- Request received17/04/2025
- Checked & confirmed29/05/2025
- Fundraising29/05/2025
- Treatment provided07/07/2025
- Invoice paid21/07/2025
- Case closed02/10/2025
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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Umar A., 2
Report publishedBlood
0
$100
About blood
Sickle cell disease is a genetic disorder that affects hemoglobin production, causing red blood cells to become misshapen and prone to breaking apart, leading to anemia, pain, and other complications. Symptoms include pain episodes, infections, organ damage, and increased risk of stroke. Management and treatment involve medications, blood transfusions, hydration, and rest to help manage symptoms and prevent complications.
Thank you for saving this life!
100%
$100 raised of $100
YOBE STATE SPECIALIST HOSPITAL DAMATURU
Damaturu, Yobe State, 6 Gujba Road, Nigeria
Background
Umar Abdulkadir is a calm and gentle child who adores his mother. For the first few years of his life, Umar seemed healthy and happy. But everything changed four days before he was brought to the hospital. He suddenly developed a high fever, his hands and feet began to swell, and he refused to eat. His mother grew increasingly worried as his condition worsened. When they arrived at the hospital, the doctors evaluated Umar - he had sickle cell disease, and he was in the middle of a painful crisis. The medical team explained that he needed emergency treatment to manage the pain and complications.
Medical history
Umar was admitted in our facility where he was diagnosed with Sickle Cell disease complications. He had his complete dosage of medications and other necessary interventions. As the treatment progressed, his condition improved as presenting symptoms subsided. He was later discharged home on his oral medications. Parents were so happy with the help received from helpster.
Prognosis
With proper treatment and management, children with sickle cell disease can lead relatively normal lives, reducing symptoms and preventing complications. Without treatment, the condition can lead to severe complications, including frequent pain episodes, organ damage, and increased risk of stroke, significantly impacting quality of life and life expectancy. With modern care, many children with sickle cell disease can live into adulthood and lead fulfilling lives, but ongoing medical management is crucial.
