Archive for April, 2019

When Lyme Disease & Ehlers-Danlos Syndrome Overlap

https://www.lymedisease.org/lyme-ehlers-danlos/

When Lyme disease and Ehlers-Danlos syndrome overlap

 

 

CDC’s Long History of Incompetence/Deception in the Management of Lyme Disease

https://www.change.org/p/the-us-senate-calling-for-a-congressional-investigation-of-the-cdc-idsa-and-aldf/u/24438160?

The CDC’s long history of incompetence/deception in the management of Lyme disease

APR 17, 2019 — 

Please see the letter below to the TBDWG and links provided.

WAKE UP AMERICA!

———- Original Message ———-
From: CARL TUTTLE <runagain@comcast.net>
To: brett.giroir@hhs.gov, tickbornedisease@hhs.gov
Cc: (98 Undisclosed recipients)
Date: April 16, 2019 at 10:13 AM
Subject: Correspondence between Doctor Edwin J. Masters and Dr. David Dennis Chief; Bacterial Zoonoses Branch

To the Tick Borne Disease Working Group,

For the record I would like to share the attached correspondence between Doctor Edwin J. Masters and Dr. David Dennis Chief; Bacterial Zoonoses Branch dated 1992 as an example of the CDC’s long history of incompetence/deception in the management of Lyme disease. The letters are in reference to Lyme disease in the South and we know now through Quest Diagnostics [1] that –

Lyme has been detected in each of the 50 United States and the District of Columbia.

Doctor Edwin J. Masters letter:

https://www.dropbox.com/s/043q3onpw82ze46/Ed%20Masters%20and%20the%20CDC%20Testing.pdf?dl=0

We are dealing with a life-altering/life-threatening infection with faulty/misleading antibody tests, inadequate treatment, no medical training and absolutely no disease control.

A plague denied; essentially classifying this disease as a low-risk and non-urgent health threat.

To gain an understanding of Dr. Masters’ background in Lyme disease you will want to read the following article: (The CDC’s manipulation of data is appalling)

Rebel with a Cause: The Incredible Dr. Masters, Part 1

He braved hand-to-hand combat with CDC over Lyme in the South.

By Pamela Weintraub Posted Jun 25, 2009

https://www.psychologytoday.com/us/blog/emerging-diseases/200906/rebel-cause-the-incredible-dr-masters-part-1

“Front and center in the debate over the existence of Lyme disease in the southern U.S.  was the country doctor, Edwin J. Masters of Cape Girardeau, Missouri, who reveled in fighting for a cause.”

Respectfully Submitted,

Carl Tuttle

Lyme Endemic Hudson, NH

Lyme Disease: Call for a “Manhattan Project” to Combat the Epidemic

Raphael B. Stricker, Lorraine Johnson

Published: January 02, 2014DOI: 10.1371/journal.ppat.100379

http://www.plospathogens.org/article/info:doi/10.1371/journal.ppat.1003796

Reference:

1. New Quest Diagnostics Data Shows Lyme Disease Prevalence Increasing and is Now Present in New U.S. States

http://newsroom.questdiagnostics.com/2018-07-30-New-Quest-Diagnostics-Data-Shows-Lyme-Disease-Prevalence-Increasing-and-is-Now-Present-in-New-U-S-States

____________________
**Comment**
Dr. Masters, like a good handful of other doctors are true rock stars in my book.  This man, fought the CDC single-handedly and the details are seriously movie material. I highly recommend you read Weintraub’s entire series on him, but I’ve highlighted it here:  https://madisonarealymesupportgroup.com/2017/10/06/remembering-dr-masters-the-rebel-for-lyme-patients-who-took-on-the-cdc-single-handedly/

 

 

 

Texas Bill Would Increase Vaccine Safety, Reject Federal Narrative

AUSTIN, Texas (April 8, 2019) – A bill introduced in the Texas Senate would prohibit vaccines from being administered unless certain safety criteria are met. Passage of the bill would significantly strengthen vaccine safety testing requirements and push back against any future federal vaccine mandates.

