Autism Therapy: safety

definition of safety: not yet defined.

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BMC Clinical Pharmacology, by Adams, JB, Baral M., Geis E., Mitchell J., Ingram J., Hensley A., Zappia I., and Newmark S., published in 2009, summarized Apr 27, 2010

A single round of DMSA chelation therapy may improve the severity of autism.

The purpose of this study was to see if DMSA therapy is safe and helpful for children with autism. The authors used five tools to assess changes in autism symptoms. Three of the tools (PDD-BI, SAS and PGI) showed improved behaviors in the children who were given one round of DMSA therapy, and those who were given seven rounds of DMSA therapy. The authors believe that one round of treatment may be enough for some children to excrete toxic metals. The children who released the most metals (thallium, arsenic, mercury, and lead) were the ones with the most improved autism symptoms.


Pediatric Review, by Brulotte, J., Bukutu C., and Vohra S., published in 2009, summarized Mar 23, 2010

Fish oil therapy may help learning and behavior in some children with neurodevelopmental disorders, including autism.

This review describes the effects of omega-3 fatty acids on the course and outcome of problems with the brain. The authors note that studies have been mixed as to whether or not children with autism have low levels of omega-3 fatty acids in their blood. There have been only a few studies that have looked at the use of omega-3 fatty acids as treatment for autism and these studies have been small and lasted only a short amount of time. Omega-3 fatty acids have a good safety profile, but they may cause nausea, nose bleeds, and a fishy burp. While doses of 3 grams of fish oil per day are considered safe for adults, parents should talk with their child’s doctor about the best dose for a child.


BMC Clinical Pharmacology, by Adams, JB, Baral M., Geis E., Mitchell J., Ingram J., Hensley A., Zappia I., and Newmark S., published in 2009, summarized Mar 4, 2010

Oral dimercapto succinic acid (DMSA) therapy may be helpful in normalizing red blood cell glutathione levels in children with autism.

This study was designed to see if DMSA therapy (9 doses over 3 days, 10 mg/kg-dose) would cause children with autism to excrete toxic metals. DMSA was very good at causing lead to be released from the body. The children seemed to have less lead in their bodies after treatment than children in other research studies. Children were given 3 rounds of DMSA treatment. Researchers said that 80% of the children may need more than three rounds of DMSA treatment in order to remove all of the toxic metals. The authors said that DMSA therapy may reduce toxic metals and improve glutathione levels with few apparent side effects.


Expert Opinion, by Kavirajan, H., published in 2009, summarized Dec 21, 2009

Memantine may be helpful for people with moderate-to-severe autism disorders.

The glutamate pathway may be out of balance in brains of people with autism. Memantine is a medication that reduces certain brain activities by blocking glutamate receptors in the brain. Two clinical trials of memantine in people with autism had different results. One trial reported that memantine was helpful for improving language and social interactions in people with pervasive developmental disorder-not otherwise specified (PDD-NOS). Another trial reported improvements in memory, irritability, and other behaviors for people with PDD. However, language was not affected in the second trial. Neither of these studies included a placebo control. Better studies are needed to find out if memantine may be helpful for people with autism.


Twin girls, diagnosed with autism, had their parents and applied behavior analysis (ABA) therapy for support. But the Halls, after moving to the Kirkland WA area, had problems finding local resources for their daughters. They have started a non-profit autism center, Olympic Peninsula Autism Center, that they hope will benefit all families in the area. The center will include water activities, physical activities, and a kitchen in which to teach some safety life skills. In addition, there are once-a-month parent support group meetings.

Read original article: Twins Inpsire Parents to Open Autism Center in Silverdale


Little City is a center in Illinois that offers support and therapies throughout the lifetime of a person with autism or other developmental issues. They were founded 50 years ago by parents searching for a solution for their children, teens, and adults. This year, over 500 volunteers from Discover are making improvements to the campus that will benefit all. For example, they are building a soccer field, they are repainting residential homes on the campus, and they are building discovery tables to be placed around the grounds that increase sensory integration. Perhaps their biggest contribution is Little City Safety Town, a mock village to teach life skills such as crossing streets and stopping at stop signs.

