:: PRISMS - Membership

Membership

Why join PRISMS? Join PRISMS to be a part of and support for all who are affected by Smith-Magenis Syndrome; help families through various stages of life faced by both children and adults with SMS by providing information, increasing public awareness, and understanding through education.

2008 Membership Form* (see below)

PRISMS membership means:

Assisting those children and families in need.
Networking with others who understand.
Utilizing our website (www.PRISMS.org) that contains a wealth of material on Smith-Magenis Syndrome for families, caregivers, and doctors.
Attending PRISMS Conferences every two or three years for face to face discussions with researchers, other experts, and most importantly other families.
Learning from our new parent membership packet and our official Spectrum Newsletter.
Sharing on our newly created SMS Discussion online member’s forum for members only where SMS issues can be discussed free of spam and accessed on-demand by category, including access to past posts.
Keeping informed by reading our monthly info mails of current SMS news.
Connecting with other families and professionals through our Parent-to-Parent program and Professional Advisory Board.
Participating in our organization as a volunteer or board member.
Finding inspiration and encouragement from fellow members.

We hope all interested people will join PRISMS!!
PRISMS is a 100% volunteer organization funded by membership and contributions.

PRISMS is only as strong as its Membership.
Help us build our membership and our strength.

PRISMS is dedicated to providing support to families of persons with Smith-Magenis Syndrome, and fostering partnerships with professionals to increase awareness and understanding of SMS

* Note: This file is in a pdf file format. If you don't already have Adobe Reader, you'll need to download and install this program in order to open this file. It's approximately an 8.7MB download.