Robin Williams' widow, Susan Schneider Williams, has penned an emotional essay about the celebrated actor and comedian's final days.
Interested in Robin Williams?Add Robin Williams as an interest to stay up to date on the latest Robin Williams news, video, and analysis from ABC News.
Williams committed suicide on Aug. 11, 2014. He was 63.
In her essay, published in the medical journal Neurology and titled "The Terrorist Inside My Husband's Brain," Schneider Williams wrote that she hopes her words will "help make a difference in the lives of others."
"Not only did I lose my husband to LBD, I lost my best friend," she wrote. "Robin and I had in each other a safe harbor of unconditional love that we had both always longed for."
Schneider Williams continued, "For 7 years together, we got to tell each other our greatest hopes and fears without any judgment, just safety. As we said often to one another, we were each other's anchor and mojo: that magical elixir of feeling grounded and inspired at the same time by each other's presence."
Robin Williams’ Widow, Susan Williams, on His Suicide: ‘No One Could Have Done Anything'
Robin Williams’ Widow Says She Was ‘Forced’ Into Legal Battle With His Kids Over Estate
Williams was diagnosed with Parkinson disease in May 2014, but a coroner’s report after his death revealed that he also had Lewy body dementia, a common but hard-to-diagnose condition that may have contributed to his decision to commit suicide, medical experts have said.
Williams' widow detailed how the disease affected his life.
"He had been struggling with symptoms that seemed unrelated: constipation, urinary difficulty, heartburn, sleeplessness and insomnia, and a poor sense of smell and lots of stress," she wrote. "He also had a slight tremor in his left hand that would come and go."
Along with "fear and anxiety," Schneider Williams said that "some symptoms were more prevalent than others, but these increased in frequency and severity over the next 10 months."
His widow even recalled an incident when Williams was filming "Night at the Museum 3" in April 2014. Williams had a panic attack on the Vancouver set.
"During the filming of the movie, Robin was having trouble remembering even one line for his scenes, while just 3 years prior he had played in a full 5-month season of the Broadway production 'Bengal Tiger at the Baghdad Zoo,' often doing two shows a day with hundreds of lines -- and not one mistake. This loss of memory and inability to control his anxiety was devastating to him," she wrote.
"He kept saying, 'I just want to reboot my brain,'" she wrote.
Schneider Williams concluded her essay by addressing researchers and doctors studying Lewy body dementia.
"You and your work have ignited a spark within the region of my brain where curiosity and interest lie and within my heart where hope lives," she said. "I want to follow you. Not like a crazed fan, but like someone who knows you just might be the one who discovers the cure for LBD and other brain diseases."
"Thank you for what you have done, and for what you are about to do," she closed.
In the years after Robin Williams’ tragic death, his widow Susan Schneider Williams has been working tirelessly to understand and spread awareness of the brain disease that led to his death – Lewy Body Disease (LDB).
In 2016, two years after Robin’s death, Williams penned a detailed and emotional essay for the medical journal Neurology entitled “The Terrorist Inside My Husband’s Brain.”
In it, Williams details the harrowing final months of the late actor’s life, and how her husband suffered from a disease he didn’t know he had. When Williams opened up to PEOPLE in late 2015 about Robin’s painful final days, she described his many misdiagnosed symptoms as “whack-a-mole,” and that “they present themselves like a pinball machine.”
In the essay, Williams writes that her husband struggled with a variety of symptoms that didn’t fit with any one disease or diagnosis: “constipation, urinary difficulty, heartburn, sleeplessness and insomnia, and a poor sense of smell—and lots of stress,” she says of his symptoms in the fall of 2013. “By wintertime, problems with paranoia, delusions and looping, insomnia, memory, and high cortisol levels—just to name a few—were settling in hard. Psychotherapy and other medical help was becoming a constant in trying to manage and solve these seemingly disparate conditions.”
Williams recalls her husband suffering a panic attack during the filming of Night at the Museum 3 and that he started to forget his lines – something that had never happened in his career. “This loss of memory and inability to control his anxiety was devastating to him,” she says.
Robin was diagnosed with Parkinson’s Disease about a month before his death. While Williams felt relief at finally knowing the cause of her husband’s suffering, she writes that her husband was not at ease.
“He kept saying ‘I just want to reboot my brain.'” Williams recalls. “When we were in the neurologist’s office learning exactly what this meant, Robin had a chance to ask some burning questions. He asked, “Do I have Alzheimer’s? Dementia? Am I schizophrenic?” and when his doctor said “No,” Robin was unsatisfied.
Williams says during his final month she could see that he “was growing weary. The parkinsonian mask was ever present and his voice was weakened,” she writes. “His left hand tremor was continuous now and he had a slow, shuffling gait. He hated that he could not find the words he wanted in conversations. He would thrash at night and still had terrible insomnia. At times, he would find himself stuck in a frozen stance, unable to move, and frustrated when he came out of it. He was beginning to have trouble with visual and spatial abilities in the way of judging distance and depth. His loss of basic reasoning just added to his growing confusion.”
Williams recounts a final perfect day with Robin after which she felt hopeful that he might be getting better. “We did all the things we love on Saturday day and into the evening, it was perfect – like one long date,” writes Williams. “By the end of Sunday, I was feeling that he was getting better. When we retired for sleep, in our customary way, my husband said to me, ‘Goodnight, my love,’ and waited for my familiar reply: ‘Goodnight, my love.’ His words still echo through my heart today.”
Williams concludes her essay with a message of warmth and respect for the neurologists, doctors and scientists who are studying and working to better diagnose LDB.
“I know you have accomplished much already in the areas of research and discovery toward cures in brain disease,” she writes. “And I am sure at times the progress has felt painfully slow. Do not give up. … If only Robin could have met you. He would have loved you—not just because he was a genius and enjoyed science and discovery, but because he would have found a lot of material within your work to use in entertaining his audiences, including the troops. In fact, the most repeat character role he played throughout his career was a doctor, albeit different forms of practice.”
She concludes: “Thank you for what you have done, and for what you are about to do.”