by PRISMS | Apr 19, 2022 | Awareness, Home Page, SMS Blog
By: Suzanne Sorenson, Colton’s Mom Being a parent of a child with Smith Magenis Syndrome (SMS) is a roller coaster. Being a parent, in general, can feel the same, but as a special needs parent, the typical traditional rights of passage and everyday milestones...
by PRISMS | Jul 14, 2021 | Awareness, Home Page, SMS Blog
By: Diane Erth, PRISMS Board Member Planning a road trip can be exciting and fun but when your road trip includes a child with SMS, much more planning is needed. Here is a bit about a trip we took recently and what I did to ensure it would be a hit! As many of you...
