Tuesday, 28 October 2014

eMiracle

hemorrhagic fevers

any of a variety of highly fatal viral diseases that are characterized by massive external or internal bleeding or bleeding into the skin. Other symptoms vary by the type of viral hemorrhagic fever but often include fever, malaise, muscle aches, vomiting, and shock. Most viral hemorrhagic fevers are geographically restricted because they are transmitted by specific animal or insect hosts (reservoirs) that occupy narrow and sometimes localized ecological niches. Viral hemorrhagic fevers are caused by viruses of four families: Flaviviridae, Arenaviridae, Bunyaviridae, and Filoviridae.

The most common viral hemorrhagic fevers are dengue and yellow fever, caused by related mosquitoborne flaviviruses. In the late 18th century, yellow fever epidemics in American coastal cities caused widespread panic, but the disease currently occurs only in developing countries of Africa and South America. It is the only major viral hemorrhagic fever for which an effective preventive vaccine exists and is widely used. Most cases of dengue, seen in tropical areas, are mild and influenza-like, but all four dengue viruses may produce dengue hemorrhagic fever or its severe form, dengue shock syndrome. Unlike yellow fever, which affects the liver and causes severe bleeding, dengue involves the liver only minimally and tends to induce only minor bleeding that is rarely fatal. However, if dengue shock syndrome occurs, patients may die when fluids and electrolytes in their vascular compartments shift into tissues, collapsing the blood volume and precipitating low blood pressure and shock. Dengue is unique among the fatal hemorrhagic fevers in that even severe cases can be effectively treated with simple fluid administration.

The arenaviruses are highly adapted to specific rodent hosts, which may become silently infected and excrete the virus in feces, urine, and saliva. However, when humans come into contact with food or soil contaminated by these rodent excreta, disease may result. The arenaviruses cause the diseases Lassa fever (occurring in Africa), Argentine hemorrhagic fever, Bolivian hemorrhagic fever, Brazilian hemorrhagic fever, and Venezuelan hemorrhagic fever.

Hantaviruses, Rift Valley fever virus (genus phlebovirus), and Crimean-Congo hemorrhagic fever virus (genus nairovirus) belong to the family Bunyaviridae. The hantaviruses, like the arenaviruses, are spread to humans by rodent contact. Hantaviruses cause Korean hemorrhagic fever and hantavirus pulmonary syndrome, which is highly fatal owing to accumulation of fluid in the lungs but features only minor hemorrhagic manifestations. Rift Valley fever, a mosquitoborne disease that is fatal in sheep and cattle, occurs in East and Southern Africa and the Middle East. Most people who contract Rift Valley fever survive, but a minority develop fatal hemorrhagic fevers, encephalitis, or severe eye disease. Crimean-Congo hemorrhagic fever, found in East and Southern Africa, the Middle East, and Russia, is a tickborne disease of cattle and other farm animals that is occasionally transmitted to humans.

The filoviruses, seen in Central and East Africa, include Ebola virus and Marburg virus. These are among the most highly fatal of the hemorrhagic fevers; some strains of Ebola cause death in up to 90 percent of victims. The filoviruses may also cause disease in primates. Marburg virus was discovered when it was transported with imported monkeys to Marburg, Germany, and caused a fatal outbreak. The origin of filovirus epidemics remains unclear; however, the virus has been found in the Old World fruit bat Rousettus aegypticus, which lives in areas throughout sub-Saharan Africa. Scientists suspect that these bats may be responsible for outbreaks of Marburg disease.


David Morens
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eMiracle

ALL YOU NEED TO KNOW ABOUT EBOLA VIRUS

Introduction

hemorrhagic fever

virus of the family Filoviridae that is responsible for a severe and often fatal viral hemorrhagic fever; outbreaks in primates, including gorillas, chimpanzees, and humans, and domestic pigs have been recorded. The disease is characterized by extreme fever, rash, and profuse hemorrhaging. In humans, certain strains of the virus can cause fatality in 50 to 90 percent of cases.


