Guest guest Posted April 2, 2006 Report Share Posted April 2, 2006 Read about on the Stories of Hope page on this site _Treating Autism_ (http://www.treatingautism.com/) You can open up the DMSA and give orally which is what we do. Kirkman brand is not bad taste or smell HTH Mandi in UK am getting ready for the switch from TD-DMPS...have been reading some good stories on Lee Silsby website about TD-DMSA... looking for some REAL stories from any of you that have them. They make it sound so awesome on the website. I guess I worry about the transdermal REALLY getting into his body to make something leave it...also, how do most of you dose it? My son is 30lbs, almost 3. I guess oral would be a nightmare as he doesnt swallow pills, also we are always fighting yeast...so TD sounds the best solution for us...if it works! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 2, 2006 Report Share Posted April 2, 2006 No miracles here with Lee Silsby TD-DMSA, but steady changes and real improvement since starting the TD-DMSA in September 2005. I have seen an accelleration in progress (we are also using supplements since 2003 and intensive in-home ABA since 2004) that I can attribute directly to chelation. Our TD-DMSA syringes say 250 mgs DMSA per ml. I give my 45 lb son about .3 ml every 4 hours. I think he could tolerate more, but I haven't upped the dose yet. I've had one DDI urine toxic metals test since starting the TD-DMSA. My son did excrete some mercury; in the green. His first DDI hair test on TD-DMSA showed a doubling of mercury excretion. Before you jump up and down, I'll tell you that he barely excreted mercury in hair pre-chelation... but I call that a measurable improvement. So, we are on our way to recovery. My son isn't a yeasty kid, so I can't tell you how TD-DMSA makes a difference there. I saw an even bigger jump in progress when I added oral ALA (dump a capsule in to some liquid or stir it into applesauce or even whipped cream!) about 2 months ago. REAL jump in progress. I'm waiting for the DDI urine metals test on this one. Take care and good luck. Pam > > I am getting ready for the switch from TD-DMPS...have been reading > some good stories on Lee Silsby website about TD-DMSA... looking for > some REAL stories from any of you that have them. They make it sound > so awesome on the website. I guess I worry about the transdermal > REALLY getting into his body to make something leave it...also, how do > most of you dose it? My son is 30lbs, almost 3. I guess oral would be > a nightmare as he doesnt swallow pills, also we are always fighting > yeast...so TD sounds the best solution for us...if it works! > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 2, 2006 Report Share Posted April 2, 2006 For oral DMSA chelation, DMSA capsules are usually opened just before the round is about to start then divided to approximate doses. A number of folks then scoop each individual dose into small bathroom size Dixie disposable cups. We found 20 ml oral syringes available for purchase (Here's ours: http://tinyurl.com/r3esc ) and just pull out the plunger slide the divided amounts " dry " into the graduated dispenser barrel then replace the plunger. Our 20ml oral syringes came packed 100 so we can dry mix an entire round. We leave the DMSA " dry " in the syringe until our lab timer goes off. At that time we carefully pull the plunger back out again and add either cranberry juice or orange juice until the graduated dispenser barrel is half full. Half full allows us to mix the dry and the wet together better and avoid any " caking " in the syringe. Too full and it's harder to mix things in the syringe up. With enough shaking we pull the plunger out once again to fill the syringe up just enough to be able to fit the plunger back in then orally dispense. We refill, shake and dispense a second syringe-full just to make sure the chelator washes out of the syringe For night dosing. A flashlight by the bedside is handy. Some folks pack a cooler and keep it by the bed. We like the flexibility of the lab timer. This is ours: http://www.control3.com/5004p.htm It's easy to learn to set and use and FWIW it's even traceable to NIST! Re: [ ] TD-DMSA-Any success stories out there? Read about on the Stories of Hope page on this site _Treating Autism_ (http://www.treatingautism.com/) You can open up the DMSA and give orally which is what we do. Kirkman brand is not bad taste or smell HTH Mandi in UK am getting ready for the switch from TD-DMPS...have been reading some good stories on Lee Silsby website about TD-DMSA... looking for some REAL stories from any of you that have them. They make it sound so awesome on the website. I guess I worry about the transdermal REALLY getting into his body to make something leave it...also, how do most of you dose it? My son is 30lbs, almost 3. I guess oral would be a nightmare as he doesnt swallow pills, also we are always fighting yeast...so TD sounds the best solution for us...if it works! Quote Link to comment Share on other sites More sharing options...
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