Mothers of babies afflicted by Zika fight poverty, despair

 

RECIFE, Brazil, Oct 17 (Reuters) - Nearly three years after a Zika outbreak in Brazil caused thousands of cases of microcephaly and other devastating birth defects in newborns, Reuters returned to check on the mothers and their children.

Zika, the first mosquito-borne virus known to damage developing fetuses, has since disappeared from headlines, but world health officials fear its spread to new populations. In Angola, dozens of babies born with microcephaly since 2017 appear linked to the same strain of Zika that hit Latin America.

In northeastern Brazil, we spoke with nearly 30 mothers who contracted the Zika virus during pregnancy. Most of them have been abandoned by their husbands and must care for their children alone.

Many of the women have largely adjusted to the initial shock of their child's disability, trading dreams of their own careers for the reality of around-the-clock care of a child who may never walk or talk.

31 PHOTOS
Mothers of babies afflicted by Zika fight poverty, despair
See Gallery
Mothers of babies afflicted by Zika fight poverty, despair
Rosana Vieira Alves and her five-month-old daughter Luana Vieira, who was born with microcephaly, pose for a picture in the sea of Porto de Galinhas, a beach located in Ipojuca, in the state of Pernambuco, Brazil, March 2, 2016. REUTERS/Ueslei Marcelino/File Photo SEARCH "ZIKA" FOR THIS STORY. SEARCH "WIDER IMAGE" FOR ALL STORIES. TPX IMAGES OF THE DAY
Jackeline Vieira de Souza, 26, holds her four-month-old son Daniel who was born with microcephaly in front of their house in Olinda, near Recife, Brazil, February 11, 2016. REUTERS/Nacho Doce/File Photo SEARCH "ZIKA" FOR THIS STORY. SEARCH "WIDER IMAGE" FOR ALL STORIES. TPX IMAGES OF THE DAY
Gabriela Alves de Azevedo, 22, holds her two-year-old daughter Ana Sophia, who was born with microcephaly, at their house in Olinda, Brazil, August 7, 2018. Gabriela had planned to finish high school and study physical therapy. Now, she spends her days caring for her child. Her husband left shortly after Ana Sophia's birth. He could not accept their child's condition, Gabriela says, and does not pay child support. "I went into depression and my family helped me," she said. "If it was not for them, I would have gone crazy." REUTERS/Ueslei Marcelino SEARCH "ZIKA" FOR THIS STORY. SEARCH "WIDER IMAGE" FOR ALL STORIES. TPX IMAGES OF THE DAY
Silvina da Silva poses with her two-year-old granddaughter Ana Sophia, who was born with microcephaly, at their house in Olinda, Brazil, August 7, 2018. Ana Sophia's mother Gabriela had planned to finish high school and study physical therapy. Now, she spends her days caring for her child. Her husband left shortly after Ana Sophia's birth. He could not accept their child's condition, Gabriela says, and does not pay child support. "I went into depression and my family helped me," she said. "If it was not for them, I would have gone crazy." Today, some relatives give moral support and Ana Sophia's paternal grandmother helps with her day-to-day care. REUTERS/Ueslei Marcelino SEARCH "ZIKA" FOR THIS STORY. SEARCH "WIDER IMAGE" FOR ALL STORIES. TPX IMAGES OF THE DAY
Gleyse Kelly da Silva, 28, holds her two-year-old daughter Maria Giovanna, at their house in Recife, Brazil, August 8, 2018. Gleyse has help from her husband and mother in caring for Maria Giovanna "Gigi" da Silva. But the burden is still great, and she was forced to leave her job as a toll attendant. "She does not sit alone, she does not roll, she does not do anything alone," Gleyse said. Gigi needs an orthopedist, but there are not enough to go around, and she's perpetually on waiting lists. Gleyse struggles with navigating her daughter's wheelchair on public transportation. Few buses have working lifts, and some drivers have refused to help her. Such struggles prompted Gleyse to help create the Union of Mothers of Angels, which provides advice and logistical support for mothers of children with microcephaly. The group now serves more than 250 families in Pernambuco. REUTERS/Ueslei Marcelino SEARCH "ZIKA" FOR THIS STORY. SEARCH "WIDER IMAGE" FOR ALL STORIES.
