This little man is Manish, a three-month old boy from Nepal. Our medical partner, Possible, tells us, “baby Manish was born with clubfoot.” Clubfoot is a congenital foot deformity is which the tendons in the foot are shorter than usual. This changes the position of the foot making it difficult to walk. “Being only three months old he does not have negative impact, but in the future he is expected to have discomfort and deformities,” says Possible. Manish lives with his mother, his older brother, and his grandparents. His father works in India to provide for his family. Manish’s grandmother says, “the doctor tells us he needs weekly plaster and even a surgery later on.” For $579, Manish will receive this necessary treatment to prevent developing deformities and discomfort later on. Possible tells us, “a cast will be put on Manish's leg every week moving the foot closer to a normal position each time.”

"Neema was born at home on December 14th, 2015," says our medical partner, African Mission Healthcare Foundation (AMHF). "She is the fourth born in the family. Neema’s parents moved away from their village three years ago due to severe drought. They managed to move with a few cows and goats and currently they are living with Neema’s grandparents (mother’s side)." "Neema has a lesion on her lower back, which can easily burst – leaking cerebral spinal fluid," AMHF says. "If not treated, Neema can easily contract infections, causing other bigger health problems." Neema's open mass is due to a condition called spina bifida. "Neema’s mother is a homemaker and his father is a livestock keeper," AMHF says. "Their two children are in primary school and they hope to be able to send all of their children to school. Currently they do not have sufficient funds to cover the cost of operation which Neema badly needs. Neema is getting on and off fevers and sometimes she vomits after breastfeeding." For $1,200, we can fund a life-saving spina bifida closure procedure for Neema. "The lesion on Neema’s back will be closed preventing her from losing CSF and easily contracting infection," says AMHF. “I hope my baby will get well, grow up like her siblings and later on go to school,” shares Neema’s mother.