So, my DD is 5 years old. She has been challenging in many ways since the beginning. She had her first two rounds of shots plus one additional shot at 9 months. None since. She had growth issues beginning at birth until about 8 months. We were encouraged to start solids early, which we did. During this time she was a different rash everyday. Body rashes, butt rashes, you name it, she had it. They continued to about 18 months. No one ever suggested eliminating foods so we didn't.
At first her poops seemed ok. But gradually, starting at about 2 years they got looser. Now her typical poop is loose, smelly and takes a while to get out (spends lots of time on the toilet). She started having behavior issues when she was around 4. We cut gluten/dairy out in January 08. We saw some improvement in the behavior but the poops never resolved. We also removed eggs for a while with no improvement. She also has somewhat dull hair and weak pealing nails. Her skin is very dry. She was on abx for 6 weeks last summer for lyme disease (had an engorged tick in her head) which didn't help things. Her hair test showed high copper & high lead.
We recently took her to a GI doctor who works with autistic kids in the hopes that he would be more "alternative".
He had us do a trial with digestive enzymes & S. Boulardii. We saw little difference on the dosage we were on.
He did bloodwork and I just got the results today:
All IgE tests were negative and her IgE marker was very low. The GI doctor felt she was not a good candidate for IgE allergies.
Other results:
Iron 56 (30-160)
Iron binding capacity 408 (228-428)
Ferritin 23 (10-200)
Plasma Sodium 142 (135-145)
Plasma Pot. 3.9 (3.4-4.8)
Plasma chloride 108 (100-108)
Plasma Carbon diox. 24.8 (23.0-31.9)
Plasma anion gap 9 (3-15)
Calcium 9.2 (8.5-10.5)
Phos 4.5 (4.5-5.5)
Mag 2 (1.4-2)
Plasma creatine .64 (.30-1.0)
Plasma glucose 66 (70-110)
Total protein 6.7 (6-8.3)
Albumin 4.6 (3.3-5.0)
Globulin 2.1 (2.6-4.1)
Uric Acid 3.9 (2.3-6.6)
Total bilirubin .2 (0-1)
Alkaline phosphatase 170 (15-350)
Transaminase SGPT 25 (7-30)
Transaminase SGOT 33 (9-32)
Vid D 11 (33-100)
Thyroxine 9.7 (4.5-10.9)
Thyroid stim hormon 1.96 (.4-5.0)
zinc 50 (60-120)
He was not concerned about any of the values outside of the Ref Range except for Vit D & zinc. He said they are finding low vit D to be a marker for malabsorption and therefore its doubly concerning.
His recommendation is to do a scope (endoscopy & colonoscopy) to check for pancreatic insufficiency, relux damage, malabsorption, inflammatory disease, etc.
I'm really torn. He mentioned that she could have inflammatory disease, which would require anti-inflammatory medications for 6-12 months (longer if its looks like Crohns).
I feel there has to be a different answer although I'm very torn. I certainly don't want her to suffer but I find it hard to believe she's suffering from a deficiency of anti inflammatory meds. He said he doesn't necessarily believe in eliminating IgG foods b/c he thinks they are just symptoms of the problem. That there is some other reason the foods are bothering you (like inflammation).
Does anyone have any thoughts? This stuff is so hard. And DS is scheduled to see him in June. I can only imagine what he'll want to do with my small fry.
At first her poops seemed ok. But gradually, starting at about 2 years they got looser. Now her typical poop is loose, smelly and takes a while to get out (spends lots of time on the toilet). She started having behavior issues when she was around 4. We cut gluten/dairy out in January 08. We saw some improvement in the behavior but the poops never resolved. We also removed eggs for a while with no improvement. She also has somewhat dull hair and weak pealing nails. Her skin is very dry. She was on abx for 6 weeks last summer for lyme disease (had an engorged tick in her head) which didn't help things. Her hair test showed high copper & high lead.
We recently took her to a GI doctor who works with autistic kids in the hopes that he would be more "alternative".
He had us do a trial with digestive enzymes & S. Boulardii. We saw little difference on the dosage we were on.
He did bloodwork and I just got the results today:
All IgE tests were negative and her IgE marker was very low. The GI doctor felt she was not a good candidate for IgE allergies.
Other results:
Iron 56 (30-160)
Iron binding capacity 408 (228-428)
Ferritin 23 (10-200)
Plasma Sodium 142 (135-145)
Plasma Pot. 3.9 (3.4-4.8)
Plasma chloride 108 (100-108)
Plasma Carbon diox. 24.8 (23.0-31.9)
Plasma anion gap 9 (3-15)
Calcium 9.2 (8.5-10.5)
Phos 4.5 (4.5-5.5)
Mag 2 (1.4-2)
Plasma creatine .64 (.30-1.0)
Plasma glucose 66 (70-110)
Total protein 6.7 (6-8.3)
Albumin 4.6 (3.3-5.0)
Globulin 2.1 (2.6-4.1)
Uric Acid 3.9 (2.3-6.6)
Total bilirubin .2 (0-1)
Alkaline phosphatase 170 (15-350)
Transaminase SGPT 25 (7-30)
Transaminase SGOT 33 (9-32)
Vid D 11 (33-100)
Thyroxine 9.7 (4.5-10.9)
Thyroid stim hormon 1.96 (.4-5.0)
zinc 50 (60-120)
He was not concerned about any of the values outside of the Ref Range except for Vit D & zinc. He said they are finding low vit D to be a marker for malabsorption and therefore its doubly concerning.
His recommendation is to do a scope (endoscopy & colonoscopy) to check for pancreatic insufficiency, relux damage, malabsorption, inflammatory disease, etc.
I'm really torn. He mentioned that she could have inflammatory disease, which would require anti-inflammatory medications for 6-12 months (longer if its looks like Crohns).
I feel there has to be a different answer although I'm very torn. I certainly don't want her to suffer but I find it hard to believe she's suffering from a deficiency of anti inflammatory meds. He said he doesn't necessarily believe in eliminating IgG foods b/c he thinks they are just symptoms of the problem. That there is some other reason the foods are bothering you (like inflammation).
Does anyone have any thoughts? This stuff is so hard. And DS is scheduled to see him in June. I can only imagine what he'll want to do with my small fry.









: But I get it all mixed up, I've never lived anywhere near the East Coast, no one in my family has. The closest was an aunt who lived somewhere in Pennsylvania for a couple years.
Thoughts not matching typing speed lately.