay for an independent assessment than to incur the expense of a due process hearing against the parents. However, it is important to know that the district may file for due process in response to a request for an IEE.

Many times, a district will deny the parents the requested IEE, but fail to bring due process. In this situation, parents often seek out a private assessment themselves and then request that the district reimburse them. They may have to file for due process against the district in order to obtain this reimbursement.

If the district agrees to fund an IEE, parents should be given the opportunity to negotiate with them regarding the independent professional who will conduct the evaluation. It is important to go with an assessor who is truly independent of both the parents and the district so that all sides feel they are getting an objective opinion. Ask other parents in your community for references in order to identify the good assessors in your area.

Once an independent assessment has been conducted, the district should convene an IEP meeting to consider the results of that assessment. If the independent assessor draws different conclusions than the district, this may strengthen the parents’ argument for a particular category of eligibility, a particular placement or additional or different services. Parents may use the independent assessment in a due process hearing against the district to establish that the district’s assessment was inappropriate or that the child has been denied services because of the district’s failure to identify his or her needs.

While trying to obtain an appropriate assessment of your child can be a frustrating experience, the law has built in a mechanism for a second opinion, which in most cases I recommend pursuing. Having more information about the student’s strengths and deficits leads to better team decision-making, better educational planning and better outcomes for the child.

What Your Future Attorney Will Want to See

September 9, 2010 in Ask the Special Ed Lawyer, Insider Insight by dianaglick

Mom and SonThis is a rather cynical title. But, in case you ever need to seek the advice of an attorney or bring litigation against the school district over your child’s special education program, there are certain documents that you will want to be able to locate and present to an attorney. On a less cynical note, it’s always good to have an organized binder with your child’s important documentation. There are professional organizers who comment on this blog about organizing your life when you have a child with special needs and nothing in this column should be construed as going against their advice. This is more of an attempt to piggy-back on the concept of organization from a legal perspective.

Some of my clients have saved every scrap of paper related to their child, but somewhere along the way became completely overwhelmed with trying to keep it all sorted. I can sympathize with this—you start by throwing a few IEPs in a folder, they multiply when you’re not looking, and suddenly you have paper coming out your ears and no sense of how to organize it.

What to Save

My recommendation is to save the following for the duration of your child’s K-12 education:

* Official report cards and progress reports (computer printouts from online grade programs can also be helpful if you regularly consult these services for updates on your child)
* Assessment Plans
* IEPs
* Assessments
* Written communication with the school or school district (including emails)

Other items of that may or may not be important, depending on the case:

* Notices of Meeting—only if the District is continually canceling meetings on you, or has a habit of convening meetings with very little notice. If you have regular, timely meetings, a notice of meeting itself is not going to be important.
* Procedural Safeguards—Districts are required by law to provide you a copy of these and some people have enough for several bird cages. I do advise parents to read these and ask questions about anything that is unclear. However, as long as you have a recent copy from the District, there is no need to continue accumulating them. Sometimes, you can even save a tree and decline them at the IEP meeting. Just remember that you will be held to knowing and understanding your rights whether you accept or decline a copy.
* Mental Health records—including progress notes from treatment, any Discharge Summaries if your child has experienced a psychiatric hospitalization, and statements, receipts and cancelled checks for your out-of-pocket expenses.
* Record of any outside services—if you seek out private tutoring or educational services for your child, keep a record of the services received, including any pre-tests or progress summaries, as well as statements, receipts and cancelled checks.

How to Save It

A simple three-ring binder with tabs separating out the school years is great way to keep your documents organized. Within the section for each school year, you can group the documents as I’ve outlined above (assessments, IEPs, report cards, etc.). Another alternative is to have a separate binder for each group of documents and then organize them according to date within each binder. Either one of these solutions will work well over the long term and will allow you easy access to documents as you need them.

What to Bring to an Intake Meeting

Special education lawsuits have a two-year statute of limitations, unless your state law specifies a different time period. State statutes of limitations prevail over the federal two-year statute and there are states with longer and shorter timeframes. California’s statute of limitations is two years, so in most cases, our office wants to see all the documentation described above from the last three school years—documents from the period covered by the statute of limitations, plus one year before that. This allows us to see what services were in place when the statute of limitations began and will usually allow us to see a triennial assessment and review.

If your attorney suspects that you have a case for pleading additional school years outside of the statute of limitations, he or she can ask for additional documentation from you and from the school district.

Disclaimer:

This column reflects the views of Diana B. Glick in her individual capacity. It does not necessarily represent the views of her law firm or her clients, and is not sponsored or endorsed by them. The purpose of this column is to assist in dissemination of information about federal special education law, but no representation is made about the accuracy of the information. The information contained in this column is provided only as general information for education purposes, and topics may or may not be updated subsequent to their initial posting.

