Moe is a 15-year-old boy from Burma. He lives with his parents, sister, and two brothers. His father works as a day labourer, while his mother is a homemaker who sometimes takes on laundry jobs to help support the family. Moe completed grade three but had to stop his education in 2024 because of his health. He was diagnosed with a heart condition that requires valve replacement. Heart valves control the flow of blood between chambers, but certain conditions may narrow the heart valve or cause the blood to flow backwards. Normal valve function is necessary to prevent long-term damage to the heart and lungs. Currently, Moe experiences fatigue, loss of appetite, dizziness, and sometimes feels uncomfortable while sleeping at night due to squeezing and radiating pain around his chest and back. Our medical partner, Burma Children Medical Fund, is requesting $1,500 to fund a heart valve replacement for Moe. The treatment is scheduled to take place on July 17th at our medical partner's care center, Kasemrad Prachachuen Hospital, and once completed, will hopefully allow him to live more comfortably. Moe's mother shared, "Thank you to the donors and the organisation for supporting my son’s surgery. We are very grateful. As day labourers, we do not have enough money. I am not healthy enough, and while doing laundry to earn extra income, I feel exhausted. Without your support, we would face unbearable financial burdens and could not afford the surgery. Thank you very much for your help.”

Hadassa is a seven-year-old girl from Haiti. She is the middle child in her family, with an older sister and a younger brother. She does not currently attend school but enjoys helping her parents around the house and watching cartoons. Hadassa has a cardiac condition called a partial atrioventricular canal defect. A hole exists between the chambers of her heart, causing blood to leak between them instead of properly circulating through the lungs to receive oxygen. This leaves her weak and short of breath. Hadassa also has Down syndrome. Hadassa needs to fly to the Dominican Republic to receive treatment. On June 24th, she will undergo heart surgery, during which doctors will repair the hole in her heart. Another organization is paying for the surgery, but her family also needs help with travel and surgery prep. Our medical partner, International Cardiac Alliance, is requesting $1,500 to cover labs, medicines, and check-up and follow-up appointments. It also supports securing travel documents for the family and travel costs for the social workers from our medical partner, who will accompany Hadassa's family overseas. Hadessa’s mother shares, “Our family is so happy to know that there is a way to fix our daughter’s heart, and we hope everything will go well!”

Nay is just like any other active one-year-old with a loving family. Except Nay was born with a heart condition, patent ductus arteriosis (PDA), a persistent opening between two major blood vessels that should close right after birth. However, Nay's remains open, which can weaken his heart and cause other cardiological and respiratory complications. Nay is one of three children. Their father is a day laborer, and their mother is a homemaker. Their incomes are just enough for basic expenses and health care, but not enough to fund heart surgery. "We are worried when we know that Nay needs surgery because we could not afford for it," Nay's parents said. To fund his surgery on October 3rd, our medical partner, Burma Children Medical Fund, is requesting $1,500. After treatment, Nay will live more comfortably and avoid potential complications. For his parents and sisters, it also means one less worry.