How to Make a Gmail Email on the Latest Android Phone

How to Create a Gmail Email | Currently email accounts are really needed, even children need e-mail. Why? Because now there are so many Android smartphone users, which as an Android user must have a Google account that is used as access to open the Play Store. And to have a Google Play store account … Continue reading “How to Make a Gmail Email on the Latest Android Phone”

How to Create a Gmail Email | Currently email accounts are really needed, even children need e-mail. Why? Because now there are so many Android smartphone users, which as an Android user must have a Google account that is used as access to open the Play Store. And to have a Google Play store account on an Android phone, the solution is to make a Gmail account. Just like the title of the article now is How to make a Gmail email on an Android phone.

The good thing about making Gmail email on an Android phone is that we don’t need to open a browser, because we can directly do it on the system application provided by the Android OS. Even the Gmail application already exists on the Android OS. We only need to update the play store if there is an update, and even then it runs automatically provided we are connected to the internet network.
In this guide I gave an example with a screenshot or a cool name as screenshot. Using the redmi note 3 android xiaomi phone, don’t worry if the cellphone is different then the display is different. In essence, all Android phones, although different brands, menus and settings are the same anyway, maybe just laying the menu is a bit different.

The following are steps to make Gmail email in a few steps, you can say it’s short but I try to be as detailed as possible. So that LCB friends can also successfully register gmail emails. Let’s make an email together, step by step;

read also: How to Delete All Gmail Emails at Once on Android

 

  1. Open the settings menu on the cellphone screen. Scroll down to find an account or add an account. (open settings – account).
  2. Look at the picture above, downward. There is a plus (+) menu, it is a menu for adding accounts or creating new accounts. Please press it, and it looks like a screenshot like this.
  3. Press the Google menu again, if I have it on the order number 4. Search on your own screen, what Google account is in the order. If you have found it, please press it, and the first step will appear to register email. Fill in the names of each, slang names don’t matter. I exemplify using zulkarnaen’s first name, and last name id.
  4. Create a username that you will create as an email ID. In other words this is a step to create an email address, to use your real name or friend’s name, write it all together without spaces.
  5. After filling in the name, click Next. then to the step of completing the birth data and type of kelaimin. I fill in April, 26th and 1988. Also choose gender or gender, male = male, female = female and other for those who do not want to mention gender.
  6. It’s time to create a password for an email account. At least 8 characters, you can use a combination of letters, numbers and unique characters like! @ # $ ^ & Etc. As long as at least 8 characters and also don’t forget, note if necessary. Match the password confirmation column with the password created above. If so, press Next.
  7. For this one step is optional, it’s up to you to enter your cellphone number or not. If you want to fill please, but in this guide I do not fill. Leave it blank and press Next.
  8. In the steps of Privacy & Terms, if you want to read, please, if you are lazy, you can immediately scroll down and go to the next step by pressing I AGREE.
  9. Confirm the username and password you made. If you feel uncomfortable with your email username and password, just back it up. But if you are sure, press Next to continue.
  10. After next, the application will load. This is a sign that the Google server is accepting new email registration, friend. Please wait, if your internet connection is good then it only takes a few seconds of the process.
  11. Steps for setting payment options, the point is if one day you want to buy a paid application in the play store. If not, please select No Thanks and Continue. Take it easy, it can be setup again if you want to buy an application in the play store.
  12. After you press continue, the application will process again and close automatically when it’s finished. Then there is no longer a new notification in the Android bar notification, friend. Please open and more or less it will appear as below.

If you also get a notification like the one above, then congratulations you have succeeded in creating a new Gmail email on your Android phone. And now you can use an email address, whether to send files to friends or receive emails from senders.

The above steps are not only for gmail e-mail lists, but also can be used as google play store accounts. To make sure you also have an email play store, please open the app play store and open the menu. You will see the email account that you managed to make, friend. I exemplify as below.

Thus the steps to make Gmail email have been completed and of course my friend has also succeeded in creating a Google Mail account. Easy, right?, It’s already easy to use it as a google play store account. You can share the article link how to make this Gmail email on Facebook or twetter, or other social media accounts that you have. Beautiful sharing, maybe some of your friends also can’t or don’t know the steps on how to make a Gmail email .

