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Girl Hoped to Have Been Cured of HIV has Relapsed

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In this undated file image provided by Johns Hopkins Medicine in 2005 Dr. Deborah Persaud, a pediatric HIV expert at Johns Hopkins' Children's Center in Baltimore, holds a vial. On Thursday, July 10, 2014, doctors and officials at the National Institutes of Health said new tests last week showed that a Mississippi girl born with the AIDS virus is no longer in remission. The girl is now back on treatment and is responding well, doctors said. (AP Photo/Johns Hopkins Medicine, File)

In this undated file image provided by Johns Hopkins Medicine in 2005 Dr. Deborah Persaud, a pediatric HIV expert at Johns Hopkins’ Children’s Center in Baltimore, holds a vial. On Thursday, July 10, 2014, doctors and officials at the National Institutes of Health said new tests last week showed that a Mississippi girl born with the AIDS virus is no longer in remission. The girl is now back on treatment and is responding well, doctors said. (AP Photo/Johns Hopkins Medicine, File)

MARILYNN MARCHIONE, AP Chief Medical Writer

A Mississippi girl born with the AIDS virus and in remission for more than two years despite stopping treatment now shows signs that she still harbors HIV — and therefore is not cured. The news is a setback to hopes that very early treatment with powerful HIV drugs might reverse an infection that has seemed permanent once it takes hold.

The girl is now nearly 4. As recently as March, doctors had said that she seemed free of HIV though she was not being treated with AIDS drugs. That was a medical first.

But on Thursday, doctors said they were surprised last week to find the virus in her blood, and there were signs that it was harming her immune system. She is now back on treatment and is responding well, they said.

The news is “obviously disappointing” and will affect a federal study that had been about to start testing early, aggressive treatment in such cases, said Dr. Anthony Fauci, director of the National Institute of Allergy and Infectious Diseases. Doctors had been considering stopping treatment if no signs of infection could be detected after two years.

“We’re going to take a good hard look at the study and see if it needs any modifications,” either in terms of length of treatment or because of ethical concerns over raising false hopes about an approach that now has suffered a setback, Fauci said. At a minimum, consent forms to join the study must be revised, he said.

Most HIV-infected moms in the U.S. get AIDS medicines during pregnancy, which greatly cuts the chances they will pass the virus to their babies. The Mississippi baby’s mom received no prenatal care and her HIV was discovered during labor. Because of the baby’s great risk of infection, doctors started her on unusually powerful treatment 30 hours after birth, even before tests could determine whether she was indeed infected.

The girl was treated until she was 18 months old, when doctors lost contact with her. Ten months later when she returned, they could find no sign of infection even though the mom had stopped giving her AIDS medicines.

Tests repeatedly showed no detectable HIV until last week, when copies of the virus were measured in her blood. Doctors say they don’t know why the virus rebounded when it did, and said it raises profound questions about what they know about HIV’s hideouts in the body.

“We are still very much in the early discovery phase of trying to achieve a sustained virological remission and perhaps even a cure. There is much, much more to learn and we remain committed to doing so,” Fauci said.

The girl’s experience still suggests that early, aggressive treatment can limit the size of the reservoir of dormant virus in the body and help control infection, said one specialist involved in the case, Dr. Deborah Persaud of Johns Hopkins Children’s Center in Baltimore.

“What we’ve learned from this case is really quite amazing,” said Jeffrey Safrit, research chief at the Elizabeth Glaser Pediatric AIDS Foundation. “They were able to suppress virus for a very long time without therapy. We need to take the positive aspects of this case and learn from them to move forward” with the federal study, he said.

In March, doctors revealed that a second baby born with HIV may have had her infection put into remission by very early treatment — in this case, four hours after her birth in suburban Los Angeles in April 2013. Nearly a year later, very sophisticated tests at multiple times suggested she had completely cleared the virus, but she remains on treatment so there is no way to know for sure.

Only one other person is thought to have been cured of HIV infection — a San Francisco man who had a bone marrow transplant in 2007 from a donor with natural resistance to HIV. He showed no sign of infection more than five years later.

___

Online:

AIDS information: https://www.aidsinfo.nih.gov

and https://www3.niaid.nih.gov/topics/HIVAIDS/

___

Marilynn Marchione can be followed at https://twitter.com/MMarchioneAP

Copyright 2014 The Associated Press. All rights reserved. This material may not be published, broadcast, rewritten or redistributed.