Read original article: Little City to Expand Therapeutic Campus Thanks to Nearly 500 Volunteers from Discover


Mom-made Toys is the brainchild of Saowapa Teeraprechakul, the mother of a child with special needs. She noticed that her son, who had few toys he could play with, loved the sound of plastic bags when he played with them. She and some other moms in Thailand began developing toys that could be used by children with autism, children who are blind, and children with cerebral palsy. They got the interest of Plan Creations/Plan Toys to create 20,000 toys in their first lot. Mothers of kids with special needs were the ones asked for input as the toys were designed. For example, toys for kids with autism are round discs shaped like heads that display different emotions. For the vision-impaired kids, there are dominoes with Braille numbers. Finally for youngsters with cerebral palsy there are weights to help them build up strength. Plan Toys makes all its toys without harmful chemicals and in adherence with international safety standards.

Read original article: Special Toys for Special Children


Did you ever think of swimming as therapy for your child with autism? Four Florida students got certified by the Dan Marino Swim Central Adaptive Acquatics program, in conjunction with Swim Central , and volunteer as instructors for Sunshine Swimming. Parents of the kids with autism find that their children learn safety in the water and see the time in the pool as therapy: "Weighted blankets and vests are among the treatments for autism, and the compression of water can have a similarly soothing effect." The swim instructors, who always emphasis fun along with learning, are Allie Shatters, Logan Shatters, Kevin Lindgren, and Colleen Lindgren.

Read original article.



Please comment on this autism topic.

Children with autism and horses

Jan 17, 2012 by Anonymous

PREFACE:

My experience working with children diagnosed with Autism has been a little like knocking on the door to their place of business. 

Option #1

Sometimes, no one answers the door and even if the hours of operation are posted, they are not always observed.

Option #2

If the door is answered, you rare sometimes invited in, but once inside you realize it is a waiting room where messages are exchanged.  There is no direct contact.  This can cause delays, miscommunication and confusion.  Patience and timing are critical.

Option #3

With enough effort and understanding you are sometimes (and hopefully) invited into the main office and speak to the boss directly.  In this setting, skills understanding and effort are still required but are less demanding and more productive.

This is the most rewarding and productive of the three options.

The equine program developed at the Westwind Rodeo Academy has facilitated the opportunity to enter the office and speak to the boss directly.  (Remember - they are not YOUR boss, but the boss of the company you need to do business with.)

I personally believe it has been a key ingredient in several instances, in moving forward and grasping the potential for the Education system to assist and direct students diagnosed with Autism in their academic efforts and opportunities.

FOLLOWING : Is a cursory description of a multi-faceted program that will hopefully provide a glimpse into these concepts.

CAUTION:  The thoughts information and data provided here are solely my responsibility and have not been endorsed, accredited, approved or even spell-checked by the Westwind School Division, the Westwind Rodeo Academy or any other authority.

Harlan (Lanny) Smith B.S.W., Family School Liaison Counselor

e-mail lannysmith56@gmail.com

The Program

More than just a riding program, the Westwind Rodeo Academy in Cardston Alberta provides a unique program centered on relationships that is based on a triad as part of a larger group of nine.  Each child that attends the program is matched with a specific horse and equine specialist EQ (horse handler) that is chosen for their skills and experience working with children with special needs as well as their command of horse knowledge and competence.  

The group of 9 is formed with 3 groups of 3 to allow for broader experience, interactive activities and comparative experiences and an ambience in the session.  The selection of which 3 students will attend together is carefully considered and may include children with a variety of challenges not limited to Autism.  The sessions are repeated for 6 consecutive weeks and may be repeated up to 4 times a year, space allows and need requires, although each section is provided as a stand alone intervention.

One of the most inspiring experiences is when children fully embrace the horse and the relationship when they take the opportunity to lay down on the horses back without saddle (sometimes with a bareback pad or blanket, but not always), and spend quiet time, just embracing the horse while the child is at rest.  This can include conversation with the EQ as originated by the child and is largely a listening activity for the EQ, or just a silent time.  This activity is sometimes suggested by the child and sometimes by the EQ and may occur at anytime during the session.  It is can be used to de-escalate the child or address stress or emotional discomfort.  It is also used as a modest celebration or reinforcement in the relationship.