Conjunctivitis – Causes, Symptoms, Diagnosis, and Treatment

eye

Conjunctivitis or pink eye is redness and swelling of the membranes of the eyelids and the surface of the eye. This layer is called the conjunctiva and inflammation of the conjunctiva is called conjunctivitis. The eye layer is usually clear and colorless. Conjunctivitis often occurs and spreads easily, especially among children, at school, especially the dormitory environment.

Because the sore eye is often contagious because of hand rubbing, hand washing is important. Sharing a washcloth, towel, or other object with people suffering from conjunctivitis can transmit the infection .

Conjunctivitis Causes

Conjunctivitis is most often caused by viruses, but other cases of conjunctivitis can also be caused by bacteria including Staphylococcus aureus , Streptococcus pneumoniae , Haemophilus species, and Chlamydia trachomatis, and fungi although less common. Dry air, allergies, smoke, and chemicals can also cause this eye disease.

Bacterial conjunctivitis is sometimes caused by a sexually transmitted infection (STI), such as Chlamydia . If symptoms do not go away after a month, this may indicate an STI. Most types of bacterial conjunctivitis will heal faster with treatment. Infective conjunctivitis is very contagious and can be easily passed on to others.

Symptoms of conjunctivitis

Symptoms of contagious conjunctivitis or pink eye include:

  • Reddish eyes
  • Itchy eyes
  • Burning in the eyes
  • Exit tears more than usual
  • Eyelashes stick together
  • Light sensitivity to light so that the eyes easily feel glare
  • The view is not blurred, if the view begins to blur there is a possibility that inflammation has reached the deeper layers of the eye, the cornea

You may have symptoms in one eye, both eyes, or symptoms can spread from one eye to another. When the contagious eye is caused by a virus, symptoms usually starting from one eye can then spread to the other eye.

If you think your eyes are contagious, contact your doctor to find out the best way to treat them. And if you wear contact lenses, make sure to be released immediately. Certain risks can increase the seriousness of the symptoms due to the use of contact lenses such as inflammation that is getting deeper due to the surface wound of the eye layer of the cornea (deeper than the conjunctiva).

Diagnosis of conjunctivitis

A doctor can usually diagnose an eye disease that is contagious by eye examination and by asking questions about your symptoms. Sometimes doctors will use cotton to take some liquid from around your eyes so that it can be tested to examine bacteria or other infections.

Some cases of infective conjunctivitis recover within a few days to 2 weeks without treatment, but some cases can take up to one month. For bacterial conjunctivitis, antibiotics can shorten recovery time and reduce the spread of infection to others. If symptoms persist for 2 weeks or more, the sufferer must return to see their doctor, who will review the diagnosis and adjust treatment.

Treating Conjunctivitis

If your doctor thinks contagious eyes are caused by bacteria, he may prescribe antibiotic eye drops or eye ointments to kill bacteria. With antibiotic treatment, symptoms usually disappear within 2-3 days. But antibiotics only work for eye diseases that are transmitted by bacteria, not for eyes that are more viral. The infectious eye virus can often heal itself in 7-10 days. If the symptoms last longer, contact a doctor.

If the contagious eye is caused by allergies or chemicals, do not go out of the house and avoid exposure to substances that cause allergic conjunctivitis. It is better to be sure to find out specific specific substance allergies by means of skin prick tests. Here’s the treatment you can do at home:

  • Home care for symptoms of contagious eye disease can help you feel more comfortable when the infection is cured
  • Wash your hands more often. Always wash your hands before and after you touch a sore or facial eye
  • Use moist cotton or a clean wet cloth to remove crust. Wipe from the inside corner of the eye. Use clean parts of cloth for each cloth. If the infection is only one eye, be careful not to spread to other eyes.
  • Place a cold or warm wet cloth on your eyes several times a day if your eyes hurt
  • Do not wear contact lenses until the sore eyes heal. Sterilize contact lenses and storage areas. Wait at least 2 days after symptoms disappear before returning to contact lenses
  • If the doctor gives antibiotic drops or ointments, use medication according to prescription and doctor’s advice, even when the eyes start to look better. Keep the tip of the bottle clean, and don’t let it touch the eye area
  • Don’t wear eye makeup until your eyes heal
  • Do not share towels, pillows, or wipes if the eyes are sore and contagious
  • Use eye drops for allergies and drugs to reduce the symptoms of contagious eye disease caused by allergies.

