Round table of India Presented pride of Telangana to Thalassemia and Sickle Cell Society, Hyderabad TSCS under Achievers NGO Category 2026
Visit of Dr. K. Laxman, Member of Parliament, Rajya Sabha, to TSCS on the Occasion of 4,000 Voluntary Blood Donation Camps.
Hyderabad, 1st October 2026: The Thalassemia and Sickle Cell Society (TSCS) had the privilege of welcoming Dr. K. Laxman, Member of Parliament, Rajya Sabha, to the Vuppala Venkaiah Memorial Blood Centre, on the occasion of the successful completion of 4,000 voluntary blood donation camps organised by TSCS.
The milestone reflects the sustained efforts of TSCS in ensuring a regular and adequate supply of blood for thalassemia and sickle cell patients who depend on regular transfusions for their treatment and well-being.
On this occasion, Dr. K. Laxman felicitated the dedicated staff of the Blood Centre for their commitment and contribution towards achieving this significant milestone. Over the years, the voluntary blood donation programme has enabled TSCS to collect nearly 3 lakh units of blood, making a substantial contribution to the healthcare needs of patients with transfusion-dependent blood disorders.
The occasion was also an opportunity to acknowledge the invaluable contribution of voluntary blood donors, blood donation camp organisers, partner organisations, volunteers and the entire TSCS team, whose collective efforts have helped sustain this life-saving initiative.
TSCS remains committed to strengthening voluntary blood donation and ensuring timely access to safe blood for every patient in need.
Thalassemia and Sickle Cell Society (TSCS), Hyderabad, had the privilege of welcoming Mr. Ajay Gandhi, a UK-based Chartered Quantity Surveyor and consultant, who has been living with Thalassaemia Major for nearly 57 years, for an inspiring interaction with our Thalassemia and Sickle Cell warriors, patients, parents and TSCS team.
Mr. Gandhi was diagnosed with Thalassaemia Major at just six months of age and has successfully built a fulfilling professional and family life while continuing his treatment. His personal journey reflects the importance of perseverance, discipline, hope, family support and adherence to medical care.
During his visit, Mr. Gandhi shared his testimonial and life journey, speaking openly about the challenges he faced, the difficult phases of his treatment and the milestones he achieved in his personal and professional life. He encouraged the patients and young Thalassemia warriors not to allow the condition to limit their aspirations, but instead to set meaningful goals in life, work towards them with determination and believe in their ability to achieve them.
He particularly highlighted that living with Thalassaemia should not prevent anyone from pursuing education, building a career, having a family and leading a meaningful and fulfilling life. His own journey—from overcoming serious health challenges to establishing a successful career, marriage and family—served as a powerful message of hope for everyone present. His closing reflection emphasizes that Thalassaemia is a part of his life, but does not define who he is.
The interaction also provided an opportunity for patients, parents and the TSCS team to engage directly with Mr. Gandhi, ask questions, share experiences and receive motivation and guidance.
Mr. Ajay Gandhi’s visit was a deeply inspiring and memorable experience for the TSCS community. His message to the Thalassemia and Sickle Cell warriors was clear: dream, set goals, remain disciplined, take care of your health and never give up on your aspirations.
TSCS sincerely appreciates Mr. Ajay Gandhi for sharing his remarkable journey and for giving hope, confidence and encouragement to our patients and families.
“Thalassaemia is part of who I am, but it does not define who I am.” – Ajay Gandhi
TSCS Conducts Orientation Workshop on Thalassemia and Sickle Cell Anaemia in Vikarabad on 24th Sept 2026
The Telangana Thalassemia and Sickle Cell Society (TSCS) conducted a one-day orientation workshop on Thalassemia and Sickle Cell Anaemia at the District Collectorate Meeting Hall, Vikarabad, in coordination with the district health authorities. Around 200 participated the meeting.
The programme was attended by officials and healthcare professionals, including Government doctors, private gynecologists, AYUSH doctors, Medical Laboratory Technicians (MLTs), DM&HO officials and staff, with a focus on strengthening early identification, diagnosis and management of Thalassemia and Sickle Cell Anaemia.
Dr. K. Sudhakar Lal, District Medical and Health Officer (DM&HO), Vikarabad, highlighted that identifying Thalassemia and Sickle Cell Anaemia during pregnancy at an early stage can help prevent severe complications through timely intervention, appropriate treatment and counselling.
Dr. Ratnavalli, Sr. Vice President of TSCS, along with Mr. Hemant Kumar, Coordinator, TSCS, conducted the orientation and educated the participating medical professionals on the early identification of symptoms, diagnostic procedures, management and appropriate referral of patients with Thalassemia and Sickle Cell Anaemia. Participants were also encouraged to attend the GANSID International Congress 2026, to be held at HICC-Novotel, Hyderabad, from October 23–25, 2026, to further strengthen knowledge, collaboration, and professional engagement in the field.
The workshop emphasized the importance of strengthening antenatal screening and early diagnosis to improve maternal and child health outcomes and move towards a Thalassemia- and Sickle Cell-free Telangana.
Mahbubnagar, September 8, 2026: An awareness programme on Antenatal Screening for Thalassemia and Sickle Cell Anaemia was organised at the IDOC Meeting Hall, Mahbubnagar Collectorate, by the District Medical and Health Office (DMHO), Mahbubnagar, in collaboration with the Thalassemia & Sickle Cell Society (TSCS).
