From Struggles with Apraxia to Honors English Tanner Geng and His Success Story
Kids Enabled May 15, 2011
From Struggles with Apraxia to Honors English
Tanner Geng and His Success Story
It is hard to navigate the world of supplements, so it is wise to turn to the experts for advice about which supplements are the most appropriate for certain conditions.
Tanner Geng’s mom Lisa, with the help of Lauren Zimet, MS, CCC/SLP, saw a significant improvement in Tanner’s speech skills (he has apraxia of speech) after he began taking fish oil supplements.
Tanner’s background from when he was 3
Lisa says, “Lauren is the one professional that witnessed the earlier dramatic surges when we started him on fish oils. So, Tanner really has responded well to essential nutrients. We always fed him very healthy – as organic as possible – but it’s not always what we eat, but what we digest and utilize.”
Join Kids Enabled as we hear of Tanner’s journey from his point of view:
Kids Enabled: What were your biggest struggles growing up? What were your toughest challenges in the classroom?
Tanner Geng: My biggest struggle was not being able to pronounce the words correctly or people couldn’t understand what I was saying if I was talking to them. In the classroom if I was asked to read something and I got stuck on a word, and I knew it the word, but I just couldn’t get it out, someone in the class would shout it out for me, which frustrated me because I knew the word. I just couldn’t say it, and they would think they were helping me because they thought I didn’t know it.
KE: What is your earliest memory of struggling in school?
TG: I don’t remember having any issues outside of reading which was in 6th grade. Reading was hard for me because, even though I knew the words, they wouldn’t come out of my mouth. I always liked to write stories and poems. My brain developed after I started taking Nutriiveda last year and I got more creative in writing my stories. I like to share the stories I write. Last year I was given more time to write, but I wasn’t into reading. I only read what I had to read. This year in junior high school I haven’t had as much time to write, but I’ve been reading more because I enjoy it. Right now I’m reading Lord of the Flies with my class. I am going to be in honors classes for high school, and my mom is really impressed especially that my teacher this year recommended me for honors English.
KE: Did your struggles ever cause your self-esteem to suffer?
TG: Sometimes I feel bad about myself because I get made fun of if I talk funny, but mainly it’s people I don’t know that would tease me, not kids that I went to school with. But, since my speech has gotten better this year, nobody even notices I have a speech problem anymore. I have lots of friends and nobody really has cared about my speech, even when I did have problems speaking.
KE: What advice would you give to parents of children who struggle with learning challenges?
TG: My advice to parents of kids who have speech problems is to be in classes with the rest of the kids in school to learn everything they learn. Although I used to not be able to speak, I still knew how to learn. My other advice is to give kids fish oils and Nutriiveda because it helps with motor planning and of course speech. It also helps with physical stuff like helping me be more coordinated.
KE: How do you define success at this point in your life?
TG: Success to me is becoming a special education lawyer to help other kids in the country who have speech and other problems and helping them get into better schools and fight for what is right for them.
From Lisa Geng:
Another Tanner update…this is just amazing! Today Tanner and I met with the guidance councilor for 9th grade; next year he will be going to high school. I knew that he was going to talk to Tanner, not me, but I was there to back him up just in case.
The first question the counselor asked was, “What do you want to do after high school?” and Tanner responded with no hesitation “I want to be a lawyer.” He wants to be a special education attorney. The questions and answers continued smoothly. Tanner was having no issues saying what classes he wanted or didn’t want, and he didn’t choose any “easy” electives either! Tanner was recommended for honors classes by his current teacher.
He currently plays varsity basketball and football and will probably continue in sports. Tanner just asked me if he can volunteer at an animal shelter over the summer. He said, “Mom, I just want to make those animals happy that have to be there.”
Tanner is fully mainstreamed and a great student, typically an A student. In the past, I had to do homework with him. I know there are others of you out there with older apraxic children that know exactly what I am talking about; reading and writing is like pulling teeth.
Since starting on the food supplement Nutriiveda (NV), Tanner is completely independent in his studies and is excelling independently; he doesn’t need my help anymore. This is far better than excelling with me for many reasons of course!
Prior to this year, if someone had asked him the question his counselor was asking today, i.e., questions about his future, college, choices of classes, etc., his standard response would have been: 1) look at me to help him answer and 2) say “I don’t know” (even if he did know but he wouldn’t want to explain) and then look at me to help him answer.
Not bad for a kid who, according to his kindergarten teachers, “wouldn’t make it in a mainstream kindergarten class and needed to be in a self-contained learning disabled class.”
Tanner was fully included for kindergarten because I really advocated for him. He not only “made it” in an inclusion class, he was one of the top students. I did follow my own advice and didn’t start him in kindergarten until age 6 years for that extra year of therapy and developmental time.
