LymeNet Flash: New New Hampshire Lyme Support Group in Manchester

LymeNet on Facebook

LymeNet on Twitter

Follow @LymeDiseaseNet

The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive

The Lyme Disease Network is a non-profit organization funded by individual donations.

»	LymeNet Flash » Questions and Discussion » General Support » New New Hampshire Lyme Support Group in Manchester

UBBFriend: Email this page to someone!

Author

Topic: New New Hampshire Lyme Support Group in Manchester

EyeBob
LymeNet Contributor
Member # 12572

posted

A friend and myself are going to start a Lyme Support Group for those affected by TBIs in Southern New Hampshire. We will meet on the third Wednesday of every month starting on June 18th. The meetings will be held at the First Congregational Church of Manchester at 508 Union Street, Manchester. Meetings will start at 6:30.

There will be no agenda per-se, the meetings are more meant to have an open format and to be informational/supportive in nature. The meeting facilitator is a very experienced facilitator who has family members affected by Lyme.

PM me if you want more information.

We hope to see you all there.

BT

Posts: 299 | From New Hampshire | Registered: Jul 2007 | IP: Logged |

bettyg
Unregistered

posted

BOB, WAY TO GO! BEST WISHES FOR A SUCCESSFUL GROUP! [group hug]

IP: Logged |

METALLlC BLUE
Frequent Contributor (1K+ posts)
Member # 6628

posted

E-mail or phone contact to reach you?

--------------------
I am not a physician, so do your own research to confirm any ideas given and then speak with a health care provider you trust.

E-mail: [email protected]

Posts: 4157 | From Western Massachusetts | Registered: Dec 2004 | IP: Logged |

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

posted

GREAT JOB!!!!

I'm glad you have been able to pull a date, time and location together for this. Hope to be there. Thanks for the information.

Cathy

--------------------
"To Dream The Impossible Dream" Man of La Mancha

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

EyeBob
LymeNet Contributor
Member # 12572

posted

PM me for more information, but essentially what I posted is what we have at this point.

I would suspect that since many of us have much to share that it should be a fairly informative and supportive meeting.

bt

Posts: 299 | From New Hampshire | Registered: Jul 2007 | IP: Logged |

Printer-friendly view of this topic

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, NJ 08534 USA
http://www.lymenet.org/