Diphtheria – Causes, Symptoms, Diagnosis, and Treatment

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Diphtheria is a serious bacterial infection that affects the mucous membranes in the throat and nose . Diphtheria is a disease that is very contagious in the nose and throat. This disease can be prevented by vaccination.

Diphtheria is a past disease in most parts of the world within 10 years, as reported by Medikal News Today . In countries where there is a lower booster vaccine uptake, however, like in India, thousands of cases remain every year. In 2014, there were 7,321 cases reported to the World Health Organization (WHO), globally.

If a person is not vaccinated against the bacteria that causes diphtheria, infection can cause serious complications, such as nervous disorders, heart failure, and even death.

Overall, 5 to 10 percent of infected people will die. Some people are more vulnerable than others, with a mortality rate of up to 20 percent in people who are infected under 5 years or more than 40 years.

Diphtheria Causes

The type of bacteria that causes diphtheria is Corynebacterium diphtheria. The condition of the disease will spread through direct contact with objects containing bacteria, such as sharing a drink cup, or the same tisue or handkerchief use. You can also be affected if there are diphtheria patients around you who sneeze, cough or runny nose from the nose. Although an infected person does not necessarily show signs and symptoms, the person is still able to transmit up to 6 weeks after the initial infection.

Bacteria often infect the nose and throat. Once you are infected, bacteria will release harmful substances called toxins. The toxin will spread throughout the body through the bloodstream and often causes a thick gray layer on the mucosa of the nose, throat, tongue, and airways.

In some cases, this toxin can also go to other organs and damage other organs such as the heart, brain, and kidneys. This can cause life-threatening complications such as myocarditis (inflammation of the lining of the heart), paralysis (muscle weakness), and kidney failure .

Diphtheria Risk Factors

Children should routinely get vaccinations to fight this disease, so there is less risk of exposure. In the United States and Europe, diphtheria vaccine has been routinely carried out so diphtheria rarely occurs, but in developing countries like Indonesia, diphtheria can still found mainly in children under 5 years of age and parents over the age of 60 years. People who have increased risk include:

  • Don’t get the latest vaccination
  • Visiting countries that do not provide immunization against diphtheria
  • Have an immune disorder such as AIDS
  • Unhealthy lifestyle or poor sanitation

Diphtheria symptoms

Symptoms of diphtheria appear within 2-5 days after exposure to bacteria. Some people have no symptoms, but some people have mild symptoms that are often the same as ordinary flu. There are typical and visible symptoms of diphtheria, such as a thick layer of gray in the throat and tonsils. Other diphtheria symptoms include:

  • Fever
  • Shivering
  • Enlargement of the gland in the neck
  • A loud sound like barking
  • Sore throat
  • Blue skin
  • Salivating continuously
  • Discomfort in the body

Additional diphtheria symptoms:

  • Difficulty breathing and difficulty swallowing
  • Change of view
  • Talk lisp
  • Signs of shock such as pale and cold skin, cold sweats, and a fast heartbeat.

You can also experience cutaneous diphtheria or skin diphtheria if you have poor hygiene and live in a tropical area. Skin diphtheria often causes ulcers (sores) and redness in the affected skin.

Diagnosis of Diphtheria

Your doctor will do a physical examination to check for enlarged lymph nodes . They will also ask about your medical history and the symptoms you feel. The doctor will also be sure that the patient has diphtheria if he sees a gray layer in the tonsils or in the throat. To confirm the diagnosis, the doctor will take a sample of the affected tissue and send it to the laboratory.

Diphtheria Treatment

If you have diphtheria, contact your doctor immediately. Diphtheria is a disease that can cause serious damage to the kidneys, nervous system, and heart, if left untreated. This disease causes fatal things from 3 percent of the cases.

