Don't IEP Alone.
I attend IEP meetings for a living and you just can't compete with that level of crazy.
Warning: I've been told I have a Philly accent. I don't hear it. Also, I curse. It's something I'm working on as far as personal development. So please don't be put off. I'm trying.
Inspired by her own son with disabilities, Lisa Lightner is an award-winning blogger and advocate. She has previously worked for her county's Arc and has served on the Boards of Directors for several disability organizations.
Currently, she is her county's chairperson for the Right to Education Task Force, a federally decreed group set up in 1971 to ensure that all children in Pennsylvania had the opportunity to an education.
When not attending IEP meetings with families or lobbying in Harrisburg and DC for disability rights, she can be found on the web at her IEP advice blog, A Day in our Shoes. She is known for her practical, realistic and implementable advice for parents.
Don't IEP Alone.
The Brain Recovery Project
I'm talking IEPs, seizures, research and more with Monika Jones from the Brain Recovery Project.
To learn more about:
The Brain Recovery Project
Our mission is simple: We help children reach their full potential after brain surgery to stop seizures
The Brain Recovery Project: Childhood Epilepsy Surgery Foundation
969 Colorado Blvd. | Suite 101 | Los Angeles, CA 90041
We help kids reach their full potential after epilepsy surgery.
Other ways I can help you with IEPs:
📊 Free IEP Data Collection Sheets
📒 Free IEP Binder for Parents
☑️ IEP Meeting Preparation Kit
🧰 IEP Toolkit for Parents
👩💻 Online Advocacy Training
🙋 Ask an Advocate your IEP Question
🧰 IEP Teacher Toolkit