Marginalised tribal communities face difficulties in accessing basic healthcare and diagnostics of Sickle cell disease (SCD)
Progress and Challenges in Battling Sickle Cell Disease in India
Sickle cell disease (SCD) stands as a formidable challenge in the realm of healthcare, casting a shadow over the lives of millions worldwide. This inherited haemoglobin disorder, characterized by the abnormal shape of red blood cells, not only inflicts physical suffering but also imposes a heavy burden on affected individuals and their families. In India, where SCD poses a significant public health concern, recent initiatives and advancements offer a glimmer of hope amid persistent challenges.
At the core of SCD lies a genetic mutation that causes red blood cells to assume a crescent or sickle shape, leading to impaired circulation and a cascade of health complications. Anaemia, organ damage, excruciating pain episodes, and premature death haunt those grappling with this condition. India, despite its vast strides in healthcare, grapples with a staggering burden of SCD, ranking third globally in the number of births afflicted with this ailment.
In response to the alarming prevalence of SCD, the Government of India launched the National Sickle Cell Anaemia Elimination Mission in 2023, setting an ambitious target to eradicate the disease by 2047. This mission represents a significant step towards addressing the multifaceted challenges posed by SCD, encompassing prevention, screening, treatment, and research.
However, the journey towards SCD eradication is fraught with obstacles. Access to essential treatments remains grossly inadequate, exacerbating the suffering of those afflicted. Hydroxyurea, a critical medication for managing SCD, faces availability issues, leaving many patients without proper care. Moreover, while blood transfusion and bone marrow transplantation hold promise as therapeutic avenues, their accessibility is marred by logistical and financial barriers.
Amid these challenges emerges a beacon of hope in the form of CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) technology. This revolutionary gene-editing tool offers unprecedented opportunities for treating SCD by rectifying the underlying genetic abnormalities. Recent approvals of gene therapies by regulatory authorities signal a paradigm shift in the approach to combating this debilitating disease.
In India, the potential applications of CRISPR for SCD treatment raise profound ethical and legal considerations. While the National Guidelines for Stem Cell Research impose restrictions on commercialization and mandate stringent regulations, research initiatives to harness CRISPR's potential are underway. The Council of Scientific and Industrial Research's efforts to develop gene-editing therapies underscore India's commitment to leveraging cutting-edge technologies in the battle against SCD.
As India marches towards a future free from the shackles of SCD, it is imperative to adopt a holistic approach that addresses existing healthcare inequities. Promoting accessibility, affordability, and inclusivity in healthcare services is paramount to ensure that the benefits of advanced therapies like CRISPR reach all strata of society. By forging partnerships, fostering innovation, and prioritizing equity, India can turn the tide against SCD and pave the way for a healthier, more resilient future.
In the relentless pursuit of progress, let us unite in our resolve to unlock hope and build a world where SCD is but a distant memory.
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