X-ray of Rosana Vieira Alves's daughter Luana Vieira, who is four months old with microcephaly, is pictured at their house in Olinda, Brazil, February 3, 2016. REUTERS/Ueslei Marcelino/File Photo SEARCH "ZIKA" FOR THIS STORY. SEARCH "WIDER IMAGE" FOR ALL STORIES.
Luana Vieira, four months old, who was born with microcephaly, is held by her mother Rosana Vieira Alves as they ride the subway after a doctor's appointment in Recife, Brazil, February 3, 2016. REUTERS/Ueslei Marcelino/File Photo SEARCH "ZIKA" FOR THIS STORY. SEARCH "WIDER IMAGE" FOR ALL STORIES.
Jackeline Vieira de Souza, 26, holds her four-month-old son Daniel who was born with microcephaly, as they walk toward their house in Olinda, near Recife, Brazil, February 11, 2016. REUTERS/Nacho Doce/File Photo SEARCH "ZIKA" FOR THIS STORY. SEARCH "WIDER IMAGE" FOR ALL STORIES.
Luana Vieira, who is two years old, and was born with microcephaly, lies on a sofa after bath at her house in Olinda, Brazil, August 6, 2018. Luana's mother Rosana Vieira Alves has three daughters. "It's hard to manage the girls. Some of them are jealous, but Luana needs more care. In time, they'll understand." Rosana does not have any family support and is overwhelmed by the cost of housing and Luana's medicines. She counts it a victory that she has managed to get a wheelchair for Luana, and worries about the four surgeries her daughter needs to correct problems with her eyes, her gut and the position of her hips and feet. The demands have taken Rosana to some dark places, and she confesses that she has considered suicide. But she still dreams of a better future, and hopes to get a degree in accounting or civil engineering. REUTERS/Ueslei Marcelino SEARCH "ZIKA" FOR THIS STORY. SEARCH "WIDER IMAGE" FOR ALL STORIES.
Jackeline Vieira de Souza, 26, uses a green bottle to stimulate her four-month-old son Daniel who was born with microcephaly inside their house in Olinda, near Recife, Brazil, February 11, 2016. REUTERS/Nacho Doce/File Photo SEARCH "ZIKA" FOR THIS STORY. SEARCH "WIDER IMAGE" FOR ALL STORIES.
Jackeline Vieira de Souza (R), 28, mother of Daniel Vieira stands by as Daniel, who is two years old, and was born with microcephaly, reacts to stimulus during an evaluation session with a physiotherapist at the Association of Parents and Friends of the Exceptional (APAE) in Recife, Brazil, August 7, 2018. A few years ago Jackeline fought to overcome a very rare complication from an earlier pregnancy, and then survived cancer. "My dream was to be a mother again," she says. In 2015, she got her wish. But during her pregnancy, she learned that her son had microcephaly. "When he was born, I fell in love with him because I knew he would be a good thing in my life, even with the difficulties I would have to face." Daniel's father separated from Jackeline shortly after learning that his son had microcephaly. He pays a small amount of family support every month, in addition to a monthly check that Jackeline gets from the government. REUTERS/Ueslei Marcelino SEARCH "ZIKA" FOR THIS STORY. SEARCH "WIDER IMAGE" FOR ALL STORIES.
Rosana Vieira Alves holds her four-month-old daughter Luana Vieira, who was born with microcephaly, at their house in Olinda, Brazil, February 3, 2016. REUTERS/Ueslei Marcelino/File Photo SEARCH "ZIKA" FOR THIS STORY. SEARCH "WIDER IMAGE" FOR ALL STORIES.
Luana Vieira, who is two years old, and was born with microcephaly, is pushed in a wheelchair by her sister Vitoria Evillen, near a sports court in the housing complex where they live, in Olinda, Brazil, August 6, 2018. Luana's mother Rosana Vieira Alves has three daughters. "It's hard to manage the girls. Some of them are jealous, but Luana needs more care. In time, they'll understand." Rosana does not have any family support and is overwhelmed by the cost of housing and Luana's medicines. She counts it a victory that she has managed to get a wheelchair for Luana, and worries about the four surgeries her daughter needs to correct problems with her eyes, her gut and the position of her hips and feet. The demands have taken Rosana to some dark places, and she confesses that she has considered suicide. But she still dreams of a better future, and hopes to get a degree in accounting or civil engineering. REUTERS/Ueslei Marcelino SEARCH "ZIKA" FOR THIS STORY. SEARCH "WIDER IMAGE" FOR ALL STORIES.
