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."

Jayden is an adorable 1-month-old baby from Kenya. He has two older siblings. His mother works as a hairdresser but currently stays home caring for Jayden, while his father works as a casual laborer at construction sites. The family shared that they do not have the insurance coverage to cover Jayden’s surgery needs and request assistance. Jayden 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, Jayden is at risk of lower-limb paralysis, exposed nervous tissue infection, tethered cord syndrome development, and possible developmental delays. Jayden will undergo spina bifida closure surgery on December 13th. This procedure will help Jayden grow up healthy and without any risks associated with this condition. Our medical partner, African Mission Healthcare Foundation, is requesting $1,151 to cover the cost of Jayden’s spina bifida closure surgery. Jayden’s mother says: “We have never seen such a condition in our family, and it is very hard to explain to people. We are hopeful that he will be treated soon.”

Lynemandy is a 28 year old woman from Haiti, who is studying for a business degree at a local university. She lives with her parents in a neighborhood of Port-au-Prince. Lynemandy has a cardiac condition called rheumatic mitral regurgitation, which is a result of a bout of rheumatic fever that she suffered as a child. One of the four valves in her heart was severely damaged as a result of this illness, and in 2018, Lynemandy underwent surgery to repair the damaged valve. The valve functioned well for four years, but now it needs to be replaced so she can live healthy in the future. The care she needs is unfortunately not available within Haiti, so Lynemandy will need to travel to undergo cardiac surgery in the United States on November 17th. Her surgery, during which a new valve will be implanted, is being funded by Baylor Scott & White Heart Hospital. Now Lynemandy and her family need to raise $1,500 to cover the costs of pre and post operative treatment, and for the social workers from our medical partner, Haiti Cardiac Alliance, who will accompany Lynemandy when she travels to the United States. Lynemandy said: "I am very grateful to everyone who is working so hard to keep me alive and healthy."

Sebastiana, who is eight years old, lives with her mother and four siblings in Tanzania. Because she is separated from her husband, Sebastiana's mother works many different jobs in order to support her children. One day, when their mother was away, Sebastiana and her siblings were busy helping out with household chores. Sebastiana got into an accident, and hot water spilled all over her arm. She received treatment for her burns - which healed - but they have left her with scars that limit the use of her arm. Sebastiana and her mother traveled a long way to meet with doctors from our medical partner, African Mission Healthcare Foundation. As a result of their visit, Sebastiana is now scheduled to undergo contracture release surgery, and the amputation of her left thumb, at Arusha Lutheran Medical Centre on October 13th. After her surgery, Sebastiana should regain full use of her hand and arm, which will be a big relief to her mother. Now we need your help to fund the $1,088 required for the surgery. Sebastiana’s mother says: “When we were leaving home, she was so happy knowing that she is going to get treatment.”

Hellen is a soft-spoken, 23 year old student, living with relatives in Gilgil Town in Kenya. Hellen's parents are elderly, and as neither they nor Hellen have a stable source of income, Hellen's relatives are paying for her studies in food and beverage. Just two weeks ago, after undergoing an MRI because of abdominal pain, Hellen learned that she has a fast growing mass in her abdomen, that has displaced her uterus. Hellen was told that she needs surgery urgently in order to remove the mass. If left untreated, the mass could become cancerous, and threaten Hellen's ability to bear children. Fortunately, our medical partner, African Mission Healthcare Foundation, is here to help Hellen access the care that she needs. On September 9th, Hellen will undergo a laparoscopic procedure at AIC Kijabe Hospital, at which time the mass will be removed. African Mission Healthcare Foundation is seeking $1,074 to fund Hellen's surgery. Hellen says: "The swelling in the stomach is growing so fast. I am scared it might be cancerous. It might also affect my ability to get kids if not treated.”

Naw Ywa is a 29-year-old woman who lives with her husband, sister-in-law, and three nieces in a refugee camp in Thailand. Naw Ywa is a homemaker, and she weaves and sells traditional Karen clothing in her spare time. Her husband also works as a homemaker and cares for his sister, who has a mobility impairment. Naw Ywa's three nieces all currently attend school in the refugee camp. This past March, Naw Ywa began to experience severe pain in her left pelvic area. This pain was accompanied by fatigue, dizziness, and trouble breathing. Although she did seek medical attention at the hospital in the refugee camp, she was only given painkillers, which temporarily alleviated her symptoms. After a few months of repeatedly being readmitted to the hospital without fully treating her condition, a doctor referred Naw Ywa to our medical partner's care center, Mae Sariang Hospital (MSH). On July 6th, she was brought to MSH and received an ultrasound. Her doctor diagnosed her with adenomyosis, a condition that occurs when the tissue that typically lines the uterus grows into the muscular wall of the uterus. She was also diagnosed with a five cm large myoma, which is a tumor that develops in or around the uterus. Her doctor has advised that she undergo a hysterectomy to remove her uterus and alleviate her symptoms. Our medical partner, Burma Children Medical Fund, is requesting $1,500 to fund Naw Ywa’s total abdominal hysterectomy. The procedure is scheduled to take place on August 17th. Once completed, she will hopefully be able to live more comfortably and confidently. Naw Ywa shares, “Me and my husband want to have children, but we agreed with the doctor’s plan. I do not want to experience this pain anymore, and my husband also does not want to see me in pain.”

