Archive for the ‘Diet’ category

New IgG Food Sensitivity Test Results

May 4th, 2011

We recently did another 96 food panel IgG Food Sensitivity Test (www.foodallergy.com).  The first test was done back in May of 2009.  So it has been close to 2 years since we retested and have had Nathaniel on the Specific Carbohydrate Diet.  Before I give you the results, let me explain why we did the IgG Food Sensitivity Test.

There are several different types of allergic reactions.  Many people are aware of IgE allergies.  IgE is responsible for the classic response for allergens. (Itchy nose and eyes, cough and for more severe cases can lead to anaphalatic shock.)  IgG  allergic reactions can immediately occur after eating offending foods but can also occur 2 to 3 days later making it difficult to determine which foods are affecting you or your child.  Your body can actually make IgG antibodies to different offending foods.  So every time you consume that food you may get headaches, brain fogginess, diarrhea, stomach aches….you name it!

Nathaniel is affected by food!  There is no doubt.  I always refer to the movie “Gremlins”.   If he gets the wrong foods he becomes a different boy.  He will start head banging, climbing walls, running in circles all while making very interesting noises.  We especially noticed this with eggs.  The crazy thing is he CRAVED eggs!  If he craves anything I am now more cautious to seeing how he reacts after eating those foods.

So here are the results: ( 3 star (very sensitive) to 1 star (low sensitivity). OLD 2009 Results in RED & 2011 Results in BLACK.

Apple  *

Blueberry *

Cottage Cheese  *

Chicken *

Swiss Cheese  *

Coconut  *

Oregano  *

Egg White  ***

Peanut  *

Egg Yoke  ***

Black Pepper  *

Garlic ***

Baker’s Yeast *

Ginger  **

Brewer’s Yeast  *

Gluten *

Cow Yogurt  *

Cow’s Milk  **

Oat  *

Peanut *

Black Pepper  *

Rye  *

Sesame  **

Strawberry *

Tuna  *

Wheat  *

Baker’s Yeast  *

Brewer’s Yeast  *

Yogurt  *

As you can see, he has a lot less food allergies than he used to have.  If you have not performed an IgG Food Sensitivity Test on your child then I would highly recommend it!  It is quite inexpensive even if it is not covered by your health insurance.  It generally costs around ~$100 when done through www.foodallergy.com .  Shop around and find the best price!  It also only requires a small sample of blood.

Hope this helps and encourages you and your family as you are on the road to recovery for your loved one!

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I Scream, You Scream, We All Scream for Ice Cream!

November 6th, 2010

Ryan & I recently enjoyed a weekend getaway together in Apalachicola, Florida.  While we were there we wandered into a bookstore.  I could not resist reading part of a book mentioning goat milk.  I know I have posted about goat milk earlier but I learned even more so of coarse I have to share.

Goat milk is wonderful for people with mal-absorption issues due to it’s fatty acids composition making the milk a lot easier to digest.  Goat milk also has wonderful anti-fungal and antimicrobial properties.  This is due to its relatively high amounts of lauric and caprylic fatty acids.

We immediately decided that we were going to get him to drink goat milk when we returned from our getaway.  This was not an easy task considering it has a strong taste but the problem was solved by making homemade ice cream.  Birthdays will never be the same!

Nathaniel cannot have egg so I came across an egg-less ice cream recipe and made some changes so it would be compliant with SCD.   So here it is!

Banana-Honey SCD Ice Cream

2 Cups of Goat Yogurt

2 Cups of Goat Milk

1 Cup (or less) of honey

1 Mashed Ripe Banana

2 Tablespoons of fresh Beet Juice (Nate loves red & no you cannot taste the beets!)

I put all these ingredients together in my ice cream maker and out comes yummy ice cream.  I now use some of the ice cream to make smoothies to sneak in the yogurt that I want Nathaniel to eat.  What did we do without ice cream? (I will post picks after I make my next batch!)