Daniel Vieira, who is two years old, and was born with microcephaly, sleeps at his home in Olinda, Brazil, August 7, 2018. During her pregnancy, Daniel's mother Jackeline Vieira de Souza learned that her son had microcephaly. "When he was born, I fell in love with him because I knew he would be a good thing in my life, even with the difficulties I would have to face." Daniel's father separated from Jackeline shortly after learning that his son had microcephaly. He pays a small amount of family support every month, in addition to a monthly check that Jackeline gets from the government. It takes several hours to travel by bus between their home in Olinda and Recife, where Daniel goes for treatments. Lately, those trips are somewhat less frequent, and Jackeline believes Daniel's health is more stable. She has no illusions that her son will ever walk, eat on his own or live a normal life. Yet in many ways she is grateful for her "miracle" baby, who she says makes her feel "happy and more accomplished." REUTERS/Ueslei Marcelino SEARCH "ZIKA" FOR THIS STORY. SEARCH "WIDER IMAGE" FOR ALL STORIES.
Luana Vieira, who is two years old, and was born with microcephaly, reacts to stimulus during an evaluation session with a physiotherapist at the Altino Ventura rehabilitation center in Recife, Brazil, August 6, 2018. Luana's mother Rosana Vieira Alves has three daughters. "It's hard to manage the girls. Some of them are jealous, but Luana needs more care. In time, they'll understand." Rosana does not have any family support and is overwhelmed by the cost of housing and Luana's medicines. She counts it a victory that she has managed to get a wheelchair for Luana, and worries about the four surgeries her daughter needs to correct problems with her eyes, her gut and the position of her hips and feet. The demands have taken Rosana to some dark places, and she confesses that she has considered suicide. But she still dreams of a better future, and hopes to get a degree in accounting or civil engineering. REUTERS/Ueslei Marcelino SEARCH "ZIKA" FOR THIS STORY. SEARCH "WIDER IMAGE" FOR ALL STORIES.
Gleyse Kelly da Silva embraces her daughter Maria Giovanna, who has microcephaly, in Recife, Brazil, January 25, 2016. REUTERS/Ueslei Marcelino/File Photo SEARCH "ZIKA" FOR THIS STORY. SEARCH "WIDER IMAGE" FOR ALL STORIES.
Gleyse Kelly da Silva holds Maria Giovanna, who has microcephaly, at their house in Recife, Brazil, January 30, 2016. REUTERS/Ueslei Marcelino/File Photo SEARCH "ZIKA" FOR THIS STORY. SEARCH "WIDER IMAGE" FOR ALL STORIES.
Rosana Vieira Alves carries her four-month-old daughter Luana Vieira, who was born with microcephaly, while taking her daughters Laiane Sophia (L) and Vitoria Evillen to their school in Olinda, Brazil, February 4, 2016. REUTERS/Ueslei Marcelino/File Photo SEARCH "ZIKA" FOR THIS STORY. SEARCH "WIDER IMAGE" FOR ALL STORIES.
Gleyse Kelly da Silva holds her daughter Maria Giovanna, who has microcephaly, at their house in Recife, Brazil, January 30, 2016. REUTERS/Ueslei Marcelino/File Photo SEARCH "ZIKA" FOR THIS STORY. SEARCH "WIDER IMAGE" FOR ALL STORIES.
Rosana Vieira Alves, 28, washes her two-year-old daughter Luana Vieira, who was born with microcephaly, at their house in Olinda, Brazil, August 6, 2018. Rosana has three daughters. "It's hard to manage the girls. Some of them are jealous, but Luana needs more care. In time, they'll understand." Rosana does not have any family support and is overwhelmed by the cost of housing and Luana's medicines. She counts it a victory that she has managed to get a wheelchair for Luana, and worries about the four surgeries her daughter needs to correct problems with her eyes, her gut and the position of her hips and feet. The demands have taken Rosana to some dark places, and she confesses that she has considered suicide. But she still dreams of a better future, and hopes to get a degree in accounting or civil engineering. REUTERS/Ueslei Marcelino SEARCH "ZIKA" FOR THIS STORY. SEARCH "WIDER IMAGE" FOR ALL STORIES.
