valymemom
Frequent Contributor (1K+ posts)
Member # 7076
posted
Just wondering how often your practitioner does it.
My son started seeing a new llmd in December who uses muscle testing and we have seen him monthly - but we only had ART done twice.
Should I be requesting it for him each visit?
I just want to figure out what supplements he needs so he can get help with inflammation/pain.
Posts: 1240 | From Centreville,VA | Registered: Mar 2005
| IP: Logged |
SForsgren
Frequent Contributor (1K+ posts)
Member # 7686
posted
I do it at every visit with my 2 practitioners that use ART as part of their work.
-------------------- Be well, Scott Posts: 4617 | From San Jose, CA | Registered: Jul 2005
| IP: Logged |
hardynaka
Frequent Contributor (1K+ posts)
Member # 8099
posted
I also see 2 ART practioners.
They do ART 90% of the time every visit.
Selma
Posts: 1086 | From Switzerland | Registered: Oct 2005
| IP: Logged |
SForsgren
Frequent Contributor (1K+ posts)
Member # 7686
posted
Hi Selma, I am actually sitting here in a room with one of your ART practitioners - maybe both. S is here at the Autism conference in Seattle... Scott
-------------------- Be well, Scott Posts: 4617 | From San Jose, CA | Registered: Jul 2005
| IP: Logged |
GiGi
Frequent Contributor (5K+ posts)
Member # 259
posted
Yes, ART is done almost through the whole visit. Very little talk - that's how the continuation of treament is determined. That's how decisions are reached whether existing meds and nutrients are still welcome by the body, etc. It avoids a lot of pitfalls.
Yes, Selma, S is here with another one of the top therapists out of the German group. I have known them for many years and they are both fabulous practitioners learning more and more at this seminar. There is constantly something new learned. Heard today that a little autistic boy started to for the first time speak many, many words that he had never spoken before ---after he had had five days of the galactose I have been talking about. It is so rewarding to hear that. Many are now being ART tested for it as are most other patients and whoever tests positive for it, is encouraged to use it.
It is fun being here with Scott - he is like a sponge learning more and more. And so am I!
Hope your doctor will continue to use ART - you will, I am sure benefit from it.
Take care.
Posts: 9834 | From Washington State | Registered: Oct 2000
| IP: Logged |
posted
This may sound really dumb....but what is ART? C Posts: 88 | From Carnation | Registered: Feb 2007
| IP: Logged |
GiGi
Frequent Contributor (5K+ posts)
Member # 259
posted
Here is an explanation of ART (Autonomic Response Testing). It is not totally telling all, but you get a pretty good sense of what it does. It is the best form of muscle testing that I know.
With this method, the problems are diagnosed, the deficiencies determined, and the most suitable medicines and nutrients determined for treatment. It avoids a lot of pitfalls and unnecessary stress of the system. It takes minutes rather than weeks and little money rather than thousands of dollars for lab testing that give no answers to "what is the problem and what will it take to start fixing this problem". The body tells what it needs to unblock the body's own regulation, i.e. help the body into a healing mode.
Take care.
Posts: 9834 | From Washington State | Registered: Oct 2000
| IP: Logged |
valymemom
Frequent Contributor (1K+ posts)
Member # 7076
posted
Thanks all! I was hoping you would respond, Gigi. My son sees someone I think you would recommend here in D.C. and I am going to start asking for muscle testing to be included at each appointment.
We switched protocols and I wish we would have ART tested to see whether to remain/change meds and supplements.
Posts: 1240 | From Centreville,VA | Registered: Mar 2005
| IP: Logged |
hardynaka
Frequent Contributor (1K+ posts)
Member # 8099
posted
Scott and Gigi, I knew S. was travelling, but I didn't know she where she was .. Now I know!!!
This internet connection is SO funny!
I asked in Reformhauser about Galactose, nope, they never heard of it. I'll go to a normal pharmacy and check. If I don't find any info, I guess I have to drop at that address in Konstanz to find out more info... Or email one of you guys later.
I'm enjoying some of dr. K's DVDs here, very very informative and easy to understand (even for bad German speakers like me).
Take care you all, Selma
Posts: 1086 | From Switzerland | Registered: Oct 2005
| IP: Logged |
The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:
The
Lyme Disease Network of New Jersey 907 Pebble Creek Court,
Pennington,
NJ08534USA http://www.lymenet.org/