LymeNet Flash: Just bought Play only verion of Under Our skin

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 » Just bought Play only verion of Under Our skin

UBBFriend: Email this page to someone!

Author

Topic: Just bought Play only verion of Under Our skin

DeafFromLyme
LymeNet Contributor
Member # 18795

posted

Just bought Play only version of Under Our skin..

Hopefully having my family watch it will get them to understand why and how I have been sick for most of my life.

Although now that I am dx'd by LLMD they are starting to come around.

Very excited to see it myself!

--------------------
Erika

IgM Band 23 +

www.24weekperfectbaby.blogspot.com

Son's blog born at 24 weeks.

Posts: 356 | From massachusetts | Registered: Jan 2009 | IP: Logged |

MariaA
Frequent Contributor (1K+ posts)
Member # 9128

posted

Here's another really good, shorter video ( a TV report in Boston) that talks about the political controversies surrounding LYme treatment:
http://www.kettmann.com/Lyme/

--------------------
Symptom Free!!! Thank you all!!!!

Find me at Lymefriends, I post under the same name.
diet: http://lymefriends.ning.com/group/healthylowcarbrecipes
Homemade Probiotics thread
Herbal Links Thread

Posts: 2552 | From San Francisco | Registered: Apr 2006 | IP: Logged |

DeafFromLyme
LymeNet Contributor
Member # 18795

posted

Thanks!

--------------------
Erika

IgM Band 23 +

www.24weekperfectbaby.blogspot.com

Son's blog born at 24 weeks.

Posts: 356 | From massachusetts | Registered: Jan 2009 | IP: Logged |

bettyg
Unregistered

posted

erika,

just out top of support here for my VIDEO LYME COLLECTION; short videos!

good for you; hope they are RECEPTIVE, and give you feedback after it, and COMFORT!

IP: Logged |

Keebler
Honored Contributor (25K+ posts)
Member # 12673

posted

-

DeafFromLyme

I hope you contacted them for a transcript so you can read what is said - since it's not closed captioned.

When I contacted the folks who made the film, they said they would be glad to send a transcript for anyone needing it.

-

Posts: 48021 | From Tree House | Registered: Jul 2007 | IP: Logged |

DeafFromLyme
LymeNet Contributor
Member # 18795

posted

Thanks Keebler I did not know they could do that... I will look into it.

I am only deaf in my right ear so I can still hear I just have to place my self correctly when sitting to be sure the left ear is closest to the TV.

Its a pain and my family gets frustrated becaue I am constantly asking what they said or making them switch sides....

I was actually told how stupid I look because when people talk to me I automatically turn my good ear to them not realizing I'm doing it, so it looks like I am giving myself whiplash! [Smile]

--------------------
Erika

IgM Band 23 +

www.24weekperfectbaby.blogspot.com

Son's blog born at 24 weeks.

Posts: 356 | From massachusetts | Registered: Jan 2009 | IP: Logged |

lymielauren28
Frequent Contributor (1K+ posts)
Member # 13742

posted

Aww Erika bless your heart!! Who cares if you look stupid as long as you can hear.

It would be far stupider (is that a word?)to try and look "normal" and not hear a thing anyone is saying!

Tell whoever told you that to crawl in a hole [Wink]

Lauren

--------------------
"The only way out is through"

Posts: 1434 | From mississippi | Registered: Nov 2007 | IP: Logged |

DeafFromLyme
LymeNet Contributor
Member # 18795

posted

Thanks Lauren!

I did! [Smile]

and it felt good. [Smile]

My family hasn't exactly been supportive through this whole thing, so I am finally at a point where I tell whoever has anything negative to say to crawl in a hole! [Smile]

--------------------
Erika

IgM Band 23 +

www.24weekperfectbaby.blogspot.com

Son's blog born at 24 weeks.

Posts: 356 | From massachusetts | Registered: Jan 2009 | IP: Logged |

liesandmorelies
LymeNet Contributor
Member # 15323

posted

Good girl Erica,

You go!!!!

--------------------
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 |

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/