Patient takes on the Speed luge for NMO…… what’s NMO?!
My name is Heidi and I was diagnosed with NMO around a year and a half ago so it’s a subject very close to my heart. However, I was surprised to hear that most people (even the GP’s) have never heard of this rare disease and so I often find myself telling them all about it.
As a result, my husband and myself would like to raise awareness of this rare disease and also raise some funds for the NMO Spectrum UK charity.
At the end of March 2015, we are taking on the challenge of an individual speed luge down the purpose built bob sleigh track in LaPlagne – but don’t worry, the site is fully accessible and lots of safety measures are carried out!
For more information about this total madness see http://www.justgiving.com/heidi-abraham.