Daniel, who is 34 years old, lives with his mother in Kawaida village in rural Kenya. He works in construction trying to get jobs whenever he can, while his mother sells groceries at a nearby market. Daniel is separated from his wife and child, which he shared has left him feeling sad and incomplete. On Sunday, July 30th, Daniel was a passenger in a Matatu (public bus), which was involved in an accident. Daniel sustained injuries to his back, right femur and his right tibia. The surgeon at the hospital where Daniel was brought told him that his back and tibia would heal over time, but the fractured femur needed to be surgically repaired. Fortunately, surgeons at our medical partner, African Mission Healthcare, can help. On August 7th, Daniel will undergo a fracture repair procedure, called an open reduction and internal fixation, at Nazareth Hospital. This procedure will ensure that Daniel's fracture will heal properly. Now, African Mission Healthcare is requesting $1,049 to fund Daniel's surgery. Daniel said: “I kindly request help because I have no one to turn to. I am hoping one day I will be able to walk again with my legs.”

Ruth is an 11-year-old girl from the Eastern region of Kenya. She is in Grade 5 and is the youngest of three children. Her father is a local farmer and her mother mother is a homemaker. They live in a traditional mud house. She is a jovial and social young girl who aspires to become a doctor in the future so that she can help children in need of different treatments. When Ruth was 7 years old, her mother began to notice an unusual knee deformity which greatly affected her mobility. Her walking style is characterized by limping, and she cannot walk long distances. This has greatly affected her studies, as she is unable to attend school which is quite a distance away. Ruth is scheduled for a knee repair surgery with our medical partner African Mission Healthcare (AMH) on July 17th. Ruth and her family are requesting $1,224 to fully fund the procedure. This surgery will enable her to walk without pain and to attend school. It will also greatly boost her self-esteem and enable her to interact with her friends at school. Ruth’s mother said, “I am pleading for support for my daughter to undergo surgery and continue with her normal life like other children.”

Kaung is a 2-year-old baby boy who lives in Burma with his grandmother, uncle, aunt, and five-month-old cousin. His grandmother is retired, his uncle is a motorbike taxi driver and his aunt is a homemaker. Kaung was born with a condition called Congenital Hydrocephalus. Congenital Hydrocephalus is caused by a brain malformation or birth condition that causes excessive cerebrospinal fluid to accumulate in brain cavities. Cerebrospinal fluid is a clear, colorless liquid that surrounds the brain and spinal cord, protecting them from injury. It carries nutrients to the brain and spinal cord and takes away waste. In a healthy person, the amount of this fluid produced by the brain is absorbed by the body. In hydrocephalus, the fluid fails to drain and accumulates, leading to pressure on the brain. Kaung's symptoms include intensifying nasal congestion and coughing with mucus. Additionally, his head is gradually increasing in size as the fluid continues to put pressure on his brain. The condition is most often treated by inserting a shunt. The shunt diverts excess cerebrospinal fluid (CSF) from the brain to another part of the body where the fluid can be reabsorbed. Kaung's family visited a doctor when he was born to address the issue. At the time, the doctor advised the family to seek further treatment. However, Kaung was never brought to a hospital or clinic due to the financial difficulties of the family. Fortunately, Kaung was able to meet with our medical partner, Burma Children Medical Fund (BCMF). With the help of BCMF and Watsi, Kaung received a CT scan at Mae Sot General Hospital. The doctor was able to diagnose his condition and scheduled Kaung to undergo surgery immediately. Kaung is scheduled for surgery on May 26th. Kaung's aunt said, "My nephew becomes cuter by the day, and he is always smiling. I tried to save money to treat him, but I could not. But now, we are so happy to have met you all at BCMF. We are happy to know that Kaung will have the opportunity to get treated because of your support.”

Ko Thaw, who is 27 years old, lives with his extended family in Burma. In early June 2022, Ko Thaw- who was working in a factory in Malaysia- developed a headache. Later that day, he also experienced chest pain, a racing heart, and an episode of vomiting. His employer brought him to the hospital, and after some testing, Ko Thaw was informed there was a problem with his aortic valve. He was given medications and a follow-up appointment. In January 2023, Ko Thaw's health deteriorated, and he was brought back to the hospital. An echocardiogram showed aortic valve regurgitation, and Ko Thaw was told that he would need surgery. His employer wouldn't pay for the surgery, and as Ko Thaw couldn't afford to pay for this on his own, he tried to manage his condition with medication. But when the medications stopped working, Ko Thaw decided to move back to Burma. Ko Thaw was referred to our medical partner, Burma Children Medical Fund. With their help, he is now scheduled to undergo mitral valve replacement surgery on May 14th at Pun Hlaing Hospital. For Ko Thaw, who currently experiences chest pain, insomnia, muscle stiffness, and headaches with fever, this surgery can't happen soon enough. Now he is seeking your help to raise $1,500 to cover the cost of his treatment. "I hope I can find suitable work soon after my surgery. I would like to say thank you so much. You all do incredible work for poor people who need assistance," said Ko Thaw.

