Dyspraxia Dialect Blog

Unfiltered thoughts direct from USA's foremost Dyspraxic - Founder and Director of Dyspraxia USA, Warren Fried. Click here

Dyspraxia USA, NFP is financed entirely through donations and member subscriptions. We are working hard to provide you with information about, and personal stories from, people and families living with dyspraxia. This information gives valuable input to families of those struggling with this condition. Your generous contribution will provide aid by funding Dyspraxia USA. Continued funding is very important because it will enable us to reach out to our friends in the 6% to 10% of the population who have dyspraxia.

Dyspraxia USA NFP hopes that, through our ideas, we can change the world for those with dyspraxia and their families. Our goal is to generate awareness about, and to help, those living with dyspraxia. We want to generate enough awareness about dyspraxia in order to ensure the earliest diagnosis possible for children.  Social and special education needs should be identified early in order to ensure educators and other professionals are aware of the condition and can provide the

We would like to eventually provide people throughout the United States who have dyspraxia with a place where they can receive support and participate in social groups and events.   Our vision is a society where developmental dyspraxia is more widely accepted and acknowledged.

Membership Fee: $30.00 yearly

Membership runs from January through December.  If you join after January, your membership would be renewed the following January.
Benefits of joining

• Receive sources and links to sources about dyspraxia
• Join other members who support each other
• Learn about events and conferences about dyspraxia and related conditions
• Your membership and donations are a very important resource for helping raise awareness about dyspraxia

Members Only:

• Warren’s Corner:  Authored by Warren Fried, a young man with dyspraxia who is also the President and founder of Dyspraxia USA NFP.
• Parent Blog: The online journal of board member Leigh Keener – a parent whose son has dyspraxia and is a rising sophomore in high school. Leigh is happy to communicate with others who are affected by dyspraxia. She will be sharing selected email questions, comments, and advice on this site.