Articles



What's New With PRC


  Posted on Sep 21, 2017 - 11:41am

Happy Fall! PRC has been busy over the summer, ensuring our language systems, access methods and support are updated to meet the needs of our clients, their clinicians and their families. So: “What’s New with PRC?” Watch the video for in-depth details, or see below for the highlights. We have new ...


    News And Updates


Welcome Orange Effect!


  Posted on Jun 28, 2018 - 11:31am

"Making sure children with speech disorders receive the speech therapy and technology they need." For Orange Effect founder Joe Pulizzi and his wife, Executive Director Pam Pulizzi, it's more than just a mission statement - it's their joy and their passion. Cleveland-based Orange Effect is the foundation they establishe...


    Blog


Two Lives, Changed


  Posted on Dec 7, 2016 - 2:42pm

The odds, they told her, were astronomical. The chances of her son having a rare disorder were the same as being struck by lightning. And then lightning struck once more. For Barrington, NJ, residents Kelly Sexton and her husband, Ryan, getting an official diagnosis for their two sons, Dylan, 7, and Logan, 5, was a myster...


    Blog


Today Is Moebius Syndrome Awareness Day


  Posted on Jan 24, 2017 - 2:37pm

Jan. 24th is Moebius Syndrome Awareness Day. According to the Children's Craniofacial Association (PDF): Moebius syndrome is a rare congenital (present at birth) developmental disorder, characterized by absence or underdevelopment of the nerves that control facial (cranial nerve 7) and eye movements (cranial nerve 6)...


    Blog   -  moebius syndrome awareness day


TOB: Words Creating Worlds


  Posted on May 1, 2018 - 10:51am

"I love him sooooo much!" I squeal and clap my hands, then stretch my fingers out and wiggle them, eyes wide, crouched, ready to tickle my six-year-old son Tobin. He looks me right in the eyes, an expectant grin growing across his face. We lock eyes for a good five seconds: I’m crouched and ready, while he stands wit...


    Blog


The Steve Gleason Enduring Voices Act


  Posted on May 19, 2017 - 3:33pm

“When a person is diagnosed with ALS, or amyotrophic lateral sclerosis, he is expected to fade away quietly and die. This is not okay.” In 2015, Congress overwhelmingly approved a bill that made sweeping changes to Medicare. Included in the bill: a provision to no longer fund the purchase of speech-ge...


    News And Updates


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