How do you set boundaries when it can feel like changing the world requires laying yourself bare? When coming out as intersex and going public in the media with my own story as a teen, I didn’t know what I didn’t know. Fellow intersex advocates share the tips and boundaries they wish they’d had. By
I drove 1,300 miles to start a new life in a red state. As a Black queer intersex person, that meant navigating new challenges for my safety, and for my vote. By Bria Brown-King  An important note: I wrote this blog in increments over a period of 2 months. It documents my moving journey
Are people with MRKH—with mostly typical sex anatomy but born without a uterus and/or parts of the vagina—considered intersex? To get anywhere, we need to be asking completely different questions. By Maddie Rose   As a teen newly navigating dating and sexuality, I received news that turned my world upside-down: a diagnosis of Mayer-Rokitansky-Küster-Hauser
Infant genital surgery made me feel like my body wasn’t mine. An eating disorder felt like a way to reclaim control. Here’s how I found my way out. By Marissa Adams Be aware: this personal essay covers infant genital surgery, medical trauma, and inpatient programs for anorexia. People with eating disorders learn to restrict
Congenital Adrenal Hyperplasia is one of the most common medical terms associated with intersex genital differences. A mom and nurse sits down with an intersex advocate to uncover common misconceptions around genital surgery. By Hans Lindahl and Stephani Lohman  ALSO AVAILABLE IN SPANISH! "Una mamá y enfermera desmiente 5 mitos sobre la cirugÃa genital
June is CAH Awareness Month. Congenital Adrenal Hyperplasia is the medical term given to one of the most common intersex conditions. We talked to five young people about their experiences with CAH, adrenal crisis, and growing up with intersex bodies. By Bria Brown-King  This essay is also available in Spanish, thanks to the translation
My name is Jackie Green and for as long as I can remember my biggest fear in life was that someone would find out that I had XY chromosomes - a fact about me that you can’t see, feel, or sense in any way.  Yet I still found myself afraid of what others would think
What Would I Have Been Like? Examining hidden preconceptions & perils of the Intersex Experience (#1) by Karen Walsh This question has morphed quite a bit over the years for me. It went from common little girl fantasies of being a traditional Mom & wife, through imagining what I’d be like if I didn’t have Complete
Guest post by: interACT Board Member, Lynnell Stephanie Long When I was a child, and in the University of Chicago Hospital, I contemplated death more than life. At the age of 14 I was told I was infertile. The doctor told me matter of fact, and never offered any sort of emotional support. I was
MTV has done an amazing thing recently by adding an intersex character to "Faking It!" In said program, the character Lauren Cooper (portrayed by Bailey De Young) has Complete Androgen Insensitivity Syndrome. This means that she has XY chromosomes, developed as female, and her body no longer produces hormones so she takes estrogen pills.
