Because a patient called one of these entities and sent an email with no return phone call or reply, this patient became extremely frustrated. Later I found out that this organization listed here as a support group no longer exists.
PLEASE PLEASE PLEASE !!
Click on YOUR state and verify that all information is correct for your organization. If you are not involved as a leader, please contact the individual who is responsible for updating this information and ask them to update. Even if there are NO changes, it would be nice if the date reflects that the information is current so we know.
My suggestion is that if you are not going to regularly update meeting dates, do not list dates, but rather include a general statement to call or email for support group meeting information.
Just my 2 cents. Thanks for listening!
Posts: 339 | From nowhere | Registered: May 2007
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posted
i have tried several times to get this added to no avail so here is the information.
Name of Support Group: Little Egypt Illinois Lyme Disease Network (LEILDN) Contact Person for this Group: Dottie L. Heffron Contact Person Telephone: (618)204-8084 Contact Person E-Mail: [email protected]
City: Centralia State or Province: Illinois Country: United States Regions of your state / province served by this group (i.e. south-east Pennsylvania): - Little Egypt Area -Southern Central Illinois Your Name: Dottie L. Heffron Your E-Mail Address: [email protected]
Other Information: Grassroots organization to educate the citizens of Southern Illinois and the surrounding areas. Speaking out to area schools about Ticks and Vector-Borne Diseases. Education is the key, and our children are the future. URL For Support Group: http://www.LymeDiseaseNetwork.com
Comments: We are dedicated to bringing education and hope to the citizens and doctors of Southern Illinois and the surrounding areas. Networking with other Lyme Disease organizations to help locate doctors and personal help for so many suffering from vector-borne diseases. Topics include: Babesiosis, Ehrlichiosis, Rickettsia(Rocky Mountain Spotted Fever), Masters Disease, Bartonella, Q-fever, and Tumaremia. Email or call us for meeting times and places. We can come to you or your group, for TOGETHER WE STAND!
The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:
The
Lyme Disease Network of New Jersey 907 Pebble Creek Court,
Pennington,
NJ08534USA http://www.lymenet.org/
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