Lymphedema Patient Day at Orthopedie Meyrignac, Paris.

The more I get involved with the lymphedema world; whether it’s meeting other patients, doctors or specialists; I am always amazed by the level of pure passion and dedication everyone has to improve the lives of people who live with the condition.

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Girl Under Pressure: Chronically Motivated For Change

I am extremely conscious of how my LE journey affects others who live with the same condition. I am not ‘The Face of Lymphedema’. I am literally one face in the millions of people who live with this condition around the globe. My story, feelings, challenges, successes and perspective will not represent yours. It’s impossible to…

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New night garment- Jobst Relax.

Wearing a compression stocking 24/7 is generally the pits. Anyone with Lymphedema can vouch for that. Day compression is different to night compression, which can present various issues for those of us still trying to figure this whole darn lympie life shizzle out. For me, night time compression has been a real pain in the butt. Sometimes…

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