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Black Press

On Your November Ballot: Prop 38 Would Allocate $8.4 Billion to Immunology and Immunotherapy Funding

“Yes on 38”, with the tagline “Californians for Life-Saving Immunology Research and Cures,” is leading the campaign for the support side of the proposition.

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California voters will decide in November whether Proposition (Prop) 38 should authorize substantial state funding for immunology and immunotherapy research.

The initiative would fund immunology and immunotherapy research aimed at harnessing the body’s immune system to develop new treatments, medical procedures and potential cures for diseases such as cancer, Alzheimer’s disease and heart disease.

More specifically, Prop 38, titled the Immunology and Immunotherapy Research Funding Initiative, is split into three main components that would go into effect if passed.

First, the initiative would authorize the state to issue $8.4 billion in general obligation bonds to support immunology and immunotherapy research. At least half of the bond proceeds, or $4.2 billion, would be dedicated exclusively to research.

Additionally, Prop 38 would make it mandatory for the state to enter into an agreement with a qualified nonprofit institute focused and dedicated to researching immunology and immunotherapy within 90 days of the initiative’s effective date. The research institute must be affiliated with the University of California. 

The third component mandates that the remaining bond revenue must be directed to California-based public and nonprofit medical institutions through a peer-reviewed grant process.  

“Yes on 38”, with the tagline “Californians for Life-Saving Immunology Research and Cures,” is leading the campaign for the support side of the proposition. 

Along with the campaign, organizations that have publicly supported the ballot initiative include the California Democratic Party, The ALS Association, Alzheimer’s treatment and advocacy organizations, California Black Health Network, Parkinson Association of Northern California and Reform California among others.

“California has an opportunity to accelerate lifesaving medical breakthroughs. Immunotherapies work differently than traditional treatments. Instead of attacking cells directly, they empower the body’s own immune system to recognize and stop disease. Today, these therapies are already treating certain cancers and chronic conditions — and researchers continue to expand what’s possible. This initiative invests in proven science so cures can move from the lab to patients faster,” said the campaign.

No on Proposition 38 is leading the campaign against the measure, with support from the League of Women Voters of California. Opponents argue that California cannot afford to assume $8.4 billion in debt for medical research that may not produce definitive results. They also object to directing more than half of the bond proceeds — $4.2 billion — to a single qualifying nonprofit research institute, arguing that funding decisions of this magnitude should be made through the state’s regular budget process.

“Medical research can save lives, but Prop 38 is the wrong way to fund it. It would authorize $8.4 billion in borrowing for immunology and immunotherapy research and require the state to make $500 million to $600 million in annual debt payments for about 20 years. Those payments would come from the General Fund, which also pays for schools, health care, and other public services,” the League of Women Voters of California said.

A “yes” vote would authorize $8.4 billion in state bonds to fund immunology and immunotherapy medical research.

A “no” vote would reject the proposed bond funding.

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Black Press

Two Looming Threats Every Alameda County Elder Should Know About

Federal changes enacted under H.R. 1 are bringing new eligibility, reporting, and coverage rules beginning in 2027. Although Californians age 65 and older and people with disabilities are exempt from the new 80-hour-per-month work requirement and will continue with annual rather than six-month renewals, that does not mean elders can ignore the coming changes.

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Alameda County elders are urged to attend the Elder Justice Symposium at Oakland City Hall on Sept. 25, from 9 a.m. to 5 p.m., for information that could profoundly affect both their health care and the legacy they hope to leave their families.

For many older adults, a lifetime of hard work has produced two things they understandably want to protect: access to health care while they are living and the home, savings, and other assets they hope to pass to loved ones when they die.

Changes already underway in California make understanding how to protect both increasingly urgent.

The first threat involves Medi-Cal.

Federal changes enacted under H.R. 1 are bringing new eligibility, reporting, and coverage rules beginning in 2027. Although Californians age 65 and older and people with disabilities are exempt from the new 80-hour-per-month work requirement and will continue with annual rather than six-month renewals, that does not mean elders can ignore the coming changes.

California has already reinstated an asset test for certain Medi-Cal recipients age 65 and older, people with disabilities and those needing long-term care. Assets must be reported when applying or renewing coverage.

And another significant change is coming.

Beginning July 1, 2027, California says the Medi-Cal asset limit for affected beneficiaries will fall from $130,000 for one person to just $21,000, and to $31,000 for two people, with certain assets excluded and special rules applying in some circumstances.

There is more. Beginning Jan. 1, 2027, Medi-Cal’s retroactive coverage period will also shrink. For most beneficiaries outside the ACA expansion adult group, coverage of qualifying medical expenses incurred before application will be reduced from three months to two.

