I started as a designer, patented inventor, and creator in the fashion, toy, and film industries, but after the early diagnosis of my young children on the spectrum, both “late talkers,” diagnosed with multiple disorders including apraxia, I entered the world of nonprofit, research, and advocacy. I am the founder of the nonprofit Cherab Foundation where I've been outreaching for over twenty years. I've hosted numerous conferences including the first for apraxia overseen by a medical director from NIH who reviewed my protocol – the use of fish oils as a therapeutic intervention, published research on my patented nutritional intervention IQed Smart Nutrition, and co-authored the book The Late Talker to share my proven protocol and help others achieve the best possible results for their communication impaired children.
When you have a child with a severe communication impairment, they probably are in therapy almost every day of their life. Too often, I’ve found parents forget children with special needs are still children. While appropriate speech therapy is critical for apraxia, children learn through play, and too often the importance of play is underestimated. What I love about The New Language of Toys is it shows us, the parents (as well as therapists) how to take typical toys found around the house to use as fun therapy tools to help bring your child a voice.
I used to work in toy design prior to being a parent so being able to use toys as therapy for speech is amazing. In addition, it helps the child’s self-esteem when you can teach them how to play, something that doesn’t always come naturally to a percentage of children with special needs. This…
I started as a designer, patented inventor, and creator in the fashion, toy, and film industries, but after the early diagnosis of my young children on the spectrum, both “late talkers,” diagnosed with multiple disorders including apraxia, I entered the world of nonprofit, research, and advocacy. I am the founder of the nonprofit Cherab Foundation where I've been outreaching for over twenty years. I've hosted numerous conferences including the first for apraxia overseen by a medical director from NIH who reviewed my protocol – the use of fish oils as a therapeutic intervention, published research on my patented nutritional intervention IQed Smart Nutrition, and co-authored the book The Late Talker to share my proven protocol and help others achieve the best possible results for their communication impaired children.
Sensory processing disorder or SPD is a difficult condition to explain as it can involve one or more of any of our senses, so can present differently in each child. It would be considered one of the neurological “soft signs” meaning that a diagnosis of SPD typically means there is more going on than a simple developmental lag. Today the majority of children diagnosed with apraxia also have coexisting soft signs such as SPD, hypotonia (low tone), and/or motor deficits in the body. It’s important if apraxia is diagnosed or suspected to take your child to either a pediatric neurologist or developmental pediatrician to confirm or rule out soft signs in the body.
When Tanner was little and his only “words” were “mmm” or “ma” we were at the Chelsea Piers in NYC. Tanner had a sensory meltdown and if you’ve never seen one it can be very intense. His…
The groundbreaking book that explains Sensory Processing Difference (SPD)–and presents a drug-free approach that offers hope for parents–now revised and updated.
Does your child exhibit…
Over-responsivity–or under-responsivity–to touch or movement? A child with SPD may be a “sensory avoider,” withdrawing from touch, refusing to wear certain clothing, avoiding active games–or he may be a “sensory disregarder,” needing a jump start to get moving.
Over-responsivity–or under-responsivity–to sounds, sights taste, or smell? She may cover her ears or eyes, be a picky eater, or seem oblivious to sensory cues.
Cravings for sensation? The “sensory craver” never gets enough of certain sensations, e.g.,…
I started as a designer, patented inventor, and creator in the fashion, toy, and film industries, but after the early diagnosis of my young children on the spectrum, both “late talkers,” diagnosed with multiple disorders including apraxia, I entered the world of nonprofit, research, and advocacy. I am the founder of the nonprofit Cherab Foundation where I've been outreaching for over twenty years. I've hosted numerous conferences including the first for apraxia overseen by a medical director from NIH who reviewed my protocol – the use of fish oils as a therapeutic intervention, published research on my patented nutritional intervention IQed Smart Nutrition, and co-authored the book The Late Talker to share my proven protocol and help others achieve the best possible results for their communication impaired children.
