Lipoedema
"The Disease They Call FAT"
Welcome to the Lipoedema information page.
My name is Gayle Clearwater, I was diagnosed with lipoedema in 2020. It has been a rollercoaster of discoveries, emotions, and plenty of fat shaming! I created this page so women like me can have an information hub to educate, empower, and inform themselves on where to seek support, help, diagnoses, and what helps to improve their quality of life.

**Disclaimer** The information and resources provided on this page are based on my personal research, experiences, and recommendations from various websites and sources. I am not a medical professional, and the content shared here should not be considered medical advice or a substitute for professional diagnosis, treatment, or guidance. While I strive to present accurate and unbiased information, some of the places or resources I recommend may reflect my own personal experiences and opinions. It is essential to consult with a qualified medical professional or healthcare provider for advice tailored to your specific condition and needs, particularly regarding lipoedema or any related medical concerns. By using this page, you acknowledge and agree to the following: - The information provided is for informational and educational purposes only and is not intended to diagnose, treat, cure, or prevent any disease. - Any reliance you place on the information provided is strictly at your own risk. I am not liable for any errors, omissions, or outcomes resulting from the use of this information. - Links to third-party websites are provided for convenience only, and I do not endorse or take responsibility for the content, accuracy, or practices of these external sites. Always verify information independently and consult professionals as needed. - Personal experiences and opinions shared on this site are subjective and may not apply universally. Results may vary depending on individual circumstances. I strongly encourage you to seek advice from licensed professionals for medical, legal, financial, or other specialized concerns. Your health and well-being are your responsibility, and any decisions made based on information from this page are at your sole discretion. This disclaimer is subject to change without notice and should be reviewed periodically for updates.
The Stages of Lipoedema
This information outlines the stages of Lipoedema, a chronic condition characterized by the abnormal accumulation of subcutaneous fat, primarily in the legs and sometimes arms, sparing the hands and feet. Here's a summary of each stage:
Stage 1
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Skin Surface: Smooth, but with enlarging subcutaneous fat tissue.
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Swelling: Intermittent, influenced by factors such as nutrition and weather.
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Additional Signs: Ankle "cuffs" (bands of fat around the ankles).
Stage 2
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Skin Surface: Uneven with visible indentations and dimpling.
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Nodules: Formation of small, bean-like nodules in the subcutaneous fat tissue.
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Tenderness: Increasing discomfort or pain.
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Additional Signs: Ankle cuffs may still be present.
Stage 3 (Moderate)
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Skin Surface: Increased indentations and deformations due to fat overgrowth.
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Fat Accumulation: Large masses of skin and fat form folds, especially around hips, thighs, and knees.
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Swelling: Persistent, with potential development of lymphedema, leading to tissue thickening and a honeycomb appearance.
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Pain: Noticeably worsens, along with reduced mobility.
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Additional Signs: Ankle cuffs are prominent.
Stage 4 (Severe)
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Complications: Significant lymphatic system compromise leading to LipoLymphedema.
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Fat and Skin Lobules: Debilitating lobules, especially on medial thighs and knees, severely restrict mobility.
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Swelling: Persistent and profuse.
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Pain: Intensified, with profound immobility challenges.
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Additional Signs: Severe ankle cuffs.
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("What is Lipedema?," 2024)
