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
“She’s a real Thumbelina” – Meet the girl who’s only 99cm tall and defied all the odds
Kenadie Jourdin-Bromley, a Canadian child from Ontario, seemed ordinary at first glance.
She had high hopes for the future, loved sports and drawing, and went to school.
Nonetheless, one characteristic set Kenadie apart from her peers: her diminutive height of 99 centimeters.
Reports state that when Kenadie was born in February 2023, she weighed a mere 2.5 pounds. Her condition was quickly diagnosed by doctors as an uncommon form of cardiovascular disease, thought to affect only 100 people globally. The nurses dubbed her “Thumbelina,” quite fittingly.
Regretfully, Kenadie had slim chances of surviving.
According to reports, the girl’s condition can lead to complications like delayed mental development, respiratory issues, and digestive issues. Doctors at the hospital where the girl was born were concerned that she wouldn’t have much time to live due to her brain injuries.
Understandably, her parents were devastated. In order to give their little girl a name in case she passed away, they chose to christen her on the day of her birth.
“We thought we were going to take her home to die, because that’s what the doctors told us,” mom Brianne explained to Barcroft TV back in 2016.
Still, as the days went by, Kenadie steadfastly refused to give up. After she triumphed over all the challenges and hardships, her parents were able to dream again that she would survive. It was nothing less than a miracle for them.
Many years later, Kenadie still astounds everyone she encounters. She is only 99 centimeters tall, her arms and legs are still immature, and she struggles to learn new things, but she is a content young girl who enjoys life to the fullest.
Kenadie reportedly enjoys bowling and ice skating. Above all, she makes people happy that she meets.
“Kenadie makes me laugh. She’s very empathetic – if you hurt your finger she comes and gives you a hug. She’s got an infectious laugh that makes you want to laugh along with her,” Kenadie’s assistant Jessica Putnam mentioned to Barcroft TV in 2016.
Naturally, Kenadie and her family face many new challenges in their lives. Despite her loved ones’ best efforts to take each day as it comes, the young girl is continuously dealing with medical issues.
“My hope for Kenadie’s future– my biggest hope for her– is I want her to be happy. I want her to smile and be successful. If we can get through today, then we’ll see about tomorrow,” her mom said.
We are happy to share Kenadie’s inspiring story!
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