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#1
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A young friend of mine is concerned for her boy now 2 1/2 years is only 24 lbs and since he was 6 months failing to grow, he has ear infections and tubes in the ears, severe asthma, vomits, abdominal pain waking him up at night, she breastfed him until he was 17 months stopping when pregnant with third baby. Five doctors are looking at his problems, and endocrinologist, an immuniologist, a pediatrician, etc. his immune system was found "normal", cystic fibrosis was rule out and soon other tests included genetic will follow. He is not showing autism, she used to care for autistic children so she knows.
Any ideas, what else doctors should rule out? |
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#2
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I would look into food allergies, possibly celiac disease or glutton problems with stomach cramps, vomiting and no weight gain.
Gina Marie |
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#3
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My first thought was milk allergy, but wouldn't 5 doctors for the last 18 months figure this out?
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#4
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Has anyone suggested an MRI to rule out Chiari Malformation? Some of the symptoms listed sound like the ones my son had. Doctors don't think of Chiari so it doesn't surprise me that they haven't figured it out yet.
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#5
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Severe reflux can cause some of these symptoms, have they checked into that?
Lisa |
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#6
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Thanks, Ktufte, Lisa:
I just finish talking to my friend. Here is another clue his bones on his hand have not change, if understand right she told me that doctors x-rayed his hand and the doctor saw bones of a 12 month old and he is 2 1/2 years. She didn't know anything about chiari. But I think, in Canada has a different name I think "herniate" I don't remember the full name I will look into that new clue too. Geneticist will follow in a few months. Lisa they did an Endoscopy and colonoscopy and was normal. Next week he is going for a bariumscopy (?). Because the baby was losing weight they were suspected of neglecting and were referred to children's aid and investigated Doctors did metabolic tests. He is developing normally as normal as anybody. He has the language skills of a 4 years old. His comprehension of language is advanced, no neurologic damage his motor skills are perfect. Physically has a an adorable face, his head size is normal to his body. He was not born a premie, he is off milk, he takes lacto-free drinks. He was also tested for celiac disease, all clear. I am going to research that clue about bones. They also tested for hormones, all clear. |
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#7
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When Asthma and Gi problems are seen at the same time...most of the physician's i've worked iwth first condsider GERD-gastroesophageal reflux,..this can be triggered by neurological problems or other reasons...have they done an upperscope or barium study.. Does your child have other health issues.
About milk....lactose intolerance and a milk allergy are different. The milk allergy will be noted on immune or allergy testing. Lactose intolerence can only be diagnosed based on history and improvement of symptoms with avoidance or a breath hydrogen test after consuming lactose products. Just a thought
__________________
Anna- Mom of 2 boys who are now 11 and 7 with more labels than most grocery stores. I really don't care what the labels are as long as they are getting the services they need in school and at home to succeed. One little girl, 5, who braves it all with a strong attitude in response. Oh my nieces and nephews are running the 50% autism rate in their house also. |
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#8
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I posted this on BT2:
Quote:
My question is what type of metabolic testing did they do? Have they actually had a consult with a metabolic specialist? Reason I ask is that along our trek to a metabolic disorder with Coley, after he was diagnosed with LKS and before PDD, a very experienced & respected neurologist told us in a consult that in his opinion Coley did not have LKS, he did not have epilepsy and that his seizures were most likely caused by a metabolic condition. He sent word back to our treating Neuro who did a metabolic work-up. All came back normal. Later we were referred to the specialist who looked at his symptoms and behaviors and diagnosed him. We altered his diet and he has not lost weight since, he just had his first spurt in height since he was an infant. He is no longer failure to thrive, he's sleeping normally (WE are sleeping normally) his development and everthing else is on track... They retest him & retest him, and there are no major differences in his labs. But all the Drs (and his teachers/therapists) agree...something that has been removed frm his diet was f'ing with his body & mind. We test him now and then with small samples, and the reaction is always the same...horrible sleep for several days, terrible behavior, very sleepy child, change in his coloring, loss of appetite......... But the thing to know about metabolics too is that it's generally not a single test kind of thing, it's a collection of results combined, and usually you need to catch those results when the body is in metabolic stress. It can be weak from not being able to metabolize componenets of food, but metabolic crisis is different, and it can easily be mistaken for a bad flu or even a severe reaction to vaccines or meds or environmental allergies, etc.... Looking back on it, and after having it explained to us better, we now know that a lot of those not so typical reactions to things was really his body super stressed out...so as long as we keep him restricted he won't show those 'metabolic stressors'...it's like the EEG that way, you gotta catch it at the right time to 'see' it. But just like our neuro knew from describing his behavior that he was having seizures, so too did the metabolic specialist know from his behavior that he had an intolerance...we didn't catch a seizure on the EEG (there was other evidence though) and we did not catch metabolic crisis in his labs.... Does that make ssense? KJ |
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#9
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I wrote a lengthy answer and was not accepted because I was told I didn't logged in when I did.
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#10
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Isabelle,
If he is seeing and endocrinologist, have they checked growth hormone? And, don't bet that the docs are going to get it right. Sorry for my inability to put all my faith in the docs, but Carly is also failure to thrive (still at age 15). For years we went to GI specialists all who wanted to give her a g-tube. The child eats plenty. In fact, she ate more than her younger brother! Through Shriners we started seeing an endocrinologist because of concerns about osteopenic bone. At age 12, when the endo asked about her showing signs of puberty, we said we werent' seeing it. He then suspected growth hormone insufficiency. We had her tested, and sure enough that was it. Not one GI specialist even suspected this or checked for this! Since starting growth hormone therapy she has put on 8 1/2 inches and 16 lbs (in 2 1/2 years). Also, Carly had a kidney condition which is triggered by an immune system problems. We went to a seminar where one doctor mentioned milk. We took her off milk and she hasn't had the kidney condition in 6 years! They won't say it's the milk, but they also are telling us to keep doing what we are doing. Gluten free has not produced many results. But, there is nothing that says you have to eat gluten or milk. There are plenty of substitues. Have they checked for Chrones disease as well? (Did I spell that right?)
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