Killer Green The Musical

Killer Green Flyer

Killer Green follows the lives of two pivotal couples in different stages of life as the two lead female characters battle a widely ignored chronic illness.  Based on biographical accounts, this musical attempts to uncover the dark truth behind how Lyme Disease affects its victims, educate viewers on the reality of these stories, and expose the widespread ignorance of the medical community.  This show has been graciously funded by The Wisconsin Lyme Network, a nonprofit organization dedicated to raising awareness for this cause.  https://wisconsinlymenetwork.org

Warning:  Killer Green depicts the reality of suicide, depression, and topics viewers might find disturbing but Lyme patients live with daily.

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Audra Cashman is a student graduating in Musical Theater at Peck School of the Arts at the University of Wisconsin Milwaukee.  Killer Green is her Senior Honors Project.

Ms. Cashman’s parents both have Tick borne illness and her mother heads a local support group for patients.  Killer Green draws upon personal experience and the experiences of many local Wisconsin patients.

 

 

 

 

 

 

https://www.lymedisease.org/canadian-lyme-consortium/

Canadian Lyme Consortium to confront escalating health crisis

Letter from the newly forming Canadian Lyme Consortium:

On behalf of a growing team of scientists, advocates, and clinicians, we wanted to let you know about a national research network that is taking shape to confront the escalating Lyme disease crisis.

The Canadian Lyme Consortium has evolved from the urgent need to accelerate progress in the understanding, detection, and treatment of Lyme disease, and to do so by meaningfully engaging patients in all levels of this process. The network unites advocates, established Lyme research groups including the Mount Allison Lyme Disease Research Network, The G. Magnotta Lyme Disease Research Lab at the University of Guelph, the Tick Microbiome Initiative at the University of Alberta, and other leaders in the fields of microbiology (Institut de Biologie Intégrative et des Systèmes (IBIS), Université Laval) and human and animal health who are eager to apply their skills to this challenging disease.

Together, we are committed to blazing a fresh trail informed by modern technologies, highly ethical research standards, and new approaches. As the Consortium develops, you can expect to see more visibility (website coming soon) as well as opportunities to contribute and participate. We look forward to working with you toward a brighter future.

Sincerely,

Vett Lloyd, Professor, Department of Biology, Mount Allison Lyme Research Network

Brenda Sterling-Goodwin, Patient representative

Roger C. Levesque, Full professor microbiology, Faculty of Medicine, Research Scholar of Exceptional Merit FRQS, IBIS, Université Laval

Melanie K. B. Wills, Adjunct Professor, Director, G. Magnotta Lyme Disease Research Lab, University of Guelph

Cezar Khursigara, Associate Professor, Department of Molecular and Cellular Biology, University of Guelph

George Harauz, Professor, Canada Research Chair, Department of Molecular and Cellular Biology, University of Guelph

Vladimir Bamm, Postdoctoral Research Associate, Department of Molecular and Cellular Biology, University of Guelph

 

https://www.ncbi.nlm.nih.gov/m/pubmed/29393980/

Bartonella henselae infection in a dog with recalcitrant ineffective erythropoiesis.

Randell MG, et al. Vet Clin Pathol. 2018. Feb 2. doi: 10.1111/vcp.12575. [Epub ahead of print]

Authors
Randell MG1, Balakrishnan N2,3, Gunn-Christie R4, Mackin A5, Breitschwerdt EB2,3.

Abstract

Ineffective erythropoiesis was diagnosed in an 8-year-old male castrated Labrador Retriever. Despite treatment with immunosuppressive therapy for suspected immune-mediated erythrocyte maturation arrest, resolution of the nonregenerative anemia was not achieved. Following documentation of Bartonella henselae bacteremia by Bartonella alpha proteobacteria growth medium (BAPGM) enrichment blood culture, immunosuppressive therapy was discontinued, and the anemia resolved following prolonged antibiotic therapy. Bartonella immunofluorescent antibody testing was negative, whereas B henselae western blot was consistently positive. The contribution of B henselae bacteremia to ineffective erythropoiesis remains unknown; however, the potential role of B henselae in the pathophysiology of bone marrow dyscrasias warrants additional investigation.

