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News
Seminar on "Iron Chelation in Thalassaemia: Present and Future Prospects" PDF Print E-mail
Wednesday, 12 December 2007
ImageBangladesh Thalassaemia Foundation and Bangladesh Society of Hematology jointly organized a seminar entitled “Iron Chelation in Thalassaemia: Present and future prospects” at BIRDEM auditorium in the city on December 12, 2007. Eminent specialist physicians of the country discussed about the importance of iron chelation in the treatment of thalassaemia.

Chairman of the Hematology Department of Bangabandhu Sheikh Mujib Medical University (BSMMU) and President of Bangladesh Society of Hematology Professor Dr Jalilur Rahman was present as the chief guest while President of Paediatric Society of Bangladesh Professor Dr M A Mannan and Secretary General of Bangladesh Society of Hematology Professor Dr M A Khan were present as Special Guests in the seminar.
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Country's first DNA Lab for Thalassemia opens at BSMMU PDF Print E-mail
Monday, 17 September 2007
ImageThe first DNA laboratory for diagnosing thalassaemia opened at Bangabandhu Sheikh Mujib Medical University on Monday, 17 September 2007. "Thalassaemia is one of the deadliest child diseases in the country. The launch of the DNA lab to diagnose the disease is a promising event," said health adviser ASM Matiur Rahman, who attended the inaugural session as chief guest. Thalassaemia is an inherited blood disease-a genetic disorder that results in a reduced rate of synthesis of one of the globin chains that make up haemoglobin. "The government is contemplating subsidising the lab to enable the poor to receive the services," the adviser said. The function was chaired by BSMMU pro-vice chancellor and head of the child Haematology and Oncology Department Dr MA Mannan.

-BDNEWS24.COM, DHAKA
 
International Thalassemia Day `07 observed in Bangladesh PDF Print E-mail
Thursday, 31 May 2007
Image
Poster
International Thalassemia Day was observed in Bangladesh as elsewhere in the world with a view to raise awareness on Thalassemia. A number of organizations held discussions, seminars, rallies, and voluntary blood donation program across the country on the occasion of the day. Thalassaemia affects more then 7% of Bangladesh's population today which means roughly 11.2 million Bangladeshi are thalassemia carriers. It is estimated that about 7,483* children are born with the disease every year with expected 3,74,154* living patients.

This year the day was marked by joint programs arranged by different organizations working on thalassemia. The association of Bangladesh Thalassemia Foundation and Hematology Society of Bangladesh with an aim to promote “Standard and Quality Care” among the physicians and patients is first time ever in Bangladesh and will have a great impact in the field of thalassemia care in the country. Another important progress was made by involvement of the telecommunication giant Grameenphone in the event by patronizing Bangladesh Thalassemia Society.
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We got a computer from Ashfaque Memorial Fund PDF Print E-mail
Monday, 28 May 2007

ImageWe have got a new computer as kind donation from Ashfaque Memorial Fund. Dr Syeda Masooma Rahman on behalf of The Fund handed over the computer at our office on May 22, 2007. With increased volume of correspondence and workload at our office we felt the need of a computer which is fulfilled with this donation. We are thankful to Dr Masooma for choosing us for the donation.

The Ashfaque Memorial Fund usually contributes in places where patients directly get the benefit. Their immediate past donation was a fine ophthalmoscope to the Unit 3 of Department of Medicine, Sir Salimullah Medical College, Dhaka. The fund was originally organized to support the bone marrow transplantation of Ashfaque Hossain, a bright medical student of 11th batch of Sher-e-Bangla Medical College, Barishal who had Acute Myeloid Leukemia (AML).

 
Weekly meeting for patients and parents PDF Print E-mail
Friday, 10 February 2006
BTF introduces weekly educational meeting for thalassemia patients and parents each Friday at 4:00 PM. The meeting will consist disscussion with patients and parent on different aspect of thalassemia.
 
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