Our Sickle Cell and Genomics Workshop designed specifically for clinicians. This online session offers insights into genomics and sickle cell disease. Additionally; it seeks to gather your valuable perspectives to aid in developing a survey that identifies the top ten priorities from the healthcare community. Participate in discussions with experts; share your views; and contribute to shaping future research and patient care strategies. Don't miss this chance to advance your knowledge and influence the direction of sickle cell genomics.
The Sickle Cell Society is the only national charity in the UK that supports and represents people affected by a sickle cell disorder to improve their overall quality of life.
First set up as a registered charity in 1979, the Sickle Cell Society has been working alongside health care professionals, parents, and people living with sickle cell to raise awareness of the disorder. The Society’s aim is to support those living with sickle cell, empowering them to achieve their full potential.
The Sickle Cell Society believes that individuals with sickle cell have the right to quality care. This can only be achieved if funding is made available to educate health carers and other professionals about the condition. The Society aims to provide this.
