LymeNet Flash: Thanks Tincup

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 » Thanks Tincup

UBBFriend: Email this page to someone!

Author

Topic: Thanks Tincup

5dana8
Frequent Contributor (1K+ posts)
Member # 7935

posted

this means the world to me.

i watch it everytime i'm being slammed by lyme
and it always makes me feel better and less alone.

Thanks also for all the lyme warriors out there.
being there when i cant be [group hug]

http://www.youtube.com/watch?v=xFWTMgcBYSo

[ 01-23-2010, 04:27 AM: Message edited by: 5dana8 ]

--------------------
5dana8

Posts: 4432 | From some where over the rainbow | Registered: Sep 2005 | IP: Logged |

Tincup
Honored Contributor (10K+ posts)
Member # 5829

posted

My heart feels good knowing you can get some good out of it. Thanks so much for saying so... it means a lot, it really does.

I watched it tonight and cried when I saw Charlie at the picnic table. I do miss him so.

But then I usually cry when I watch it.. and really cried when putting it together.

We've all been though so much ... but we keep on going.

And ya know what?

2010 is the year of change. It is.

I can feel it and see it coming. Once it happens things will be better for our docs and for all of us.

And most importantly, things will be better for the dear children....

[group hug]

--------------------
www.TreatTheBite.com
www.DrJonesKids.org
www.MarylandLyme.org
www.LymeDoc.org

Posts: 20353 | From The Moon | Registered: Jun 2004 | IP: Logged |

5dana8
Frequent Contributor (1K+ posts)
Member # 7935

posted

thanks again Tinnie for putting the time & efforts into this.

it must have been hard for you to put this togeather...so many memories.

double thanks for your positive optimism for change in 2010. your a treasure

(( warm hugs))

[group hug]

Ps' sorry i havent been around for a while
what happened to Charlie?

--------------------
5dana8

Posts: 4432 | From some where over the rainbow | Registered: Sep 2005 | IP: Logged |

Lymetoo
Moderator
Member # 743

posted

Thanks TC!!

and hi to my good friend, Dana!!! [hi]

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96222 | From Texas | Registered: Feb 2001 | 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/