These days most families of young children with disabilities are using social media to connect with one another. It is important that family leaders and the professionals who provide services and supports to families have discussions about the pros and cons of social media. In fact, it is essential that technical assistance programs get involved in social media and provide families with assistance on how to protect their privacy.
FERPA
Every child who benefits from publicly-funded education services is covered by FERPA or the Federal Education Rights and Privacy Act. FERPA limits who can share information and what information they can share about a child and/or family receiving services funded with federal education dollars. Thus children enrolled in early intervention or IDEA (Individuals with Disabilities Education Act) Part C or birth to three programs are covered by FERPA. Additionally, Parent Training and Information centers and Technical Assistance centers which receive funding under Part D of IDEA have to follow FERPA.
What About Privacy Settings?
Every social media site, whether Facebook, YouTube, Google+, Twitter, Tumblr, Instagram, Vimeo or LinkedIn has its own privacy settings. These settings change over time too! It is important to help families to figure out how to find and use the privacy controls on different sites. Facebook, for instance, allows users to designate their Facebook "Friends" as close or acquaintances. In addition, users can decide whether to share their posts with only their friends, or to share posts publicly.
What happens in Vegas, stays on Facebook, Flickr...
It is important to remind families that once they have shared something on a site, they no longer have control over who see's what they have shared or who can re-share their post, picture or video. Anyone can grab a screenshot, download or forward their information. And in this day and age, most folks won't simply forward, but they may add their own comments or opinions.
So, you want me to stay off the internet?
No! Social media can be an incredible avenue for supporting and informing families with young children with disabilities. It can also create movements for system change. However, it is important that families understand that they do have rights, and that there are ways to minimize what gets shared and with whom. Finally, it is essential that we remind families that they are sharing on behalf of someone else. A minor child. As that child grows up it is important that families have regular check-ins with their child and discuss how much and with whom information is shared on the internet.
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