Furzeacre579, thank you for your questions. I agree that you are right to be concerned about your granddaughter. Sadly, because lipoedema affects almost exclusively women (although a very few men do have it), it has been something of a Cindarella condition as far as the medical profession is concerned - even today not that many gps know about it and are often very sceptical about it. Nurses are often much more helpful. It is a condition that affects between 5-10% of women and has been known about since the end of the second world war yet, until recently, hardly any research into it and most of the research that has been done has been funded by Facebook lipoedema groups. Can you imagine a condition that affected between 5-10% of men being so unknown and unresearched over the best part of a century? It is a hormonal condition that is generally hereditary and gets worse with each hormonal change. It typically first appears in puberty and starts with the "treetrunk" thighs. The earlier it is diagnosed, the better the chances of intervention taking effect. I didn't even know about it until 2014 when I read an article about it in the newspaper and the light bulb switched on in my head. By this stage, l had been through puberty, four pregnancies (one was a miscarriage) and had just had menopause. Because of this, I had developed lipoedema almost everywhere it was possible to get it. My legs are affected all the way down but, for me, the areas l dislike most are my saddlebag hips, large bottom and abdomen. I am around size 14-16 and many affected ladies are far larger. Far too many doctors dismiss lipoedema as obesity - it is a common co-morbidity of lipoedema - and tell you to eat less and move more. If only it were that simple! Please, please carry on trying to get your daughter to see the problem. You could always join one of the lipoedema groups on Facebook for some ideas, too.