Welcome Shannon, AAC Institute/ICAN Talk Clinic!
From: aacpa...@googlegroups.comSent: 3/7/2014 11:41 AMTo: Digest RecipientsSubject: Digest for aacpa...@googlegroups.com - 3 Messages in 1 Topic
Group: http://groups.google.com/group/aacparents/topics
scarney <sca...@aacinstitute.org> Mar 06 10:07AM -0800
Hello to Everyone,
My name is Shannon and I am the new administrator for the AAC Parent Google
Group. I have just moved to Pittsburgh from Vermont where I lived for 10
years. I was active in a group known as the Vermont Family Network. I was
a parent support person and had my own support group for the town where I
lived. I am currently the office manager for the AAC Institute/ICAN Talk
Clinic, too.
My daughter has cerebral palsy as well as other diagnoses. She is
currently in her second year of college studying Human Services. She would
like to be an advocate some day. She has developed my passion for helping
those who may need help finding their own voice.
I would like to get some feedback as to how you would like to see this
group move forward. Are you happy the way it is? What kinds of things
would you like posted to keep you informed? What type of information do
you find most valuable to support your child using AAC? Are you in need of
someone to talk to?
You may have noticed already that we launched our new ICAN Talk Clinic
website, and the AAC Institute has started the process to update our
primary website. Some parent requested information has been made
available at *www.icantalkclinic.com* <http://www.icantalkclinic.com/> as
we as we start redesigning our new site, resources and services. In the
meantime, I will be sharing information about our AAC summer camp for those
of you already asking how to register for the full parent group to have
access.
I look forward to “meeting” all of you in conversation.
Best regards,
Shannon
Gayle Rich <gayle...@carpedrm.com> Mar 06 05:04PM -0500
Hi Shannon,
Welcome to the group. My name is Gayle and I have been a nominal member for years - my daughter Sarah is 31 years old with severe quadriplegic cerebral palsy and is now living in a facility with many other young adult disabled folks. She has always been just a functional communicator with her Dynavox (v-max) but since she is at her new home (almost 2 years), she has virtually stopped using it altogether. She has the capability, but not the motivation.
She has an iPad and they are investigating communication programs on it as she seems much more interested in using it than her vmax. I would be interested in information on people using the iPad as a communication device and what has been successful for others, as well as strategies for encouraging use of communication tools in general. She seems perfectly happy to drive around, smile and wave to both staff and other residents when her life could be so much richer if she would communicate with them.
Look forward to more conversation from the group,
Gayle
On Mar 6, 2014, at 1:07 PM, scarney wrote:
Terry Street <terr...@verizon.net> Mar 06 05:30PM -0500
Gayle,
My 8 year old uses Touch Chat on the iPad. It is a fabulous communication device and is super for her to use in her daily school work as well. I homeschool and am very pleased with the app. She is beginning to make more complex sentences with Touch Chat.
Terry
Sent from my iPad
--
You received this message because you are subscribed to the Google Groups "AAC Parents" group.
To unsubscribe from this group and stop receiving emails from it, send an email to
aacparents+...@googlegroups.com.
To post to this group, send email to
aacpa...@googlegroups.com.
Visit this group at
http://groups.google.com/group/aacparents.
For more options, visit
https://groups.google.com/d/optout.