LymeNet Flash: Mass LD Hearing - ATTN: People who live in the Berkshires

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 » Medical Questions » Mass LD Hearing - ATTN: People who live in the Berkshires

UBBFriend: Email this page to someone!

Author

Topic: Mass LD Hearing - ATTN: People who live in the Berkshires

Rhausta
Member
Member # 7920

posted

If you live in the Berkshires, and would like to attend the hearing please give me a call or email asap.

If you cannot afford the bus or overnight accomondations, please call me anyway.

My number is 413-569-5800.
Please be sure to leave a message and I will call you back. Please speak loudly and slowly.

Email: [email protected]

Carla

Posts: 24 | From Southwick, MA | Registered: Sep 2005 | IP: Logged |

sizzled
Frequent Contributor (1K+ posts)
Member # 1357

posted

Up!

Posts: 4258 | From over there | Registered: Jul 2001 | IP: Logged |

Rhausta
Member
Member # 7920

posted

Does anyone even have a contact in the Berkshires or know of a support group?
Carla

Posts: 24 | From Southwick, MA | Registered: Sep 2005 | IP: Logged |

henson2
Frequent Contributor (1K+ posts)
Member # 463

posted

Up.

I think a tick bite I got at Tanglewood may have infected me. I spent a summer there; I knew nothing about Lyme then, did no tick checks, and our conditions were spartan. I spent so much time in the grasses and brush and beautiful rural environment w/o ever knowing a thing about ticks.

It's awfully endemic out there....

Thanks for your offer Carla.

I'm on the other side of the state.... but I sure hope folks will make the trip.

We will all spend a few days crashed afterward, but seeing so many sick and suffering people make the effort to get there will speak volumes to the Legislature.

If you're waffling, or on the fence, or waiting to see, please decide now.

It's so important now. We need EACH of you. I'll be with you in finding it hard to physically move to make the trip, as short as it is for me.

Your efforts and sacrifice matter.

Solidarity, and Thanks
[Smile]

Posts: 1066 | From East Coast | Registered: Dec 2000 | IP: Logged |

FightFireWithWater
Frequent Contributor (1K+ posts)
Member # 5781

posted

Please don't give up if you try to contact someone regarding a ride or other arrangements for the hearing and you don't get a reply.

Try another means of reaching the person or try to get a message sent through one of the other organizers for the hearing.

--------------------
"Help Or Be Helpless" Please visit "Activism" board daily. See the threads regarding the IDSA Guidelines crisis and the threads about Dr. Charles Ray Jones and decide how best to help today!

Posts: 1265 | From does not list | Registered: Jun 2004 | IP: Logged |

dontlikeliver
Frequent Contributor (1K+ posts)
Member # 4749

posted

I just WISH I could be there. I just do not have the funds for a plane ticket right now.

I hope that those of you in a position to go are able to make a big impact!

Good luck

DLL

Posts: 2824 | From The Back of Beyond | Registered: Oct 2003 | 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/