Naw Aye is a 28-year-old woman who lives with her husband, son, sister-in-law, brother, two nephews, and two nieces in a refugee camp in Mae Hong Son Province, Thailand. Originally from across the Burmese border in a conflict-area called Karen State, she fled to the refugee camp with her family in February 2023 due to airstrikes on her village. Her husband and her brother are unemployed, while her son, nieces, and nephews go to school. She and her sister-in-law are homemakers. During her free time, she loves to play with her son and enjoys planting vegetables in her small garden. She is currently expecting her second child. Her doctors recommended that she deliver via cesarean section because In January 2020, when Naw Aye was pregnant with her first child, her water broke prematurely which put her baby's life at risk. She was brought to a hospital in Burma, where she gave birth to her son through a caesarean section (C-section). In February, after they had fled to the refugee camp, Naw Aye became pregnant. She went to the hospital in the refugee camp regularly for antenatal care. She was told during one of her visits that although her pregnancy was going well, she would need to give birth through a C-section to ensure the safety of both mother and child. Our medical partner, Burma Children Medical Fund, will help ensure a safe C-section on November 3rd. This procedure costs $1500, and Naw Aye needs your support. “I want to sell sacks or Mohinga (Burmese soup) for extra income soon. But I don’t have enough cash to start doing that, and I am pregnant. I hope I can do that after I give birth,” Naw Aye said.

Sokha is a 62-year-old woman from Cambodia. She has one daughter and five grandchildren. She lives with her daughter near the Vietnamese border and spends most of her time listening to the radio and helping around the house. Her family earns a small income, with her daughter selling boiled corn on the roadside and her son-in-law working at a nearby construction site. Sokha had to stop working due to her deteriorating vision but hopes to return to selling eggs in the market as soon as possible. A year ago, Sokha developed a cataract in her left eye, causing her itchiness, tearing, and blurry vision. She has difficulty seeing things clearly, including colors and faces, and is worried about falling when walking, so she cannot go places on her own. When Sokha learned about our medical partner, Children's Surgical Centre (CSC), she traveled for four hours seeking treatment. On August 7th, doctors will perform cataract surgery and an intraocular lens implant in her left eye. After recovery, she will be able to see clearly. CSC is requesting $253 to fund this surgery. Sokha contributed $50 to her care. Sokha said, "I hope, after surgery, I can see clearly again. I could help my daughter sell corn or return to work at the market."

Juan, an 11-month-old boy from Bolivia, lives with his mother and five older siblings in a neighborhood in the mountains above La Paz. Juan was born with a cardiac condition called ventricular septal defect, in which a hole exists between the two lower chambers of his heart. Blood leaks through this hole without passing through his lungs to obtain oxygen, leaving him weak and making it difficult for him to gain weight. To address Juan's condition, congenital heart surgery is the only viable treatment option. Skilled doctors at Hospital del Niño Dr. Ovidio Aliaga Uría will perform the surgery by closing the hole in his heart using a patch. However, due to Juan's low weight, the surgeons have determined that it is unsafe to proceed with the procedure. As a result, he will be hospitalized for several weeks before the surgery to receive proper nutritional support, enabling him to gain weight and prepare for the operation. Our medical partner, Haiti Cardiac Alliance, is actively seeking your generous support to raise $1,500 to support Juan's cardiac care. Your contribution will play a vital role in enabling Juan to receive the life-changing congenital heart surgery he urgently requires. By partnering with Haiti Cardiac Alliance and making a financial contribution, you can make a significant difference in Juan's life and overall well-being. Juan's mother shared, "I am very hopeful that after this surgery, my son will gain appetite and start growing and gaining weight more normally!"

Celeste is a 3 month-old infant from Colombia. She was born in Medellín, lives with her parents, grand parents and great grandparents in a little house full of 4 generations. Even though she is so young she is a lovely girl who already smiles and laughs with everyone that comes and tells her she is cute. Celeste has clubfoot of both feet. Clubfoot is a condition in which the foot is twisted out of shape. This causes difficulty walking and even wearing shoes. Fortunately, Celeste's family traveled to visit our Medical Partner Clínica Noel. There, surgeons will perform clubfoot repair surgery on December 18th. Our medical partner, Clínica Noel, is requesting $1500 to fund Celeste's bilateral clubfoot repair. After treatment, she will be able to learn how to walk properly and without pain as she grows up. Her mother said, "I hope you can help my little princess, since I found out at my pregnancy I have tried to learn about her condition so I can help her not to suffer and recover properly."

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.

Godson is a 4-month-old baby boy, the youngest in a family of six children. He lives with his parents and siblings in Singida, Tanzania. Both parents are farmers. They grow corn and sunflowers, which they use to make cooking oil. They sell cooking oil to earn money to support their family. Godson was born with a congenital condition in which his feet are twisted out of shape. The parents have been very concerned for their son. They've been to several different hospitals in the past three months seeking treatment with no success. Two weeks ago, while Godson's mother was out for a walk, a stranger saw Godson and approached the mother. The stranger explained his experience with his daughter who had a similar condition. After a brief conversation, the man directed her to the care center of our medical partner, African Mission Healthcare (AMH), for a consultation. Godson's parents wasted no time traveling over 400km and finally arrived at AMH's care center with excitement. The doctors at AMH diagnosed Godson with clubfoot in both of his feet. Godson requires a treatment that involves a series of casting. Fortunately, AMH is able to provide treatment. After a brief talk with our team, Godson's parents understood the diagnosis and what treatment would be needed. The surgeons at AMH will perform clubfoot repair surgery on April 21st. AMH is requesting $935 to fund Godson's clubfoot repair. After treatment, he will be able to walk easily. Godson’s mother says, “After seeing my son I thought this will be his future. I am happy to know that his condition can be treated.”

