This is a problem - Healers Who Share
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Muscles are controlled by nerves so this could more accurately be called nerve function. For purposes of understanding and ease of reference we have separated this from the nerve section.
SUMMARY OF REMEDIES
(with range of mega bottles needed)
Acetylcholine Scelrosis CPX 6
Actin Assassination Disease
Complex 6
Bone Nerve Muscle Malady 4-6
Dorsal Muscle Dystrophy 5-6
Dystonia A 6
Dystonia B 6
Dystonia C 6
Dystonia D 6
Familial Amyloidotic
Polyneuropathy 5-6
Fatal Neuropathic Amyloidosis 5-6
Hypophosphatemia 1 thru 6 5-6
Inclusion Body Myopathy 1 5-6
Inclusion Body Myopathy 2 5-6
Inclusion Body Myopathy 3 5-6
Continued on Next Page
PARALYSIS-LIKE DISEASES
Many nerve diseases have not one singular cause, but several factors working together. Often they contain muscle and nerve weaknesses together.
Acetylcholine Scelrosis Complex - When the choline protein wears out in the bone, the Thymus can no longer synthesize choline from the missing protein. The absence of choline has created a miasmic disease we call Acetylcholine Sclerosis. When this neural transmitter hardens, all nerves and muscles begin to stiffen and malfunction, like a Dystonia.
Actin Assassination Disease Complex Actin is one of the two most important ingredients in muscles.The remedy is for an aggressive enzyme disorder that destroys actin.
Bone Nerve Muscle Malady A wide-spread, bone-based "age-related" disease that dissolves strength and firmness. In Latin this could be called a "myomyelo" disease.
Dorsal Muscle Dystrophy The muscles in the area of genitals and anus/rectum begin to deteriorate. The chief symptoms are a feeling of pain near the tail bone, rectal internal bulging, reduced bladder holding ability, prolapsed uterus, impotency and (in late stages) prolapsed rectum. Dystonia A through D is our way of distilling the 23 recognized Dystonia diseases into 4 choices. All of the dystonias resemble Stiff Man Syndrome or Stiff Muscle Disease in some way. People can hardly bend any joints and even walking is a chore. The 4 Dystonias may well cover both diseases.
Familial Amyloidotic Polyneuropathy - Usually manifesting itself between 20 and 40 years of age, it is characterized by pain, paresthesia, muscular weakness and autonomic dysfunction followed by kidneys and the heart afflictions.
Fatal Neuropathic Amyloidosis - Symptoms include weakness or fatigue, sometimes weight loss, heart damage (congestive heart failure), shortness of breath, swelling of the feet and legs, chest pains, irregular heart rhythm, light-headedness (due to lowering of blood pressure during sudden position changes), abnormal sensations of the arms, feet, or legs, symptoms related to autonomic neuropathy (e.g. gastrointestinal symptoms such as bloating, diarrhea, etc.).
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PARALYSIS-LIKE DISEASES
Leigh 5 Disease - Subjects have muscle pain (loosely described as fibromyalgia), ossein pain (connective tissue of the bone), headaches and difficult breathing (not enough blood to lungs because of weakened heart).
Ligament Malacia - A bone disease that causes ligaments to soften and lose their supporting role to muscles and bones. Contrast this to the gall bladder disease that hardens ligaments (Ligament Sclera). The closest medical terminology seems to be Benign Hypermobility Joint Syndrome.
Ligament Sclera - The Gall Bladder can form inherited conditions with current fungi and viruses to strangle assimilation of what it takes to feed a ligament. The condition mimics arthritis
Ligaments/ Tendons/ Joint Fluid - A combination of the revival of base cells for these non-bone joint supporting elements. Most noticed when climbing stairs and laying in bed. Often felt as a “separation” of the left shoulder joint.
Lymphangioleiomyomatosis - LAM is called a rare disorder in which abnormal smooth muscle cells grow rapidly in lung and lymph tissue almost exclusively in women. The disease is strongly associated with Angiomyolipomas and Tuberous Sclerosis. The lung abnormalities resulting from LAM may cause difficulty breathing (dyspnea), chest pain, and coughing, which may bring up blood (hemoptysis). Many women with this disorder have recurrent episodes of collapsed lung (spontaneous pneumothorax). There are non-lung manifestations shown to right.
Lysosome Myeloma Complex - Lysosomes are made in the bone and are dispersed throughout the body. This disease or other forms of lysosome damage result in wasting diseases in the body, especially in bones. Muscular Dystrophy is considered an example. Derived from lysosomes are sphingophospholipids the only phospholipids not derived from glycerol in humans. Sphingolipids include sphingomyelins, cerebrosides and gangliosides. Insufficient conversion by enzymes of any of the forms results in nervous tissue and membrane deterioration.
Muscle Malacia - Used for a common disease that makes muscles weak.
Muscle Nerve Degeneration - Animal-based virus that locks on to the nerves of muscles and slowly withers them. Often accompanied by sore muscles after exertion.