Strains of Ebola

The virus takes its name from the Ebola River in the northern Congo basin of central Africa, where it first emerged in 1976. Ebola is closely related to the Marburg virus, which was discovered in 1967, and the two are the only members of the Filoviridae that cause epidemic human disease. Five strains of Ebola virus, known as Ebola-Zaire, Ebola-Sudan, Ebola-Côte d'Ivoire, Ebola-Reston, and Ebola-Bundibugyo, named for their outbreak locations, have been described.

Ebola-Zaire causes death in 80 to 90 percent of cases, and Ebola-Sudan causes death in 50 percent of cases. Ebola-Côte d'Ivoire, found in dead chimpanzees in the Taï National Park in southwestern Côte d'Ivoire, can infect humans, although only two human cases have been documented, and both individuals survived. Ebola-Reston, which was originally discovered in laboratory monkeys in Reston, Va., in 1989, was also detected in laboratory monkeys in other locations in the United States in 1990 and 1996, as well as in Siena, Italy, in 1992. All the monkeys infected with Ebola-Reston have been traced to one export facility located in the Philippines, although the origin of the strain has not been identified. Similar to Ebola-Côte d'Ivoire, Ebola-Reston does not appear to cause death in humans. The fifth strain, Ebola-Bundibugyo, was discovered in November 2007 in an outbreak in Bundibugyo district, near the border of Uganda and Congo (Kinshasa); it causes death in about 25 percent of cases.


Outbreaks

The first outbreaks in 1976 in Zaire (now Congo [Kinshasa]) and The Sudan resulted in more than 400 deaths. A subsequent outbreak in Congo (Kinshasa) in May 1995 prompted temporary quarantine of the Kikwit region, and more than 250 people died. Later outbreaks in Uganda in 2000 and in Congo (Kinshasa) in 2002 also resulted in several hundred deaths. In September 2007 an outbreak was confirmed in Congo (Kinshasa) in the Kasai-Occidental (West Kasai) province, located in the south-central region of the country. However, while Ebola was detected in blood samples from some people that fell ill, other people were found to be infected with Shigella, the bacterium that causes dysentery—a disease whose symptoms are similar to the early symptoms of Ebola. As a result, although several hundred people became ill and more than 160 people died during the Ebola outbreak, it was unclear how many of the deaths were actually caused by Ebola. Less than two years later, in December 2008, a second outbreak of the disease was confirmed in the Kasai-Occidental province. Ebola had been detected in just four people by early 2009; however, another 42 cases were suspected, and some 200 people were under close observation for infection. Although 13 deaths had been reported in association with the outbreak, samples collected from the victims did not test positive for Ebola.

In 2008, tissue samples from pigs that died of unknown causes in the Philippines were analyzed and found to contain Ebola-Reston virus. This was the first time that the virus was found in a mammalian species other than primates. Infections in pigs were unexpected and raised concerns about transmission of the virus from pigs to humans. In January 2009, antibodies to Ebola-Reston were found in five Filipinos, four of whom worked on pig farms and one of whom worked in a slaughterhouse. All five individuals were believed to have been infected with the virus through direct contact with infected pigs. The infected people were healthy and did not show signs of infection at the time antibodies to the virus were detected. In order to stop the spread of Ebola-Reston among pigs, Philippines officials authorized the slaughter of thousands of potentially infected swine.


Course of infection

Viewed through an electron microscope, the Ebola virus appears as long filaments, sometimes branched or intertwined. The virion (virus particle) contains one molecule of noninfectious, single-stranded RNA (ribonucleic acid). It is not known how the Ebola virus attacks cells; however, it has been postulated that the virus produces proteins that suppress the immune system, allowing reproduction of the virus to continue unhindered. Viral hemorrhagic fevers similar to Ebola typically are carried by arthropods and rodents; however, the natural reservoir for the Ebola virus has yet to be discovered. Among the suspected reservoirs for Ebola are bats, primates, rodents, and insects that inhabit tropical forests in Africa and Asia. Ebola can be transmitted through contact with infected blood, bodily fluids, and possibly respiratory secretions. The virus has also been detected in the organs of patients after recovery from the fever. Unsanitary conditions and lack of adequate medical supplies may be factors in the spread of the disease.

