Davide GerbaudoUNIVERSAL FUND MEMBER
Davide's Story

Davide joined Watsi on September 14th, 2013. Nine years ago, Davide joined our Universal Fund, supporting life-changing treatments for a new Watsi patient every month. Davide's most recent donation traveled 6,200 miles to support Ly, a 62 year old man from Cambodia, to fund hand surgery.

Impact

Davide has funded healthcare for 123 patients in 14 countries.

patients you have funded

Elinipa is a beautiful two-year-old girl. She is an incredibly friendly child who loves to play with her five older siblings. At birth, she was a healthy child. It wasn't until she was learning to walk however, that her mother noticed that her legs were slightly curved, yet even so they did not seek treatment assuming it was a minor problem that she would outgrow. Elinipa has now been diagnosed with bilateral valgus, which is a condition caused by an excessive accumulation of fluoride in the bones, which often stems from contaminated drinking water. As a result of her condition, Elinipa's legs bow inward to the point that her knees touch. This makes walking persistently more difficult as she continues to grow. Through our medical partner's outreach program her parents learned that their daughter needs surgery to correct her legs. Elinipa's parents are small scale famers who depend entirely on what they harvest to make a living. As a result, their income is not enough to afford to take Elinipa to the hospital to treat her condition. Our medical partner, African Mission Healthcare, is requesting $880 to fund corrective surgery for Elinipa. The procedure is scheduled to take place on May 13th at our medical partner's care center, Arusha Lutheran Medical Centre. With this treatment Elinipa's mobility will hopefully be restored, thus allowing her to participate in a variety of activities, and greatly decreasing her risk of future complications. Elinipa’s father says, “I am worried with how her legs continue to bend inward. Please help us.”

$880raised
Fully funded

Nimo is a 3 year old girl, living with her grandmother in Ethiopia. When she was just a few months old, Nimo's parents gave her to her grandmother, as with four other children already at home and Nimo's medical condition, they were unable to take care of Nimo. Nimo's grandmother, who has a small business, was already supporting four other people, so she shared that it is hard for them to survive from day to day. Nimo was born with a congenital malformation, that led to a blockage in her intestines. At first, when Nimo began to show signs of this condition, her family didn't have the funds to take her to the hospital. By the time someone provided funds so that Nimo could get to the hospital, she was weak and underweight from malnourishment. An emergency colostomy was performed, and over time, Nimo gained strength, and is now able to run and play with her friends. However, she still has multiple issues that require medical attention and additional surgery to help her fully heal. Nimo is scheduled to undergo surgery to correct her condition on July 5th, at BethanyKids Myungsung Christian Medical Centre. Our medical partner, African Mission Healthcare, is requesting $1,500 to cover the total cost of Nimo's procedure and care. After her recovery, Nimo will no longer experience bowel dysfunction, or be at risk of developing related health complications in the future. Nimo's grandmother says: “When she heals, I will go to my home and celebrate with my family. ”

$1,500raised
Fully funded

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.”

$1,151raised
Fully funded