View Xynamic Motorsport Photography Yearbook '14 by Gary Parravani / Jake Yorath / Neil CunninghamPreview
Preview

Xynamic Motorsport Photography Yearbook '14

In conjunction with Racing4MND

by Gary Parravani / Jake Yorath / Neil Cunningham

Hardcover, ImageWrap
Hardcover book with full-colour design printed directly on the casewrap
Quantity:
VAT will be added at checkout.
About the Book
Photobook consisting of artistic photography from the 2014 Motorsport Season.
Photos from British GT, Blancpain GT, European Le Mans series amongst others.
The book is produced in conjunction with Neil Cunningham's Charity - Racing4MND.
100% of the profit from this book go to the charity.
For more information on the charity go to the 'Author Website' link below.
Author website
http://racing4mnd.org/
Features & Details
  • Primary Category: Arts & Photography Books
  • Project Option: Standard Portrait, 8×10 in, 20×25 cm
    # of Pages: 50
  • Publish Date: Feb 16, 2015
  • Language English
  • Keywords british gt, motorsport, photography, ferrari, lamborghini, audi, bentley, mercedes, aston, martin, gt3, blancpain, elms, bss, bes, bgt, xynamic, charity, racing4mnd
See More
About the Creator
racing4mnd
Racing4MND

My name is Neil Cunningham and I was a professional racing driver for 27 years, and latterly a stunt driver for Top Gear Live. I also worked on the Bond movie Quantum of Solace. In 2010 I was diagnosed with Motor Neurone Disease. The Heaton-Ellis Trust in conjunction with Racing4MND aims to find a cure for Motor Neurone Disease. The Trust’s goal is to help raise awareness and funds to help the research programme headed by Professor Chris Shaw at the department of Clinical Neuroscience at King’s College Hospital, London. Since starting in 2009, the trust has reached its initial goal of £1million and Professor S haw’s team has made incredible advances. We now know the causes of two-thirds of familial-related cases, with most being identified since 2011. Our current goal aims to help ensure that by 2015 the cause of over 95% of familial MND will be known. Your support will help make this happen.

Continue reading