For an elder facing hospitalization, long-term care or an unexpected medical crisis, misunderstanding these rules could have enormous financial consequences.

The second threat concerns what happens to everything you worked so hard to acquire.

Many people believe, “I have a will and a living trust, so my family is protected.”

It may not be that simple.

An estate plan is only as effective as the way it has been structured, maintained and implemented. How assets are titled, whether a trust has actually been funded, beneficiary designations, Medi-Cal eligibility and long-term-care planning can all affect whether a person’s wishes are ultimately carried out.

A will by itself does not automatically avoid probate, and simply possessing trust documents does not mean every asset has been properly protected or positioned to pass as intended.

That is why elders should learn the rules before a medical crisis, incapacity or death makes planning far more difficult.

At the Elder Justice Symposium, experts will explain these changes in understandable language and discuss steps that elders and their families should consider now.

Attendees will have an opportunity to learn what questions to ask about Medi-Cal eligibility and renewals, asset limits, estate planning and protecting the legacy they intend for their families.

Do not assume the rules you learned years ago are still the rules governing you today.

Come to Oakland City Hall on Sept. 25, from 9 a.m. to 5 p.m.

Bring your questions. Bring your family. Most importantly, bring a willingness to prepare.

The decisions you make before these changes take full effect could profoundly affect your health care, your financial security, and what remains for the people you love.

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Advice

Outdoor activities keep you active, but UV exposure can accelerate chronic eye conditions

BLACKPRESSUSA NEWSWIRE — Never underestimate signs of eye problems because if left unaddressed, they can lead to vision impairment or vision loss. Some symptoms should even prompt you to get immediate professional help, as they may indicate emergency sight-threatening conditions.

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Outdoor activities, if done for prolonged periods without adequate ultraviolet (UV) protection, can accelerate eye conditions like cataracts and age-related macular degeneration (AMD). Eye/eyelid cancers are other solar radiation risks of unprotected outdoor time. 

You’d want to implement the above UV vision protection strategies more than ever, as the number of days with high ultraviolet index values is on the rise. The World Meteorological Organization notes that measurements show a significant uptick in the number of days with high UV indices over the past decades.

What Are Some Common Eye Conditions? 

Refractive errors are among the most common eye conditions that result from the eyes being unable to bend (refract) light correctly. They can occur due to certain physical traits, including:

  • The eyeball either being too short or too long
  • The cornea’s shape either being too flat or too steep
  • The flexibility of the lens inside the eye changing as a result of getting older (e.g., the lens becomes stiff due to advancing age) 

Refractive errors are so common they impact over 150 million people in the U.S., per the NEI (National Eye Institute). Some have nearsightedness, also called myopia, while others have farsightedness, also known as hyperopia. In older people, presbyopia, which makes close-up things look blurry, is also prevalent.

Astigmatism is another common refractive error that causes blurriness with both near and far vision. It results from the eyes having an irregular shape (egg or oval shape instead of round). Some people may also have this alongside another refractive error. 

What Are the Signs of Serious Eye Problems? 

Never underestimate signs of eye problems because if left unaddressed, they can lead to vision impairment or vision loss. Some symptoms should even prompt you to get immediate professional help, as they may indicate emergency sight-threatening conditions.

If you, a family member, or a friend ever experiences any of the following, please seek the help of an emergency optometrist, ophthalmologist, or eye hospital right away. 

  • Partial or total loss of sight
  • Sudden double vision
  • A dark curtain, veil, or shadow that moves across the vision
  • A sudden, unexplained increase in eye floaters and flashes
  • Intense pain in and around the eyes
  • Severe redness and inflammation
  • Extreme light sensitivity
  • Physical trauma to the eyes, particularly deep punctures, cuts, or chemical splashes

What Chronic Eye Conditions Can Unprotected Outdoor UV Exposure Cause or Accelerate? 

Spending time in nature doing outdoor activities has become more popular among folks in the U.S., with participation rates increasing over the years.

A new report from the Outdoor Industry Association (OIA), for instance, shows that in 2025, 183.2 million Americans got outside. It represents nearly six in ten people aged 6 and older and reflects an increase of 30 million from 2019’s total participants. 

Nature time and outdoor activities have undeniable health benefits, from lowering stress to supporting better heart health. They can, however, still pose safety risks, particularly if people ignore basic precautions, such as those for outdoor lens safety, skin protection, and dehydration prevention. 

