Lupus Still Disparately Affects Black Women


( – Many chronic diseases are the result of the body’s immune system mistakenly perceiving that the body is under attack from foreign bodies. A counterattack is then launched — an inflammatory response meant to vanquish the intruder. In reality, the immune system has misinterpreted the threat and is actually attacking the body’s own cells and tissue.

Immune system disorders cause abnormally low activity or over activity of the immune system. In cases of immune system over activity, the body attacks and damages its own tissues (autoimmune diseases). Immune deficiency diseases decrease the body’s ability to fight invaders, causing vulnerability to infections.

There are more than 80 known autoimmune diseases. Many of them have similar symptoms which makes them hard to diagnose. They usually fluctuate between periods of remission or no symptoms, and flares where symptoms become worse.

More and more, we are all hearing about friends, family, and even celebrities, like Nick Cannon, who are “victims” of autoimmune disease – especially Lupus.

Lupus is a systemic autoimmune disease driven by inflammation in which the immune system indiscriminately attacks “self-tissues” throughout the body. It is estimated that more than 16,000 people are diagnosed with lupus each year in the United States. Approximately 1.5 million Americans, and 5 million people worldwide, currently live with lupus. Anyone can get lupus, but it most often affects women. Lupus is also more common in women of African American, Hispanic, Asian, and Native American descent than in Caucasian women. Women of color are two to three times more likely to develop lupus than Caucasians.

Lupus autoimmunity can cause variable symptoms from person to person. Parts of the body frequently affected by lupus include the skin, kidneys, heart and vascular system, nervous system, connective tissues, musculoskeletal system, and other organ systems. Lupus is not contagious, not even through sexual contact. You cannot “catch” lupus from someone or “give” lupus to someone.

Your immune system is the network of cells and tissues throughout your body that work together to defend you from invasion and infection. You can think of it as having two parts: the innate and the acquired immune systems.

When the immune system is working properly, foreign invaders (antigens) provoke the body to produce proteins called antibodies and specific types of white blood cells that help in defense. The antibodies attach to the invaders so that they can be recognized and destroyed.

Normally the immune system’s white blood cells help protect the body from harmful substances, called antigens. Examples of antigens include bacteria, viruses, toxins, cancer cells, and blood or tissues from another person or species. The immune system produces antibodies that destroy these harmful substances.

What causes the immune system to no longer tell the difference between healthy body tissues and antigens is unknown. One theory is that some microorganisms (such as bacteria or viruses) or drugs may trigger some of these changes, especially in people who have genes that make them more likely to get autoimmune disorders.

These diseases tend to run in families. Women – particularly African-American, Hispanic-American, and Native-American women – have a higher risk for some autoimmune diseases. The diseases may also have flare-ups, when they get worse, and remissions, when they all but disappear. The diseases do not usually go away, but symptoms can be treated.

An autoimmune disorder may result in: the destruction of one or more types of body tissue; abnormal growth of an organ; and/or changes in organ function.  Autoimmune diseases can affect almost any part of the body, including the heart, brain, nerves, muscles, skin, eyes, joints, lungs, kidneys, glands, the digestive tract, and blood vessels.

The classic sign of an autoimmune disease is inflammation, which can cause redness, heat, pain, and swelling. How an autoimmune disease affects you depends on what part of the body is targeted. If the disease affects the joints, as in rheumatoid arthritis and psoriatic arthritis, you might have joint pain, stiffness, and loss of function. If it affects the thyroid, as in Graves’ disease and thyroiditis, it might cause tiredness, weight gain, and muscle aches. If it attacks the skin, as it does in scleroderma/systemic sclerosis, vitiligo, and systemic lupus erythematosus (SLE), it can cause rashes, blisters, and color changes.

Diagnosing lupus can be difficult. It may take months or even years for doctors to piece together the symptoms to diagnose this complex disease accurately. Making a correct diagnosis of lupus requires knowledge and awareness on the part of the doctor and good communication on the part of the patient. Giving the doctor a complete, accurate medical history (for example, what health problems you have had and for how long) is critical to the process of diagnosis. This information, along with a physical examination and the results of laboratory tests, helps the doctor consider other diseases that may mimic lupus, or determine if you truly have the disease. Reaching a diagnosis may take time as new symptoms appear.

