Founded in 2021 as We Are Not Alone (WANA), our initiative grew from the determination of thalassemia patients and parents who wanted to break the silence surrounding this disease. In 2025, we became officially registered as BTPWA under the Department of Social Services, Government of Bangladesh (Registration Number: DHA-010087, Date: 19 March 2025).
With the slogan “We Are Not Alone”, the Bangladesh Thalassemia Patients and Parents’ Welfare Association began its journey on December 25, 2021. Over the past four years, the organization has conducted a range of impactful programs, including thalassemia carrier screening and awareness campaigns, patient and parent meetups, medical consultation sessions with specialists, Zakat-based financial assistance, distribution of winter clothing, as well as TV appearances and online awareness initiatives.
Our activities include-
Thalassemia Patients and Parents’ Meet-up: Since our journey began in 2021, we have been organizing meet-up programs every year. In addition to thalassemia patients and their families, doctors, researchers and experts, representatives of pharmaceutical companies, diagnostic labs, blood banks and treatment centers, thalassemia activists and well-wishers, and many others participate in these programs.
Thalassemia Carrier Screening and Awareness: We have been organizing awareness seminars and carrier detection (through hemoglobin electrophoresis test) programs among students of various educational institutions and with various professionals in offices in Dhaka and outside Dhaka.
Zakat, Donations and Winter Clothes Distribution: Zakat and donations are collected and financial assistance is provided to poor thalassemia patients for regular treatment or to make them self-reliant. In addition, winter clothes are distributed among patients during winter and new clothes are given to child patients and their mothers during Eid.
Medical consultation program with thalassemia or hematologists: Programs are regularly organized online with expert doctors to solve various problems of thalassemia patients and improve their quality of life. Such programs are organized so that patients living outside Dhaka from all over Bangladesh can easily get advice from experienced hematologists in Dhaka. In these programs, patients and their guardians get various advice on the disease through direct question and answers
Conduct thalassemia prevention awareness programs in educational institutions in Dhaka and outside Dhaka
Organize meetings and consultative events with specialist physicians to improve the quality of thalassemia treatment
Arrange voluntary blood donation programs for thalassemia patients and develop donor pools involving patients’ family members
Broadcast thalassemia awareness documentaries through social media and mass media
Implement joint awareness campaigns across different parts of the country in collaboration with social welfare organizations and professionals from various fields
Hold meetings with the Honorable Minister of Health to raise demands related to thalassemia treatment
Engage celebrity figures as goodwill ambassadors and disseminate their individual awareness messages on thalassemia
Conduct awareness campaigns in mosques and other religious places of worship with the support of religious leaders of all faiths
Collect Zakat and donations to provide financial assistance to underprivileged thalassemia patients and distribute winter clothing
Arrange awareness-building and skill-oriented training sessions and workshops for patients
Facilitate hemoglobin electrophoresis testing for unmarried individuals and students through government, private, or individual initiatives
Coordinate with the Ministry of Social Welfare regarding employment opportunities and national registration for thalassemia patients and draw the attention of the government