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Navigating the Journey of Dyslexia Advocacy

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October is Learning Disabilities Awareness Month—a dedicated time to raise community awareness about learning disabilities and provide support for all children.

While awareness is crucial, parents of children with dyslexia are intimately familiar with their children’s day-to-day struggles. For these parents, another “A” word holds even greater power—advocacy.

As a parent, no one understands your child better than you do. In advocating for your child’s needs, it’s essential to recognize your unique role and the importance of being their strongest advocate. This blog will guide you through the process of advocating for your child with dyslexia, offering valuable insights, tips, and key information.

  1. Know Your Child’s Rights Under the Individuals with Disabilities Act (IDEA):

Under the Individuals with Disabilities Act (IDEA), our nation’s special education law, children and their parents or guardians are guaranteed certain protections and rights. Once your child is identified as having a qualifying disability, schools are legally obligated to provide special education services. IDEA also grants parents procedural safeguards, ensuring they are informed and have a voice in every aspect of their child’s special education evaluation and IEP (Individualized Education Program) process. It’s crucial to understand these rights and the associated documentation thoroughly. Don’t hesitate to seek clarification before signing any documents.

  1. Stay Organized with a Binder:

An essential aspect of effective advocacy is staying organized. Maintain a binder containing all relevant documentation about your child’s diagnosis and evaluations. This should include test results, doctor’s notes, educator’s observations, report cards, writing samples, and academic skill data. This binder keeps essential documents organized and records progress and communication with your child’s educational team.

  1. Be Prepared for Special Education Meetings:

Being well-prepared for special education meetings is paramount. Your seat at the table matters because you know your child best. Prepare questions in advance and be ready to speak up if answers aren’t clear. Meetings often move swiftly, so don’t hesitate to request additional meetings for clarification. Taking notes during these meetings demonstrates your active involvement and commitment to your child’s special education services.

  1. Summarize and Follow Up via Email:

After special education meetings, send a summary email outlining the main discussion points and decisions. This ensures everyone is on the same page and provides an opportunity for clarification. If anything remains unclear, your email can initiate further conversation. Request follow-up meetings as needed to address any outstanding issues.

  1. Establish Clear Expectations:

Communicate with teachers about your expectations, your child’s expectations, and the school’s expectations. Prevent miscommunication and surprises by setting honest, positive, and realistic expectations for your child’s success. Maintain objectivity when receiving feedback from teachers and professionals to foster productive discussions.

In conclusion, October’s Learning Disabilities Awareness Month is an excellent opportunity to underscore the importance of advocacy for children with dyslexia. As a parent, you are uniquely positioned to champion your child’s educational journey. By understanding your child’s rights, staying organized, preparing for meetings, communicating effectively, and setting clear expectations, you can be the most effective advocate for your child’s success.

Keywords: Learning Disabilities Awareness Month, dyslexia, advocacy, parents, special education, IEP, individualized education program, educational rights, communication, expectations

 

Parents as Advocates: Tackling Dyslexia

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Parents as Advocates: Tackling Dyslexia

Parents whose children suffer from dyslexia are plenty aware of the struggles their children face on a day-to-day basis. That is why another “A” word can be even more powerful for families—advocacy.

No one knows your child better than you do. Keep this in mind when advocating for your child’s needs. In parents’ efforts not to come across as a “helicopter parent,” they sometimes assume it is in their child’s best interest to follow the expert’s lead, avoid making waves and be passively agreeable. They do not want to be the bulldog. These fears are common, but that doesn’t make them true.

You are your child’s greatest advocate, and here’s how to accomplish that.

Know Your Legal Rights

Under the Individuals with Disabilities Act, our nation’s special education law, children and their parents or guardians are guaranteed certain protections and rights. Once identified as having a qualifying disability, schools are legally required to provide special education services to your child.

Also, under IDEA, the law provides parents with something called procedural safeguards, which are put in place so that parents are aware of and have a voice in every aspect of their child’s special education evaluation and IEP process. As part of the process, the school must provide you with documentation and an explanation of your rights—STUDY UP ON THESE DOCUMENTS.

It is commonplace for IEP meetings to move quickly, with a “sign here if you don’t have any questions” style of rapid wrap-up. It is your job to closely review these documents and to seek clarification before signing anything.

Be Organized

Another best practice for advocacy that goes hand in hand with knowing your child’s legal rights is to stay organized. Keep a binder of all necessary documentation regarding your child’s diagnosis and any other evaluative documents that you accumulate as you work through the process.

Items such as test results, doctor’s notes and recommendations, educator’s observations, report cards, writing samples, and any data concerning your child’s academic skills should be kept for future reference.

The binder is also a great resource for you to use for note taking during IEP or 504 meetings. Not only will you have your own notes to refer back to after the meeting, but the process of taking notes shows that you are actively listening and invested in your child’s special education services. When parents demonstrate this level of involvement and support, it’s the child who benefits.

