Sickle Cell Disorder – Information and Support Links
Resources » Sickle Cell Society Sickle Cell Disorder Resources for Patients | NHLBI, NIH Sickle cell disorder – NHS Let’s Keep Talking – Living your life with Sickle Cell Disease […]
Life Insurance and Sickle Cell
Important Disclaimer:The NE & Y HCC does not provide financial, legal, or insurance advice. We are not responsible for the content of external websites or organisations mentioned below. This information […]
Help for Children and Young Person’s with Sickle Cell Disorder
These videos are designed for young people to help them understand Sickle Cell Disease in a simple and engaging way. They explain what the condition is, how it affects the […]
What is Sickle Cell?
Sickle cell disorder (SCD) is a genetically inherited red blood cell disorder. That means it is passed down from a parent’s genes. SCD changes the shape of red blood cells, […]
Thalassaemia & Rare Inherited Anaemias
The NE & Y HCC is a network for SCD only. The hospitals and clinical teams are part of the North Egland Thalassaemia & RIA HCC – North of England Haemoglobinopathy […]
Citizen’s Advice
Benefits What benefits can I claim? There are a number of different benefits checking services available which can help you to explore your benefit entitlement: ● https://www.entitledto.co.uk/ ● https://www.turn2us.org.uk/ Can […]
Exercise for Sickle Cell patients
Supporting Healthy Movement and Physical Development for People with Sickle Cell Disorder Being active and moving your body regularly can help you stay healthy, strong, and feel good. For people […]
Nourishing Your Wellbeing: Nutrition and Sickle Cell Disorder
While there’s no specific diet that can cure sickle cell disorder, the food and drinks you consume play a significant role in managing your health, reducing the risk of complications, and promoting overall wellbeing.