We imagine a world where ALS is a treatable, manageable illness rather than an underfunded, terminal disease that devastates the lives of individuals and their families every 90 minutes. 90 Foundation A Non-Profit 501c3. ALS in not an incurable disease. it is an underfunded disease. With your help we can change that.

Sombrero en Crochet, inspiración. Tejí este sombrero hace semanas y desde entonces se ha convertido en mi favorito, porque es único. Por ahora, aquí les comparto unas bonitas fotos del sombrero y yo. Espero se inspiren y si quieren saber cualquier detalle del sombrero me lo dejen saber en los comentarios abajo.

The Real Housewife of Santa Monica. After 20 years in the Castro, my dad decided to leave for a flatter, easier life. Allison met me in San Francisco a couple of weeks ago to help.

Husband, father, brother, son, living with ALS. Beyond the Ice Bucket Challenge. So in many ways, this year is going to be about logistics. What do we have to do to keep our heads above water? Once we figure out the logistics, my third year with this disease will be remembered as the one in which we find a cure! November 14, 2014. Then there was Deb Quinn, a patient who movingly spoke about her family being ravaged by famil.

View from Below - Part 2. Getting Set Up at My Desk. When I got back to my desk, my office neighbor, Vasanti, was one of the many who immediately wondered just what the hell was going on.