Surviving the Holidays with Chronic Illness

The holiday season for chronic illness warriors is stressful and hard. Here are some tips on surviving the holidays with chronic illness without flaring. Continue Reading →

Invisible in Taiwan: Living in Taipei with Chronic Illness

Invisible in Taiwan: Living in Taipei with Chronic Illness – What it’s like to live in Taipei and New Taipei with chronic illness and mobility challenges. Continue Reading →

Figuring, Completing, Boring, Cuddling, Chatting – August 2018 Linkup Party for People with Chronic Illnesses

A Chronic Voice hosts a link-up party each month for those of us who are chronically ill. Sheryl’s writing prompts for August are: Figuring, Completing, Boring, Cuddling, and Chatting. Continue Reading →

My Flare Survival Kit

This is my flare survival kit, which includes medications, supplements, and things I need to make myself comfortable when flares hit suddenly. Continue Reading →

What Is A Flare?

A friend recently asked me, “What is a flare?” Flares are a sudden increase in symptoms from my normal day-to-day levels of energy, fatigue and pain. Continue Reading →

My Several Worlds Is Heading In A New Direction

Finding joy in the aftermath of incurable illness has been very hard, but I am still a global citizen of the world, and I have much to offer readers that are interested in expat life and teaching abroad, and in regards to living with chronic illness. Continue Reading →

Chronic Illness – Pacing For Pain Management

Today’s post is about chronic illness and pacing for pain management and why it’s important to people who are chronically ill, like me. Continue Reading →

Fibro-What? Kicking Fibromyalgia To The Curb (Not Really)

My struggle with the severe and debilitating symptoms of Fibromyalgia in Taiwan as a Canadian expat. Continue Reading →

70 Facts About My Invisible Illness You Might Not Know

Today’s post is for everyone who suffers from invisible illness and chronic illnesses. Here are 70 facts about my invisible illness you might not know. Continue Reading →

Living with AS and Why We Need to Keep Moving

I have Ankylosing Spondylitis, a form of autoimmune arthritis. My team, The Walking Spondies, is looking for walkers to join in the Walk Your A.S. Off 2015 Walk-a-thon. Continue Reading →