Beware of online sickle cell disease ‘advocacy’ that aims to trick you

Can people who don’t have sickle cell disease (SCD) advocate for the community? Absolutely. However, I think there is an important distinction that deserves attention. Usually, most advocates are patients, caregivers, healthcare professionals, or family members of people living with the disease. However, I’ve recently seen an influx of people joining online support groups and […] The post Beware…