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Utterly New Insight About Milk & Autism

July 21st, 2010

This is one of my favorite articles on milk and how dairy products affect children with autism.  I have seen the physical effects when Nate used to be addicted to milk.  (I did not see how milk was affecting him until I removed milk because he had milk everyday ALL day and his behaviors were normal to me.  It was from removing milk that I was able to do any type of comparison at all and all I can say is WOW!!!  Good bye, cow’s milk!)

This article talks about the science behind those physical manifestation we can see after autistic children have dairy products.  (I keep holding myself from going into details of what those physical manifestations look like so that this is not too long of a post.  I really think it is important to read this article so I will go into more details in later posts.)  This article also explains why we are using goat milk in Nathaniel’s diet and are not seeing any reactions.  Enjoy the article!!!

(Used by Permission from Julie Matthews, CNC)

As an autism nutrition consultant, I’ve been supporting clients following the Gluten-Free Casein-Free (GFCF) diet for years. Some of my clients would report that their child could handle goat’s milk or raw milk without allergic reactions. I began to wonder if all milk was created equally.

I conjured various theories: could the protein in goat’s milk be different than cow milk, was it the pasteurization process (absent in raw milk) that made the difference, was it something else, or a combination of factors? Then, one of my clients introduced me to A1 and A2 beta-casein.

There are various types of casein. Goat’s milk, as well as sheep and buffalo milk, contain A2 beta-casein. Raw milk, while often from cows, is typically produced from small herds of Jersey and Gernsey cows, both of which contain a high percentage of A2 beta-casein compared to most dairies that use mainly Holstein cow’s that produce a majority of A1 beta-casein. Here’s what I have learned through my research about casein and A1 versus A2 beta-casein.
Beta-casein is a protein that contains bioactive peptides and opioids. Bioactive peptides are important for protecting the undeveloped immune system of newborns, and stimulate the growth and development of organs like the gastrointestinal tract and gut. Bioactive peptides have also been shown to kill bacteria that normally cause immune system infections. Opioids have pain-killing effects, sedative properties, induce sleep, and play a role in the control of food intake. Opioids can be produced by the body in the form of endorphins, or be absorbed from digested food, such as milk and wheat, in the form of casomorphins and gluteomorphins (opioid proteins). Several forms of beta-casein exist and make up 25-30% of the proteins in cow’s milk. There are approximately 13 beta-casein variants, with A1 and A2 variants being the most commonly occurring. A1 beta-casein contains the amino acid histidine at position 67 in the protein, while A2 beta-casein instead contains the amino acid proline at the same position. Studies have shown that when digested, A1 beta-casein breaks down to a casomorphin protein called beta-casomorphin-7 (BCM7). This is a direct result of the histidine amino acid that A1 beta-casein contains, as A2 beta-casein does not form BCM7 (1).

Several enzymes in the digestive tract process beta-casein including DPPIV, (dipeptidyl peptidase IV) and cause the break down of bioactive peptides and opioids. Studies suggest that the digestion of cow’s milk (containing A1 beta-casein), leads to the release of opioids, such as BCM7, and can cause harmful effects in children with autism (2) where DPPIV function may be impaired. As this amino acid structure is more difficult to breakdown, those with compromised or weak digestion may accumulate opioids more readily. Additionally, when the gut is “leaky” (referring to increased gut permeability), these opioids end up in the blood stream in much greater concentrations than in those people with a healthy gut wall that does not leak. BCM7 is not produced when A2 beta-casein is digested, so goat’s, buffalo’s, and sheep’s milk that contain A2 beta-casein but not A1 beta-casein should not cause these harmful effects. There are other opioids that may also be formed; however, BCM7 appears to be the strongest.

As Jon Pangborn, Ph.D. describes, the enzyme DPPIV, which is also called CD26, has several other functions in the body, including involvement in signal transmission via lymphocyte receptors, and assisting the enzyme, ADA, in processing adenosine as an ADA binding protein. DPPIV is impaired by toxic heavy metals like mercury, lead and cadmium, a milk allergy, organophosphate insecticides, and yeast. Children with autism have greater toxic metal burdens, and one theory is that these heavy metals knock out this DPPIV enzyme, and the impaired DDPIV leads to improper processing of dairy and wheat. A supplemented plant analog version of DPPIV cannot substitute for the animal version completely, but it can certainly help.

