This Tribute is supporting Turner Syndrome Support Society. If you want to help please make a Donation or consider creating a Fundraising Event. We are asking for donations for the TSSS as Emma was diagnosed with Turners Syndrome when she was 13 years old but has had it her whole life. It occurs when a baby girl is born with one X chromosome instead of 2. TS can cause other complications such as heart problems, restriction of height and other things. There isn't much explanation in to why or how TS occurs, but by lots of research girls with TS are able to increase their height by taking daily injections of growth hormone and hormone replacement for estrogen via tablets.

Add an event or occasion to Emma's Tribute.

Light a candle for Emma and leave a message. You can choose from a variety of candles & colours. Your candle will appear in the candles gallery

Choose a virtual gift to add to Emma's gifts gallery. There are lots of different gifts to choose from and you can add a message to display with your gift.

Contribute to Emma's lifestory and add a memory or anecdote. You can also upload pictures, videos and music to accompany your story.

Send a thought to Emma's thoughts gallery

Add your pictures to the pictures gallery

Add your videos to the video gallery

Add music to the music gallery