Hana is a cute and happy baby who loves playing with toys and interacting with the people around her. Her favorite foods are porridge with bread and pasta. She is the only child of her parents. Her mother used to sell candles at church gates, and her father is in the military, though he currently has no contact with the family. Last year, Hana started refusing her mother’s milk, and her abdomen began to swell. Her mother was extremely concerned about her baby's condition and immediately took Hana to the clinic. Hana was diagnosed with Hirschsprung's Disease, a condition in which missing nerve cells in the large intestine cause intestinal blockage. Further referrals led her to our medical partner, African Mission Healthcare, who will help Hana and her mother with a treatment plan. Now, African Mission Healthcare is asking for $1,500 to help fund Hana's Hirschsprung's pull-through surgery scheduled for March 16th. Hana's mother said, “After her surgery, I want her to be well and to grow healthy. I will send her to school. I will try my best to give her a better life, and I don’t want her to suffer as I did. I hope she will be wise and independent in her future.”

Sephania is a baby from Simanjiro, Arusha in Tanzania. He lives among the Maasai people. He comes from a large family of six siblings, raised by a single mother. His father died shortly after he was born, and his mother depends on her brothers, who are cattle breeders. They help provide basic needs for the family since his mother does not work and has no means to earn a living. Sephania was born with both his legs twisted inward and downward. His mother was informed that there was treatment for the condition. She could not afford transport money at the time and had to wait for almost 2 years before she was able to collect enough money to travel to a medical center. She arrived at our center with an escort, who helped her translate as she only speaks Maasai. After a brief assessment with our team, we set up a treatment plan for Sephania, starting with a series of castings. Sephania has clubfoot on both feet. Clubfoot is a condition in which the foot is twisted out of shape. This causes difficulty walking and even wearing shoes. Fortunately, Sephania traveled to visit our medical partner's care center, Arusha Lutheran Medical Centre. There, surgeons will perform clubfoot repair surgery on May 12th. Our medical partner, African Mission Healthcare Foundation, is requesting $935 to fund Sephania's clubfoot repair. After treatment, he will be able to walk easily. Sephania’s mother says, "It has taken a while to be able to come for treatment. I hope my son will get treatment that will help with his foot’s condition."

Peter is a 5th grade student from Kenya. He is an only child being raised by his single mother, who works as a hotel waitress earning about $70 per month. The family also has a small tea plantation in their ancestral home, but are unable to raise the funds needed for Peter's surgery. Peter has been diagnosed with hydrocephalus, a condition in which excess cerebrospinal fluid accumulates in the brain and increases intracranial pressure. As a result of his condition, Peter has been experiencing difficulty in holding things and walking. The condition has affected his appearance, with a change in the color of his eyes. Over time, he has developed urine and stool incontinence. His worried mom decided to seek treatment from several hospitals. Doctors determined that Peter needs a special surgery that will relieve pressure from the skull. Without treatment, Peter will experience severe physical and developmental delays. Our medical partner, African Mission Healthcare Foundation, is requesting $720 to cover the cost of surgery for Peter. The procedure is scheduled to take place on January 11th, and will drain the excess fluid from Peter's brain. This will reduce intracranial pressure and greatly improve his quality of life. With proper treatment, Peter will hopefully develop into a strong, healthy young boy. Peter’s mother says, “Peter has been sickly and has been missing school for almost a year now. This condition is affecting his school life. He needs this treatment to recover and go back to school.”