The dust on the shoes.
I just pass a finger on the hard leather. I should put the cream on to soften it.
Read 0
22 March 2019
ProQR Doses First Patient in Phase 1/2 STELLAR Trial of QR-421a for Usher Syndrome Type 2
Original text here
LEIDEN, Netherlands and CAMBRIDGE, Mass., March 11, 2019 (GLOBE NEWSWIRE) — ProQR Therapeutics N.V. (Nasdaq:PRQR), a company dedicated to changing lives through the creation of transformative RNA medicines for the treatment of severe genetic rare diseases, today announced the first patient dosed in the Phase 1/2 STELLAR clinical trial for QR-421a in patients with Usher syndrome type 2 or non-syndromic retinitis pigmentosa (RP).
Read 17 February 2019
Assistance for the disabled: the first or last moment of a trip
(transalted from Italian by Sophia Boccard)
I just got back from an incredible solo trip to Thailand. I have not traveled alone since my trip to Peru in 2016.
Read 25 January 2019
Will my children have Usher Syndrome?
This text is taken from Usher Syndrome Coalition website, where you can find more information about genetics for Usher syndrome
Children receive one copy of each chromosome from their mother (shown in green) and one copy from their father (shown in blue).
Read How accessible are the cities and the places we live in? How could accessibility be improved? How difficult or easy is to travel in a given destination?
With the #YellowTheWorld map we collect stories of user experiences, to share best practices and help others to choose their travel destinations. Navigate the map, read other user experiences and tell us your story.
We care about you, we care about moving easily and safely. We want to #YellowTheWorld.
Read & Contribute
Here is a collection of videos that explain how a person with low vision sees.
It is ofteh nard to explain to other people how you see, but surely these videos are helpful to understand Retinitis PIgmentosa, Stargardt or Macular Degeneration.
The association La Girobussola, born in Bologna in october 2013, promote mobility of people with visual disability, intended as an opportunity to live a complete experience of travel, meeting, dialogue and exchange with a community, outside of the mainstream tourist networks and organized “all inclusive” tours.
The vEyes project was born on June 20th, 2012 in order to initially create an open hardware / software platform, on which to integrate “building blocks”, that are solutions based on wearable technologies that can support people with visual impairment in daily actions (reading a text on paper, moving about avoiding obstacles, accessing drug information leaflets or label information on food products, integrating and making accessible biomedical devices such as glucometers or sphygmomanometers, etc.).
The aim of Artemisia is to create a network of Italian parents with disabled children, so that they can support each other and share personal experiences and useful information.
Every drop counts!
Your donation will help NoisyVision to grow bigger and develop more projects. We are all working as volunteers and we need your help. We have a lot of great ideas and we need also money to make some dreams come true.
Your donation will support our current and future projects. Here some of the areas where we are constantly needing funding:
Donate now!
And you can support us also purchasing something in our shop - who said that a good cause can not look great?
Shop now!