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**Comment**

All I could think of when I read this article was, “You lucky dog.”  How many Lyme/MSIDS patients have anemia due to an undiagnosed Bartonella infection?  Hard to say, but I’ll bet there’s a lot out here in Lyme-land.

Notice this lucky dog gets Dr. Breitschwerdt, the Bart Guru, taking care of him and using his special growth medium to detect Bartonella to begin with.  People don’t even get that.  Then, the lucky dog is put on prolonged antibiotic therapy, directed by someone who knows what he’s doing, and will live another day to chase squirrels.

Can I be a dog, please?

https://www.lymedisease.org/morgellons-month/

February is Morgellons Awareness Month

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The Charles E. Holman Morgellons Disease Foundation has designated February as Morgellons Awareness Month.

Morgellons, which appears to have a connection to Lyme disease, is a controversial diagnosis in the medical world. Sufferers are often dismissed by their doctors as being delusional.

According to the foundation, Morgellons Disease (MD) is a multi-system illness uniquely characterized by the formation of unusual fibers within the skin. MD is a debilitating, painful and life impacting condition consisting of slow-healing skin lesions, overwhelming fatigue, GI disturbances and an array of neurological deficits. Patients with Morgellons may shed unusual appearing particles from the skin described as fibers, sand or seed-like, black specks, or crystalized particles.

Holman Foundation President Cindy Casey and others from the organization have been heavily involved with a documentary film project (still being edited) called Skin Deep: The Battle Over Morgellons. You can watch a trailer of the film here:

http://

The 11th Annual Medical-Scientific Conference on Morgellons will be held on April 14-15, 2018 at the Wyndham Garden Hotel in Austin, Texas. This conference brings physicians, scientists, nurses, patients and their families together for 2 days of presentations. The very latest in research and treatment of Morgellons will be presented.

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More on Morgellons:  https://madisonarealymesupportgroup.com/2016/12/10/morgellons-in-dogs/

https://madisonarealymesupportgroup.com/2016/10/27/research-on-morgellons/

https://madisonarealymesupportgroup.com/2016/06/17/morgellons-believe-it/

https://madisonarealymesupportgroup.com/2016/12/05/new-book-on-morgellons/

 

 

https://www.curetalks.com/event/rsvp/Highlights-from-the-International-Lyme-and-Associated-Diseases-ILADS-18th-Annual-Scientific-Conference-Boston/292/?upcoming=yes  (Click here to hear talk.  Audio is located under the pictures of the doctors)

The Global Lyme Alliance is pleased to present Highlights from ILADS 18th Annual Scientific Conference, our expert panel of leading physicians will provide their insights and a summary of key data and research presented at this conference.

Physician Panel:
Dr. Kenneth Liegner, Physician, Author and Patient Advocate https://www.curetalks.com/cu/pub/profile/240/
Dr. Thomas Moorcroft, Co-founder of Origins Of Health, an Osteopathic wellness center https://www.curetalks.com/cu/pub/profile/242/
Dr. Leo J Shea III, Clinical Associate Professor of Rehabilitation Medicine at Rusk Institute, a division of the New York University-Langone Medical Center https://www.curetalks.com/cu/pub/profile/243/
Dr. Samuel Shor, Associate Clinical Professor, George Washington University Health Care Sciences https://www.curetalks.com/cu/pub/profile/241/

Patient Panel:
Jackie Bailey, NP at Apheresis Associates of Northern Virginia (AANV)
Jennifer Crystal, Writer and Educator

Lyme Disease talks are conducted in association with Global Lyme Alliance.

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**Comment**

Great info!  Thank you Global Lyme Alliance, physicians and patients for putting this on!