Saika is a 17-month-old baby from Haiti. She is an interactive happy child. She lives with her 3 sisters and 2 brothers. Saika 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, Saika's parents have been worried about her increasing head circumference and the pressure this could be putting on her brain. Without treatment, Saika will experience severe physical and developmental delays. Our medical partner, Project Medishare, is requesting $897 to cover the cost of surgery for Saika 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 February 27th. This critical treatment will drain the excess fluid from Saika's brain to reduce intracranial pressure and greatly improve her quality of life. With proper treatment, Saika will hopefully develop into a strong, healthy young girl. Her parents are looking forward to her being able to be healthy enough to go to school when she is older.

Vanila is a 17-year-old girl. She comes from a sizable family that includes five siblings, with her being the second-to-last born. She is a student and recently completed her secondary education with the hope of going further in her education. Her parents work as farmers, relying on their harvest for sustenance. Additionally, her father engages in casual day-to-day jobs to supplement their income. Three of Vanila’s siblings are independent and working, and they occasionally assist their parents in covering household expenses. Vanila’s journey began when, as a baby, her parents noticed both of her legs twisting inward and downward. Unfortunately, financial constraints prevented them from addressing her medical needs. In September 2023, Vanilla’s family learned about Kafika house, and the services offered. They visited, and she was diagnosed with bilateral clubfoot, a condition that significantly limited her mobility. With both legs affected, she commenced treatment for her left foot first, starting with manipulation and casting. In October 2023, she underwent surgery, and her treatment progressed well, showing positive results. Currently, Vanila is on the verge of beginning treatment for her right foot. She will undergo a similar process to correct the defect in her right foot. The team will begin clubfoot treatment for Vanila on December 29th. Our medical partner, African Mission Healthcare, is requesting $935 to fund Vanila's clubfoot repair. After treatment, her mobility will significantly improve. Vanilla says: “I’m looking forward to the day that I will be walking comfortably.”

Lydiah is a 36-year-old fruit vendor from Kenya. Her husband is a motorcycle driver, and they have two children, ages eleven and seven. For seven months, Lydiah has been experiencing pain and abnormal bleeding in a sensitive area. After seeking treatment, Lydiah was diagnosed with a left ovarian benign cystadenoma and uterine fibroids. To relieve her pain, Lydiah needs to undergo a hysterectomy, a procedure in which surgeons will remove her uterus. However, Lydiah does not currently have medical coverage and cannot afford the proposed procedure. Fortunately, our medical partner, African Mission Healthcare (AMH), can help. On July 21st, Lydiah will undergo gynecological surgery at AMH's care center. Once recovered, Lydiah will be able to resume her daily activities free of pain. Now, AMH is requesting $1260 to fund Lydiah's surgery. Lydiah said, “These stomach pains are unbearable and very uncomfortable. I cannot go to the market to sell fruits because of the pain. I hope to get this surgery to ease the pain and get back to my job.”

Yesica is an 8-year-old girl who lives with her parents and 2 younger brothers in a mining city high in the mountains of central Bolivia. Her father works in construction, and her mother is a homemaker. Yesica is in second grade and loves attending school and learning about science. Yesica was born with 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 her weak and short of breath. Yesica needs surgery to heal this condition. Fortunately, our medical partner International Cardiac Alliance (ICA) can help. Yesica is scheduled for cardiac surgery on October 11th, during which doctors will sew the hole closed so that blood can no longer leak through it. After surgery, she will be able to be more active and grow up to be a strong young woman. Yesica's family and ICA need help raising $1,500 to fund the procedure and her follow-up medical care. Her mother shared, "Our family is very hopeful that Yesica will be stronger and healthier after her surgery."

Renatus is a seven-year-old boy in grade 1 from Tanzania. He is smart, charming, and enjoys playing with everyone he interacts with. Whenever engaged in conversation, he exudes confidence. Renatus is the younger child in a family of two siblings. His parents are farmers and livestock keepers, making every effort to provide for their family. However, inflation makes it challenging for them to meet all their needs. During his early growth stages, Renatus effortlessly went through crawling, standing, and beginning to walk. However, as time passed and he started walking more, his legs began to show signs of bowing. This concerned his mother, leading her to take him to the hospital for evaluation. The doctor advised starting him on calcium therapy, but unfortunately, the treatment proved ineffective. Consequently, the mother sought another medical opinion from various medical centers, but the condition continued to worsen as Renatus grew older, making it increasingly difficult and painful for him to walk. Renatus and parents traveled 6 hours to seek treatment. He was diagnosed with a wind-swept deformity, which affects both of his legs, leading to reduced stability while walking. He was also diagnosed with clubfoot of both feet, a condition in which the foot is twisted out of shape. These conditions cause difficulty in walking and wearing shoes. He has become less confident during playtime, as he frequently trips and falls. Our medical partner African Mission Healthcare (AMH) determined that the best course of action is corrective surgery to improve Renatus’s quality of life. Surgeons will perform clubfoot repair surgery on August 2nd. AMH is requesting $935 to fund Renatus's clubfoot repair. After treatment, he will be able to walk and play easily. Renatus’s mother said, "I wish my son to have a good life ahead free from any defect. I hope this treatment will make it possible for him to have a good future.”

