Christina Applegate’s candid revelations about the impact of multiple sclerosis left us deeply moved. The 51-year-old actress bravely shared how the disease affects her daily life, emphasizing that ’’With the disease of MS, it’s never a good day”. Her openness about her fears and vulnerabilities only heightened our admiration for her courage.
Fear is part of her everyday life.
During a recent interview, Applegate reflected on the small blessings she used to overlook before being diagnosed with MS in 2021.
She noted that people ask her why she doesn’t take showers, and she explains that ’’getting in the shower is frightening.’’ The Dead to Me star added, ’’You can fall, you can slip, your legs can buckle. Especially because I have a glass shower. It’s frightening to me to get in there.’’
The 51-year-old went on admitting ’’There are just certain things that people take for granted in their lives that Itook for granted’’. She stated that some of them are simple daily tasks such as going down the stairs or carrying things.
The actress revealed that she can still manage to drive short distances and carry food upstairs to her daughter Sadie Grace who is 12, but she made it clear that she struggles with going ’’down, never up.’’
She pointed out ’’Gravity can just pull you down and take everything down with you.’’
Christina Applegate shares new details about living with MS.
In a recent appearance on ABC News, Applegate opened up about her journey with the degenerative disease. She revealed that even the act of sitting for the interview was challenging for her.
«I’m not out a lot, so this is a little difficult, just for my system,» she shared. «But of course, the support is wonderful, and I’m really grateful.»
She continued, «I’m not putting a time stamp on it. I’m never going to wake up and go, ’This is awesome!’ I’m just going to tell you that. It’s just not going to happen. I wake up and I’m reminded every day.»
She added, «I’m isolating and that’s kind of how I’m dealing with it by not going anywhere because I don’t want to do it. It’s hard.»
«(MS) can be very lonely because it’s hard to explain to people. I’m in excruciating pain, but I’m just used to it now.»
She’s not surrounded by too many people.
Despite the assumption that the actress has a support system of friends and family to assist her with everyday tasks, she revealed that she has kept her inner circle small since being diagnosed with MS. She admitted, ’’I actually don’t want to be around a lot of people because I’m immunocompromised.’’
Applegate shared that her friend lives with her during the week and assists her in taking care of Sadie. And on the weekends, a caretaker comes in.
Christina also mentioned that she prefers to avoid overstimulation of her nervous system as it can be overwhelming for her. Therefore, she tries to maintain a quiet and relaxed environment as much as possible.
She explained, ’’Imagine just being in a crowd of people and how loud that is. It’s like 5,000 times louder for anyone who has lesions on their brains.’’
Christina Applegate found unwavering support from her husband during her struggles with MS and breast cancer. His love and strength were pillars that upheld their family’s happiness, even in the face of adversity.
Preview photo credit VALERIE MACON/AFP/East News
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
Leave a Reply