What an SMA Patient Really Needs
In this Muscular Dystrophy UK video, Dr. Ros Quinlivan from the Queen’s Square Centre for Neuromuscular Diseases in…
Wendy is a proven blogger and social media manager who has helped to build online communities for businesses and organizations. She currently heads the website’s social outreach online through social media platforms such as Facebook, Twitter, and Pinterest.
At Bionews we’re committed to providing the most accurate, relevant, and up-to-date reporting for our patient communities. Our goal is to ensure that everyone has access to disease-specific information that is both trustworthy and easy to understand. You can read more about our editorial policy here.
In this Muscular Dystrophy UK video, Dr. Ros Quinlivan from the Queen’s Square Centre for Neuromuscular Diseases in…
Spinal muscular atrophy (SMA) is a genetic condition which affects a child’s range of movement due to the ongoing degeneration…
In this Huffington Post video shared in July 2015, meet artist Dwayne Szot and his amazing painting invention.
Earlier this year, when lingerie company Panache asked women to nominate role models, hundred of names poured in,…
While there is currently no cure for spinal muscular atrophy (SMA), there are ways to manage the disease to improve…
When a child is diagnosed with spinal muscular atrophy (SMA), a tremendous amount of stress and burden is heaped on the entire family.
https://www.youtube.com/watch?v=wOTFiztJBuI Nine-year-old Izzy Zahn wanted to help someone, so she decided to make a book of her photography and sell…
Spinal muscular atrophy (SMA) is a genetic disease that affects about 1 in 10,000 babies. The neurodegenerative disease is…
This MediaStorm documentary is all about Philly Mayer. Philly is a bright and happy nine-year-old boy who was…
In this video from the DNA Learning Center shared in July 2012, attorney Steve Mikita recalls attending Duke…
Get regular updates to your inbox.