Luz is a three-year-old girl from a mining town in central Bolivia. Her mother is a farmer and her father sadly passed away from a heart attack soon after she was born. Luz has a cardiac condition called ventricular septal defect, in which a hole exists between the two lower chambers of her heart. Blood leaks through this hole without passing through her lungs to obtain oxygen, leaving her weak and dependent on an external oxygen tank. Fortunately, our medical partner, The International Cardiac Alliance can help. Luz is scheduled to undergo heart surgery on March 21st. Our medical partners are requesting $1,500 to fund her procedure. Luz's mother says, "I am looking forward to my daughter being able to play normally and start preschool after her surgery!"

Su is a 12-year-old boy from Burma who lives in an Internally Displaced Persons (IDP) camp with his family. Su had to discontinue his studies while in fourth-grade, and his family was forced to leave their home because of the conflict in Burma. Su’s grandparents are his primary caregivers as his parents divorced, got remarried and moved away. His half-brother, uncle, aunt, and infant cousin also live with the family. Su’s grandmother and aunt take care of their home, while his grandfather, uncle and half-brother work as day laborers. Su initially noticed signs of his condition in January, when he felt pain on the left side of his mouth, and had a slight swelling on the left side of his face. One month later, he was taken to the clinic by his aunt, where it was discovered that he had three cavities on the left side of his mouth. The doctors removed the decayed tooth on the top jaw but left the lower two as the swelling was significant. Su stayed in hospital for one week to recover, while receiving antibiotics. He was released from the clinic once the pain and swelling had decreased, but shortly after, the symptoms resurfaced, more intense than before. Presently, the left side of Su’s face is significantly swollen, and he feels acute pain. He has difficulty eating and can only chew from the right side of his mouth. He cannot lay down on the left side due to the swelling and pain, which gets worse at night. Su also feels pain in his neck when he drinks or swallows food. Su needs to undergo a CT scan, a procedure in which X-ray images taken from several angles are combined to produce cross-sectional images of the body. This will help doctors diagnose his condition and formulate an appropriate treatment plan. Su's family is however unable to raise the required funds needed for the imaging procedure. Our medical partner, Burma Children Medical Fund, is requesting $414 to cover the cost of Su's CT scan and care, scheduled for March 25th. Su is keen to return to school when his condition is treated. He loves to paint and draw in his free time and would like to be an artist someday. Su's grandfather is worried about his condition, but hopeful about his future. He says, “Whatever he wants to do in his future, I will support him fully, as his parents are gone.”

Samuel is a smart, playful boy aged one year and eight months old. He loves martial arts and can recite the entire alphabet. He loves to pray with his mother. Before he was born, a prophet told his mother that she would give birth to a son named Samuel. She was very happy to have a son as her older children are all girls. Samuel's mother cleans the street for a living. She carries her son on her back and cleans the street early in the morning. Sometime back, Samuel contracted pneumonia due to the cold mornings, and she stopped working for a while. She has recently resumed to help support her family. Her husband works as a day laborer, but he does not have consistent work. The family lives in a rented single-room mud house. Their income is minimal, and they struggle to meet their daily expenses. They receive government donated food on public holidays. An international organization supports one of her school-going daughters, paying for her education and donating some food every month. Samuel was born with a congenital condition called epispadias, where the urethra does not develop into a full tube, and the urine exits the body from an unusual site. As a result of this condition, Samuel experiences constant urinary leakage and is unable to urinate while standing like other boys. Samuel is scheduled for epispadias repair but his family is not able to meet the surgery costs. Fortunately, our medical partner, African Mission Healthcare, is helping Samuel receive treatment. On March 12th, surgeons at their care center BKMCM will perform an epispadias repair surgery so that Samuel can live more comfortably and confidently. Now, Samuel's family needs help to fund this $1,040 procedure. Samuel's mother says, "I love him so much that I pray every day that he will be fine after the surgery. I am worried that I might lose him during the surgery, but I want him to heal and become like other boys, so I consented to him having the surgery. I wish for him to become continent, and attend school someday."