The Body Emotions 

Emotion Code Body Code Practitioner  

  Tom Heintz cecp cbcp Practitioner 

Alternative Medicine Holistic Energy Therapist

Emotion Code & Body Code

Tom@TheBodyEmotions.com

 

 

 

 

 Toxins - What are they?

 

 

 

Prions -

A prion is a  protein that can fold in multiple, structurally distinct ways, at least one of which is transmissible to other prion proteins. It is this form of replication that leads to disease that is similar to viral infection. Prions are not considered living organisms because they are misfolded protein molecules which may propagate by transmitting a misfolded protein state. If a prion enters a healthy organism, it induces existing, properly folded proteins to convert into the misfolded prion form. In this way, the prion acts as a template to guide the misfolding of more proteins into prion form. 

In sessions it is identified as either Stage 1 or Stage 2 and can be located in any part of the body. Identifying the location is not normally required in a session, just the fact that there is a presence and at what stage it currently is.

In a session summary, a Stage 1 refers to an Infectious state where proteins are being misfolded and Stage 2 refers to the Saturated or Disease level. Both forms can be released in Energetic Holistic Healing due to the fact that it is all energy. Identifying and releasing the underlying causes of the Prion Toxin and the releasing of the actual toxic energy can clear the body of this imbalance. 

In more technical terms: 

A tiny proteinaceous particle, likened to viruses and viroids, but having no genetic component, thought to be an infectious agent in bovine spongiform encephalopathy (Mad Cow Disease), Creutzfeldt-Jakobdisease, and similar encephalopathies.

A particle composed of protein, similar to a virus but lacking DNA or RNA. Prions are thought to be the agent of infection of some diseases of the nervous system.   Some of these proteins have been implicated in the ontogeny of age-related degenerative disorders such as  amyotrophic lateral sclerosis (ALS), frontotemporal lobar degeneration with ubiquitin-positive inclusions (FTLD-U), Alzheimer's disease, and Huntington's disease. This has given rise to the 'prion paradigm', where otherwise harmless proteins can be converted to a pathogenic form by a small number of misfolded, nucleating proteins.

 

 
     
 

 

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