From the field
Real moments from our outreach, news from our programmes and events you can join.
Field StoryCommunity members are encouraged to access screening and obtain accurate information about sickle cell status to support early diagnosis, informed decisions, and appropriate healthcare.
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Field StoryThe initiative has encouraged community members to know their sickle cell status, seek appropriate healthcare, and share accurate information about SCD to promote early screening, informed decisions, and stigma-free communities.
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UpdateJosepha was a Co-Founder of TASIWA and dedicated sickle cell warrior who championed Sickle Cell Disease awareness and supported families affected by the condition. Her compassion and commitment to the sickle cell community will forever remain in our hearts.
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UpdatePascazia Mazeze has been nominated for the FISA Awards 2019 in the Youth Humanitarian Support category in recognition of her humanitarian contribution.
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UpdateThis recognition celebrates her commitment to sickle cell advocacy and TASIWA’s efforts to raise awareness, amplify the voices of people living with Sickle Cell Disease, and promote better health and well-being.
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Field StoryThe training aimed to strengthen the group’s understanding of SCD and its ability to support affected children and their families.
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Field StoryJosepha Kwila Chokara shares a powerful personal story of living with Sickle Cell Disease, beginning with his diagnosis at the age of two and a half. His early experiences reveal the challenges caused by misconceptions, traditional beliefs, stigma, and limited awareness of sickle cell disease.
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EventTheir valuable contribution, expertise, and commitment helped strengthen awareness and understanding of SCD. This partnership highlights the importance of collaboration between healthcare professionals and community organizations in addressing misconceptions and improving support for individuals living with SCD and their families.
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EventThe initiative recognized their influential roles in families, schools, and communities, equipping them with accurate information to raise awareness, challenge misconceptions, and promote support for people living with SCD.
Read moreWarriors, parents and volunteers — we'd love to hear and share your experience.
