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.
Merchandise - Lipoedema
Supporting Lipoedema Awareness
All profits from merchandise purchased through my website are dedicated to raising awareness about Lipoedema. Your support helps cover the costs of printed flyers, informational cards, and exhibition expenses, enabling us to share valuable resources and stories with a broader audience. Together, we can make a difference in bringing visibility to this often-overlooked condition.

Who Ate All the Pies Series
This series of designs came from a very raw and personal place. During an appointment with an anesthetist, I was told I needed to lose weight and consider weight-loss surgery. I explained, “I eat healthy, exercise, and I don’t sit down and eat pies all day!” His response? “Well, clearly you must be eating more than you should. At least you carry it in your legs and not around your stomach.”
I left that appointment in tears.
Looking back now, I know I was in the early stages of lipoedema. No medical professional fat-shames me anymore, and I use my experiences to raise awareness and empower others.