The binder keeps essential documents organized and acts as a paper trail of progress and correspondence among your child’s team.

Be Prepared

It is also essential for parents to be fully prepared for special education meetings. Because of this, the binder’s benefits are two-fold: paper trail and parent playbook [or however you want to define the two benefits].

Of all members of your child’s academic team, you are the person that knows him best, so your seat at the table matters most. Advocating for your child means preparing questions ahead of time and speaking up if they aren’t answered clearly. Meetings tend to move quickly, so request an additional meeting if you haven’t gotten clear answers.

Do not assume that the team will automatically clarify for you, so be prepared to ask follow-up questions if needed.

Follow up

Another helpful advocacy move is to email a summary of the main discussion points that you took away from the meeting afterwards. This keeps everyone on the same page regarding the decisions that were discussed and allows you to share your own perception of how the meeting went.

If anything is unclear, your email will start that conversation and provide clarification. In that email, ask about a follow-up meeting so that dates can be arranged and any other necessary steps can be taken.

Keep Open Communication with Teachers

Speak to teachers about your expectations, your child’s expectations, and the school’s expectations. This will prevent any miscommunication and unfortunate surprises.

When setting expectations for your child’s success, it is important to be honest, positive, and realistic about the growth that you’d like to see. It will be difficult, but as much as possible, remain unemotional and unbiased about the feedback that you get from your child’s teachers and other professionals—cool heads prevail.

Parents as Advocates: Tackling Dyslexia

/in , , , , , /by

October is Learning Disabilities Awareness Month—31 days dedicated to building community awareness about learning disabilities in an effort to provide supports for all children. As important as awareness is, however, parents whose children suffer from dyslexia are plenty aware of the struggles their children face on a day-to-day basis. That is why another “A” word can be even more powerful for families—advocacy.

 

No one knows your child better than you do. Keep this in mind when advocating for your child’s needs. In parents’ efforts not to come across as a “helicopter parent,” they sometimes assume it is in their child’s best interest to follow the expert’s lead, avoid making waves, and be passively agreeable. They do not want to be the bulldog. These fears are common, but that doesn’t make them true.

 

You are your child’s greatest advocate, and here’s how to accomplish that:

 

  • Under the Individuals with Disabilities Act, our nation’s special education law, children and their parents or guardians are guaranteed certain protections and rights. Once identified as having a qualifying disability, schools are legally required to provide special education services to your child. Also under IDEA, the law provides parents with something called procedural safeguards, which are put in place so that parents are aware of and have a voice in every aspect of their child’s special education evaluation and IEP process. As part of the process, the school must provide you with documentation and explanation of your rights—STUDY UP ON THESE DOCUMENTS. It is commonplace for IEP meetings to move quickly, with a “sign here if you don’t have any questions” style of rapid wrap-up. It is your job to closely review these documents and to seek clarification before signing anything.
  • Another best practice for advocacy that goes hand in hand with knowing your child’s legal rights is to stay organized. Keep a binder of all necessary documentation regarding your child’s diagnosis and any other evaluative documents that you accumulate as you work through the process. Items such as test results, doctor’s notes and recommendations, educator’s observations, report cards, writing samples, and any data concerning your child’s academic skills should be kept for future reference. The binder keeps essential documents organized and acts as a paper trail of progress and correspondence among your child’s team.
  • It is also essential for parents to be fully prepared for special education meetings. Because of this, the binder’s benefits are two-fold: paper trail and parent playbook [or however you want to define the two benefits]. Of all members of your child’s academic team, you are the person that knows him best, so your seat at the table matters most. Advocating for your child means preparing questions ahead of time and speaking up if they aren’t answered clearly. Meetings tend to move quickly, so request an additional meeting if you haven’t gotten clear answers. Do not assume that the team will automatically clarify for you, so be prepared to ask follow-up questions if needed.
  • The binder is also a great resource for you to use for note taking during IEP or 504 meetings. Not only will you have your own notes to refer back to after the meeting, but the process of taking notes shows that you are actively listening and invested in your child’s special education services. When parents demonstrate this level of involvement and support, it’s the child who benefits.
  • Another helpful advocacy move is to email a summary of the main discussion points that you took away from the meeting afterwards. This keeps everyone on the same page regarding the decisions that were discussed and allows you to share your own perception of how the meeting went. If anything is unclear, your email will start that conversation and provide clarification. In that email, ask about a follow-up meeting so that dates can be arranged and any other necessary steps can be taken.
  • Speak to teachers about your expectations, your child’s expectations, and the school’s expectations. This will prevent any miscommunication and unfortunate surprises. When setting expectations for your child’s success, it is important to be honest, positive, and realistic about the growth that you’d like to see. It will be difficult, but as much as possible, remain unemotional and unbiased about the feedback that you get from your child’s teachers and other professionals—cool heads prevail.