While it is possible that A2 milk may also release opioids, Japanese and German scientists were unable to release BCM7 from A2 milk (1, 3). It appears that human breast milk may not release BCM7 either. Interestingly, this may explain why breastfeeding does not seem to cause a casein reaction to sensitive babies when dairy is avoided in a mother’s diet. In addition to affecting autism, research suggests that BCM7 may lead to the onset of several diseases, such as heart disease, diabetes, and schizophrenia (4).

Studies have also shown that wheat products, which contain gluten, also cause health problems for children with autism (5) Gluten has long been established as a problematic protein for many individual, most well studied in celiac patients, causing inflammation in the gut, diarrhea, constipation, abdominal pain, digestive problems, and the improper absorption of nutrients. Similar responses are seen in many children with autism (that are not diagnosed with celiac). Gluten, along with an autistic person’s already compromised digestive system, can exacerbate the ability of the body to break down beta-casein.

Scientists believe that opioids like gliadomorphin (a gluten opioid) and BCM7 (a casein opioid) are toxic for children with autism due to the fact that these children have an abnormal, leaky, gastrointestinal tract (6). Instead of completely digesting and excreting these opioid proteins, some of the partially digested gluten and casein proteins leak out of the gut and are transported to other parts of the body before they can be completely digested. These opioid proteins travel through the bloodstream, cross the blood brain barrier (the barrier between the brain and the rest of the body), enter the brain, and stimulate morphine-like effects. Casein proteins (BCM7) negatively affect the brain by causing inattentiveness, unclear thinking, and irregular sleeping and eating patterns (7).

In children with autism, gliadomorphin and BCM7 can also cause the release of histamine, a chemical that regulates immune cell communication. Histamines are normally released in the body in response to an allergic reaction. This mis-regulation of immune cells weakens the immune system’s ability to ward off harmful viruses and bacteria that cause diseases. This is consistent with the experience that many children with autism get frequent infections and illness. Antibodies are also released to help target and remove unwanted opioid proteins. IgA is an antibody that can be found in blood, saliva, tears, and mucous membranes of the respiratory system and gastrointestinal tract. IgG antibodies are the most common antibodies in the body, and can be located in all bodily fluids. IgG antibodies are the only form of antibody that can cross the placenta in pregnant woman to protect a fetus (unborn baby). IgG antibodies also play a major role in fighting viral and bacterial infections. When the immune system detects foreign particles such as viruses, bacteria, fungi, or cancer cells it stimulates the production and release of antibodies. These antibodies attach to the foreign particles, labeling them as hazardous so that they can be destroyed and removed from the body (8). So while the peptides from casein or gluten trigger an IgG immune response, the opioids trigger an IgA immune response. So it is not just opioids that trigger an immune response, casein and gluten protein can do so also, just using different types of antibodies.

Studies have shown that in autistic and schizophrenic patients, large amounts of gliadomorphin and BCM7 can be detected outside the gut (8). This further indicates that their bodies are not able to properly break down and utilize these opioid proteins. These studies also showed that in 86% of schizophrenic patients, IgA antibodies that were targeting gluten were released into the body, and 67% had IgA antibodies that were targeting casein. In patients with autism, approximately 30% of the patients had IgA antibodies targeting gluten and casein present in the body. The release of IgG antibodies targeting gluten and casein were also detected in these patients. More than 80% of the autistic and schizophrenic patients had elevated levels of IgG antibodies in their blood.

In recent years, the adverse effects of gluten and casein led researchers and to believe that autistic and schizophrenic patients should be placed on a gluten-free/casein-free diet, and this has become a widespread treatment for both diseases (9). Case studies that involved putting patients with schizophrenia and autism on a gluten-free/casein-free diet normally lead to some improvement of symptoms, but more clinical trials need to be performed to get a better picture of why this is the case. There is not enough data yet to understand all of the complexity behind gluten and casein and the challenges with them, but the experience of thousands of patients support the science we know so far: that a gluten-free/casein-free diet helps. And of course implementing the diet always depends on the patient’s needs, the caregiver’s willingness to try it, and professional supervision (10).