Actual riding occurs during these sessions but is not the object or the goal.  Many sessions pass without the child being on horseback as the situation dictates.   Each session is focused on the child's orientation to the world around them as far as they can express through words, body language, choices or actions, their needs and concerns as well as interests and inclinations.  Although safety is an over riding principal, convenience to the horse or EQ is secondary to the child's expressed or perceived preference.  

We have witnessed EQ's trotting beside the horse as ridden by the child who has expressed a desire to have the horse move at faster than a walk.

(Again, safety is paramount which necessitates one or more EQs running beside the horse. In this case, the child's skills and aptitude to remain safely on the horse is previously determined.  We also consider the horses history and attitude and performance on that particular day as part of the decision making process.)  

This can be physically demanding and inconvenient for the EQ but a major contributor to the child's experience and benefit.  The results the child experiences, the more effort required by the EQ to facilitate without imposing or tainting the child's experience.

The other component of this system is the support of a Mental Health Practitioner and supervision by the Facility Director.  This completes the formal team.  Decisions about activities, concepts and specific goals are managed by the Facility Director and Bahavior Specialist and the EQ's in consultation.

We have also encouraged with some success, the attendance to at least one of the sessions in each section by a significant family member as well as the students classroom teacher and possible other support personnel.  These individuals are given direction about the concepts of non-interference and non-projecting on the child's experience while acknowledging the elements the child is embracing.  They meet the horse, the EQ and observe the activities.  We often take pictures or video and encourage this experience to be talked about at home and in the classroom.

Of course this is a snapshot of the experience in condensed form and there are many details and intricacies that cannot be explained or properly presented in this format.  Overall, the development of this process has been  most rewarding and inspiring and worth the investment of time, money and effort.  It requires many elements working in concert to achieve this model.  We are fortunate that these things have come together thus far.

Questions or comments leading to discussion and education are appreciated.


 


These well trained registered therapy dogs, Lottie Dot and Dora travel all over the Mid South area with their owner, trainer and handler, Patricia Belt, providing comfort, motivation to special needs children.  These special dogs also teach children about Fire Safety and Dog Bite Prevention for example, how to stop, drop and roll, and how to safely approach and pet a dog.


  They visit schools, libraries, hospitals, assisted living facilities, Fire Stations, camps, and visit children upon special invitations.


http://tnsafetyspotters.org


 


 


Spooktacular!

Nov 4, 2008 by dankohn

            It has been a rather eventful time for us since I last wrote.  The Halloween Spooktacular was a lot of fun and the kids had a good time playing the little games.  I made what was surely a very tasty and attractive pumpkin spice cake with cream cheese frosting for the Cake Walk, which we struggled valiantly (and in vain) to win back.  When we finally did win, we were allowed to pick only a small treat because they were only giving away the big cakes on the quarter-hour.  We were bummed and all we got for our efforts were three lousy cookies.  It was nice to know that my cake was one of the “good” prizes, though.

            Thomas’ teacher was at the fun fair conducting the Mummy Autopsy in the Haunted Courtyard.  She was really funny and had a very convincing witchy cackle.  Thomas was a little freaked out at first, but he (and Hayley) finally recognized the teacher and she watered her character down a bit so as not to scare my children in particular.  Thomas really seemed to enjoy all of the festivities and after we finished up at the Spooktacular, we went to Grandma’s cottage.

            Thomas had a difficult time at the cottage.  There were a lot more people there than he was used to (good for us pier-workers, bad for the autistic boy) and all of the noise and bustle in the house was confusing and hard for him to handle.  On Saturday, when we went outside to work, he did a lot better just being in the more open space and fresh air.  The weather was actually pretty great.  If there’s anything worse than working on that pier, it’s working on that pier when there’s drizzle stinging your face.

