TSCS

Thalassemia and Sickle Cell Society -
Kamala Hospital and Research Centre,
Vuppala Venkaiah Memorial Blood Centre
(1)

Thalassemia and Sickle Cell Society (TSCS) is a registered NGO (Reg. no. 5359 Dt. 22/10/1998) established in the year 1998 with the pledge to help the Thalassemia patients. Thalassemia is a genetic blood disorder and affected patients depend on regular blood transfusion for survival, usually every 2 to 3 weeks. Our objective is to treat all thalassemia children and add years to their lives.

01/03/2026

🌟 Thalassemia Free India by 2035 – This bold vision is the heartbeat of ATC 2026, igniting hope across the nation!
We're thrilled by the overwhelming positive feedback from prestigious participants, including global experts, policymakers, and advocates who praised the conclave's impactful sessions, collaborative spirit, and actionable strategies for eradication.

Mr. Aleem Baig - Senior Joint Secretary, TSCS-Hyderabad speaking about the success of ATC2026!!

Together, at TSCS Hyderabad, we're accelerating towards a healthier future! 💙

[Thalassemia, SickleCellSociety, HyderabadNGO, PatientSupport, AwarenessCampaigns, BoneMarrow, Transfusions, GeneticScreening, CommunityOutreach, ScreeningPrograms, FamilyCounseling, AdvocacyWork, DonorRegistry, ResearchFunding, WellnessInitiatives]

27/02/2026

🌟 Thalassemia Free India by 2035 – This bold vision is the heartbeat of ATC 2026, igniting hope across the nation!
We're thrilled by the overwhelming positive feedback from prestigious participants, including global experts, policymakers, and advocates who praised the conclave's impactful sessions, collaborative spirit, and actionable strategies for eradication.
Together, at TSCS Hyderabad, we're accelerating towards a healthier future! 💙

[Thalassemia, SickleCellSociety, HyderabadNGO, PatientSupport, AwarenessCampaigns, BoneMarrow, Transfusions, GeneticScreening, CommunityOutreach, ScreeningPrograms, FamilyCounseling, AdvocacyWork, DonorRegistry, ResearchFunding, WellnessInitiatives]

24/02/2026

"Hope, Innovation, and a Cure." ✨

Dr. Sunil Bhat shares his thoughts on the monumental success of ATC 2026 held at Novotel Hyderabad Airport & Kamala Hospital and Research Centre (10th-11th Jan).

When the brightest minds in pediatric care and research come together with a shared goal, miracles happen. We are marching toward a Thalassemia-Free Bharat, one breakthrough at a time.❤️

👇 Drop a 🙏 if you support this mission!

[Genetics, Hematology, Blood Transfusion, Bone Marrow Transplant, Prenatal Screening, Hemoglobinopathy, Clinical Research, Community Outreach, Health Equity, SustainableDevelopment, RareDiseases, MedicalEducation, AdvocacyGroups, VoluntaryDonation, TherapeuticInnovation]

19/02/2026

Thalassemia-Free India by 2035

The conclave, held January 10–11, 2026, in Hyderabad, earned rave reviews from global experts and policymakers for its powerful sessions and practical strategies toward eradication.

Dr. Pietro Sodani highlighted the event's collaborative energy in his testimonial: "Together, we are accelerating towards a healthier future!

[Genetics, Hematology, Blood Transfusion, Bone Marrow Transplant, Prenatal Screening, Hemoglobinopathy, Clinical Research, Community Outreach, Health Equity, SustainableDevelopment, RareDiseases, MedicalEducation, AdvocacyGroups, VoluntaryDonation, TherapeuticInnovation]

16/02/2026

Dr. Sushil Patil and a nine-member team from PATH (Maharashtra and Madhya Pradesh) visited the Thalassemia and Sickle Cell Society (TSCS) on 11–12 February 2026 for exposure visit. The program provided insights into the functioning of a well-established comprehensive care center and the end-to-end delivery of services for thalassemia management, with emphasis on transitioning from event-based interventions to a longitudinal continuum of care.
The team observed multidisciplinary patient care, safe transfusion practices, follow-up systems, and prevention initiatives including antenatal screening, carrier detection, and community awareness. The visit enabled knowledge exchange and offered valuable learning on comprehensive care and prevention strategies for thalassemia.

International Federation

Blood Disorders

15/02/2026

Wishing everyone a very Happy Mahashivratri! 🌿
On this auspicious day, the Thalassemia and Sickle Cell Society prays that Lord Shiva blesses every family with resilience, courage, and renewed hope. Just as the Lord conquered the darkest poison to protect the world, we draw inspiration to fight the challenges of blood disorders with strength and determination.
May this holy night bring health, positivity, and spiritual growth to you and your loved ones. Remember, the HbA2 test is available for Free at our centers in Hyderabad and Khammam.
For more information, reach out to us at 040-29885658 / 29880731 / 29885458 or email us at tscs@tscsindia.org.
Follow us for more updates.