Sen. Bob Hall (R) introduced Senate Bill 2350 (SB2350) on March 8. The legislation would only permit a health care provider to administer a vaccine if all of the following criteria are met.

  • The study the U.S. Food and Drug Administration (FDA) relied upon for approval of the vaccine evaluated the vaccine against a placebo control group or against another vaccine or substance that the FDA approved based upon a placebo-controlled study;
  • The study relied upon by the FCA for approval of the vaccine evaluated the safety of the vaccine for a sufficient time to identify potential autoimmune, neurological, or chronic health conditions that may arise on or after a year from the vaccine being administered;
  • The vaccine has been evaluated for its potential to cause cancer, mutate genes, affect fertility, cause infertility and cause autism spectrum disorder;
  • The Texas Department of State Health Service has posted on its website disclosure of any known injuries or diseases caused by the vaccine and the rate at which the injuries or diseases have occurred; and
  • The chemical, pharmacological, therapeutic, and adverse effects of the vaccine and the rate of injury of the vaccine when administered with other vaccines, have been studied and verified.

Effect on Federal Policy

After recent comments by former FDA Commissioner Dr. Scott Gottlieb in February of 2019 just prior to his resignation, some believe that federal vaccine mandates are imminent.  According to CNN, Gottlieb said,

“[I]f states don’t require more schoolchildren to get vaccinated, the federal government might have to step in.” Gottlieb also reportedly said, “You could mandate certain rules about what is and isn’t permissible when it comes to allowing people to have exemptions.” [1]

As discussed below, current vaccine safety testing requirements are far less stringent than most would assume.  Passage of SB 2350 would bolster these requirements and make enforcement of any federal vaccine mandates more difficult.

Number of Recommended Vaccines Steadily Rise Since Removal of Liability

Vaccine mandates are generally based upon the vaccine schedules recommended by the Centers for Disease Control and Prevention (CDC). Because vaccines pose a risk of injury or death, liability is associated with them. Many Americans are unaware that the pharmaceutical industry is shielded from liability for harm caused by most vaccines. This unique legal protection was put into place as a result of legislation passed in 1986, after extensive lobbying by the pharmaceutical industry. Manufacturers of other products don’t enjoy this freedom from liability. Due to lack of liability, vaccines are the pharmaceutical industry’s most lucrative product.

The 1986 law also created the National Vaccine Injury Compensation Program (NVICP), which is essentially a special system outside of the normal litigation process to hear claims of harm caused by vaccines. Any compensation granted by the NVICP is paid by the public, through a surcharge on vaccines, and not by vaccine manufacturers. To date, over four billion dollars has been paid under this system to compensate for harm caused by vaccines. [2]

Further, although discovery is a right afforded to litigants in most other legal forums, discovery is not permitted in the NVICP process. This protects vaccine manufacturers from having to search for, and produce, relevant information, including damaging information. In cases involving prescription medication, which are heard in other legal forums, information unfavorable to the pharmaceutical industry has come to light through discovery, such as the damaging e-mails which were required to be produced in the Vioxx litigation. [3]

In the absence of pharmaceutical industry liability for most vaccines, the number of vaccines recommended by the industry and the CDC is steadily rising. For example, in 1983, the CDC recommended that children receive 23 doses of seven vaccines. By 2017, the number of vaccines it was recommending rose to 69 doses of 16 vaccines starting on the day of birth to age 18, with 50 doses of 14 vaccines given before age 6. [4] Since 2002, a CDC adult vaccine schedule has also existed. [5] Like with the childhood schedule, the number of recommended vaccines and doses on the adult schedule has continued to rise. Furthermore, there are hundreds of new vaccines in the developmental process and the number of CDC recommended vaccines is expected to continue to rise.

