You may notice that a paypal button has been added to the site. This is to give you the opportunity to contribute to the expenses of running and maintaining this soon to be non-profit website. We hope to be a growing resource for those living with dysautonomia and those who care for them, and also initiate the awareness of dysautonomia in the public. New interactive programs are being developed and more research articles added daily, plus fun stuff you’ll love to explore.

We want it to be your, the patient’s, website and all suggestions and feedback are welcome. At present we are filing papers with the state for official non-profit status and there are considerable fees to pay. The website designer (he is also the webmaster) and his wife who suffers from dysautonomia have been privately paying all the necessary fees to bring this service to the web. I’m sure others of us would like to help, so we are making it easy through Paypal.

Thanks to all the members for their interest and support.