Season’s Greetings from Robin Marshall, ASI Executive Director
For me personally, it is the time of year when I think about family. I am reflecting once more on what family really means. And I am realizing and appreciating what all of you, my Alström Family, have taught me about leading a more meaningful and fulfilling life. Thank you! As we all know, Alström […]
News from the Schiafone Family
View a documentary film about Alström Syndrome produced by Journalism students at Ryerson University in an effort to explain “The Monster Disease“. http://rbnonline.ca/media/8225/
“We ourselves feel that what we are doing is just a drop in the ocean. But the ocean would be less because of that missing drop. “ ~ Mother Theresa
Welcome to the Alström Syndrome International blog… This blog will be your source for all ASI happenings, news, and shared information. We hope you find this new news format easy to use and informative. Anyone with questions or comments about this blog should contact Jan Marshall (ja**********@ja*.org). Permanant information can be and always will be […]
