Happiness's baby is a newborn who is barely two weeks old. Happiness and her husband, James, have been blessed with a new baby, expanding their family to two children. They reside in Morombo, located in the Arusha region of Tanzania. Happiness is a stay-at-home mother managing the household and caring for their children, while James works diligently on their farm to provide food and sells surplus harvests for additional income. In addition to farming, James seeks casual day jobs to supplement their finances, yet despite their efforts, they find their income insufficient to cover all expenses. At times, they struggle to afford medical bills, particularly when faced with a poor harvest, making providing adequate meals for the family challenging. Happiness's baby was born with clubfoot of both feet, causing his feet to twist inward and downward. Concerned for their son’s future, the parents sought advice from the attending doctor, who recommended seeking treatment, as the condition is treatable. They were referred to our medical partner's care center for help. Clubfoot is a condition in which the foot is twisted out of shape. This causes difficulty walking and even wearing shoes. Fortunately, Happiness traveled to visit our medical partner's care center, Kafika House. There, the team will begin clubfoot treatment on February 16th. Our medical partner, African Mission Healthcare, is requesting $935 to fund Happiness's baby's clubfoot repair. After treatment and as he grows, the baby will be able to wear shoes and walk properly. Happiness says: “I want my baby to grow up with normal feet and never bear the burden of the condition he is born with.”

Koem Long is a 21-year-old who works in construction - ever since his motorcycle accident he hasn't been able to work. He is an only child and lives with his elderly grandparents. Currently, he stays at home to assist his grandparents and enjoys watching TV in his free time. Two months ago, Koem Long collided with another motorbike on his way home from work. He fell on the pavement, fracturing his jaw and injuring his right shoulder. He went to a local government hospital to repair his fractured jaw but was told they could not repair his shoulder. He has been diagnosed with a brachial plexus injury on his right side. The brachial plexus is a nerve network that transmits signals from the spine to the shoulder, arm, and hand. Injuries to this nerve network can result in loss of function and sensation. Two months later, his right arm is still non-functional. He cannot lift his shoulder or move his arm. Koem Long feels pain and is very disappointed that he cannot help his grandparents or find a job in his current condition. Koem Long traveled to Kien Khleang National Rehabilitation Centre to receive treatment. This is the only center in Cambodia where this treatment is available. On February 20th, he will undergo a brachial plexus repair surgery. After recovery, he hopes to have movement in his hand and be able to find work. Our medical partner, Children's Surgical Centre, is requesting $709 to fund this procedure. Koem Long said, "After surgery, I hope I will be able to move my hand easily, ride my motorbike, spend time with my friends, and find work."

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.”