Schizophrenic patients who were put on a gluten-free/casein-free diet or treated with dialysis, a process that cleans the blood in order to rid the body of gliadomorphin and BCM7, were relieved of their symptoms, and low levels of the opioid proteins were detected. Approximately 81% of patients with autism who were put on a gluten-free/casein-free diet for at least 3 months were also relieved of their symptoms. A few parents, who stated that their child with autism had seizures before going on the diet, noticed that the frequency of the seizures either decreased or ceased all together. As previously stated, opioid proteins can cause an allergic response in the body, which leads to the release of histamines. Histamines have a direct effect on immune cell regulation. The disturbed immune response leads to a higher production of antibodies, such as IgA and IgG, as a means of further breaking down and excreting harmful gliadomorphin and BCM7 particles. In other words, the high levels of antibodies that are detected in patients with autism are a direct result of complications that occur when gluten and A1 beta-casein are consumed (8).

A vast majority of children that consume dairy consume cow milk products so removal of dairy on the GFCF diet would be the removal of A1 beta-casein in most instances. This may be the reason the GFCF diet is so successful for children on the autism spectrum. I’d like to pose a new hypothesis, maybe it is not ALL casein but the A1 beta-casein that is actually the primary problem with milk for children with autism.

With that said, there are most likely are other reactions and problems with dairy for some (if not many) individuals, so I do not think this preliminary information justifies abandoning the GFCF diet. (In fact, I hesitated writing and talking about this topic for a long time, as I did not want to confuse parents new to diet.) I have seen many wonderful results from GFCF and know many clients that cannot seem to tolerate goat or raw dairy. I don’t want children to miss out of the full benefit from diet by not trying a GFCF diet.

Through my clinical experience, I have found that it is very important to give the GFCF diet a complete trial, free of any infractions. Once a child has been on this diet for 3-6 months and you see what progress can be made with it, then and only then, do I feel that a parent may experiment with diet and try adding goat’s milk or some other A2 milk back. It seems that for some children, their casein sensitivity is mild and A2 milk works well. For others, once the gut is healed, they are able to consume small amounts of A2 milk. I often hear that as a child’s digestive systems improve, they are able to handle goat’s milk yogurt or raw milk. It is possible that the BCM7 issue is a primary factor for some people, and that A2 milk may provide an option for some individuals.

While milk is not “necessary” in the diet, dairy has health benefits when the individual is not intolerant to it. (Note that when people are intolerant, it can be very harmful regardless of the “benefits.”) If there is a way to include some dairy in some children’s diets, there can be a positive benefit to having this flexibility and nutrition in the diet. Dairy makes wonderful probiotic-rich fermented foods such as yogurt and kefir to support a healthy intestinal tract—and often nuts, nut milk and coconut-based fermentations are not tolerated. Dairy contains essential fatty acids, fat-soluble vitamins A, D, and K, and calcium.

Additionally, as I describe in Nourishing Hope for Autism butyrate, (also butyric acid), found in dairy, “has been shown to clear ammonia and nitrogen, modulate local electrolyte flux, supports the reduction of diarrhea and improves very large, hard stools. Butyric acid also supports and fuels the intestinal walls to support a healthy gut and is used as an anti-candida substance.” Raw dairy contains phosphatase (an enzyme important for calcium absorption), probiotics, unadulterated protein, and higher nutritional content (because of what is normally destroyed during pasteurization and because they are pasture-grazed). This new A1 and A2 information may allow some children with autism to receive the benefits of milk without the problems it can cause.

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Homemade Goat Yogurt Recipe

July 16th, 2010

Nathaniel is on the Specific Carbohydrate Diet.  Homemade goat yogurt is considered to be a legal food.  It is full of of beneficial bacteria used to help heal the gut.   I am about to post more information on the difference between cow’s and goat’s milk for those of you who are interested.  Till then here are some step by step directions for making goat yogurt.

