Anyone successfully use his protocol????? Stories? Experience?
Posted by SForsgren (Member # 7686) on :
There isn't really a "protocol". There are some basic things that he does, but he individualizes this for each person using labs, ART, etc.
I have been a patient for 3 years and have found that he has been a great part of my improvement.
I am still being treated, but off all antibiotics now for almost 1 year and still doing well overall.
His theories on toxins and emotions being an equal factor to infection in illness has been a key driver in my own approach to recovery.
It is not all about Lyme or about killing bugs...
Posted by Brussels (Member # 13480) on :
I'm with Scott. So far the best approach for chronic infection diseases for us at home. Both me and daughter are now in remission again. We did a few courses and now can do the energetic tests by our own.
My lyme doctor said he never has seen anyone that was so sick like I was recovering so fast in his life.
We though added photons to speed up recovery since January. Dr. K. still doesn't use homeopathy through photons as far as I know. Scott also used that and got free of abx only after using the Bionic.
I treated heavy metals (still doing that), root canals, cavitations, scars, ancient physical 'wounds', EMRs, switchings, psychological problems (many!), psychological blockages, and loads of acupuncture points all over my body. ART is a great tool.
Posted by lymie_in_md (Member # 14197) on :
I've followed Dr. K. for sometime, I may not have done many of the things he recommended, but I feel I'm really close to remission in part because of the information he puts out. Some of that information is archived within lymenet from many of his patients. Who I've learned quite alot from including both Scott and Brussels.
He's also had great impact with LLMDs who now treat for metals, sometime ago they didn't. You can thank Dr. K. for much of that change and many others.
By the way, all the good Dr.s talk to each other constantly about difficult patients and to get ideas. We don't see this as patients. He is one of the important contacts many doctors have.
Dr. K. is also continuing to learn and evolve, recently many of us are doing the KPU protocol. You wouldn't have seen this except within the past 6 months for lyme.
I've had symptoms now for 3 years. I think I could have reduced that dramatically if I was more open to the alternative and to use many of the techniques we now know about.
Hopefully Dr. K. will create a protocol to use photons.
Posted by richedie (Member # 14689) on :
What is ART?
Also, where is he located? Should I mention him to my doctor?
Posted by randibear (Member # 11290) on :
are there any doctors here in the u.s. that use the protocol?
or can you do it alone?
Posted by seekhelp (Member # 15067) on :
Located in WA, impossible to get into for the most part.
quote:Originally posted by richedie: What is ART?
Also, where is he located? Should I mention him to my doctor?
I agree with seek -- very difficult to find practioners. I'm fortunate to have worked with a practioner around Baltimore.
The best way to find if there are practioners within your area is to call Dr. K.'s office for practioner's within you area.
Posted by GiGi (Member # 259) on :
Be back later with a couple of comments.
Posted by richedie (Member # 14689) on :
Lymie in MD??? Baltimore? My doc is in Baltimore. Can you PM me some info?
Posted by GiGi (Member # 259) on :
Richedie, you may want to contact http://www.andreannarainville.com/about.html She has been teaching a group/clinic in Baltimore, New York, etc. She has been Dr. K.'s right hand for many years, and I get her assistance when needed for family and friends. She has her own practice in Bellevue, WA.
Good luck.
P.S. If you are looking for someone who has had her life renewed via ART and the Klinghardt method, think of me. I am completely recovered, and am only active here on a limited basis to help a few who want help. I still take a very active part in attending all Klinghardt seminars and if I can't reach him because he is in another part of the world and I don't want to bug him, I contact Andreanna to get answers or advice.
Posted by bigdreams87 (Member # 20493) on :
Gigi, I have some questions is there a way I can get in contact with you?
Posted by GiGi (Member # 259) on :
Bigdreams, my e-mail is [email protected] Please do.
Posted by Marnie (Member # 773) on :
His protocols AND THOSE OF Dr. B changed over the years...as they should.
In other words...we're still learning, still trying to figure out what works, what doesn't and why.
Some of you might find the book, "Hippocrates' Shadow" interesting.
We know what HELPS, but we are still looking for a CURE...not remission...CURE.
Hopefully the safest, most effective and cheapest cure for the masses.
I understand that many here CANNOT AFFORD the doctor's visits, co-pays for drugs and treatments and all the supplements recommended by doctors (plural).
I don't believe ANY American should go bankrupt trying to get well (and many have!). This is a MORAL issue that HAS to be addressed.