Chanseth is a 23-year-old factory worker who lives with his parents and four siblings in Kampong Speu province in Cambodia. His older brother works with his parents on a rice farm; Chanseth and two of his sisters work in a local factory, and their 10-year-old sister is in grade three at the local public school. When he is not working in the factory, Chanseth helps his brother and parents on the rice farm. In August 2022, Chanseth was injured in a motorcycle accident, fracturing his left humerus (upper arm bone), and sustaining multiple superficial wounds on his arm. Originally, his arm was just splinted. Two months later, Chanseth went to a local government hospital to see if they could help with the repair of the fracture. It has now been eight months, and Chanseth's arm is still non-functional. He cannot raise his shoulder or use his arm. Chanseth was diagnosed with a brachial plexus injury on his 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. Because of the damage to his tendons and nerves, Chanseth is unable to work. He will require a nerve and tendon transfer to improve his shoulder function to regain the use of his hand. Chanseth sought help at our medical partner, Children's Surgical Centre. On March 28th, he will undergo brachial plexus repair surgery at Kien Khleang National Rehabilitation Centre, the only facility in the country where this treatment is available. Children's Surgical Centre is requesting $709 to fund this procedure. Chanseth said: "After surgery, I hope that they can fix my fracture and I can use my hand to go back to work."

San is a 43-year-mother of two from Thailand. San and her husband stay apart and San works as an agricultural day laborer. Her son lives with his own family and her daughter is a second grader. During her free time, San used to read the news on her phone. In 2020, San began to experience occasional abdominal pain and an urge to vomit, along with tiredness and unusual colored urine. She was then diagnosed with multiple gallstones and cholecystitis, an inflammation of the gallbladder. San has been advised to undergo a surgery to remove the gallbladder. If left untreated, San's symptoms will continue to worsen and put her at risk for further health complications in the future. After seeking treatment through our medical partner, Burma Children Medical Fund (BCMF), San is scheduled to undergo her surgery on September 14th. BCMF is requesting $1,500 to cover the cost of San's procedure and care. San cried and said, "Thank you for helping me. It is not just saving me but also saving my daughter from becoming a motherless child. You have helped me continue my life with my loved ones. I do not know how to express my heartful and profound gratitude to you all. Thank you so much.”

Beatrice is a one-month-old baby from Kenya. She is the youngest in a family of nine children. Due to the ongoing rain shortage, the parents have had to go out of their way to do casual jobs to provide for the family. The family has no insurance and cannot raise the required funds for her surgery. Beatrice was born at home, and immediately, her mother noticed she had swelling on her back. Referred by a friend to BethanyKids, her family traveled for two days and brought her in for an examination. Beatrice was born with spina bifida, a type of neural tube defect in which the spine does not properly close around the spinal cord. Without treatment, Beatrice is at risk of lower-limb paralysis, infection of the exposed nervous tissue, development of tethered cord syndrome, and possible developmental delays. Our medical partner, African Mission Healthcare Foundation, is requesting $1,151 to cover the cost of Beatrice's spina bifida closure surgery. The procedure is scheduled to take place on March 8th. This procedure will hopefully spare Beatrice from the risks associated with her condition, allowing her to grow and develop along a healthy trajectory. Beatrice’s mother says, “I was confused when I first saw the condition my child has, and I did not know what to do. I’m really looking forward to her surgery.”

Meet Clerize: a beautiful and bright 4-year-old. She is the 1st born in a family of two and her family hails from a small village in rural Kenya. We met her at our Nyandarua medical camp outreach accompanied by her grandmother. Clerize's grandmother is a farmer while her father, who is separated with his wife, works as a boda boda (motorcycle taxi) driver. Clerize was born healthy however at the age of three, her grandmother noticed an unusual walking style. She stared tiptoeing and would fall every time she tried to walk. For lack of information and because of the distance, they didn’t take her to the hospital. Later their family heard about CURE hospital medical camp in Nyandarua and brought her to be seen by the doctors. The medical team diagnosed Clerize with clubfoot. Clubfoot is a condition in which the foot is twisted out of shape. This causes difficulty walking and even wearing shoes. Fortunately, Clerize's family has now traveled to visit our medical partner's care center, AIC Cure International Hospital. There, surgeons will perform clubfoot repair surgery on February 26th. Our medical partner, African Mission Healthcare Foundation, is requesting $1,286 to fund Clerize's clubfoot repair. After treatment, she will be able to walk more easily and is looking forward to attending school. “I am pleading for help to help my granddaughter undergo surgery so that she can resume with her normal life and walking,” Clerize's grandmother told us.