Leah is a 48-year-old mother of four from Kenya. She buys and sells old newspapers for a living. Her husband works as a casual laborer on construction sites. Leah lives in a two-room monthly rental house with her family. She does not currently have active medical cover. About three months ago, Leah noticed a painful lump on her right breast while taking a bath. She visited a nearby facility for a checkup, and was referred to Kenyatta National Hospital in Nairobi. However, she had difficulty receiving prompt medical. Three weeks ago, Leah realized the lump was growing and more painful, and sought care again. She visited Kijabe Hospital, where she underwent review by the general surgery team, and several tests, including a mammogram and core biopsy, were requested. Ultimately, Leah was diagnosed with breast cancer. She needs surgery to remove the cancerous mass, but cannot currently afford the amount required for her to undergo the procedure. Fortunately, our medical partner, African Mission Healthcare (AMH), can help. On August 21st, Leah will undergo a mastectomy at AMH's care center. During the procedure, surgeons will remove the impacted breast tissue to rid her body of breast cancer and to prevent the cancer from metastasizing. AMH is requesting $1110 to cover the cost of Leah's procedure. After treatment, Leah will hopefully return to a cancer-free life. Leah said, “I am in so much pain, especially on my right breast. The cancer has greatly affected the whole chest, and I feel so worried. I need to get surgery to stop these cells from spreading. ”

Devie is a 31-year old woman from the Philippines. She has three children that she loves and supports alongside her partner. In 2018, Devie began to experience troubling symptoms, including discomfort in her neck, shortness of breath, easy fatigability, palpitations, and difficulty swallowing. Unfortunately, due to financial constraints, she couldn't seek medical consultation. Due to her condition, she cannot work. As time went on, Devie's condition worsened, and in 2019 she noticed a visible lump on her neck. This made it even more challenging for her to carry out her daily tasks. Devie traveled to Our Lady of Peace Hospital, where she underwent a thorough examination. She was diagnosed with Colloid Adenomatous Goiter, a thyroid gland disorder characterized by the development of multiple nodules or lumps within the thyroid tissue. These nodules are made up of abnormal thyroid cells that form small, fluid-filled sacs called colloid cysts. She needs surgery to prevent her symptoms from getting worse. Fortunately, our medical partner, World Surgical Foundation Philippines (WSFP), is helping Devie receive treatment. She is scheduled to undergo a thyroidectomy on July 22nd at Our Lady of Peace Hospital. Surgeons will remove all or part of her thyroid gland. The Philippine Health Insurance Corporation is covering a portion of the cost of Devie's treatment, and WSFP is raising the remaining $935. Devie shared, "I am grateful to Watsi and World Surgical Foundation Philippines because I have been enduring this illness for a long time, waiting for someone to help and for something to happen, and they are my answered prayer. Please never get tired of helping less fortunate people like me."

Dormaha is a four year old preschooler from Haiti. She lives with her parents in a neighborhood of Port-au-Prince, and likes dancing and watching cartoons. Dormaha suffers from a cardiac condition called ventricular septal defect. Blood leaks through a hole that exists between the two lower chambers of her heart, bypassing her lungs without obtaining the oxygen Dormaha requires. She needs surgery to prevent her from experiencing the weakness and shortness of breath that she currently lives with. The surgery that Dormaha needs is not currently available in Haiti, so she will be flying to the Dominican Republic to receive treatment. Fortunately, on May 18th, she will undergo cardiac surgery at Hospital CEDIMAT, during which surgeons will sew a patch over the hole to close it. Our medical partner, Haiti Cardiac Alliance, is contributing $8,000 to pay for the surgery. However, Dormaha's family also needs help to fund the costs of many other aspects of Dormaha's care. They are seeking $1,500 to pay for the lab tests, medicines, checkup and follow-up appointments, that are all part of Dormaha's critical treatment. This money will also go towards obtaining passports, and for the social workers from our medical partner, who will accompany Dormaha's family overseas during her care. Dormaha's mother said: "Our family has been hoping for this surgery ever since our daughter was a small baby, and we are very glad the chance has arrived!"

Srey Tey is a playful 3-year-old from Cambodia. She lives in Svay Raing province with her parents and two older siblings. Her mother cares for the children at home, while Srey Tey's dad earns a living as a taxi driver. Srey Tey's favorite things include ice cream, cartoons, and playing with her siblings! Srey Tey's mom had a long and difficult delivery with shoulder dystocia, a condition where one or both of the baby's shoulders get stuck in the birth canal. Since birth, she noticed that Srey Tey has limited movement in her left arm. Srey Tey has been diagnosed with a brachial plexus injury on her left 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. Currently, she cannot move her left hand and has limited strength and function in her arm. Srey Tey's family brought her to our medical partner's care center for treatment. This is the only center in the country where this treatment is available. On May 11th, she will undergo a brachial plexus repair surgery. After recovery, she will have improved function in her arm and hand. Our medical partner, Children's Surgical Centre (CSC), is requesting $709 to fund this procedure. Srey Tey's family contributed $100 to her care. Srey Tey's mother shared her hopes that, after surgery, Srey Tey will be able to move her hand more easily and start preschool.

Aaron is a 16-month-old baby boy from Haiti. He lives in Port-au-Prince with his two loving parents and three older sisters. His parents describe him as a happy and outgoing baby. Aaron was born with a congenital heart defect called Aortic coarctation, where a major blood vessel leading from the heart is too narrow. It forces the heart to pump harder to move blood through the aorta. Often, this condition can go undiagnosed and result in fatality later in life. Fortunately, Aaron was diagnosed by our medical partner, Haiti Cardiac Alliance (HCA), and a treatment plan has been created. On April 17th, doctors will perform the surgery and use a balloon attached to a catheter to stretch the aorta to a more appropriate size. HCA is requesting $1500 to fund the procedure. After the surgery, Aaron should live more comfortably and his parents with less worry. His mother says, "We are very excited to know that this surgery will finally be possible for our son!"