Grant to Fund Research on Ultra-Rare Hypophosphatasia “Soft Bone” Disease
Did you ever consider who funds medical research? Most people assume that it's funded by the government. But, in fact, over half of the more than $100 billion (yes $100…
Did you ever consider who funds medical research? Most people assume that it's funded by the government. But, in fact, over half of the more than $100 billion (yes $100…
Have Neurogenic Orthostatic Hypotension or other MSA? Join the LIVE FEED and Watch the annual MSA Patient & Family Conference on Facebook On October 13-14, the Multiple System Atrophy (MSA)…
When it comes to treating a chronic and serious disease like idiopathic pulmonary fibrosis (IPF), sometimes you have to fight fire with fire. Or, as in this case micro fibrosis…
Researchers at the at Indiana University-Purdue University Indianapolis are studying slime. That's right. And it's not just any slime. It's the slime produced by bacteria that keeps antibiotics from being…
Jenn Keeton was a longtime Children's nurse, surrounded by common and rare diseases among the youth. She never thought her own child would be born with one. Her and her…
Americans prize the ability to improvise, adapt, and overcome obstacles. We like it when people are faced with seemingly insurmountable odds yet find a way to maybe not cheat the…