Support

Encouraging Stories

Melanie’s update: Nutriiveda…a life saver!

If you have a child on nutriiveda and seizure medication, please contact me lisa@cherab.org There are doctors now that want to study what you are about to read) Nutriiveda…a life saver! Robin Ketchum called me from the ICU at a Georgia hospital today. “Our 26 year old ‘Real Life Little Mermaid’ Mel is in intensive [...]

Permalink // Comments (1) // March 27, 2010 at 2:31 pm

Late Talker vs. Apraxia-A Garden of Stories

Subject: my apraxic son My name is Gerri and I live in Yarmouth Maine. A friend of mine recently sent me an article from the Star Ledger highlighting your son’s disability. Until recently, we lived in Chatham, NJ. My son, Brian, who is 11 years old, also has apraxia. He too attended the early intervention [...]

Permalink // Comments (0) // July 27, 2006 at 9:44 pm

Editorial Opinion – "Work With Your Child"

By Lisa and Glenn Geng I know you have heard this statement before, and if you didn’t, you will, many times. It is always important to “work” with your child even if he or she does not have any challenges, but even more so if they do, especially the first 5 or 6 years of [...]

Permalink // Comments (0) // July 27, 2006 at 9:42 pm

To the heroes, starting or running a support group for apraxia

Cherab Foundation would like to applaud and encourage the heroes: The people who step forward to start or run a support group for apraxia! Because of these people, parents and professionals can gain personal support and information, which is invaluable to the parents and professionals who care for apraxic children. Parents and Professionals may believe [...]

Permalink // Comments (0) // July 27, 2006 at 9:36 pm

Success Stories

Many parents who have young children diagnosed with apraxia worry about their child’s future. You can help to inspire and raise hope by sharing your success story. Please email your success stories. The families on this page have generously offered to reach out to help others via email. Because these parents and children all can [...]

Permalink // Comments (0) // July 14, 2006 at 6:50 am

A Reason to Know the Signs of Oral Apraxia

By Lisa Geng, a parent of two (beautiful) late talkers, (one with apraxia) Founder and President of two nonprofits for children with communication impairments, Children’s Apraxia Network, and the Cherab Foundation , Co-Founder of Speechville.com, and Co-Author of The Late Talker book I just received an email from a parent who has a child that [...]

Permalink // Comments (0) // June 26, 2006 at 9:23 pm

Silent No More

Message from the President, Missouri Speech-Language-Hearing Association Silent No More he spoke to me yet he was utterly silent mute, soundless, wordless he was the most quiet child (a very powerful quiet) at the same time, he was the most loud child (a very powerful quiet loud) screamed silently at the top of his lungs [...]

Permalink // Comments (0) // June 26, 2006 at 7:16 pm

Our Fourth Child

Written by Susan Loyd* “Thoughts from a mom with 4 special needs kids” Our fourth child was going to be normal. I just knew it after all our other three children were neurologically impaired and no way would God give us a fourth. Our fourth child was going to be able to say her name [...]

Permalink // Comments (1) // June 26, 2006 at 6:03 pm

A Letter To Parents Who Have A Child That Is A Late Talker First Written 7/4/00 and Update from 10/03

Acknowledgment from The Late Talker book: “”…Thanks to my two boys, Dakota and Tanner. Your communication delays were a motivating wake-up call to do something to help both of you and others. Your success from early intervention is an inspiration, providing hope for all late talkers. Without you there would not have been a Cherab Foundation and the [...]

Permalink // Comments (2) // June 25, 2006 at 9:20 pm

Suggestions for a Pre-School Teacher who has a Child with Apraxia in Class

1. Send home a picture of the activity centers, and all the children and teachers, so the child can be more specific about what he or she did during the day. 2. Recognize the child’s strengths, not just his or her needs. 3. Start on teaching the child some signs to use in the classroom [...]

Permalink // Comments (0) // June 25, 2006 at 8:20 pm

JOIN OUR COMMUNITY

The Cherab Foundation BigTent Community
The Cherab Foundation Facebook Group
Follow The Cherab Foundation on Twitter

The Cherab Foundation

P.O. Box 8524
Port St. Lucie, Florida 34952-8524
Phone: 772-335-5135

A proud member of Consumers United for Evidence-based Health Care (CUE)
A national coalition of health and consumer advocacy organizations
and part of the Cochrane Collaboration