LymeNet Flash: UNDER OUR SKIN trailer! Please watch

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 » UNDER OUR SKIN trailer! Please watch - youtube

UBBFriend: Email this page to someone!

Author

Topic: UNDER OUR SKIN trailer! Please watch - youtube

luvdogs
LymeNet Contributor
Member # 9507

posted

http://youtube.com/watch?v=sxWgS0XLVqw

I hope you guys can access this - this is part of the documentary that is supposed to be coming out soon... (Under our Skin)

[ 30. April 2008, 03:41 PM: Message edited by: luvdogs ]

Posts: 588 | From Rhode Island | Registered: Jun 2006 | IP: Logged |

Clarissa
Frequent Contributor (1K+ posts)
Member # 4715

posted

Thanks for sharing...that was like looking into a mirror. I feel completely vacant and sad...this is just a nightmare.

I forwarded it to the Larry King request email. This movie trailer says it all...I pray this movie opens some eyes.

It really hit home. [Frown]

--------------------
Clarissa

Because I knew you:
I have been changed for good.

Posts: 1625 | From Florida | Registered: Oct 2003 | IP: Logged |

Wildthing
LymeNet Contributor
Member # 6791

posted

OMG-This is SOOOO sad [Frown]

What about Montel Williams, This is a guy that has been through some tough medical times...I'm going to look at his website, see if I can get a link of this video over to him

--------------------
Powerful Women's Motto: Live your life in such a way that When your feet hit the floor In the morning, Satan shudders & says� 'Oh ****!...She's Awake!!

WildThing
www.wildthingstodo.com

Posts: 160 | From Royersford,PA,USA | Registered: Jan 2005 | IP: Logged |

groovy2
Frequent Contributor (1K+ posts)
Member # 6304

posted

I wrote Larry -

make sure to give stats on US infections
and include Famous people who have lyme -
bush ect- Jay-

Posts: 2999 | From Austin tx USA | Registered: Oct 2004 | IP: Logged |

KS
LymeNet Contributor
Member # 12549

posted

brought me to tears....tears of sadness, frustration, anger....

I think it is a very good idea to try to send this to as many TV shows and news stations as possible. This movie can really make a difference in terms of sparking awareness and the right kind of discussions.

Let's all work together!!

Posts: 561 | From mass | Registered: Jul 2007 | IP: Logged |

luvdogs
LymeNet Contributor
Member # 9507

posted

I posted this on Oprah's Lyme discussion but don't know if she will see - how do I send to her?

Posts: 588 | From Rhode Island | Registered: Jun 2006 | IP: Logged |

Wildthing
LymeNet Contributor
Member # 6791

posted

Let's get together on this and try to send as to as many tv shows as possible...

Montel Williams: http://www.montelshow.com/mail/

Oprah: https://www.oprah.com/plugger/templates/BeOnTheShow.jhtml?action=respond&plugId=B2100004

Elen Degeneres: http://ellen.warnerbros.com/show/respond/?PlugID=8

Come on everyone, add your shows!!!

--------------------
Powerful Women's Motto: Live your life in such a way that When your feet hit the floor In the morning, Satan shudders & says� 'Oh ****!...She's Awake!!

WildThing
www.wildthingstodo.com

Posts: 160 | From Royersford,PA,USA | Registered: Jan 2005 | IP: Logged |

KS
LymeNet Contributor
Member # 12549

posted

I just emailed Dr. Phil...really played on the psychological component of the disease and children (i.e. autism).

http://www.drphil.com/shows/page/contactdrphil/

Posts: 561 | From mass | Registered: Jul 2007 | IP: Logged |

KS
LymeNet Contributor
Member # 12549

posted

Just contacted Dateline....let's go and help our heros, who made this film, get the attention it deserves. Every email, call and letter does make a difference!!

[email protected]

Posts: 561 | From mass | Registered: Jul 2007 | IP: Logged |

inseattle
Member
Member # 12743

posted

I sent this clip to several people this last month, including my HMO doc who doesn't "get" Lyme, but several recipients said they were not able to open it. I used the address below. Did I do something wrong? I contacted two Seattle TV stations last week with Lyme info, and will send this, too.

www.openeyepictures.org/underourskin/index

Kate

Posts: 22 | From seattle | Registered: Aug 2007 | IP: Logged |

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

posted

Inseattle..

I can't open that site either or get it to work.. so I send the utube one that was originally posted up top.

[Big Grin]

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

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

luvdogs
LymeNet Contributor
Member # 9507

posted

I just emailed Oprah, Elen and Montel. Will somebody come on the show with me if they call [Smile]

I'll need somebody's hand to hold...

Posts: 588 | From Rhode Island | Registered: Jun 2006 | IP: Logged |

Clarissa
Frequent Contributor (1K+ posts)
Member # 4715

posted

I'll go on the show with you...(but only if you bring the purple capsule with us for strength).