I credit therapy for so much. Tanner has done a lifetime of therapy in the past 10 years, both traditional and alternative with a focus on speech, but I also know that therapy doesn’t work as well if a child doesn’t get the essential nutrients.
More background on Tanner
My son at 13 was considered a success, but there were issues.. He was mainstreamed and I no longer had him in speech therapy even though he would once in a while see a therapist. He accepted how he spoke, and so did we. We accepted that he could communicate well enough to have friends, be in school mainstreamed without support, read the menu and order his own food at a restaurant. And we also knew that nobody would know Tanner had a speech issue if he kept his answers short- not unless he let his guard down and tried to talk in complex thoughts.
But what my son was like a year ago -this is what we accepted that is all gone now -he’s normalized:
1. Lags in both reading and writing. He was on level on both and tested to be above average in his concepts -but his expression was lagging. Reading outloud or writing was not enjoyable to him and I had to work with him with his homework. It was a struggle.
2. He didn’t pick up abstract type humor if we were watching adult TV shows like say The Office. He was more literal- he enjoyed America’s Funniest Home Videos for example.
3. He was also literal in his ability to listen. If a teacher said he had to do something like unplug unused appliances around the house to help save the planet- he would unplug appliances around our house and if I asked him what he was doing he would say “Mom don’t you care about planet Earth?!” If the teacher said “OK class after we are done I don’t want anyone to leave until you help me clean up” Everyone would leave when they were done and I was told by a few very proud teachers that “He was the only one that helped me” I was the strange parent that wasn’t happy to hear that compliment. I knew he wasn’t normal and wanted him to stray into abstract thought a bit more!!
4. His ability in sports was clumsy but committed. Poor little guy would push himself till he was literally exhausted but his abilities were far short of other boys his age. He didn’t run well, nor would you use the word effortless or graceful to describe him when he was playing sports. While his brother and all the other neighborhood kids wore Heelys and used skate boards, Tanner would have his own but would never use them. His reflexes were sluggish as well.
5. He would tire easily and take naps when home from school.
6. Tanner never felt pain like others. He was called the “tough kid” when he got shots because he didn’t cry, but he would say “ow” and cringe away if you tickled his arm, or patted his head. A few years ago he was at a sleep over and broke his finger playing football, but the family didn’t know it was broken because he didn’t tell them he hurt it. The next day when I went to pick him up he wanted to stay and swim, still not saying anything was wrong with his finger. The only reason I found out was because he couldn’t “really bend it” anymore so I took him to the hospital where even when the doctor touched where the break was he didn’t flinch, but it was a broken finger.
All these things we started to accept were who he was, and while I think any typeof story of progress is great -until every rock is unturned if a new one pops up I think it’s worth exploring. Then if that doesn’t work you know that you helped your child get to as far as potentially possible.
And maybe the only reason I did try something was because I wasn’t trying to help Tanner’s speech or motor skills or anything else at this point. Probably not but maybe.
My son has had within the one year on NV surges across the board that are SO profound that every single person that meets him now that knew him just 18 months ago is SHOCKED. He quickly on NV developed a tremendous surge in complex language, independence and excellence in academics, grace and abilities in sports in basketball, football to the point if you didn’t know it was him you’d never know it was him on that field, quick reflexes, fully developed mature abstract sense of humor that he both understands if he hears it and knowledge in how to make others laugh in this area, passion for music, interest in current events and wanting to discuss them, tremendous growth from a stocky 5 foot 7 slightly overweight child who had been on a healthy organic diet but was that way regardless to a muscular SIX FOOT ONE 14 year old.
Tanner feels pain normally now -he’s not really thrilled about it –he said to me “wouldn’t you rather not feel pain all the way?” And I told him it was a warning system for his body -so pain is a good thing to feel normally -besides he did feel pain before -for stuff he shouldn’t feel pain about -like a pat on the head or a tickle etc. (for more documentation on ability to feel pain and normalization in this area read more here)
And cherry on top -he was recommended for honors classes for high school and of all things honors English too. He gave a verbal report in school and got an A and her just wrote to YADA about it.
“I’m not in speech therapy. I gave a verbal report today and the teacher wrote down that I was nice and loud and with a clean voice. Sometimes if I am tired my speech messes up.”
Two years on Nutriiveda original-9th grade and in benchmark testing done by his high school where he is mainstreamed, fully independent and in honors, even though his grades were already honors level (average grade 88) he went up another 6 points in English and 16 in math! He’s on his HS debate team (debate…a former child with apraxia!) and…he placed second in December of 2011!! Tanner’s on debate because he wants to be a special education attorney to help other children like him in the future!
