Guest guest Posted July 7, 2005 Report Share Posted July 7, 2005 Dear Nani, Namaste. Thank you for your email. Medical Background: Synonyms and related keywords: short stature, chondrodystrophy, skeletal dysplasia, osteochondrodysplasia, disproportionately short stature, dwarfism, rhizomelic shortening of limbs, disproportionately long trunk, trident hands, midfacial hypoplasia, prominent forehead, frontal bossing, thoracolumbar gibbus, megalencephaly, caudal narrowing of interpedicular spaces, chondrodysplasia. Source: Joo-Hee Grace Park, DO., Robert Wallerstein, MD. Achondroplasia is a common nonlethal form of chondrodysplasia. It is transmitted as an autosomal dominant trait with complete penetrance. De novo mutations cause 75-80% of cases. The mutation rate is estimated to be 0.000014 per gamete per generation. Main features include short stature, rhizomelic shortening of the arms and legs, a disproportionately long trunk, trident hands, midfacial hypoplasia, prominent forehead (frontal bossing), thoracolumbar gibbus, true megalencephaly, and caudal narrowing of the interpedicular spaces. It is caused by mutations in the gene for fibroblast growth factor receptor-3 (FGFR3). The gene has been mapped to band 4p16.3. The common mutations cause a gain of function of the FGFR3 gene, resulting in decreased endochondral ossification, inhibited proliferation of chondrocytes in growth plate cartilage, decreased cellular hypertrophy, and decreased cartilage matrix production. G1138A and G1138C mutations account for approximately 99% of the mutations resulting in a specific amino acid substitution (G380R). A rare mutation is the novel missense mutation (Lys650Met) in the tyrosine kinase region, which results in a disorder termed severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN). Another mutation, Gly380Arg has been reported in a Spanish population. Mortality/Morbidity: Sudden death in the first year of life is attributed to abnormalities at the craniocervical junction causing spinal cord compression. The rate of unexpected death in infants with achondroplasia is less than 3%. Angular deformities of the extremities, premature degenerative joint disease, and spinal disorders are common clinical features. Pranic Healing: Source - Advanced Pranic Healing by Master Choa Kok Sui. The general rule for healing genetic ailments is to use EV or LEV. The younger the patient, the faster the rate of healing, however, the treatment must be applied very gently and carefully by an advanced, proficient pranic healer. 1. Invoke and scan before, during and after treatment. 2. Touch you heart with the pads of the fingers of your passive hand. Smile. Project loving kindness to the patient for several seconds. 3. General gentle sweeping with LEV. Pause for a few minutes. 4. Localized through sweeping on the front and back solar plexus chakra. Energize with LEV. 5. Localized sweeping on the front and back heart chakra. Lightly energize through the back heart with LEV. 6. Localized thorough sweeping on the crown, back head and throat chakras. Lightly energize with white. 7. Localized thorough sweeping on the ajna. Energize the ajna gently with LEV, simulataneously gently and firmly instruct the ajna to normalize. 8. Localized thorough sweeping on the bones of the head, spine, arms, legs, and ribs with emphasis on the affected areas. 9. Localized thorough sweeping on the sex chakra and navel chakras. Energize with white. 10. Localized thorough sweeping on the basic chakra. Energize the basic with LEV, simultaneously visualize the energy going to the bones of the spine, skull, arms, legs and ribs. Apply distrubutive sweeping to the front and back and to the sides. 11. Stabilize and release projected energy. 12. Repeat treatment 1 to 3 times per week. Love, Marilette --- Institut für Energiearbeit <office wrote: > Dearest Marilette, > Namaste! > I think maybe you didn't receive my below E-Mail > that's why I kindly ask for > an answer on my E-Mail from 02.06.2005, could you > please let me know a > treatment-protocol for Achondroplasia. > Thank you very much, > love and greetings to you > Nani > > _____ > > Von: Institut für Energiearbeit > [office] > Gesendet: Donnerstag, 02. Juni 2005 12:29 > An: 'marilette_ph' > Betreff: Achondroplasia = Parrot-Kaufmann-Syndrom > > > > Dear Marilette, > > Namaste! > > Would you please be so kind to send us a pranic > healing protocol for the > treatment of ACHONDROPLASIA for a 15 month old boy? > > Arms and Legs are to short, he has a hump in the > spine at the level from > back-solar-plexus to the meng-mein-chakra and a > contraction in level of the > cervikal-spine, which will be operated in the age of > 4 years. > > The aim of the treatment is, to lengthen the arms > and legs and to prevent > the operation of the cervikal-spine. > > The boy is very bright and has no pain. > > Many thanks in advance, > > Nani > > ******************************************** > Institut für Energiearbeit > Mag. Claudia Dieckmann > Schopenhauerstraße 52, 1180 Wien > TEL & FAX +43 1 408 54 55 > MOBIL +43 664 336 11 76 > <office > office > <http://www.energie-institut.com/> > www.energie-institut.com > ******************************************** > > > 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. Discover Stay in touch with email, IM, photo sharing and more. Check it out! http://discover./stayintouch.html Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.