Srinivas MuddanaUNIVERSAL FUND MEMBER
Srinivas' Story

Srinivas joined Watsi on December 15th, 2014. Eight years ago, Srinivas joined our Universal Fund, supporting life-changing treatments for a new Watsi patient every month. Srinivas' most recent donation supported Angel, a four-year-old girl from Kenya, to fund clubfoot surgery and care.

Impact

Srinivas has funded healthcare for 105 patients in 13 countries.

Patients funded by Srinivas

Vath is a 14-year-old boy from Cambodia. He is an only child who lives with his mother and grandparents, while his father works long hours at a public hospital in Phnom Penh, two hours from where they live. To support the family, his mother sells groceries from their home. Vath is currently in 7th grade and enjoys studying the Khmer language. He loves playing soccer with his friends at school. Vath was born with double "S" scoliosis, an abnormal double curvature of the spine, and macrodactyly, a rare congenital condition that causes toes to be abnormally large. Due to the condition of his spine, his rib cage presses against his lungs, making breathing difficult. Vath was first seen by our medical partner, Children’s Surgical Centre (CSC), where he underwent surgery on his right foot, including a toe amputation in January 2024. His family is now seeking further treatment for his scoliosis, which has inhibited his growth. It is difficult for him to walk or keep up with friends, and he often experiences shortness of breath, especially while at school and around other boys his age. On September 3rd, Vath will undergo a fusion procedure of his spine. The damaged vertebra will be removed and the spine will be fused to correct the curvature and stabilize his spine. Timely treatment in adolescence can prevent progression and reduce the need for more invasive measures later in life. Vath and his family are able to contribute $50 but need help to raise $1,450 more to fund the cost of the surgery, spinal implants, medications, and post-op care. Vath said, "I want to run and play soccer with my friends again soon and return to school to study."

$738raised
$712to go

Oliver is a married mother of four children, all of whom are married with children except the last one who is still in school. She is a farmer together with her husband. Her second child, a daughter, has been there for her support throughout her illness. Oliver likes chatting with her daughter and enjoys eating nsima made from cassava maize flour served with fresh fish. Oliver was well until one year ago when she noted a small lump on her right breast that was not painful. She visited her nearest hospital where some pain medication was provided. She visited many other hospitals after noting that the growth was becoming bigger as time passed. At one of the hospitals, a diagnosis of suspected breast cancer was made before proceeding to Kamuzu Central Hospital for further assessments. At Kamuzu Central Hospital (KCH), different tests were done, and a diagnosis of invasive ductal carcinoma was made followed by four cycles of neoadjuvant therapy. Oliver was later scheduled for surgery on January 15th this year but unfortunately, she did not report back since she did not have the funds. On January 29th, Oliver went back to KCH where she was referred to our medical partner's care center Partners in Hope Medical Center (PIH) so that she can undergo surgery more urgently. Of late, Oliver has been experiencing needle pricking pains, and weakness affecting her farm work plus household chores as a mother. On January 30th, Oliver reported to PIH and met the surgeon who confirmed the need for a modified radical mastectomy. Modified radical mastectomy is the removal of the entire breast, including the nipple, areola, and skin plus most axillary lymph nodes. Oliver believes the surgical operation will help her get back home in a good condition and enable her to resume her farm work. Oliver said, “Kindly remove this breast for me to have my peace of mind after getting rid of these bad symptoms that I experience, I would rather be able to move on in my age.”

$1,194raised
Fully funded

Khin is a 49-year-old refugee living with her father, her daughter and her younger sister in a refugee camp, in Tak Province along the Thail-Burma border. Her family fled from Karen State, Burma to Thailand in 2017 because of the conflict in their area. Khin’s father is retired and her daughter is a student. Khin’s sister looks after their retired father at home. Khin Mar is a day labourer in the camp. However, the job is not available every day. Every month her family receives 1,200 baht (approx. 40 USD) on a cash card from the organization The Border Consortium. This amount combined with her monthly salary is enough to cover their daily needs. They receive free basic health care provided by the International Rescue Committee in the camp but surgical care is not available there. In the middle of 2023, Khin noticed pain in her lower abdomen. Still, she did not go to the hospital or clinic as she thought the process was normal for women who are getting older and close to menopause. However, in the beginning of November, she noticed that the pain worsened and now the pain is constant. She visited the hospital in the camp, where the medic gave her some medication and she returned home. The pain did not resolve and continued. On 13 November, she returned to the hospital in the camp where she met with the doctor and the doctor performed an ultrasound for her and told her that there is a mass in her uterus. The doctor told her that they will refer her to Mae Sot Hospital (MSH) where she received another ultrasound, and the doctor diagnosed her with uterine myoma - a benign tumour in the uterus and also told her that she needs surgery to remove the mass as well as her whole uterus. Khin has been experiencing lower abdominal pain and back pain almost every day now. She cannot sleep as she worries that if she receives surgery, she will not be able to work and will not have income. At the same time, she also feels hard to perform her job well as she feels that her back pain makes it worse for her when she washes clothes. If left untreated, Khin's symptoms will continue to worsen and put her at risk for further health complications in the future. Fortunately, Khin is scheduled to undergo her hysterectomy which will heal her condition on December 4th. Our medical partner, Burma Children Medical Fund, is requesting $1,500 to cover the cost of her procedure and care. After surgery, she will no longer in pain and she will be able to continue her job comfortably like before. Khin said, “if I do not work, I worry that I will not have enough income for my family and also when I heard that I need surgery, I worry about the surgery cost. When I heard that there will be a donor for me, my father and I are very happy as we know we cannot afford to pay for this expensive surgery.”

