Help and Advice

How Would It Be Seen?

September 11, 2026|Categories: Help and Advice|Tags: , , , , |

Christie's Endometriosis Story For everyone living with endometriosis, there is a private language of pain that the outside world almost never gets to read. It is a condition that can colour entire days, relationships, and futures, and yet leaves no outward mark on the body it lives in. This [...]

Every Body Deserves Care – World Sexual Health Day

September 4, 2026|Categories: Help and Advice, Blog|Tags: , , , |

Sexual health is not a topic many of us are taught to talk about openly, and for people living with endometriosis or adenomyosis, that silence can be even harder to break. Pain, fatigue, bloating and unpredictable symptoms can all affect intimacy, and yet conversations about sex and chronic illness [...]

When Summer Hits Harder: Endometriosis and Invisible Illness Comorbidities

August 12, 2026|Categories: Help and Advice|Tags: , , , , |

Understanding POTS, EDS, MCAS, and autoimmune conditions in the heat If you live with endometriosis, you may already know that it rarely travels alone. Alongside a diagnosis of endometriosis, often arriving after years of being dismissed or misdiagnosed, many people find themselves accumulating further diagnoses: POTS, EDS, MCAS, lupus, thyroid [...]

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