By using this column you understand that this information is not provided in the course of an attorney-client relationship and is not intended to constitute legal advice. This blog site should not be used as a substitute for competent legal advice from a licensed attorney in your state. This column is not intended to be advertising and Diana B. Glick does not seek to represent anyone desiring representation based upon viewing this blog site in a state where this blog site fails to comply with all laws and ethical rules of that state.

To Sign the IEP or Not to Sign — this is the question!

August 20, 2010 in Ask the Special Ed Lawyer, Insider Insight by dianaglick

Whew! You made it through the IEP meeting and are still standing. Now that the meeting is over, you are being asked to sign the IEP so the District may implement the proposed services, accommodations and goals. Should you sign or not? And, why does it matter?

Your Rights

The District must obtain your consent before providing the services indicated in the IEP. However, parents are under no obligation to sign the IEP, particularly if they disagree with its terms. Parents may sign, refuse to sign or authorize certain services without agreeing that the IEP provides your child a free appropriate public education.

The Ideal Scenario

Student raising her handIn the ideal IEP meeting, each of the following occurs:

* The designation makes sense and is back up by appropriate assessments
* Each of the professionals has given a report and there are offers of services that address all of your child’s areas of need
* There are measurable, understandable goals for each of your child’s areas of need
* If necessary, there are modifications and accommodations to the curriculum (homework, class work, testing) that will allow your child access
* The District has presented you with a written document reflecting all of these items, plus a narrative that contains the main points of discussion during the meeting.

When this kind of a meeting has occurred and you feel good about the outcome, by all means, give your consent. It is when one or more of these items is missing or has gone awry that you should consider not signing and instead developing a strategy to address the unresolved issues with the IEP team.

Your Options

Option 1: Sign the IEP. See you next year for the annual review!

Option 2: Authorize the implementation of goals and services, but do not agree that the IEP provides a free appropriate public education.

This is a very helpful middle option that can serve to move the process forward and extend protections to parents and student without compromising any potential legal claims in the future. It also serves to keep the conversation alive if there are items pending resolution. This response can be made with a simple sentence written on the signature page, or can be written up in a “Parents’ Addendum to the IEP,” which lays out your concerns in greater detail while still providing authorization to implement what the District has proposed.

Option 3: Do not sign at all.

Some parents opt to take the IEP home and review it carefully before signing it. This is a great idea if you would like some time to digest the information presented at the meeting and make sure you understand everything before signing. If you are satisfied with the document, make sure to sign and get it back to the District as soon as possible.

In other situations, parents fully disagree with some aspect of the IEP and do not want to provide their consent or authorization. If you find yourself in this situation, you will want to consider your next steps. Would you like to have another meeting to discuss specific aspects of your child’s program? Would you like to see revisions to the goals, more goals or perhaps fewer goals? Are there assessments necessary to determine what your child needs? Let the District know, preferably in writing, what you would like to see happen next and emphasize the importance of collaboration in getting an appropriate document with a plan to address your child’s needs.

Some Pitfalls of Not Signing

While not signing your child’s IEP is a right you have and one that can be exercised in the face of an inappropriate plan, there are some potential pitfalls you’ll want to be aware of as you are making your decision.

First, if this is an initial IEP finding your child eligible for special education, refusing to sign or authorize implementation means that your child is not yet considered eligible for special education. This may be important if your child is experiencing significant behavioral difficulties. As I will describe in greater detail when we talk about discipline, the IDEA provides special protections for children with IEPs when they have committed disciplinary infractions. If your child is racking up multiple suspensions, the safest course of action is to authorize the implementation of the IEP and agree in writing that your child is eligible while you continue to hammer out the details of the plan.

Second, if you decline to provide consent or authorization (no signature at all), the District is not legally able or required to implement the services offered in the IEP. For example, if the District is offering speech therapy for 30 minutes per week and you believe your child should get 60 minutes per week, it might be better to authorize the District’s offer of service while you continue to negotiate, instead of rejecting all services by not signing. If you refuse to agree to your child’s annual IEP, the District is required to provide the placement and services offered in the last IEP that you signed and that was implemented. If this is an initial IEP, there is fallback IEP to implement.

Finally, refusing to sign an IEP can create an atmosphere of tension among the members of the IEP team. The District wants and needs your signature in order to move forward and some of the team members may feel insulted or offended that you have refused to sign. This should not deter you from advocating for your child, but it’s good to understand how your actions could be perceived by the District. The most important thing you can do once you decide not to sign your child’s IEP is to keep the lines of communication open with the District and indicate clearly what you would like to see happen to resolve the conflict.

