Chaica is a 13-month-old baby girl from Haiti. She is the youngest child in the family and loves to smile. Chaica has been diagnosed with hydrocephalus, a condition in which excess cerebrospinal fluid accumulates in the brain and increases intracranial pressure. As a result of her condition, Chaica has been experiencing Increasing head circumference. Without treatment, Chaica will experience severe physical and developmental delays. Our medical partner, Project Medishare, is requesting $897 to cover the cost of surgery for Chaica at Hospital Bernard Mevs that will treat her hydrocephalus. This is the only site in the country where this care is currently available and the procedure is scheduled to take place on January 26th. This critical treatment will drain the excess fluid from Chaica's brain to reduce intracranial pressure and greatly improve her quality of life. With proper treatment, Chaica will hopefully develop into a strong, healthy young girl. Her family is looking forward to Chaica being able to grow up healthy and they hope this care will help their daughter.

Gareth, who is four years old, lives with his parents and three siblings in central Bolivia. His parents are shopkeepers and have so much love for their family. Gareth was born with ventricular septal defect, a heart condition that creates a hole between the two lower chambers of the heart. Blood, which should circulate through his lungs to obtain oxygen, simply leaks out through the hole, leaving Gareth weak and short of breath. In addition to his heart condition, Gareth was born with Down syndrome. Doctors at our medical partner, Haiti Cardiac Alliance, are scheduled to operate on Gareth on January 19th, at Hospital del Niño Dr. Ovidio Aliaga Uria. During the procedure, surgeons will sew a patch over the hole in Gareth's heart, so that his blood will flow normally. Gareth's family needs your help to fund the $1,500 to cover the costs of his care. Gareth's mother said: "Our family is very grateful to everyone who is making it possible for Gareth to have this surgery."

Erick is a 10-year old boy, and the oldest of four siblings. He and his family live in Tanzania, where Erick particularly enjoys studying Kiswahili, civics and mathematics, with an eye towards becoming a businessman when he grows up. When he isn't studying, he is out playing with his friends, or helping to do chores around the house. Erick's parents work as farmers, an occupation that has proved increasingly daunting, in light of the drought that has lasted for three years already. Erick has been diagnosed with a right clubfoot. A surgery he underwent previously caused his right leg to be slightly twisted downward and inward, making it difficult and painful for him to walk long distances. He requires another procedure to help correct his right leg, but his parents are unable to afford the medical bill, and are appealing for help. Fortunately, Erick sought assistance from our medical partner, African Mission Healthcare Foundation, at Arusha Lutheran Medical Centre. It is there, on December 15th, that surgeons will perform clubfoot repair surgery, which will enable Erick to walk more easily, to continue with his studies, and to pursue his dreams, without having to contend with his clubfoot. Now Erick's family needs your help to fund his procedure, which will cost $935. Erick says: "I feel like it will be hard for me to achieve my dreams with my current foot condition. I appeal for your support."

Noah is a young boy from Ngarenanyuki, a small village in the rural parts of Arusha, Tanzania. He is a member of a big family with seven siblings. His father is a livestock keeper and at their home, the young children are responsible for helping around with light house chores. In 2021, Noah was in the kitchen with some of his siblings, and he accidentally fell into a pot of boiling water. He was badly burnt on his left side of the elbow near the chest. His parents provided first aid to Noah, because they live in a remote area, and it was hard for them to get to the nearest hospital. Noah’s wounds healed eventually, but left him with a burn scar contracture. The contractures tighten the skin around the burn area, and it is difficult to move his arm. Noah came to our center during a medical camp and was assessed to find out if he was fit for the required treatment to help with the burn scar contracture. Noah's parents cannot afford treatment and are appealing for help. Fortunately, our medical partner, African Mission Healthcare Foundation, is helping Noah receive treatment. On October 12th, surgeons at their care center will perform a burn contracture release surgery to release the tightening and help him move his hand easily. Now, he needs help to fund this $874 procedure. Noah’s mother says, "I was worried that that my boy will grow up with that deformity but with what I have seen here, he is going to be better.”

Naima is a smiley and playful baby girl from Ethiopia. She loves to breastfeed and play with her seven older siblings and her mother. Her dad is a retired driver and the community elder, and her mother stays home to care for the children. Because Naima's father has no source of income, their older children support them financially. Naima was born with an anorectal malformation, a congenital abnormality that leads to a complete or partial intestinal blockage. She needs to undergo a series of procedures to eliminate bowel dysfunction. Naima developed bowel obstruction because of her condition and an emergency colostomy was done. She has had multiple issues with her colostomy care and associated complications. As a result, she cannot make stool in a typical way. Her parents have been very troubled because of her condition and are asking for support. Naima is scheduled to undergo surgery to correct her condition on September 22nd. Our medical partner, African Mission Healthcare Foundation, is requesting $1,500 to cover the total cost of Naima's procedure and care. After her recovery, Naima will no longer experience bowel dysfunction or be at risk of developing health complications in the future. Naima's father says, “I hope my child will get the treatment and heal. Once she finishes her treatment, I hope she will be relieved from her pain and suffering and lead a healthy life.”

Walendjina is an adorable two-year-old toddler from Haiti. She lives with her parents, who are both market vendors, and her two older siblings in a small village in the mountains of northwestern Haiti. Walendjina has Tetralogy of Fallot, a rare condition caused by a combination of four congenital heart conditions. These conditions include a hole between the two lower chambers of the heart and a muscular blockage of one of the valves. On August 15th, Walendjina will fly overseas to the Cayman Islands to receive treatment. During this cardiac procedure, surgeons will close the hole in her heart with a patch and remove the muscular blockage from her valve. A portion of the cost of Walendjina's treatment is being supported by Have a Heart Cayman, and our medical partner, Haiti Cardiac Alliance, is raising the remaining $1,500 to cover the cost of Walendjina's labs, medication, followup appointments, and travel fees for her and her family. Walendjina's father shares, "Our family has been very scared for our daughter's health ever since she was born. We will all be very glad to be able to stop worrying so much about her heart!"

Rosa hails from Guatemala. She has a gentle smile and speaks Kaqchikel, an indigenous Mayan language. Recently, during a routine screening, Rosa's medical examiners found a precancerous lesion on her cervix. Rosa needs a colposcopy to complete her diagnosis and enable her doctors to prevent the progression of this lesion into cervical cancer. Rosa can't afford to pay for the medical care she needs. For only $220, Rosa will receive treatment and be able to move forward with her life.

Four year old Rose is one of the youngest of nine children! She has bilateral "genus varus" or bowleggedness. Due to this condition, she experiences severe knee pain and is unable to run or walk normally. Though Rose loves to play with other children, her problems with her joints make it more difficult for her to join in physical activities. Her parents cannot afford the cost of surgery themselves, due to their large family. In order to correct this condition, we are donating $500 towards surgery and the application of long leg casts to Rose's legs. After surgery, her providers expect that Rose will be able to walk normally and will avoid experiencing premature osteoarthritis.