- Request received23/05/2025
- Checked & confirmed02/06/2025
- Fundraising02/06/2025
- Treatment provided03/06/2025
- Invoice paid30/05/2025
- Case closed26/08/2025
Why is treatment sometimes done earlier than the payment?
When a case is urgent and vital, hospitals often proceed with delivering medical care right away to save a life, even before the finalisation of admission procedures. Usually, when this happens, hospitals put the bill on our credit until the funds are transferred to their accounts. That’s why the chronology can sometimes be in disorder.
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Michael N., 18
Report publishedBlood
0
$475
About blood
Sickle cell anemia is a genetic blood disorder where red blood cells are abnormally shaped and sticky, like sickles, and don't last as long as normal red blood cells. This condition results in a constant shortage of healthy red blood cells, leading to anemia and other serious complications.
Thank you for saving this life!
100%
$475 raised of $475
Background
Michael is an 18-year-old student living with sickle cell disease. He came to the clinic with complaints of joint pain and frequent fatigue. Over the past year, he has been admitted twice due to sickle cell crises and once for severe anemia, which required a blood transfusion. This year, he has already had one admission related to a sickle cell crisis. He also reports occasional chest pain. Despite his health challenges, Michael is determined to keep up with his studies, although he missed several weeks of school last term because of fatigue and recurrent infections. Michael is currently in Form Four at a rural day school. He comes from a humble background, his parents earn less than KSh 150 per day. The family lives in a modest two-room mud-walled hut and relies on a stream, a 20-minute walk away, for drinking water. Despite the hardships, Michael is a cheerful and ambitious young man who enjoys spending time with his friends and dreams of becoming a medical professional one day if given the necessary support.
Medical history
Michael, who has sickle cell disease, was diagnosed with moderate anemia. He was treated with antibiotics, rehydration fluids, and medication specific to sickle cell management. As his condition improved, he was discharged to continue his recovery at home. During a follow-up call, a Helpster volunteer spoke with his relieved and happy mother, who shared that Michael has fully recovered and returned to his usual routine, including going back to school. She added, “I was so scared when he got sick and wasn’t improving even after using local herbs. Receiving proper hospital care has been the greatest blessing for our family. Thank you so much.”
Prognosis
He was treated and given drugs needed and if this could have not done on time it could have resulted toorgan damage, pain, and increased risk of infection .
