Remembering Katarina Pavelek: A Life Lost to ME

Today I read something that broke my heart.

It was about a young woman who made the devastating decision to end her life through assisted suicide. Her name was Katarina Pavelek, and while I couldn’t place her straight away, I’m sure I’ve seen her on screen before—she was an actress in The Mindy Project and appeared in other shows like Togetherness and The Last Sharknado: It’s About Time.

From this moment on, I don’t think I’ll ever forget her name.
Because Katarina, like me, was living with Myalgic Encephalomyelitis. And like so many of us, she was suffering in ways that are hard to put into words.

You can read more about her story here:
Who was Katarina Pavelek – Slovakian Actress Dies in Assisted Suicide

A Life Remembered

What struck me most wasn’t just the article—it was the tribute from her friends. Fourteen of them gathered on a beach, brought drinks, flowers, and a poster to write farewell messages. They shared memories, laughter, tears… and love. So much love.

Katarina may not have had starring roles on screen, but in the lives of those who knew her, she was a light. A presence. A friend. That’s what matters most.

This Isn’t About Judgement

I’m not here to debate her decision.
Because I know all too well the pain that comes with this illness—not just physically, but emotionally, mentally, spiritually. Only Katarina knew the full weight of what she was carrying. And whatever that looked like, I want to honour her—not question her.

If You’re Struggling, Please Don’t Carry It Alone

If you are in a dark place right now, I want you to know: you’re not alone.

I’ve been there. So low I couldn’t see the point in anything. ME can take everything—your energy, your independence, your identity. But I promise you, even when it doesn’t feel like it, there is still hope. There is still love. There are people who care—even if it’s a stranger at a bus stop or someone reading this blog.

Please, talk to someone. Anyone. It doesn’t have to be perfect or pretty. Just don’t hold it in.

I’m always here if you need to talk. I’m not a professional, but I will always listen.
📧 ask@alishawhittam.com

If you’re in the UK and need immediate help, please visit:
NHS Help for Suicidal Thoughts

To Katarina—
Thank you for the light you shared while you were here.
You will be remembered.
With love,
Alisha 🫶

more Blog Posts

A recent Dragons’ Den episode pitched ear seeds as a cure for Myalgic Encephalomyelitis—an illness I live with every day. Here’s why that claim is not only wrong, but dangerous. Let’s raise awareness, push for better education, and demand accurate
Meet Alfie the Black Labrador from Liverpool, the heartwarming canine companion of Alisha, who lives with Myalgic Encephalomyelitis. Follow their new YouTube channel for adorable videos, inspiring stories, and the unbreakable bond between a dog and his chronically ill owner.
The worst Christmas of my life. I share my story in the hope that you manage this sort of situation better than I did. Not a Holly Jolly Christmas in my house this year.
Christmas used to mean laughter, lights, and being surrounded by the people I love. But since being diagnosed with Myalgic Encephalomyelitis, the festive season has become one of the hardest times of the year. While the world celebrates, many of
Join me for Vlogmas Days 14 & 15 as I share festive moments with Alfie the cuddly Black Labrador, catch up on his advent calendar, and reveal a brilliant Christmas coffee deal! Through the highs and lows of chronic illness,
Dr Paul Hwang's latest ME/CFS research offers new hope for those living with chronic fatigue. Discover how his unexpected findings on mitochondria and the WASF3 protein could reshape our understanding of energy production in Myalgic Encephalomyelitis—and why this matters for