Galloway-Mowat
Syndrome Community

For the last year of our lives, we have spent countless hours doing research on Galloway-Mowat Syndrome (GAMOS). Because of how rare it is, we were unable to find any helpful information. All we found was the doom and gloom and all the negative. All the medical articles and papers written, nothing helpful. We wanted to build a site that shared a more personal experience of what we're dealing with on a daily basis in hopes of helping another family who may be going through the same thing.