The genetic condition of sickle cell disease (SCD) results when sickle cell genes are inherited from each parent. We connected with Dr. Seethal Jacob about a study on maintaining an immune response against pneumococcal bacteria in children with SCD.

When it comes to health insurance, not everyone has access to equitable healthcare in the U.S. Here’s a look at where we are and ways to make improvements in health insurance coverage and health disparities.

During the COVID-19 pandemic there was a large drop in cancer screenings. This reduction could potentially decrease the chances of detecting many cancers at earlier stages and possibly lead to a greater amount of suffering from undiagnosed or late-stage diagnoses.

ADHD goes as an undiagnosed and untreated struggle more often for girls, women, and certain Black, Indigenous, and People of Color (BIPOC) groups. Here's a look at ADHD and health disparities of female and BIPOC individuals.

Here’s a look at early U.S. immunization history, the significance of COVID-19 vaccinations, the Delta variant, and Onesimus.

After largely being an unknown risk previously, medical researchers examined MGUS and familial risk in a study. Here’s a look at what was learned from the study, other MGUS incidence information, and MGUS screening recommendations.

Study of the stress hormone cortisol is entering into research studies, and we at DHH find it a timely topic for its impacts to some BIPOC groups. Here’s a look at cortisol, the health impacts of cortisol, and ways to reduce cortisol levels.

As the most commonly occurring blood disorder in the world, sickle cell trait primarily impacts those in the BIPOC community with African ancestry. We connected with Dr. Pavlos Msaouel about a study on high-intensity exercise in those with sickle cell trait.

Distrust in healthcare has been America’s hard pill to swallow especially for the BIPOC community. But how can members of healthcare, like physicians, regain the trust of their BIPOC patients?

Will telemedicine remain as a mainstay for myeloma patients after the pandemic? Learn the prime points from the Myeloma TelemEDucation Empowerment Resource Center.

When faced with the diagnosis of breast cancer for the first time, it can be overwhelming. Dr. Regina Hampton explains key players in the breast cancer treatment game.

New research from Heinz Ludwig, MD et al explores the global interrelations between Multiple Myeloma (MM) mortality and countries’ economic resources, patient empowerment, and health access and quality. The study is intended to inform about the associations between these factors, and to improve diagnosis, management, and outcome of patients globally.

The Prostate Cancer TelemEDucation Resource Center helps improve prostate cancer patients’ and care partners’ familiarity with healthcare, and thus increase quality of care regardless of the COVID pandemic, geographical location, or racial disparities. The program focuses on the specific needs of Black men and other vulnerable communities to most effectively reduce healthcare disparities.

Black American women have less breast cancer but die at higher rates than our white counterparts. Why is there a disparity?

Studies centering on vaccinations for myeloma patients have been limited in the past due to their low participation rate in trials coupled with negligent measures of patient outcomes. Learn about compilation of vaccination data.

Access to low-cost nutritious food stores is limited in BIPOC communities, but efforts are underway to dismantle the inaccessibility.

Months into the coronavirus pandemic in the U.S., what have we learned about the effects of the virus on Black, Indigenous, and People of Color (BIPOC) populations?

Blood transfusions, organ transplants, and bone marrow transplants can be detrimental situations for any person who needs one. But what special considerations are there for those who are of BIPOC and mixed races?

Blood transfusions, organ transplants, and bone marrow transplants can be detrimental situations for any person who needs one. But what special considerations are there for those who are of BIPOC and mixed races?

Dr. Andrew Campbell shares the reasons that drive him to help people with sickle cell disease in this Heart Behind the White Coat (HBWC) program.