We always have new events going on! For more information and details about these current events head over to our Current Events page!

Upcoming Meeting Information!
Bookmark this page to get the latest information on the next meeting!
We will be providing information here for each upcoming meeting going forward!

Latest Event: Under Our Skin Viewing
The National Capital Lyme and Tick-Borne Disease Association has sponsored viewings of the Under Our Skin and Under Our Skin 2: Emergence documentaries in Harrisburg, NC.
Click here for more information.

Potential Lyme Disease Support Groups in Fayetteville and Asheville

Recently, the NC Lyme Disease Foundation has received interest from members in starting support groups in the Fayetteville and Asheville areas. We are not aware of any such groups in these cities and are very interested in facilitating this effort. In this respect, we have agreed to collect the email addresses of members who may be interested in attending meetings in either of these two cities.

If you may be interested in attending future Lyme Disease support group meetings in either of these two cities, please contact us using the form on the right and state which city you are interested in. We will then gather those addresses and send them to the individuals who are interested in spearheading this important initiative. Thank you in advance for participating in this important effort.

Looking For Information?

If you want more information about Lyme Disease feel free to browse our site and the provided information after reading our disclaimer.

Want To Join The NCLDF?

If you are interested in joining the NCLDF please use the form to the right to send us an email. We can inform you of the next meeting that is planned so that we can see you in person!

Already A Member?

Head over to the Group Activity page and sign up to view the calendar and the forums.

An (active) email address is required to sign in and notifications of meetings.

The North Carolina Lyme Disease Foundation, Inc. is a non-profit organization that works to increase community awareness and provide support to those with Lyme Disease.

The foundation was started in September of 2002 by Dr. Beth Jordan and Fonda Notch, who have both battled the disease and wanted to reach others who are trying to find out more about this controversial illness.

The NCLDF is not affiliated with any other organizations, and the purposes for which the Foundation is organized are exclusively charitable, scientific, literary, and educational. The intention of this website is to provide materials to educate the public about Lyme Disease. For more information please read our disclaimer.