The Ebola virus has an incubation period of 4 to 16 days. The onset is sudden and harsh. Infected persons develop fever, severe headaches and muscle aches, and loss of appetite. Within a few days the virus causes a condition known as disseminated intravascular coagulation, which is marked by both blood clots and hemorrhaging. In the case of Ebola fever, clots are concentrated in the liver, spleen, brain, and other internal organs, forcing capillaries to bleed into surrounding tissue. Nausea, vomiting and diarrhea with blood and mucus, conjunctivitis, and sore throat soon follow. A maculopapular rash (discoloured elevations of the skin) appears on the trunk and quickly spreads to the limbs and head. The patient is then beset by spontaneous bleeding from body orifices and any breaks in the skin, such as injection sites, and within the gastrointestinal tract, skin, and internal organs. Death is usually brought on by hemorrhaging, shock, or renal failure and occurs within 8 to 17 days.


Treatment

There is no known treatment for Ebola fever, although immune plasma may be beneficial. Current therapy consists of maintenance of fluid and electrolyte balance and administration of blood and plasma to control bleeding.

Drugs designed to disrupt Ebola virus replication have been developed and tested in Ebola-infected monkeys. One such therapy was found to protect more than 60 percent of rhesus monkeys infected with Ebola-Zaire when the agent was administered within 30 to 60 minutes following infection. The treatment, which in 2010 was approved for safety trials in humans, was promising for persons who become accidentally infected in laboratory or hospital settings.

The spread of Ebola virus can be contained by barrier nursing, handling of infected blood and tissue in isolated laboratory units, and proper decontamination of reusable equipment.
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Wednesday, 24 September 2014

eMiracle

FREE 910mb on mtn for pc and android

MTN free browsing tweak coming from the New package line from MTN giving you over 900mb of Free data. The new packages include Jumia, Hellofood, Jovago, Lamudi, Carmudi,kaymu and Easitaxi

The new packages come with 130MB free data allowance each (100MB monthly, 25MB weekly and 5MB daily).

This is very simply to make use of the Free data allowance available on each of the packages once each of them gets exhausted.When you exhaust the 100MB free data on Jumia package you subscribe for the 100MB free data on Jovago package. Just like that till you do same on all the seven packages giving you a total free data of 700MB.

After which you go with the weekly 25mb free data on all the packages as well as the daily 5MB free data on each of the packages.It does not follow any sequence, you may decide to use the Jumia package first (100MB monthly, 25MB weekly and 5MBdaily) before using Jovago, hellofood and the rest or you can exhaust the individual 100MB on all the packages before the 25MB followed by the 5MB packages the choice is yours.



When you must have exhausted the whole Data available on all the packages you must have enjoyed up to 910MB free data.

The above data from the MTN packages above cannot work ordinarily on its own but needs another application to work. The application that powers it is none other than Simple Server or TunnelGuru and to make it also work on android devices simple server android application is required or android equivalent of Tunnelguru which is TroidVPN.

The various applications are totally different from each other and can work independent of each other. The choice is your to choose which one you like and want to connect with. Though simple server is proxy inclined and can only work when you configure your browsers and other system application to work with proxy while on android most android applications may not work using simple server on the other hand Tunnelguru and Troidvpn are VPN inclined and when connected through it you need not configure any other thing. Like I earlier said the choice is your.

To get started you need to first of all get into any of the packages.

