Picture in your mind the most painful thing that has ever happened to you. Now zero in on exactly what the pain felt like, looked like, or even smelled like. For me, there is no greater pain than having ulcerated wounds. I never really knew the feeling of true…
When I was diagnosed with scleroderma at 19, it was dumped into my lap. The doctor simply looked at me and said, “Get your affairs in order and work as long as you can. Scleroderma has no cure and will ultimately take your life.” To say I was affected mentally…
We all face a lot of pressure to appear perfect — educated, attractive, healthy, capable, and independent. This can be a big pair of shoes for a “normal,” healthy person to fill. Now imagine how difficult it is for someone with a chronic, debilitating illness to check all of those…
When the COVID-19 pandemic hit the U.S. in March 2020, it was like time stood still. Many chronic illness patients were on high alert, constantly afraid of contracting the virus. Given the complexity of my disease, scleroderma, even the common cold can land me in the hospital, fighting for…
As young adults, my friends and I used to play a drinking game called Never Have I Ever. The rules were simple: Someone calls out something they’ve never done. If you haven’t done it, either, you do not take a sip of your beverage. However, if you have participated in…
My traveling days have been few and far between since I was diagnosed with systemic scleroderma in 2001. Now, it’s even more difficult due to the COVID-19 pandemic. However, I was invited to participate in an ad that will promote clinical trials, so last month, I traveled from my home…
I am a scleroderma patient. Saying or writing that is hard for me. It took 20 years of being a patient to feel confident enough to say it out loud. I’ve had systemic scleroderma my entire adult life, and it’s changed the way I live, how I do my…
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