Meet Gianna, a lovely, four year old girl from Kenya. Gianna lives with her grandmother, while her mother works at a local hotel, and her father is a casual laborer on construction sites. Gianna was born with Osteogenesis imperfecta, also known as brittle bone disease. A child born with this condition has soft bones that break easily. Gianna has never walked, and lives in near constant pain. When she did try to walk using support, she fractured some bones. Our medical partner, African Mission Healthcare Foundation, is here to help Gianna access the care that she needs. On January 16th Gianna will undergo a procedure at AIC Cure International Hospital, that will provide greater support for Gianna's bones, and which may even enable her to gain sufficient strength to walk. Gianna's family is seeking your support to fund the $1,224 needed to pay for the surgery. Gianna's grandmother said: "Gianna has never walked, and my desire is to see her walk like other children. Your financial support to help her undergo surgery will be greatly appreciated."

Agnes is a college student and is in her final year pursuing an architectural course. She lives with her parents and is the second born in a family of three children, all of whom are in school and rely on their parents for school fees and upkeep. Her father is a carpenter in their hometown, Kimende, and his income is inconsistent and not enough to cover the cost of the required surgery. Her mother is a small-scale farmer. Agnes was heading home in the evening last night when she remembers hearing screams and was hit by an unknown motorist from behind. She has no recollection of what happened after that. She lost consciousness and could not recognize her surroundings. She was brought to our medical partner's care center Kijabe Hospital and had an x-ray that revealed a left distal femur fracture. Doctors have recommended an urgent fracture repair surgery since the wound is open and she is in extreme pain. Today, she has regained her consciousness but cannot sit or walk due to the fracture. Fortunately, surgeons at our medical partner are here to help. On October 14th, Agnes will undergo a fracture repair procedure, called an open reduction and internal fixation. This procedure will help get rid of the pain and she will eventually be able to sit and walk easily again. Now, our medical partner, African Mission Healthcare, is requesting $1,500 to fund this procedure. Agnes says, “I am in so much pain and I cannot walk. I don’t remember what happened, I just found myself bedridden with lights all over. I am unable to go back home because of the fracture.”

Kay is 43-year-old woman and garment factory worker. She lives alone on the border of Thailand and Burma. Kay supports her parents in Burma by sending them money every month. In her free time, she enjoys reading books about Buddhism. In the middle of 2021, Kay began experiencing pain and abnormal bleeding. By September of 2022, the pain and symptoms had worsened. Kay has been diagnosed with myoma, or a noncancerous growth in the uterus. She has been advised to undergo a total abdominal hysterectomy, which would surgically remove her uterus and cervix. If left untreated, Kay's symptoms will continue to worsen and put her at risk for further health complications in the future. Fortunately, Kay is scheduled to undergo her hysterectomy on September 19th. Our medical partner, Burma Children Medical Fund, is requesting $1,500 to cover the total cost of her procedure and care. Once recovered, she will no longer experience pain or abnormal bleeding. She will be able to go back to work, and to continue supporting her family. “When I recover fully, I will continue to work in the garment factory. I will save my money and I will pay back my debt. I will try to continue supporting my parents,” said Kay.

Jonathan is a courageous fire officer from the Philippines. He lives with and helps support his siblings and elderly mother. He works to provide their family's sole income. Last month, Jonathan began to experience pain and other troubling symptoms that caused him to seek medical attention. He was diagnosed with mixed hemorrhoids, or a combination of internal and external hemorrhoids. This condition causes the veins of the lower rectum to become swollen. He requires surgery to prevent his symptoms from getting worse. Fortunately, our medical partner, World Surgical Foundation Philippines (WSFP), is helping Jonathan receive treatment. He is scheduled to undergo a hemorrhoidectomy on August 20th at WSFP's care center. During this procedure, surgeons will remove his hemorrhoids. A portion of the cost of his treatment is being supported by the Philippine Health Insurance Corporation, and WSFP is raising the remaining $1,137 to cover the cost of Jonathan's procedure and care. Jonathan shares, "This disease hinders me from doing my job. I'm the only one who works in our family. If I can't work, I won't be able to provide for our needs, so this surgery is a big help for me. To Watsi and World Surgical Foundation Philippines, thank you so much for your kind hearts. May you not get tired of helping the needy."

Naw Eh is a 32-year-old woman who lives with her parents, her husband, and her children in a refugee camp. She supports her family by caring for her children and managing their home. Her husband is currently unemployed. Three of her children are enrolled in primary school, but her fourth child is too young to attend. During her free time, Naw Eh enjoys sewing clothes. Naw Eh is currently expecting a new baby and her doctors recommend that she undergoes a caesarean section to deliver her child because she is already 40 weeks pregnant and her baby is still in the wrong position, laying horizontally instead of vertically. With a C-section, doctors will be able to ensure the safety of both Naw Eh and her baby during the delivery. Our medical partner, Burma Children Medical Fund, is helping Naw Eh undergo a C-Section on July 7th. This procedure will cost $1,500, and Naw Eh's family needs your support to help fund her care. Naw Eh shares, “In the future, I will search for a job in the refugee camp, and I will also take good care of my children.”

