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 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.

Blog 3: Sickle Cell Crisis by Debbie Omodele What words come to mind when you hear the words ‘sickle cell’? I can almost guarantee that many of you thought of the word pain amongst many. Pain is one of the most common complications of Sickle Cell Disorder (SCD).  As mentioned in blog 1 and 2, … Read more Blog 3: Sickle cell crisis. Third in the series of blogs by Debbie Omodele, Children’s Haemoglobinopathy Nurse Specialist, Barking, Havering and Redbridge University Hospital Trust.

Genotypes Did you know that a couple who are both carriers of the sickle haemoglobin (Hb) gene (HbAS) carry a 25% chance of having a baby with Sickle Cell Disorder (SCD)? These chances are the same with every pregnancy they have together. Your genotype is the set of genes that determines whether you have SCD, … Read more Blog 2: Genotypes, Compatibility and Sickle cell disorder. Debbie Omodele

This is the first of  a series of Blogs written by Debbie Omodele, Children’s Haemoglobinopathy Nurse Specialist, Barking, Havering and Redbridge University Hospital NHS Trust. Keep an eye out for follow ups on topics such as preconceptual screening, managing conditions, psychological well-being, pain management and transition looking at the importnace of family wihtin this process. Enjoy. … Read more Blog 1: Shining the light on Sickle Cell on Rare Disease Day