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 | 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...
by PRISMS | Jun 6, 2022 | Clinics, Education, From PRISMS, Home Page, Research
By Robert Miller, Advisor on Clinic Relations PRISMS is pleased to announce the online publication of its first in a series of family-friendly treatment recommendations. This series is designed to provide essential information to parents, caretakers, and other...
by PRISMS | Nov 11, 2021 | Awareness, Home Page, SMS Blog
By: Michelle Larscheid, Program Coordinator Ann C.M. Smith, M.A., D.Sc (Hon), CGC, Chair Emeritus of PRISMS Professional Advisory Board and co-founder of PRISMS, was the keynote speaker for the PRISMS Virtual Summit on September 10, 2021. With over 107 views and...
