Protecting our children from Bullying who have a Rare Disease~ LET US DO MORE THAN SIGN A PETITION TO STOP RDB LETS JOIN A MOVEMENT
To provide awareness and education to schools and the community about Rare Diseases. To educate the community by visiting schools and talking about Rare Diseases. The more educated others are the more our children do not feel alone WE will CHANGE the opinions of others so they do not feel the need to bully. Although we can’t eliminate it 100% we can provide the tools to help and provide the reassurance that “our” children are not alone.
Company Overview
We at recognize the need to help our children feel ABLE even when labeled disABLE. Bullying is a huge factor for the children who have a RARE or “invisible” disease. They are often “outsides” and labeled. This group is to help other children understand that different is good, help them understand all children with a rare disease endure. We want to let “our” children know we understand and support them and most importantly “Show” them they are not alone!!

To join please go to FB page StopRareDiseaseBullyingNow/StopCAIDnow or please email Barbie Marshall at for more information .
StopCAIDnow is glad to be continuing its partnership/relationship with the Global Genes Project to help stop the bullying for the Rare Disease Community…Take the ying out of bullying and the only BULL should be Bringing understanding & Learning 2 Love 4 all that are different!

Leave a Reply

Looking for something?

Use the form below to search the site:

Still not finding what you're looking for? Drop a comment on a post or contact us so we can take care of it!

Visit our friends!

A few highly recommended friends...