Lifestyle
Dolores Catania mentioned that she needs to start using Ozempic again because she thinks she’s gained about 20 pounds over the summer. She said she’s going to get back on it quickly.
Dolores Catania is about to get her next Ozempic dose. She told Page Six at the MTV Video Music Awards that she’s taking her shot the next day and mentioned she’s overdue for it but hasn’t stopped using it.
Dolores Catania, 53, said she gained a few pounds this summer because of her Travels. She visited South Africa for conservation work and Lisbon, Portugal for fun.
She mentioned that she’s probably 20 pounds heavier now and needs to start using Ozempic again right away.
Dolores Catania supports her decision to use Ozempic for weight loss, saying that many celebrities do the same, whether openly or privately.
She feels good using it and mentioned that she’s researched it thoroughly and spoken to many doctors, none of whom have said it’s bad for her. She also shared that her boyfriend, Paul Connell, has had great results with Ozempic. He lost 50 pounds and no longer needs blood pressure medication.
Dolores Catania was one of the first celebrities to openly say she uses Ozempic for weight loss, but she told Page Six in April 2023 that she does it for medical reasons.
She explained that she’s dealing with menopause, thyroid issues, and iNFLaMMAtion, which make it hard for her to lose weight. Despite working out and eating well, she was still gaining weight due to these issues.
While Catania has had good results with Ozempic, some people have warned about possible side effects.
Sharon Osbourne has said she’s lost too much weight from using Ozempic and now struggles to gain weight back.
Recently, Lottie Moss, Kate Moss’s younger sister, had to go to the hospital after getting very dehydrated and having a seizure because she took too much of the drug.
A recent study also found that Ozempic has been connected to 162 deaths in the US.
A Man Who Was Called “The Tree Man” Was Able to Hold His Daughter Again After Many Surgeries
“The Tree Man” is a man whose life has been defined by a rare malformation in his hands. Once dubbed for his distinctive condition, he has undergone numerous surgeries, overcoming tremendous challenges on his journey. Now, with unwavering determination and the skilled hands of medical professionals, he has reclaimed a simple yet profound joy—holding his daughter once again.
Abul Bajandar has a rare condition called ’Tree Man’ Syndrome.
Abul Bajandar, a man hailing from Bangladesh, is afflicted with an extraordinary and rare condition known as ’Tree Man’ Syndrome. This hereditary condition, though non-contagious, is unfortunately incurable, and surgical interventions offer only temporary relief. Abul is not alone in his struggle, as there are others worldwide grappling with the challenges posed by this syndrome.
This syndrome manifests through the development of wart-like skin growths that bear a striking resemblance to tree bark. These growths, while initially small, have the potential to grow significantly in size, resulting in considerable disability for those affected.
He has it from a young age.
The onset of his condition began during adolescence, with small warts appearing on his body at the age of 13-14. Regrettably, as he advanced in age, the affliction rapidly escalated, affecting various parts of his body.
After 16 surgeries he was able to hold his daughter again.
After undergoing a series of 16 surgeries between 2016 and 2017 at Dhaka Medical College Hospital in Dhaka, Bangladesh, Abul Bajandar achieved a poignant milestone—he could once again hold his daughter. The surgical procedures aimed to remove the bark-like lesions from his hands and feet, offering a glimmer of hope in his battle against Tree Man Syndrome.
Bajandar shared the profound joy he experiences spending time with his daughters, emphasizing, “If I recover from this, I want to work again, to build a small business to help my daughters in her studies and to give them a good life.” These words reflect not only his determination to overcome the challenges posed by his rare condition but also his unwavering commitment to providing a better future for his family.
Throughout Abul Bajandar’s challenging journey with Tree Man Syndrome, he draws strength from the unwavering support of his wife and mother. In the face of the condition’s recurrence, their steadfast presence provides him with comfort and encouragement. Bajandar reflects on the transformative power of fatherhood, sharing, “When my daughter was born, she brought me the hope of life again. I didn’t want to leave her as an orphan. I felt like I must live for her.”
Abul Bajandar’s condition returned but he remains hopeful.
Despite facing the disheartening recurrence of his condition, Abul Bajandar maintains a resilient sense of hope. Doctors, initially uncertain about the possibility of the condition’s return, witnessed its reappearance. Undeterred, Bajandar expresses his unwavering optimism, declaring, “My only dream is to recover from this situation and live a healthy life.”
His poignant words reflect not only the personal challenges he endures but also a universal desire for health and well-being. Bajandar’s enduring hope shines through as he states, “All I can say is that I truly believe and hope that a cure exists for this disease.” In the face of adversity, his spirit remains unbroken, embodying the strength of individuals confronting rare and challenging medical conditions.
Another person born with a rare condition has defied societal norms and emerged as a symbol of extraordinary resilience. Meet the girl affectionately referred to as “Voldemort” due to being born without a nose.
Preview photo credit Tansh / Alamy Stock Photo, ZUMA Press, Inc. / Alamy Stock Photo
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