by PRISMS | Jun 12, 2023 | Awareness, Home Page, Newly Diagnosed, SMS Blog
By Amy Pereira, PRISMS Board Member I remember vividly 13 years ago when I was first introduced to PRISMS. Joey was just 15 months when we received his diagnosis and admittedly, I was lost and frantic. As a newly diagnosed parent, my life had...
by PRISMS | Apr 11, 2023 | 30th Anniversary, Awareness, Home Page, SMS Blog
By: Michelle Larscheid Kevin Sperry didn’t realize the neighbor boy from down the street, who knocked on his door over 5 years ago and asked if he could go for a walk, would become his best friend. That best friend is Coulter Daniel. Sperry said he knew Coulter...
by PRISMS | Apr 4, 2023 | Awareness, Home Page, Newly Diagnosed, SMS Blog
Caring for a child with Smith-Magenis Syndrome most likely will be the most challenging and rewarding job you will ever have. You might feel as if you are the only person who can do the job and doubt that anyone else could meet your child’s needs the way you can....
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 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...
