Guest guest Posted December 23, 2010 Report Share Posted December 23, 2010 I think that DAN kids probably only amount to 50% at most, JMHO, have you looked at Yasko stuff? It means major time input from the parent, Sam (also not a DAN kid) did well until we got to the stage of needing weekly testing that we could not afford and HHI refused to work with Caudwell. We still use many of the prinicples in his supps, chelate per Cutler and are 4 months into TST FWIW Mandi x Thank for this info Tracey.. .My son is 6 yrs we have been doing DAN 4 yrs now i believe now he is not a DAN kid and i need a new approach.. Thanks again for feedback Caroline.. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 23, 2010 Report Share Posted December 23, 2010 I think that DAN kids probably only amount to 50% at most, JMHO, have you looked at Yasko stuff? It means major time input from the parent, Sam (also not a DAN kid) did well until we got to the stage of needing weekly testing that we could not afford and HHI refused to work with Caudwell. We still use many of the prinicples in his supps, chelate per Cutler and are 4 months into TST FWIW Mandi x Thank for this info Tracey.. .My son is 6 yrs we have been doing DAN 4 yrs now i believe now he is not a DAN kid and i need a new approach.. Thanks again for feedback Caroline.. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 23, 2010 Report Share Posted December 23, 2010 We were seeing him for about a year.. Very expensive supp regime nearly £250 per month and NO improvements... We saw him in Cambridge and became frustrated with his lack of notes to support earlier visits with him and his constantly changing views on what problems were and how to treat them. It often felt like he had a flavour of the moment.. We were told to buy a green light laser..first visit, second visit was all about wearing clothes with silver fibres and third time all about cryogenics. We went specifically about epilepsy.. as he said seizures would be controlled within a year.. for us this did not happen and he suddenly decided DD should go to Germany to have her tonsils cryogenically removed... though DD had never had tonsilitis nor a throat problem. It was at this point we stopped seeing him and did not take his advice on tonsils. The frustration and hassle of sourcing all the meds he prescribed was the final straw.. Many are his own meds and generally they need to come from USA. His prescriptions at that time could not be supplied even by the places he suggested in USA.. and we spent so many hours phoning his offices trying to make it possible to get hold of the meds. When we had poor reactions to the meds there was no means of contacting him to get feedback of suggestions on how to alter Medication regime he suggested. I am sure that some may have found his approach and treatment good, for us it was an expensive period in which there were NO improvements and thankfully we have found a therapy which has begun to make massive improvements in using TST. Best Wishes Tracey Have any of you consulted with Dr Klinghardt .. In relation to lyme or other? Thanks Caroline Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 23, 2010 Report Share Posted December 23, 2010 We were seeing him for about a year.. Very expensive supp regime nearly £250 per month and NO improvements... We saw him in Cambridge and became frustrated with his lack of notes to support earlier visits with him and his constantly changing views on what problems were and how to treat them. It often felt like he had a flavour of the moment.. We were told to buy a green light laser..first visit, second visit was all about wearing clothes with silver fibres and third time all about cryogenics. We went specifically about epilepsy.. as he said seizures would be controlled within a year.. for us this did not happen and he suddenly decided DD should go to Germany to have her tonsils cryogenically removed... though DD had never had tonsilitis nor a throat problem. It was at this point we stopped seeing him and did not take his advice on tonsils. The frustration and hassle of sourcing all the meds he prescribed was the final straw.. Many are his own meds and generally they need to come from USA. His prescriptions at that time could not be supplied even by the places he suggested in USA.. and we spent so many hours phoning his offices trying to make it possible to get hold of the meds. When we had poor reactions to the meds there was no means of contacting him to get feedback of suggestions on how to alter Medication regime he suggested. I am sure that some may have found his approach and treatment good, for us it was an expensive period in which there were NO improvements and thankfully we have found a therapy which has begun to make massive improvements in using TST. Best Wishes Tracey Have any of you consulted with Dr Klinghardt .. In relation to lyme or other? Thanks Caroline Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 23, 2010 Report Share Posted December 23, 2010 Thank for this info Tracey.. .My son is 6 yrs we have been doing DAN 4 yrs now i believe now he is not a DAN kid and i need a new approach.. Thanks again for feedback Caroline.. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 23, 2010 Report Share Posted December 23, 2010 Thank for this info Tracey.. .My son is 6 yrs we have been doing DAN 4 yrs now i believe now he is not a DAN kid and i need a new approach.. Thanks again for feedback Caroline.. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 23, 2010 Report Share Posted December 23, 2010 Hi Caroline... DD was not benefitting from supps.. this is why TST approach of working on improving breathing to allow body and brain to function at a higher level has been a Eureka moment for us.. We have tried tens of different therapies.. even getting to the point of considering brain surgery... as nothing would control DDs seizures.... because her problems lay with low blood oxygen reaching her brain.. I have read articles on how similar her hypoxic epilepsy is to many of the challenges faced by ASD kids too. I really hope that you find the key to unlocking your little lad too.. TST has done this for us... DD is a high functioning young lady , no ASD diagnosis, but very ASD like behaviours and socialisation issues in the past. Best Wishes Tracey Thank for this info Tracey.. .My son is 6 yrs we have been doing DAN 4 yrs now i believe now he is not a DAN kid and i need a new approach.. Thanks again for feedback Caroline.. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 23, 2010 Report Share Posted December 23, 2010 Hi Caroline... DD was not benefitting from supps.. this is why TST approach of working on improving breathing to allow body and brain to function at a higher level has been a Eureka moment for us.. We have tried tens of different therapies.. even getting to the point of considering brain surgery... as nothing would control DDs seizures.... because her problems lay with low blood oxygen reaching her brain.. I have read articles on how similar her hypoxic epilepsy is to many of the challenges faced by ASD kids too. I really hope that you find the key to unlocking your little lad too.. TST has done this for us... DD is a high functioning young lady , no ASD diagnosis, but very ASD like behaviours and socialisation issues in the past. Best Wishes Tracey Thank for this info Tracey.. .My son is 6 yrs we have been doing DAN 4 yrs now i believe now he is not a DAN kid and i need a new approach.. Thanks again for feedback Caroline.. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 24, 2010 Report Share Posted December 24, 2010 Hi Mandi well we did the yasco testing and i also apply it to our supplements but never went 100 % into it .. I feel Adam is a lyme guy o am going to tackle it head on in 2011.. Happy Christmas to u all xx Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 24, 2010 Report Share Posted December 24, 2010 Hi Mandi well we did the yasco testing and i also apply it to our supplements but never went 100 % into it .. I feel Adam is a lyme guy o am going to tackle it head on in 2011.. Happy Christmas to u all xx Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 19, 2011 Report Share Posted July 19, 2011 Yes, I have, Amy. My dentist has studied extensively with Dr. Klinghardt and has recently begun teaching with him. I've had both dental and medical. As you probably know, Dr. K uses a sophisticated form of muscle testing, which I have found invalueable. so much so that I feel I've been spoiled in regard to using other doctors. What specifics were you looking for? > > Has anyone done dr Klinghardts treatements medical or dental? > > I'd like to hear how it went. > > thanks, > Amy > Quote Link to comment Share on other sites More sharing options...
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