Diphtheria therapy
Diphtheria is a serious condition, so doctors will provide therapy quickly and aggressively. The first step of therapy for diphtheria treatment is antitoxin injection. This antitoxin injection will fight the toxins produced by bacteria in the body. Be sure to tell your doctor if you have an allergy to certain drugs. If there is an allergy, the doctor will be careful when giving antitoxin, starting with a small dose and increasing gradually. Doctors can also prescribe antibiotics such as penicillin and erythromycin, to help eradicate infections in the body.

During the treatment of diphtheria, doctors can also advise hospitalized patients in isolation rooms so that patients will not potentially transmit the infection to others.

Diplopia – Causes, Symptoms, and Complications

eye

Diplopia is a condition when you see two images of the same object. This condition is commonly called double vision . Usually, this vision problem is the result of the underlying condition. Identifying and treating the cause can help you restore your vision and stop other symptoms from occurring.

There are two types of diplopia: monocular diplopia and binocular diplopia. You can find out what type of diplopia you have with a simple test. In binocular diplopia, when double vision occurs, close one left eye, double vision still exists, and when closing one right eye, double vision is still present. In monocular diplopia, close your left / right eye, if double vision disappears when you close only 1 eye, you have monocular diplopia.

Monocular diplopia is the result of problems with one of your eyes. Problems in the brain or nerves in your eyes may be a cause of binocular diplopia. Once your doctor identifies your type of double vision, they can begin to look for the cause.

Cause

Causes of monocular diplopia
Monocular double vision occurs due to one eye problem and is rare compared to binocular diplopia. Many people with monocular diplopia report that sometimes seeing things will be very clear, while other images will fade or faint.

Possible cause:

  • Heavy (cylindrical) astigmatism
  • Changes in the shape of the cornea (keratoconus)
  • Cataract
  • Dry eyes
  • Pterygium, as there is meat growing in the lining of the eye

Binocular diplopia causes:

  • Nerve damage
  • Diabetes
  • Cranial nerve weakness
  • Myastenia gravis
  • Grave’s disease
  • Strabismus (crossed eyes)

Complications

Every possible cause for double vision has potential complications. The causes of double vision can range from something that is easily treated to something more complicated, such as chronic disease. Some people with double vision may experience nausea or vertigo because the field of vision changes. Other people may experience eye strain and sensitivity to light or sound.

Life-threatening conditions such as infections or brain tumors can cause double vision, but these cases are rare. In this case, severe eye pain or headaches often occur along with visual changes. Any headaches accompanied by changes in vision are considered life threatening and require immediate medical care.

Double vision always requires a doctor’s evaluation to determine the cause. Double vision is a symptom of something abnormal happening in your eyes, brain, or nervous system. Double vision problems require complete evaluation to uncover the cause.

In many cases, the additional images you see in your field of vision are the result of conditions that are treated. But sudden changes in your vision require immediate medical attention.

Some conditions require urgent medical care to prevent permanent vision loss or life-threatening complications.

Diagnosis

Diagnosing double vision as monocular or binocular diplopia can usually be done immediately. However, determining the cause may be more difficult. If you have double vision, telling your symptoms and vision experience will help in the diagnosis.

When you visit your doctor, your doctor will pay attention to your symptoms and perform several tests to look for additional vision problems. Doctors are also likely to have a short test to diagnose this type of diplopia.

After you have a diagnosis of diplopia, the job of finding a cause begins. To do this, your doctor will probably do three types of testing:

After you have a diagnosis of diplopia, the job of finding causes begins. To do this, your doctor will probably do three types of testing:

  1. Check your current health condition

You and your doctor may spend some time exploring your medical history. This includes:

A complete history of your symptoms : Explaining fully your vision problems to the doctor can help them eliminate possible causes and decide what tests can help. Be sure to tell your doctor about unusual symptoms that you experience, even though you are not sure they are related to your vision problems.

Your personal health history : Your doctor may consider underlying factors such as diabetes, thyroid problems, or neurological disorders that can cause your vision problems.

Your family’s health history : If family members have vision problems or disorders that can lead to double vision, let your doctor know. These problems can be a good starting point for your own diagnosis.