The programme focused on prevention, early detection, genetic counselling, and appropriate management of inherited blood disorders, supporting the goal of a Thalassemia-Free Telangana.
The sessions were conducted by Dr. Suman Jain, Founder Member, Chief Medical Research Officer & Secretary, TSCS; Mrs. Ratnavali, Founder Member & Vice President, TSCS; and Dr. G. Padma, Head of Research, TSCS. They highlighted the importance of systematic antenatal screening, carrier identification, timely counselling, and preventive interventions.
DMHO Dr. Srinivasulu and Programme Officer Dr. Shankar attended along with Medical Officers, Community Health Officers, Health Supervisors, and Laboratory Technicians. Around 180 healthcare personnel participated actively in the programme.
TSCS has so far screened approximately 25,000 antenatal women in Mahbubnagar, identifying a carrier frequency of around 2.5%. These efforts help enable early identification, counselling, and preventive measures to reduce affected births.
The TSCS team was felicitated by the DMHO in recognition of its contribution to antenatal screening and prevention. Participants were also encouraged to attend the GANSID International Congress 2026, to be held at HICC-Novotel, Hyderabad, from October 23–25, 2026, to further strengthen knowledge, collaboration, and professional engagement in the field.
Sankalp India Foundation, Bengaluru, celebrated the milestone of 1,000 successful Bone Marrow Transplants (BMTs) through the “1000 Beginnings Scientific Meeting: Building the Path to Eliminate Severe Hemoglobin Disorders,” held on 5 September 2026 in Bengaluru.
The event brought together healthcare professionals, patient-support organizations, experts, and stakeholders working towards improving outcomes for individuals living with severe hemoglobin disorders.
Representing the Thalassemia and Sickle Cell Society (TSCS), Hyderabad, Dr. Suman Jain, Chief Medical Research Officer and Secretary, Mr. Manoj Rupani, Treasurer, and Dr. Saroja K, Medical Officer, participated in the celebrations.
Dr. Suman Jain delivered an insightful talk on “Value in Blood Services: Are We Investing in the Right Things?”, highlighting the importance of strengthening blood services and ensuring that investments translate into meaningful and sustainable benefits for patients.
TSCS congratulates Sankalp India Foundation on this remarkable achievement and its continued commitment to improving access to quality treatment and care for patients with severe hemoglobin disorders.
Together, we can build a path towards a future free from the burden of severe hemoglobin disorders.
Turning wishes into moments of joy, confidence and hope
A Wish Can Change a Day. A Dream Can Change a Life.
For children and young people living with thalassemia and sickle cell disease, life often involves regular treatment, hospital visits and challenges that can overshadow the simple joys of childhood. The Thalassemia and Sickle Cell Society (TSCS), Hyderabad, facilitates the connection between its patients and the Make-A-Wish Foundation, helping eligible patients share their dreams and supporting the wish-fulfilment process. Make-A-Wish then works to turn those wishes into reality, bringing moments of happiness, confidence and hope to our warriors.
Through this ongoing initiative, our Thalassemia and Sickle Cell warriors are given an opportunity to dream beyond their illness—to experience happiness, confidence and the feeling that their wishes matter. Make-A-Wish helps turn those personal dreams into memorable experiences and meaningful gifts.
From Everyday Joys to Big Dreams
The wishes of our patients are as unique as their personalities. Some dream of something that can bring everyday happiness, while others imagine themselves in inspiring professions and roles of responsibility.
Wishes expressed by our warriors include receiving bicycles, mobile phones, televisions and laptops, as well as
| Wish / Dream | What it Represents |
|---|---|
| Bicycles | Freedom, fun, confidence and the joy of being |
| Mobile phones | Connection, communication and a sense of independence. |
| Televisions | Entertainment, relaxation and shared family moments. |
| Laptops | Learning, education, creativity and future opportunities. |
| Dream careers | Hope and ambition—such as aspiring to become a loco pilot or Commissioner. |
A Continuing Journey of Wishes
The partnership with Make-A-Wish is not a one-time activity. The Thalassemia and Sickle Cell Society (TSCS), Hyderabad, facilitates this initiative for its patients on a regular basis, helping identify and coordinate eligible wishes. Once every quarter, wishes of our patients are supported and fulfilled, creating repeated moments of joy throughout the year. Each fulfilled wish is a reminder that our warriors are seen not only as patients, but as children and young people with dreams, talents and ambitions.
By making these wishes possible, Make-A-Wish contributes to a positive and uplifting experience for the warriors and their families. The smiles captured during wish fulfilment events reflect the emotional value of these moments.
Every gift carries a story. Every smile carries a dream.
26th August 2026 – Milad Blood Donation Camp
On the auspicious occasion of 12th Rabi-ul-Awwal (Milad), a voluntary blood donation camp was organised by Forum for Cultural Upgradation & Social Service (FOCUSS) and Tanzeem Irshad-ul-Muslimeen at the Central Library, Afzalgunj, Hyderabad, on 26th August 2026.
The camp received an overwhelming response, with around 650 units of blood collected for the treatment and support of Thalassemia patients.
Thalassemia and Sickle Cell Society (TSCS) sincerely appreciates and thanks the organisers and all the voluntary blood donors for their continued support and commitment towards Thalassemia patients. Their valuable contribution helps ensure a steady and timely supply of blood for patients who depend on regular transfusions.
A meaningful gesture of compassion, service, and humanity that truly made a difference.