Yoon is a bright and loving 12-year-old girl. She lives with her mother and uncle in Karen State of Burma near the border with Thailand. She was a student in grade three but stopped studying in August 2020 when she was no longer able to walk. Yoon enjoys painting pictures and reading books. In the future, she wants to go back to school and continue her studies. She helps out her mother with household chores. Her uncle is unemployed whereas her mother is an agricultural day labourer. One day at home, Yoon fell down when she tried to stand up to go to the bathroom. Her feet felt painful and were pointing downwards. After that, she did not try to stand up again and would move around her house on her knees. Her mother would have to carry her to the bathroom. Due to their financial situation, her mother was not able to seek treatment despite being very worried for her daughter. Over time, Yoon noticed that her feet were increasingly pointing downwards and were stiff. Her legs would feel painful and were also stiff. Sometimes, she could not stretch out her legs due to feelings of tightness and pain. Her mom shared that she would cry whenever her legs pained, and she would have to wait until the pain lessened by itself. Additionally, her hands began to weaken until she could not hold food with her hands. At the same time, her speech became slurred and her voice became hoarse. On June 17, Yoon arrived at our medical partner's care center, Mawlamyine Christian Leprosy Hospital (MCLH), and was admitted that same day. She received a physical examination and was diagnosed with cerebral palsy and tightness of Achilles tendon in both of her legs. The doctor recommended she receive surgery on both of her feet, which would help her walk again, and scheduled the procedure for June 21st. When Yoon’s mother told the doctor that they cannot afford to pay for surgery, the doctor referred Yoon to Burma Children Medical Fund (BCMF) for assistance accessing further treatment. Our medical partner, BCMF, is requesting $1,500 to cover the cost of an Achilles tendon lengthening procedure for Yoon. This procedure will elongate her Achilles tendon, allowing increased motion at the ankle joint. Without treatment, Yoon's condition will continue to cause her discomfort and will further limit her movement. Her mother said, “I cried almost every night when I saw my daughter in this condition. She always cried and complained about her feet. She always asked me to bring her to the hospital to get treatment. Whenever she asked me, I felt very sad and I would cry in secret. I want her to get treatment, but I cannot afford to pay for it. Due to COVID-19 and the current fighting in Burma, I cannot make enough money or save it. Often, I would only eat fishpaste and rice, but give her meat so that she can have something nutritious. When I heard that she has donors who will help her receive treatment, I felt very happy and thankful to BCMF for this kindness. I never thought she would receive such an opportunity. It makes me so happy that I do not know how to express it in words.”

Thay is a one-year-old girl from Burma. She lives with her parents, grandfather, three sisters and a brother in a village. Thay's mother looks after her and her brother at home, her grandfather is retired, and her sisters go to school. Thay's father works as a porter, but has has difficulty finding work for over a month. With the increasing number of internally displaced people settling in their village due to the humanitarian crisis, there are now many individuals competing for the same work. When Thay was around eight months old, her parents noticed that her head was increasing in size. As a result, Thay cannot yet sit up or crawl. She is only able to turn her head, and will cry if she cannot see her parents. Thay was recently diagnosed with hydrocephalus, which has causes fluid to build up in her brain. Without immediate surgery to alleviate the intracranial pressure, Thay is at risk of developing severe, potentially fatal medical complications. Our medical partner, Burma Children Medical Fund, is requesting $1,500 to fund the insertion of a ventriculoperitoneal shunt for Thay, which will drain the fluid that has accumulated in her brain. The procedure is scheduled to take place on May 20th and, once completed, will greatly improve Thay's quality of life as she grows up. Thay's father said, "I am thankful to every organisation and everyone for supporting my daughter’s treatment cost. Because of you, I believe that my daughter will receive surgery and be healthy and live a normal life after treatment."

Gatguon is an 8-week-old baby girl from a remote area of South Sudan. The civil war in South Sudan has made it difficult for many to access healthcare and treatment, including Gatguon's family. Gatguon was born with swelling in the back of her head. Upon referral to Old Fangak Clinic, the doctor diagnosed Gatguon with spina bifida, a type of neural tube defect in which the spine does not properly close around the spinal cord. Without treatment, Gatguon is at risk of lower-limb paralysis, infection of the exposed nervous tissue, development of tethered cord syndrome, and possible developmental delays. Gatguon urgently needs spina bifida repair surgery to correct the condition and reduce risk of infection. Unfortunately, this treatment is not available for her in South Sudan. Dr Jill Seaman and her team at Old Fangak Clinic facilitated Gatguon’s travel to Kenya – a long and difficult journey for a sick baby. Now, doctors at our medical partner's care center in Kenya will perform the surgery she needs. Gatguon’s parents have two kids. Her mother is a stay-at-home mom and her father is a vegetable farmer. They are hopeful that baby Gatguon will be treated and that they will continue taking care of her and loving her unconditionally. Our medical partner, African Mission Healthcare, is helping Gatguon's family raise $1,151 to cover the cost of spina bifida closure surgery. The procedure is scheduled to take place on April 20th and will hopefully spare Gatguon of further complications and allow her to grow and develop along a healthy trajectory. Gatguon’s mother shared, “We hope that our child will be treated.”