Health Charities That specialise in Sickle cell

Information, counselling, caring and advocacy support for those with sickle cell disorders and their families.

OSCAR Birmingham Ltd raises awareness of Sickle Cell and Thalassaemia, both red blood cell disorders and provides support and befriending services to those affected by these conditions. OSCAR educates, provide advocacy and raises awareness by organising community events, presentations in schools,colleges. We work with public and private agencies to further our work in uand around Birmingham

The prinicpal activities is to provide relief of sickness, distress and poverty and enhancement of life, of members of Afro-Caribbean and Asian Community affected by the disorders of Sickle Cell and Thalassaemia, within Wolverhampton and the surrounding areas. Work with families identified by Staffordshire County Council through their 0-19 Family Support Service - offering support and guidance

Plasma of Hope is a UK registered charity supporting individuals that are living with Sickle Cell Disease or other related illnesses. We advocate for people living with genetic blood disorders such as Sickle Cell and Thalassemia, and survivors of associated complications including stroke and other health issues resulting to disability. We also help their carers and those in their support network.

We help children with health challenges . Example children suffering from sickle cell disease in ENGLNAD and Ghana. We also do educational programmes for children of school going age.

?SICKLE CELL CARE MANCHESTER WILL STRIVE TO SUPPORT PEOPLE DIAGNOSED WITH SICKLE CELL DISEASE (SCD), THEIR FAMILIES AND CARERS, IN ORDER TO EMPOWER AFFECTED INDIVIDUALS AND TO ENHANCE THEIR QUALITY OF LIFE. SICKLE CELL CARE MANCHESTER WILL ALSO WORK TO IMPROVE AWARENESS OF SCD,WE ALSO WISH TO IMPROVE KNOWLEDGE AND UNDERSTANDING OF SCD, AND TO FOSTER ACCEPTANCE OF THOSE LIVING WITH THE CONDITION.?

To assist the haematology staff at Kings College Hospital with the provision of much needed laboratory equipment, particulary in the areas of Sickle Cell Disease and Thalassaemia.

Support for people affected by Sickle Cell and Thalassaemia genetic blood disorders. Provision of counselling, advice and information, screening, education and training, health promotion, self help groups, social activities, volunteers, student placement and work experience.

a) to promote the relief of children and young people with sickle cell disease and their families and carers, in particular but not exclusively by the provision of support, education and practical advice;b)to develop the capacity and skills of the members of the socially and economically disadvantaged community of Whythenshawein such a way that they are better able to identify, and help them

Supporting families affected by Sickle cell in the Thames Valley area and raising awareness of Sickle Cell through our fundraising and awareness events.

We provide social events for clients; advocacy; advice and support for clients, family and carers; Heamoglobinopathy counselling for individuals with carrier status; we are part of the service improvement group with the hospital and provide awareness and general information for the general public.

TEF is made up of 3 pillars:Provide people who have Sickle Cell Disease and their families access to traditional therapies, counselling and emotional well-being coursesWork with schools, councils and hospitals to educate on the policies that will encourage better practices and support for the community.Run events and campaigns to educate and raise money so we can help everyone impacted by

To spread the good news in relation to Christianity.Also very much involved in helping the youth in the community.Giving generously to other charities for sickle cell research.Bringing people together to live as a family.

Bringing awareness to Thrombotic Thrombocytopenic Purpura(TTP) and other rare blood conditions such as Sickle Cell Anemia and auto immune disease such as Lupus SLE, supporting those affected by TTP, aiming to research and find cure for TTP.

To support, advice to those affected by sickle cell disorders. We aim to educate and give information to the general public cell disorders and thalassaemia. We visit affected person at home or in hospital.

Provide support for sickle cell and thalassaemia suffers.

Create, stimulate and foster public awareness of sickle cell disease in the UK and Sierra Leone. Educate private and public sectors about sickle cell diseaseAdvocate in the care and support of sickle cell patients and their familiesCounsel sickle cell patients and their familiesIdentify babies at risk of sickle cell by newborn screeningPromote medical and social research on sickle cell.

To support families living with children and young people diagnosed with special needs such as autism, sickle cell and the like.

The charity provides support for those directly and indirectly affected by Sickle Cell and Thalassaemia in Leicester,Leicestershire and Rutland. This is achieved via a number of initiatives such as monthly coffee mornings, quarterly support group meetings, workshops, training days, research participation, educational forums, outreach, children-led initiatives and bespoke client programmes

THE RELIEF OF PERSONS SUFFERING FROM SICKLE CELL DISEASE AND THE PROVISION OF FACILITIES FOR RECREATION, AND THE RELIEF OF POVERTY FOR SUCH PERSONS AND THEIR IMMEDIATE FAMILY MEMBERS HAVING NEED FOR SUCH FACILITIES DUE TO THE EFFECT/IMPACT OF SICKLE CELL.

Holistic Massage services,Nutritional advice, 1-1 support, training and information, Hospital and home services, personal development and the provision of support for carers.We run a social activity centre with drop in facilities. We provide outreach support in the form of light house work and DIY etc...Help with form filling and benefits.We also provide opportunities for volunteering

TO RELIEVE THE NEEDS OF PEOPLE AFFECTED BY SICKLE CELL DISEASE, THEIR FAMILIES AND CARERS FOR THE PUBLIC BENEFIT BY: 1) IMPROVING AWARENESS OF SICKLE CELL DISEASE FOR THE GENERAL PUBLIC, SERVICE AND HEALTH CARE PROVIDERS; 2) ENABLING PEOPLE AFFECTED BY SICKLE CELL DISEASE TO RAISE AWARENESS OF THEIR NEEDS IN THEIR LOCAL AND WIDER COMMUNITIES; 3) SUPPORTING THE PROVISION OF SUITABLE ADJUSTMENTS TO

GoAbiye Limited objectives as set out in our Memorandum & Articles of Association is to relieve the needs of those suffering from sickle cell disease, their families and carers, for the public benefit by providing financial assistance and support. Our mission is to reduce the mortality and morbidity secondary to sickle cell disease in Africa and to amplify sickle cell awareness campaign globally.

Sickle Cell and Young Stroke Survivors support the social and psychological needs of children and young people living with Sickle Cell disease and childhood Stroke in the UK. We proactively address the day-to-day needs of the children and their families to reduce isolation. We work mainly in England and are keen to provide free medical treatment and drugs to children in Africa.

We provide home tuition for children and young people affected by Sickle Cell disorder. We organise outing activities where young people have the opportunity to learn more about the area where they live in. We organise sporting activities that provide young people affected by Sickle Cell disorder the opportunity to be fit and mix with other young of their ages.