SICKLE CELL AND THALASSAEMIA SUPPORT PROJECT (WOLVERHAMPTON)

Support | SCTSP

We are a community organisation supporting individuals and their families living with Sickle Cell or Thalassaemia blood disorders. 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
1077687
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1999
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sctsp.org.uk
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SCTSP
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Sickle Cell and Thalassaemia Support Project (Wolverhampton)

The Sickle Cell and Thalassaemia Support Project (SCTSP) is a UK nonprofit organisation dedicated to addressing health disparities and providing support for families affected by sickle cell disease or thalassaemia. Established in 1990, the organisation operates primarily in Wolverhampton, Walsall, and Dudley.

Charity Overview

  • Charity Number: 1077687
  • Registration History: The project was officially registered as a charity on 5 October 1999[4].
  • Operational Areas: The SCTSP serves communities across Wolverhampton, Walsall, Dudley, and surrounding areas, focusing on improving health outcomes and quality of life for those affected by these blood disorders[1][5].

Mission and Activities

The SCTSP's mission is to provide comprehensive support to individuals and families living with sickle cell or thalassaemia. This includes offering resources, services, and advocacy to address the unique challenges faced by these families. The organisation engages in community outreach, education, and advocacy efforts to enhance awareness and understanding of these conditions[1][5].

Community Engagement

  • Patient Experience Surveys: The SCTSP conducts surveys to gather insights from patients living with sickle cell disease, aiming to improve services and support based on their experiences[5].
  • Partnerships and Events: The organisation participates in various community events and partnerships, such as supporting employee resource groups in fundraising challenges like the Tough Mudder[5].

Governance and Operations

The SCTSP operates as a registered charity with a structured governance framework. It files annual accounts and returns, which are accessible through charity registries[2][3].

[1] https://www.sctsp.org.uk/about-1 [2] https://register-of-charities.charitycommission.gov.uk/en/charity-search/-/charity-details/3959621/charity-overview [3] https://find-and-update.company-information.service.gov.uk/company/03575079/filing-history [4] https://register-of-charities.charitycommission.gov.uk/en/sector-data/top-10-charities/-/charity-details/3959621/full-print [5] https://www.sctsp.org.uk

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Poslední komentáře

Awesome work you're doing for the community! Supporting those with Sickle Cell and Thalassaemia makes such a positive impact. 💙 #CommunityHeroes
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So grateful for organizations like yours that bring awareness and support to families affected by these blood disorders. Keep up the incredible work! 🌟 #SickleCellAwareness
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Poslední diskuze

What strategies can we implement to raise awareness about sickle cell and thalassaemia screening among young men in our community?
Odpovědí: 3, Naposledy před 1 den detail
How can we improve support services for families affected by sickle cell and thalassaemia in the Wolverhampton area?
Odpovědí: 3, Naposledy před 1 den detail

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HOME About Us Information and Support Get Involved Events and Activites Supporters Contact More We are a community organisation supporting individuals and their families living with sickle cell or thalasseamia blood disorders across Wolverhampton Walsall Dudley and surrounding areas Sickle Cell and Thalassaemia Support Project Quick Facts Traits are healthy carriers of sickle cell and thalassaemia most people who carry the trait do not know they have it. Treatments are improving quickly people can live a long life if they receive the right treatment. Because sickle cell and thalassaemia are genetic diseases they can occur in any population. You only get sickle cell or thalassaemia by inheriting genes from your parents.

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