Top Posts & Pages
- Wristbands
- New genetic discoveries tell us more about what causes MND – Part 2 — MND Research Blog
- ALS Ice Bucket Challenge
- The Real ALS Challenge
- Motor Neurone Disease Wristbands / MND Wristbands
- ALS Ice Bucket Challenge
- Helen Carter's Story
- World record bid charity match in memory of Karen
- Asbestos Awareness Week
- MND Wristbands - Another grateful buyer
-
Recent Posts
Email
Any Questions or Queries drop me an email at ly1405@my.bristol.ac.ukRaising Awareness of Motor Neurone Disease
Twitter Updates
Tweets by lyellmnd-
Join 13 other subscribers
Blog Stats
- 15,505 hits
Archives
- July 2016
- August 2014
- June 2014
- March 2014
- February 2014
- January 2014
- November 2013
- October 2013
- September 2013
- August 2013
- June 2013
- May 2013
- April 2013
- March 2013
- February 2013
- January 2013
- December 2012
- November 2012
- October 2012
- September 2012
- August 2012
- July 2012
- June 2012
- May 2012
- April 2012
- March 2012
- February 2012
Search
Monthly Archives: April 2012
Eye Gaze
This Video was done to gain awareness for MND (Motor Neurone Disease) and to promote ‘Eye Gaze’ to show people suffering with the disease that they can still be productive at their worst. Eye Gaze is a way for people … Continue reading
Posted in Uncategorized
Leave a comment
31 Ways in 31 Days
Remember, ALS and MND are the same disease, the terms are used interchangeably but usually ALS in America and MND in the UK. May = ALS Awareness month in the US June = MND Awareness month in the UK
An ALS Love Story
The Trailer to the ALS Love Story, very powerful and insightful. ‘There’s nothing that will take the wind out of your lungs quite like somebody telling you that one day your best friend will die, in one of the worst possible ways … Continue reading
Posted in Uncategorized
Leave a comment
The truth behind the Secret Disease
Inspiring Documentary on the truth about ALS “One of the most powerful pieces of film I have ever seen! What a thoroughly awesome, incredible group of people. While I did not know Tim in some ways I feel- through the … Continue reading
Posted in Uncategorized
Leave a comment
How Was I to Know?
A poem written by Natalie Fognani, a woman diagnosed with ALS 5 years ago was turned into a song by Lucas Hoge and Corey Barker. Natalie’s last wish was to have her poem put to music and Country Artist Lucas … Continue reading
Posted in Uncategorized
Leave a comment
Another Turning Point a Fork Stuck in the Road
ALS UNDERGROUND “I AM A CAREGIVER FOR MY HUSBAND WHO HAS THE “NO CURE” DISEASE ALS, MND AKA LOU GEHRIG’S DISEASE. I AM NOT A NURSE OR MEDICALLY EDUCATED, I HAVE BEEN THROWN INTO THIS ROLE BECAUSE OF ALS & … Continue reading
Posted in Uncategorized
Leave a comment
If you’re on Twitter follow these four to keep up to date with the latest news on MND/ALS/LouGehrigs @laurayell @liampdwyer @MNDAssoc @mndresearch Thank you
Posted in Uncategorized
Leave a comment
Emma Berry Goodman, Aged 17, died of Motor Neurone Disease
The family and friends of Emma Berry Goodman were devastated when she became the youngest person in Britain to die of the deadly degenerative condition Motor Neurone Disease. As the first anniversary of the 17-year-old’s tragic death approaches, a charity … Continue reading
Posted in Uncategorized
Leave a comment
ALS motor neurons made easy?
For more than 150 years, ALS has been recognized by experts as a motor neuron disease. But scientists still remain unsure why these cells are especially vulnerable to destruction in people with ALS or why they ultimately fail during the course of … Continue reading
Posted in Uncategorized
Leave a comment
In Memory of William Tyler
Rothley Park Golf Club raised a massive £19166.76 in aid of William Tyler a beloved Husband, Father and Friend, who was diagnosed with Motor Neurone Disease during his year as captain at the club. May he Rest In Peace
Posted in Uncategorized
Leave a comment