The idea of EndoArmy came about after Founder (Kianna Scott) experienced 11 years of pain without a diagnosis. Like many, she had to figure out what disease she had on her own. She saw 7 doctors with no answers. She had to fight unrelentingly until she found one that would believe her pain. After she got her answers, she started a new battle. Learning about a disease most people, including those in the medical industry, know little to very little about. This journey inspired her to start an organization. This organization’s purpose is to create recognition for, give a voice to, and empower the dreams of warriors with endometriosis.
In 2019 Kianna hosted her first EndoArmy gathering in northern Virginia where she met Karen Scoggins. Karen and her husband had a similar dream as Kianna. Together they joined funds, forces, and expertise to turn EndoArmy into a 501 (C)(3) nonprofit organization made by patients for patients!
To create recognition for, give a voice to, and empower the dreams of warriors with endometriosis.”
As the journey of creating this organization began, fellow warriors started to join. The mission began to take shape. No one person can change how endometriosis is treated. We started to see that in order to win this battle and make a change, we will all need to come together. We are each a warrior but a battle has never been won alone. We must raise our voices as weapons. We must not stay silent. We must hold each other up. Our pain is strong, our bodies are weak, but our love can change the world! EndoArmy is an organization powered not by one endo activist, but many. The goal is to provide approachable, patient-centered public education and community groups.
We are each warriors but a battle has never been won alone. We must raise our voices as our weapons. We must not stay silent. We must hold each other up. Our pain is strong, our bodies are weak, but our love can change the world!”
Kianna remembers the feeling of complete hopelessness when she was told by medical professionals they didn’t have the answers. The despair she felt when she was told to give up on her dreams. Her biggest fear in life was not death. Like many warriors, her biggest fear was to be alive yet unable to live, love, and laugh. After 30 years of pain and improper treatment, Karen knows what it means to suffer a lifetime of pain due to a lack of support and knowledge regarding this disease. Together with countless other warriors who share our story, our hope is that this campaign will make it so no one has to face that fear alone. Our dream for EndoArmy is summed up well using a quote from Jonathan Swift “May you live all the days of your life”
May you live all the days of your life” – Jonathan Swift
1 in 10, that is how many are affected by endometriosis. You are not alone. Come together, let us raise our voices and fight for change.
Endo Army seeks to raise awareness both inside and outside the endometriosis community by partnering with and encouraging warriors who influence an array of audiences through their sports, hobbies, art, and businesses to speak up and share our campaign. If you have an audience you would like to reach and are interested in partnering with us please feel free to contact us for more information. Our current campaign is our “ride campaign” to learn more about it, or to find out how you can help follow the link below.