Moving is always challenging, and getting used to a new neighborhood or city can be a little overwhelming. I’m writing this column while sprawled out in bed two weeks after I moved from New York to Michigan. Due to Cushing’s disease, my use of mobility aids, and the cost…
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_.
On Nov. 25, I gave birth to a beautiful baby girl through an emergency cesarean section. However, the story doesn’t start there. Two weeks earlier, I awoke in the middle of the night to my water breaking at only 25 weeks pregnant. My husband and I rushed to the…

I’m currently in the process of frozen embryo transfer, which is usually the second half of an in vitro fertilization (IVF) cycle. Because I have both Cushing’s disease and polycystic ovary syndrome, having children naturally would’ve been a huge struggle, so my husband and I leaned into IVF. We…
I love the summer because June is Pride Month for the LGBTQ+ community and July is Disability Pride Month, two huge parts of who I am. For those of you who don’t know, I’m pansexual and genderqueer, with a preference for they/them pronouns. Cushing’s disease changed my body entirely.
Last week, my husband and I sent all of our stuff away in a pod. A few days later, he packed up our car with all of our belongings, kissed me goodbye, and drove off to Michigan to close on our new house and start a new job. I’m staying…
I’m not fantastic at asking for help. I pride myself on my capabilities and have always struggled with feeling like a burden because of my Cushing’s disease. However, my husband and I are in the midst of a move from New York City to Chelsea, Michigan, and on top…
I’ve been open about my experience going through in vitro fertilization. I have Cushing’s disease and polycystic ovary syndrome, and they each come with their own brand of fertility issues. My husband and I did an egg retrieval procedure last year, and we hope to do a frozen embryo…
My husband and I figured out a while ago that we can’t live in New York City forever. As much as I adore this city, my illness and disability make it impossible for me to take the subway, which is a major travel limitation. On top of that, the city…
When I was diagnosed with Cushing’s disease, I felt completely alone, like I was on an island surrounded by raging waves I couldn’t possibly swim through. In response, I built a community of understanding people, via this column and on social media, as well as by meeting up with…
My white blood cell count was high during my first tumor with Cushing’s disease, back in 2020. Now, with my second tumor, it’s happening all over again. For that reason, I’ve added a hematologist to my doctor rotation to make sure there isn’t any cancer and that Cushing’s is…
I have Cushing’s disease and polycystic ovary syndrome (PCOS), both of which cause fertility issues. With Cushing’s, my periods stopped entirely and my hormones are obviously completely messed up. With PCOS, I had cysts and calcified fibroids on my ovaries. I was told I had a chance to…
I’ve been open about my current journey with in vitro fertilization (IVF). A few months ago, my husband and I went through the first part of it, freezing our embryos, and now we’re at the beginning stages of an embryo transfer. I, somewhat naively, thought that was going to…
I turned 29 last week, and for the first time, I no longer feel like I’m waiting for life to happen. In the past, Cushing’s disease took over every aspect of my life. I was diagnosed in 2020, though I’d been experiencing symptoms for years. After undergoing…
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