Yadesa is an 80-year-old man from Ethiopia. He is a retired merchant who spent his life working hard and building an independent life. Since the deeply sad loss of his beloved wife, he has found comfort and support by moving in with one of his two brothers. One year ago, Yadesa developed a cataract in his right eye, causing him blurry vision and burning sensation. A cataract is a clouding of the lens of the eye, blurring vision. For a man who spent his whole life actively connecting with the world through buying and selling, this slow darkening of his sight is truly heartbreaking. It has made it incredibly hard for him to talk and spend time with his loved ones, enjoy the world around him, and hold onto the dignity and independence that have always defined who he is. Fortunately, Yadesa is scheduled to undergo cataract surgery with the help of our medical partner, Saglan Wajee General Hospital. Surgeons will remove and replace the blurred lens. After recovery, he will be able to see clearly. Now, he needs help to raise $150 to fund this procedure. Yadesa shared, "I hope to regain the independence I so deeply miss, allowing me to navigate my home and enjoy the company of my brother with newfound ease and confidence."

Nan Maw is a 24-year-old woman from Burma. She lives with her friends in Bangkok in an apartment rented by their employer. She works as a waitress, while her brother and mother still live in their village in Karen State, Burma. When Nan Maw was healthy and working full-time, she would send half of her salary home to support her mother. She dreams of building a concrete house back home for her family. Nan Maw was born with an atrial septal defect (ASD), a condition in which a hole exists between the two upper chambers of the heart. Sometimes ASDs may close on their own during development, but sometimes this condition requires surgery to repair the hole and prevent long-term damage to the heart and lungs. Due to her condition, she can only engage in part-time work as she gets tired too easily. Nan Maw is scheduled to undergo heart surgery on August 31st at our medical partner's care center, Kasemrad Prachachuen Hospital, to correct her atrial septal defect and improve her quality of life. Our medical partner, Burma Children Medical Fund, is requesting $1,500 to help cover the cost of Nan Maw's procedure and care. Nan Maw said, “I would like to thank your organization, BCMF, and your donors for your help. If you do not help me, I would have had to give up on my treatment because I know that I could not afford it by myself. I am very happy and thankful to all the donors. You have helped me feel that I can dream again. Before I developed these symptoms, I dreamed of working hard, saving money, building a house back home, and opening my own restaurant. Since I first noticed my symptoms, it felt like my dreams were lost. But now, I can dream again.”

Albertina is a two-week-old girl from Tanzania, and the youngest child in her family of nine children. Her mother maintains their home and cares for the children, while her father works as a fisherman to provide for the family. Albertina was born with clubfoot on her left foot, a congenital condition in which the foot is turned inward. Without appropriate treatment, this condition can affect her ability to wear shoes and walk comfortably as she grows. Soon after her birth, Albertina's family was referred to our medical partner's care center, Kafika House, for assessment and treatment. The referral gave the family hope that their newborn daughter could receive the specialized care she needed. Albertina is scheduled for treatment, and will be fitted with a foot abduction brace (FAB), which she will wear as part of her treatment plan until the age of five to help prevent her clubfoot from recurring. The treatment will begin on October 20th, and our medical partner, African Mission Healthcare, is requesting $341. After treatment, Albertina will have the opportunity for better mobility, and enjoying her childhood milestones. “We are grateful that our daughter has a chance to receive treatment, and grow up like other children,” said Albertina's mother.