Without proper preparation and long-term ocular protection, your eyes can take a hit from UV overexposure, as this can increase the risk of or accelerate the following eye conditions.   

Cataracts 

Prolonged or consistent exposure to UV rays without any protection can trigger oxidative stress in the eyes. Over time, the sun’s UV light can damage the protein inside your eyes’ lenses. The damage breaks down the proteins and causes them to clump up and form cataracts.

Cataracts are highly common, with the risk increasing with age. The longer they go untreated, the more vision loss they can cause and may even lead to blindness. 

Age-Related Macular Degeneration 

The oxidative stress caused by unprotected UV exposure can contribute to the development or acceleration of AMD. It’s a progressive disease that damages the eyes’ macula (central part of the retina at the back of the eye), blurring central, straight-ahead vision.

Developing AMD can put you at risk of experiencing difficulty:

  • Reading
  • Recognizing faces
  • Driving
  • Completing focus tasks

Eye/Eyelid Cancers 

Prolonged exposure to the sun’s potent UV rays can harm the sensitive areas of the eyes, including the delicate tissues in and around the eyelids. In some cases, this damage can trigger the development of certain cancers. 

How to Safeguard Your Vision From Harmful UV Rays 

Making it a habit to wear sunglasses whose label states “100% UV protection” or “UV400” should be one of your top priorities to protect your eyes from the sun’s UV rays. If you’re not keen on having to switch from prescription specs to sunglasses, don’t worry, as you can get specialty glasses.

You can, for example, fit stylish designer pieces, whether it’s Gucci, Prada, or Versace eyeglasses, with prescription sun care, UV-protective tinted lenses. There are also photochromic (transition) lenses that automatically darken when exposed to UV. 

Wear a wide-brimmed hat to maximize sun protection, too. It can safeguard not just your eyes but also your face and even neck from direct sunlight. 

Frequently Asked Questions

Can You Reverse UV-Related Eye Conditions? 

Some UV-related eye conditions are reversible, such as eye dryness and surface irritation caused by an isolated incident of overexposure to the sun’s rays. Another is photokeratitis, which is similar to a sunburn, except it affects the eyes. 

Resting (moving to a dimmer area) and applying cool, damp compresses to the eyes can help relieve these conditions’ temporary symptoms. 

Many other UV-related eye conditions, however, are chronic or permanent. Cataracts and AMD, for instance, are non-reversible. They are, however, treatable. There’s surgery for cataracts, while AMD’s management often involves injections or laser therapies.

What Is the Most Common Degenerative Eye Disease? 

AMD is the most common degenerative eye disease. 

The latest statistics cited by the American Macular Degeneration Foundation put the number of Americans 40 years and older diagnosed with some form of macular degeneration at 20 million. It further notes that close to 1.5 million people have late-stage, vision-threatening AMD. 

Don’t Let UV Rays Ruin Your Eyesight

UV radiation can contribute to or accelerate various eye conditions, some of which could be permanent, such as cataracts and AMD. It should be enough reason for you to always wear sunglasses with a UV400 or 100% UV protection rating. 

Find more health and lifestyle guides or the latest events and news impacting the Black community by checking out the rest of our platform. 

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Black History

BOOK REVIEW — Curved Air: A Biography of Sickle Cell Anemia and the Quest to Cure the First Molecular Disease

OAKLAND POST — Over decades, researchers worked haphazardly. Papers were written, treatments were tried, used, or discarded. Doctors discovered that genetic testing could prevent new cases, a heartbreak for would-be parents. Researchers discovered that “a perfect storm” of confluence spread SCD: malaria, human population, and mosquitoes.

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Book Cover of Curved Air
Book Cover of Curved Air.

Copyright: c.2026, Publisher: The Belknap Press of Harvard University Press, SRP: $29.95, Page Count: 338 pages

Four weeks of testing, and you’re exhausted.

Two gallons of blood, maybe three, have been removed. No lie. You’ve laid on tables, slid through machines, been scanned so much you lost count and finally, your doctors have a diagnosis. As in the new book “Curved Air” by Kevin Davies, you have hope there’s a what next?

Though the disease was known in parts of Africa and likely existed here in the United States for hundreds of years, sickle cell disease (SCD) is a relative newcomer in disease research.

Says Davies, “Sickle cell was first identified more than 120 years ago” and it was considered as a “Black disease.” Because of that, discrimination followed “sickle cell warriors” and research was scant, though white people can and do get SCD.

