Selective Mutism Foundation, Inc

 


Selective Mutism Foundation Mission
Our mission, as conscientious co-founders, is to promote further  research, advocacy, social acceptance, and the understanding of Selective Mutism as a debilitating disorder.

Through raising our children (who are now grown and on their own), networking, educating the public, and ongoing research
participation, we have contributed immensely to society, including effecting DSM criteria and renaming of the disorder.

We continue to focus on Selective Mutism, exclusively, and remain steadfast with our goals and in providing assistance and
membership in the most cost effective manner possible.  We are not motivated by monetary gain, but rather by the silent cries for
help from the children
.  We are particularly grateful to so many of you who contact us or send letters of gratitude acknowledging
our sincerity. 

We are proud to have been the ones that have pulled Selective Mutism out of the dregs of neglect, misconceptions, and negativity
and elevated it into the limelight.  We are proud to have given Selective Mutism a home among other recognized disorders, and
dignifying it with credibility, integrity and attention.  More importantly, we are proud of our adult children and the countless others
we help.  Through them we developed the greatest wealth of all, an abundance of inner strength, motivation, patience and
perseverance against all obstacles.

In recent years, the Internet has advanced from a luxury to a necessity for many.  The Internet is un-equivalent to any other means
of mass communication, yet it is this form of communication that is a detriment to our population as it inadvertently suppresses
verbalization. 

And so, through our site we invite you to utilize our information, experience, and support, as your tool to empower yourselves.  We
are here to advocate for and bring about acceptance, verbal and social interaction, community inclusion, integration, and
productivity for
our unique population.  

Together we continue to make a difference!

 Sue Newman and Carolyn Miller
Co-Founders/Directors

 

Selective Mutism Foundation, Inc. | What is Selective Mutism | Mission Statement | Guest Book | About Non-Profits | Co-Founders | Officers | Media | Consultation & Sensitivity TrainingAdvisory Board | Free Selective Mutism Treatment | Book | Newsletters | Web Mall | Research/Ethics | View Selective Mutism in the DSM | Sound Advice/Treatment | Common Myths | Related Links | Contact Us for Parent Packet | Join Selective Mutism Foundation, Inc. | Disclaimers | Bulletin Alert | Younger Years  | SMF Brochure  | Advocating for Your Child | Benefits of Membership | School Blues | Summer Camp  | Circle of Friends | College | PreCollegeHidden Disabilities | Donating to SMF | Features of SM | Why is the DSM Important | How did this Rare Disorder become Known | Life After SM | Common Myths | HealthCare Providers | SelfHelp Links | Rehabilitation | Take the Self Test | Teacher Skills | Special Education | Is SM a Speech Disorder | SSI  Benefits | Teacher Talk | Teen Volunteers | 504 Plan

Selective Mutism Foundation is a charitable 501(c)(3) not-for-profit organization and is not affiliated with any other organization or website.  
All donations are tax deductible as allowed by law. 
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©2012