Moringe is a 13-year-old boy from a Maasai family in Tanzania. Moringe is the seventh child of his mother and comes from a large family. His father, a livestock keeper, works hard to support his children and family. The Maasai community in Kiteto primarily relies on livestock farming, and Moringe’s father is a respected cattle breeder. Unfortunately, Moringe is currently facing a debilitating physical condition that severely affects his mobility and hampers his ability to walk long distances. In 2022, Moringe began to experience pain in his feet. Shortly after, his knees began to bow inward, leading to the development of a condition commonly known as knee knocking or Genu Valgus. This condition often stems from an excessive accumulation of fluoride in the bones, which often occurs because of contaminated drinking water. Morinfe's condition affects his daily activities and restricts his participation in important community events and educational opportunities. Due to limited financial resources and the high cost of medical care, Moringe's family hasn't been able to get Moringe the support he needs. Thankfully, our medical partner, African Mission Healthcare, can help. African Mission Healthcare is requesting $880 to fund corrective surgery for Moringe. The procedure is scheduled for June 6th, and treatment will hopefully restore Moringe's mobility, allow him to participate in the activities he's missed out on, and decrease his risk of future complications. Moringe says, "I hope this chance I got will help change my life for the better. I hope when I go home, I will be able to do most of my activities without feeling any pain in my leg."

Paulo is a 17-year-old boy from Tanzania. He lives with his parents and his four siblings. His parents are farmers who grow food for their family and sell the excess to support their family. Due to limited funds, Paulo and his siblings had to stop attending school. Paulo experiences difficulty with his mobility. When Paulo was enrolled in school, he was often unable to walk the distance to class. Paulo's parents were inspired to seek treatment for Paulo after attending an outreach seminar held by our medical partner, African Mission Healthcare (AMH). Doctors at AMH's care center determined that Paulo's limited mobility is due to the shape of his legs, and Paulo was diagnosed with genu varus. Genu varus is typically caused by an excessive accumulation of fluoride in the bones which often stems from contaminated drinking water. Fortunately, AMH can help. AMH is requesting $880 to fund corrective surgery for Paulo's legs. Paulo's procedure is scheduled to take place on June 6th, and will hopefully restore Paulo's mobility, allow him to participate in a variety of activities, and decrease his risk of future complications. Paulo says, "I hope that one day I will be able to walk without feeling any discomfort."

Leonard is a 14-year-old boy from Mpanda, Tanzania. Leonard's parents manage a small farm that provides their family with food. They also take on various additional jobs during the day, including helping on other people's farms, washing clothes, and cleaning yards, to support their family. Despite their hard work, Leonard's parents have a hard time supporting their five children and Leonard's grandparents. Leonard was diagnosed with genu varus, a condition where his legs bow outwards. This condition is typically caused by an excessive accumulation of fluoride in the bones, which often stems from contaminated drinking water. Due to his condition, Leonard has difficulty walking and participating in daily activities. However, as a result of financial constraints, Leonard's family has been unable to seek treatment for him. An outreach team directed by our medical partner, African Mission Healthcare (AMH), visited Leonard's village and spread the news about available treatment for genu varus. As a result, Leonard's parents were motivated to seek treatment for their son at AMH's care center. AMH is requesting $880 to fund corrective surgery for Leonard. Leonard's procedure is scheduled for June 6th. This treatment will reduce the discomfort in his legs, restore his mobility, greatly decrease his risk of future complications, and allow him to resume his daily activities. Leonard says, "I am glad that after a long wait, I get to have treatment that will make my legs better. I can't wait to enjoy playing soccer with my friends and helping my parents at the farm."

Jeremy is a two-year-old toddler from Haiti. He lives with his parents, who run a small grocery kiosk in Port-au-Prince. He is their only child. Jeremy was born with ventricular septal defect (VSD). VSD is a cardiac condition where there is a small hole in the wall that separates the heart's lower chambers. Due to this hole, oxygen-rich blood mixes with oxygen-poor blood, causing weakness and shortness of breath. On June 12th, Jeremy will undergo cardiac surgery in the Dominican Republic. During this procedure, surgeons will sew a patch over the hole in Jeremy's heart so that his blood can't leak through it. Our medical partner, Haiti Cardiac Alliance (HCA), is contributing $8000 to pay for surgery. However, Jeremy's family needs help to fund the costs of surgery prep and transport. Jeremy's family is requesting $1,500 to cover labs, medicines, and preoperative and postoperative appointments. This sum will also support passport obtainment and the social workers from HCA who will accompany Jeremy's family overseas. Jeremy's mother said: "Our family is very excited to know that our son has been chosen for surgery. We're all praying for him."