SUMMARY OF REMEDIES
(with range of mega bottles needed)
Leigh 5 Disease 6
Ligament Malacia 5-6
Ligament Sclera 5-6
Ligaments/ Tendons/
Joint Fluid 5-6 Lymphangioleiomyomatosis 5-6
Lysosome Myeloma Complex 5-6
Muscle Malacia 5-6
Muscle Nerve Degeneration 5-6
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Lymphangiomatosis on Tongue
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Liver hygroma, lymphangiomatosis
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PARALYSIS-LIKE DISEASES
Muscular Dystrophy is a general approach to undefined cases. Over time we have made very specific forms for maximum effect. Actin Assassination Disease Complex may resemble a muscular dystrophy
Lysosome Myeloma Complex covers many of the presumed causes of muscular dystrophy and may round out the edges of specific diseases. Leigh 5 Disease is a Mitochondria disease and may present with similarities to lysosome diseases.
SUMMARY OF REMEDIES
(with range of mega bottles needed)
Actin Assasination Disease CPX 5-6
Leigh 5 Disease 5-6
Lyosome Myeloma Complex 5-6 Muscular Dystrophy
Autosomal Dominant 5-6
Muscular Dystrophy 5-6
Muscular Dystrophy Beckers 5-6
Muscular Dystrophy
Congenital 5-6
Muscular Dystrophy Emery-
Dreifuss X-Linked 5-6
Muscular Dystrophy
Limb-Girdle 5-6
Muscular Dystrophy Duchene 5-6
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SUMMARY OF REMEDIES
(with range of mega bottles needed)
Myotonic Dystrophy 1 6
Myotonic Dystrophy 2 6
Myotonic Dystrophy 3 6
Myotonic Dystrophy 4 6
Myotonic Dystrophy 5 6
PARALYSIS-LIKE DISEASES
Myotonic Dystrophy 1-5 presents with hypotonation of muscles while Dystonia usually display with hypertonation. We have also seen Mytonic Dystrophy resemble Restless Leg Syndrome.
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The digestive tract and uterus (womb) often are affected in Myotonic Dystrophy. These organs contain involuntary muscles, which can weaken or develop myotonia (trouble relaxing). Abnormalities in the brain can lead to excessive sleepiness or apathy. The heart (especially the “electrical” part) also can be affected.
Weakness and wasting (shrinking) of voluntary muscles in the face, neck and lower arms and legs are common in myotonic muscular dystrophy. Muscles between the ribs and those of the diaphragm, which moves up and down to allow inhalation and exhalation of air, also can be weakened.
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SUMMARY OF REMEDIES
(with range of mega bottles needed)
Hypophosphatemia 5-6
Paralysis Antidote
Hypokalemia Type 1-5 5-6
Paralysis Antidote Lentiform
Nucleus Sclerosis 5-6
Paralysis Antidote Motor
Nerve Interrupt # 1 5-6
Paralysis Antidote Nucleus
Tractus Solitaris 5-6
Paralysis Antidote Oculofacial
Progressive Congenital 5-6
Paralysis Antidote
Progressive Bulbar 5-6
Paralysis Antidote Motor Nerve
Interrupt #1 5-6
Spinal Muscle Atrophy 5-6
Stiff Man Syndrome 5-6
Stiff Muscle Disease 5-6
Strong Tissue 5-6
PARALYSIS-LIKE DISEASES
Some are an assembly of paralysis-like diseases so we demystified them by starting the name with “Paralysis Antidote”.
Paralysis Antidote Hypokalemia Types 1-5 involve low serum potassium.
Paralysis Antidote Lentiform Nucleus Sclerosis symptoms resemble the “Stiff Man Syndrome”.
Paralysis Antidote Motor Nerve Interrupt # 1 is for weakened motor nerves that cause the pelvis and spine to go out of alignment.
Paralysis Antidote Nucleus Tractus Solitaris is for central sleep apnea and the usual accompanying snoring. Subjects often nap easily and can doze of when driving.
Paralysis Antidote Oculofacial Progressive Congenital involves trouble with the eyelids and sometimes other facial muscles. Experience shows this condition will also affect the health of the teeth. Paralysis Antidote Progressive Bulbar involves the muscles of lips, tongue, mouth, pharynx and larynx. We have seen cases where one leg will draw upwards and make the leg appear to be shorter than the other leg.
Paralysis Antidote Motor Nerve Interrupt #1 is usually marked by the propensity of spine and sacrum joints to go out of alignment. Hypophosphatemia remedies often add to nerve paralysis or contraction.
Spinal Muscle Atrophy - seems to have ligament deterioration as a hallmark.
Stiff Man Syndrome – Is a more general form of the Dystonias mentioned previously.
Stiff Muscle Disease - Designed for Myotonia Congenita (Thompsen's Disease). Painless muscle stiffness mostly in hands, legs and eyelids. Handgrip releases slowly. Improves with exercise. Leads to always tight muscles.
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PA Oculofacial Progressive Congenital
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Ehlers Danlos
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Strong Tissue – Is designed for Ehlers-Danlos condition where people are frequently spraining ankles. The remedy has worked very well since 2002 for the condition. Subjects maintain that their backs are always going out of place as well as joints are easily hyperextended or out of socket. Benign Joint Hypermobility Disease is more relevant to all ligaments, so we made Ligament Malacia.
Hypophosphatemia 1 thru 6 - Causes a slow muscle wasting, difficulty breathing, hemolytic anemia, some mental/emotional confusion. The body needs phosphorus in order to use calcium. Bone weaknesses, white blood cell dysfunction weaken many other functions.
INCLUSION BODY MYOPATHY 1-3 - A muscle vacuole disease with filamentous inclusions. It is characterized by adult-onset, slowly progressive distal and proximal weakness.
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