Frequestly Asked Questions

Sickle Cell Anemia is a genetic blood disorder that affects the production of hemoglobin in red blood cells. The abnormal hemoglobin causes the red blood cells to become stiff and sickle-shaped, which can block blood flow and cause damage to organs and tissues.

Sickle Cell Anemia is an inherited disorder that is passed down from parents to their children. A child can only inherit Sickle Cell Anemia if both parents carry the gene for the disease. If both parents carry the gene, there is a 25% chance that their child will inherit the disease.

The symptoms of Sickle Cell Anemia can vary from person to person and can range from mild to severe. Common symptoms include pain, fatigue, jaundice, and swelling of the hands and feet. Individuals with Sickle Cell Anemia are also at increased risk of infections, stroke, and organ damage.

Currently, there is no cure for Sickle Cell Anemia. However, there are treatments available that can help manage the symptoms and complications of the disease. Treatment options include pain management, blood transfusions, and bone marrow transplants.

Certainly! At Favoured, the Lord Delights in You Foundation, we believe that awareness and sensitization are critical in the fight against Sickle Cell Anemia. We carry out various awareness campaigns to educate people about the disease, its symptoms, and how to manage it. Our awareness campaigns include: 1. Media campaigns: We use various media platforms, including radio, TV, and social media, to create awareness about Sickle Cell Anemia. We produce and broadcast jingles, documentaries, and public service announcements to reach a wide audience. 2. Community outreach: We organize community-based programs and events to engage with people at the grassroots level. We partner with local leaders, schools, and religious organizations to create awareness and provide education about the disease. 3. Sensitization workshops: We conduct sensitization workshops for healthcare workers, teachers, and other professionals who work with people living with Sickle Cell Anemia. These workshops provide them with the knowledge and skills to manage the disease effectively. 4. Advocacy: We engage with policymakers and stakeholders to advocate for policies and programs that support people living with Sickle Cell Anemia. We also advocate for increased funding for research and treatment of the disease. Our awareness campaigns have been successful in reaching a wide audience and raising awareness about Sickle Cell Anemia. We believe that through continued education and sensitization, we can reduce the prevalence of the disease and improve the quality of life for those living with it.

We appreciate your interest in getting involved with Favoured, the Lord Delights in You Foundation! There are several ways you can support our mission of creating a Sickle Cell free Society: 1. Make a donation: Your financial support can go a long way in helping us provide care and support for people living with Sickle Cell Anemia, as well as creating awareness and sensitization programs. You can make a donation on our website or contact us for more information on how to donate. 2. Volunteer: Our organization relies on the support of volunteers to help us carry out our programs and services. We welcome volunteers with a passion for our cause, and we offer a variety of roles that can fit different skills and schedules. Contact us to learn more about our volunteer opportunities. 3. Spread the word: You can help us create awareness about Sickle Cell Anemia by sharing our message on social media, telling your friends and family about our organization, and participating in our events and campaigns. 4. Partner with us: We welcome partnerships with organizations and individuals who share our vision and goals. If you would like to explore partnership opportunities, please contact us to discuss further. Thank you for your interest in supporting our organization. Your involvement can make a significant difference in the lives of people living with Sickle Cell Anemia.

There are several misconceptions about Sickle Cell Anemia that we have encountered in our work at Favoured, the Lord Delights in You Foundation. These misconceptions include: 1. Sickle Cell Anemia is contagious: Sickle Cell Anemia is a genetic disorder and is not contagious. It is inherited when both parents carry the sickle cell trait. 2. People with Sickle Cell Anemia cannot have children: While people with Sickle Cell Anemia may face challenges in having children, it is not impossible. With proper medical care and counseling, many people with the disease have healthy children. 3. Sickle Cell Anemia only affects Africans: Sickle Cell Anemia is most prevalent in people of African descent, but it also affects people of Hispanic, Middle Eastern, and Mediterranean descent. 4. Sickle Cell Anemia is only a childhood disease: While Sickle Cell Anemia is often diagnosed in childhood, it is a lifelong chronic condition that requires ongoing medical care and management. 5. Sickle Cell Anemia is curable: There is currently no cure for Sickle Cell Anemia, but treatment options such as medication, blood transfusions, and bone marrow transplants can improve the quality of life for people living with the disease. It is important to address these misconceptions to create a better understanding of Sickle Cell Anemia and reduce the stigma associated with the disease. Through our awareness and sensitization programs, we aim to educate people and dispel these myths.

People with Sickle Cell Anemia may face several challenges in having children, including: 1. Increased risk of passing the disease to their children: Sickle Cell Anemia is an inherited genetic disorder. If both parents carry the sickle cell trait, there is a 25% chance of passing the disease to their children. 2. Increased risk of complications during pregnancy: Women with Sickle Cell Anemia may have a higher risk of complications during pregnancy, including miscarriage, premature birth, and stillbirth. 3. Increased risk of maternal and fetal complications: Sickle Cell Anemia may increase the risk of maternal complications such as anemia, infections, and pre-eclampsia. It may also increase the risk of fetal growth restriction, low birth weight, and neonatal death. 4. Need for specialized medical care: People with Sickle Cell Anemia require specialized medical care, which may include regular blood transfusions and medication. This can be challenging during pregnancy and may require close monitoring by a medical team. 5. Emotional and psychological challenges: The challenges of managing Sickle Cell Anemia during pregnancy can take a toll on a person's emotional and psychological well-being. People with the disease may experience anxiety, depression, and stress related to the pregnancy. It is important for people with Sickle Cell Anemia who are planning to have children to seek counseling and medical advice to understand the risks and options available to them. With proper medical care and support, many people with the disease have healthy pregnancies and children.

There are several ways to support individuals and families affected by Sickle Cell Anemia. You can donate to organizations that provide education, advocacy, and support for those living with the disease. You can also volunteer your time and skills to help raise awareness and provide support to individuals and families affected by the disease. Lastly, you can help spread awareness about Sickle Cell Anemia by sharing information and resources with your friends, family, and community.