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Feeding Aversion by Lori Overland, MS, CCC-SLP

Feeding Aversion by Lori Overland, MS, CCC-SLP

For most of us, mealtime is a rewarding and enjoyable time of the day. We look forward to both the food and the social interaction. Imagine walking into your home and smelling fresh cookies baking or soup simmering. You hear the clanking of pots and pans and the whirl of the food processor. You ay associate the sounds and sells with familiar food and start to salivate. Your first thought may be, “How long until dinner?” For many of the clients we work with, mealtimes are frightening and challenging rather than enjoyable. Over the years, I have received countless numbers of referrals for children who reportedly had “behavioral feeding aversions. The vast majority of these clients have feeding aversions or “behavioral feeding issues. In some cases, well meaning families or therapists have actually created these aversions. Strict behavioral intervention programs may not recognize or treat the sensory or motor etiology of feeding disorders.

Consider the cases outlined below:
Jason is a five year old boy with a diagnosis of pervasive developmental delay. He is extremely hyper-sensitive to high pitched sounds. As his mother begins the preparations or dinner, Jason puts his fingers in his ears and begins rocking back and forth. The hum of the microwave and the buzz of the blender increase the intensity of Jason’s protests. Jason screams as his parents try to put him in a chair for dinner. Jason’s pediatrician suggests that he has behavioral issues. A more accurate assessment of Jason’s feeding aversion may be that his hearing sensitivities are so significant that the kitchen has become an unpleasant place for him to be.

Sarah is a ten-month-old baby girl. Initially she had trouble with bottle feedings which required several nipple and formula changes. She has a history of gastrointestinal reflux, which was addressed with position changes, thickened formula and eventually resolve with medication. She was also a difficult to calm baby who required complicated routines for bath time, dressing/undressing and bedtime. At six months of age, rice cereal was introduced. Sarah gagged and spit up. Her parents tried a variety of baby cereals, fruits and vegetables over the next few months. Sarah’s reaction was generally the same. She turned her head, pushed the food away and gagged on anything her parents were able to get into he mouth. Her parents were advised to ‘give her time and sell get used to food.” Her doctor was not overly concerned because he weight was staying on the charts due to her formula intake. Her parents were frantic. Through a sensory diet program we discovered that Sarah’s reaction to baby applesauce was very different if we put it in the freezer for fifteen minutes prior to a meal. She actually became an active participant in the mealtime experience! While dining in an Italian restaurant, her mother discovered that “Penne ala Vodka” was her favorite food. The bland taste of baby food and lukewarm temperature did not give Sarah enough information to be able to handle food successfully. In addition, her early bout with reflux made feeding an uncomfortable time of the day. Addressing underlying medical concerns improved her ability to handle feeding. A sensor diet which respected Sarah’s need for increased information made food considerably more enjoyable.

Alexandra is a two-year-old girl with a diagnosis of Down Syndrome. She reportedly did “fine” on a bottle and with pureed foods. When solid foods were introduced at approximately nine months of age, Alexandra had repeated incidents of gagging and choking. Initially, she would try any solid foods presented, but she reportedly became a “picky eater.” By fifteen months of age, she would only eat pureed foods or crunchy, salty foods, such as Goldfish and crackers. She will sometimes put a solid food she deem acceptable into her mouth, suck on it and push it out with her tongue. As I observe Alexandra eating, I note her primary pattern continues to be a suckle with both pureed foods and solid foods. Her mother has been told that Alexandra only eats purees because he “gets away with it.” I suspect Alexandra is afraid to eat solid foods. Due to low muscle tone, reduced strength and mobility in her jaw, lips, cheeks and tongue, she does not have the motor skills to chew food effectively. She is willing o eat highly salted snacks which will break down easily in her mouth. Other high tasty foods may be explored to experience the flavor and then pushed out the oral cavity using an infantile suckle pattern. As Alexandra has learned to chew, other food textures have become safe and acceptable to her.

In all of these case presentations, sensory and motor limitations contributed significantly to the “feeding aversion.” Families and therapists frequently give children with special needs foods that they do not have motor skills to handle or foods that do not address their sensory deficits. The response is often gagging, choking and throwing up. The subsequent learned reaction is to refuse to eat these food textures or tastes when they are presented. Sell meaning therapists and families are so concerned with nutrition that they miss the underlying issues which limit a child’s ability or willingness to eat. The practice of “force feeding” clients is another factor which contributes to behavioral feeding problems. The message we give children is, “I bigger thank you and I can make you eat.” The result is a lack of trust the child has for the therapist or caretaker. Our clients cannot always communicate their needs effectively, and we may miss subtle communication attempts. The diagnosis of feeding aversion or behavioral feeding problem does not always adequately represent the issues.

A comprehensive feeding evaluation must include assessment of both motor and sensory skills. Adequate respiration and postural stability are your first considerations, as stability in the body will support mobility in the mouth. Then, oral phase skills such as lip closure, tongue retraction tongue bowling, tongue lateralization and tongue tip elevation should be assessed. A five-day baseline diet, analyzed in terms of taste, texture and temperature should serve as an initial exploration of a client’s sensory preferences. Your therapy plan should focus on facilitating the motor skills required to handle feeding. Exploration of taste, texture and temperature variables should be done slowly, with only one change made at a time. Use sensory variables, such as taste and temperature, to facilitate changes in motor skills. (For example, in Sarah’s case, the addition of cold temperature to her applesauce gave her more information and encouraged increased lip closure on the spoon and more effective tongue retraction to move the bolus back in the oral cavity.) As changes are noted in motor development, a client will be better ale to handle an increased variety of textures; the client will have been an active participant in sensory exploration in the feeding interaction. Improved feeding skills will b supported by the development of trust in the caretaker/client or therapist/client relationship. For clients with underlying sensory and motor issues, behavior management approaches should be considered as secondary to sensory/motor goals.