            Thomas really liked using the leaf-blower, which we let him do because we’re idiots (again).  Actually, it wasn’t that idiotic and it helped him.  The vibration of the motor and loud noise really kept him focused and he did a good job blowing the leaves into the fire.  Yeah, we had a fire going too.  Jonathan was supervising and Thomas and Hayley both know to stay away from fires.  Hayley actually learned about fire safety in preschool (where they CONTINUE to spell her name wrong…) and runs around the house saying, “Oops!  Your arm is on fire!  You better stop, drop and roll!”

            After we finished with the pier, we went to the little country pumpkin farm.  We don’t even go to the big, commercialized pumpkin “farm” near our house anymore.  You should see how much they want for a pumpkin these days!  So we go to the little country pumpkin farm up north and choose pumpkins.  This place is so cool…you pay on the “honor system” meaning that there is no personnel manning the check-out counter.  You just figure out what you owe and put the dough in a box.  They have a tiny hay-maze, a big old tractor for the kids to sit on and this year, they had a little silo filled with corn and trucks.  As you can imagine, getting Thomas out of the corn was a chore, but he loved playing in it.

            We came home on Sunday and started getting ready for Halloween.  As is characteristic of Thomas, he was not excited about Halloween.  He still didn’t want to trick-or-treat, but as the week went on, I just didn’t let it go.  We kept talking about the party at school on Friday so that by the time Friday came around, he was excited about going.  Hayley and I walked Thomas to school, then I went to Hayley’s school to watch her costume parade and take pictures and then I booked back to Thomas’ school to help with his party.  I put on my Cleopatra costume in the hallway before entering Thomas’ room.  His teacher was a very fetching Snow White and one of the other moms was a pumpkin so I wasn’t the only goofy grown-up there.  Thomas did really well; he participated in the craft (a little magnetic Candy Corn with his name on it), played Pin the Nose on the Pumpkin and played Spooky Bingo.  We then went on a classroom parade, going through the other, big-kid classrooms.  Then it was back to the room for cupcakes and cookies, not to mention all of the candy that other kids brought to share with their chums.  Then we walked to go get Hayley (I, still wearing my Cleopatra costume.  And pulling the wagon…) and then we walked home.  Hayley’s backpack was really heavy and I couldn’t imagine what was in there until we got home and opened it.  It was full of around five pounds of snacks and candies that classmates had brought.  I felt like a deadbeat because I didn’t bring anything, but it looked like the kids had more than enough.  With the amount of candy they brought home, we really didn’t NEED to trick-or-treat at all.  But we did.  My niece Julia looked adorable in her girl’s pirate costume.  The kids did a good job, except that Thomas had the same problem as last year with staying by us on the sidewalk.  He was running ahead and then running back to us but sometimes he would run a little too far ahead.  I know it was definitely not his fault, what with all the sugar in his little body.  I would also like to take this opportunity to thank all of the parents out there who gave out pretzels and whole-wheat crackers!  God bless!

            When we got home from trick-or-treating on Halloween night, the kids were absolutely wired.  We tried to get them to eat some form of protein – anything at all that could be considered good – and were only partially successful.  Hayley chose scrambled eggs which I whipped up with the enthusiasm of a TV chef.  Thomas I believe finally settled on some kind of bread product and wouldn’t be induced to eat any kind of meat.  Oh well.  Halloween only comes once a year, followed shortly by the holidays.  But seriously, only once a year.  Like Easter.  And vacation.  And Valentine’s Day…

            We had a party for Jonathan’s birthday on Saturday.  His family came over and we had a very pleasant dinner for him.  Thomas was okay with the whole thing, sort of.  He didn’t want anybody to have any cake, EVER.  I just wish I knew what that meant.  He says stuff like that, but it’s one of those things where you know he doesn’t mean what he’s saying; he means something else.  I just can’t figure out what he means.  I’m still working on it.