Reach is a five-year-old pre-schooler who lives in Kampong Speu with his parents and older brother. His mother works in a hair salon, and his dad is a security guard. At home, Reach loves watching YouTube and playing with toy cars. In 2020, he accidentally pulled the boiling rice pot down and burned multiple areas on the left side of his body. He received initial treatment at a nearby pediatric hospital, including skin grafts and wound care. However, burn scar contractures have developed, tightening the skin around his burns, especially around his wrist and hand. The contractures make it difficult to hold objects and perform everyday tasks. When his family learned about our medical partner, Children's Surgical Centre, they traveled for two and a half hours seeking treatment. On June 15th, surgeons at CSC will perform a burn contracture release surgery to improve the function of his hand. Now, his family needs help to fund this $495 procedure. His mother shared, "I hope Reach can use his hand like before and feel good about himself like before the accident."

Pendo, a baby girl, resides in the Ngorongoro region of Tanzania. Her family follows the Maasai tradition and sustains themselves primarily through subsistence farming and livestock rearing. Pendo was born with clubfoot, a congenital condition that causes her foot to be twisted inward and downward, which causes difficulty walking and even wearing shoes. Unfortunately, due to limited medical facilities and awareness in her village, the condition went unnoticed by doctors at birth. Pendo's mother noticed her bent leg a few days later. Despite the concern of the village grandmothers, her father initially believed it was part of God's plan and resisted any intervention. However, during an outreach program conducted by our medical team in her village, Pendo's mother learned about the treatment options available for her daughter. Realizing the potential for improved quality of life for Pendo, she sought medical assistance and brought her to our partner's center. Fortunately, Pendo is now being seen by our medical partner's care center, Arusha Lutheran Medical Centre. There, surgeons will perform clubfoot repair surgery on June 16th. Our medical partner, African Mission Healthcare Foundation, requests $935 to fund Pendo's clubfoot repair. After treatment, she'll be able to walk easily as she grows and live a full life ahead. Pendo's mother says, "Thank you for the chance to receive the treatment for my daughter. I hope her future will be good."

Japhet is a baby and the last born in a family of five children living in Ngorongoro, Tanzania. His father works as a livestock keeper and farmer, cultivating crops for sustenance while selling part of the harvested produce to meet household expenses. Meanwhile, Japhet's mother fulfills the role of a homemaker, taking care of the children and managing house and family. Despite the father's efforts to provide for the family, there are difficulties in affording education and healthcare for their children, leading to their reliance on traditional remedies for medical treatment. Japhet was born with clubfoot, a condition where the foot is twisted out of shape, causing difficulty walking and even wearing shoes. This situation concerns his parents as they contemplate their child's future. While attending church, they received information about visiting specialists organizing a clinic specifically for children with treatable disabilities. Japhet's mother was able to attend the clinic, feeling relieved upon hearing about potential treatment options. With the church's assistance, transportation was arranged for them to travel to the hospital, and they arrived at our medical partner's center, where they were warmly welcomed. After assessing Japhet, he was diagnosed with clubfoot, specifically in his left foot. He will undergo manipulation and casting to gradually correct the foot's angle, followed by a tenotomy surgery to heal his condition. Thankfully, on June 16th, skilled surgeons at our medical partner, Arusha Lutheran Medical Centre, will perform clubfoot repair surgery. African Mission Healthcare is seeking $935 in funding to cover the costs associated with Japhet's treatment. This procedure will significantly improve Japhet's prospects for a better future. Japhet's mother says, "I hope my child will have the best treatment, and this treatment will make his future life better."

Thaw is a 5-year-old boy who lives with a large family in Burma. His whole family works as agricultural day labourers. He has not yet started his schooling because he is young and because of his health condition. Thaw enjoys playing with other children in their neighborhood. He also enjoys practicing writing the Burmese alphabet, which his brother has taught him. Thaw was born with a congenital condition affecting his lower digestive tract. He underwent surgery a few days after he was born and again when he was two years old. Now the doctor wants to perform a reverse colostomy, an operation to improve the function of his lower digestive tract. Our medical partner Burma Children Medical Fund (BCMF) is requesting $1,500 to cover the cost of Thaw's surgery scheduled for June 12th. Thaw's father said, "Both us [my wife and I], have to watch him constantly because we are worried that he will get an infection... Currently, half of our income goes towards his medical expenses, which makes it difficult for our family to survive."

