We get this question a lot. It’s a question that no statistic, no graphic and no medical documentation can answer. What is it like to live with Endometriosis? It hit me the day before my 4th surgery… my life often feels as though it revolves around surgery, pills and doctors. And, unfortunately, this probably isn’t … Continue reading
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Turn it Yellow for Endo Awareness
It’s March and we’re back… bringing you more posts than ever this year! Your support is most appreciated!! October is typically known for Breast Cancer Awareness and pink is found everywhere. Well, this month we are dedicated to turning social media and everything yellow to raise awareness for Endometriosis. So what can you do to … Continue reading
Guest Post – Suffering Through Misdiagnosis
Guest Post by Rose Thomas – I connected with Rose over email and it has truly been a blessing to read her story. I can actually relate to Rose’s suffering through Endometriosis and being misdiagnosed. Read as she shares her story of pain, loss and hope! — Have you ever wondered “why me?” Over the … Continue reading
Raising Awareness for Endometriosis
This week is National Endometriosis Awareness Week. I have a strong desire to help other women that are undiagnosed or recently diagnosed find the right help and answers. Let’s start with some facts and stats first: 1 in 10 women have Endometriosis (also known as Endo) Endo cannot be OFFICIALLY diagnosed without surgery. A doctor … Continue reading
How to Process Endometriosis
Your life changes when you receive a medical diagnosis. Since everyone processes things differently, here is what I’ve learned over the last 15 years of dealing with chronic pain and finally finding the answers. 3 weeks prior to marrying my best friend, I opted to have exploratory surgery. The result was Endometriosis (read more here). … Continue reading
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