If you have raw goat milk you will want to heat your goat milk up to 180 degrees Fahrenheit and keep it there for a minimum of 2 minutes.  (You do not want to exceed 185 degrees Fahrenheit or you will burn the milk.)  By keeping your milk at 180 degrees Fahrenheit for 2 minutes you will pasteurize your raw goat milk.

Once you have pasteurized the goat milk let the milk cool.  (I like to speed up the process by putting the milk  in a cool water bath.)  You do not want to add the GI ProStart (SCD legal yogurt starter from GI Pro Health) until the milk is near room temperature otherwise the bacteria in the starter will die and you will have a bad batch of yogurt.

Once the milk has cooled add the yogurt starter and mix it in with a whisk.  The directions for the GI ProStart is 1/8 teaspoon per 2 quarts of milk which is 1/4 teaspoon per gallon of milk. Make sure that you mix the starter thoroughly.

Then put the milk in your yogurt maker or in my case some Mason jars that I place in my food dehydrator.  I have an economy size  Excalibur Food Dehydrator that has 9 trays.  What I like about having this dehydrator is that it I can make up to 2 & 1/2 to 3 Gallons of yogurt at a time.

I keep the bottom tray in the dehydrator to make sure air is flowing all around the yogurt.  Now keep a consistent temperature between 100-110 degrees Fahrenheit for 24 hours.  (Do not exceed 30 hours.)  After 24 hours remove the yogurt and store it in your refrigerator.  You have now officially made some amazing goat yogurt!

Hope you enjoyed this post!

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What Is All The Talk About The Gluten Free Casein Free (GFCF) Diet?

March 18th, 2010

If you have a child with autism or if you have interest in people with autism it is quite likely that you have heard about the Gluten Free Casein Free (GFCF) diet.  Some parents have heard about it but do not really understand how the milk proteins (casein) and the wheat proteins (Gluten) can affect child with autism.  Just the idea of removing wheat and milk from a picky eating autistic child can seem overwhelming but let me encourage you that for MANY autistic children the benefit can outweigh the difficulty of doing the diet.

Casomorphin & Gliadorphin: Many children with autism have a difficult time digesting milk and wheat proteins.  When these proteins are not broken down completely they they become peptides called Casomorphin (derived from casein) and gliadorphin (derived from gluten).  Do you recognize a word in casomorphin?  It should make you think of morphine.  The peptides from gluten and casein are important because they can react with opiate receptors in the brain, which can mimic the effects of opiate drugs like heroin and morphine.  You may have noticed some autistic children can look and act a little high.  Well that is not acting.  They are high and you may also notice that they crave milk or wheat often through their day and start falling apart if they do not get the foods they want.  They are starting to experience withdrawal and that is not a good feeling.

Having a hard time believing this?  You can do a Gluten/Casein Peptide test.  I have also heard that a urine drug test will come back positive for opiates.  (I have not tried this so I would go with the peptide test .  I have recently seen that drug stores now sell home drug tests.  I would be very interested to hear from someone who has used this method of testing.  I do not remember these tests being available years ago before changing our son’s diet and there is no way on earth I would introduce these foods to him since he has improved so dramatically!)

It always gets worse before it gets better: I am a fond believer that negative behaviors get worse before they get better when introducing an autistic child on a new diet.  It many ways  this can mean that you are actually on the right road.  They are going to have to get those milk and wheat proteins out of their bodies and it is not always pleasant.  Some negative reactions that  may occur can be but are not limited to headaches, nausea, cold sweats, flu like symptoms, increase negative behaviors etc.

Benefits that may be seen after being on the diet: Many parents have reported several benefits to their children being on the GFCF diet.  Many children who were non-verbal have become verbal.  Parents have reported increased eye contact, less brain fogginess, decrease in negative behaviors, more stable moods, increased interest in people etc.

How to make the leap: Here are a few suggestions for changing your child’s diet.

