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Researchers Create Artificial Blood:
Significant Aid Against Undead Virus

(ZWN-AP) 29/04/14

A $9m' Forward Trust' research project has successfully created red blood cells that are safe for transfusion into humans.

This latest breakthrough in biological engineering could revolutionize medicine in its fight against the necro-mortosis worldwide pandemic. It could enable factories to mass produce blood, rather than relying on human donation. Disease free, this manufactured blood could also be tailored to individual blood types.

Principal researcher on the project, Professor James Bridge, found that induced pluripotent stem cells (iPS) could be matured into the universal blood type O.

Speaking about this pioneering research, Bridge said: “Although similar research has been conducted elsewhere, this is the first time anybody has manufactured blood to the appropriate quality and safety standards for transfusion into a human being test subject.”

Clinical trials will aim to conclude in 2016, early 2017, and will most likely involve the treatment of three patients with a blood disorder called Thalassaemia. Treatment for this condition includes regular blood transfusions. The trial will monitor any reaction to the artificial blood, and the clinical trial doctors are able to remove the blood from the system at any time if necessary.

Additionally, in a 'project only partnership', pharmaceutical giant Amcalon has posted on their website a press release stating that they will be testing 12 necro-mortosis sufferers monitoring the results of complete blood transfusions. This type of research has been done in the past with negative results. The brain and connected nerves suffer too much damage due to the rapid onset of the mortosis virus. 'Rapid atrophy ' is the term for this.

The ability to create blood cells in the lab could significantly reduce the cost to healthcare providers transfusing patients. However, Bridge warns that whilst this breakthrough is an exciting step for medicine, the industrial processes to manufacture blood on a mass scale are not yet in place.

“A single unit of blood contains a trillion red blood cells. There are 2 million units of blood transfused in the UK each year.”

Dr Joyce Yen-Wright, Director of Technology Transfer at the 'Forward Trust,' also noted the difficulties involved in moving this process from the lab to global production. Financial backers are in place, including Amcalons R&D division. Also, several countries have expressed their principle support of establishing a manufacture and distribution chain.

“One should not underestimate the challenge of translating the complex science into streamlined procedures of manufacture,” she said. “Nowhere is this more apparent than in the challenge Professor Bridge and colleagues have set out to address, which is to replace the human blood donor as the source of supply for life-saving transfusion, and possibly reversing the effects of advanced necrosis.”

If this trial is successful, however, it is possible that in the future blood for human transfusion will be created and shipped out from factories. The impact this could have on stemming the spread of necro-mortosis, or even reversing its effects could be profound.



President Obama announced the awarding of $5 billion in grants for research into cures ranging from necro-mortosis, cancer, heart diseases, and autism among other diseases.


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Obamacare and necro-mortosis
- where do you stand?

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XL-6 drug Suspended

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Amcalon starts 'Phase 4' XL-6 inhibitor testing
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The World Health Authority site is the official Necro-Mortosis education site:
Visit it here for essential information on the virus.

Highlights of the recently released WHA report.

Upon infection, the exposed usually succumbs to reanimation within 4 - 48 hours. First stage symptoms feel like flu. Migraine, hot flushes, aching muscles.

Second stage is followed by severe chills, extreme lethargy, some disorientation, a gradual slowing of the heart rate. early onset dementia, extreme pain in their joints and muscle cramping. At this point, many fall into coma or suffer stroke or heart failure. This is due to the massive shock to the bodies immune system. Necrosis and mortification follow shortly afterwards.

Reanimation can occur within minutes. Studied subjects have nearly always reanimated within the first hour of death.

Source: World health Authority report



Baby Born With Necro-Mortosis Cured By Drug Combination
ZWN (AP) - Posted March 15/2014

Child born from necro-mortosis infected woman is cured using combination drug

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Necro-Mortosis (corpse/dead), also known by the names Mortuus Ambulare" (walking dead) and "Corpus Vigere" (active/awake corpse)

We do know that the 'Necro-Virus' (Necro Mortosis) was first discovered in the West Indies - Haiti in 2006

The cause of the virus remains unknown at this point.

Three predominant theories suggest it's origin

A: Voodoo (Vodou). Considering the source of the outbreak is Haiti, this first theory is expected. However, no scientific facts support this theory or give it any credibility.

B: Viral anomalistic. Possibly a hybrid or chimera virus. Possibly crossed species. If this is the case, It remains unclear how the virus originated or mutated.

C: A bi-product of chemical/bacterial warfare. This again seems unlikely. No country or credible terrorist organization has claimed responsibility for the virus at this time.

Read the full explanation of the virus here



 


Index of Other Major Non-Related Diseases & Conditions

ADHD
Arthritis
Asthma & Allergies
Autism
Avian Influenza
Birth Defects
Cancer
Chlamydia
Chronic Fatigue Syndrome
Diabetes
E. coli
Epilepsy
Fetal Alcohol Syndrome
Flu (Influenza)
Genital Herpes (Herpes Simplex Virus)
Giardiasis
Gonorrhea
Heart Disease
Hepatitis
HIV/AIDS
HPV (Human papillomavirus)
Necro-Mortosis
Meningitis
Norovirus Infection
Obesity
Salmonella
Scabies
Sexually Transmitted Diseases
Stroke
Trichomonas Infection (Trichomoniasis)
Tuberculosis (TB)

Main Content Source: Centers for Disease Control and Prevention







Facts about necro-mortosis

Mortosis is transferable through the exchange of blood, saliva orother bodily fluids, including bites.Mortosis can be contracted through sharing of needles. Virus can be sexually transmitted

There is no known antidote at this point (Beware internet scams claiming to sell cures or inhibitors)

Mortosis is NOT airborne

Only infected people will reanimate upon death.

None infected people or people who die of natural causes do NOT rise.

If bitten, (or otherwise infected) on an arm or leg, severing the affected appendage may remove the infection, but only within the first few minutes of exposure. Burning the affected wound will only act to cortorize the wound. Not remove the infection.

Animals exposed to the Necro-Mortosis virus will become sick and die but do not reanimate. Livestock exposed must be destroyed.

Upon infection, the exposed usually succumbs to reanimation within 4 - 48 hours. First stage symptoms feel like flu. Migraine, hot flushes, aching muscles.

Second stage is followed by severe chills, extreme lethargy, some disorientation, a gradual slowing of the heart rate. early onset dementia, extreme pain in their joints and muscle cramping. At this point, many fall into coma or suffer stroke or heart failure. This is due to the massive shock to the bodies immune system. Necrosis and mortification follow shortly afterwards.

Reanimation can occur within minutes. Studied subjects have nearly always reanimated within the first hour of death.

Source: World health Authority report

 


The different levels of a mortosis outbreak:

Mortosis outbreaks can be separated into three categories, depending on how easily they can can spread and the severity of death they cause. Category A outbreaks are considered the highest risk and Category C outbreaks are those that are considered emerging threats or easily containable.


Category Level 'A'

These high-priority outbreaks pose the highest risk to the public and national security because: They can be easily spread or transmitted from person to person
They result in high death rates and have the potential for major public health impact
They might cause public panic and social disruption
They require special action for public health preparedness.


Category Level 'B'
These outbreaks are the second highest priority because:
They are moderately easy to spread
They result in a moderate rate of death and/or low death rates
They require specific enhancements of Center for Disease Control's laboratory capacity and enhanced disease monitoring.

Category Level 'C'
These third highest priority outbreaks include emerging threats that could be spread in the future because:
They are easily transferable
They have potential for high morbidity and mortality rates and major health impact.
Source: CDC - Center for Disease Control and Prevention

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