by PRISMS | Mar 22, 2023 | 30th Anniversary, From PRISMS, Home Page, SMS Blog
Our work at PRISMS would not be possible without the expertise of our amazing Professional Advisory Board, also known as the PAB. The PAB consists of ten individuals representing the diverse needs of the Smith-Magenis syndrome (SMS) community. It is an...
by PRISMS | Feb 20, 2023 | 30th Anniversary, Awareness, SMS Blog, Uncategorized
By: Kimberly Caulkins Every year since 1961 the city of La Crosse, Wisconsin holds a traditional German Oktoberfest. Born in Munich in the 19th century, Oktoberfest first made its way to La Crosse in 1961. What started as a simple community event has turned into...
by PRISMS | Feb 4, 2023 | 30th Anniversary, Awareness, Home Page, SMS Blog
By: Maggie Miller, Vice President PRISMS Board of Directors and Co-Founder, PRISMS This year PRISMS marks 30 years of serving the Smith-Magenis Syndrome (SMS) community. This wonderful community includes persons with SMS, parents and family members, professionals, and...
by PRISMS | Feb 1, 2023 | 30th Anniversary, Awareness, Home Page, SMS Blog
By: Brandon Daniel, PRISMS Board President It is hard to believe it has been 30 years since the founding of PRISMS! In some ways that seems like a long time ago and in other ways it does not seem that long ago at all. When I think of PRISMS, I think about my first...
by PRISMS | Jan 29, 2023 | Awareness, Home Page, SMS Blog
Can you tell us a little bit about yourself, your family, and your SMS individual? My name is Leah Baigell and along with my husband Henry, we have two boys – Max who is 33, and Zach, our 30 year old with SMS. Max married Havens and they have our 2 amazing...