$1,500raised
Fully funded

Kelita is a single mother with four children, aged 18,14,12, and 8. Kelita shared that she separated from her husband in 2017 because she would not adhere to cultural chieftaincy rules that wives are supposed to follow. Kelita refused to stop going to church; hence her family broke apart, and her husband married another woman. He does not provide support for his children so Kelita works hard to support her family on her own. Kelita sells cooked green maize in the nearest markets, earning about $37.00 per month. She and her four children live in a three-room house without water or electricity. Kelita does extra work in people’s gardens for her family's support and shared that she enjoys eating nsima (ugali) with vegetables prepared with groundnut flour. Kelita was well until 2011, when, after the delivery of her third child, she noted a fast-growing swelling on her neck. She did not seek medical care as there was no pain. As time passed, the swelling grew, but was not painful. In 2021, Kelita started experiencing neck heaviness and breathlessness, frequent coughs, and pains when carrying heavy items on her head. This affected her daily activities and business since she could no longer carry a basket of maize on her head. Kelita stopped her cooking business and relied on doing piece work in people’s gardens to support her family. However, even this is difficult now, as bending has become a challenge. In November 2021, Kelita visited her nearest hospital and was referred to Kamuzu Central Hospital, where an ultrasound scan revealed a bilateral complex mass in her thyroid. Kelita was sent for thyroid function tests but since she did not have the money required for the tests, she returned home to try traditional medicine, to no avail. In July, Kelita met a Partners in Hope (PIH) beneficiary who guided her to visit PIH for potential support from Watsi. On August 14th, Kelita met the surgeon at PIH. After the required tests were completed, a diagnosis of goiter was confirmed. Kelita was told she needed to have a surgical intervention called thyroidectomy, the removal of part or all of the thyroid gland. Due to her financial challenges, Kelita was referred to Watsi's medical partner, African Mission Healthcare, for support. Kelita could smile much bigger after hearing about the planned surgery and committed to a co-pay $27.64 from her savings. Kelita hopes to be well again after the surgical operation. Kelita looks forward to the peace of mind that will enable her to support her children as a single parent. “I need my peace of mind for me to resume my business and be able to carry items on my head again. Kindly help me,” Kelita says.

$1,015raised
Fully funded

Hapyness is a charming 9-month-old girl, born to hardworking farmers in the remote village of Igot, in the Ulanga district of Tanzania. Her family's daily life revolves around the cultivation of maize and millet, which not only sustains their meals, but also provides a modest income for the family’s necessities. Unfortunately, her father, who is advancing in age, cannot work extended hours, so her mother toils diligently on the farm, to ensure they yield bountiful harvests. Hapyness was born with a clubfoot, a condition in which the foot is abnormally twisted, making it difficult for her to crawl and eventuall to walk. At the time of her birth, the nurse in attendance recommended immediate medical attention. However, locating such specialized care in their isolated village proved to be impossible. After months of searching, Hapyness' father crossed paths with a young boy who had had a clubfoot which had been successfully treated, and he was able to provide Hapyness' father with the information he had been seeking. As a result of this meeting, Hapyness' parents brought her to the Plaster House, where her treatment will begin on October 6th. Our medical partner, African Mission Healthcare Foundation, is requesting $935 to fund Hapyness' clubfoot repair. After treatment, she will be able to crawl and to walk comfortably as she grows. Hapyness’s mother says: “I am glad there is a chance for my daughter to get treatment. I hope she doesn't have to live with this disability for the rest of her life.”

$935raised
Fully funded