Kits Blanc

Northeast LGBT volunteer coordinator

Hey! I'm Kits, I'm The King of Endo and I am transgender with endometriosis. I am a transman, which means I was assigned "female" at birth and I transitioned into a man. I bring awareness to endometriosis while promoting unconditional self love within the transgender community. I am 30 years old and live in Pittsburgh, PA. My pronouns are he/him/his. I am a contractor by trade and own my own contracting company, Reality Contracting, LLC. I am engaged to be married Oct. 2025 and I have an active non profit with my fiancé called "Genesis Gifts" in which we gift children who are grieving their parent(s) during the holidays. I attended SCAD (Savannah College of Art & Design) Atlanta, however I was unable to finish due to financial difficulties. I believe in 100% transparency and use that to bring awareness to endometriosis. I started back in 2017 when I had a doctor tell me that they believed I had it for the first time in my life. I dove deep into a rabbit hole of what the disease was and what could be done, only to find out endometriosis is a big mystery to the world. I couldn't believe it! I had experienced these symptoms since elementary school and always felt alone and like I was crazy. There's no cure, it takes close to 10 years for a diagnosis, there's not a lot of research, and those suffering from it are treated inhumane. Turned away simply due to the health care system not caring about women's health. I couldn't sit back and do nothing. I needed answers, I needed to help my future children from suffering in silence the way I had to, I needed to make sure the other endo warriors of the world knew they were not alone. I was officially diagnosed with stage 4: thoracic, diaphragmatic, bowel, hepatic, and sciatic endometriosis in 2018 when I had my laparoscopy surgery to have it removed. At that time I still identified as "female", but was struggling internally with the pain of feeling like I'm a male trapped in a woman's body mixed with the physical pain brought on by the endometriosis. I was told by my surgeon that I had the "worse case on endometriosis" he had ever seen. They made me aware at that time that they were unable to remove all of the endometriosis because of me having it on my lungs, diaphragm, and further up where they were unable to reach. I was told there are only 3 surgeons in the world with the expertise to remove the endometriosis for me. located in Atlanta, Oregon, and Brazil. I chose the surgeon in Atlanta, Georgia since I graduated high school there and I have been trying to afford to have my second surgery since. So while I saved up for that I turned to social media, spreading factual information about endometriosis and recordings of myself having flareups. No matter how embarrassing or uncomfortable it made me feel. I did that for years with no real traction on social media and not many followers at all. It wasn't until 2022 when I finally had the courage to come out as a transgender man that my views, likes, and comments started to flood in. I was sharing my journey as I usually do and all of a sudden the algorithm started boosting my content, people are commenting hate and support, I am being shared, and people are interested. All because my videos said "Transman" and I am bringing awareness to an illness that people believe is a "woman's disease". I jumped at the realization and started including the fact that I am a transgender man and I wanted the world to see how the testerone would effeft a transman transitioning with endometriosis. I was named "The King of Endo" by my followers on TikTok and it just stuck. Being a man bringing awareness to endometriosis is a task but I am up for it! proving to the world that everyone suffers from endometriosis and once we realize it is a human disease and not just a woman's disease, then maybe we can see a change in how the heathcare system sees endometriosis and gender identity when it comes to chronic illnesses. I put myself in a position to be seen, studied, and questioned through my transparency. I feel that the best way to bring awareness to anything is by showing it first hand. People only believe what they can see. So I show you all. I see a future where endometrisosis is as known as cancer, where there is early testing & preventative care, where all patients are believed no matter their age or gender, where there is financial assistance and/or Paid time off at work for those that suffer from endometriosis, where there is medication designed just for endo warriors, and no one has to feel alone again. I do this for the whole world and I will not stop until my goals are met. Join me in my journey and fight to change how Endometriosis is seen and treated! Follow me @KitsBlanc on all Facebook, TikTok, and Instagram.

Hey! I'm Kits, I'm The King of Endo and I am transgender with endometriosis. I am a transman, which means I was assigned "female" at birth and I transitioned into a man. I bring awareness to endometriosis while promoting unconditional self love within the transgender community. I am 30 years old and live in Pittsburgh, PA. My pronouns are he/him/his. I am a contractor by trade and own my own contracting company, Reality Contracting, LLC. I am engaged to be married Oct. 2025 and I have an active non profit with my fiancé called "Genesis Gifts" in which we gift children who are grieving their parent(s) during the holidays. I attended SCAD (Savannah College of Art & Design) Atlanta, however I was unable to finish due to financial difficulties. I believe in 100% transparency and use that to bring awareness to endometriosis. I started back in 2017 when I had a doctor tell me that they believed I had it for the first time in my life. I dove deep into a rabbit hole of what the disease was and what could be done, only to find out endometriosis is a big mystery to the world. I couldn't believe it! I had experienced these symptoms since elementary school and always felt alone and like I was crazy. There's no cure, it takes close to 10 years for a diagnosis, there's not a lot of research, and those suffering from it are treated inhumane. Turned away simply due to the health care system not caring about women's health. I couldn't sit back and do nothing. I needed answers, I needed to help my future children from suffering in silence the way I had to, I needed to make sure the other endo warriors of the world knew they were not alone. I was officially diagnosed with stage 4: thoracic, diaphragmatic, bowel, hepatic, and sciatic endometriosis in 2018 when I had my laparoscopy surgery to have it removed. At that time I still identified as "female", but was struggling internally with the pain of feeling like I'm a male trapped in a woman's body mixed with the physical pain brought on by the endometriosis. I was told by my surgeon that I had the "worse case on endometriosis" he had ever seen. They made me aware at that time that they were unable to remove all of the endometriosis because of me having it on my lungs, diaphragm, and further up where they were unable to reach. I was told there are only 3 surgeons in the world with the expertise to remove the endometriosis for me. located in Atlanta, Oregon, and Brazil. I chose the surgeon in Atlanta, Georgia since I graduated high school there and I have been trying to afford to have my second surgery since. So while I saved up for that I turned to social media, spreading factual information about endometriosis and recordings of myself having flareups. No matter how embarrassing or uncomfortable it made me feel. I did that for years with no real traction on social media and not many followers at all. It wasn't until 2022 when I finally had the courage to come out as a transgender man that my views, likes, and comments started to flood in. I was sharing my journey as I usually do and all of a sudden the algorithm started boosting my content, people are commenting hate and support, I am being shared, and people are interested. All because my videos said "Transman" and I am bringing awareness to an illness that people believe is a "woman's disease". I jumped at the realization and started including the fact that I am a transgender man and I wanted the world to see how the testerone would effeft a transman transitioning with endometriosis. I was named "The King of Endo" by my followers on TikTok and it just stuck. Being a man bringing awareness to endometriosis is a task but I am up for it! proving to the world that everyone suffers from endometriosis and once we realize it is a human disease and not just a woman's disease, then maybe we can see a change in how the heathcare system sees endometriosis and gender identity when it comes to chronic illnesses. I put myself in a position to be seen, studied, and questioned through my transparency. I feel that the best way to bring awareness to anything is by showing it first hand. People only believe what they can see. So I show you all. I see a future where endometrisosis is as known as cancer, where there is early testing & preventative care, where all patients are believed no matter their age or gender, where there is financial assistance and/or Paid time off at work for those that suffer from endometriosis, where there is medication designed just for endo warriors, and no one has to feel alone again. I do this for the whole world and I will not stop until my goals are met. Join me in my journey and fight to change how Endometriosis is seen and treated! Follow me @KitsBlanc on all Facebook, TikTok, and Instagram.