Below are the various codes to opt in to any of the packages;

USSD CODES FOR MONTHLY 100MB

*662*6*1*3# for jumia

*662*6*2*3# for hellofood

*662*6*3*3# for jovago

*662*6*4*3# for carmudi

*662*6*5*3# for lamudi

*662*6*6*1*3# kaymu

*662*6*6*2*3# easitaxi


USSD CODES FOR WEEKLY 25MB 

*662*6*1*2# for jumia

*662*6*2*2# for hellofood

*662*6*3*2# for jovago

*662*6*4*2# for carmudi

*662*6*5*2# for lamudi

*662*6*6*1*2# kaymu

*662*6*6*2*2# easitaxi

USSD CODES FOR DAILY 5MB

*662*6*1*1# for jumia

*662*6*2*1# for hellofood

*662*6*3*1# for jovago

*662*6*4*1# for carmudi

*662*6*5*1# for lamudi

*662*6*6*1*1# kaymu

*662*6*6*2*1# easitaxi

On a successful subscription for any of the package you will receive a notification from MTN.

Now Download Simple Server HERE

However, if you already have simple server on your system, simply open the folder of the simple server open the server.ini file and change the VALHDR0 and IQUERY to

VALHDR0 = 'jumia.com.ng'

IQUERY = 'jumia.com.ng'

or better still download the per-configured simple server.ini file HERE and use it to replace the one in the simple server folder. That is, delete only the Simple server.ini file in the simple server folder you already have and replace it with the one downloaded HERE.

Run the simple server and when it is ready you can start to browse but before then set you browser and applications to use this proxy
HTTP Proxy:127.0.0.1

Port: 8080



If you do not want to bother yourself with proxy settings of your browser and applications and want this to support every application on your system then you need to use Tunnelguru.

Download TunnelGuru HERE

Extract it to a location on your system.

Download and install Java runtime on your system if this is the first time you are running Tunnelguru on your system. Download Javaruntime HERE

Signup for a Free TunnelGuru account HERE if this is the first time you are using it.

Launch the TunnelGuru and Configure it as follows:

SERVER: Choose any server Location with [ALL] attached to it.

RPORT: 80

LPORT: 0

User: Your Tunnelguru Username

Password: Your Tunnelguru password

Untick TunnelDNS Query

PROTOCOL: TCP

Tick Use Proxy and Enter: 10.199.212.2:8080

HEADER: host:jumia.com

Click on START



ANDROID SETTINGS

To use this on your android device, you need to use either Simple server android application or TroidVPN (Tunnelguru android version)

ANDROID SIMPLE SEVER SETTINGS

Download Simple server Android Apk HERE

Open it, Tap on Settings and configure it as follows;

Listen port: 8080

Proxy Host: 10.199.212.2

Proxy Port: 8080

Enable Proxy: YES

Injection Method:GET

Injection Query: http://jumia.com.ng

Injection Host: jumia.com.ng/home.php

Injection line: Just press enter 4 times and leave it empty

Enable Injection: Tick to Enable

Buffer Size: 8092

Log Level: DEBUG


TROIDVPN SETTINGS



Download TroidVPN HERE

Launch it and configure it as follows

Enter your Tunnelguru username on the First Space and Your Password on the second space

Choose any server location with [ALL]

RPORT: 80

LPORT: 0

Choose TCP

Click on Advance

Tick Use Proxy for TCP connection

Proxy Host: 10.199.212

Proxy Port: 8080

Header Custom:host:jumia.com

Click on Save

Now Connect


TroidVPN powers all android applications while Simple server may not.

The main trick here is, after exhausting the 910MB total free data available on a single MTN Sim, get another Sim and do the same to it. The more MTN sim the more MB and Free data you get to enjoy.


