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The Charity Commission for Northern Ireland
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TunMicro Sickle Cell Foundation

  • Status

    Received: 16 days late

  • Income

    £0.1K

  • Spending

    £0.0K

Charity no. 106477 Date registered. 08/06/2017

Public benefits

TunMicro SCF promotes research which is contributing to the scientific and medical understanding of SCD/SCT and its causes. We also support the development of new treatments that may provide relief from the effects and symptoms of SCD, leading to better health outcomes for those diagnosed with SCD/SCT. TunMicro is also promoting the welfare of

those suffering from SCD/SCT, and these include improved quality of life, access to good health services and well-being outcomes for families, friends and carers who have been directly or indirectly affected with SCD/SCT. We recognise our unique talents in delivering Biomedical services on a day to day basis in Northern Ireland, and that's why we are advancing education about Sickle Cell Disease/Trait (SCD or SCT) to Africa particularly Nigeria, as well as offering Free Sickle Cell Screening. Our Team from the Pathology department of South Eastern Health and Social Care Trust, Ulster Hospital I Belfast commenced on preparatory charity mission in December 2015 to the Public Health Centre Oshodi Local Government Council in Lagos, Nigeria to offer free sickle cell screening and counselling. Nigerians need our medical professional talents because provision of providing free genetic screening particularly sickle cell gene, practical support and interventions in assisting sickle cell patients are lacking. The benefits to the public of a charity such as this is to ensure people of Nigeria who otherwise would die of a preventable sickle cell disease are given opportunity to have life to live. These benefits are demonstrated through the publication of results of research projects and about progress via the frequent feedback from our service users and other collaborators such as health professionals and the families and carers of people with sickle cell disease. We are unaware of any harm that may flow from these purposes. Other who may benefit include friends, family , and carers of those living with SCD/SCT in Northern Ireland and indeed those living outside of Northern Ireland (specifically in the rural Africa-focused project), who may also benefit from the outcome of research to which the charity may contribute. Most of our trustees who are participating in the activities of the organisation are also benefitting in that way because they access those services on equal terms with all other service users. We have given our trustees and staff training to ensure good governance and the efficient delivery of high-quality services that may be transferable to other areas of the their lives. We recruit volunteers to deliver our services. We do not currently have staff.

What your organisation does

TunMicro Sickle Cell Foundation provides a varied programme of support and information services to individuals living with Sickle Cell Disease or Sickle Cell Traits, their families and carers. The unique focus of TunMicro SCF is that it is managed by health professionals with a keen interest/background specialising in the diagnosis of blood

diseases and also by people from the local BME communities all of whom are directly or indirectly affected by Sickle Cell Disease (SCD)/Sickle Cell Trait (SCT). Therefore, when people access our support, they will have the opportunity to meet and talk to others who are technically experienced or have been facing that same challenges. TunMicro is all about taking practical actions to deal with SCD/SCT as well as informing and educating beneficiaries about prevalence and management. Some of our programmes are geared towards breaking myths and taboos around SCD as well as tackling social isolation faced by those affected. TunMicro provides services which include, counselling, raising awareness, complementary therapies, advocacy/peer support. This can include hospital, home visits, and telephone support, health improvement sessions, bereavement support, carer's support, welfare, tailored support for families with babies affected by SCD, fatigue management, relaxation/stress management, signposting to other sources of support - health improvement training and workshops - outreach health improvement events e.g. talks, stalls, drama presentations - facilitating beneficiaries to share their experiences in order to improve future Sickle Cell Disease services in the regions of focus. We also support research and surveys into the prevalence, causes and treatment of SCD in the regions of focus.

The charity’s classifications

  • The advancement of education
  • The advancement of health or the saving of lives

Who the charity helps

  • Asylum seekers/refugees
  • Ethnic minorities
  • General public
  • Overseas/developing countries
  • Youth (14-25 year olds)

How the charity works

  • Advice/advocacy/information
  • Counselling/support
  • Education/training
  • Medical/health/sickness
  • Research/evaluation
  • Volunteer development

Charity accounts & reports for financial year end 31 March 2024

Independent examiners report Charity accounts Trustee annual report

Charity accounts & reports for financial year end 31 March 2023

Independent examiners report Charity accounts Trustee annual report

Charity accounts & reports for financial year end 31 March 2022

Independent examiners report Charity accounts Trustee annual report

Charitable purposes

The Foundation is established to raise awareness about Sickle Cell Disease/Trait (SCD/SCT) in the community among the people of Black and Ethnic Minority (BME) groups and mixed heritage people living in Northern Ireland. Also, to create sickle cell awareness among the Northern Ireland public health bodies and Health Practitioners for early screening in new born baby. To advance education about Sickle Cell Disease/Trait (SCD or SCT) in Africa, particularly Nigeria, as well as offering free sickle cell screening. Also, provide practical support and interventions in assisting communities to better managing Sickle Cell Disease.

Governing document

Constitution

Other name


  • 3 Trustees
  • 0 Employees
  • 0 Volunteers

Contact details

Public address

  • Mr Ismaila Olatunji Sule, 7 Moatview Crescent, Dundonald, Belfast, BT16 2BG

Trustee board

Trustee
Mr Ismaila Olatunji Sule
Mr Taiwo Taofeeq Yusuf
Mrs Victoria Abiola Ladi-Taiwo

Areas of operation

List of regions

  • In Ireland
  • In Northern Ireland
  • In The Uk
  • Internationally
  • Nigeria
  • Republic Of Ireland