Guest guest Posted August 5, 2004 Report Share Posted August 5, 2004 Amy, I'd have to say that the biggest red flag in your post was the carb addiction. I don't know if I'd trust the test results..... something is not right here! He is hooked on those foods because his brain/body is getting something out of it..... ie; a big hit of serotonin or something. The sensory issues he has (which even though the pattern doesn't seem to make sense, it does seem clear that he has some sort of sensory problems) mean that there is some disruption in neurotransmitters going on...... for what reason, it's unclear. But, I'd think it's obvious you need to steer him away from the starchy carbs he's craving. It sounds like the starches allowed on GF/CF have actually made matters worse. Whenever I hear about a kid having that " heroin addict " behavior for things like regular bread, I'm thinking.... it's the gut bugs. They're telling him what he needs. I'm not sure about cases where the tests might be wrong or misleading...... but...... like I said, SOMEthing is NOT right in this picture! I might be a little predjudiced but...... I'd say ignore the test results and do SCD anyway. Being so limited, his current diet can't be a good thing. My daughter didn't have any obvious GI issues when we started either (she has multiple neurologically based disabilities, but not autism)....... and yet SCD has made a positive difference in seizure control. You're probably thinking that his severe self limiting and the gagging with meat, etc. that you've seen will make it terribly difficult to do this diet, but I promise you there is a way. I'd suggest making a batch of the fabulous cashew butter muffins from the pecanbread website...... they're very fluffy and " breadlike " . There's all kinds of ways to " sneak " veggies and even meats into muffins and pancakes..... pureed and mixed in so they are totally disguised. They've fooled the pickiest of the picky! Quite a few other families here have been in the same boat.... with SERIOUSLY picky kids that they thought would NEVER eat any SCD foods..... and many of them have been surprised. My best advice? Listen to your Mommy instincts (which I believe have a lot more weight than test results and doctor's opinions:)) .....and do what you feel is right for him. Patti, mom to Katera, SCD 14 months Is SCD for us? HELP! recently got the rest of my son's lab tests back. We found that as per the urine and stool tests, he has no dybiosis at all. His yeast and bacterial levels are all within normal ranges. Note also that he has never really had an obvious, apparent gut/bowel issue either. I spoke at length with his doc (Dr. Usman) about the test results and what it means for us going SCD. But I am still unsure. Sorry so long - but I am really torn up about this. Any advice will be GREATLY appreciated All the best, Amy Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 5, 2004 Report Share Posted August 5, 2004 >>>he placed a small piece of grilled chicken breast on his tounge. He immediately began to gag and then vomited. Here are some ideas: Putting a food in your mouth is completely different from swallowing it. Swallowing means you are putting in in your body! It also requires a different set of muscles and feelings than just having it in your mouth. Meat can be tough too. My younger son had a time with meat. He had GERD and a gagging up reflex. He acutally improved with enzymes about the third month. I don't know what helped exactly except maybe it helped to quiet his nervous system down and the food was better digested...not as chuncky in the gut. How does your son do with soft or squishy foods? Breads and nut butters are squishy and don't sit as chunks in the gut. Does your son do better if the meat is broken up really fine or cooked so it is really tender. If you are interested in enzymes, here is the site www.enzymestuff.com The smell is another sensory item you hit on. I am very sensitive to smells, and smell has a lot to do with tastes and eating. That might be something to explore. >>>The docs think it might be an eating disorder. Might be worth exploring. Eating disorders have a component of control to them (the person is trying to establish some control in their world and environment). My son was very logical/literal. So when he would say, " I hate this food. " I would answer, " That's fine, you can hate it. But you still need to eat it to stay healthy. I eat foods I don't like too. So do most people. " When he would say, " I will not eat this broccoli. " I would say, " Fine. But you need to eat a green vegetable. Which green vegetable do you want. That is the next thing to eat. It is green vegetables turn. " I used a system of each food group gets a 'turn' because kids understand 'taking a turn'. When my son would say, " I want a banana instead. " I would say, " Bananas are good. Of course you can have a banana when it is the Fruit Group's turn. The next time it is Fruit's turn, you can have this banana. " ...and so on. The idea is to establish some law of nature or third party you both are abiding by so your child isn't in a power- struggle with YOU. good luck with this. . Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 6, 2004 Report Share Posted August 6, 2004 Patti - Thank you for your thoughtful reply. I agree that his body is definitely trying to tell me something! Your point that the starches allowed on the GF/CF is WELL taken! Like your child, my son is not " classically " autistic. He has been diagnosed with abnormal EEGs and is currently under the care of a neurologist. His symptoms may be all related to that - or not. They are mailnly autistic-like symptoms, though - singificantly delayed language, moderate to severe sensory processing and regulation issues. However he is - and always has been - a very well-connected (attached) little boy, big cuddler, wicked sense of humor. I think you are right about just doing it. We have definitely psyched pourselves up for SCD - even have our 6 year old on board (promised him he could still eat fries once in a while...just not at home or infront of his brother). We all intend to be SCD at home. By the way, the test results were all obtained through Dr. Anju Usman and Great Smokies Labs - we did the Comprehensive Digestive Stool Analysis and a urine analysis, the Metabolic Analysis Profile. Thanks again! Amy > Amy, > I'd have to say that the biggest red flag in your post was the carb addiction. I don't know if I'd trust the test results..... something is not right here! He is hooked on those foods because his brain/body is getting something out of it..... ie; a big hit of serotonin or something. The sensory issues he has (which even though the pattern doesn't seem to make