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Success! Mursale from Tanzania raised $838 to fund surgery on his legs.

Mursale
100%
  • $838 raised, $0 to go
$838
raised
$0
to go
Fully funded
Mursale's treatment was fully funded on December 26, 2019.

Photo of Mursale post-operation

October 22, 2019

Mursale underwent surgery on his legs.

Mursale had a successful surgery has helped straighten his left leg that had significant genu varus. This was making his walking difficult and painful. His right leg has mild genu valgus which had also been scheduled for surgery but there was a last-minute change of plan by the surgeons and decided to only operate the left leg which was severely affected. In case after correcting the left leg and the right does not improve he will be scheduled for another surgery to correct the remaining right leg.

Mursale’s mother says, “I am grateful for coming in and helping fund my son’s treatment cost so that he can be able to walk again. Thank you very much.”

Mursale had a successful surgery has helped straighten his left leg that had significant genu varus. This was making his walking difficult a...

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September 19, 2019

Mursale is a child from Tanzania. Mursale is a three year old little boy and a third born child in his family, he is a calm but happy baby. Mursai’s father does small business in his hometown where by he sells construction sand and his mother is a small business woman, she own a small restaurant.

Mursale was diagnosed with windswept deformity. His legs bow in a way to seem as though they are blown by the wind. This condition is typically caused by an excessive accumulation of fluoride in the bones, which often stems from contaminated drinking water. As a result, he has difficulty walking.

Our medical partner, African Mission Healthcare, is requesting $940 to fund corrective surgery for Mursale. The procedure is scheduled to take place on September 19. Treatment will hopefully restore Mursale’s mobility, allow him to participate in a variety of activities, and greatly decrease his risk of future complications.

Mursale’s father says, “Please help my son get this treatment so that he is able to walk without difficulty.”

Mursale is a child from Tanzania. Mursale is a three year old little boy and a third born child in his family, he is a calm but happy baby. ...

Read more

Mursale's Timeline

  • September 19, 2019
    PROFILE SUBMITTED

    Mursale was submitted by Joan Kadagaya, Curative Medical Support Program-Partner Representative at African Mission Healthcare, our medical partner in Tanzania.

  • September 20, 2019
    TREATMENT OCCURRED

    Mursale received treatment at Arusha Lutheran Medical Centre (ALMC). Medical partners often provide care to patients accepted by Watsi before those patients are fully funded, operating under the guarantee that the cost of care will be paid for by donors.

  • September 24, 2019
    PROFILE PUBLISHED

    Mursale's profile was published to start raising funds.

  • October 22, 2019
    TREATMENT UPDATE

    Mursale's treatment was successful. Read the update.

  • December 26, 2019
    FULLY FUNDED

    Mursale's treatment was fully funded.

Funded by 22 donors

Funded by 22 donors

Treatment
Fluorosis - Genu Valgus / Varus
  • Cost Breakdown
  • Diagnosis
  • Procedure
On average, it costs $838 for Mursale's treatment
Hospital Fees
$789
Medical Staff
$15
Medication
$11
Supplies
$0
Labs
$23
  • Symptoms
  • Impact on patient's life
  • Cultural or regional significance

​What kinds of symptoms do patients experience before receiving treatment?

Patients with genu valgum (or "knock-knees") have knees that bend inward and cause an abnormal walking gait. Patients with genu varum (or bowleggedness) have knees that bend outward and cause knee or hip pain and reduced range of motion in the hips.

​What is the impact on patients’ lives of living with these conditions?

The patient's mobility is hindered, which can prevent the patient from making a living through physical labor. The patient may also develop arthritis later in life.

What cultural or regional factors affect the treatment of these conditions?

In the United States, supplemental fluoride is added to the water to improve dental health. However, in areas of northern Tanzania, there is too much naturally-occurring fluoride in the water, which causes bone curvature.

  • Process
  • Impact on patient's life
  • Risks and side-effects
  • Accessibility
  • Alternatives

What does the treatment process look like?

After surgery, the patient will stay in the hospital for 4-5 days. During this time, the surgical wound will be monitored for swelling and infection. The patient will complete physiotherapy to help him or her walk or move the limbs. A series of X-rays will be performed over several months to monitor the healing process.

What is the impact of this treatment on the patient’s life?

The bones and joints will be aligned, and long-term disability will be prevented.

What potential side effects or risks come with this treatment?

This procedure is not risky, but it is time-consuming. The rehabilitation process can take several months.

How accessible is treatment in the area? What is the typical journey like for a patient to receive care?

Care is not easily accessible. Most patients live in remote, rural areas and are identified through mobile outreach. The pediatric surgical program at Arusha Lutheran Medical Centre was started to meet the large burden of pediatric disability in the region.

What are the alternatives to this treatment?

There are no alternatives. Although some cases can heal on their own, the patients submitted to Watsi require dedicated treatment.

Meet another patient you can support

100% of your donation funds life-changing surgery.

