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 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 | 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 | Nov 22, 2021 | Awareness, Home Page, SMS Blog
By Jennifer Klump November is National Adoption Month. It is the month when the broader community acknowledges the efforts of those whose lives have been impacted by adoption. It also helps spread awareness and encourages all of us to learn about adoption. ...
by PRISMS | Sep 7, 2018 | Awareness, Newly Diagnosed, SMS Blog
Trevor Gritman, Father to Boston (8) In 2010, my wife and I had our first son. We already had an amazing three-year-old daughter and then, we were getting a boy, I was beyond excited! I immediately started thinking about the cool things I was going to teach him and...
