Welcome to Sickle Cell Solutions International

Together, Let's Make a Difference.

At Sickle Cell Solutions International,
we aim to
uplift the quality of life for low-income families with chronic sickle cell disease.

We aim to extend the lives of those suffering from this condition by imparting knowledge about effective care management and reducing the frequent and often life-long crises associated with the disease.

STORY

THE PROBLEM

Sickle cell disease is an often misunderstood and overlooked genetic condition that targets millions worldwide, predominantly those of African, Middle Eastern and Asian descent. The disease is characterized by a life-long battle with immense pain, with the possibility of no definitive medical cure.

Sickle cell disease doesn't care about your income status. It is chronic and debilitating, and the obstacles littering the path to effective management manifold - from lack of awareness and education about the disease, disparities in access to necessary preventive and pain management care, to a vacuum in nutritional knowledge essential for reducing painful episodes.

what we do

We are here to help you navigate through the storm. Sickle Cell Solutions International focuses on:

1

Providing education on crisis prevention care to parents of children with sickle cell disease.

2

Facilitating access to fundamental medical care for children experiencing acute sickle cell crises.

3

Offering low-cost resource tools to mitigate episodes of debilitating pain crises in children living with sickle cell disease.

Meet the Team

We are led by a dedicated team of professionals, experienced and passionate about making a meaningful difference in the lives of those battling sickle cell disease. Meet our President and Executive Director, Professor Aseye Djokotoe, Ph.D, and our Vice President and Operations Director, Hilda M Djokotoe, MS, VRC.

Where we work

Currently, we are focused on working within communities in Ghana, with plans to expand into the neighboring countries in the long term.

how we work

We use resources efficiently and sustainably by using volunteer healthcare providers in the local communities. We partner with community health nurses and medical professionals in local health centers in our target locations. We raise the needed funds to pay for travel and meals for volunteer health workers to make regular home visits and continue to partner with parents and caregivers of children with sickle cell disease in areas with limited access to healthcare. These local healthcare providers serve as resources on the ground to communicate next steps and strategies for maximizing the impact of our resources.

We also hold community education events in partnership with specialists to provide information to patients of all ages and their caregivers.

Who we serve

We work to support low-income children and adults living with sickle disease in different ways. We play a more hands-on role with babies and teenagers by providing tangible resources including food, access to medication, access to basic supplies that are hard to come by, and connections to healthcare systems.

For adults, we mainly provide education on self-care and connections to the appropriate healthcare partners to help them manage their condition for optimal health.

TOGETHER, WE CAN FIGHT SICKLE CELL DISEASE

Join us in our mission. Your generous involvement and contribution can fuel the change we wish to see in the world.

Every contribution brings us closer to a better future for children with sickle cell disease. Thank you for deciding to make a difference today.