Disclaimer:

This column reflects the views of Diana B. Glick in her individual capacity. It does not necessarily represent the views of her law firm or her clients, and is not sponsored or endorsed by them. The purpose of this column is to assist in dissemination of information about federal special education law, but no representation is made about the accuracy of the information. The information contained in this column is provided only as general information for education purposes, and topics may or may not be updated subsequent to their initial posting.

By using this column you understand that this information is not provided in the course of an attorney-client relationship and is not intended to constitute legal advice. This blog site should not be used as a substitute for competent legal advice from a licensed attorney in your state. This column is not intended to be advertising and Diana B. Glick does not seek to represent anyone desiring representation based upon viewing this blog site in a state where this blog site fails to comply with all laws and ethical rules of that state.

Everything You Need to Know About Your Child’s IEP

August 6, 2010 in Ask the Special Ed Lawyer by dianaglick

IEP Basics

When people reference your child’s IEP, they may be speaking about the meeting (“Are you going to the IEP today?”), the document (“Here is your copy of the IEP.”) or the process as a whole (“Your child may need an IEP.”). There is also an IEP team that is the decision-making body for your child’s services and supports. Because this term seems to be everywhere you turn, you’ve probably already guessed that the IEP process and the document generated by this process are the basis for your child’s experience in special education.

I’ve discussed the general IEP process in my prior columns, starting with the initial assessment. Remember that the legal obligation of the school district is to provide “FAPE”—a free appropriate public education—to students who are eligible for special education. Once the eligibility determination has been made, the District must offer whatever combination of placement, services and supports that are necessary to allow children with disabilities a basic floor of educational opportunity. While the District and parents may agree that the child is eligible for special education, there may be significant differences of opinion regarding the child’s placement, service and accommodations. These are the issues that are worked out through the IEP process.

The IEP Team

There are a few main points to remember about the IEP team. First, as a parent, you are an integral part of the team and should be involved in all the major decisions during the process.

Federal law also requires the presence of the following team members at the IEP meeting: your child’s mainstream teacher, at least one special education teacher and/or support professional (such as a speech-language pathologist or occupational therapist), and an administrator with decision-making power. The presence of the administrator as key—you want to make sure that someone who can offer special education services on behalf of the District is present at the meeting.

The IEP Meeting

KindergartenerSometimes, parents are intimidated by the committee of experts facing them in the meeting (those kid-sized chairs don’t help either!). I try to empower my clients and remind them that they are the parents—who knows their child better? No one! It’s always important to listen to the assessors, teachers and other service providers who are working with your child, but let your gut be your guide. This means that you should feel confident about asking questions and expressing any disagreements you have about your child’s abilities and needs. For example, an IEP will indicate your child’s “present levels of performance.” If a blanket statement is made such as, “Sam is a delightful child with many friends,” and you happen to know that Sam is a delightful child with such a severe language disorder that he cannot participate in age-appropriate conversations and therefore does not have many friends, speak up about this.

Parents are allowed to invite others to the IEP meeting for personal support or advocacy. I encourage this if you believe you will feel intimidated or overwhelmed by the District personnel in the room. It’s always good to have another set of eyes and ears with you and it may boost your confidence to have more support in the room.

In addition, state law may allow you to make a tape (or digital) recording of the meeting. In California, parents may record if they have given 24 hours written notice to the District of their intent. This is recommended in situations where there have been misunderstandings in the past about statements made during the IEP or when you anticipate hearing a lot of evaluation reports that you may need time to digest and want to hear again after the meeting.

The IEP Document

It is often said “If it’s not in the IEP, it doesn’t exist.” This is a good maxim to keep in mind. If someone offers a service during the meeting, but it’s not written down as part of the formal offer of FAPE, it may not happen and there will be no written record of the discussion.

The “service page” of the IEP describes your child’s placement and the services (including amount and frequency) the District is offering to provide. This section is the heart of the document and you’ll want to make sure you understand its terms before signing your consent.

Other important sections of the IEP document include your child’s designation, any accommodations and modifications to the curriculum and the goals. I’ll discuss with greater detail these sections of the IEP in future columns.

At the end of the document is a place where parents can sign their consent to the IEP. Your signature means that you agree that the District’s offer provides your child with FAPE and that you authorize the District to implement the services specified within. In the ideal scenario, you understand the terms of the IEP and agree that they are designed to help your child access the curriculum; therefore, you provide your consent and the District moves forward on the basis of what is written in the IEP. When there is disagreement about any element of the IEP, parents have the right to withhold their consent to the document and seek other avenues to resolve the conflict with the District. Next month, I will continue this discussion and describe the various options parents have when it is time to sign the IEP.

