I am 35 years old and I was diagnosed with lipoedema last year and have been struggling to come to terms with it. I always knew there was something going on with my legs but no doctor ever diagnosed me with this,until last year, when I was referred to professor Mortimer's clinic.
Initially I was told I have Lipedema and a lymphoscintiography was performed last year in August 2015. I was given compression garments and asked to do water exercises etc. I received my report for lymphoscintiography last month, it says I have lymphlipoedema.
I read an article last month about WAL and how it has improved life for lipoedema patients and I am keen to go that way. It is an expensive procedure though so I am raising money that will help me with this. Thanks for your support.