With “agonizing” pain as a major symptom, “SCD is one of roughly seven thousand genetic diseases” currently known to science. When someone has SCD, a genetic mutation causes their red blood cells to curve and get stuck in blood vessels, rather than flowing freely as they should. This diminishes the oxygen supply “to various parts of the body… which causes inflammation and pain,” jaundice, stroke, and damaged organs. Anemia, Davies says, can leave a patient fatigued and short of breath. Anticipating pain crises causes anxiety and PTSD.

Says Davies, “More than forty million people carry” one copy of the genetic mutation that causes SCD, and “five hundred thousand affected” babies are born with the disease per year, worldwide.

Over decades, research was done haphazardly. Papers were written; treatments were tried, used, or discarded. Doctors discovered that genetic testing could prevent new cases, a heartbreak for would-be parents. Researchers discovered that “a perfect storm” of confluence spread SCD: malaria, human population, and mosquitoes.

There was always hope that someday, sickle cell disease might be cured.

Then, Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) gene-editing therapy was approved by the FDA, and a brave volunteer named Victoria Gray stepped forward…

So, you want to – need to – learn more about sickle cell disease? Is it imperative for you? Then, this is your book. But there are things you’ll want to know before you dive into “Curved Air.”

Because author Kevin Davies is the editor of The CRISPR Journal, you can expect up-to-date, cutting-edge information; but that’s a two-sided coin: the information is heavy-duty, not always easy to grasp, and it’s burdened by acronyms that can be overwhelming. Yes, that’ll inform you, but it may also send you elsewhere for further understanding, which really should’ve come from this book.

And yet, if you or someone you love has SCD, this is your book. It explains where the disease came from, why it hasn’t been completely cured yet, and what kind of hope you can hold. It’s a good start on a path to comprehension.

Also, be aware that the narrative here is sometimes padded with journalistic fluff that might annoy you if you’re eager to get to the science. Indeed, “Curved Air” will teach you. Then again, it also might test you.



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Black Press

Prostate Cancer is Twice as Likely to Kill Black Men. Talking to Your Doctor Could Help Save Your Life

BLACKPRESSUSA NEWSWIRE — The American Cancer Society recommends that African American men speak with their doctor at age 45 about whether prostate cancer screening is right for them. Men at even higher risk should have that discussion at age 40, especially those with one or more close relatives who were diagnosed at an early age.

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American Cancer Society board member Dr. Robert Winn discusses risk factors for the disease and why too many Black men still aren’t getting screened

September is Prostate Cancer Awareness Month, and as both a Black man and a cancer center director, I know many men in our community think it’s bad luck to talk about cancer. But I’m here to tell you it’s bad luck not to talk about it.

We, Black men in the U.S., are nearly 70% more likely than White men to be diagnosed with prostate cancer. We’re also twice as likely to die from the disease.

But I’m telling you, if you’re diagnosed early, you can still enjoy a long, happy life doing the things you love, whether that’s playing with grandkids or staying active in your community. That’s because although it can become a serious illness, most men diagnosed with prostate cancer won’t die from it.

In fact, more than 3.5 million U.S. men who’ve been diagnosed with prostate cancer are still alive today. And when it’s diagnosed early, you boost your odds of survival. It’s that simple.

Generally, prostate cancer is most likely to develop after age 50, but when it develops in Black men, they tend to be younger. That means we need to be on the ball about understanding our personal risk. The risk factors include a family history of prostate cancer and certain genetic health risks that come from a parent.

When it comes to family medical history, we need to get a lot better at talking. For me, it turned out I had uncles who’d died from prostate and other cancers, but I didn’t always know that, so I couldn’t use that information to help me make smarter screening choices.

The American Cancer Society recommends that African American men speak with their doctor at age 45 about whether prostate cancer screening is right for them. Men at even higher risk should have that discussion at age 40, especially those with one or more close relatives who were diagnosed at an early age.

Look, I get that no one looks forward to a screening, but it typically starts with just a simple blood test, called a prostate-specific antigen, or PSA.

Even if you end up needing a digital rectal exam, it takes less than a minute and could save your life. So, what I say to people is, what’s the price of your life? Isn’t it worth a minute of being uncomfortable?

Brothers, this is essential for you to know: just because you’re feeling good doesn’t mean you don’t have early-stage prostate cancer. By the time you start to actually experience symptoms, the disease could be at an advanced stage and might be harder to treat.”

Prostate cancer is significantly impacting our fathers, our brothers, and our sons. That’s why the American Cancer Society is working with health systems and professionals in your community to help remove barriers in the fight against the disease.