            Thomas’ report card came home yesterday and it was very good.  He has either mastered or is progressing as expected in most skills.  He still needs more work on remember his address, phone number and birthday.  He also needs to work on holding writing utensils properly, but other than that, he’s really doing well.  I meant to ask his teacher if he’s being evaluated just as his classmates are or if she uses a more lenient scale for Thomas.  I would like to assume that he is graded on a par with his peers, but whenever I’m in class, I can tell that she’s being a little more patient with him than she is with some of the other kids.  That could just be because I’m in class or it could be because she knows that certain things are harder for Thomas.  I volunteered in class today and meant to ask, but forgot.  She kept me busy filing, cutting, laminating and working with certain kids on recognizing letters.  I had not a moment to think!

            Coming up, we have…very little.  My birthday is in a few weeks and I need to think about what we’re going to do for that.  I hate making these decisions.  It feels like I’m trying to throw myself a party.  We used to go out for birthdays, but a couple of years ago Jonathan and I decided that it’s easier with the kids and everything if we just stay in and order pizza.  Well, staying in and ordering pizza evolved into staying in and hosting a dinner party and Jonathan’s birthday party was every bit as stressful and required almost as much preparation as one of the kid’s birthdays.  So I’m thinking of just saying that we’ll all go to Chili’s for my birthday because I don’t want to have to do as much work for my birthday as Jonathan and I had to do for his.

            One thing I will do gladly, however, is accept gifts.


School Lunches for Kids with ASD

Sep 11, 2008 by Anonymous

SCHOOL LUNCHES FOR KIDS WITH ASD: DELICIOUS, HEALTHY & POSSIBLE.

THE CHALLENGE:

With only twenty minutes to eat, kids with autism spectrum disorder (ASD) should have "fast" foods that are healthy, tasty, loaded with nutrients and free of the culprits that are common problems: gluten, milk products, soy, and artificial additives and coloring. Add to the list sensory issues involving food texture, color and taste along with unusually picky appetites so common in ASD - and the task seems insurmountable. Beyond the challenges with foods are the safety issues of the food containers themselves, especially plastics containing phthalates and bisphenyl A (BPA). And of course there is the "cool" factor which affects pre-school through high school. Food that is different is totally uncool for kids who already face so many social and learning stigmas.

Knowing the challenges, we can now focus on the solutions.

THE SOLUTIONS:

Basics

As is the case with any meal, there are some basics to follow. Blood sugar control is critical. All people are affected by rapidly rising blood sugar which then cascades down too quickly and too low. The most noticeable effects are on brain function especially mood and attention. As the blood sugar drops too quickly, there can be irritability, hunger headaches, lack of focus, behavior problems, and cravings for a "quick sugar fix" which keeps the cycle going. This interferes with learning and can be disruptive to the class. Protein and fiber stabilize blood sugars. Below is a summary of the basic rules for any meal including school lunch.

Assumptions

All food suggestions are GFCF (gluten-free, casein-free). Glutens include wheat, oat, barley, rye, spelt and kamut. Milk products and milk casein include milk, yogurt, cheese, creams, ice cream, cream sauces, and butter.

Avoids

Glycemic foods which raise blood sugar (glucose) quickly include: sugars, sodas of any kind, candy, sweets, juices, and any refined grains (pretzels, bread, crackers, bagels, chips) on an empty stomach. Limit the sugars and keep the refined carbohydrates limited. If small amounts are consumed at the end of the meal, the negative effect is less.

A word on sodas - both regular and diet. They have no place in a healthy diet. They are high in phosphorus which depletes healthy nutrients. Consider them removers of electrolytes, not drink options. Water is best, but other good choices include: dilute juices, seltzer water with juice to flavor, vegetable juices (V8)

Promote Protein at every meal or snack

Choices include fish, poultry, meat, eggs, beans, nuts and seeds.

Avoids: milk products

The serving size for protein for each person is the size of the palm. A child's may be 1 to 2 ounces of meat/chicken/fish and a teen and adult may be 3 to 5 ounces. See the chart for guidelines

For beans, the serving size is two cupped palms full. See the chart for guidelines.

Fabulous Fiber at every meal

Choices include fruits, beans, nuts, seeds and grains.

