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 Types of Lipoedema
The five types of lipoedema describe how the condition affects different body areas. Here's a detailed breakdown:
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Type I
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Affects primarily the buttocks.
Type II
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Involves the buttocks, hips, and thighs, extending up to the knees.
Type III
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Affects the buttocks, hips, thighs, and calves extending up to the ankles.
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Feet are spared, maintaining a clear distinction between affected and unaffected areas.
Type IV
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It involves the upper arms and usually accompanies Type III, meaning both the arms and lower body are affected.
Type V
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Focuses on the calves, specifically from the knees to the ankles.
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This classification helps identify the progression and distribution of lipedema, guiding tailored treatment approaches.
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("What is Lipedema?," 2024)
