
Jemma Newman
Articles
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2 months ago |
ankylosingspondylitisnews.com | Alexandra Fendrich |Lisa Marie Basile |Jemma Newman |Margarida Maia
One evening in December, I scrolled through photos on my phone, looking back at each moment in time.
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Sep 16, 2024 |
ankylosingspondylitisnews.com | Esteban Cerezo |Alexandra Fendrich |Jemma Newman |Patricia Inacio
Lower socioeconomic status is associated with more severe disease, longer diagnosis delays, and permanent disability in people with ankylosing spondylitis (AS), a Spanish study showed. Even with similar access to disease-modifying anti-rheumatic drugs (DMARDs), socioeconomic status may be a significant factor for understanding health outcomes differences between AS patients, the scientists suggested.
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Jul 9, 2024 |
ankylosingspondylitisnews.com | Alexandra Fendrich |Margarida Maia |Jemma Newman
It’s summer, which means I want to spend more time outside, preferably near water with an ice cream in hand. Living with ankylosing spondylitis (AS) has required me to have a different form of “hot girl summer,” though, as I manage the ups and downs of flares — periods of disease when my pain and stiffness increase. Beyond trying various medications, I’ve identified strategies to help me function amid periods of high inflammation. They’ve been crucial to how I navigate my disease.
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Apr 22, 2024 |
ankylosingspondylitisnews.com | Margarida Maia |Patricia Inacio |Jemma Newman
Nearly half of patients admitted to the hospital for ankylosing spondylitis (AS) are discharged to somewhere other than home or return to the hospital within three months, according to a study from over 150 hospitals under HCA Healthcare. Receiving medications such as opioids and steroids during a hospital stay were among the factors that stacked the odds against being discharged home, whereas having a surgical procedure, among other factors, increased the odds of being readmitted.
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Mar 5, 2024 |
ankylosingspondylitisnews.com | Jemma Newman |Margarida Maia |Lindsey Shapiro
When I was diagnosed with ankylosing spondylitis (AS) in December 2019, I frequently felt anxious, miserable, and utterly exhausted about my future. But if I could go back and tap myself (gently) on the shoulder at that difficult time, I’d have some encouraging thoughts to share. If anyone reading this column is in a similar cave of darkness because of AS, I hope that a bit of positivity will help to balance out the challenges. “Psst,” I’d whisper in the ear of my younger, pain-riddled self.
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