Sickle cell disease (SCD) is a common inherited blood disorder of public
health concern in India. Individuals with SCD may encounter stigma,
discrimination, and misconceptions about their condition, leading to
feelings of isolation and frustration. It is important to note that the
psychological impact of SCD can vary among individuals. Some may develop
resilience and coping strategies to manage the challenges, while others
may require additional support from healthcare professionals,
psychologists, or support groups to address their psychological needs.
The multidisciplinary approach involving medical care, psychological
support, and social interventions is crucial in improving the overall
well-being of individuals living with sickle cell disease. While the
clinical aspects of SCD are significant, it’s also important to consider
the psychological aspects that can affect individuals with the
condition. In this context, there is a pressing need for societal
support pillars which empower SCD patients and improves their quality of
life. In this context, there is a pressing need for societal support
pillars which empower SCD patients and improves their quality of life.
The impact of societal support pillars on SCD patients is substantial.
Strengthening healthcare systems, fostering robust social support
networks, facilitating inclusive educational environments, and raising
public awareness are integral components of comprehensive care for
individuals living with SCD. All these pillars can significantly improve
the quality of life and outcomes for SCD patients, ultimately leading to
a more inclusive and supportive society.