An interesting post on Dr. Urano's blog today marking 2 years since he has joined the Washington University in Saint Louis. I think it is worthwhile to read the blog posts about the Life of a Wolfram mom and the other blogs about People Living with Wolfram syndrome on the Jack and JT Snow foundation page. I had not read them before because they do not directly apply to the science of MANF, but very moving stuff, glad that AMBS is working to help cure this disease. I am excited AMBS is partnered with some of the best research medical universities in the US as well. I am a medical school student and consider myself to be fairly smart, but I had absolutely no shot of getting into Washington University and probably not Miami either.