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!"

Nwe Ni is a 43-year-old woman who lives with her mother, her two sisters, and her older brother in Karen State, Burma. Nwe Ni used to work as a homemaker, but stopped once the goiter in her neck became enlarged. Her discomfort began in November 2019, when Nwe Ni started to experience neck stiffness and swelling. Currently, she also has trouble with insomnia, leaving her tired and prompting her to rest during the day. At the same time, she has lost her appetite and, with her neck swollen, at times it feels constricted. In February 2023, Nwe Ni was referred to the Mae Sot General Hospital for further investigation. The doctor there diagnosed her with a multinodular goiter and told her that she would require surgery. Nwe Ni’s mother told the doctor that they could not cover the cost of surgery, and they were referred to Burma Children Medical Fund, which is seeking $1,500 to fund Nwe Ni's thyroidectomy, which is scheduled for March 8th, at Mae Sot General Hospital. She and her family are looking to you to help cover the costs of her life-changing procedure. Nwe Ni said: “I am so delighted when I heard that I could have this mass removed. It feels so heavy, and I am not comfortable living like this. I would like to say thank you so much [to the donors] and you will always be in my prayers for your assistance.”

Ye Min is is a 2-month-old baby from Thailand. His father works at a hotel and his mother is a homemaker. After being delivered, doctors assessed that Ye Min began to experience poor vision in both eyes. These symptoms have made it increasingly difficult for him to see clearly. Ye Min has been diagnosed with retinal detachment, a condition in which the retina pulls away from the supportive tissue in the eye, resulting in vision loss. If left untreated, he could lose vision completely. Ye Min is scheduled to undergo surgery to reattach his retina on January 26th. Our medical partner, Burma Children Medical Fund (BCMF), is requesting $1,500 to cover the total cost of his procedure and care. After his surgery, Ye Min's vision will hopefully be restored, and he will resume his daily activities comfortably. Ye Min’s mother said, “I am worried about my son’s condition because he is too young to receive the surgery. I cannot wait to stay with him and take care of him well. I want my son to get better soon. I was very happy when I hear that this organization will help pay for my son’s treatment. I am really thankful to all of the donors who will help my son receive surgery.”

Baraka is a two-year-old boy from Kenya. He is cheerful baby and an only child to his single mother. Baraka lives with his mother and grandmother. His mother sells clothes in their neighborhood. Baraka was diagnosed with cryptorchidism, a condition in which one or both of the testicles remains undescended. If left untreated, Baraka has an increased risk of developing hernias, testicular cancer, and fertility problems in the future. Baraka will be receiving assistance from our medical partner, African Mission Healthcare Foundation (AMHF). Fortunately, he is scheduled to undergo corrective surgery on February 12. AMHF is requesting $459 to cover the total cost of his procedure and care. His mother says, "I have gone round many hospitals but have been unable to raise money for the surgery. I pray for help because I was told if he grows up like that he may not father children. I hope my boy can be helped to grow up like other boys."

Diego lives alone with his mother in a one-room adobe house that is rented from family members. Diego's mother does not work, and is currently borrowing money from family members to pay for living expenses. She does not have enough money to buy much food for herself some days, and buying formula is just not something that she could ever afford, even if she sold all of her belongings. Diego's step father has left Diego's home and has not been back (we have verified that Diego and his mother are in a safe home situation). His mother is unable to breastfeed Diego. Now, Diego is losing weight extremely quickly and faces the life-threatening danger of getting diarrhea, fever, or an acute respiratory infection. Our community health worker had to give Diego empirical treatment before beginning formal treatment with out nutritionist to prevent a life-threatening situation. With $1016, Diego can receive proper nutrient supplementation. Although Diego's condition is severe, it is very treatable. He will receive formula which will give him the calories, nutrients, and protein he needs to grow and develop normally. His mother will receive motivational nutrition education so she knows what and when to feed her child to prevent future cases of malnutrition. Diego's mother shared: "I dream that my son will be a good student and be able to become a professor."

Jane felt a lump on her left breast two months ago and had a mammogram test done. She had a breast lumpectomy, but she still experiences slight pain and is not able to engage in hard labor or tend to her farm due to the pain. The lump was confirmed as cancer. Jane is a middle aged woman, a wife and a mother of three children. Her husband works as a government chief while she is a farmer. Jane's husband no longer can support the family, which has greatly affected their socioeconomic lifestyle. Jane is the only provider for her family, and her condition is getting in the way or supporting her children. If not treated, Jane is at risk of having cancer spread to other parts of her body and this might result into premature death. Surgeons now recommend a wide local excision on her left breast. Unfortunately, Jane is not able to get the full amount needed to meet the $740 treatment cost on her own. Once Jane is able to receive the treatment she needs, the potentially fatal risk of cancer spreading to other parts of her body will be reduced. She will be free to farm and take care of herself and family. “I pray to get well soon and be able to continue supporting my children," Jane said.