Stuart Haygarth hangs his spectacle chandelier at The Lighthouse, Scotland's national Architecture Design Centre on November 29, 2007 in Glasgow, Scotland. The 7ft chandelier is made of over 1000 pairs of glasses, and is one of a range of products the designer has made out of recycled products. (Photo by Jeff J Mitchell/Getty Images)

India's Central Reserve Police Force personnel take part in a rehearsal for the Republic Day parade on a cold winter morning in New Delhi January 8, 2014. (Photo by Ahmad Masood/Reuters)

Cha Huilan, a 40-year old Lisu woman, and her daughter leave Lazimi village with a zipline across the Nu River in Nujiang Lisu Autonomous Prefecture in Yunnan province, China, March 24, 2018. Chinese mountain villagers, cut off from shops and churches by a raging river, use a zipline to cross its violent rapids and jagged rocks. (Photo by Aly Song/Reuters)

Keira Knightley attends the premiere for “A Dangerous Method” at The 55th BFI London Film Festival at The Odeon West End on October 24, 2011 in London, United Kingdom. (Photo by Dave Hogan/Getty Images)

Two Bunny Girls from the Playboy Club and two Penthouse Pets from the Penthouse Club prepare to take part in the annual Good Friday waiters and waitresses race in Battersea Festival Gardens, London, 28th March 1972. (Photo by Ian Showell/Keystone/Hulton Archive/Getty Images)

Eight-year-old handicapped Chinese girl Qian Hongyan crawls with two home-made props and part of a basketball at Zhuangxia Village on January 5, 2005 in Luliang County of Qujing City, Yunnan Province, China. The girl who lost both of her legs in a traffic accident in 2000 at the age of three, struggles to live her life with a basketball as an underprop, “walking” between school and home by herself. The girl's story is widely reported in the country, and experts from China Rehabilitation Research Center has come to Qian's home to help her for rehabilitative treatment early 2005. (Photo by China Photos/Getty Images)

Tessa Evans was born without nose, a very rare facial anomaly called 'arhinia'. The little girl, who is now 18-months-old, has helped in spreading awareness about her condition across the globe.