Living with an invisible chronic illness isn’t easy: you end up having rehearsed answers to lots of questions about your health, you know what it’s like to live with permanent fatigue, big worries about the future are just things you think about every day, you are incredibly good at collecting water samples in tiny bottles and you are probably on first name terms with a few of the nurses at your local hospital. Earlier this year I decided to add a baby into this craziness and the last 7 months have been the biggest learning curve of my life.
Blog 4: Closing the Education Gap: Promoting Compassionate Care for Individuals with Sickle Cell Disease by Debbie Omodele, Children’s Haemoglobinopathy Nurse Specialist, Barking, Havering and Redbridge University Hospital Trust.
Despite existing for many decades, sickle cell disease (SCD) still faces a knowledge gap among the public and healthcare professionals (HCPs). Educating HCPs about SCD pathophysiology, care, and management is crucial to bridge this gap and breaking down healthcare-related stigmas. In this blog, we will hear directly from patients, shedding light on their experiences and … Read more