Eric Dane has passed away at the age of 53 following a battle with ALS (update: last words)

Eric Dane has passed away at the age of 53 following a battle with ALS. Dane confirmed his ALS diagnosis last April, in a big People Magazine interview and cover story. The older I get, the younger “53” seems, damn. Dane is best known for his role as “McSteamy” in Grey’s Anatomy, but he also worked a lot in recent years, in projects like Euphoria and other TV shows, probably to bank some money for his family and keep in good standing for his SAG health insurance. He is survived by his wife Rebecca Gayheart and their two daughters.

Eric Dane, the actor best known as the charming plastic surgeon nicknamed McSteamy on the wildly successful ABC medical drama “Grey’s Anatomy,” has died. He was 53.

His death was confirmed by his publicist Melissa Bank. He had been treated for A.L.S., a neurological disorder also known as Lou Gehrig’s disease, which breaks down a patient’s ability to control muscles, speak and eventually breathe without assistance.

“He spent his final days surrounded by dear friends, his devoted wife, and his two beautiful daughters, Billie and Georgia, who were the center of his world,” Ms. Bank said in the statement.

Mr. Dane died 10 months after revealing his A.L.S. diagnosis in People magazine in April 2025. He later spoke in interviews and on social media about the challenges of living with that progressing condition. Patients with amyotrophic lateral sclerosis, or A.L.S., typically live for only two to five years, though clinical trials for potential therapies have provided hope that lives can be extended by several months.

“I will never forget those three letters,” Mr. Dane said in a 2025 interview with Diane Sawyer on “Good Morning America.” “It’s on me the second I wake up.” During the interview he described the loss of function in his right arm. “It’s not a dream,” he added.

[From The NY Times]

I’m glad Rebecca and their girls were there for him in the end. Eric and Rebecca’s marriage had a lot of ups and downs, breakups and makeups. I feel strongly that Rebecca and Eric agreed to stay married so that she could be there for him in his final months/years. My thoughts are with Rebecca and their daughters.

Note by CB: It’s hard to believe that Eric has passed so young. He helped so many people by going public with his ALS diagnosis and being open about how quickly it progressed and was affecting him. I learned a lot about this disease from him and his legacy will live on in his work and advocacy.

Update by CB: Eric Dane spoke with Brad Falchuk for Netflix’s Famous Last Words. His episode is available on Netflix now. Here’s the incredible message he recorded for his daughters and I’m including the transcript below in case you can’t listen at work.

Billie and Georgia, these words are for you. I tried. I stumbled sometimes, but I tried.

Overall, we had a blast, didn’t we? I remember all the times we spent at the beach.The two of you, me, and Mom in Malibu, Santa Monica, Hawaii, Mexico. I see you now playing in the ocean for hours, my water babies. Those days, pun intended, were heaven.

I wanna tell you four things I’ve learned from this disease, and I hope you won’t just listen to me. I hope you’ll hear me.

First, live now, right now, in the present. It’s hard, but I learned to do that.

For years, I would wander off mentally, lost in my head for long chunks of time,wallowing in worry and self-pity, shame, and doubt. I replayed decisions, second-guessed myself. “I should have done this.” “I never should have done that.” No more. Out of pure survival, I am forced to stay in the present. But I don’t wanna be anywhere else.

The past contains regrets. The future remains unknown. So you have to live now. The present is all you have. Treasure it. Cherish every moment.

Second, fall in love. Not necessarily with a person, although I do recommend that as well. But fall in love with something. Find your passion, your joy. Find the thing that makes you wanna get up in the morning. Drives you through the entire day. I fell in love for the first time when I was about your age. I fell in love with acting.

That love eventually got me through my darkest hours, my darkest days, my darkest year.
I still love my work. I still look forward to it. I still wanna get in front of a camera and play my part. My work doesn’t define me, but it excites me. Find something. Find something that excites you. Find your path. Your purpose. Your dream. Then go for it. Really go for it.

Third, choose your friends wisely. Find your people and allow them to find you, and then give yourselves to them. The best of them will give back to you. No judgment. No conditions. No questions asked. I’m so thankful for my very close family and friends. Every single one has stepped up.

I can’t do even the little things I used to do. I can’t drive around town, go to the gym, get coffee, hang out. I’ve learned to embrace alternatives. My friends come to me. We eat together, watch a game, listen to music. They don’t do anything special. They just show up. That’s a big one. Just show up. And love your friends with everything you have. Hang on to them. They will entertain you, guide you, help you, support you, and some will save you.

Finally, fight with every ounce of your being and with dignity. When you face challenges, health or otherwise, fight. Never give up. Fight until your last breath. This disease is slowly taking my body, but it will never take my spirit.

The two of you are different people. But you’re both strong and resilient. You inherited resiliency from me. That’s my superpower. You knock me down, I bounce right up, and I keep coming back. I get up again and again and again. Mark says I’m like a cat. Except a cat has nine lives, and I’m on number 15 easily. So when something unexpected hits you, and it will, because that’s life, fight and face it with honesty, integrity, and grace, even if it feels or seems insurmountable.

I hope I’ve demonstrated that you can face anything. You can face the end of your days. You can face hell with dignity. Fight, girls, and hold your heads high.

Billie and Georgia, you are my heart. You are my everything. Good night. I love you. Those are my last words.

[From YouTube]

Photos courtesy of Backgrid, Craig Sjodin/Avalon, Cover Images, Avalon.red.

