Guest guest Posted August 1, 2006 Report Share Posted August 1, 2006 Dear Marilette Atma Namaste A child of 12 years named " Yash Modi " is suffering from LUQUE DYSTROPHY. last year he had undrgone treatment from a healer in bombay for 3 months. However he has not shown any improvement. I have done my advanced 6 months back. please advice about the treatment. I would be grateful to you. thank you so much love tikku ======================= Dear Tikku, Namaste. Thank you for your email. Medical Background: Muscular Dystrophy (MD) is the name of a group of muscle disorders that are characterized by progressive weakness and wasting of the voluntary muscles that control body movement. As muscle tissue weakens and wastes away, it is replaced by fatty and connective tissue. Anyone can be affected. Contrary to popular belief, muscular dystrophy is not exclusively a childhood disorder. While some types of MD are first evident in infancy or early childhood, other types may not appear until later in life. Specific disorders within this group vary in many ways. Which muscles are chiefly involved is different from disorder to disorder. The severity of the symptoms, the age at which the symptoms appear, how fast the symptoms progress and what pattern of inheritance the disorder follows are all factors which differ between the various forms of muscular dystrophy. Muscular dystrophies are genetic diseases. They are not contagious. Forms of muscular dystrophy can be passed on from generation to generation, or they can occur spontaneously in a single individual as the result of a mutation of a particular gene. In any case, they are not anyone's fault. Each form of muscular dystrophy is caused by an error in a specific gene associated with muscle function. specific types of muscular dystrophy? Becker Muscular Dystrophy: The genetic transmission of the disorder is X-linked recessive. It is caused by mutations in the same gene as DMD. The onset of symptoms is generally later in BMD than in DMD, and can occur anywhere from 5 years of age to young adulthood. As in DMD, in families where there is a positive history of muscular dystrophy, BMD can be detected or ruled out in infants by means of a blood test. Initial Symptoms: Again, initial symptoms are similar to Duchenne, only milder in severity. Progression: The rate of progression is slow. Many people with Becker muscular dystrophy are able to walk well into their teens and adult years. Life expectancy is, in many cases, normal. Limb-Girdle Muscular Dystrophy Type of Inheritance: This is a group of inherited forms of muscular dystrophy. Most are autosomal recessive, but some forms of limb-girdle muscular dystrophy follow a dominant pattern of inheritance. Clinical Onset: The onset of symptoms is extremely variable, becoming evident anywhere from early childhood to adulthood. Usually, affected members of a family have about the same age of onset and degree of severity. Initial Symptoms: Some forms of limb-girdle MD affect the lower extremities initially. Symptoms include difficulty with gait, running, climbing stairs and rising from the floor. Other forms affect the shoulder muscles predominantly with resulting difficulty in lifting the arms. Progression: Progression of limb-girdle muscular dystrophy is variable. In some cases, it progresses very slowly, while in others, progression is rapid. Life span is often unaffected. Facioscapulohumeral Muscular Dystrophy (FSH) Type of Inheritance: FSH is an autosomal dominant type of muscular dystrophy. The gene for the most common type of FSH is located on chromosome 4. Clinical Onset: This disorder generally appears when a person is in early adolescence, but it can also appear in young adulthood or childhood. It can usually be detected earlier by clinical examination in a family where there is a positive family history. Initial Symptoms: Lack of facial mobility (smiling, whistling), difficulty in raising arms over the head and forward slope of the shoulders are some of the common initial symptoms. Progression: The progression of facioscapulohumeral muscular dystrophy is typically slow, with long periods of time when the disorder seems to stop progressing altogether. As the trunk and leg muscles become involved, persons with this disorder may lose their ability to walk. Life span is often normal. There are more than 100 forms of muscular dystrophy. The Luque procedure is an example of surgery for scoliosis. Pranic Healing: 1. Invoke and scan before, during and after treatment. 2. General sweeping twice. 3. Localized thorough sweeping on the front and back solar plexus chakra and the liver. Energize the solar plexus chakra with LWG, LWB then ordinary LWV. Apply more localized thorough sweeping on the front and back solar plexus chakra. 4. Localized thorough sweeping on the spine and both sides of the spine with emphasis on the affected parts of the spine alternately with LWG and LWO. Do not apply O on the head or above the neck area. Energize the affected parts of the spine with LWR. 5. Localized thorough sweeping on the muscles: from the neck and below but not on or near the heart or spleen, sweep alternately with LWG and LWO. For muscles on the head, on or near the heart and on or near the spleen sweep alternately with LWG and ordinary LWV. 6. Localized thorough sweeping on the minor chakras of the arms and legs alternately with LWG and LWO. Energize them with LWR. 7. Localized thorough sweeping on the basic chakra alternately with LWG and LWO. Energize the basic chakra thoroughly with LWR simultaneously visualize the basic chakra becoming brighter. 8. Localized thorough sweeping on the front and back spleen chakra and the navel chakra. Energize the navel chakra with LWR. 9. Localized thorough sweeping on the kidnys and the meng mein chakra. Energize the kidneys with W. 10. Localized thorough sweeping on the front and back heart chakra. Energize the heart chakra through the back heart chakra with LEV or EV. 11. Localized thorough sweeping on the ajna chakra, forehead chakra, crown chakra, backhead minor chakra, jaw minor chakras and throat chakra. Energize them with LWG then with more of ordinary LWV. 12. Stabilize and release projected pranic energy. 13. Repeat treatment 2 to 3 times per week for as necessary. 14. Play the Meditation on Twin Hearts cd. Encourage the patient to practice the Meditation on Twin Hearts after each Pranic Healing treatment. This will facilitate proper assimilation of healing energy. Love, Marilette 1. Pranic Healing is not intended to replace orthodox medicine, but rather to complement it. If symptoms persist or if the ailment is severe, please consult immediately a medical doctor and a Certified Pranic Healer. 2. Pranic Healers who are are not medical doctors should not prescribe nor interfere with prescribed medications and/or medical treatments. ~ 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 Reference material for Pranic Healing protocols are the following books written by Master Choa Kok Sui: Miracles Through Pranic Healing, Advanced Pranic Healing, Pranic Psychotherapy, Pranic Crystal Healing. Ask or read the up to date Pranic Healing protocols by joining the group through http://health./ MCKS Pranic Healing gateway website: http://www.pranichealing.org. Quote Link to comment Share on other sites More sharing options...
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