Our team of specialized doctors and healthcare professionals are experienced in managing thalassemia and providing personalized treatment plans.
We offer complete support, including blood transfusions, iron chelation therapy, and regular monitoring to ensure optimal health.
We focus on the physical and emotional well-being of patients and their families, offering counseling and guidance throughout the treatment process.
With state-of-the-art diagnostic tools, we ensure early detection and provide genetic counseling to help prevent the spread of thalassemia.
We offer financial aid programs to support patients with the costs of treatment, making care more accessible to all.
We are committed to raising awareness and educating communities about thalassemia to promote early intervention and prevention.
Thalassemia is a genetic blood disorder that affects the production of hemoglobin, leading to anemia. It is inherited when a person receives the defective gene from both parents. The condition can vary in severity, with some individuals requiring regular blood transfusions and treatments for lifelong management.
Symptoms of thalassemia include fatigue, weakness, pale skin, delayed growth, and bone deformities. In severe cases, individuals may also experience organ damage due to iron buildup from frequent blood transfusions. Early diagnosis can help manage symptoms and prevent complications.
Treatment for thalassemia depends on the severity of the condition. Mild cases may require little intervention, while severe cases often involve regular blood transfusions, iron chelation therapy, and other medical treatments to manage anemia and prevent complications. Genetic counseling and early diagnosis are also important for managing the disease.
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