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Living with endometriosis can feel incredibly isolating. The pain is invisible, the journey is long, and too often you’re left carrying questions that no one around you can answer. Podcasts have become a lifeline in the endo community, a way to feel less alone, more informed and validated while lying on the couch during a… Continue reading My Top 5 Podcasts for Endometriosis: Voices That Truly Get It

Endometriosis isn’t just a physical condition it affects your mental health, your relationships, your identity and how confident you feel navigating the healthcare system which I am all to aware of. These books each offer something a little different: practical tools, emotional validation, science-based insight, and a sense of being understood. You can find them… Continue reading My Top 5 Endometriosis Books Worth Reading

There is a particular kind of hurt that comes from being in invisible pelvic pain like endometriosis, adenomyosis, pudendal neuralgia, myofascial pelvic pain syndrome and other chronic illness - unforeseen by the human eye but felt deeply and then being made to feel like that pain is an exaggeration. Not because someone outright says, “you’re… Continue reading When Invisible Chronic Pelvic Pain Is Real But You’re Treated Like You’re Being Dramatic 

There is a particular kind of guilt that comes with living in a body that is in chronic pelvic pain and it feels even heavier when you are a mother, creative/artist selling products to make money and studying a diploma in councilling to eventually work in the field of woman’s mental health. Which is important… Continue reading The Guilt of Being a Mother, Artist, Blogger and Studying Living With Chronic Pelvic Pain

Life is loud. Not just the noise you hear, but the constant pull on your attention. The needs. The notifications. The expectations. The silent pressure to keep going even when you’re running on empty. Somewhere in the middle of the chaos, many of us stop paying attention to the one person who is always there.… Continue reading Attention to Being in the Moment: Do You Pay Attention to Yourself in the Chaos of Life and Motherhood.

With increasing painful symptom’s of tethered endometriosis of the bladder and bowel, chronic inflammation, pudendal neuralgia nerve involvement and myofascial trigger points and being misunderstood become apart of my life it gets very real. This happens with multiple diagnosis’s pelvically. So let’s talk about it! There is a particular kind of unwanted suffering that comes… Continue reading Living with Endometriosis and Pudendal Neuralgia – the Cross over of symptoms.

Fatigue has been one of the hardest parts of living with chronic pelvic pain, not because it’s the most visible part of chronic pelvic pain, but because it’s the least understood part of having endometriosis, pudendal neuralgia and myofascial pelvic pain. When you live with endometriosis and pudendal neuralgia any pelvic condition, exhaustion isn’t just… Continue reading Fatigue, Pelvic Pain, and the Quiet Way My Body Shuts Down

Don’t let a bad doctor make you feel like your to blame for your chronic pelvic pain I’ve gone back and forth for a long time about whether to write this.  Because speaking honestly about medical harm from a doctor often comes with consequences of disbelief people find it hard to understand that someone medically… Continue reading Leaving A Toxic Doctor – This Is What Happened, And This Is What I Carry Forward

This week I received MRI results that confirmed something I’ve been quietly bracing myself for: my endometriosis has returned and this time, it’s affecting both my bladder and bowel. The scan showed a lesion on the dome of my bladder, attached by an adhesion, and evidence of endometriosis or adhesions involving the sigmoid colon. Anyone… Continue reading My MRI Revealed Reoccurring Endometriosis: Navigating Bladder and Bowel Involvement and the Road to Specialist Care