Htay

Htay is a 54-year-old single woman from Burma. She lives with her sister, three nephews and a niece in Mudon Township, Mon State, Burma. Her nephew and her sister work on a rubber farm while her two other nephews go to school. Her oldest nephew also works in a phone shop. Htay is a homemaker and she does not have income. She lives and eats with her nephews and niece. Htay was diagnosed with a heart condition that involves a malformation of her mitral valve, the valve between the left atrium and left ventricle. This valve controls the flow of blood, but certain conditions may cause blood to flow backward or the valve to narrow. When Htay was 30 years old, she started to feel tired, and experienced shortness of breath and difficulty breathing at night. She went to the Yangon General Hospital for treatment. At the hospital, she was diagnosed with mitral valve stenosis and she underwent a procedure called a balloon valvotomy to widen the too narrow valve in her heart. She was fine after her treatment. Four years later, she started to experience shortness of breath, difficulty breathing and could no longer do household chores. However, she did not go to the hospital as she could not afford to pay for further treatment. On the 5th of July 2019, her niece’s husband suggested she seek treatment at Pinlon Hospital, where he had also received surgery in the past. She followed her niece’s husband’s advice and went to Pinlon Hospital. At the hospital she received another screening and the doctor told her she needs to replace one of the valves in her heart. Our medical partner, Burma Children Medical Fund, is requesting $1,500 to fund a mitral valve replacement for Htay. The treatment is scheduled to take place on February 19th and, once completed, will hopefully allow her to live more comfortably. Htay said, “After I went to Yangon Hospital several times and the doctor said that I had to have surgery as soon as possible, I felt so sad, but I tried to keep up my courage to stay strong. I secretly sold three acres of my farmland which my parents gave me. [However, I did not receive surgery] because if I would have died after surgery, my sister would have had difficulty paying for my funeral, so I was waiting and praying to meet with donors for a long time. Now, I feel less stressed since I talked to Burma Children Medical Fund staff. Thank you everyone for helping me!”

85% funded

85%funded
$1,280raised
$220to go
Philomena

Philomena was diagnosed with ARM at birth. With this condition, the little one was found to lack an anal opening and instead was passing stool through her vagina. A few hours after birth, Philomena, one in a set of twins, was noted to have a distended abdomen. The doctor quickly checked on the baby and discovered she lacked an anal opening. To keep Philomena from getting a fistula, the doctors put in a colostomy at three days. Philomena’s parents paid for this through some family savings they had. When they left for home, Philomena’s twin sister developed a persistent cough which was later found to be a hole in the heart. "I have never felt this drained ever in my life. Since I gave birth I am always in hospitals with either one of my two babies,” says Philomena’s mother. Due to lack of finances, Philomena’s parents shared their plight with their church members and one of them advised that they visit Watsi Partner Care Center BethanyKids Hospital. At BethanyKids a surgery to create an anal opening has been recommended. If not treated, Philomena will not lead a normal life and will be forced to use a colostomy for life. The surgery is a cost Philomena’s parents cannot bear. Philomena’s father is a carpenter while her mother closed her grocery store to tend to the children. Together they have five children with three currently in school. With very limited income and having exhausted their savings, Philomena’s parents are not able to raise the funds needed. They had defaulted on paying the national health insurance premiums as they could not keep up, but they’ve been advised to try to maintain this coverage in the future given their family's health needs. “Please help us. It is quite a stressful time for us but we believe we will come from it as victors,” says Philomena’s mother.

50% funded

50%funded
$355raised
$353to go

Meet another patient you can support

100% of your donation funds life-changing surgery.

Htay

Htay is a 54-year-old single woman from Burma. She lives with her sister, three nephews and a niece in Mudon Township, Mon State, Burma. Her nephew and her sister work on a rubber farm while her two other nephews go to school. Her oldest nephew also works in a phone shop. Htay is a homemaker and she does not have income. She lives and eats with her nephews and niece. Htay was diagnosed with a heart condition that involves a malformation of her mitral valve, the valve between the left atrium and left ventricle. This valve controls the flow of blood, but certain conditions may cause blood to flow backward or the valve to narrow. When Htay was 30 years old, she started to feel tired, and experienced shortness of breath and difficulty breathing at night. She went to the Yangon General Hospital for treatment. At the hospital, she was diagnosed with mitral valve stenosis and she underwent a procedure called a balloon valvotomy to widen the too narrow valve in her heart. She was fine after her treatment. Four years later, she started to experience shortness of breath, difficulty breathing and could no longer do household chores. However, she did not go to the hospital as she could not afford to pay for further treatment. On the 5th of July 2019, her niece’s husband suggested she seek treatment at Pinlon Hospital, where he had also received surgery in the past. She followed her niece’s husband’s advice and went to Pinlon Hospital. At the hospital she received another screening and the doctor told her she needs to replace one of the valves in her heart. Our medical partner, Burma Children Medical Fund, is requesting $1,500 to fund a mitral valve replacement for Htay. The treatment is scheduled to take place on February 19th and, once completed, will hopefully allow her to live more comfortably. Htay said, “After I went to Yangon Hospital several times and the doctor said that I had to have surgery as soon as possible, I felt so sad, but I tried to keep up my courage to stay strong. I secretly sold three acres of my farmland which my parents gave me. [However, I did not receive surgery] because if I would have died after surgery, my sister would have had difficulty paying for my funeral, so I was waiting and praying to meet with donors for a long time. Now, I feel less stressed since I talked to Burma Children Medical Fund staff. Thank you everyone for helping me!”

85% funded

85%funded
$1,280raised
$220to go