Kiberian is a 3-year-old boy from Kajiado County who needs surgery to help him walk well. He comes from a large pastoralist family with many siblings. His father is a farmer/herder, while his mother takes care of their family and home. Kiberian was born with a deformity in his legs that has greatly affected his mobility. His knees bend inward, while his ankles remain apart. He cannot walk long distances and often falls while walking. Kiberian's father took him to a satellite clinic for treatment and the doctors recommend procedures that will reposition the femur and tibia of each leg into alignment. Our medical partner African Mission Healthcare (AMH) is requesting $1,224 to cover the cost of the surgery, scheduled for June 20th. This treatment will be impactful to Kiberian because he will be able to walk well, play with other children, and continue with his education. Kiberian’s father shared, “The joy of a father is to see his children growing well without any challenge or deformity and I would love to see my boy walking well.”

Levina is a charming 4-year-old girl and the youngest child of three in her family. Sadly, Levina had a twin brother who suffered from a high fever when they were about nine months old and tragically passed away. Levina, too, faced challenges during her early years, as her overall health showed many challenges. However, she managed to survive and gradually saw improvements in her general well-being as she grew older. Levina has been diagnosed with right valgus, meaning that her right leg bows inward. This condition is typically caused by an excessive accumulation of fluoride in the bones, which often stems from contaminated drinking water. As a result, she experiences difficulty in walking. In April 2022, Levina visited our partner's care center and began receiving treatment to correct her leg deformity, as her legs were severely bowed. However, given the severity of her condition, her initial surgery proved insufficient to fully heal her condition. Consequently, she has returned for another surgery in order to progress further with her treatment plan. Levina’s parents are once again seeking assistance to cover the costs of the treatment she began when she was three years old. Our medical partner African Mission Healthcare (AMH) is requesting $880 to fund her treatment, which will hopefully restore Levina's mobility, allow her to participate in a variety of activities, and greatly decrease her risk of future complications. Levina’s mother says, "Thank you so much; the first treatment has helped my daughter so much. We have hope that when she completes her treatment, she is going to be able to walk freely."

Woodyson is a young student from Haiti. Woodyson lives with his mother and older siblings in central Haiti's rural, mountainous area. He is in the tenth grade and would like to become a teacher. Woodyson has a cardiac condition called rheumatic mitral regurgitation. Woodyson underwent surgery six years ago to replace his aortic valve and repair his mitral valve due to a rheumatic fever that severely damaged his heart. Although his repaired mitral valve served him well for six years, he now needs to have his mitral valve replaced with an artificial implant. The surgery he needs is not possible in Haiti, so Woodyson will fly to the United States to receive treatment. On July 7th, he will undergo cardiac surgery, during which surgeons will remove Woodyson's damaged valve and implant an artificial mechanical valve. Another organization, Baylor Scott and White Heart Hospital is contributing $20,000 to pay for his surgery. Woodyson's family also needs help to fund the costs of surgery prep, travel, and followup. The $1,500 bill covers labs, medicines, checkups, and follow-up appointments. It also supports passport obtainment and the social workers from our medical partner, Haiti Cardiac Alliance, who will accompany Woodyson overseas. Woodyson shared: "I am excited to be able to have this surgery so that I can feel completely normal and healthy again."

Lucy, a 3-year-old girl, is shy with a heart full of joy. As the third and youngest child in her family, Lucy brings delight to her loved ones. Her mother shared that Lucy enjoys singing, spending time with her friends, engaging in playful activities, and assisting with household chores. Lucy's father is a farmer, while her mother oversees the household. During our medical partner's encounter with Lucy at the Nyahururu clinic, she was accompanied by her mother, who expressed concerns about a leg deformity. Her mother mentioned that Lucy has recently been limping and frequently complains of pain when walking and playing with her friends. Lucy was diagnosed with clubfoot on the right foot. Clubfoot is a condition in which the foot is twisted out of shape, which causes difficulty walking and even wearing shoes. Fortunately, Lucy's family visited our medical partner's care center, AIC Cure International Hospital. There, surgeons will perform clubfoot repair surgery on July 12th. Our medical partner, African Mission Healthcare Foundation, requests $1,286 to fund Lucy's clubfoot repair. After treatment, she can walk without pain, continue her education and play with friends. "It would bring me joy to have Lucy walking and playing like other children," Lucy's mother told us.