Gabriela Alves de Azevedo bathes her four-month-old daughter Ana Sophia, who was born with microcephaly, at their house in Olinda, Brazil, March 2, 2016. REUTERS/Ueslei Marcelino/File Photo SEARCH "ZIKA" FOR THIS STORY. SEARCH "WIDER IMAGE" FOR ALL STORIES.
Rosana Vieira Alves, 28, feeds her two-year-old daughter Luana Vieira, who was born with microcephaly, at their house in Olinda, Brazil, August 9, 2018. Rosana has three daughters. "It's hard to manage the girls. Some of them are jealous, but Luana needs more care. In time, they'll understand." Rosana does not have any family support and is overwhelmed by the cost of housing and Luana's medicines. She counts it a victory that she has managed to get a wheelchair for Luana, and worries about the four surgeries her daughter needs to correct problems with her eyes, her gut and the position of her hips and feet. The demands have taken Rosana to some dark places, and she confesses that she has considered suicide. But she still dreams of a better future, and hopes to get a degree in accounting or civil engineering. REUTERS/Ueslei Marcelino SEARCH "ZIKA" FOR THIS STORY. SEARCH "WIDER IMAGE" FOR ALL STORIES.
Gabriela Alves de Azevedo holds her four-month-old daughter Ana Sophia, who was born with microcephaly, at their house in Olinda, Brazil, March 2, 2016. REUTERS/Ueslei Marcelino/File Photo SEARCH "ZIKA" FOR THIS STORY. SEARCH "WIDER IMAGE" FOR ALL STORIES.
Maria Giovanna "Gigi" da Silva, who is two years old, and was born with microcephaly, sits in her home in Recife, Brazil, August 8, 2018. Gigi needs an orthopedist, but there are not enough to go around, and she's perpetually on waiting lists. Her mother Gleyse Kelly da Silva struggles with navigating her daughter's wheelchair on public transportation. Few buses have working lifts, and some drivers have refused to help her. "People do not respect my daughter's rights," she said. Other mothers have told her similar stories, including a bus passenger who refused to ride with "that demon," referring to a baby with microcephaly. REUTERS/Ueslei Marcelino SEARCH "ZIKA" FOR THIS STORY. SEARCH "WIDER IMAGE" FOR ALL STORIES.
Gabriela Alves de Azevedo, 22, holds her two-year-old daughter Ana Sophia, who was born with microcephaly, at their house in Olinda, Brazil, August 7, 2018. Gabriela had planned to finish high school and study physical therapy. Now, she spends her days caring for her child. Her husband left shortly after Ana Sophia's birth. He could not accept their child's condition, Gabriela says, and does not pay child support. "I went into depression and my family helped me," she said. "If it was not for them, I would have gone crazy." REUTERS/Ueslei Marcelino SEARCH "ZIKA" FOR THIS STORY. SEARCH "WIDER IMAGE" FOR ALL STORIES.
Houses stand in the Morro da Conceicao neighbourhood in front of high rises in Recife, Brazil, August 10, 2018. REUTERS/Ueslei Marcelino SEARCH "ZIKA" FOR THIS STORY. SEARCH "WIDER IMAGE" FOR ALL STORIES.
Luana Vieira, who is two years old, and was born with microcephaly, reacts to stimulus during an evaluation session with a physiotherapist at the Altino Ventura rehabilitation center in Recife, Brazil, August 6, 2018. Luana's mother Rosana Vieira Alves has three daughters. "It's hard to manage the girls. Some of them are jealous, but Luana needs more care. In time, they'll understand." Rosana does not have any family support and is overwhelmed by the cost of housing and Luana's medicines. She counts it a victory that she has managed to get a wheelchair for Luana, and worries about the four surgeries her daughter needs to correct problems with her eyes, her gut and the position of her hips and feet. The demands have taken Rosana to some dark places, and she confesses that she has considered suicide. But she still dreams of a better future, and hopes to get a degree in accounting or civil engineering. REUTERS/Ueslei Marcelino SEARCH "ZIKA" FOR THIS STORY. SEARCH "WIDER IMAGE" FOR ALL STORIES.
