Faith is a cheerful 20-year-old student from Kenya and the youngest of three siblings. Hailing from Makueni County, she has just finished high school, achieving a grade that allows her to pursue her dream of becoming a teacher. Faith's parents are both small-scale farmers, primarily growing maize and beans to support their family. Faith was born healthy, but when she was seven years old, she began experiencing pain in her right foot. Initially, her parents took her to a nearby hospital, where they were told that her foot was fine. Concerned but without a solution, they sought help from APDK, where Faith received a brace, but her condition did not improve. Eventually, a friend recommended our medical partner's care center, AIC CURE Hospital. Faith has clubfoot in her right foot, a condition that twists the foot out of shape, making walking and wearing shoes difficult. She is currently undergoing serial casting to prepare for surgery to correct her condition. Our medical partner, African Mission Healthcare, is helping Faith receive treatment. On November 12th, surgeons will perform clubfoot repair surgery to help Faith regain her foot's function. Now, Faith's family needs help to fund this $1,286 procedure. Faith says, "I am looking forward to complete healing so that I can walk easily, continue my studies, and achieve my dream career."

Jasmin is an 11 year-old girl from Bolivia who needs heart surgery. Jasmin lives with her father, a police officer, and her mother, a nurse. She has one older brother and one younger sister in La Paz. Jasmin likes to paint, draw in coloring books, and help her family with errands. Jasmin was born with Down syndrome, and also a cardiac condition called patent ductus arteriosus, in which a hole exists between two major blood vessels near the heart. Blood leaks through this hole, leaving Jasmin weak and short of breath. Our medical partner International Cardiac Alliance is requesting $1,500 to fund surgery to repair Jasmin's heart. During surgery, doctors will sew the hole closed so that blood can no longer pass through it. Once her heart is repaired, Jasmin will be able to breathe easier and have more energy and ability to make the most of everyday. Jasmin's mother shares: "we're so happy that the time has finally arrived for her surgery, our family has been waiting a long time for this moment."

Chan Bora is an angelic baby boy from Cambodia. He lives with his parents, his 10-year-old sister, and his 8-year-old brother in Phnom Penh province. His parents work as fruit sellers at the local market, often taking Chan Bora with them when his siblings are in school. His favorite pastime involves playful interactions with items left on the floor, especially his siblings' toys. Additionally, he has a fondness for nutritious duck eggs prepared by his mother. Chan Bora has clubfoot of both feet. Clubfoot is a condition in which the foot is twisted out of shape. This causes difficulty walking and even wearing shoes. Fortunately, Chan Bora's family traveled one and a half to visit our medical partner, Children's Surgical Centre (CSC). There, surgeons will perform bilateral tendo-achilles lengthening and casting to correct the foot equinus (pointing down) position on January 9th. CSC is requesting $444 to fund Chan Bora's clubfoot repair. After treatment, both of the affected tendons in his feet will stretch and grow into the right position, allowing him to walk as he grows. Chan Bora's mother said: "I hope after surgery and taking off the cast, he can run around like other children."

Festus is a three-month-old infant from Kenya. His mother gave birth to him while she was still in high school, and she had to discontinue her studies to care for him. Festus and his mother were driven out of their home by his grandfather, and although a relative has provided them with shelter, they lack the financial means to support themselves or cover their medical expenses. Festus' mother got to know about our medical partner's care center, BethanyKids, through a mobile clinic in their locality, following which they were referred to the hospital for treatment. At BethanyKids, Festus was diagnosed with spina bifida, a congenital neural tube defect in which the spine does not properly close around the spinal cord. Without treatment, Festus is at risk of lower-limb paralysis, infection of the exposed nervous tissue, development of tethered cord syndrome, and possible developmental delays. Fortunately, our medical partner, African Mission Healthcare, is helping Festus receive treatment. On March 20th, surgeons at BethanyKids will perform a spina bifida closure surgery to alleviate the risks associated with the condition, allowing him to grow and develop along a healthy trajectory. Now, Festus' family needs help to fund this $1,151 procedure. Festus’ mother says “It is very painful seeing him with the swelling at the back. I wish to see him healed so he can grow up as other children.”