steveevans35.blogspot.com
Steve Evans Blog: Regaining a little independence
http://steveevans35.blogspot.com/2015/06/regaining-little-independence.html
Tuesday, 2 June 2015. Regaining a little independence. The system comprises a mechanical hand which is moved by tiny servos. This was manufactured by Patrick using his 3D printer. Then there's a processing unit, again constructed and programmed by Patrick. The system connects to the eyegaze computer by USB. Finally a screen grid was made to allow eye selection. The system is still in its early stages of development but early tests are promising. The next video was made in the seafront carpark at my flat.
steveevans35.blogspot.com
Steve Evans Blog: We Are Not Alone
http://steveevans35.blogspot.com/2015/04/we-are-not-alone.html
Monday, 6 April 2015. We Are Not Alone. Filming My Father In Life And Death. Click to watch on demand until March 2016. I know from other MND sufferers, the Isaac's and our experience isn't universal but I suspect it's representative of many families dealing with this disease. I am so grateful for your honesty - thank you does not begin to cover it but I dont know what else to say. Thank you. 12 April 2015 at 00:18. Subscribe to: Post Comments (Atom). For those of you who really want to, you can check ou...
steveevans35.blogspot.com
Steve Evans Blog: November 2014
http://steveevans35.blogspot.com/2014_11_01_archive.html
Sunday, 16 November 2014. Perseverance, patience and acceptance” – PatientsLikeMe member Steve shares what it’s like to live with MND. Posted November 14th, 2014. Looking back over the last 7 years since your diagnosis with ALS/MND, is there anything you’d like to have known sooner that has helped you along your journey? You’ve documented your experiences in your film “My Motor Neuron Disease Made Easier” – can you share a little about your inspiration for the project? Eyegaze is undeniably an incredible...
steveevans35.blogspot.com
Steve Evans Blog: August 2014
http://steveevans35.blogspot.com/2014_08_01_archive.html
Tuesday, 26 August 2014. Enduring Motor Neurone Disease. Monday, 25 August 2014. Daniel's and Tracy's ice bucket challenge. Thursday, 21 August 2014. Finally I was determined to make a 60 second version, with the view to getting it on TV as an ad campaign to raise awareness and funds. BUT the minimum cost of airtime for a realistic ad campaign is £25k. So if anyone knows of any organisations who could contribute a few grand, let me know. Wednesday, 6 August 2014. Jake Nailing Muse Again.
steveevans35.blogspot.com
Steve Evans Blog: April 2014
http://steveevans35.blogspot.com/2014_04_01_archive.html
Thursday, 3 April 2014. Just like old times. Almost. So yesterday I decided to return. We drove to Hampton Court station where there are very conveniently placed disabled parking spaces, hopped on a train with the help of the train's guard and was at Waterloo 35 minutes later. We only spent about an hour looking around, not wanting to push our luck. It was nice having made it there again albeit not under my own steam anymore. As always I can't help feeling many of the exhibits fall into "The Empo...After...
steveevans35.blogspot.com
Steve Evans Blog: Enduring Motor Neurone Disease
http://steveevans35.blogspot.com/2014/08/enduring-motor-neurone-disease.html
Tuesday, 26 August 2014. Enduring Motor Neurone Disease. Wow, thats stunned us. Good luck with the campaign. Anna P. 4 September 2014 at 23:55. A very moving video indeed. very moving. I hope youre doing OK at the moment. All the best, Adrian. Ember Gdns. 6 September 2014 at 08:09. Subscribe to: Post Comments (Atom). For those of you who really want to, you can check out my "status" on my web link. Finally, PLEASE leave comments, even if brief as its the only way I know its being read!
steveevans35.blogspot.com
Steve Evans Blog: Quick update
http://steveevans35.blogspot.com/2015/03/quick-update.html
Sunday, 29 March 2015. Subscribe to: Post Comments (Atom). For those of you who really want to, you can check out my "status" on my web link. Finally, PLEASE leave comments, even if brief as its the only way I know its being read! View my complete profile. Pauline's life with MND.
steveevans35.blogspot.com
Steve Evans Blog: December 2014
http://steveevans35.blogspot.com/2014_12_01_archive.html
Wednesday, 10 December 2014. Subscribe to: Posts (Atom). For those of you who really want to, you can check out my "status" on my web link. Finally, PLEASE leave comments, even if brief as its the only way I know its being read! View my complete profile. Pauline's life with MND.
steveevans35.blogspot.com
Steve Evans Blog: June 2015
http://steveevans35.blogspot.com/2015_06_01_archive.html
Tuesday, 2 June 2015. Regaining a little independence. The system comprises a mechanical hand which is moved by tiny servos. This was manufactured by Patrick using his 3D printer. Then there's a processing unit, again constructed and programmed by Patrick. The system connects to the eyegaze computer by USB. Finally a screen grid was made to allow eye selection. The system is still in its early stages of development but early tests are promising. The next video was made in the seafront carpark at my flat.
steveevans35.blogspot.com
Steve Evans Blog: September 2014
http://steveevans35.blogspot.com/2014_09_01_archive.html
Thursday, 11 September 2014. The last event of the summer was Wheels and Wings at Dunsfold Aerodrome. Tracy had advised them of my situation and they offered complementary VIP parking and access to the covered veterans enclosure if it was raining. Totally opposite experience to Farnborough. The highlight of the show was the two remaining airworthy Lancaster bombers flying together. Although when the Vulcan is flying it always steals the show. Subscribe to: Posts (Atom). View my complete profile.
SOCIAL ENGAGEMENT