Author Archives: Lisa Marie Basile

I left a really challenging job situation last year. The job was making me physically sicker and sicker, like the blood in my veins was slowly draining. My ankylosing spondylitis (AS) has never been as horrific as it was during my nearly two years at that job. It wasn’t…

There are many great things about social media. It connects people who would never otherwise meet or talk, creates shared experiences, and can be used as a tool for support and empathy. On social media, the great “we” can be parsed into parts; suddenly the faceless many with ankylosing spondylitis…

When I was officially diagnosed with ankylosing spondylitis (AS) two years ago, I’d been having symptoms for the better part of a decade. The diagnosis came at a time when I finally had health insurance and could book myself in to see a rheumatologist at one of the best…

I was put on biologic medicine to treat ankylosing spondylitis a little over a year ago. I started the biweekly injections and slathered myself in hand sanitizer everywhere I went. Living in New York City, I’m surprised I wasn’t sicker more often! Everyone warned me that biologics were the gateway…

Life can be affirming and beautiful, but it also can be hard, random, and totally unfair. We all know this. And all of that is extra real when living with a chronic disease like ankylosing spondylitis (AS). We may wonder: How does everyone have so much energy all the time…

Getting diagnosed with ankylosing spondylitis (AS) wasn’t just about figuring out (finally!) which disease was causing me to feel like a hot garbage fire — it was about accepting one unchangeable reality and creating a new one. The unchangeable reality came with a thousand variables: Your body will…

I’m a wellness writer and editor. Some of my work has appeared in publications including The New York Times, Good Housekeeping, and here at Ankylosing Spondylitis News — my favorite! My last full-time gig was as editor of a wellness retailer’s blog. The brand wanted to be seen as a trustworthy authority…

I was anxious as I walked into my first ankylosing spondylitis meetup, sponsored by the Spondylitis Association of America. I had no idea what type of people would be there or the severity of their disease. I worried that I’d be too young or too old, or too mobile,…

When I search for “autoimmune disease” or “immune-mediated disease” on YouTube, I get a lot of results, but very few of them are about ankylosing spondylitis (AS). It’s disappointing that so few videos are made by people with AS. I’m looking for someone to connect with, who understands, and…

Around the time of my “official” AS diagnosis (I stress “officially,” because most of us have this disease for years before diagnosis), I joined AQUASTUDIO in New York City. It’s an intimate, friendly, and low-impact studio dedicated to holistic wellness and water workouts. The majority of classes are on bikes…