sense, it does seem clear that he has some sort of sensory problems) mean that there is some disruption in neurotransmitters going on...... for what reason, it's unclear. But, I'd think it's obvious you need to steer him away from the starchy carbs he's craving. It sounds like the starches allowed on GF/CF have actually made matters worse. Whenever I hear about a kid having that " heroin addict " behavior for things like regular bread, I'm thinking.... it's the gut bugs. They're telling him what he needs. I'm not sure about cases where the tests might be wrong or misleading...... but...... like I said, SOMEthing is NOT right in this picture! > > I might be a little predjudiced but...... I'd say ignore the test results and do SCD anyway. Being so limited, his current diet can't be a good thing. My daughter didn't have any obvious GI issues when we started either (she has multiple neurologically based disabilities, but not autism)....... and yet SCD has made a positive difference in seizure control. You're probably thinking that his severe self limiting and the gagging with meat, etc. that you've seen will make it terribly difficult to do this diet, but I promise you there is a way. I'd suggest making a batch of the fabulous cashew butter muffins from the pecanbread website...... they're very fluffy and " breadlike " . There's all kinds of ways to " sneak " veggies and even meats into muffins and pancakes..... pureed and mixed in so they are totally disguised. They've fooled the pickiest of the picky! Quite a few other families here have been in the same boat.... with SERIOUSLY picky kids that they thought would NEVER eat any SCD foods..... and many of them have been surprised. > > My best advice? Listen to your Mommy instincts (which I believe have a lot more weight than test results and doctor's opinions:)) .....and do what you feel is right for him. > > Patti, mom to Katera, SCD 14 months > Is SCD for us? HELP! > recently got the rest of my > son's lab tests back. We found that as per the urine and stool > tests, he has no dybiosis at all. His yeast and bacterial levels > are all within normal ranges. Note also that he has never really > had an obvious, apparent gut/bowel issue either. I spoke at length > with his doc (Dr. Usman) about the test results and what it means > for us going SCD. But I am still unsure. > > Sorry so long - but I am really torn up about this. Any advice will > be GREATLY appreciated > > All the best, > > Amy > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 6, 2004 Report Share Posted August 6, 2004 - Thanks for your words of confidence. We actually have just started Sam on enzymes - from Houston, we are using the AFP Peptizyde and the HN Zyme-Prime. We've been using them for just a few weeks now. We've tried a bunch of things regarding texture, size, etc. He loves crunchy potato chips or veggie chips. He adores french fries, of course, but particularly seeks out the really well-done ones. He also likes mushy texture - he likes nut butters so much that he eats them straight from the jar. He will also eat applesauce once in a GREAT while. The other few things he will eat are the occasional banana, GF/CF waffles, GF/CF pizza, GF/CF chicken nuggets (but of course, no plain chicken!). No consistent pattern. Fortunately his SLP in preschool has a background in feeding issues (interned at the children's hospital). Sam starts school in a few weeks and we will be consulting with her on this too. The control thing is right on the money. He is so stubborn about taking a bite if he does not want to that he is often immune to bribes - even for a Mc's french fry (the ULTIMATE bribery tool). We don't want power struggles over food, so I never force him to eat anything. Thus he usually goes without eating dinner (I do not make him special food for dinner - he gets what we get). I recently purchased a book called " Just Take a Bite " and it looks to be quite interesting - it is more of the sensory/theraputic approach to feeding issues. For exapmle, they espouse regular, set eating schedules, a clear, clutter-free eating environment (HA!), and so on. The ultimate irony is that he is still in the 90th percentile for height and 75th percentile for weight. Go figure. (but we KNOW his overall nutrition is in the crapper). Thanks again - Amy > >>>he placed a small piece of grilled chicken breast on his tounge. > He immediately began to gag and then vomited. > > Here are some ideas: > > Putting a food in your mouth is completely different from swallowing > it. Swallowing means you are putting in in your body! It also > requires a different set of muscles and feelings than just having it > in your mouth. Meat can be tough too. My younger son had a time with > meat. He had GERD and a gagging up reflex. He acutally improved with > enzymes about the third month. I don't know what helped exactly > except maybe it helped to quiet his nervous system down and the food > was better digested...not as chuncky in the gut. > > How does your son do with soft or squishy foods? Breads and nut > butters are squishy and don't sit as chunks in the gut. Does your son > do better if the meat is broken up really fine or cooked so it is > really tender. If you are interested in enzymes, here is the site > www.enzymestuff.com > > > The smell is another sensory item you hit on. I am very sensitive to > smells, and smell has a lot to do with tastes and eating. That might > be something to explore. > > > >>>The docs think it might be an eating disorder. > > Might be worth exploring. Eating disorders have a component of > control to them (the person is trying to establish some control in > their world and environment). > > My son was very logical/literal. So when he would say, " I hate this > food. " I would answer, " That's fine, you can hate it. But you still > need to eat it to stay healthy. I eat foods I don't like too. So do > most people. " > > When he would say, " I will not eat this broccoli. " I would say, " Fine. > But you need to eat a green vegetable. Which green vegetable do you > want. That is the next thing to eat. It is green vegetables turn. " I > used a system of each food group gets a 'turn' because kids > understand 'taking a turn'. > > When my son would say, " I want a banana instead. " I would say, " Bananas > are good. Of course you can have a banana when it is the Fruit > Group's turn. The next time it is Fruit's turn, you can have this > banana. " ...and so on. The idea is to establish some law of nature or > third party you both are abiding by so your child isn't in a power- > struggle with YOU. good luck with this. > > . Quote Link to comment Share on other sites More sharing options...
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