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Welcome!
Hey there! I'm Kailey.
Back in 2016, after years of dealing with unexplained pain, I heard the word "Endometriosis" for the first time. It was (and still is) a tough journey and but I did not let it bring me down. Instead, I started Hello Endo Chick.
Hello Endo Chick is a resource dedicated to raising awareness and providing support for those living with endometriosis and their loved ones. Our mission is to empower individuals to take control of their health and become well-informed about their condition. Here, I share my own personal journey and experiences living with endometriosis, as well as stories from fellow endo warriors.
We strive to create a safe and open space to talk about the struggles and triumphs of living with Endometriosis. We are passionate about bringing awareness to this often misunderstood condition and connecting with fellow Endo Chicks to create a strong, supportive community with a good dose of fun.
What We Do
Organize fun, informative events and workshops to promote endometriosis awareness and create community.
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Host a support group for endo warriors and supporters to connect with those who get it.
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Advocate and push for legislative reform in the state of Connecticut and beyond.
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Design apparel and accessories to empower.
Updates and Info
Connect on Instagram
![📢 CALL FOR SUBMISSIONS: Share Your Endometriosis Story! 💛✨
Hey #EndoWarriors, caregivers, and loved ones! 💛 I’m creating a project of hope, strength, and resilience for the endometriosis community, and I’d love for YOUR story to be part of it.
💬 Have you…
✔ Fought for a diagnosis after years of being dismissed?
✔ Found strength in friendships, love, or community?
✔ Discovered ways to manage symptoms or reclaim joy?
✔ Used art, advocacy, or creativity to turn pain into purpose?
If so, I’d love to feature your story in my new project for a collection of real-life experiences from those living with endometriosis AND the people who support them.
📖 How to Submit:
➡ Click the link to share your story: [Insert Google Form Link Here]
➡ Choose to remain anonymous or include your name.
➡ Stories from patients, caregivers, partners, professionals & advocates are welcome!
➡ Selected stories will be featured in a published book to inspire and support the endo community.
✨ Because you are NOT alone. Your story matters. And together, we are stronger. ✨
Tag someone who should share their story! 💛💬 #EndoTogether #EndometriosisAwareness #EndoWarrior #YouAreNotAlone #EndometriosisStories #ChronicIllnessCommunity](https://scontent-sea1-1.cdninstagram.com/v/t51.75761-15/488647497_18154544560360015_5593499058633047843_n.jpg?stp=dst-jpg_e35_tt6&_nc_cat=108&ccb=7-5&_nc_sid=18de74&_nc_ohc=lUWNbdyflF0Q7kNvwF9tfO6&_nc_oc=AdnAfXtZfRaCGU0XEjCJMqU7zbkwD98pB2p0VgtjCrda9zuLs2ltaDew8PYPChKsvvk&_nc_zt=23&_nc_ht=scontent-sea1-1.cdninstagram.com&edm=ANo9K5cEAAAA&_nc_gid=DfwUNodTCmA2qU942dYP_w&oh=00_AfKfOhlxhQGnFTHRksDWr8JxGp7jkpWf7l43__5rDq0OcQ&oe=6830FDDA)
![It’s been a long road…I finally had excision with an expert for endometriosis. ✨It’s not the end but a major milestone in my journey!😁
Excision is when the endometriosis is excised or cut out entirely and is considered the surgically gold standard of treatment. Is it a highly advanced technique requiring extensive training (CEC). My previous surgeries were ablation, in which the tissue is burned off, allowing the disease and subsequent pain to recur because it was not entirely removed. It’s like a weed, it will regrow if you burn the surface, but if you remove the weed and its roots, it won’t. (although endo may come back, it is far less likely in skilled hands with excision vs. ablation).
Endo is a chronic disease with no cure. This will give me the best chance at pain management. I also had a partial hysterectomy for Adenomyosis, a.k.a. endos evil twin. It is the presence of endometrial glands and stroma within the myometrium” [Gong et al., 2022]. The myometrium is the medical term for the muscular portion of the uterine wall. There are ways to manage Adeno symptoms, and removal of the uterus is a cure. For me, it was time. My uterus felt like a constant weight, significantly affecting my day-to-day life. I could no longer exercise without pain or even walk a mile.
I’m excited and hopeful for the journey ahead. ✌️ I’ll be posting recovery video updates. Keep in mind everyone’s endo journey is unique and we cannot compare one to the other. I am here for support and to support you all. Please message me with any questions! I’d love to share my experiences with you. Keep on fighting 💜💛💜 #endometriosisawarenessmonth #endometriosis #adenomyosissucks #adenomyosis #endowarriors #endometriosis #endoupdate #endostrong #adenomyosis #chronicillness #chonicpain #endometriosisstory #endosupport #endometriose #endostrong🎗 #endojourney](https://scontent-sea1-1.cdninstagram.com/v/t51.36329-15/337429860_773939463944746_7011837870271607404_n.jpg?stp=dst-jpg_e35_tt6&_nc_cat=105&ccb=7-5&_nc_sid=18de74&_nc_ohc=BNe4kGEZ6TcQ7kNvwGzabkY&_nc_oc=AdlgDPJkwWDcwax-fRgmIRRDZxtzBNkrYN_uF_L77jfxJWgEaplc6qnWqW-OEMz9leo&_nc_zt=23&_nc_ht=scontent-sea1-1.cdninstagram.com&edm=ANo9K5cEAAAA&_nc_gid=DfwUNodTCmA2qU942dYP_w&oh=00_AfLV9DjWQjcdpBtf1QVlFbu0-dcdztMjURHFjO_A-Vohow&oe=68310745)
Endometriosis in Connecticut
For more information on Endometriosis legislation and research developments in Connecticut, please visit the links below.
Headed by State Representative Jillian Gilcrest, The Endometriosis Working Group has announced several priorities to create greater awareness and expand access to care.
Through research and advocacy, JAX and our partners in Connecticut are committed to improving the lives of those impacted by endometriosis.
This is a support group for those living in and around Connecticut with Endometriosis. Friends and family members of those affected are welcome to join. The group's goal is to support, empower, and connect those affected by the disease. We will host monthly meetups and social activities across the state.
EndoRISE is a groundbreaking, Connecticut state supported initiative to address Endometriosis, a highly invasive, under-diagnosed and under-researched disease. Whether a patient, researcher, provider, or simply interested in learning more, we welcome you to join us in the effort to impact the lives of the over 200 million people suffering from this disease.
JOIN OUR BOOK CLUB
This Facebook group is for all Endometriosis warriors who want a positive place to share their favorite books or podcasts. Each month or two we will vote on a book to read related to endo, chronic illness, mental health, motivation, etc. We will share our ideas through discussion posts and virtual reading parties.
If you're interested in supporting CT Endometriosis awareness and events, consider donating or buying us a coffee. Your contribution will make a big difference in helping us raise awareness and provide support for those affected by this condition. Thank you so much!