I recently had what I call a “day of doctors.” I had multiple specialist appointments coming up, so I planned them all for the same day. First, I met with a hematologist to figure out why my white blood cell count has been so high. The doctor offered several possibilities,…
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_.
Last June, my partner and I moved from New York City to Michigan. I was very involved with the healthcare system in New York, for better or worse. I was diagnosed with Cushing’s disease in 2020, and even though my main doctor is in Los Angeles, I still…

I spend a lot of time talking with other people who are chronically ill. There’s something special about having a friend who truly understands everything I’ve been through with Cushing’s disease. Recently, I’ve noticed a pattern in my discussions with the Cushing’s community: There’s a lot of frustration…
Last weekend, my husband and I took a trip upstate to see my family. We left late, so by the time we were on our way, it was dark outside. With an iced coffee in hand, I relaxed into my seat, singing songs with my husband and enjoying the darkness…
My health has been drowning me lately. Not only did I have to deal with COVID-19, but also it’s the time of year when many of my regular medical appointments take place. I have an annual pituitary MRI to gauge the size and location of the tumor…
I looked around my apartment last week and realized I had medication everywhere. My coffee table had piles of pill bottles, my counter was full of Sharps containers and syringes, and my drawers were chock-full of vitamins. Everywhere I looked, there was something related to my Cushing’s disease. I’ve…
Last week was one of the worst weeks I’ve had in a long time. My husband and I were supposed to visit my brother and his family in Michigan. I looked forward to seeing my nephew and other relatives and getting a break from New York City. Unfortunately, before we…
The constant, overwhelming feeling starts in my stomach and spreads throughout my entire body. I have to take several deep breaths so that I can focus. My anxiety has been taking over several times a day, every day, since I started showing symptoms of Cushing’s disease in 2018.
It took me over two years to receive my Cushing’s disease diagnosis, mostly because my doctors weren’t well-versed in Cushing’s and didn’t know what to look for. I know that so many in the Cushing’s community have experienced that same sort of pain: We go to a…
Having Cushing’s disease is a full-time job. On many days, I just want to curl up in bed, pull a blanket over me, and sleep all day because my body is so tired and aches all over. However, life goes on, even with my illness, and I can’t ask…
I grew up in New York City, which has continued to be my home. My parents have a gorgeous house on Staten Island. I went to high school and college in Manhattan. I spent endless time at my best friend’s house in Brooklyn. Eventually I moved to upper Manhattan and,…
I’ve been living with Cushing’s disease since 2018. Over the years, I tried out multiple doctors until I formed my perfect care team, which includes endocrinologist Theodore Friedman, MD, PhD. He helped me obtain my diagnosis in 2020, pushed for my endoscopic transsphenoidal surgery to…
Choosing a doctor, or a team of them, is a personal decision. Finding them can be an intimidating process, and it’s exhausting when we have to deal with people who are dismissive, who engage in medical gaslighting, or who misdiagnose us. Throughout my diagnosis and treatment journey with …
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