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posted in <<Autoimmune Disease > Chemical Sensitivity > Chronic Fatigue Syndrome / ME > Electrical Sensitivity > Fibromyalgia > Gulf War Syndrome > Lyme & Co-Infections > Mold Illness > TREATMENTS


Neural Therapy

developed by: Ferdinand and Walter Huneke (brothers from Germany)


Neural TherapyOriginally developed in Germany by the Huneke brothers, neural therapy involves the injection of a common local anesthetic (Procaine/Novocain), into various points of the body. It is based on the theory that trauma can produce long-standing disturbances in the electrochemical function of tissues. The areas affected by trauma include autonomic ganglia, peripheral nerves, scars, glands, acupuncture points, trigger points, skin and other tissues. A correctly administered injection can often instantly and lastingly resolve chronic longstanding illness and chronic pain.

Neural therapy is often very effective for medical illnesses such as chronic pain, allergies, vertigo, asthma, sinusitis, eczema, rheumatoid arthritis, lupus, chronic bowel problems, kidney disease, prostate and female problems, infertility, tinnitus (ringing in the ears), and many other conditions.

Even though regional anesthesia, epidural injections, and trigger-point injections (neural therapy procedures) are widely used in the U.S., neural therapy as a comprehensive healing system is virtually unknown to most American practitioners. However, in Europe’s German speaking countries it has become one of the most widely used modalities in the treatment of chronic pain and intractable illness.

Excerpted from Dr. Klinghardt’s lecture “Neural Therapy C: Treating the Brain” presented at the American Academy of Neural Therapy in Seattle, December 1998:

Neural Therapy (NT)

NT can be used in several different ways:

1. Electric field effect: to generate strong electric fields within the brain or portions of the brain (segmental therapy). Various functional parts of the brain communicate rapidly with other parts of the brain by emitting electric fields (which travel at the speed of light). These are in the neighborhood of 20-40 millivolts. A procaine injection to the scalp generates a stable field of approximately 180 millivolts (for 30 minutes). These fields overlap with the brain’s own fields and facilitate the growth of dendrites (increases number of new synapses) and can also activate dysfunctional synapses. The intravenous injection of procaine has a strong effect on the electric activity of the brain, leading to a more stable and synchronized brain wave pattern. The “adenoid injection” can strongly activate pituitary and hypothalamic function.

2. Anti-focal effect: A scar injection (or injection to a tooth, ganglion or other dysfunctional structure) can stop abnormal neurological signals (from scar, tooth or other dysfunctional group of cells). Abnormal signals stemming from a often remote untreated focal area are often the cause of ANS dysfunction in the brain, leading to areas of vasoconstriction, impaired transport in the ground system and inhibition of trans-membrane transport and impaired transit of nutrients across the ground system or matrix. This in turn creates a focus-specific vulnerable area within the brain with decreased immune function, decreased oxygen and nutrient uptake, and decreased detoxification abilities. The outcome is a region with increased toxic metal (and other toxin) deposition and uninhibited growth of fungi, bacteria and viruses.

3. Nutrient uptake enhancement: NT can be used to selectively increase blood flow and nutrient uptake in areas of the brain. The sympathetic ganglion blocks to the anterior neck (superior cervical ggl., stellate ggl.) are most commonly used, but injection to any of the other cranio-facial ganglia or the adenoids or sinus points may be the curative procedure. Segmental therapy is again very helpful, especially over the brainstem. The intravenous injection of procaine can be used to have a general vasodilating effect on the intracranial vessels.

4. Detoxification: NT can be used, to mobilize compartmentalized mercury and other metals or toxins (to detoxify ANS ganglia and nerves). We could show that after injection of a mercury toxic stellate ganglion (demonstrated by the use of ART or the bi-digital O-ring test) with procaine, urine excretion of Hg increased form 0 to 28 micrograms/liter of urine in the first urine voided after the injection. This result could further be improved dramatically, by adding the appropriate complexing agent into the injection. Also simple trigger point injections and segmental therapy injections can have the same effect. Therefore, NT can be used to selectively mobilize compartmentalized toxin residues, such as lead or mercury.

5. Axonal transport for targeted drug delivery: NT can be used to introduce nutrients, healing agents and detoxifying agents into the periphery of a cranial nerve or autonomic nerve and have the substance be transported axonally into the brain or brainstem – thus effectively bypassing the blood-brain barrier.

sources: Huneke Neural Therapy, Klinghardt Academy Neural Therapy

see also: Neural Therapy Part I (PDF) and Part II (PDF) by Dietrich Klinghardt, MD, PhD, Neural Therapy C: Treating the Brain by Dietrich Klinghardt, MD, PhD, Neural Therapy with Bee-Venom, Mike Dessin’s Recovery From Severe ME Using Neural Therapy, A New Day support group discussing Mike Dessin’s recovery treatment

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Comments

  • Julie Laffin

    October 31, 2009 at 2:32 pm

    This article really speaks to me. I would like to try this. I have a lot of cervical spine and cranial nerve issues. It would be great to learn more about this. J8

  • sandra

    April 16, 2010 at 8:13 pm

    Dear Planet Thrive,
    Julie I love what you have done. I am trying to find someone who treats or had and was treated for bad autonomic nervous system dysfunction. Please let me know at my email address if you know. Thank you.
    Sincerely,
    Sandra

  • earthwalker

    April 16, 2010 at 8:28 pm

    Thanks so much Sandra! I’m sorry but I don’t know of anyone for autonomic nervous system dysfunction. Maybe someone else can recommend someone here in the comments section. You could also ask on our forums in the community section. Best to you Sandra! x Julie

  • KATHY VESTER

    January 7, 2011 at 1:05 am

    I have xmrv and have had since 2001 also lupus, renal cell cancer and am awaiting kidney removal surgery, The doctors,even oncologist have never heard of xmrv but yet they could not identify with what they found in my blood when they tried to type and cross match for surgery,It’s so scary that someone who is a hematologist/oncologist prescfibing chemo conncoctions has never even heard of xmrv and tries to make me look like a dumbass because he’s never heard of it. It’s doctors like him that have killed sufferers likke me.Someone should start a website wher the idiots could be reported and then flooded with info. I think they recieve their degree and never again pick up another publication unless it’s in regards to a free golf trip from a pharmacuetical company

  • Paulvon

    September 4, 2012 at 11:35 am

    Hello Kathy Vester,

    I can certainly appreciate your golf trip comment…

    I have been researching the damaging effects of electromagnetic exposures on human DNA and autoimmune functions for several years. I must say I had never encountered a reference to xmrv until reading your post. Here’s what Wikipedia has to offer. >

    http://en.wikipedia.org/wiki/Xenotropic_murine_leukemia_virus-related_virus

    The viral mutations seen in lab study results, could very well be related to double-strand breakage in DNA -caused by electromagnetic exposures.

    You would do well to investigate this possible EMF/XMRV relationship, particularly for the fact that the occurrence of this new disease, is concurrent with these new and dangerous levels of cell phone and wi-fi induced radiation in the general population.

    Best regards,
    Paul Von

  • Pam Lee

    October 6, 2013 at 7:57 pm

    What can you do for bacterial spinal meningitis? My daughter was near death from an inner ear infection which became chronic……her ear drum burst into the spinal fluid and her blood stream. 5 days in ICU, 10 days of rehab and 10 more days of liquid antibiotics…..high dses of steroids in the beginning, slowly lessening. She has chroinc back pain, loss of hearing, fatigue, ear achs and headaches every day……hair loss too……help! and thank you for listening, P.L.

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