I glance at the clock for the 15th time. It’s 2 a.m. I need to wake up in two hours to feed the baby, and my eyes are stinging with exhaustion. I’ve tried everything. I count sheep. I manifest. I put on the sounds of oceans, forests, and birds. I…
Chronically Yours— Noura Costany

Noura Costany (they/them) is a writer from Queens, New York. They were originally diagnosed with cyclical Cushing’s disease in 2020, and their pituitary adenoma recurrence was confirmed in 2022. Noura is hoping the column “Chronically Yours” will help spread the word about cyclical Cushing’s disease, create an online community for those struggling with chronic illnesses, and bring light to inequality that is often overlooked in healthcare systems. You can catch Noura on TikTok and Youtube @chronicallyyours_.
A few weekends ago, my family and I all crammed into a car and drove to Pennsylvania from our home in Michigan for my beloved grandmother’s funeral. Since we had a toddler and a 7-month-old in the car, eight hours turned into 12. That long car ride was followed by…

Note: This column describes the author’s own experiences with diet, exercise, and supplements. Not everyone will have the same response. Consult your doctor before starting or stopping a therapy or health regimen. Nothing has motivated me to focus on my health more than having a daughter. I look down at…
I have very odd eyesight problems that are caused by Cushing’s disease, including visual snow, floaters, halos, and night blindness. According to neuro-ophthalmologists that I’ve seen, my actual eyesight is fine. My issues are caused by the high levels of cortisol in my body. My body responds to stress with…
Brain fog is one of the most frustrating issues I face with Cushing’s disease. It’s not one thing, but a collection of symptoms, such as memory lapses, confusion, trouble focusing, mental cloudiness, and unease. I didn’t realize that Cushing’s disease was causing my brain fog at first. I…
Being queer and chronically ill are two huge parts of who I am. I’m proud of both of the identities that influence my community and my life. For a long time, these two parts of me felt like a Venn diagram where the circles didn’t even touch. However, over time,…
The term “flare-up” is used to describe the sudden onset of aggravated symptoms. Although I’m medicated for Cushing’s disease, I still have significant flare-ups. Often, they’ll happen when I overexert myself, fail to rely on my mobility aids, or overestimate how good I feel. I also have flare-ups during…
I love it when kids ask me questions about my Cushing’s disease, because it’s a great chance to educate them. Kids are super curious, especially about my mobility aids and medications. In my experience, children generally understand why older adults or people…
Cushing’s disease significantly affects the menstrual cycle. When people hear that statement, they often think that the disease affects only periods, but it actually alters every part of the menstrual cycle. The first sign of Cushing’s disease for me was a complete loss of my period. One month, I’d…
Cushing’s disease can look different from one person to the next. One may use a wheelchair, while another is in remission. Someone might be on 50 medications, and another person might need only one. Therefore, simply saying I have Cushing’s disease doesn’t really explain how it affects my body.
Despite achieving success, some people experience impostor syndrome — the feeling that they’re not good enough or haven’t earned it. They may feel like a fraud, like they’ve tricked people into believing they’re good at something. For those of us with chronic illness, impostor syndrome may cause us to wonder…
Editor’s note: This story includes discussion of suicide. If you or someone you know needs help, the national suicide and crisis lifeline in the U.S. is available by calling or texting 988. There is also an online chat at 988lifeline.org. Internationally, find a suicide prevention helpline at findahelpline.com.
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