Rosana Vieira Alves, 28, holds her two-year-old, daughter Luana Vieira, who was born with microcephaly, at a supermarket in Olinda, Brazil, August 9, 2018. Rosana has three daughters. "It's hard to manage the girls. Some of them are jealous, but Luana needs more care. In time, they'll understand." Rosana does not have any family support and is overwhelmed by the cost of housing and Luana's medicines. She counts it a victory that she has managed to get a wheelchair for Luana, and worries about the four surgeries her daughter needs to correct problems with her eyes, her gut and the position of her hips and feet. The demands have taken Rosana to some dark places, and she confesses that she has considered suicide. But she still dreams of a better future, and hopes to get a degree in accounting or civil engineering. REUTERS/Ueslei Marcelino SEARCH "ZIKA" FOR THIS STORY. SEARCH "WIDER IMAGE" FOR ALL STORIES.
Daniel Vieira, who is two years old, and was born with microcephaly, is greeted by his brother at their house in Olinda, Brazil, August 7, 2018. During her pregnancy, Daniel's mother Jackeline Vieira de Souza learned that her son had microcephaly. "When he was born, I fell in love with him because I knew he would be a good thing in my life, even with the difficulties I would have to face." Daniel's father separated from Jackeline shortly after learning that his son had microcephaly. He pays a small amount of family support every month, in addition to a monthly check that Jackeline gets from the government. It takes several hours to travel by bus between their home in Olinda and Recife, where Daniel goes for treatments. Lately, those trips are somewhat less frequent, and Jackeline believes Daniel's health is more stable. She has no illusions that her son will ever walk, eat on his own or live a normal life. Yet in many ways she is grateful for her "miracle" baby, who she says makes her feel "happy and more accomplished." REUTERS/Ueslei Marcelino SEARCH "ZIKA" FOR THIS STORY. SEARCH "WIDER IMAGE" FOR ALL STORIES.
Gleyse Kelly da Silva, 28, rests on the baby carriage of her two-year-old daughter Maria Giovanna, while waiting for a medical appointment in a hospital in Recife, Brazil, August 8, 2018. Gleyse has help from her husband and mother in caring for Maria Giovanna "Gigi" da Silva. But the burden is still great, and she was forced to leave her job as a toll attendant. "She does not sit alone, she does not roll, she does not do anything alone," Gleyse said. Gigi needs an orthopedist, but there are not enough to go around, and she's perpetually on waiting lists. Gleyse struggles with navigating her daughter's wheelchair on public transportation. Few buses have working lifts, and some drivers have refused to help her. "People do not respect my daughter's rights," she said. Other mothers have told her similar stories, including a bus passenger who refused to ride with "that demon," referring to a baby with microcephaly. REUTERS/Ueslei Marcelino SEARCH "ZIKA" FOR THIS STORY. SEARCH "WIDER IMAGE" FOR ALL STORIES.
Rosana Vieira Alves, 28, smiles with her daughter two-year-old Luana Vieira, who was born with microcephaly, during an evaluation session with a physiotherapist at the Altino Ventura rehabilitation center in Recife, Brazil, August 6, 2018. Rosana has three daughters. "It's hard to manage the girls. Some of them are jealous, but Luana needs more care. In time, they'll understand." Rosana does not have any family support and is overwhelmed by the cost of housing and Luana's medicines. She counts it a victory that she has managed to get a wheelchair for Luana, and worries about the four surgeries her daughter needs to correct problems with her eyes, her gut and the position of her hips and feet. The demands have taken Rosana to some dark places, and she confesses that she has considered suicide. But she still dreams of a better future, and hopes to get a degree in accounting or civil engineering. REUTERS/Ueslei Marcelino SEARCH "ZIKA" FOR THIS STORY. SEARCH "WIDER IMAGE" FOR ALL STORIES.
HIDE CAPTION
SHOW CAPTION
of
SEE ALL
BACK TO SLIDE

