Janel Parrish discusses her endometriosis diagnosis, surgery, and recovery, emphasizing living in the present, gratitude, and spreading awareness for the underdiagnosed disease while navigating fertility challenges.
“ living in the present and just being grateful every day that I wake up and I get to do what I love with people that I love,” Parrish, 37, exclusively shared withdocumentary on Wednesday, June 3.
“We don’t know what the future brings, and I am just trying to really stay in the present and follow what makes me happy and follow my joy, and that’s been bringing me so much happiness. ”Pretty Little Liars’ Janel Parrish Recovering From Endometriosis Surgery Pretty Little Liars star Janel Parrish is opening up about her recent endometriosis diagnosis and subsequent surgery — and for a good reason.
“It is my hope to continue to spread awareness about #endometriosis so here we are,” Parrish, 37, wrote via Instagram on Friday, December 19. “I want to share my story in the , the often-painful condition occurs when tissue that is similar to the inner lining of the uterus grows outside the uterus. The misplaced tissue can thicken and bleed with each menstrual cycle, leading to pain, inflammation and scarring.
, Parrish and other leading voices aim to spotlight one of the most underdiagnosed, underfunded and misunderstood diseases in women’s health.nearly six months after having surgery for the condition.
“I’m feeling really good. I don’t feel any symptoms and I’m doing everything that I can to try to keep living as healthily as I can, and just being positive. ” When she first learned about her diagnosis, Parrish was trying to start a family with her now-ex. Because fertility problems often arise in endometriosis patients, the diagnosis proved to be difficult but physically and emotionally for the actress.
“This thing happens to your body, and then all this pain hits,” she recalled. “I didn’t know what was causing it. I knew that it wasn’t working out. We weren’t getting pregnant, but I didn’t know that I had endometriosis until about two years later when the pain hit.
”, a nonprofit dedicated to transforming how endometriosis is researched, treated and understood through funding multidisciplinary research and creating programming that reshapes the cultural conversation around the disease. Us about her life today.
“The endometriosis is gonna be a part of me, and we’re just gonna have to kind of take it as it comes. As of now, as far as I know, I am healthy and happy, and I’ll just take it as it comes. ”
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