  1. Physical examination

A complete physical examination can help your doctor find and identify possible causes for your double vision. This check may include:

  • Blood tests to look for infection
  • Vision check
  • Eye movement test
  • Toxicity test
  • Blood sugar reading
  • Imaging tests, such as CT scans or MRIs

Before deciding on treatment, it is important for you and your doctor to find the cause of the vision problem. In many cases, vision problems can be lost once you repair or handle a fundamental problem.

The most common treatments for diplopia include:

  • Corrective lenses : Glasses or special lenses can correct vision problems.
  • Blindfold: Covering one eye can stop double vision. Although this may not be a long-term solution, eye patch can help manage double vision until there is a more permanent solution.
  • Eye training : If your vision problem is the result of strained or weakened eye muscles, your doctor can give you “exercise” that can help you regain eye muscle strength. When muscles become stronger, your vision problems will increase.
  • Surgery: Depending on the cause, you may need surgery to correct any physical problems. Also, people with problems such as cataracts or problems in the eye may need surgery at some point. Operations to deal with these problems can also improve double vision.

Prognosis

People with double vision often recover completely. Some people will recover with minimal care depending on the cause. Other people may need more care.

After the underlying cause is treated, double vision and any other symptoms that you experience can be lost. In some cases, you need additional treatment, but most attempts to treat diplopia are successful.

Some common causes of double vision can return. This includes cataracts and cranial nerve weakness. In this case, it is important to consult a doctor to identify the problem immediately after diplopia starts so that you can start treatment if vision problems return.

Haemochromatosis

strong man

Hereditary haemochromatosis is a genetic disease that causes the body to absorb too much iron from food eaten. Excess iron is stored in the body’s organs, especially the liver, heart and pancreas.

Too much iron-damaged organ damage causes life-threatening disorders such as cancer, heart disease and liver.

Cause
Hereditary haemochromatosis is caused by mutations of genes that control the amount of iron that the body absorbs from food. Mutations that cause hereditary hemochromatosis are passed on from parents to their children.

Genes that mutate in people with hereditary hemochromatosis are called HFE. A child inherits one HFE gene from each parent. If both parents pass the mutated HFE gene to their child, the child can develop hemochromatosis.

The HFE gene has two common mutations, C282Y and H63D. Genetic testing can reveal whether a person has a mutation in the HFE gene or not.

If someone inherits two abnormal genes, he can develop hemochromatosis, but not everyone with two abnormal genes has signs and symptoms of hemochromatosis.

If a person inherits an abnormal gene, he will not experience hemochromatosis. But the body may absorb more iron than normal. He is considered a carrier of gene mutations and these mutations can be passed on to his children.

How does haemochromatosis affect the organs?
Iron plays an important role in several body functions, including helping blood formation. Most people absorb about 10 percent of the iron that is swallowed. When the body has enough to store iron, the body reduces the amount of iron absorbed by the intestine to avoid excessive buildup.

In patients with hereditary hemochromatosis, the body absorbs as much as 30 percent of the iron that is swallowed. Because the body cannot use or remove additional iron, iron is stored in organ tissues, especially the liver.

Finally, the body can accumulate five to 20 times more iron than normal. Over the years, excessive iron stockpiled can damage organs, cause organ failure and chronic diseases such as liver cancer and diabetes .

Types of hemochromatosis
Other forms of hemochromatosis include:

  • Juvenile haemochromatosis – In this hemochromatic, iron accumulation begins much earlier and symptoms usually occur between the ages of 15 and 30 years. Although hemochromatosis is also an inherited disease, the genetic disorder that causes it does not involve the HFE gene, but is caused by mutations in the gene called hemojuvelin.
  • Neonatal haemochromatosis – In this disorder iron accumulates rapidly in the baby’s liver and can cause death.

Symptoms
Early signs and symptoms of hereditary hemochromatosis are similar to other common symptoms, making it difficult to diagnose. Signs and symptoms include:

  • Fatigue
  • Loss of sex drive (libido) or impotence
  • Menstrual lack of normal (amenorrhea)
  • Pain in the right upper abdomen

Some sufferers of hereditary hemochromatosis have no symptoms, while others experience various problems. These symptoms vary in people and may be different for men and women.

Although hereditary hemochromatosis is present at birth, most people do not experience signs and symptoms until later on, usually between the ages of 30 to 50 years in men and after age 50 in women. Women generally experience symptoms after menopause, when they no longer lose iron through menstruation and pregnancy.