Many struggle to get by on a monthly disability check of just over 954 reais (roughly $250), which must cover shelter, food, medications and transportation to frequent doctor visits.

Some seek comfort among mothers whose children share the same affliction. Others expressed gratitude for family members or friends who offer a break from the daily grind. Many confessed to despair and depression, and some considered suicide. But they share a fierce love for their children and a hope for a better life.

Four of them provided us a glimpse of their daily life in simple homes on the outskirts of Recife and Olinda, two cities in the state of Pernambuco.

MORAL SUPPORT

Gabriela Alves de Azevedo, 22, lives outside of Olinda with her daughter, Ana Sophia, now three years old.

Ana Sophia has microcephaly, a rare birth defect marked by small head size that signifies arrested brain development during gestation. Before Zika, such birth defects had never been linked to a mosquito-borne disease. Besides developmental issues, Ana Sophia has vision and hearing problems and trouble swallowing.

Gabriela had planned to finish high school and study physical therapy. Now, she spends her days caring for her child. Her husband left shortly after Ana Sophia's birth. He could not accept their child's condition, Gabriela says, and does not pay child support.

"I went into depression and my family helped me," she said. "If it was not for them, I would have gone crazy."

Today, some relatives give moral support and Ana Sophia's paternal grandmother helps with her day-to-day care.

Gabriela does physical therapy exercises at home with her daughter and thinks her health has improved.

"Nowadays, I treat my daughter like a normal child. I know she has her deficiency, but I pretend she does not." 'DON'T EVER GIVE UP' Gleyse Kelly da Silva, 28, has help from her husband and mother in caring for three-year-old Maria Giovanna "Gigi" da Silva. But the burden is still great, and she was forced to leave her job as a toll attendant.

After Gigi was born, there were many consultations with medical teams trying to understand the full implications of Zika. Those visits are less frequent, but Gigi's medical challenges are significant.

"She does not sit alone, she does not roll, she does not do anything alone," Gleyse said.

Gigi needs an orthopedist, but there are not enough to go around, and she's perpetually on waiting lists.

Gleyse struggles with navigating her daughter's wheelchair on public transportation. Few buses have working lifts, and some drivers have refused to help her.

"People do not respect my daughter's rights," she said. Other mothers have told her similar stories, including a bus passenger who refused to ride with "that demon," referring to a baby with microcephaly.

Such struggles prompted Gleyse to help create the Union of Mothers of Angels, which provides advice and logistical support for mothers of children with microcephaly. The group now serves more than 250 families in Pernambuco.

Gleyse says some mothers have abandoned their children due to the many hardships, sending them to live with grandparents or other relatives. She is determined to make a place for in the world for children like Gigi. Her advice to other mothers: "Don't ever give up.”

MIRACLE BABY

A few years ago, Jackeline Vieira de Souza, 28, of Olinda, fought to overcome a very rare complication from an earlier pregnancy, and then survived cancer.

"My dream was to be a mother again," she says.

In 2015, she got her wish. But during her pregnancy, she learned that her son, Daniel Vieira de Oliveira, had microcephaly.

"When he was born, I fell in love with him because I knew he would be a good thing in my life, even with the difficulties I would have to face."

Daniel's father separated from Jackeline shortly after learning that his son had microcephaly. He pays a small amount of family support every month, in addition to a monthly check that Jackeline gets from the government.

It takes several hours to travel by bus between their home in Olinda and Recife, where Daniel goes for treatments. Lately, those trips are somewhat less frequent, and Jackeline believes Daniel's health is more stable.

She has no illusions that her son will ever walk, eat on his own or live a normal life. Yet in many ways she is grateful for her "miracle" baby, who she says makes her feel "happy and more accomplished."

HOPE AND DESPAIR

Rosana Vieira Alves, 28, has three daughters, but nearly all of her attention goes to her youngest, Luana Vieira da Silva, age three.

"It's hard to manage the girls. Some of them are jealous, but Luana needs more care. In time, they'll understand."

Rosana does not have any family support and is overwhelmed by the cost of housing and Luana's medicines. She counts it a victory that she has managed to get a wheelchair for Luana, and worries about the four surgeries her daughter needs to correct problems with her eyes, her gut and the position of her hips and feet.

The demands have taken Rosana to some dark places, and she confesses that she has considered suicide. But she still dreams of a better future, and hopes to get a degree in accounting or civil engineering.

"I'm sure one day I'll get there," she said.

(Reporting by Ueslei Marcelino in Recife; Writing by Julie Steenhuysen in Chicago; editing by Diane Craft)

Read Full Story