Three years on Nutriiveda original -10th grade -benchmark testing done by his high school where he is mainstreamed, fully independent and in honors, continues to go up. His GPA so has now risen to a 3.85 and he is almost a straight A student in honors classes. Again no IEP or any accommodations of any kind. Tanner is still focused on his goal of being a special education attorney and wants to continue to raise his GPA.
PS. After I read this I asked Tanner “Why did you use the word motor planning in your interview? I typically hear you say things about improvements in your speech, your school work, athletics, and jumping over a bush! What do you think motor planning means?” (because I figure he hears me say it) So Tanner says “It’s when your brain tells your body what to do” So at this point he was putting his socks on and I said “You mean like I can motor plan with my brain to tell my foot to step on your foot?” And at this point I was trying to step on his one foot but he kept moving it away and we were both laughing. And then Tanner says to me when I gave up “ My brain is faster at motor planning than yours“
Special Thanks to Kids Enabled
A Note About Oral and Verbal Apraxia
Tanner was diagnosed with both oral as well as verbal apraxia. While verbal apraxia is a lot more common than people today appreciate, oral apraxia is a diagnosis given much less frequently. Many people don’t know what Verbal Apraxia is, and even less know what Oral Apraxia is. Not all children with verbal apraxia will have oral apraxia, but it’s pretty much a given that all children with oral apraxia will have verbal apraxia. Before Tanner learned how to smile he didn’t even try much and most times just had a blank look on his face as you’ll see on the photo on the left. We called him the “serious baby” at this point not knowing he had classic signs of oral apraxia. On the right is a photo of Tanner smiling. Like others with oral apraxia you’ll see, he was able to smile once in awhile, just not often, and not on command.
Below is me with my sons Tanner on the left, and his brother Dakota on the right on their first day of school. We were all so excited, and you can see the school bus in the background. Tanner had to learn how to smile due to his oral apraxia. When Tanner was learning to smile he would smile and close his eyes. We’d then say “Tanner open your eyes” and he’d open his eyes and open his mouth. Then we’d say “Smile again” and again he’d smile and scrunch his face like in this photo again which was his classic smile for awhile.
Tanner’s background is here which is a letter I wrote to parents years ago to raise awareness about oral and verbal apraxia. But most don’t know what oral apraxia is or how it can affect a child and his family. The impact it can have in school when that “blank look” is taken by the teacher as not understanding. Tanner’s oral apraxia affected him for most of his life up till recently. At age 11 after years of therapy his one therapist Dr. Renai Jonas even tried hooking electrodes to his face to stimulate the nerves with little help. Tanner responded to nutrition through NV somehow which is remarkable after the years of therapy. We are so thankful!
Like Tanner on this site there are two other children diagnosed with both oral and verbal apraxia which are very well documented with video and photos.
Possible Oral Apraxia or Oral Motor Warning Signs from the Cherab Foundation
There are two types of oral motor problems.
Oral Apraxia is a disorder where the child, who typically is a “late talker” is unable to coordinate and/or initiate movement of their jaw, lips and tongue (articulators) on command.
An Oral Motor Disorder, which could be a different oral motor problem than apraxia (could be from weakness/dysarthria for example) is the second type, in which the child is unable to coordinate and/or initiate movement of normal eating movements (vegetative activities.)
Here are some possible warning signs of the two types of oral motor problems, written by Lisa Geng, the parent of two children who were diagnosed by a neurologist (Trever. DeSouza MD) and a neurodevelopmental pediatrician (Marilyn Agin MD) with two different types of oral motor problems, with help from Cherab’s advisor, Sara R. Johnson, CCC/SLP.
Can your child do the following regularly or on command:
If your child cannot do all or some of the above, this may be a sign of Oral Apraxia, which is worth looking into with medical and speech professionals.
Or does your child…
If your child does all or some of the above, this may be a sign of Oral Motor problems, which is worth exploring with medical and speech professionals.
If you are seeing any of the above signs, seek out the services of a Speech Language Therapist for an evaluation of these skills. This can be done through your State’s Early Intervention Programs, a free federally funded program for qualified children from birth to three years of age or through your school district’s preschool disabled program, a free program for qualified children between the ages of three to 6 years. You can also contact the American Speech Language-Hearing Association in Rockville, Maryland for a list of certified clinicians in your area. It is very important to have an ACCURATE assessment completed by a skilled clinician. You may also want an evaluation from a developmental pediatrician, or pediatric neurologist to look for signs of low tone (hypotonia).
More about Oral as well as Verbal Apraxia
Written by Lisa Geng, mother to two boys that were both “late talkers” who are doing great today. President and Founder of the Cherab Foundation, and Co Author of The Late Talker book St Martin’s Press