Thalassemia and Sickle Cell Society provides free consultation, free blood and transfusion facilities, counselling, investigations and food for around 70 – 80 patients daily. We are proud to have eminent doctors, specialists, hemato-oncologist, paediatric endocrinologist, cardiologist, paediatrician, pathologists, ophthalmologist, dentist, radiologists and research scientists associated with us in helping to provide best comprehensive care and cure for our patients.
Thalassemia and Sickle Cell Society is putting its heart and soul in getting BMT (Bone Marrow Transplantation is the only cure for Thalassemia) done for the patients by doing free HLA typing, counselling them for BMT and helping them financially. Which is a great social, mental and emotional support and relief to the family.
To undergo BMT procedure patients should have fully matched Human Leukocyte Antigen (HLA) sibling/parent. The treatment is an expensive and an unaffordable procedure for our patients. Setting up BMT centre is very expensive and complex affair. Hence, TSCS made Memorandum of Understanding (MoU) with Sankalp Foundation, for BMT treatment at Bhagwan Mahaveer Jain Hospital, Bangalore initially. Also we made MoU with other reputable hospitals, such as Narayana Hrudayala, Bangalore and Rainbow Children Hospital, Hyderabad, where HLA Fully matched and Haplo matched types of BMT procedures are available.
We express our gratitude to Electronics Mart India (Bajaj Electronics) for their continued support for BMT.
Thalassemia and Sickle Cell Society was established (1998) in the city to promote appropriate treatment and quality life for every thalassemia affected child. Thalassemia is an inherited condition affecting the blood. Good treatment is important to prevent complications, this treatment is for lifelong until the child goes through successful Bone Marrow Transplantation.
Thalassemia and Sickle Cell Society is dedicated to ensuring the best quality treatment and quality of life for patients suering with Thalassemia and Sickle Cell Anemia. Moving ahead to reach our goal of Thalassemia free Telangana and Andhra Pradesh.
We have opened a branch of TSCS at Kurnool run by well experienced medical staff. TSCS started this center to support Thalassemia and Sickle Cell patients of Kurnool and surrounding districts.
![🩸 THALASSEMIA AWARENESS 🩸 Early detection can make all the difference. Thalassemia is a serious genetic blood disorder that requires lifelong care. Being aware of its symptoms like dark urine, slow growth, fatigue, abdominal swelling, pale or yellowish skin, and facial bone deformities can help in seeking early treatment and improving the quality of life. If you or a loved one notice any of these signs, please consult a healthcare provider promptly. Remember, early intervention is key! ❤️ Let’s spread awareness, support the cause, and stand together for a healthier future....#TSCS #ThalassemiaAwareness #ThalassemiaSupport #BloodDisorderAwareness #GeneticDisorders #ChildHealthMatters #PediatricCare #HealthEducation #KnowTheSymptoms #EarlyDetectionSavesLives #BloodHealthMatters #HealthcareForAll #ChronicIllnessAwareness #SupportThalassemiaWarriors #HyderabadHealth #StayInformedStaySafe #HealthFirst #ThalassemiaCare #FightThalassemiaTogether #CommunityHealthCare...[thalassemia, anemia, TSCS, Hyderabad, awareness, health, blood donation, early diagnosis, symptoms, patient care, children health, support group, healthcare, medical support, nonprofit]](https://www.tscsindia.org/wp-content/plugins/instagram-feed/img/placeholder.png)
