I just want to rest, wrote the 20-year-old as she lay in her hospital bed last week, adding updates to her popular blog, Just Call Me Coco... After more than two years and 1,000 pages, those would be her final words.
They were a far cry from the excitable, upbeat demeanour of her previous posts, in which she would bravely describe her condition, hopes and fears and frequent treatment – as well as answer questions about her personal life from her army of inquisitive blog followers.
In a YouTube video, titled Living with Cystic Fibrosis, uploaded in 2010, Emma described her symptoms, life-expectancy and relationships with friends.
"I think it's pretty safe to say I'm deteriorating pretty rapidly," she said in response to questions about her health. "Probably more than most.
"Hopefully, I'll exceed doctors' expectations of five years, though.
"It's not long."
It was one of thousands of posts about her condition – one of the more "depressing ones," as she described it.
But Emma continued to raise awareness of cystic fibrosis, which affects more than 10,000 people in the UK.
She had publicly battled her affliction through her blog, YouTube and Twitter for years, but also campaigned for the Cystic Fibrosis Trust and the Organ Donor Register, which she did not get the chance to join.
Her prolific blogging included scores of photographs in hospital and receiving treatment, but also included her thoughts on her hobbies and interests.
Posts about fashion, make-up and music would break up her honest accounts of living with a debilitating condition.
Emma, from Desford, died at Glenfield Hospital on Monday, surrounded by her family. She had typed her final blog post days before, at 1.17pm on July 4.
"You know the things you think you'll think about when you're threatened with the prospect of death? Yeah, well I'm not thinking about them," she wrote.
"Like what my last meal would ideally be, or who would be here when I finally died (other than my parents), or what I'd hoped to achieve by said day, what I wish I'd done or said, etc.
"I've been trying to think about my best life moments but it's not flashing before my eyes. Weird experience. Really weird.
"I just want to rest."
The former Bosworth Academy student had battled with the disease, which affects the lungs, since she was a small child and knew it was unlikely she would live past 25.
The heartbreaking final words on her blog reflect the bravery and acceptance she had shown since she began documenting her battle with the condition, in August 2010.
Scores of people who followed her blog and YouTube channel left messages of disbelief and shock at the sad news.
Commenting on her YouTube site, Georginiou wrote: "Emma, RIP. In one of the lowest parts of my life you showed life is worth it. I took comfort in knowing someone like you existed in this world.
"To be aware of something so beautiful gave me hope. I will not forget you and you changed me forever. I am better for knowing of you.
"Wherever you are, there will be a place in my heart for you."
Another Tumblr friend commented: "One of the people I followed died today. Emma suffered from cystic fibrosis and was a lovely girl.
"She has sent me messages before, telling me not to give up and I'm so sad she is gone."
Staff at Bosworth Academy also paid tribute to the former pupil. Assistant principal Nick Palmer said: "She approached everything with enthusiasm and with a sense of humour, never once allowing herself to miss out or be disadvantaged in any way.
"It is impossible to remember a time she was not smiling or laughing. She never gave up on anything or anyone.
"She was a fantastic role model for young people, who simply refused to be defined by her disability."
Tutor Ursula Manning said: "Emma was a bubbly and bright student whose enthusiasm and determination to succeed made her a natural leader. She was liked and respected by the staff and students and we shall all miss her terribly."
Russell Baker, head of science at the school, said: "Everyone at Bosworth Academy who had the pleasure of knowing Emma is devastated to hear of her tragic death.
"We remember her with great fondness and affection, not only as an extremely conscientious, creative and popular student, but also as someone who was always positive, happy and cheerful despite having to cope with damaging effects of her cystic fibrosis."
Cystic fibrosis affects mostly the lungs and digestive system, clogging them with sticky mucus and making it hard to breathe and digest food.
Cystic Fibrosis Trust spokeswoman Louise Banks said: "Emma was willing to put herself forward to help us raise awareness of both cystic fibrosis and the need to increase the number of lungs available to people with cystic fibrosis who reach transplant stage.
"We are so sad to hear that she has succumbed to the effects of cystic fibrosis. Emma was waiting to be put on to the transplant waiting list." See Emma's site JUST CALL ME COCOJust Call Me Coco... A selection from Emma's blog over the past few weeks JUNE 30, 9.11pm If you live in the UK, text CFWK13, followed by £2, £5 or £10 to 70070, to make a donation to the Cystic Fibrosis Trust, aiding research into a cure, preventative medication, family aid and awareness across the country. A nice way to end the CF Awareness Week I reckon! JULY 1, 8.30am Just woken up and coughed out what can only be described as a toad. Never seen anything like it in my life. These meds are playing havoc with my insides. One minute I feel great and full of air and energy… Next minute, I'm full of roid rage and choking on amphibian shaped/coloured mucous. Oozing sex appeal as ever… JULY 2, 11.49am @Coco is a nickname given to me by about three people and it was simply because of two things, depending on who said it. Either a) the colour of my hair or b) the fact that I used to always wear coco mademoiselle. That's literally it. Not exciting at all. x July 3, 12.59am My note for the day: It's all got very serious and scary in camp CF, for me at least. Had some conversations about assisted breathing, ventilation and other big scary things. Had bizarre fits of breathing and passed out and all sorts. It's been bizarre to say the least. All you really need to know about my day, though, the weirdest part, is that… I've been catheterised. Yep. Lol. July 3, 7.25am High flow oxygen – aka the noisiest piece of kit ever. July 3, 3.19pm Looking particularly fetching with an ice pack on my 'ead. July 4, 4.16am I've started to have the moments where I'd be okay if it all just stopped. I don't want to be in this pain any more. It's gotten way beyond control. I wouldn't go as far as "euthanise me", but I'm creeping ever closer to DNR (do not resuscitate). July 4, 4.21am I'm half expecting a message like "I've been worse than you and I was fine''. You might've been. Docs just told me I might be nearing the end yesterday though, so I'd say I'm allowed to be terrified. JULY 4, 4.21am It's all very sudden. Everything is. July 4, 1.17pm You know the things you think you'll think about when you're threatened with the prospect of death? Well I'm not thinking about them. Like what my last meal would ideally be or who would be here when I finally died (other than my parents), or what I'd hoped to achieve by said day, what I wish I'd done or said. I've been trying to think about my best life moments but it's not flashing before my eyes. Weird experience. I just want to rest.
For more information about the charity, visit:
www.cysticfibrosis.org.uk
To register for organ donation, visit: www.organdonation.nhs.uk