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Feeding Strategies in Babies with Down Syndrome

Feeding Strategies in Babies with Down Syndrome

Babies with Down Syndrome commonly have developing difficulties with speech and swallowing which may be addressed very early. Your baby is likely to have low oral tone including the muscles of the oral cavity. The lips and tongue are especially at risk to develop less strength that is needed as your baby grows, necessary for breast or bottle feeding, eating and speech. Because of the low tone, the tongue appears oversized, flaccid with a rounded tip and frequently at rest between the gums.

The tongue is very important in feeding. The soft palate or roof of the mouth is a soft spot growth plate like the fontanelles on he head, which eventually close as your baby grows. The stimulation of sucking the tongue against the palate is important to stimulate this closure. There is also a connection with fluid in the ears, another common problem in babies with Down Syndrome. It is critical that she sits upright to feed, with her ears higher than the mouth, to reduce the likelihood of ear fluid. Place the nipple lower than your baby’s mouth. If the tongue stimulates the palate during sucking adequately, which will also occur with proper positioning, the palate will develop in a smooth, arched manner. If her mouth is closed, her tongue is in an active phase of toning against the palate. If not, a high narrow palatal vault with a bony notch will develop. If fed in a reclined posture, your baby is susceptible to ear infections. Reclined feeding may encourage mouth breathing thereby generating more mucous in the nose which would the drain to the ear by way of the Eustachian tube.

For young infants, use a Playtex Nurser with the bag liners. Take the baby’s lead. When he sucks, press the bag to increase the volume of liquid drawn in by the tongue. He will exercise his tongue every time you press. Don’t press if the baby stops to breathe or swallow. Let the baby rest when he needs to because his endurance may be poor. Your baby will be exercising his tongue every time you press, and increase the strength of his tongue.

Babies over 8 months may be ready to use a straw which will exercise their tongue by sucking through it. It will help her retract or pull back her tongue while pursing he lips. The first straw should be straight and short, and the baby may need to tae a large amount of the straw in her mouth. As the baby increases her tongue strength, allow les and less of the straw to go into her mouth, so the tongue can be further challenged. As the baby improves her ability to use only” of a straw into her mouth to suck, give her a longer straw. The Party stores sell all kinds of straws with twists and turns that are colorful and attractive. Gradually add more complex straws as your child is able to use each one.

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Interactive Metronome

Interactive Metronome

Improves attention, focus, timing, motor planning and language processing because of the brain’s neuroplasticity. It is accomplished by having the clients perform a variety of 13 exercises in high repetition while hitting sensors on the hands and feet at the exact moment a cowbell is heard through headphones. Patients require 10 to 15 hours of treatment and can be used with children as young as 6 years of age.

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Orofacial Myofunctional Therapy

International Association of Orofacial Myology

Orofacial Myofunctional Therapy

International Association of Orofacial Myology

The mission of the IAOM is to improve the health of the public by advancing the art and science of Orofacial Myology by:
1. Increase the awareness and ensure access to quality primary health for the treatment of orofacial myology disorders
2. Maintain the highest professional standards possible through promotion of educational opportunities an administration of the certification process
3. Increase the body of knowledge through scientific research
4. Represent professional interests of orofacial myologists
5. Promote and encourage interdisciplinary relationships with allied health professionals.

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International Association of Tongue Tie Professionals

International Association of Tongue Tie Professionals

An organization of professionals of various disciplines whose focus in on tongue-tie and upper lip tie to faciliate the health and well being of newborns through all age adults. This includes surgeons, IBCLCs, orofacial myologists, academics and bodyworkers. They are committed to the most up to date information about tongue-ties.

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Childhood Apraxia of Speech

The Cherab Foundation

Childhood Apraxia of Speech

The Cherab Foundation

The Cherab Foundation is a world-wide nonprofit organization working to improve the communication skills and education of all children with speech and language delays and disorders. Our area of emphasis is verbal and oral apraxia, severe neurologically-based speech and language disorders that hinder children’s ability to speak. The Cherab Foundation is committed to assisting with the development of new therapeutic approaches, preventions and cures to neurologically-based speech disorders. We bring together parents and medical, research, and educational professionals. Please join us and help to give our children a smile and a voice.

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ADDA

ADDA

ADDA provides information, resources and networking opportunities to help adults with Attention Deficit/Hyperactivity Disorder (AD/HD) lead better lives.

We provide hope, empowerment and connections worldwide by bringing together science and the human experience for both adults with AD/HD and professionals who serve them.

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Autism Society

Autism Society

The mission of the Autism Society of America is to promote lifelong access and opportunity for all individuals within the autism spectrum, and their families, to be fully participating, included members of their community. Education, advocacy at state and federal levels, active public awareness and the promotion of research form the cornerstones of ASA’s efforts to carry forth its mission.

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