MAC-SALVE Sickle Cell Foundation

Frequently Asked Questions

Frequently Asked Questions (FAQ)

Below, you'll find the questions that people frequently ask regarding our foundation and the mission we champion. These inquiries shed light on our cause, providing insight into our work and the impact we strive to make in the community affected by sickle cell disorder.

Sickle cell disorder is a genetic blood disorder that affects the shape of red blood cells. It can lead to various health complications due to the abnormal shape of the cells.

Sickle cell disorder is inherited in an autosomal recessive manner, meaning both parents must pass on the mutated gene for a child to have the disease.

Common symptoms include chronic pain, fatigue, jaundice, and susceptibility to infections.

Currently, there is no cure for sickle cell disorder, but ongoing research is leading to promising treatments.

You can support us by donating, volunteering, or participating in our fundraising events. Your contributions help us further our mission.

To become a volunteer, please visit our "Get Involved" page and fill out the volunteer form. We'll get in touch with you with more details.

Yes, we greatly appreciate donations. You can make a donation through our website's donation portal.

Donations are used to fund research, provide support to individuals and families affected by sickle cell disease, and raise awareness about the condition.

Yes, we have support groups where individuals and families can connect, share experiences, and find emotional support. Check our events page for upcoming meetings.

You can reach us through our "Contact Us" page on the website or by sending an email to info@macsalve.org.