Guest guest Posted November 2, 2004 Report Share Posted November 2, 2004 Dear Namita, Namaste. Thank you for your email. The pranic healing protocol below is given by Grand Master Choa for genetic ailments of this type. Medical Background: Cystinosis is a rare autosomal recessive genetic disease affecting both children and adults. " Autosomal recessive " escribes a trait or disorder requiring the presence of two copies of a gene mutation at a particular locus in order to express observable phenotype; specifically refers to genes on one of the 22 pairs of autosomes (non-sex chromosomes). Cystinosis is usually diagnosed in early infancy. It is estimated that 2,000 individuals worldwide have cystinosis, but exact numbers are difficult to obtain since this disease often goes undiagnosed. With early detections and proper treatment, children and adults with cystinosis can avoid serious health complications, such as kidney failure and neurological damage. The disease is characterized by elevated levels of intracellular cystine due to a defect in the lysosomal cystine transporter. Accumulation of cystine results in multiple organ damage with renal damage being the most pronounced in the first decade of life. Individuals with cystinosis experience both tubular dysfunction (renal Fanconi Syndrome) and glomerular deterioration. The renal Fanconi Syndrome usually occurs within the first year of life. Glomerular deterioration progresses throughout the first decade of life resulting in end-stage renal failure. There are two main types of Cystinosis. 1. Nephropatic -Infantile Nephropathic Cystinosis Children with Infantile Nephropathic Cystinosis generally appear normal at birth and during the first 6-8 months of life. As a proximal renal tubular defect in sodium and water resabsorption develops, leading to polyuria and polydipsia, affected children become especially vulnerable to dehydration. This, and a defect in sweat production, often leads to recurrent fevers as a presenting symptom. By 1 year of age children usually show growth retardation, rickets, metabolic acidosis, and other chemical evidence or renal tubular abnormalities, such as increased renal excretion of glucose, amino acids, phospathe and postassium. Less overt clinical and biochemical evidence of the disease can be found at a much earlier age by careful examination of children known to be at risk because of an affected older sibling or other relative. As the children age, failure to thrive is prominent. Without specific therapy children remain below the third percetile in both height and weight throughout life. The typical patient with infantile nephropathic cystinosis has short stature, retinopathy, photophobia, and onset of renal Fanconi syndrome in the 1st year of life. By 1-2 years of age corneal cystine crystals and rickets are apparent. Glomerular failure progresses slowly with end-stage renal disease by an average age of 9 years. -Late-onset Nephropathic Cystinosis child (4-5 yrs) adolescent (12-13 yrs) adult-onset (25 yrs) When more than one sibling has this condition, their age of onset and symptoms are similar. The most usual age of presentation has been 12-13 years. These patients have crystalline deposits in the cornea and conjunctiva, and have cystine crystals within bone marrow aspirates. Patients with late-onset cystinosis often do not develop the complete Fanconi syndrome, but their renal failure progresses to require renal transplantation, as in infantile nephropathic cystinosis. They are usually in end-stage renal failure within a few years of diagnosis. 2. Benign Non-Nephropathic Cystinosis Other patients have this form of cystinosis (formerly refered to as Adult Cystinosis) that is usually discovered by serendipity when an opthalmologic examination reveals crystalline opacities within the cornea and conjunctiva. These patients may suffer from photophobia similar in character to that of patients with the nephropathic forms of cystinosis, but their photophobia may not begin until middle age, and is usually not as debilitating. Since the only patients found to have this condition are those who have slit-lamp examination, it is possible that many such patients have no eye symptomatology and are never diagnosed. Benign cystinosis patients have crystalline deposits in their bone marrow and leukocytes, but do not develop renal dysfunction or retinopathy. University of California, San Diego, Department of Pediatrics, Division of Metabolic Disease. June 18, 2004. U.S.Library of Medicine Pranic Healing: Before and during treatment, play the OM CD. 1. Invoke and scan before, during and after treatment. 2. General sweeping with LEV or EV. 3. Localized thorough sweeping on the front and back heart chakra. Energize the heart chakra through the back heart chakra with LEV or EV. Visualize the pranic energy entering and going deeply into the heart chakra. 4. Localized thorough sweeping and energizing with EV on the front and the back solar plexus chakra. 5. Localized thorough sweeping on the front, sides and back of the lungs with EV. Enegrize the lungs through the back of the lungs with EV. 6. Localized thorough sweeping on the meng mein chakra with white. Do not energize. 7. Localized thorough sweeping and energizing on both kidneys and other affected areas with EV. 8. Localized thorough sweeping and energizing on the front and back spleen with white. If the patient experiences pain or radical reaction, immediately apply localized sweeping until there is complete relief. 9. Localized thorough sweeping on the basic chakra and the perinium minor chakra alternately with LWG and LWO. Energize with LWG, LWO and LWR. 10. Localized thorough sweeping on both arms and both legs with emphasis on their minor chakras alternately with LWG and LWO. Energize the minor chakras with LWG, LWO and LWR. 11. Localized thorough sweeping on the navel chakra and the lower abdominal area. Energize with EV. 12. Localized thorough sweeping on the brain, the eyes with EV. 13. Localized thorough sweeping on the crown, ajna, forehead, back head minor and the throat chakras with EV. Energize the chakras with EV and gold. While energizing the ajna chakra, gently but firmly instruct the ajna to normalize and harmonize all the other chakras and organ systems. 14. Stabilize and release projected pranic energy. 15. Repeat treatment 2 to 3 times per week for as long as necessary. Supplemetary: 16. Introduce the parents and older family members to the proper regular practice of the Meditation on Twin Hearts and blessings. Include the child's proper healing in the list of blessings. 17. Regular physical exercises. 18. Balanced nutritious diet with proper amounts of water. Love, Marilette ====================================================== namu_39in > dear marilette, > namaste!i have a patient 5yr old girl,she has less > physical growth.medical diagnose is Cystinosis.pls > guide me the treatment so i can heal treat her as > soon > as possible.thanks. > > > > luv, > namita. ===== Pranic Healing is not intended to replace orthodox medicine, but rather to complement it. If symptoms persist or the ailment is severe, please consult immediately a medical doctor and a Certified Pranic Healer . ~ Master Choa Kok Sui Miracles do not happen in contradiction to nature, but only to that which is known to us in nature. ~ St. Augustine Ask or read the uptodate pranic healing protocols by joining the group through http://health./ For the latest International Information regarding GMCKS Pranic Healing, visit http://www.pranichealing.org. Check out the new Front Page. www. Quote Link to comment Share on other sites More sharing options...
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