Jane is a polite and calm 17-year girl from a family of four children. Jane’s father is a small-scale farmer of maize and vegetables and practices livestock keeping. Jane completed her primary education late last year and started secondary school, but had to stop because the walk to school grew to be too painful. Jane was diagnosed with left Genu Valgus meaning her leg is bent causing her knees to knock against each other when walking. This condition is typically caused by an excessive accumulation of fluoride in the bones, which often stems from contaminated drinking water. As a result, Jane experiences pain and exhaustion after just a short distance walk. Our medical partner, African Mission Healthcare, is raising $880 to fund corrective surgery for Jane. The procedure is scheduled to take place on July 5th. Treatment will hopefully restore Jane's mobility, allow her to participate in a variety of activities, and greatly decrease her risk of future complications. Jane shared, “I would like to continue with my studies because I want to be either a teacher or a nurse.”

Thu Zar is a 21-year-old woman who lives with her parents, three sisters, and three nieces in Mae Sot near the Thailand-Burma border. Her family moved from Shan State in Burma to Thailand in 2008 in search of better opportunities. She used to work at a logistics company until two weeks ago when she quit due to her condition. Her parents run a small shop from their home, and her oldest sister is a cleaner at a restaurant. One of her other sister’s is unemployed and her third sister as well as her three nieces all go to school. In 2015, Thu Zar felt a small mobile mass in her chest. She did not feel any pain at the time and forgot about the mass. In 2019, she attended a workshop about reproductive health at her school, run by Mae Tao Clinic (MTC). During the workshop she remembered the mass and later when she was alone, she checked to see if it was still there. She felt the mass and thought that it had increased in size, but she did not experience any pain. The next day, she told the workshop trainer about the mass. The trainer told her to go to MTC for treatment. However, Thu Zar decided she did not want to take time off from school to go to the clinic, since she thought the mass was not causing her any pain or discomfort. Now, Thu Zar's condition has worsened and causes her great pain. She can only sleep on her back, because if she sleeps in any other position she experiences immense pain. Thu Zar sought treatment through our medical partner, Burma Children Medical Fund. She is now scheduled to undergo mass removal surgery on June 9th to heal her condition. She is raising $1,500 to cover the total cost of her procedure and care. Thu Zar is very worried about her health and told us, "I feel very sad and depressed with this condition."

Lhory, a 30-year-old woman from the Philippines, experienced severe right-side abdominal pain starting in January. She went to the closest hospital and was advised to undergo a whole abdominal ultrasound. The test showed that she has gallstones that need to be surgically removed. With her husband’s limited income as an Air Conditioner Technician, they’re unable to cover the cost of her treatment. Fortunately, she was able to reach out to our medical partner, the World Surgical Foundation Philippines. Lhory is now scheduled on May 3rd to undergo surgery to treat her condition. Our medical partner, World Surgical Foundation Philippines, is requesting $1,253 to cover the total cost of Lhory’s procedure and care. After her recovery, Lhory will no longer experience severe abdominal pain or be at risk of developing severe health complications in the future. “My current condition hinders me from doing my usual day-to-day chores. My condition makes it hard for me to bend, sit or lift objects," Lhory shared. "We don’t have the capacity to finance my surgery. So, I’d like to thank the World Surgical Foundation Philippines and Watsi for helping me. I hope that after this surgery, I can fully take care of my family again,” says Lhory.

Bb Lafleur is a newborn baby from Haiti. She has an older brother and two loving parents. Bb Lafleur 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, Bb Lafleur has been experiencing an increasing head circumference. Without treatment, she will experience severe physical and developmental delays. Our medical partner, Project Medishare, is requesting $957 to cover the cost of surgery for Bb Lafleur 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 April 7th. This critical treatment will place a shunt to drain the excess fluid from Bb Lafleur's brain to reduce intracranial pressure and greatly improve her quality of life. With proper treatment, Bb Lafleur will hopefully develop into a strong, healthy young girl. Her family hopes that this early treatment of their baby's hydrocephalus will allow her to grow up without any health problems and have a full life ahead.