This personal journey is the one I am most nervous to share, but I feel it is the most important. If I can support one person who is going through similar symptoms to not feel alone, and help advocate to encourage one person to receive an earlier diagnosis, then this is all worth it. Here is my Lichen Sclerosus journey.
The symptoms and impacts of Endometriosis are different with each individual who has it. Each journey is valid. In this blog post I share my story with this disease and the 15 years it took for a diagnosis. Even though I have been living with Endo for two decades, I still struggle to find the right words to articulate my experience with this elusive disease. I hope my story can provide support and encouragement to anyone who needs it. 💛
“Support and encouragement to reclaim our lives” What a bold statement. But what does it even mean? Why is this even needed?
In today’s new blog post, I break down EndoColumn’s mission statement. Let me know your thoughts 💛