Disclaimer:
This column reflects the views of Diana B. Glick in her individual capacity. It does not necessarily represent the views of her law firm or her clients, and is not sponsored or endorsed by them. The purpose of this column is to assist in dissemination of information about federal special education law, but no representation is made about the accuracy of the information. The information contained in this column is provided only as general information for education purposes, and topics may or may not be updated subsequent to their initial posting.
By using this column you understand that this information is not provided in the course of an attorney-client relationship and is not intended to constitute legal advice. This blog site should not be used as a substitute for competent legal advice from a licensed attorney in your state. This column is not intended to be advertising and Diana B. Glick does not seek to represent anyone desiring representation based upon viewing this blog site in a state where this blog site fails to comply with all laws and ethical rules of that state.

Getting Started in Special Education: The Initial IEP Meeting

May 25, 2010 in Ask the Special Ed Lawyer, Insider Insight, Latest Articles by dianaglick

In my first “Getting Started” column, I described the process for getting your child assessed for special education. Once the assessment is completed, the District will convene an Individualized Education Plan (IEP) meeting to discuss their findings and allow the IEP team to determine eligibility and services, if necessary. The initial IEP meeting is an opportunity for parents and professionals to come together, identify your child’s strengths and challenges and determine a course of action, including services, accommodations and supports, to provide educational access.

The key determination of the initial IEP meeting is whether your child is eligible for special education. Eligibility hinges on two factors: 1) the child must have a qualifying disability and 2) the disability must interfere with the child’s ability to access his or her education, making special education services necessary to provide a basic floor of educational opportunity.

Qualifying Disabilities:

Federal statutes and regulations describe twelve specific disabilities that will make a child eligible for special education. These twelve are:

1) mental retardation

2) hearing impairment

3) speech or language impairment

4) visual impairment

5) serious emotional disturbance (also known as “emotional disturbance”)

6) orthopedic impairment,

7) autism

8.) traumatic brain injury

9) specific learning disability

10) other health impairment

11) deaf-blindness

12) multiple disabilities

States have also been given the option to include developmental delays for children ages three to nine as a separate category.

Interference with Educational Access:

This is a tricky provision. If your child has a problem articulating certain sounds but is doing just fine in school, the District will likely determine that she is not eligible for special education. However, it is important that the team not interpret your child’s school performance too narrowly. For example, if your son is passing his classes, but is calling you crying every afternoon and asking to come home, that is not educational success.

Typically when there is a disagreement, it is because parents believe their child to be eligible while the District asserts otherwise. If you find yourself in this situation, here are some good questions to ask and areas that deserve further scrutiny:

1. Was the assessment appropriate? The law contains a series of requirements for assessments, including that they be conducted in the first language of the student, that the determination not rely on a single testing instrument and that assessments include parental input. These are all areas to explore if you are faced with an assessment that you believe does not accurately reflect your child.

2. What are the qualifications and credentials of the person conducting the assessment? For example, if there is a dispute about whether a child has a speech or language impairment, you will want to make sure that the person conducting the assessment was a licensed speech and language pathologist. States have different licensing requirements, but many also have an online directory of licensed professionals, which can help you confirm the qualifications of your child’s assessor.

3. Is the District considering the full educational experience of my child? This includes not only grades, but standardized testing and peer relationships as well.

4. Parents can ask themselves: have we been the glue holding this whole operation together? Sometimes parents go to great lengths to make sure their children pass their classes, including hiring private tutors, paying for expensive private therapies and even doing homework for them. While I can certainly understand the desire to help your child, this approach tends to backfire if you are seeking a special education designation for your child. Unfortunately, there are situations in which parents have to “let their child fail” in order to establish that he truly does need the intervention.

If the team remains at an impasse on the issue of eligibility, there are many things parents can do to continue advocating for their child, including requesting an independent assessment, working with the school on a 504 plan and seeking out legal advice, among others. I will touch on each of these approaches in future columns.

Author Diana B. Glick

Disclaimer:

This column reflects the views of Diana B. Glick in her individual capacity. It does not necessarily represent the views of her law firm or her clients, and is not sponsored or endorsed by them. The purpose of this column is to assist in dissemination of information about federal special education law, but no representation is made about the accuracy of the information. The information contained in this column is provided only as general information for education purposes, and topics may or may not be updated subsequent to their initial posting.

By using this column you understand that this information is not provided in the course of an attorney-client relationship and is not intended to constitute legal advice. This blog site should not be used as a substitute for competent legal advice from a licensed attorney in your state. This column is not intended to be advertising and Diana B. Glick does not seek to represent anyone desiring representation based upon viewing this blog site in a state where this blog site fails to comply with all laws and ethical rules of that state.

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