Published • loading... • Updated
The Struggle of Lourenço and His Mother for a Life with Fewer Obstacles
Summary by The Best Project Ever.
This story is only covered by news sources that have yet to be evaluated by the independent media monitoring agencies we use to assess the quality and reliability of news outlets on our platform. Learn more here.1 Articles
1 Articles
Lourenço Sousa is a 19-year-old native of Azambuja who was born with Pelizaeus-Merzbacher's disease, a rare and degenerative genetic pathology of the central nervous system. He does not speak, does not walk, does not eat alone and depends entirely on his mother. A solidarity campaign aims to raise funds to adapt the bathroom at home, to provide more security and comfort in the day-to-day life.
Coverage Details
Total News Sources1
Leaning Left0Leaning Right0Center0Last UpdatedBias DistributionNo sources with tracked biases.
Bias Distribution
- There is no tracked Bias information for the sources covering this story.
Factuality
To view factuality data please Upgrade to Premium