Treatment
Treatment can be done with treatment and medication.

Blood reduction
Treatment of hereditary hemochromatosis can be done by removing blood from the body regularly, just like donating blood. This method is called phlebotomy. But in this case, the goal is to reduce iron levels above normal.

The amount of blood taken depends on age, overall health and severity of iron overload. Some people need lots of phlebotomy to achieve normal iron levels.

The initial schedule of treatment
Initially, blood can be taken once or twice a week in a hospital or doctor’s clinic. After iron levels return to normal, patients may need to get blood intake four to six times a year.

Treating hereditary hemochromatosis before damage to organs can prevent serious complications such as liver disease, heart disease and diabetes.

If the patient already has one of these complications, the process of bleeding can slow the progression of the disease, and in some cases even cure. If the patient already has liver cancer, the doctor can recommend periodic screening by performing an abdominal ultrasound and blood test.

Drug
In certain situations, the patient may not be able to undergo the process of removing blood or having heart complications caused by hemochromatosis. Doctors can recommend drugs that help the body remove some iron from the blood.

The medicine can be injected into the body by a doctor or taken in pill form. This drug causes the body to release iron through urine or feces in a process called chelation. Side effects can cause pain and redness where the drug is injected, as well as symptoms of flu.

Blighted Ovum (Empty Pregnancy)

pregnancy

Blighted ovum is a condition where a woman feels pregnant but there is no baby in the womb. A woman who experiences it also feels pregnancy symptoms such as menstrual delay, nausea and vomiting in early pregnancy ( morning sickness ), hardened breasts, and abdominal enlargement. Even during pregnancy tests both test packs and laboratory results are positive.

At the time of conception, mature eggs (ovum) meet sperm. However, due to various factors, the fertilized egg sperm cannot develop fully, and only a fluid-filled placenta is formed. Nevertheless the placenta remains embedded in the uterus. The placenta produces the hormone HCG ( human chorionic gonadotropin ) where this hormone signals the ovaries and brain as a notice that there are already conception results in the uterus. The HCG hormone which causes the appearance of pregnancy symptoms such as nausea, vomiting, cravings and causes the pregnancy test to be positive. Because pregnancy tests both test packs and laboratories generally measure levels of the hormone HCG ( human chorionic gonadotropin ) which is often referred to as a pregnancy hormone.

Until now there is no way to detect early blighted ovum pregnancy. A new woman can be indicated to have blighted ovum if she has done a transvaginal ultrasound examination. But this action can only be done during pregnancy entering the age of 6-7 weeks. Because at that time the diameter of the pregnancy sac was greater than 16 millimeters so that it could be seen more clearly. From there it will also appear, there is a pregnancy sac that is empty and does not contain the fetus.

Because the symptoms are not specific, blighted ovum is usually found only after a spontaneous miscarriage will occur where bleeding complaints occur. In addition to blighted ovum, an enlarged abdomen such as pregnancy, can be caused by pregnant wine (hydatidiform mole), uterine tumor or intestinal disease.

About 60% of blighted ovum is caused by chromosomal abnormalities in the process of fertilizing eggs and sperm. TORCH infection, rubella and streptococci, uncontrolled diabetes (diabetes mellitus), low levels of beta HCG and immunological factors such as the presence of antibodies to the fetus can also cause blighted ovum. The risk also increases if the age of the husband or wife gets older because the quality of sperm or ovum drops.

If you have been diagnosed with blighted ovum, then the next action is to remove the conception from the uterus (curettage). The results of curettage will be analyzed to determine what causes blighted ovum and then overcome the cause. If due to infection it can be treated so that this incident does not recur. If the cause is antibodies, an immunotherapy program can be done so that later you can get real pregnancy.

To prevent the occurrence of blighted ovum, it can be done several precautions such as TORCH examination, rubella immunization in women who want to get pregnant, if they suffer from cured disease first, controlled their blood sugar, perform chromosomal examinations, especially if over 35 years of age, stop smoking for quality sperm / ovum is good, checking for a routine pregnancy and getting used to a healthy lifestyle.