Guest guest Posted April 3, 2006 Report Share Posted April 3, 2006 Dear Charlotte and Marilette Namaste Please advice on the treatment for Neurofibromatosis, where tumours surround the nerves throughout the body and cause a great deal of pain and stops parts of the body from working. Thanking You Best regards Vinay Gudka ================================================= Dear Vinay, Namaste. Thank you for your email. Medical Background: Also known as Von Recklinghausen's Disease. The neurofibromatoses are genetic disorders of the nervous system that primarily affect the development and growth of neural (nerve) cell tissues. These disorders cause tumors to grow on nerves and produce other abnormalities such as skin changes and bone deformities. Although many affected persons inherit the disorder, between 30 and 50 percent of new cases arise spontaneously through mutation (change) in an individual's genes. Once this change has taken place, the mutant gene can be passed on to succeeding generations. Scientists have classified the disorders as neurofibromatosis type 1 (NF1) andneurofibromatosis type 2 (NF2). NF1 is the more common type of the neurofibromatoses. In diagnosing NF1, a physician looks for changes in skin appearance, tumors, or bone abnormalities, and/or a parent, sibling, or child with NF1. Symptoms of NF1, particularly those on the skin, are often evident at birth or during infancy and almost always by the time a child is about 10 years old. NF2 is less common. NF2 is characterized by bilateral (occurring on both sides of the body) tumors on the eighth cranial nerve. The tumors cause pressure damage to neighboring nerves. To determine whether an individual has NF2, a physician looks for bilateral eighth nerve tumors and similar signs and symptoms in a parent, sibling, or child. Affected individuals may notice hearing loss as early as the teen years. Other early symptoms may include tinnitus (ringing noise in the ear) and poor balance. Headache, facial pain, or facial numbness, caused by pressure from the tumors, may also occur. Present medical treatments for both NF1 and NF2 are presently aimed at controlling symptoms. Surgery can help some NF1 bone malformations and remove painful or disfiguring tumors; however, there is a chance that the tumors may grow back and in greater numbers. In the rare instances when tumors become malignant (3 to 5 percent of all cases), treatment may include surgery, radiation, or chemotherapy. For NF2, improved diagnostic technologies, such as MRI, can reveal tumors as small as a few millimeters in diameter, thus allowing early treatment. Surgery to remove tumors completely is one option but may result in hearing loss. Other options include partial removal of tumors, radiation, and if the tumors are not progressing rapidly, the conservative approach of watchful waiting. Several years ago, research teams located the exact position of the NF1 gene on chromosome 17. The product of the NF1 gene is a large and complex protein called neurofibromin. One portion of this protein is similar to a family of proteins called GAP (guanosine triphosphatase-activating protein). Scientists have demonstrated that GAP proteins play a significant role in tumor suppression in certain cancers. The similarity of the NF1 protein to GAP proteins suggests that the NF1 protein may have a similar switching role in the development of neurofibromas. Scientists theorize that defects in the gene may lessen or inhibit the normal output of its protein and allow the irregular cell growth that may lead to tumor development. Intensive efforts have led to the identification of the NF2 gene on chromosome 22. The NF2 gene product is a tumor suppressor protein. Basic studies in molecular genetics may lead one day to nonsurgical or pharmacologic treatments aimed at retarding or suppressing tumors associated with the neurofibromatoses. The Interinstitute Medical Genetics Research Program at the NIH Clinical Center conducts NF2 family history research. Using specimens from some of the families, scientists have isolated and sequenced the NF2 gene and have described two different patterns of clinical features in NF2 patients. Investigators are continuing to study these patterns to see if they correspond to specific types of gene mutations. Source - National Institute of Neurological Disorders and Stroke Pranic Healing: 1. Invoke and scan before, during and after treatment. 2. General sweeping several times with LWG. 3. Localized thorough sweeping on the ajna chakra, corwn chakra and forehead chakra alternately with LWG and ordinary LWV. Energize the ajna with EV. 4. Localized thorough sweeping on the front and back heart chakra. Energize the back heart with EV. 5. Localized thorough sweeping on the liver alternately with LWG and LWO. 6. Localized thorough sweeping on the front and back solar plexus chakra alternately with LWG and LWB. Energize the solar plexus chakra with LWG, ordinary LWV then LWB. 7. Localized thorough sweeping on the basic and perineum chakras with LWG then with LWB. Energize the basic chakra with W. 8. Localized thorough sweeping on the affected part(s) thoroughly and alternately with LWG and LWO. Energize the affected part(s) with LB for localizing effect. Then energize the affected part with LG then LO. If the affected part is delicate, then just use EV for cleansing and energizing it. 9. Stabilize and release projected pranic energy. 10. Repeat treatment 2 to 3 times per week for as long as necessary. 11. For Patient: - Practice the Meditation on Twin Hearts (MTH) properly once per day. Use the MTH with self healing alternately with MTH for psychological well-being. Healing of diseases with strong genetic component is facilitated when there is a high, constant dose of EV. The regular proper practice of the MTH brings down tremendous amounts of EV to the practitioner. - Blessing may be done several times per day, everyday to generate more healing energy. - Regular low impact physical exercise to facilitate cleansing and energizing of the physical body. - Eat healthy nutritionally balanced diet with plenty of fresh water. Source - Advanced Pranic Healing by Master Choa Kok Sui. Love, Marilette 1. 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. 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: Science and Art of Modern 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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