Avoid: glutens

If your child eats very few vegetables, fruits, grains, nuts, seeds and beans, added fiber is important. Fiber as pure guar gum is easy to add to any recipe and also to drinks. It is GFCF and more fine than sugar, mixing completely in water or juice. See the table for fiber intake suggestions.

Favorite Foods at every meal or snack

Include at least one food that is a favorite in order to promote more interest in the meal.

Fun Meals - Part of the Cool Factor

Take a tip from the fast food marketers and include a surprise gift in the lunch. It might be a small collectible such as cars, baseball cards, characters, hair clips, stickers, or child's ring or bracelet. Home made "giftlets" (tiny gifts) are perfect.

Guidelines and Ideas

Go organic as much as possible. "USDA Organic" means the food is produced without the use of harmful pesticides, artificial fertilizers, antibiotics, growth hormones human waste, or sewage sludge, and that they were processed without ionizing radiation or food additives. Children with ASD are already coping with their own excess metabolites and really can not handle the burden of harmful chemicals in the environment and foods. The less the exposure the better. Anything you can do for your child is a benefit.

There are numerous resources for GFCF foods and recipes online and in many books. Utilize all of these to find the commercially available foods your child will eat as well as recipes that are not just GFCF, they are nutritious and delicious. Test them at home - not in the school lunch. There are GFCF juice boxes, pretzels, breads, wraps and snacks.

Establish three to five basic lunches that work. If your child is willing and interested, engage him or her in the process. Test new foods out at home until you have the food right and the combination of foods right.

Use freezer packs for keeping foods cold and thermos for hot foods. Include non-toxic hand sanitizers which are commercially available (avoid the commercial sanitizers). You can also send two paper towel pieces - one moistened with soap and one moistened with water..

Packaging - a good opportunity to Go Green!

Again - go with the marketers - jazz it up! Select a lunch container your child loves. Young children love to decorate a lunch box with stickers and paints. Make the lunch box the child's own work of art personalized with a name. Reusable containers and boxes are the green way to go. Older children will definitely want to select whatever is considered cool. The most cool may be a paper bag or small recycled bag carried in a back pack. Go with the trend and your child's own choice. There are companies who make safe, BPA-Free, safe lunch box sets with inserts for the different foods.

To avoid plastic wraps for sandwiches, use wax paper or parchment paper. Avoid containers with BPA by avoiding items with the recycle number 7. There are many BPA -Free containers which can be washed and reused. Your child will need to know to bring these back home rather than throw them away.

For napkins, use washable cloth napkins or dishcloths, or choose processed chlorine-free (PCF), post-consumer-waste (PCW) paper napkins available in stores and on line. If utensils are needed, use stainless steel appropriate to the child's skill level and age.

Nutritious Can Be Delicious - Even for the Picky Eater - The Trojan Horse Technique

Remember Odysseus from seventh grade mythology? Seeking to gain entrance into Troy, he cleverly ordered a hollow wooden horse so large that the Greek army could hide inside. What looked like a huge horse was really a disguise to conquer the city. We have used this concept for decades to hide nutritious food to nourish picky eaters.

Rather than introduce a new food in its natural form, begin by hiding a very small amount (about a tablespoon) of it as puree mixed or blended into a well-liked and well-tolerated food. This approach allows the body to accept the new food. As the child accepts the taste, include more. Children who have food texture issues are especially good candidates for blended foods because their sensory development may be younger than their chronological age. Adapt to the sensory level and return to purees until sensory issues improve. Rather than focusing on getting a child to tolerate foods that he perceives as "lumpy" or unpleasant to chew, the goal is getting a child to eat nutritious food, however you can.

Match the Color and Texture

Assume the new food is a vegetable, use organic baby food purees or make your own. Puree the new food into an established food that does not change the overall color, texture, smell, or taste. If a child eats nothing but white food, start with very light-colored vegetables including squash, cauliflower and corn. If the child likes ketchup or tomato sauce, then introduce deeper-colored vegetables such as beets, greens, peas and beans. Pureed vegetables can be beaten into batter for pancakes, muffins, brownies, and cookies or into tomato and other pasta and pizza sauces, and even into ketchup.

