Carrie and Craig Kosinski responded positively when a long-lost family friend requested them to watch her infant twins.
Carrie and Craig offered to temporarily assume custody of the adorable girls.
Days turned into weeks, and weeks into months, and eventually the girls were a permanent part of the family.
For Carrie and Craig, having children had always been a dream, but they had no idea how their journey would turn out.
The births of Adalynn and Kenna occurred on February 28, 2014. The twins were born via emergency C-section, and at the age of three months, the Kosinkis were granted legal custody of the infant girls.
After a few years of parenting their adoptive twins, Carrie and Craig got a call from their original mother, who revealed that she was dealing with yet another tragic circumstance.
She was battling to make everything work while dealing with serious challenges in her life. She asked the couple if they would be open to adopting her two younger kids, Cece and J.J., twins who are two years old.
The younger twins were biologically related to Kenna and Adalynn.
From Union Grove, Wisconsin, Carrie and Craig had to consider their options carefully.
The couple had made numerous unsuccessful attempts to become pregnant before beginning the adoption process with Kenna and Adalynn.
They sought medical attention because they had no idea what was wrong for a while, and the doctor broke some devastating news.
The medical professional informed Carrie that due to her severe endometriosis, she was unable to conceive naturally. Therefore, having biological children was essentially out of the question; this is why they initially turned to adoption.
“It was a difficult decision. We were trying to get pregnant ourselves. But they were siblings so that was definitely was part of our consideration — we wanted to keep the siblings together,” Carrie told The Journal Times.
Carrie and Craig, however, put aside their private worries and informed the mother that they would be delighted to adopt the younger twins.
But not long after welcome Cece and J.J. into the family, Carrie started to feel off and knew she needed to see a doctor.
An ultrasound in September 2015 confirmed Carrie’s own pregnancy. Actually, there were two fetuses visible on the screen! In the past five years, she and Craig have welcomed three sets of twins.
”We were in shock, but super happy,” Carrie Kosinski explained.
Craig and Carrie understood their pregnancy was a gift from a higher power, despite their first overwhelm. All six of the children would be raised in a secure, loving home, the parents resolved.
But destiny would soon bring the family back, and their medical professionals could hardly believe what had transpired.
Unbelievably, the other two sets of twins’ birth dates, February 28 and March 1, were shared by biological twins Karraline and Clarissa.
”We were very shocked. We were like ‘oh my God we are going to have three sets of twins. What are we going to do with ourselves?’”, Carrie recalled.
The fact that all of Carrie and Craig’s kids have the same birthday is proof positive that this was meant to be, according to the delighted parents.
The Journal Times quotes Carrie as saying, “God certainly has a sense of humor.”
In week 25 of her pregnancy, Carrie used in vitro fertilization to give birth to Karraline and Clarissa. Sadly, their biological twins had to stay in neonatal intensive care for several months. Karraline and Clarissa, however, were in good health and shape when they were finally permitted to return home.
Three pairs of twins living under one roof is obviously expensive, but several members of the neighborhood have offered financial assistance.
Kind strangers from across the nation provided the family with financial assistance to cover their rising bills and expensive charges through fundraising websites like GoFundMe and AdoptTogether.
”I have to be very organized and keep to a schedule, or things get out of hand,” Carrie says.
Craig and Carrie believe that someone from above had a particular plan for their family because all six of their children were born on the same day: Cece and J.J. on February 28, 2013, Adalynn and Kenna on February 28, 2014, and Karraline and Clarissa on February 28, 2016.
”We believe that because God adopted us into His family that we were meant to adopt these children into our family,” Carrie said. ”It’s such a huge blessing to us. We love all our children the same. We wouldn’t want our lives to be any different.”
Today, this family is enjoying life, and to see all these beautiful kids grow up must be such a blessing for Carrie and Craig.
These bugs come out at nighttime, and attacking victims, they silently kill or leave them with a lifelong infection
When Emiliana Rodriguez was a little girl, she recalls watching friends play a nighttime soccer match when one of the players abruptly died on the pitch.
Unaware of what had transpired, Rodriguez, a native of Bolivia, developed a phobia of the dark and the “monster”—the silent killer known as Chagas—that she had been told only appears at night.
Chagas disease is a unique sort of illness that is spread by nocturnal insects. It is also known as the “silent and silenced disease” that infects up to 8 million people annually, killing 12,000 people on average.
Emiliana Rodriguez, 42, discovered she had to live with Chagas, a “monster,” after relocating to Barcelona from Bolivia 27 years ago.
“Night is when the fear generally struck. I didn’t always sleep well,” she admitted. “I was worried that I wouldn’t wake up from my sleep.”
Rodriguez had specific tests when she was eight years old and expecting her first child, and the results indicated that she carried the Chagas gene. She recalled the passing of her buddy and remarked, “I was paralyzed with shock and remembered all those stories my relatives told me about people suddenly dying.” “I wondered, ‘What will happen to my baby?’”
Rodriguez was prescribed medicine, though, to prevent the parasite from vertically transmitting to her unborn child. After her daughter was born, she tested negative. Elvira Idalia Hernández Cuevas, 18, was unaware of the Mexican silent killer until her 18-year-old son was diagnosed with Chagas.
Idalia, an eighteen-year-old blood donor from her birthplace near Veracruz, Mexico, had a positive diagnosis for Chagas, a disease caused by triatomine bugs, often known as vampire or kissing bugs and bloodsucking parasites, when her sample was tested.
