LymeNet Flash: Under Our Skin Screening

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 » Under Our Skin Screening - Today in Lyme

UBBFriend: Email this page to someone!

Author

Topic: Under Our Skin Screening - Today in Lyme

thatbrian
Member
Member # 23520

posted

Where else should you see a screening of Under Our Skin but Lyme, CT? Film starts at 2:00 - details below.

See you there!

Lyme Public Hall

March 21 (Sunday) 2PM - 4:30PM
Under Our Skin - Lyme Disease Documentary

"Under Our Skin" is a film that exposes the hidden story of Lyme disease. Information on the film can be seen on "www.underourskin.com".
A presentation by Lyme disease experts, Kim Ruggiero and Dr. Eva Sapi, Ph.D., will follow the film. Kim Ruggiero, artist and gallery owner, is a victim of Lyme disease who was misdiagnosed for years before receiving treatment. Subsequently, Kim has spent many years educating the public about the disease. Dr. Eva Sapi, professor of biology and environmental studies at the University of New Haven, will discuss her pioneering research on the bacteria that causes Lyme Disease.

Posts: 20 | From Stamford, CT | Registered: Dec 2009 | IP: Logged |

Robin123
Moderator
Member # 9197

posted

Wow - talk about bringing coals to Newcastle - let us know what the True Lymies said! And where is Polly Murray?

Posts: 13171 | From San Francisco | Registered: May 2006 | IP: Logged |

kam
Honored Contributor (10K+ posts)
Member # 3410

posted

Wow!

Posts: 15927 | From Became too sick to work or do household chores in 2001. | Registered: Dec 2002 | IP: Logged |

thatbrian
Member
Member # 23520

posted

After talking with several people before and after the film, I was amazed by what I heard. Believe it or not, people that live in the town that the disease was named after have had the same difficulty getting a dx as the rest of us have had!!!

Posts: 20 | From Stamford, CT | Registered: Dec 2009 | IP: Logged |

thatbrian
Member
Member # 23520

posted

quote:
Originally posted by Robin123:
Wow - talk about bringing coals to Newcastle - let us know what the True Lymies said! And where is Polly Murray?

Polly Murray did not make it, but we were told that she would be at the conference in May:

The 2010 Lyme Disease Symposium Saturday, May 8th, 2010

Dodds Hall Auditorium
The University of New Haven

8:30 AM - 8:00 PM

Posts: 20 | From Stamford, CT | Registered: Dec 2009 | 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/