Mix Fruits and Vegetables

Vegetable juice makes a healthy addition to fruit juice. Try mixing carrot juice with orange juice, and then adding a teaspoon or so of another vegetable juice. Serve in a brightly colored sippy cup to camouflage any color changes. Blend pureed vegetables into cooked fruits such as applesauce or pearsauce, into meatballs, and even into nut butters. Expand ideas as tolerance improves. Be sure to carry out the Trojan Horse technique out of the sight of your child!

Muffin Casseroles

Many families have developed what we call muffin casseroles. One resourceful mother developed a GF/CF muffin for her child who ate only breads and muffins, and then gradually added fruit puree to the batter. As he tolerated fruits, she moved to vegetable purees, and finally added pureed meat. Until he was able to transition to eating foods in a traditional manner, he ate his muffin casseroles at every meal and snack-and loved them!

Increase Protein

The Trojan Horse technique is especially useful for kids who need more protein in their diets. Add eggs, especially the high-protein whites, and rice-protein powders to batters, breads, smoothies, meat sauces and meatballs. Do not add raw eggs to smoothies.

Gradually Move On

AS your child expands to eating vegetables, try vegetables dipped in honey or mayo/ketchup mix or hommus. It is a start . As a child accepts an increasing number of foods presented in a sneaky manner, eventually, he/she will accept the food alone - we promise! All it takes is patience, and a lesson from Greek mythology!

Choose one from each section. This list is GFCF. Also avoid any foods which provoke reactions or those forbidden at school (nuts for examples) or foods The "Other" section is optional.

Some Protein Choices: chicken strips, GFCF chicken nuggets w/ketchup to dip, meat slices rolled up, shrimp (send frozen, will thaw by lunch) w/seafood sauce to dip, organic "deli" chicken slices, hommus plain, on bread or crackers or as dip for veggies, muffin "pot pies", soy yogurt, egg salad, hard boiled eggs or deviled eggs, peanut butter on crackers or apples, nuts - all varieties - almonds, cashews, pecans, pistachios, hazelnuts. Hot food for thermos: chili or soups, turkey hot dogs cut up, GFCF pizza.

Some Vegetables & Fruit Choices: These can be eaten plain or dipped in GFCF sauces, ketchup or honey. Foods include: cup of vegetables, baby carrots or carrot strips, broccoli "trees", apples, bananas, berries, oranges, peaches, grapes, pineapple, melon, natural fruit cocktail in natural juice, raisins, apricots,  applesauce in cups, any blended fruit sauce.

Drink Choices: water, fruit juice, V8, V8+fruit, seltzer w/juice, fruit smoothie, other milk (soy, rice, coconut, almond), and keep drinks partially frozen so they will remain cold. 
Other: GFCF pretzels, rice crackers, baked tortilla chips, GFCF dry cereal, GFCF vegetable gummies, small GFCF cookie.

The above is an excerpt from the book The Kid-Friendly ADHD & Autism Cookbook: The Ultimate Guide to the Gluten-Free, Casein-Free Diet
by Pamela J. Compart, M.D. and Dana Laake, R.D.H., M.S., L.D.N.
Published by Fair Winds Press; November 2006;$24.95US/$32.50CAN; 978-1-59233-223-6
Copyright © 2008 Pamela J. Compart, M.D. and Dana Laake, R.D.H., M.S., L.D.N

Author Bio
Pamela J. Compart, M.D., is a developmental pediatrician in Columbia, Maryland. She combines traditional and complementary medicine approaches to the treatment of ADHD, autism, and other behavioral and developmental disorders. She is also the director of HeartLight Healing Arts, a multidisciplinary integrated holistic health care practice, providing services for children, adults, and families.

Dana Godbout Laake, R.D.H., M.S., L.D.N., is a licensed nutritionist in Kensington, Maryland. Within her practice, Dana Laake Nutrition, she provides preventive and therapeutic medical nutrition services. Her practice includes nutritional evaluation and treatment of the full spectrum of health issues affecting adults and children with special needs.



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