24/10/2026
If you're living with lipoedema, or you've started to wonder whether it might be what's going on for you, this one is for you.
It can feel isolating to live with a condition so many people don't fully understand. I've supported women with lipoedema for over five years, and I see again and again how much it helps to feel understood, and to have a plan that fits your body rather than a generic one.
In my latest blog post I look at where genetic testing fits for lipoedema. It can't diagnose lipoedema, and it doesn't give one single answer, but it can give us more information about how your body may handle inflammation, hormones and nutrients, so we can personalise your plan. I also cover where nutrition sits alongside the medical and physical care you need.
If this resonates with you, you can read it here: https://carriereedy.com/blog-posts/f/lipoedema-and-your-genes-a-perfect-storm
And if you'd like to talk through your own situation, my free, no obligation chat is always open.
General information only. Lipoedema should be diagnosed and managed with your doctor or a qualified specialist.