David Cassidy, despite his struggles with substance abuse and frequent legal issues, believed he was a good father to his son. He once talked openly about their relationship and shared what he told his child after finding out he had a mental illness.
David Cassidy became famous as a teen idol when he starred as Keith Partridge on the hit 1970s show “The Partridge Family.” On the show, he played the eldest sibling in a family that performed music together. His real-life stepmother, Shirley Jones, also starred in the series, playing the role of the mother.
David Cassidy’s rise to fame began with the success of “The Partridge Family,” which led to the release of eight studio albums. Although many cast members were part of the show, only David and Shirley Jones, his real-life stepmother, provided the vocals. Interestingly, David was chosen for his role because of his looks, but he soon became the lead singer on the albums.
However, David’s fame soon became a burden. Unlike many teen idols who get tired of fame over time, David resented it from the start. He wanted to be seen as a serious actor but felt trapped in his role as Keith Partridge.
In the 1980s, David admitted, “I was pigeonholed as a teen idol, and there’s no credibility.” He also talked about the personal toll fame had on him, calling it “a very empty, isolated, lonely existence.”
David’s fame isolated him, but it also led to struggles with substance abuse. In 2008, he admitted that he had a problem with alcohol. This was followed by legal trouble, including a DUI charge in 2010 and two more in 2013 and 2014.
In 2014, David entered rehab to address his addiction. By 2015, he had to file for bankruptcy and faced charges for a hit-and-run later that year. In an interview on the “Dr. Phil” show, David revealed that his drinking had hurt his relationship with his son, Beau Cassidy.
“I was the ideal father. I would do anything for him. He’s the love of my life and probably the reason I didn’t kill myself. Because of him,” David said. He also had a daughter, Katie Cassidy.
In 2017, David’s challenges deepened when he announced he had been diagnosed with dementia. Both his grandfather and mother had suffered from the disease, and David admitted, “I was in denial, but a part of me always knew this was coming.”
Reflecting on his mother’s battle, David remembered, “In the end, the only way I knew she recognized me was with a single tear when I walked into the room.” This memory filled David with fear that he would suffer the same fate.
David shared his deepest fears with his son, Beau, telling him, “Promise me you’ll find a way to let me go. Don’t let me live like that.”
Tragically, David passed away in November 2017 at the age of 67 due to organ failure. He had been hospitalized in Florida for several days, and his kidneys and liver failed.
David’s publicist, Jo-Ann Geffen, confirmed his death, sharing a statement from the family: “It is with great sadness that we announce the passing of our father, our uncle, and our dear brother, David Cassidy. David died surrounded by those he loved, with joy in his heart and free from the pain that had gripped him for so long.”
Despite the challenges he faced, David’s estate turned out to be worth more than expected. His son, Beau, inherited nearly $1.68 million, including $230,000 in assets, $450,000 from David’s retirement plan, and a $1 million life insurance policy. David had left most of his estate to Beau, excluding his daughter Katie.
David’s love and pride for his son were clear, especially as Beau followed in his footsteps to pursue a career in entertainment. In a 2012 interview, David reflected on fatherhood, saying, “As a father, I do everything my dad didn’t do. My son Beau’s birth changed my life. I’ve gone to every baseball and basketball game, every performance.”
David was proud when Beau left college to follow his dream of becoming a musician. Beau formed a band called the Fates, and David was excited about his son’s future success.
Beau continued to make a name for himself, even participating in “The Voice.” He was praised as “a really talented performer.”
Fans on social media also noticed Beau’s striking resemblance to his father, often commenting on how similar they looked.
One fan said, “Beautiful smile, young man… keep happy and creating your music,” while another noted, “Just as handsome as his father.” Others echoed similar sentiments, calling Beau “a Handsome Young Cassidy” and commenting, “You look just like your handsome Dad, David!”
David Cassidy’s life had its ups and downs, but his love for his son, Beau, never wavered. Despite the struggles he faced, from teen idol fame to battling addiction and illness, David’s legacy lives on through Beau, who continues to carry on his father’s musical talent and charm.
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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