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‘A skeleton covered in skin’ - that’s how a mom described the daughter she lost to bulimia.

It had been seven years since she’d tasted solid food and she was determined to make the most of it.

BBC News Published image sourceSophie Robehmed Sophie Robehmed spent most of 2018 with chronic abdominal and lower back pain, symptoms she'd had before but never for more than a week or so. Then she was diagnosed with pelvic congestion syndrome - a condition no doctor had mentioned in the many years she'd been seeking medical help. It's Tuesday 14 August 2018 and I am sedated, lying on an operating table, while metal coils are being inserted into my ovarian and pelvic veins via a catheter in my neck. I have recently been diagnosed with pelvic congestion syndrome (PCS), or ovarian vein reflux ...

Loretta's flatmate amy is a photographer. together they;ve been posting loretta's recipes on instagram, where she is the nil by mouth foodie. loretta has quite a following, she's become a so—called influencer. for so long, i had no hope. so to now get to a point where life has become enjoyable and i'm actually looking forward to what's to come is, like, huge. the final part of every cooking session, amy does the taste test. i could just keep eating for hours. from the darkest despair, loretta is now successful as the chef

Of us it will be in the high teams to low 20s. creating and trying new recipes is important for any chef, but for the last six years loretta harmes hasn't been able to taste her food after being diagnosed with a genetic disorder which means she uses a feeding tube. despite this, she hasn't lost her passion for cooking and has a growing following on instagram, where she's known as the �*nil—by—mouth foodie'. breakfast�*s graham satchell has been to meet her. the kitchen is my happy place. it's like an outlet, like therapy for me. when you are so passionate about something, nothing reall...