Support groups by State
Click on your State for List of Support Groups, Websites, Events and More…
If you are looking for support groups in another country besides the US please visit:
Global Lyme and Invisible Illness Organization
If you have a group you would like added, please place in comments below or contact us here.
Support Groups by State
Click on your state to learn about Lyme disease support groups, news, research, legislation.
- Alabama
- Alaska
- Arkansas
- Arizona
- California
- Canada
- Colorado
- Connecticut
- Delaware
- Florida
- Georgia
- Idaho
- Illinois
- Indiana
- Iowa
- Kansas
- Kentucky
- Louisiana
- Maine
- Maryland
- Massachusetts
- Michigan
- Minnesota
- Missouri
- Montana
- New Hampshire
- New Jersey
- New Mexico
- New York
- North Carolina
- Oklahoma
- Ohio
- Oregon
- Pennsylvania
- Rhode Island
- South Carolina
- Tennessee
- Texas
- Utah
- Vermont
- Virginia
- Washington
- West Virginia
- Wisconsin
Lyme Information by Country
- Australia
- Austria
- Czechoslovakia
- Denmark
- England
- Finland
- France
- Germany
- Ireland
- Italy
- Japan
- Netherlands
- New Zealand
- Norway
- Poland
- Scotland
- Sweden
- Switzerland
- Wales
Websites
- Empire State Lyme
- Georgia Lyme Disease Association
- Global Lyme and Invisible Illness Organization
- Ilads (International Lyme and Associated Disease Society)
- Kansas Tick Borne Disease Advocates
- LDA (Lyme Disease Assocation)
- Lyme 411
- Lyme Aware
- LYMEDISEASE.org
- Lyme Friends
- Lyme Support Network
- Madison Area Lyme Support Group
- May 12 Interational Awareness Day
- National Capital Lyme Disease Association
- TBDA Tick Borne Disease Alliance
- United States Worldwide Lyme Awareness Protest Facebook Page and Website
- What is Lyme Disease?
- Wisconsin Lyme Network
- Worldwide Lyme Borreliosis
Thanks for providing this list.This collection of events, news, research, and support groups for Lyme disease patients is a wonderful way to get in touch with each other and discuss the issue.
Under the California listing, please remove Nor-Cal Chico Lyme and replace with Chico Lyme Disease Support Group on Facebook. We are in N. California, Butte County.
Thank you,
Dee Ohliger
Got it, thank you!
UPDATE FOR FRESNO LYME SUPPORT GROUP IN CALIFORNIA…
Here is the correct address. Sorry for the previous error.
https://www.facebook.com/groups/FresnoLymeSupport/
Thank you Leslie, I got it changed.
Hello, I recently started a Lyme disease support group in Fresno, CA. Please, add us to the list for California as “Fresno Lyme Disease Support Group”. We can be found on Facebook under the same name. http://www.facebook.com/FresnoLymeDiseaseSupportGroup
Error on web address.
Corrected info…
https://www.facebook.com/groups/FresnoLymeSupport
Hi,
I’ve had New Mexico Lyme Disease Support since 2007. However, it’s never been listed. I emailed above over a year ago, as well. Thanks ahead of time!
Diane J Marie
Public email address: dianemarie555@gmail.com
Oh sorry Diane, I did do a post for you last year.. but just forgot to add it to this list .. Ill add it now. <3 Here is the post I did last year so you don't think I ignored you. Thanks for all you do! http://whatislyme.com/new-mexico-lyme-support-group/ Let me know if anything has changed since then. Actually i just noticed your email is changed now so Ill update it from the one i had to the one you listed here.
I am in the process of starting a support group that focuses on awareness in the Fox Valley (Appleton) area. Any help would be greatly appreciated.
Private support group in Montrose Pa
Montroselymegroup@gmail.com
Got it on there, thank you!
Please update Oregon Lyme Disease Network facebook page
Please update Oregon Lyme Disease Network current information. 501(c)3 since 2003, are affiliates of LDA and work with ILADS and CALDA since 2001. We have set up support groups around Oregon that meet face to face, and online. Our support groups are located in Hood River Oregon, Portland OR, Bend OR, Salem OR, Eugene Or (NOT LDEO) and Medford OR. Current phone 541-410-2585. We also have an Oregon Lyme Disease Network facebook page only for Oregonians
https://www.facebook.com/groups/869280209779701/
❤Lymily❤ is my emotional support group group from Pa ……
Please enter our group on this page. It’s OK to use my email address. Thank you.
New Mexico Lyme Disease Support
dianemarie555@gmail.com
Also, Lisa, did you know about Lyme-Aware? It’s here and click on the shape of a state on the map to get to any state support group:
http://www.lyme-aware.org
The page for New Mexico Lyme Disease Support is here:
http://lyme-aware.org/news/in-the-lymelight/933-new-mexico-lyme-disease-support-group.html
We are a Lyme disease support Group on the GULF COAST OF FLORIDA. ( The Culf Coast Lyme Disease Support Group)The Support Group has Been in Operation for about 9 years. Information about the Support Group and the Administrator. Adjunct Professor Emeritus Carol Fisch can be found at the Web site which is used for contact info. We also have three Web sites, on Facebook. Carol Fisch, Lyme disease Education and Awareness, Carol Fisch Lyme disease Conversation and Carol fisch the Lighter Side of Lyme. PLEASE ADD THESE TO YOUR FLORIDA LIST…… Thank You Carol Fisch
The web site is; http://www.FloridaLyme Support.com for the Gulf Coast Lyme disease Support Group… Thank You Carol Fisch
Hello Lisa,
Thank you for creating this list. Please add my FB group LEAF- Lyme Expressions And Fellowship.
Thanks for all you do!
Lizzie
LEAF
Please add http://www.kentuckyindianalymesupport.org to your list. We serve Kentucky and Southern Indiana Lyme patients
Got it on both Kentucky and Indiana, thank you Pam!
Sure wish their was a support group in Indiana:(
Hey Jewell, did you see this page? http://whatislyme.com/lyme-in-indiana/
Please add http://flda.org as the florida lyme disease association’s site. It has info, resources as well as listing some of our local support groups.
Thank you Wendy! Got it added. 🙂
I noticed there is no support group listed for Louisiana and am having trouble finding support groups here. My son passed away from long term untreated lyme disease almost 2 years ago and I am looking for a way to show support in this area.
Here is the information we have collected on Louisiana. http://whatislyme.com/lyme-in-louisiana/
I am so sorry that you lost your son. There are no words… just sorry.
We do have a Lyme memorial on here if you would like to write something up to honor him we will make a page for your son.
~Lisa Hilton