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The genetic change of Duchenne/Becker type and its hope through WMDROC session and first and second genetic test results

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  These days, everyone's life has become a mess because of COVID-19.     Even if I do not point out, even though they deny it, some humans in a certain country scientifically researched these things with an unclear purpose, artificially synthesizing the genes to create the worst coronavirus. And because the important management was negligent and spread all over the world, there was no room for anyone to doubt that such a great incident occurred.      These events have ushered in a gloomy era called Corona Blue.  If it wasn't for this Corona Blue, I would have posted a few more, if not many, useful research data or information. I have regrets about this.   I have been studying for a long time to stop the muscle destruction in patients with Duchenne or Becker type and some other types of muscular dystrophy, and to increase the weight while using this stop as an inflection point to regenerate the destroyed muscle again. Among these research processes and experiences, the most curi
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[New] The project for curing myotonic muscular dystrophy by WMDROC

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Please, refer to ; Episode 1 https://www.youtube.com/watch?v=3i3ChcmMFcQ&t=126s Episode 2 https://www.youtube.com/watch?v=GWKIg3VKny4&t=73s Episode 3 https://www.youtube.com/watch?v=ClbDJd1tZ8Q&feature=youtu.be Episode 4 https://www.youtube.com/watch?v=4QFWk_Twkkc&t=11s Everything in there. Comparison of difference between pre-treatment and during  3-session sessions by WMDROC
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World First Cure Project For Duchenne Muscular Dystrophy With Mitochondrial Myopathy by WMDROC[Currently ongoing in progress ]

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patient Name ; J. E Lee Date of birth ; 09, 13, 1978 Residence ; Busan, South Korea Gender ; Male Outline of outbreak 1. Lower extremities weak since he was a child.   did not able to run well. 2. Pseudo hypertrophy in the calf from the infant. 3. 08. 05, 2005 diagnosis of biopsy ;  Mitochondrial myopathy. 4. 2005. Diagnosis of Genetic Test ; Duchenne type MD. 5. 01-26-2018 ; Serum test Result ; SGOT ; 66 (H)           U/L SGPT  ; 60(H)              " LDH  ; 297(H)             " CPK  ; 1,688(H)           " T3 ;   0.50(L)              ng/ml   Result of genetic examination ; Duchenne Muscular Dystrophy -> exon 45, 46, 47, 48 deletion.  Report of biopsy result ; Mitochondrial Myopathy 7. Weight of patient ; 51.3 kg before start WMDROC treatment. 8. Height of patient ; 169 cm tall before start WMDROC treatment 9. The disease of patient progressed very rapidly(quickly lose muscle) b y taking the he
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