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Creating impactful change for the endometriosis community
Living with endometriosis and previously having worked with chronic pain patients as an Allied health professions our founder is driven by the current lack of knowledge within both society and medicine, resulting in not only a delayed diagnosis and/or misdiagnoses of endometriosis, but the negative impact on the well-being and the quality of life that people with endometriosis endure due to, a lack of medical research, limited clinical knowledge, and societal bias regarding; invisible illnesses, women’s health & wellbeing, and menstrual health.
About Endometriosis
What is Endometriosis
Endometriosis is a medical condition in which tissue similar to the lining of the uterus (endometrium) is found elsewhere in the body. These cells can grow on the surface or infiltrate deep inside organs, nerves, muscles, ligaments etc. Endometriosis has been found on every single organ in the body (including the brain, heart, lungs etc), and can bind organs together. Endometriosis has been listed as one of the top 10 most painful medical conditions. Despite this there is no cure for endometriosis, only management strategies and surgery to reduce / limit the effects of endometriosis.
Effects & Complications of Endometriosis
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​Loss of organs
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Stoma
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Urostomy
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Chronic pain
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Fatigue
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Medical trauma
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Nerve damage
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Nausea / sickness
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Shortness of breath
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Chest pain / tightness
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Infertility
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Ovarian cysts (which can {& do} explode)
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Bloating (Endo belly)
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Burning up
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Frozen pelvis
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Fused organs
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Misdiagnosis
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Medical anxiety
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UTIs
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Depression / low mood
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Blood in stools
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Heavy bleeding
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Painful sex
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Bleeding during / after sex
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Painful ovulation & mensuration
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Pain opening bowels
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Migraines
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Black outs
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Sciatica / nerve pain
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Acute flare up of pain
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Adhesions
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Pneumothorax
Misconceptions of Endometriosis
Endometriosis has many misconceptions both within the medical profession and society which not only delays vital treatment, but can result in outdated and / or inappropriate medical treatment and advice, further prolonging the suffering of those with endometriosis. The main misconceptions are:
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Endometriosis is just a painful period that can cause infertility.
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Endometriosis only affects menstruating women.
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The pill, coil, or pregnancy will reduce / slow down / reverse /stop the growth of endometriosis.
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A Hysterectomy or menopause will cure endometriosis.
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Endometriosis is only found in the womb & ovaries (reproductive organs).
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It is too rare for endometriosis to be found outside of the pelvic cavity.
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Endometriosis only effects women in their 30s who have not had children.
It is vital that these misconceptions are abolished, and that everyone has a factual baseline knowledge of endometriosis.
Lets stop the silence together!
Our collaborative art and literature project, has given a voice to the 1-in-10 people living with endometriosis, in which 170+ people shared their lived experiences with endometriosis through art and literature pieces with the aim of:
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Raising awareness for both symptoms & the lived experiences of endometriosis.
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Debunk misconceptions.
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Highlighting the urgent need for updated medical research and upskilling of medical professionals.
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Reducing the ‘average’ diagnosis period down from 8 years (for many this can be 20-30 years until diagnosis).
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Create a safe space for people with endometriosis to be heard, seen, and validated.
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Creating impactful changes for the next generation.
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Increase knowledge and provide education to change societal bias regarding, invisible illnesses, women’s health & wellbeing, and menstrual health.
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Increase empathy for the endometriosis community and have an awareness on the impact of sufferers’ families, careers, friendships, physical and mental well-being, futures etc.
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