Showing posts with label Special Education Advocate. Show all posts
Showing posts with label Special Education Advocate. Show all posts

Friday, September 12, 2014

There are always so many questions around Assistive Technology for students.  This is a wonderful opportunity to attend a very informative event!

https://www.eventbrite.com/e/2014-gate-seminar-tickets-12740702785

Event Details

The Georgia Assistive Technology in Education (GATE) Seminar is a FREE comprehensive venue for Educators, Therapists, Parents and Community Members to gather and learn about Assistive Technology to help achieve student success in the classroom. This seminar will feature a hands-on exhibit hall including national and local vendors in all areas of Assistive Technology. Specialists in the field will present a variety of sessions that focus on best practices, product demonstrations and classroom implementation strategies that will support each student as they reach for their “Accessible Tomorrow”.
For more information on event parkinglunch optionslodgingContinuing Education Units (CEUs), and Certified Rehabilitation Credits (CRCs), please visit our Wiki page here.
**Wireless Internet will be available for a charge of $3.00.  Debit or Credit Card ONLY, NO CASH accepted.  Wifi access can be purchased on location on the day of the event.  Instructions for Wifi access will be included in your attendee packet.
***While admission is free, we are collecting $1.00 cash donations for a LAST RESORT FUND.  This fund helps pay for assistive technology for people in need.  Contributors will be included in the drawing for DOOR PRIZES sponsored by our GATE exhibitors.
Tweeting about GATE Seminar 2014?  Use the hashtag: #GATE2014
**If you are a vendor wanting to register for space in the exhibit hall, please use THIS VENDOR REGISTRATION LINK

Saturday, August 23, 2014

Keeping Vigilant...

I have been trying to capture the right words to describe my week up in Virginia's William and Mary College of Law, for the ISEA (Institute for Special Education). While the week was both inspiring and informative, there is no doubt every parent, every family, every community will need to continue to be vigilant to assert their rights, if their child is to receive a fair and appropriate education.  After meeting attorneys and a sprinkle of advocates from across the United States, the theme across our Country is disparaging – bordering on egregious.  If you have a child with special needs, you MUST understand YOU WILL HAVE TO PURSUE these rights for your child.

One of my goals from the training, is to make sure I provide you with a road-map and resources.  Having an active Advocacy and Educational Consulting practice, kiddos come first and the blog the least important on the to do list. I now realize, to help as many as possible, I need to drop in more often. We are in this together, you are not alone and you can learn how to work with your School or District.  And if that is not possible, you can learn the best remedy you have.

Along with keeping the blog current, I am bringing back quarterly workshops.  I am sincerely grateful for the overwhelming demand for the return of my workshops.  I will be including both previous workshops (please remind me if you were on the waiting list) as well as a series where we dive deeper into individual groups. Next week I will post a calendar of subjects and dates. However, we will launch in September with the infamous "Binder Workshop".  Managing your child's paperwork NOW and not when when in crisis.  This workshop tends to be an eye opener, and where parents find out what evaluations their child is missing, or out of date. How to manage all the work samples you are saving and also how to build an effective communication log. This workshop is relevant to parents of children with special needs - as well as parents who have their children in a private school setting, and are looking to transition back to public school.

Remember to Keep Calm and Advocate!  Robin

Wednesday, December 25, 2013

A Holiday Message



What every Holiday you celebrate - I send a wish to you of Peace and Joy.  And as you gather with your families - celebrate the Special Child in your life.

To My Son Myles,

The day you were born I expected to love you unconditionally, and to find joy in holding you, and to feel happiness just by watching you grow......

.....but I never expected to be so in awe of the way you affect the world around you, and I certainly didn't realize just how much you would teach me.......

I'm so proud of the special person you are and all the wonderful things you do.

You inspire me - Thank you for the gift of being you.

All My Love - Mom




Sunday, September 29, 2013

It started: DSM5 used to revoke autism diagnosis 
Share your story to stop the DSM5

As many of us expected, the new definition of “autism” laid out in the Diagnostic and Statistical Manual, Fifth Edition (DSM5) is being used to deny services and educational placements to people with autism. We are receiving more and more reports from around the US (Buffalo, Dallas, Utica, etc.) of schools, Medicaid providers, insurance companies and local government service providers using the DSM5 to deny services to people who have an autism spectrum disorder.
If you are facing difficulties or the loss of services as a result of the DSM5 please let us know. Please contact us at jgilmore@autismactionnetwork.org with your stories. Your stories will be a crucial component in stopping the DSM5.
All the studies on how the DSM5 will affect people with autism have shown huge numbers will lose their diagnosis, their services, Medicaid and educational placement along with it. One study from the Child Study Center at Yale University showed a 55% reduction, including 30% of those categorized as low-functioning.
We have had bills introduced in several states including New York, New Jersey and Connecticut to require the continued use of the DSM4 and other diagnostic tools such as the ICD. We are working on getting bills introduced in other states. Illinois has already passed legislation prohibiting the use of the DSM5 to deny services. And we are working to prevent the federal government from using the DSM5.
The DSM5 discards the labels of “Asperger syndrome” and “pervasive developmental disorder not otherwise specified (PDD-NOS)” Schools and insurance companies and Medicaid providers are using these changes to tell people who have an Asperger’s or PDD-NOS diagnosis that they no longer have “autism” and are losing insurance coverage, placements in special education and other services.
The DSM5 is wrapped in controversy. The federal National Institute of Mental Health considers the DSM5 so flawed that they will not spend any research dollars on studies that use it. We do not have to put up with this.
Please share this message with friends and family and please post to Facebook and other social networks.

Monday, September 2, 2013

Gwinnett STOPP Retreat - August 23, 24 2013



Last weekend I attended a working retreat for Gwinnett SToPP. (Gwinnett Parent Coalition to Dismantle the School to Prison Pipeline) Professionals from all counties where interviewed and 10 were selected to be a part of their 4th year initiative.  We have made an 8 month commitment towards a project to benefit students and their education - however more important - an investment in a child's future.   Though the majority of attendees reside in Gwinnett - there were additional participants (myself included) who attended from a different county.  The statistics are both staggering - and appalling.

  • Georgia students lost 1.7 million days of instructional time to in or out of school suspensions during 2010-2011 school year.
  • 2,143 Kindergarteners were suspended in Georgia during the 2010-2011 school year. 
  • The graduation rate for Georgia was only 67.4 percent for the 2010-2011 school year.  Only a sixth of Georgia high schools graduated more than 80 percent of students.


I feel privileged to be a part of this initiative for year 4 - and will keep you informed as the weeks go by.