6 March 2016
The need to talk, to vent and … to laugh
Talking, talking, talking.
There is the need to talk.
There is the need to share the phases and the moments of this degenerative disease, so maybe it feels less heavy.
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3 March 2016
Geographical distribution of Usher Syndrome.
I have a passion for maps and globes. Maybe because I love to travel, or because they help me to dream of other possible lives.
Read 26 February 2016
The Gods like it Yellow. The story goes on.
Did yo hear about The Gods like it Yellow ?
We launched the event with this post
And here you can read the detailed description of the project
There are still three months to go, but we want to keep informed NoisyVision readers because this event is not only an adventure for the visually impaired .
Read 21 February 2016
#YellowTheWorld again above 5000 metres. Perù I am coming!
A year after the #YellowTheWorld expedition to the Everest Base Camp it is time for a new adventure.
Why? Where is it written that you have to go somewhere?
Read 12 February 2016
Blind date with a blind.
We met on the internet, through a series of contacts. Only after writing each other a few emails we found out we both lived in Berlin.
Read 10 February 2016
Help NoisyVision with 3 clicks
I regret having to write this post, but I have to try.
According to 2.0 strategies is wrong to ask “Likes” and shares, but when NoisyVision reached nearly 800 “Likes” Facebook has changed algorithm and now you have to pay to make sure that users see the posts.
Read 29 January 2016
NoisyVision.org is online!
Five years after the birth of NoisyVision it was time to modernize the site, to catch up with the times.
Read #YellowTheWorld is an awareness campaign initiated by NoisyVision, with the aim to promote the mobility of the visually impaired.
We want to spread awareness and understanding of low vision and problems related to eye disease, with particular attention to accessibility facilitation of mobility.
Read 5 December 2015
The Visionary Europe
Visual impairment is an invisible disability. It is hard to talk about it as it is a borderline disability. It is not common to have people from all over Europe to share their experiences and daily life problems.
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