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21 Responses to “Eric Dane has passed away at the age of 53 following a battle with ALS (update: last words)”

  1. Christine says:

    I am so sorry for everyone who this horrific disease has touched. Wow, that was so fast. I hope he is at peace, he really fought and made sure we heard his voice.

  2. Aimee says:

    Heartbreaking. It was so quick! I guess that was a blessing for him and his family. Rest in peace.

    • sasha says:

      He likely had medical assistance in dying. This is not a disease you live out until your last breath if you can help it.

      • Elle says:

        I agree with you, Sasha.

        It is, ironically, the 12 year anniversary of my father’s death. He was on a ventilator and had been in the ICU for five weeks. The doctors called for a family meeting and told us that there was no way he was going to ever leave the hospital. That we could attempt to keep him “alive” but even that was getting difficult. They had already accidentally violated his DNR once. My brother wanted to keep trying and I reminded everyone of his DNR, and that he wouldn’t want to be “living” like this. The doctor came in that evening, administered morphine or whatever it was, unhooked the machines, and he passed quietly, painlessly, quickly. He easily could have “lived” for a few more days, weeks, possibly months. But the doctors and nurses respected HIS wishes.

        I bring this personal story up because I have no doubt that something similar happened here. May he rest in peace. A very talented man.

  3. Julie says:

    This is a very sad news. I loved him in Grey’s but even more in The last ship.

  4. sunny says:

    This is very sad news. He was so young. I hope his family finds peace.

  5. Eleonor says:

    53 is young.
    So sad to hear ASL is an awful disease.

  6. Ameerah M says:

    This is so sad. And I am shocked at how quickly it happened. He was one of my favorite characters on Grey’s and I actually stopped watching the show when he left. RIP to Eric and my condolences to his daughters and Rebecca.

  7. Jayna says:

    He was so brave in the face of it. Still going out there and interacting with the world, attending what he could, still working until he couldn’t, not hiding away as his disease progressed, as long as he could. He handled this illness with such grace and dignity and also tried to use his time to raise awareness of it and highlight organizations. I so admire that.

    RIP, Eric, and I hope it helps your young children to see how much people loved the fighter your dad was and all of the joy he brought people through his body of work.

    “It’s imperative that I share my journey with as many people as I can because I don’t feel like my life is about me anymore,” he said.

    “I have no reason to be in a good spirit at any time, on any given day, I don’t think anybody would blame me if I went upstairs in my bedroom, crawled under the sheets, and spent the next two weeks crying,” Dane admitted. “And I was a little bit pleasantly surprised when I realized that I wasn’t built like that, because I thought for sure that was gonna be me.”

    “I make sure that people are aware of what ALS is and what it’s about, and more importantly, what we can do to combat it and improve the landscape, because it’s so rocky and littered with hurdles and bureaucracy and all this other nonsense that we’re trying to sift through so we can get to a place where we go, start working on solution.”

    Rebecca was the one dealing with the medical insurance for him with his treatment and the bureaucracy he’s talking about, and all of the hurdles, and it was daunting. She talked about it. That’s what families often have to deal with in getting the treatment for their loved ones. She said they were family, and, yes, they were.

  8. Kay Dozier says:

    Heartbreaking. When I first saw it, I thought it was a hoax. I still can’t believe it, he was so young. My heart goes out to his wife and daughters.

  9. AB says:

    Damn he went so quickly. What a cruel disease. Devastating.

  10. Denise says:

    Today is my Mom’s anniversary for dying from ALS. And I wake up to this news. Absolutely heartbreaking.

    I’m praying for a miracle, for a cure to this terrible disease

  11. Chaine says:

    So tragic. It is shocking that his disease progressed this quickly as it seemed when he broke the news last year it was mainly just affecting his arm. I assumed he still had time left.

    • kerfuffles says:

      In his interview with Diane Sawyer, he spoke about how it took 9 months from when he first noticed symptoms (weakness in his hand) to getting a diagnosis. So by the time he was public about his diagnosis, he had probably had the disease for at least a year.

      It’s still shockingly fast, but I think he’d been struggling with this for much longer than it was known publicly. As others have said, he may have chosen medical assistance in dying.

      What a horrid disease. May his public battle with this disease help spur research into finding a cure or at least a good treatment to slow its progression.

  12. Kirsten says:

    This is so very sad. I’m glad that he and his family got to be together. RIP

  13. Mel says:

    ALS is a terrible way to die. RIP to him, condolences to his family.

  14. DrYoko says:

    This news breaks my heart. My mother died of ALS 11 years ago and it is a horrific disease for the individual and the family. To have no hope of a cure is a tragedy. I wish Eric peace on his journey to Yonder, and I wish his family all the best as they navigate the terribly mixed feelings of gratitude that their father/loved one didn’t suffer for too long and the grief of losing him.

  15. Barbara Beimann says:

    One of the toughest things for my husband, diagnosed four years ago, is the frustration with the loss of function and communication. He recently told me “you don’t understand”. I responded, “you are right,I do not….But I am trying with everything I have”. It is that gap between being a Caretaker and significant other. we started ALS/MND programme from Limitless healthcenter. co m 5 months ago, he has regain some functionalities, we noticed his speaking has gotten better since we started on this treatment programme, it didn’t make the ALS go away but it gave him a better quality of life. I also understand that God does not give us more than we can handle…

  16. Bumblebee says:

    He was 2 years younger than me! That is young!! All the good ones go too soon.

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