There are more than 80 types of autoimmune diseases, and some have similar symptoms. This makes it hard for your health care provider to know if you really have one of these diseases, and if so, which one. Getting diagnosed can be frustrating and stressful. In many people, the first symptoms are being tired, muscle aches and low fever.

Most autoimmune diseases are chronic, but many can be controlled with treatment. Symptoms of autoimmune disorders can come and go. When symptoms get worse, it is called a flare-up.

If you or someone you love is living with an autoimmune disorder, it’s important to get all the facts on the condition. Though researchers don’t know exactly what causes autoimmunity, much has been learned about the risk factors involved. After an autoimmune disease diagnosis, your main priority should be getting the care you need to manage your particular disorder, and that may mean finding medical experts who specialize in your autoimmune condition.

Remember, I’m not a doctor. I just sound like one. Take good care of yourself, and live the best life possible!

The information included in this column is for educational purposes only. It is not intended nor implied to be a substitute for professional medical advice. The reader should always consult his or her healthcare provider to determine the appropriateness of the information for their own situation or if they have any questions regarding a medical condition or treatment plan. Glenn Ellis, is a Health Advocacy Communications Specialist. He is the author of Which Doctor?, and Information is the Best Medicine. A health columnist and radio commentator who lectures, nationally and internationally on health related topics, Ellis is an active media contributor on Health Equity and Medical Ethics. Listen to Glenn, every Saturday at 9:00am (EST) on, and Sundays at 8:30am (EST) on For more good health information, visit:









Doubts Raised About Highly-Praised Malaria Vaccine Headed for Africa


May 7, 2017

Doubts Raised About Highly-Praised Malaria Vaccine Headed for Africa

( – With much fanfare, the world’s first injectable vaccine against malaria will be introduced in three countries – Ghana, Kenya and Malawi – starting in 2018.

The vaccine – known as RTS,S or Mosquirix, trains the immune system to attack the malaria parasite, which is spread by mosquito bites. It was developed by the British pharmaceutical company, GlaxoSmithKline.

The World Health Organization (WHO) said the vaccine could potentially save tens of thousands of lives.

But its demanding regime – once a month for three months and then a fourth dose 18 months later – is raising concerns that it may be a logistical nightmare in the poorest parts of the world. In fact, the drug failed to get a green light from the world health body in 2015 when the manufacturer had planned to roll out the drug in a major campaign.

Further testing in pilot projects has been ordered by the WHO which can take up to 5 years to complete.

An earlier clinical trial of the vaccine in 2012 produced disappointing results. Only about a third of the vaccinated infants had fewer infections than a control group.

Moncef Slaoui, chairman of research and development at Glaxo, called the trial’s outcome at that time “less than we’d hoped for”. “But if a million babies were vaccinated, we would prevent 260,000 cases of malaria a year. This is a disease that kills 655,000 babies a year — 31 percent of that is a very large number,” he was quoted to say.

Other preventative malaria treatments include the drug camoquin, used by the group Doctors Without Borders (MSF) in 2014 in Sierra Leone. Sierra Leone has the fifth highest prevalence of malaria globally, and the disease is the biggest killer of children under five in the country.

Issues with the vaccine, including low protection and high required amount of doses, does not make the vaccine suitable for wide rollout in the areas that need it most (high disease burden, low resource settings). MSF calls for more research and development into a malaria vaccine that can give good protection and is easy to use in low resource contexts as a priority.

GLOBAL INFORMATION NETWORK creates and distributes news and feature articles on current affairs in Africa to media outlets, scholars, students and activists in the U.S. and Canada. Our goal is to introduce important new voices on topics relevant to Americans, to increase the perspectives available to readers in North America and to bring into their view information about global issues that are overlooked or under-reported by mainstream media.

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