Seriously, I have no fear of public speaking and am good "on the spot". I'm in if you need me!!

Any my story is a good one to tell becaue my father, mother, brother, niece, nephew, aunt, cousin and best friend's husband and I, all have/had Lyme and coinfections.

Just give me the word,

--------------------
Clarissa

Because I knew you:
I have been changed for good.

Posts: 1625 | From Florida | Registered: Oct 2003 | IP: Logged |

Clarissa
Frequent Contributor (1K+ posts)
Member # 4715

posted

I just emailed Ellen but I didn't get any "confirmation" or anything.

I hope it went through!!!

--------------------
Clarissa

Because I knew you:
I have been changed for good.

Posts: 1625 | From Florida | Registered: Oct 2003 | IP: Logged |

luvdogs
LymeNet Contributor
Member # 9507

posted

Thanks Clarissa!

OK.. we'll tell her that we will only speak if we can have the purple capsule on the table in front of us for support.

Kind of like a blanky.

OK, you can do most of the talking, and sometimes, when, and if, I remember something important, I'll raise my hand and say "I have a thought" or something like that. And then we can hope that the thought stays long enough to let it out.

Kool! We have it figured out.

Other people can come if they want! We can all share the purple capsule.

Posts: 588 | From Rhode Island | Registered: Jun 2006 | IP: Logged |

luluMN
LymeNet Contributor
Member # 12703

posted

Count me in !! I daydream of this: going on TV

sometime and telling everyone the truth about

what we have really gone through on a day to day

basis! I hope we get to shout it out to the

world...

As my daughter would say: "ME too, ME too!"

Laura

Posts: 232 | From MN | Registered: Jul 2007 | IP: Logged |

Clarissa
Frequent Contributor (1K+ posts)
Member # 4715

posted

"kind of like a blanky"

Luvdogs, you CRACK ME UP!!!

--------------------
Clarissa

Because I knew you:
I have been changed for good.

Posts: 1625 | From Florida | Registered: Oct 2003 | IP: Logged |

luvdogs
LymeNet Contributor
Member # 9507

posted

I'll bring the blanky and you can bring the memory, k?

Posts: 588 | From Rhode Island | Registered: Jun 2006 | IP: Logged |

lymeHerx001
Frequent Contributor (1K+ posts)
Member # 6215

posted

Unfourtunatelly it brought tears to my eyes too.

I wanna hit someone!

Posts: 2905 | From New England | Registered: Sep 2004 | IP: Logged |

IMHisda
LymeNet Contributor
Member # 6998

posted

I called our public television station here and asked them to play it.

--------------------
RV

Posts: 249 | From Healing in USA | Registered: Mar 2005 | IP: Logged |

liesandmorelies
LymeNet Contributor
Member # 15323

posted

SO SO SAD!!!!!!I will share this with others. [Frown]

--------------------
aka: Lyme Warrior

In order to do "real" science, you have to have a "real" conversation with nature.

Well Behaved Women Rarely Make History!

"Just Demand your Rights"

Posts: 869 | From nor - cal | Registered: Apr 2008 | IP: Logged |

Tracy9
Frequent Contributor (1K+ posts)
Member # 7521

posted

I wanna come too!!!

I have years and years of public speaking experience, including many radio and national TV shows.

I'm in!!!

--------------------
NO PM; CONTACT: [email protected]

13 years Lyme & Co.; Small Fiber Neuropathy; Myasthenia Gravis, Adrenal Insufficiency. On chemo for 2 1/2 years as experimental treatment for MG.

Posts: 4480 | From Northeastern Connecticut | Registered: Jun 2005 | IP: Logged |

luvdogs
LymeNet Contributor
Member # 9507

posted

Maybe you should have spoken on Monday! Lord knows that gal in the black dress was a nervous wreck.

You're hired! Come with! - when we ever hear from them [Smile]

Posts: 588 | From Rhode Island | Registered: Jun 2006 | IP: Logged |

bettyg
Unregistered

posted

and don't forget me!

IP: Logged |

Larkspur
LymeNet Contributor
Member # 5131

posted

I wanna come on Ophrah too! I think I would be good.

And I want Nate to redo my bathroom (but that's another show, I guess)

--------------------
"We must be willing to get rid of
the life we've planned, so as to have the life that is waiting for us" - e.m. forster

Posts: 921 | From PA | Registered: Jan 2004 | IP: Logged |

Tracy9
Frequent Contributor (1K+ posts)
Member # 7521

posted

LMAO!!!!

--------------------
NO PM; CONTACT: [email protected]

13 years Lyme & Co.; Small Fiber Neuropathy; Myasthenia Gravis, Adrenal Insufficiency. On chemo for 2 1/2 years as experimental treatment for MG.

Posts: 4480 | From Northeastern Connecticut | Registered: Jun 2005 | 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/