In an interview with the Guardian, Hernandez stated, “I started to research Chagas on the internet because I had never heard of it.” When I read that it was a silent murderer, I became really afraid. I had no idea where to go or what to do.
She is not alone in this; a lot of people are ignorant of the diseases that these unpleasant bugs can spread. The term Chagas originates from Carlos Ribeiro Justiniano Chagas, a Brazilian physician and researcher who made the discovery of the human case in 1909.
Over the past few decades, reports of the incidence of Chagas disease have been made in Europe, Japan, Australia, Latin America, and North America.
Kissing bugs are mostly found in rural or suburban low-income housing walls, where they are most active at night when humans are asleep. The insect bites an animal or person, then excretes on the skin of the victim. The victim may inadvertently scratch the area and sever the skin, or they may spread the excrement into their mouth or eyes. This is how the T. cruzi infection is disseminated.
The World Health Organization (WHO) estimates that between 6 and 7 million people worldwide—roughly 8 million people in Mexico, Central America, and South America—have Chagas disease; the majority of these individuals remain oblivious to their illness. These estimates are provided by the Centers for Disease Control and Prevention (CDC). The persistent infection might be fatal if untreated. According to the Guardian, Chagas disease kills over 12,000 people year, “more people in Latin America than any other parasite disease, including malaria.”
Despite the fact that these bugs have been found in the United States—nearly 300,000 people are infected—they are not thought to be endemic.
While some people never experience any symptoms, the CDC notes that 20 to 30 percent experience gastrointestinal or heart problems that can cause excruciating pain decades later.
Furthermore, only 10% of cases are detected globally, which makes prevention and treatment exceedingly challenging.
Hernández and her daughter Idalia went to see a number of doctors in search of assistance, but all were also uninformed about Chagas disease and its management. “I was taken aback, terrified, and depressed because I believed my kid was going to pass away. Above all, Hernandez stated, “I was more anxious because I was unable to locate any trustworthy information.”
Idalia finally got the care she required after receiving assistance from a family member who was employed in the medical field.
“The Mexican government claims that the Chagas disease is under control and that not many people are affected, but that is untrue,” Hernández asserts. Medical practitioners misdiagnose Chagas disease for other heart conditions because they lack knowledge in this area. Most people are unaware that there is Chagas in Mexico.
The World Health Organization (WHO) has classified chagas as a neglected tropical disease, which means that the global health policy agenda does not include it.
Chagas is overlooked in part because, according to Colin Forsyth, a research manager at the Drugs for Neglected Diseases Initiative (DNDi), “it’s a silent disease that stays hidden for so long in your body… because of the asymptomatic nature of the initial part of the infection.”
Forsyth went on to say, “The people affected just don’t have the power to influence healthcare policy,” making reference to the impoverished communities. It’s kept hidden by a convergence of social and biological factors.
Chagas, however, is becoming more well recognized as it spreads to other continents and can also be transferred from mother to child during pregnancy or childbirth, as well as through organ and blood transfusions.
The main objective of the Chagas Hub, a UK-based facility founded by Professor David Moore, a doctor at the Hospital for Tropical Diseases in London, is to get “more people tested and treated, and to manage the risk of transmission, which in the UK is from mother to child,” according to Professor Moore.
Regarding the WHO’s 2030 aim for the eradication of the disease, Moore stated that progress toward it is “glacial” and added, “I can’t imagine that we’ll be remotely close by 2030.” That seems improbable.
Two medications that have been available for more than 50 years to treat chagas are benznidazole and nifurtimox, which according to Moore are “toxic, unpleasant, not particularly effective.”
Although the medications are effective in curing babies, there is no guarantee that they will prevent or halt the advancement of the condition in adults.
Regarding severe adverse effects, Rodriguez remembers getting dizziness and nausea as well as breaking out in hives. She completed her therapy, and she gets checked out annually.
Moore goes on to say that while creating stronger anti-Chaga drugs is crucial to stopping the disease’s spread, pharmaceutical companies are currently not financially motivated to do so.
As president of the International Federation of Associations of People Affected by Chagas condition (FINDECHAGAS), Hernández is on a mission to raise awareness of the condition until there is a greater need on the market for innovative treatments.
In Spain, Rodriguez is battling the “monster” as part of a campaign to increase public awareness of Chagas disease being conducted by the Barcelona Institute for Global Health.
“I’m tired of hearing nothing at all,” Rodriguez declares. “I want Chagas to be discussed and made public. I’m in favor of testing and therapy for individuals.
They are being heard, too.
World Chagas Disease Day was instituted by the WHO on April 14, 1909, the day Carlos discovered the disease’s first human case.The WHO states that “a diversified set of 20 diseases and disease categories are set out to be prevented, controlled, eliminated, and eradicated through global targets for 2030 and milestones.” And among them is Chagas.
To prevent a possible infestation, the CDC suggests taking the following steps:
Close up any gaps and fissures around doors, windows, walls, and roofs.
Clear out the rock, wood, and brush piles close to your home.
Put screens on windows and doors, and fix any tears or holes in them.
Close up gaps and crevices that lead to the exterior, crawl areas beneath the home, and the attic.
Keep pets inside, especially during the evening.
Maintain the cleanliness of your home and any outdoor pet resting places, and check for bugs on a regular basis.
If you believe you have discovered a kissing insect, the CDC recommends avoiding crushing it. Alternatively, carefully put the bug in a jar, fill it with rubbing alcohol, and then freeze it. It is then recommended that you bring the bug’s container to an academic lab or your local health authority so that it can be identified.
Please tell this tale to help spread the word about an illness that goes unnoticed!
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