LymeNet Flash: Lyme Support Groups by State Online

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»	LymeNet Flash » Questions and Discussion » General Support » Lyme Support Groups by State Online

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Author

Topic: Lyme Support Groups by State Online

nan
Frequent Contributor (1K+ posts)
Member # 63

posted

http://www.geocities.com/playpub/SL-US-Support.htm

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nan

Posts: 2135 | From Tick Country | Registered: Oct 2000 | IP: Logged |

imanurse
LymeNet Contributor
Member # 7022

posted

Wow the Iowa information is really, really outdated. Who can one contact with the current info?

Thanks.

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**Eat Chocolate**

Posts: 942 | From USA | Registered: Mar 2005 | IP: Logged |

yourtroubl
LymeNet Contributor
Member # 11087

posted

Of course, I am in West Virginia and there is none in my state.

Posts: 347 | From WV | Registered: Jan 2007 | IP: Logged |

Melanie Reber
Frequent Contributor (5K+ posts)
Member # 3707

posted

Thanks Nan!

Really great information all in one place, HUGE kuddos on this wonderful effort!

But yes...some need to be updated.

This is typical, as many groups' and advocates' activity levels fluctuate over time.

To contact Washington Lyme for any changes:
[email protected]

My best,
melanie

Posts: 7052 | From Colorado | Registered: Mar 2003 | IP: Logged |

playpup
Member
Member # 1768

posted

Thanks Melanie

I appreciate your kind words.

Over time, I found I was spending tons of hours trying to locate local group for out-of-state patients who needed local support.

I eventually figured out that I just need to create an easy way for me to get to this information.

So I figured if it helped me ... it might help others. So I decided to just make it a gift for the entire Lyme Community, and hope it helps people, patients and other support group leaders to find the support they are looking for.

But I can't take all the credit, I had help from other support group leaders and patients who helped me in creating this listing for our Lyme Community.

It sounds like I will be getting some updated information, which is always good news.

By all means ... feel free to drop me a line to
Add, Update or Delete Info.

But also be patient with updates, as I have Lyme and have to wait for good brain days.

Enjoy!

Alexis
[email protected]

Posts: 38 | From Seattle, WA | Registered: Oct 2001 | IP: Logged |

nan
Frequent Contributor (1K+ posts)
Member # 63

posted

For clarification....this was sent to me via email. It sounds as though some of this info is outdated.

Sorry...I don't now who is responsible for it, but, Like Melanie, I thought it was great to find it all in one place!

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nan

Posts: 2135 | From Tick Country | Registered: Oct 2000 | IP: Logged |

nan
Frequent Contributor (1K+ posts)
Member # 63

posted

You certainly do deserve credit, Alexis! A very nice and useful gift to the Lyme community....thanks so much for your efforts!

[kiss]

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nan

Posts: 2135 | From Tick Country | Registered: Oct 2000 | IP: Logged |

Lisianthus
LymeNet Contributor
Member # 6631

posted

The only thing for Michigan is the MLDA.... Ya right!

They want no information on Dr. J. Refuse to sign petitions. And when I posted the petition about the ILDA guidelines I was yelled at and told not to post them. They don't want any information about lymenet posted at all! Or anything to do with the LDA.

So I left the group.

Its a shame that these people are reaping the benefits for what other people are fighting for (ILADS)

Sorry just makes me mad [Mad]

And I wish there were another group for MI.

I had to leave the state to get a LLMD (I traveled to NY)

Lisi

[ 02. February 2007, 05:29 PM: Message edited by: Lisianthus ]

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yahoo 360 http://360.yahoo.com/my_profile-UqSNGiA9crUMRW.lFNGN5Jk-?cq=1

Posts: 986 | From Michigan | Registered: Dec 2004 | IP: Logged |

playpup
Member
Member # 1768

posted

Thanks Nan [Smile]

I appreciate your words of support.

It's certainly a team effort. [group hug]

One by One we are finding each other
One by One we are finding we are not alone
Together we ARE making a difference.

Blessings,
Alexis

Posts: 38 | From Seattle, WA | Registered: Oct 2001 | IP: Logged |

tdtid
Frequent Contributor (1K+ posts)
Member # 10276

posted

Wonderful job Alexis! And thank you Nan for bringing it to our attention. Definitely a keeper!

Cathy

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"To Dream The Impossible Dream" Man of La Mancha

Posts: 2638 | From New Hampshire | Registered: Oct 2006 | IP: Logged |

bettyg
Unregistered

posted

this is the perfect time to check on your state's info. get the newest info, and provide to alexis so in the future; she can update your state's info when she feels up to it!

it's a win-win situation; you provide the resources; she provides the work of entering it in there plus all the others who assisted when she started this job! KUDOS TO ALL! [bow]

IP: Logged |

strongerangel
Member
Member # 10037

posted

the LDA of Greater KC is still current. I know bc they're the ones who recommended my doctor, and basically saved my life!

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-Em

"Thank you, Oh Lord, for giving me the power to control my pain"

Posts: 59 | From Missouri | Registered: Sep 2006 | IP: Logged |

playpup
Member
Member # 1768

posted

If possible, perhaps you would like to help us to make it a better and more up-to-date list.

If so ... let us know.

Posts: 38 | From Seattle, WA | Registered: Oct 2001 | IP: Logged |

CJ
LymeNet Contributor
Member # 169

posted

How do they find the information?
Where do they do their searches?
I would like to go look at my own name and see what comes up.
Thanks! That was very good information.

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here's hoping today is better than yesterday and tomorrow is even better!

Posts: 239 | From Evansville, IN | Registered: Oct 2000 | IP: Logged |

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