05/06/2026
You may be aware that June is Lipoedema Awareness Month, and as a sufferer of this condition, I hope you will forgive my self-indulgence when it comes to posting over the coming weeks, about the struggles, symptoms and support available for those diagnosed or those questioning whether they should visit the GP for a diagnosis.
I fully understand the obstacles - both in terms of physical and mental health - that this condition poses, and I am thankful that with the spotlight on lipoedema, understanding and recognition increases annually.
If you would like to visit your GP and are concerned that they may not be entirely aware of the condition, please click the following link, where you can print off a letter to take along to the appointment with you: https://www.talklipoedema.org/diagnosis
If you are looking for support with your mental health, your physical pain, or would like to make an appointment for lymphatic drainage, please visit our website, where you will find a list of practitioners who are here to assist you. www.kbtherapyclinic.com
Whilst there is currently no cure for this condition, there are treatments, organisations, and community forums, that make you feel less alone in your battle.
What is Lipoedema and what are the symptoms?
Lipoedema is a chronic connective tissue disorder that causes painful, abnormal fat buildup, most commonly in the legs, thighs, buttocks, and arms.
🚫 It’s not the same as obesity and not caused by overeating or inactivity.
📍 Key Symptoms
✔️ Disproportionate lower body size
✔️ Pain, heaviness, and tenderness
✔️ Easy bruising
✔️ Fat that doesn’t respond to diet/exercise
✔️ Swelling that worsens throughout the day
🖐️ Hands and feet are usually not affected
It’s important to note that not everyone with lipoedema suffers from every symptom. People can experience lipoedema in other areas of the body too, like the arms or abdomen.
For more information on lipoedema, head to our website: www.talklipoedema.org
