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Ella Henning

MONTHLY DONOR

United States   •   Born on November 24

Ella's Story

Ella joined Watsi on November 11th, 2014. Five years ago, Ella joined our Universal Fund, supporting life-changing treatments for a new Watsi patient every month. Ella's most recent donation traveled 8,800 miles to support Chhorn, a mom-of-four from Cambodia, to fund a hip replacement after a serious fall.

Impact

Ella has funded healthcare for 64 patients in 11 countries.

All patients funded by Ella

Israel

Israel is a baby boy from Tanzania and the last-born in a family of two children. His mother delivered him at home with the help of midwives and soon noticed her son's left foot was not straight. She was scared to tell her husband or her parents-in-law as she was scared they might accuse her of bringing disability into their family. It took her almost two months to be able to summon up the courage and inform her husband about their son's condition. Her husband was understanding and they decide to seek a doctor's advice at a local hospital near their village. They were informed that the condition was treatable but they would have to be referred to the district hospital. They inquired on the cost of the treatment but the cost turned out to be too expensive for them to afford. Thus they were forced to return home hoping they would be able to raise the money one day and have their son's foot corrected. Both parents depend on small-scale farming for their living, which they shared is barely enough to meet their basic needs. They heard about the Plaster House from a relative and decide to try seeking help. The medical team shared that Israel has clubfoot of his left foot. Clubfoot is a condition in which the foot is twisted out of shape. This causes difficulty walking and even wearing shoes. Fortunately, surgeons at our medical partner's care center, Arusha Lutheran Medical Centre, will perform clubfoot repair surgery on September 2nd. Our medical partner, African Mission Healthcare Foundation, is requesting $935 to fund Israel's clubfoot repair. After treatment, when he grows up, he will be able to walk easily. Israel’s mother says, “I am scared my son would be discriminated if he does not have this condition corrected. Please help us.”

69% funded

69%funded
$654raised
$281to go
Catherine

Catherine is a 17-year-old student from Tanzania, the youngest in her family of three children. She is currently in Form Four and hoping to graduate secondary school this year. She is a shy but bright young girl. Catherine’s father is a construction worker and her mother owns a shop at their home where she sells day-to-day household stuff. Catherine 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, Catherine has been experiencing headaches for the past two weeks continuously. She was originally taken to the hospital and was tested for a UTI and malaria but found to have nothing wrong. Her headaches got more severe, followed by vomiting and irritability and could not control her urination. Her family was told to do a CT scan test but the surgeons were not satisfied with the results and needed to do an MRI. The MRI showed that there is build up of CSF fluids causing pressure in her brain and the doctors shared that Catherine needs surgery as soon as possible. Without treatment, Catherine will experience severe physical and developmental delays. Our medical partner, African Mission Healthcare Foundation, is requesting $1,238 to cover the cost of surgery for Catherine to treat her hydrocephalus. The procedure is scheduled to take place on April 29th and will drain the excess fluid from Catherine's brain. This will reduce intracranial pressure and greatly improve her quality of life. With proper treatment, Catherine will hopefully develop into a strong, healthy young girl. Catherine says, “I would really like to get better and continue with school. Please help me get well.”

100% funded

$1,238raised
Fully funded
Mya Mya

Mya Mya is a 40-year-old-woman who lives and work with her elder sister for a herbal medicine production workshop in Sanchaung Township, Yangon Division in Burma. They are originally from Bago Division and moved a few years ago. Since Mya Mya was 18 years old she has felt bronchial asthma and suffered from difficulty breathing. Sometimes she feels severely tired. She went to a health worker at her village and the health worker told her to go and see heart specialist in Yangon. However, at that time she did not have money to go to Yangon, so she did not go. She has only used herbal medicine for treating difficulty breathing since she was 18-year-old, which did help her feel better. For the last four months at night she has severe difficulty breathing, so she woke her sister up and asked her sister to send her to a private clinic called Yaung Chi Oo in Yangon. After the doctor's examination, she was told her that she needs to go and see heart specialist doctor. Then the doctor gave her an injection and some oral medication. Then, she went to Thiri Sandar Private Hospital on January 31, 2020 where she received an echocardiogram. The doctor told her that she has heart disease and she needs surgery. On February 5, Mya Mya went to Kan Thar Yar Hospital (KTYH) as suggested by the doctor at Thiri Sandar Hospital. The doctor at KTYH performed another echo before diagnosing her with large ventricular septal defect (VSD). The doctor at KTYH also told her that she needs surgery. Unfortunately, Mya Mya and her family cannot afford to pay for the surgery. After talking to the nurses and doctor about her problem, the nurses who know Watsi Partner Burma Children Medical Fund (BCMF) refered her to BCMF. Mya May needs to stop working because of her tiredness. She is worried about her parents because if she cannot work. She shared, "If I recover from my disease, I need to work for my parents, to support them.”

100% funded

$1,500raised
Fully funded