by PRISMS | Apr 28, 2024 | Clinics, Education, From PRISMS, Home Page, Research
PRISMS is pleased to announce another online publication in its series of family-friendly treatment recommendations. This series is designed to provide essential information to parents, caretakers, and other professionals who may be providing services to an individual...
by PRISMS | Aug 10, 2023 | 30th Anniversary, From PRISMS, Home Page
Rare diseases like Smith-Magenis syndrome may affect a small number of individuals, but their impact can be devastating. These conditions are characterized by their scarcity, which poses unique challenges for research, diagnosis, and treatment. However, one of the...
by PRISMS | Jul 24, 2023 | 30th Anniversary, From PRISMS, Home Page
PRISMS is proud to announce a new addition to the Board of Directors, Eric Rogers. Eric will serve as a Member-At-Large. Eric and his wife Jessica live in Mount Juliet, TN with their son Wyatt (9) who has SMS, and daughter Adelyn (5). Eric attended Cumberland...
by PRISMS | Jun 20, 2023 | 30th Anniversary, From PRISMS, Home Page
The new 2022 PRISMS Annual Report has just been released. The annual report highlights all the hard work and achievements that have been accomplished in the past year. At PRISMS, we are committed to complete transparency by making our financial records and...
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 | Sep 27, 2022 | Awareness, Education, From PRISMS, Home Page, Newly Diagnosed, SMS Blog
By: Michelle Larscheid, Program Coordinator The 11th PRISMS International Conference brought together the Smith-Magenis syndrome (SMS) community for three days of connection and education. It Is the largest conference specifically focused on SMS in the...
