The Willis family has gone through a lot during these past months, and their struggles are far from over.
Ever since the Die Hard star was diagnosed with a condition that affects one’s ability to communicate, the world fell silent. His family provided him with extreme support and has been updating his fans of Bruce’s condition regularly.
Bruce withdrew from from the spotlight, and later on, he was diagnosed with a more specific condition; frontotemporal dementia.
“Our family wanted to start by expressing our deepest gratitude for the incredible outpouring of love, support and wonderful stories we have all received since sharing Bruce’s original diagnosis,” his daughter Rumer Willis posted on the social media.
“In the spirit of that, we wanted to give you an update about our beloved husband, father and friend since we now have a deeper understanding of what he is experiencing.
“Since we announced Bruce’s diagnosis of aphasia in spring 2022, Bruce’s condition has progressed and we now have a more specific diagnosis: frontotemporal dementia (known as FTD).”

As Bruce’s wife, ex-wife, and his daughters were as well affected by his illness, his daughter Tallulah, whom the actor shares with Demi Moore, is experiencing issues with her mental health and they get worse as her father’s health condition worsens.
Tallulah spoke openly of her anorexia after she was dumped by her fiancè Dillon Buss less than three months after her father’s aphasia diagnosis.
As per reports, Bruce is being aware of his daughter’s suffering.
“Bruce could see her wasting away and it only made his own problems worse,” a source said, as reported by Radar.
“Bruce was shattered when he saw Tallulah’s suffering,” the insider went on.
“It got to the point where the family thought it would be better if they weren’t around each other at all.”

Tallulah has been diagnosed with borderline personality disorder after she checked into an in-patient facility following the breakup.
In the essay she penned for Vogue Magazine, Tallulah explained that her struggles with body dysmorphia began when she started taking medication for ADHD.
“I felt smart for the first time,” Tallulah said of taking her medication, “but I also started to enjoy the appetite-suppressant side effect of the meds. I saw a way to banish the awkward adolescent in favor of a flighty little pixie. And like so many people with eating disorders, my sense of myself went haywire.
“There’s an unhealthy deliciousness at the beginning of losing weight rapidly. People are like, ‘Oh wow!’ And then quickly it turns to, ‘Are you okay?’ My friends and family were terrified, and I dismissed it.”

The 29-year-old added: “By the spring of 2022, I weighed about 84 lbs. I was always freezing. I was calling mobile IV teams to come to my house, and I couldn’t walk in my Los Angeles neighborhood because I was afraid of not having a place to sit down and catch my breath.”
We truly hope Tallulah would be able to overcome her health issues.
Céline Dion Shares Raw Video of Stiff-Person Syndrome Crisis in Never-Seen Footage from New Documentary

In a devastating moment from “I Am: Céline Dion,” the famous person battles through an unexpected and horrifying SPS episode.

Fans are getting an unheard-of glimpse inside Céline Dion’s tribulations during the last few years of her life.
After being diagnosed with stiff-person syndrome in August 2022, the 56-year-old superstar tentatively but proudly returns to the recording studio in a devastating sequence towards the end of her new documentary, I Am: Céline Dion (available for streaming globally on Prime Video).
Shortly after, as part of her continuous treatment regimen, she makes her way to physical therapy and her foot starts to hurt.
Dion’s body locks up, indicating that she is in severe agony while her care team gives her a diazepam nasal spray during the SPS crisis episode. One of her teammates says, “We’ll do a 9-1-1 if she goes back into a spasm.”
In the movie, Dion subsequently remarks, “Every time something like this happens, it makes you feel so embarrassed.” “I’m not sure how to say it. You know that you dislike losing control of yourself?
The five-time Grammy winner thought back on the horrifying moment that director Irene Taylor’s crew captured on camera during her PEOPLE cover interview.
“Overstimulation—whether it be happiness, sadness, sound, or a surprise—can put me into a crisis—that’s one part of the [SPS] condition,” Dion explains, adding that she “did not see” the crisis episode coming that day. “Before something triggered, I was fine.”
Taylor’s understanding of the condition deepened when she was “two feet away” from Dion during the crisis.
Taylor remarks, “That was really amazing, not just for Céline to go through it, but for me to see as well.” “I continued to film because that is how I work, and I thought we would decide later whether or not to incorporate that into the movie.”

Dion and Taylor had developed a close relationship by the time the movie was in post-production, and according to Taylor, “I knew that putting it in the film was really not a risk because she believed in me at that point.” “I really can only thank her for that because she is an open book, was there, and didn’t hold anything back.”
Dion is attempting to humanize the uncommon illness through the movie and contribute to fund-raising efforts for scientific studies in the pursuit of a solution.
Neuropathy has a very broad spectrum. For this reason, I’m making a lot of effort to raise money so that people can speak with their husbands, friends, or neighbors about it,” Dion explains.
Adds Dr. Amanda Piquet, the doctor who diagnosed Dion and director of the University of Colorado Anschutz Medical Campus’s program on autoimmune neurology: “There are many exciting things in store for SPS, and the future looks bright.”
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