The burden of Thalassemia is overwhelming in India, with more than 10,000 thalassemic children born every year. In India, DKMS partners with like-minded NGOs and transplant centers, providing care for Thalassemia patients. These partners organize thalassemia awareness camps.
A DKMS-supported thalassemia awareness camp is a collaborative intervention conducted in partnership with local organizations to:
In this process, partners lead end-to-end execution (patient mobilization, venue, permissions, and on-ground coordination and execution of camps), while DKMS supports diagnostic access, technical expertise, and program oversight to all of their partners.
In these local thalassemia camps for pediatric thalassemia patients, the patient families travel from far places, sometimes from very remote corners of India. At these camps, the patients and their parents and siblings provide buccal swab samples for HLA typing to identify whether there is a suitable family donor. Samples from the camps are analyzed in the DKMS laboratory, and clinical matching reports are provided. In case, if there is no match within the family then we also support with free unrelated donor searches.
Financially underprivileged thalassemia patients in India who are:
Patients must meet the following criteria to be eligible for HLA typing:
Patients who meet the above eligibility criteria can write to our Thalassemia program managers at thalprogram@dkms-india.org. NGOs and Transplant Centers that are interested in knowing more about this program can also write to thalprogram@dkms-india.org
