Guest guest Posted May 28, 2006 Report Share Posted May 28, 2006 Even at 60 lbs. last summer he was taking 2 capsules every 8 hrs. That's 200 mg. No pharmacist has even said anything to me. Do you think this is why his white blood cell count drops too low to chelate right after the first 3 rounds? He has to do a blood test every 3 rounds. And, inbetween he has to do DDI stool samples. Last summer when he chelated they sent urine test kits instead of stool test kits and even with that it showed lots of lead coming out. So really I could use one capsule 3 times and only 3 capsules per round? Every 4 hours would be easier and less capsules would be too. He will eat yellow apples. I won't let him have the red apples because of the phenols. Bananas, but they seem to make him constipated and he already has those issues. Pears for my mom. I don't buy them because he usually doesn't eat them for me. Great Value brand potato chips Mc's Fries and s and Sonic 's and Sonic chicken strips and nuggets Banquet brand chicken strips and nuggets turkey fried okra and sometimes other fried foods. If it wasn't fried he wouldn't even try it. sometimes pretzels Little Debbie Fancy Cakes - we cheat there with the dairy At school they have been giving him Teddy Grahams bread Waffles He will only drink water. It is well water and has been tested twice in 6 years. He is very resistant to foods that have any color. When he was totally GFCF he would hunt for the bread. A few times like now when I was on the computer and I thought it got a little too quiet I would find that he had devoured a loaf of bread. It never truely showed up on the Great Plains tests and other tests that he really had a problem with gluten, but his behavior used to really change if he accidentally ate gluten. So, I kept him off of it. In March he did a Genetics Celiac's test. One way would 100% prove he didn't have Celiac's disease. The other way would be uncertain and require scoping for a definant answer. April -- In , " Shepard Salzer " <_Shepard@...> wrote: > > > April, > That's way too high a dose of DMSA even for an adult. Does it make sense to do something you don't have to pay for that will probably make things worse? As someone else mentioned you can cut way back on the dose and dose every three hours (ALA's half life is 3 hours, DMSA's in 4 hours, easier to dose both together. You need not tell the doc until he notices the improvements. Andy Cutler recommends 1/8-1/2 mg per lb, so the highest your son should be taking is 33 mg every 3 hours. By dosing every 8 hours you run a high risk of redistributing the toxins into the brain rather than chelating them out of the body. > > What are the foods he'll actually eat? > S S > > > > > weighs 65 lbs.<BR> > Oral DMSA and ALA<BR> > 300mg DMSA and 50 mg. ALA every 8 hrs. 3 days on 11 days off. I know <BR> > everyone one this board probably uses every 4 hours but our DAN! doctor <BR> > won't do that.<BR> > Diet : Has been horrible since going GFCF since 2y3m old. He is now<BR> > 8 1/2 years old. He was GF til 2 years ago. He would never expand his <BR> > diet. Even therapists helped. Once again his OT that he has had for a <BR> > year is going to work on food issues this summer. He is still CF. <BR> > I am not consistant with most of the supplements. He gets magnesium <BR> > and pro mineral support everyday. I just started using L- glutithione <BR> > again. Put him back on No-Phenol. He has to take Benefiber. <BR> > Yeast Protocal? I don't have one. When he was younger I could tell <BR> > yeast was a problem. Now, I am not sure.<BR> > Approval? I go through 's DAN! doctor so I can get it paid for <BR> > by Medicaid. I don't pay for any of it. <BR> > April<BR> > > > _______________________________________________ > Join Excite! - http://www.excite.com > The most personalized portal on the Web! > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 28, 2006 Report Share Posted May 28, 2006 Ditto to what said. I hope you'll consider reducing the dose and changing the dosing schedule. in Illinois Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 29, 2006 Report Share Posted May 29, 2006 You need to get empty capsules and divide the capsules you have. 1/8-1/2 mg per lb at 60 lbs would be 7.5-30 mg per dose so consider dividing a 100 mg capsule into 4 (25 mg) or 5 (20 mg) doses. You would dose every 3 hours if ALA and DMSA and every 4 hours if DMSA only. That would mean dosing 8 times in a 24 hour period with both or 6 times with DMSA only. Were his white blood cells an issue before you began chelation? Bananas are constipating. Have you considered digestive enzymes? HNI in particular might prove helpful. Certainly sound like a gluten seeking diet. The gluten intolerance that many on the spectrum have is not regular celiac. S S Even at 60 lbs. last summer he was taking 2 capsules every 8 hrs. <BR> That's 200 mg. No pharmacist has even said anything to me. Do you <BR> think this is why his white blood cell count drops too low to chelate <BR> right after the first 3 rounds? He has to do a blood test every 3 <BR> rounds. And, inbetween he has to do DDI stool samples. Last summer <BR> when he chelated they sent urine test kits instead of stool test kits <BR> and even with that it showed lots of lead coming out. So really I <BR> could use one capsule 3 times and only 3 capsules per round? Every 4 <BR> hours would be easier and less capsules would be too. <BR> He will eat yellow apples. I won't let him have the red apples <BR> because of the phenols.<BR> Bananas, but they seem to make him constipated and he already has <BR> those issues.<BR> Pears for my mom. I don't buy them because he usually doesn't eat <BR> them for me.<BR> Great Value brand potato chips<BR> Mc's Fries and s and Sonic<BR> 's and Sonic chicken strips and nuggets<BR> Banquet brand chicken strips and nuggets<BR> turkey<BR> fried okra and sometimes other fried foods. If it wasn't fried he <BR> wouldn't even try it.<BR> sometimes pretzels<BR> Little Debbie Fancy Cakes - we cheat there with the dairy<BR> At school they have been giving him Teddy Grahams<BR> bread<BR> Waffles<BR> He will only drink water. It is well water and has been tested twice <BR> in 6 years.<BR> He is very resistant to foods that have any color.<BR> When he was totally GFCF he would hunt for the bread. A few times <BR> like now when I was on the computer and I thought it got a little too <BR> quiet I would find that he had devoured a loaf of bread.<BR> It never truely showed up on the Great Plains tests and other tests <BR> that he really had a problem with gluten, but his behavior used to <BR> really change if he accidentally ate gluten. So, I kept him off of <BR> it.<BR> In March he did a Genetics Celiac's test. One way would 100% prove <BR> he didn't have Celiac's disease. The other way would be uncertain <BR> and require scoping for a definant answer.<BR> April<BR> _______________________________________________ Join Excite! - http://www.excite.com The most personalized portal on the Web! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 29, 2006 Report Share Posted May 29, 2006 - Yes, I will be calling the doctor's office tommorow when they open and ask lots of questions. Thanks to everyone. April -- In , " mmc2315 " <m.chelap@...> wrote: > > Ditto to what said. I hope you'll consider reducing the dose and changing the > dosing schedule. > > in Illinois > Quote Link to comment Share on other sites More sharing options...
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