Omake Chapter: The FDA Report
1000hrs, 15 August 2014, White Oak, Maryland, United States.
Food and Drug Administration
Center for Biologics Evaluation and Research
Cellular and Gene Therapy Products
Abridged Analysis and Report on "Healing Solution Mark I"
For Press Release
Background:
The development of the Healing Solution was first developed by the Japanese Government, but was taken over by the Nakanishi Biological Research Labs, which was a top secret and highly compartmentalized organization of the group, only known to the top company officers. This Healing Solution was created sometime in 2011 or 2012, but specific data concerning the research and development of this particular solution has been lost. However, the data with the specific makeup, sequencing and production methods was recovered after the battle for the Nakanishi stronghold on the island of Socotra was concluded. The solution was issued almost immediately to Nakanishi private military contractors in large quantities in 2013, as well as the United States Military who had significant contracts with the Nakanishi Group. The Nakanishi Group sold the fluid exclusively to the military at a high markup, making millions of dollars in the process. The FDA was excluded from testing this solution due to political interference, and was issued to troops in the field nonetheless. Despite the involvement of the Nakanishi Group in developing this solution, many other pharmaceutical companies have been producing the Healing Solution, Mark I which was released in an open source format earlier this year by the US Government on the experience with the solution when issued to the military. The FDA approved of this release and for use on humans, seeing that from the usage in the military was having no ill effects and that it had the huge potential to save lives. However, after several deaths resulting from the use of Healing Solution, Mark I in several military hospitals last year that were recently reported by media outlets, and the uptick in cancer cases among both civilian and military personnel has led the FDA to reexamine its evaluation on the Healing Solution, Mark I.
Analysis:
The fluid is made up of several different organic compounds, which can be found in the appendix adjoining this particular report. One ounce is sufficient to treat minor gashes, cuts and bruises, completely healing them within thirty seconds. Forty gallons are required to treat the most extreme cases, including burns, severed limbs and internal injuries. This sort of treatment requires that the patient be completely immersed in the solution, which is then disposed of after thirty seconds. In the case of the military, personnel were immersed in special tanks containing about forty gallons of the fluid in order to treat burns, severed limbs and other injuries suffered in the line of duty. Most of these personnel were then released, but then had to come back to the hospital complaining of pain and other maladies five to six months later.
A six month test on lab rats and mice was conducted from 1 January 2014, when the healing solution was first given to the FDA until 1 June 2014. During this time, test animals were subjected to numerous injuries on a weekly basis, from falls, to cuts, and burns. Test animals were then exposed to one ounce of the solution that would cure them of their injuries.
The results showed that cancerous growth appeared in almost one-hundred percent of the cases at about five months, which were untreatable even with the Healing Solution, and subsequently led to death of the test animals. The types of cancer were seemingly random, with lung, stomach, brain and throat cancers occurring most often. The lab animals suffered excruciating pain whilst in the last stage of the testing period, and required more and more fluid to treat them until the dosage became so high that it was impossible to treat them. This was not the case for the vast majority of the test; it was only until about the fifth month that the vast majority of the lab animals developed the cancerous conditions and perished. Other effects were that the animals would often refuse food, their reproductive health dropped dramatically, with sperm and egg counts reaching zero in all cases, and experienced disorientation and became aggressive, causing them to act erratically. These matched with the cases reported by military personnel last year when being treated with the Healing Solution for an extended period of time.
Conclusion:
The Healing Solution Mark I is to be immediately discontinued by all pharmaceutical companies currently in possession of the Healing Solution formula. Persons who have been using the Healing Solution, Mark I, should cease dosage immediately and contact their physicians for examinations and treatment, if necessary. Prolonged exposure to this substance is an extreme health risk to patients; under no circumstances should this solution be used to treat open wounds or cancerous growths. Even the small one ounce tubes pose a significant risk to humans, and might make wounds even worse in the long run.
More testing is needed to examine the causes of the cancerous growths, and for other effects that the Healing Solution might possess.