  • Join a support group.  (Local or on the internet.  Ask other parents how they would recommend starting the diet.
  • Understand and write down all the ingredient names that have gluten and casein.  (You can find these list by a simple google search.
  • Make some foods in advanced that you can readily give your child if they are hungry.
  • Go grocery shopping and stock up on GFCF foods.
  • Figure out what foods are served that are GFCF from your local restaurants and fast food chains.  http://www.glutenfreerestaurants.org/find.php
  • Journal the experience

I know that the first step can be a difficult one but once you have figured out foods your child can eat and enjoys eating then it becomes a lot easier.  Before you know it you may see your child blooming before your eyes and that is what is important.  Not that cooking may become a little more challenging but that your child is REALLY benefiting from all your extra work and effort.  You can do it!!!

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Cooking for the Specific Carbohydrate Diet

October 15th, 2009

Last Friday I had a phone consultation with a Specific Carbohydrate Diet (SCD) counselor. We discussed the food that Nathaniel was currently eating and the direction we need to go in.

I am a mama on a mission to get Nathaniel to eat fruits and vegetables and enjoy eating them. Many of you know that children with autism struggle with eating different foods. They have a difficult time with the different flavors, smells, textures and visual appearance of food. Yet many of these children are starving for nutrients so diet is a main concern for our family when it comes down to Nathaniel’s overall well being.

If your child has just recently been diagnosed then I would suggest 100% that diet be step #1. I had a hard time even thinking of changing Nathaniel’s diet and thought it would be awful but I was so WRONG. I am getting to know Nathaniel and see his personality come out more and more and diet is part of the equation.

I have mentioned before that feeding Nathaniel the wrong foods is like feeding a Gremlin after midnight. (I hope I have not mentioned too old of a movie. I realize I am getting older when people start asking what is a Gremlin? Hehe) Nathaniel will literally run into walls or try to climb them for 2 weeks if he has a piece of cake. This is not an overstatement. I am amazed that I initially did not think changing his diet would help but all the grey lines for behavior due to food are now black and white since we started his diet.

Every now and then, I am going to post what is cooking in our kitchen. It is mostly to encourage those other mamas out there that they can take the next step and work on diet. (YOU CAN DO IT!!!!!) It is also for people who are just curious. If I can do this so can you. I am not a chef and have always had a difficult time enjoying cooking but it is worth it to see the whole family healthy. Now I am discovering that I am enjoying cooking and experimenting with different foods.

Let me mention a few challenges that I have for cooking for Nate that will hopefully be helpful for you.

First of all, we are just entering stage 2 of SCD.

Secondly, Nathaniel has a very hard time trying new foods. He would eat bread all day if he was allowed to eat bread. He used to be a carbohydrate junky. (Him loving carbohydrates so much was my first red flag that he needed to be on a diet.)

Third, he now has a whole list of IgG food allergies so I am learning to cook without these foods. Cooking without eggs is exceptionally hard but I am learning.

Butternut Squash

Butternut Squash


So here we go! We have just recently been able to get Nathaniel to eat butternut squash. I never would have believed it was possible but he has probably eaten a little over a whole butternut squash over a weeks time! This is the time to buy butternut squash (I found them for 78 cents a pound) so if you find that your child will eat butternut squash then stock up and freeze some.

Butternut Squash fries being cooked

Butternut Squash fries being cooked


We cut up each butternut squash in the length and shape of french fries. We then used a little olive oil on a skillet and cooked them till they were FULLY cooked and were a little crispy. (Early in the diet, try to use fats sparingly to aid in healing so try not to use too much oil.) Then we salted them but if your child likes things that are more sweet than salty then you could always try a touch of honey.
Yum!  They are actually really tasty.

Yum! They are actually really tasty.

Soon we will be baking the butternut squash and having it be in the same size and shape. Our goal is that he is getting used to the taste and texture and eventually will eat butternut squash no matter how it is cooked. We are taking one step at a time.

I plan on freezing a couple bags to save time and money.

I plan on freezing a couple bags to save time and money.

But we can’t stop here. There are too many other veggies and fruits that have yet to be explored! (This is me using self-motivation. Hehe) I’ll let you know what we experiment with next.

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