[Kamala Hospital and Research Centre, India, Haemoglobinopathy, Genetic Disorder, Blood Disorder, Free Medical Camp, Haemoglobin Test, Patient Support, Courage and Resilience, Community Health, Transfusion Services, Paediatric Care, Hyderabad Events, Khammant Centre, Spiritual Strength]

14/02/2026

This Valentine's Day, let your love flow and make a difference that truly saves lives. 💖
❤️ TSCS, Hyderabad brings you a heartfelt opportunity to celebrate the season of love by donating blood and supporting those battling Thalassemia and Sickle Cell Disease. Your single donation can be the reason someone gets a second chance at life.

This February, visit TSCS and turn compassion into action. Also, avail the free HbA2 test at our Hyderabad and Khammam centers. Because the greatest gift you can give is the gift of life.

Let’s come together and spread hope! 🩸✨

[Thalassemia, Sickle Cell, Patients, Transfusion, Screening, Awareness, Hemoglobin, Treatment, Support, Donors, Health Camp, Khammam, NGO, Prevention, Counselling]

10/02/2026

"Thalassemia Free India by 2035" is the bold vision driving ATC 2026.

The conclave, held on January 10–11, 2026, in Hyderabad, received exceptional feedback from global experts and policymakers for its impactful sessions and actionable eradication strategies.

In her testimonial, Ratnavali Kottapalli, Vice President of the Thalassemia and Sickle Cell Society (TSCS), Hyderabad, emphasized the power of the collaborative spirit displayed during the event and beyond.

Together, we are accelerating towards a healthier future! 💙

[Genetics, Hematology, Blood Transfusion, Bone Marrow Transplant, Prenatal Screening, Hemoglobinopathy, Clinical Research, Community Outreach, Health Equity, SustainableDevelopment, RareDiseases, MedicalEducation, AdvocacyGroups, VoluntaryDonation, TherapeuticInnovation]

07/02/2026

At the Thalassemia and Sickle Cell Society (TSCS) in Hyderabad, we are moving Beyond Transfusions.

Towards a Cure. Our dedicated Kamala Hospital and Research Centre is a beacon of hope, having successfully performed 204 Total Bone Marrow Transplants (BMTs). This incredible milestone includes 157 Matched Family Donor transplants, 39 Haplo Transplants, and 8 Matched Unrelated Donor Transplants. We are committed to providing comprehensive care and advancing treatment options.

Remember, HbA2 tests are provided free of cost at our centers in Hyderabad and Khammam.
Join us in our mission to turn hope into healing.

[Treatment, Hematology, Cure, Transplant, Donor, Research, FreeTest, Hospital, Society, Support, Awareness, Genetic, BloodDisorder, PatientSupport, Lifesaving]

Address

Door No. 8-13-95/1/C, Opp Lane To National Police Academy, Raghavendra Colony, Shivarampally, Rajendranagar Mandal, Telangana
Hyderabad
500052

Telephone

+914029885658

Website

https://www.tscsindia.org/contact-us/

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Our Story

Thalassemia is a genetic blood disorder, people who are affected with Thalassemia have low hemoglobin which might lead to a severe anemia. Hemoglobin is found in 'Red Blood Cells' which helps in carrying 'Oxygen' to every individual body parts, when there isn't enough hemoglobin in the 'Red Blood Cells', oxygen cannot get to all parts of the body, where organs starve for 'Oxygen' and couldn't function properly. Patients who are affected by Thalassemia should go through regular blood transfusions for survival, usually every 2 to 3 weeks.

We at Thalassemia and Sickle Cell Society (TSCS), a registered NGO since 1998, strive hard to treat all the children who have been suffering from Thalassemia. We have just started with 20 patients at Banjara Hills, Hyderabad, whereas the number kept on increasing from day to day, in order to give quality service to the patients, now we have shifted to a bigger accommodation in 2009 so that we could provide the patients a safe and hygienic treatment.

We are equipped with the latest diagnostic and treatment facility which helps us in providing fast and risk-free treatment to the patients for free of cost. The society also provides medicines at subsidized rates, and record regular growth of children. Often there will be free medical and genetic counseling, and a team of specialized Doctors conducts medical checkups every now and then.

TSCS is now located at Door No. 8-13-95/1/C, Opp Lane to National Police Academy, Raghavendra Colony, Shivarampally, Rajendra Nagar, Rangareddy Dist – 500052, Telangana. Ph. 040-29885658 / 29880731 / 29885458