REMEMBER TO SHARE THIS WITH YOUR FRIENDS
ENJOY!!!!!
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Monday, 8 September 2014

eMiracle

ENTEROVIRUS 68

The rare virus suspected of sickening 1,000 kids in 11 states can start out like the common cold but quickly evolve into something much more serious, health officials say. The virus, known as enterovirus 68, is similar to the rhinovirus that causes the common cold, according to the U.S. Centers for Disease Control and Prevention. But unlike a cold, the infection can lead to severe respiratory symptoms like wheezing. "It’s the wheezing you have to watch out for," said ABC News’ chief health and medical editor, Dr. Richard Besser, referring to the whistling sound generated when air moves through narrowed breathing tubes. Unidentified Respiratory Virus Likely to Hit Kids Across Country Respiratory Virus Sickening Children in Colorado Doctors at Children's Hospital Colorado in Denver have seen more than 900 pediatric patients with symptoms of the virus in the emergency room since mid- August, according to officials. The hospital admitted 86 kids with severe symptoms and a handful ended up in intensive care. Beyond Colorado, suspected cases have also been reported in Missouri, Kansas, Illinois, Kentucky, Iowa, Ohio, Oklahoma, Atlanta, Utah and Georgia, according to the CDC. North Carolina has been removed from the list of affected states, the agency said today, but the list is expected to grow. "If your state doesn't have it now, watch for it, it's coming," said Besser. Here are five things you should know about the outbreak. Georgia and Pennsylvania reported clusters of enterovirus 68 almost exactly five years ago in September 2009, according to a 2011 CDC report . Arizona had a small cluster of cases in August and September 2010, according to the same report. This Isn’t the First Enterovirus 68 Outbreak in the U.S. While this isn’t the first time enterovirus 68 has popped up in the U.S., health officials are still trying to figure out why the virus has reemerged. "This is a very common time for outbreaks. Kids come back to school, they like to share things, they bring them home to their little brothers and sisters," said Besser, adding that most enterovirus outbreaks occur in the summer. "But this one, this particular enterovirus is very rare, and they have no idea why it showed up this year." No One Knows How It Started Studies on enterovirus 68 are limited, and so is knowledge about how the virus spreads. Most enteroviruses spread through contact with respiratory secretions like saliva and mucous as well as feces, according to the CDC. The Department of Health and Senior Services in Missouri, where at least 300 suspected cases have been reported, recommends washing hands thoroughly and often, avoiding close contact with people how are sick, disinfecting frequently-touched surfaces and staying home with feeling sick. No One Knows How It Spreads There are no anti-viral medications for enterovirus 68, and no vaccines to prevent the infection, according to the Missouri Department of Health a Senior Services. Instead, health care providers are tasked with treating the symptoms of the infection – a job that may require hospitalization. "The important thing is to recognize the signs of respiratory distress," said Besser, describing how difficulty talking, audible wheezing and bluish lip color can signal distress. "There are treatments to improve respiration." There’s No Specific Treatment Young children and people with asthma may be particularly vulnerable to enterovirus 68, health officials say. Dr. Raju Meyappan, a pediatric critical care physician at Rocky Mountain Hospital for Children in Denver, said he's seen multiple asthmatic children end up on breathing tubes in intensive care unit after contracting the virus. "As a pediatric ICU doctor, we try our best not to intubate kids with asthma at any point in time," Meyappan said. "They all needed it. The onset [of the virus] is severe." Children also appear to be more susceptible than adults, according to a CDC report released today about cases in Missouri and Illinois. The ages of those infected ranged from 6 weeks to 16 years, with most of the illnesses occurring in children aged 4 and 5.
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eMiracle

NEW CODES FOR ALL NETWORKS

Mobile phone users to use common codes from today Monday 8th September , 2014 10:12 am All mobile phone users regardless of the network will use a common short code to check their credits, top up and assess call centres from today. This follows the National Communications Authority’s (NCA) move to harmonize all short codes for general customer services across all networks. The NCA however says the existing short codes for the various telecommunicati on networks will run concurrently with the new one until April 2015. To recharge, subscribers will use 134. To check balance, subscribers will need to dial 124 and 100 for the call centre. The others are 600 for number portability, 400 for verification of SIM, 108 for Voice Mail Deposit and 109 for Voice Mail Retrieval. There have been complaints from users about the number of short codes they have deal with, prompting an investigation by the NCA, which eventually decided to introduce common codes.
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