If you’re facing Christmas with Myalgic Encephalomyelitis (ME), please know this: you are not alone.
The festive season can feel like a spotlight on everything ME has taken from us—family time, fun, independence, and the simple joy of being present.
📺 While TV shows and magazines show picture-perfect holidays full of laughter and celebration, the truth for many of us is very different. For millions living with chronic illness, Christmas can feel isolating, painful, and overwhelmingly lonely.
I was diagnosed with ME in 2012. I’ve cried through Christmases alone. I’ve missed birthdays, weddings, and even funerals of people I love. This illness took my career, my freedom, and changed everything for my husband and daughter, too.
✨ But here’s the thing—I see you. I feel you. And if you’re hurting this Christmas, please know my inbox is always open.
No pressure, no expectations—just a fellow spoonie who understands. If you need a safe space to talk, message me using my contact page or email me: alisha@alishawhittam.com.
I may not have all the answers, but I can listen. 💌
With love and solidarity this Christmas,
Alisha 🫶