Becoming a parent and feeling loved by our parents is what we often hope for in a family. But life can be unpredictable, as was the case for Alba.
Alba was abandoned by her mother when she was very young. Despite being taken in by twenty families, they all eventually turned her away. However, a ray of hope entered her life.
Luca Trapanese, a gay man from Italy, faced many challenges when he decided to adopt a child. Despite the obstacles he faced from society, he was eventually allowed to adopt a young girl. This girl happened to have Down syndrome, but Luca didn’t hesitate. They formed a strong bond that everyone could see.
Luca had been told he could only adopt a child with a serious illness, significant disability, or behavior issues. But any of those options would have made him happy.
Finally, when Alba was just 13 days old in 2017, Luca officially became her father. By then, twenty families had already said no to adopting her because of her physical condition. But for Luca, Alba brought him immense joy and fulfillment, and he was honored to be her father. He took his role as a father very seriously.
Becoming a father had been a long journey for Luca, even though he had experience working with special needs. It all started when his best friend died of cancer at 14, motivating Luca to help others. He now helps people through his work with a Catholic charity.
When the opportunity to adopt a young girl came up, Luca committed to being her father wholeheartedly, even though he didn’t have a partner or live with anyone. Alba is a lively girl who loves to sing and dance and is very outgoing.
Although Luca was scared the first time he held a newborn, he knew instantly that they belonged together. He shares updates about their adventures on Instagram, where he has hundreds of thousands of followers. Together, they survived the challenges of a pandemic and became stronger.
We wish Luca and Alba a long and happy life together, filled with love and joy.
These Deadly Insects Attack Victims At Night, Killing Them Quietly Or Leaving Them With A Lifelong Infection
Emiliana Rodriguez’s childhood memories are a blend of joy and sorrow, intertwined with the haunting specter of a silent killer lurking in the darkness. Growing up in Bolivia, she vividly remembers evenings spent watching her friends play soccer under the moonlit sky. But one fateful night, the game was abruptly halted by the tragic passing of a player, a victim of the insidious disease known as Chagas.
For Rodriguez, the incident cast a long shadow of fear over the night. In the folklore of her upbringing, Chagas was depicted as a monstrous presence that emerged under the cover of darkness, claiming lives without warning. This narrative became all too real when she learned that her friend had succumbed to this silent and silenced disease, one of the thousands who perish annually from its grasp.
Now, at 42 years old and living in Barcelona for over two decades, Rodriguez still grapples with the specter of Chagas that haunts her past. “The terror would grip me at night”, she confides. “There were times when sleep eluded me, fearing that I might never wake up again.”
Her own confrontation with the disease came to light eight years ago, during her first pregnancy. The revelation of her status as a carrier sent shockwaves through her, evoking memories of her childhood trauma. “I felt paralyzed with fear”, she recalls. “The thought of what might happen to my unborn child kept me awake at night.”
Yet, despite the looming threat, Rodriguez embarked on a journey of treatment to safeguard her child from the same fate. Thanks to medical intervention, her daughter emerged unscathed, spared from the clutches of the silent killer that had haunted her family’s history.
Rodriguez’s story is not unique. Across the globe, individuals like Elvira Idalia Hernández Cuevas of Mexico find themselves thrust into the unfamiliar terrain of Chagas disease. For Idalia, the journey began with a routine act of altruism, donating blood. Little did she know that this act would expose her to a hidden danger lurking within her own community.
“When I first heard the diagnosis, I was terrified”, Idalia recounts. “I had never even heard of Chagas before, let alone imagined that I could be its victim.”
Her experience echoes a broader reality, one where awareness of Chagas remains dangerously low, even in regions where the disease exacts its heaviest toll. Originating in the Americas, Chagas has since spread its reach to other continents, ensnaring millions in its silent grip.
In the face of this silent epidemic, efforts to combat Chagas are hindered by a lack of awareness and resources. Outdated treatments offer little solace to those afflicted, with medications often proving toxic and ineffective, particularly for newborns.
Yet, amidst the darkness, there are glimmers of hope. Champions like Emiliana Rodriguez and Elvira Idalia Hernández Cuevas are raising their voices to break the silence surrounding Chagas. Through advocacy and awareness campaigns, they seek to shine a light on this neglected disease, urging communities to confront the monster lurking in their midst.
As the world grapples with the challenge of eradicating Chagas by 2030, the road ahead remains daunting. But with each voice raised in solidarity, the hope for a future free from the shackles of Chagas grows stronger.
In the battle against this silent killer, knowledge is our most potent weapon. By arming ourselves with awareness and understanding, we can confront Chagas head-on, ensuring that no more lives are claimed by the darkness.
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