We can help you find low-cost or free screening locations. And for men who need cancer treatment, the American Cancer Society can reduce the financial burden of traveling to medical appointments by providing free rides and, if you live far away from where you receive treatment, a free place to stay.

When it comes to prostate cancer screening, one size doesn’t fit all. So, it’s important for all men – and especially Black men – to talk to their doctor about what’s best for them based on their age, risk, and health history. Please make that appointment, because we don’t want you to risk missing out on the best years of your life.

For more information, call the American Cancer Society’s 24/7 helpline at 1-800-227-2345 or visit cancer.org.

Dr. Robert Winn is a nationally recognized physician-scientist and researcher. He currently serves as cancer center director at Temple Health’s Fox Chase Cancer Center. Since 2021, he has served on the board of directors for the American Cancer Society, a leading cancer-fighting organization with a vision to end cancer as we know it, for everyone.

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Black Press

Prostate Cancer is Twice as Likely to Kill Black Men. Talking to Your Doctor Could Help Save Your Life

BLACKPRESSUSA NEWSWIRE — The American Cancer Society recommends that African American men speak with their doctor at age 45 about whether prostate cancer screening is right for them. Men at even higher risk should have that discussion at age 40, especially those with one or more close relatives who were diagnosed at an early age.

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Prostate Cancer is Twice as Likely to Kill Black Men. Talking to Your Doctor Could Help Save Your Life

American Cancer Society board member Dr. Robert Winn discusses risk factors for the disease and why too many Black men still aren’t getting screened

September is Prostate Cancer Awareness Month, and as both a Black man and a cancer center director, I know many men in our community think it’s bad luck to talk about cancer. But I’m here to tell you it’s bad luck not to talk about it.

We, Black men in the U.S., are nearly 70% more likely than White men to be diagnosed with prostate cancer. We’re also twice as likely to die from the disease.

But I’m telling you, if you’re diagnosed early, you can still enjoy a long, happy life doing the things you love, whether that’s playing with grandkids or staying active in your community. That’s because although it can become a serious illness, most men diagnosed with prostate cancer won’t die from it.

In fact, more than 3.5 million U.S. men who’ve been diagnosed with prostate cancer are still alive today. And when it’s diagnosed early, you boost your odds of survival. It’s that simple.

Generally, prostate cancer is most likely to develop after age 50, but when it develops in Black men, they tend to be younger. That means we need to be on the ball about understanding our personal risk. The risk factors include a family history of prostate cancer and certain genetic health risks that come from a parent.

When it comes to family medical history, we need to get a lot better at talking. For me, it turned out I had uncles who’d died from prostate and other cancers, but I didn’t always know that, so I couldn’t use that information to help me make smarter screening choices.

The American Cancer Society recommends that African American men speak with their doctor at age 45 about whether prostate cancer screening is right for them. Men at even higher risk should have that discussion at age 40, especially those with one or more close relatives who were diagnosed at an early age.

Look, I get that no one looks forward to a screening, but it typically starts with just a simple blood test, called a prostate-specific antigen, or PSA.

Even if you end up needing a digital rectal exam, it takes less than a minute and could save your life. So, what I say to people is, what’s the price of your life? Isn’t it worth a minute of being uncomfortable?

Brothers, this is essential for you to know: just because you’re feeling good doesn’t mean you don’t have early-stage prostate cancer. By the time you start to actually experience symptoms, the disease could be at an advanced stage and might be harder to treat.”

Prostate cancer is significantly impacting our fathers, our brothers, and our sons. That’s why the American Cancer Society is working with health systems and professionals in your community to help remove barriers in the fight against the disease.

We can help you find low-cost or free screening locations. And for men who need cancer treatment, the American Cancer Society can reduce the financial burden of traveling to medical appointments by providing free rides and, if you live far away from where you receive treatment, a free place to stay.

When it comes to prostate cancer screening, one size doesn’t fit all. So, it’s important for all men – and especially Black men – to talk to their doctor about what’s best for them based on their age, risk, and health history. Please make that appointment, because we don’t want you to risk missing out on the best years of your life.

For more information, call the American Cancer Society’s 24/7 helpline at 1-800-227-2345 or visit cancer.org.

Dr. Robert Winn is a nationally recognized physician-scientist and researcher. He currently serves as cancer center director at Temple Health’s Fox Chase Cancer Center. Since 2021, he has served on the board of directors for the American Cancer Society, a leading cancer-fighting organization with a vision to end cancer as we know it, for everyone.



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