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...I’ve spent much of the last two years feeling an overwhelming sense of loneliness and isolation. Though the online community has helped me greatly, I still felt as though I...

...One of the hardest aspects of my diagnosis was breaking the news to my mother. Having lived most of her adult life with ulcerative colitis, Mum knew firsthand the misery...

...I've previously spoken about the mental challenges of having AS and being immunosuppressed during the pandemic. Unfortunately, that was just the tip of the ice berg. Here are some more (of the many) aspects...

...Ankylosing spondylitis has taught me something incredibly valuable — that one day will never be the same as the next. I used to think if I was on a streak...

...I've always been an active, outgoing person, so when I lost my job of 8 years, I became very depressed for a whole year. Then I realized there's still life...

...The start of a new school year is coming up quickly. Far more quickly than expected (wasn’t it just June?). And, that means getting back into a schedule. For many...

...Sometimes, you just gotta let it out. That comes from a caregiver myself as well as seeing my husband go through so much frustration during diagnosis, treatment, and multiple surgeries...

...I recently returned from Los Angeles, a valid business trip, but my daughter and I also chose to see the sights as well. We flew in Sunday for Monday-morning business...

...Summer time for me always comes with a lot of traveling. Day trips, extended weekends trip, or a quick flight somewhere. Over the years living with AS, I have learned...

...A few years back, I wrote about my dating experiences while having AS. Guess who’s back for another article on dating! Since identifying as a disabled person, my experiences with...

...I don’t know where you live, but recently, we’ve had a massive heat wave where I live in Canada. The humidity has been into the 40s Celcius (100s Fahrenheit), and...