As a parent of a child diagnosed with apraxia, you probably have heard, “what’s wrong with him?” at least once. If not, be prepared, because when you hear it and you aren’t ready for it, it can feel like someone knocked the wind out of you. I didn’t only love the Chicken Soup for the Soul books for me, but I also would share the stories I felt were of interest with my boys who both were diagnosed as young children with severe special needs. What these books brought me and my boys was pride, hope, and inspiration that from a rough beginning, there can be a bright future. Actually, in some cases, these stories share it’s due to a rough start that the person ended up becoming a better person.
While my son Tanner was little and I read stories to him from the Chicken Soup for the Soul…
The classic New York Times bestseller that started it all- and according to USA Today one of the top five books in the past quarter century "that leave a legacy." The Original... with 20 new bonus stories for the next 20 years!
Everyone is talking about it. Twenty years after its creation, this bestseller continues to change lives around the world. Rediscover the power of inspiration with timeless stories about the everyday miracles that illuminate the best of the human spirit.
Whether you're discovering Chicken Soup for the Soul for the first time, or you are a long-time fan, this…
I started as a designer, patented inventor, and creator in the fashion, toy, and film industries, but after the early diagnosis of my young children on the spectrum, both “late talkers,” diagnosed with multiple disorders including apraxia, I entered the world of nonprofit, research, and advocacy. I am the founder of the nonprofit Cherab Foundation where I've been outreaching for over twenty years. I've hosted numerous conferences including the first for apraxia overseen by a medical director from NIH who reviewed my protocol – the use of fish oils as a therapeutic intervention, published research on my patented nutritional intervention IQed Smart Nutrition, and co-authored the book The Late Talker to share my proven protocol and help others achieve the best possible results for their communication impaired children.
Unlike parents who have a child that is born deaf or blind where protocols are in place by law, if you have a child with a communication impairment like apraxia, you have to advocate a lot for your child or they may not receive the therapies and placement that are appropriate for them. To make it even more complicated, there is no one set classification for a child with apraxia. If your child is deaf or has a diagnosis such as autism, the school system has a classification for those diagnoses. For just about any other communication impairment your child can be classified from “other health impaired” to “developmentally delayed” Some schools may have communication or speech impairments as a classification, but not all.
This book is a start to helping you learn how to become an advocate for your late talker child. After advocating for both of my special…
Drawing on decades of experience, a special education attorney and sought-after special education advocate help parents of students with disabilities navigate their school systems to get the services they need for their children.
Parents will find no other book on special education like Your Special Education Rights. Julie and Jennifer demystify the federal laws that govern the rights of public school children with disabilities and explain how school districts often ignore or circumvent these laws. They pull the curtain back on the politics of special education, exposing truths that school districts don't want you to know, such as the fact…
I always intended to be a fiction writer (and have written ten novels, both YA and adult) but my oldest child is autistic, which led to my meeting and then collaborating on several non-fiction books with Dr. Lynn Kern Koegel, who’s an expert in the autism field, currently at Stanford University. Finding myself writing non-fiction wasn’t the only way having an autistic child changed my life. When my son was first diagnosed, I didn’t know what that meant for his future, and I desperately wanted information—and even entertainment—that made me feel inspired and hopeful. I needed to find my way toward feeling positive and not anxious, for both our sakes.
So, in the interest of full disclosure, I should mention that I haven’t read this entire book, but I did read the original article that the book came out of and other articles by and about the Suskinds.
Ron Suskind did exactly what Lynn Koegel and I believe all parents should do: he observed his son’s interest and used it as a bridge for communication and connection.
Disney was a huge part of our family life when our kids were little (and still plays a role in our lives today since one of my sons is a children’s television writer and another one has his own theme park video channel), so I love that it was Disney movies that brought the Suskinds together.
Pulitzer Prize-winning author Ron Suskind tells the story of how his autistic son was able to regain the ability to speak through the medium of Disney animated films.
"Ron Suskind's "Life, Animated" is an extraordinary saga of an exceptional boy from a remarkable family and their compelling journey through autism."-David Royko, Chicago Tribune
Imagine being trapped inside a Disney movie and having to learn about life mostly from animated characters dancing across a screen of color. A fantasy? A nightmare? This is the real-life story of Owen Suskind, the son of the Pulitzer Prize-winning journalist Ron Suskind and his wife,…