Inadequate Vaccine Safety Testing

Lack of adequate safety testing is a common concern of opponents of mandatory vaccines and SB 2350 addresses this critical issue.

Many Americans believe that vaccines undergo the same safety testing as drugs prior to their approval. However, this is incorrect. In fact, vaccines and drugs are subject to different rules because the FDA has chosen to classify vaccines as “biologics” rather than “drugs.” Drugs are required to undergo multi-year, double-blind inert placebo studies, widely known as the gold standard of safety science, prior to licensing. Vaccines, on the other hand, are not required to undergo inert placebo-controlled studies for approval. [6] Furthermore, unlike the lengthy periods required for drug safety studies, vaccine safety studies monitor for adverse reactions for very short periods of time, often of fourteen days or less. [7] Additionally, although children frequently receive multiple vaccines at the same time in accordance with the CDC’s recommended schedule, vaccine manufacturers are not required to test the safety of the vaccines in these combinations. [8]

In fact, there is a multitude of reasons, in addition to inadequate safety testing, to question the mandating of vaccines. For example, the ingredients in them are often cited as a source of concern. The ingredients in each type of vaccine differ but, generally, vaccines contain a myriad of toxic or concerning substances such as aluminum, antibiotics, formaldehyde, Polysorbate 80, bovine extract, egg protein, monosodium glutamate (MSG), squalene, and aborted human fetal tissue. [9], [10]. Additionally, several recently published books set forth scientific information which raises concerns about vaccines, including the book Miller’s Review of Critical Vaccine Studies: 400 Important Scientific Papers Summarized for Parents and Researchers by Neil Z. Miller, which contains over 400 peer-reviewed scientific studies. [11] In another book, Vaccines – A Reappraisal, Dr. Richard Moskowitz, a family physician with over fifty years of experience, discusses a wide range of troubling information concerning vaccines, such as:  epidemiological research which indicates that vaccines may interfere with the normal development of a healthy immune system; information concerning the role that vaccines can play in causing infectious disease outbreaks; and evidence of the surprisingly low effectiveness levels of many vaccines. [12] J.B. Handley’s book How to End the Autism Epidemic also contains a wealth of information concerning potential harm caused by vaccines, particularly focusing on aluminum, a toxic metal used as an adjuvant in many vaccines, and on evidence of a causal link between vaccines and autism. [13] As these works clearly indicate, the science is not settled with regard to whether vaccines are safe or necessary.

State Action Needed

Federal regulation becomes ineffective when states enact contradictory policies. If multiple states ban mandatory vaccinations or pass laws which conflict with the CDC’s recommended schedules, it will become extremely difficult for the federal government to enforce future federal mandates. Such state laws will also undermine the federal narrative and make it harder for the feds to generate support for nationwide mandatory vaccine policies. By passing SB 2350, Texas has the opportunity to lead on this important issue and to become the potential standard bearer for resisting federal vaccine policy at the state level.

NOTES

[1] Cohen, Elizabeth and Bonifeld, John, “FDA chief: Federal government might step in if states don’t change lax vaccine laws.”  CNN.com. Cable News Network. Web. 20 Feb 2019, https://www.cnn.com/2019/02/20/health/vaccine-exemptions-fda-gottlieb/index.html.  Accessed 7 April 2019.

[2] Children’s Health Defense. “$4 Billion and Growing:  U.S. Payouts for Vaccine Injury and Deaths Keep Climbing.” www.ChildrensHealthDefense.org. Web. 19 Nov. 2018,   https://childrenshealthdefense.org/news/4-billion-and-growing-u-s-payouts-for-vaccine-injuries-and-deaths-keep-climbing/. Accessed 7 April 2019.

[3] Berensen, Alex, “Jury Finds Merck Liable in Vioxx Death and Awards $253 Million.”  nytimes.com. Web. 19 Aug. 2005, https://www.nytimes.com/2005/08/19/business/jury-finds-merck-liable-in-vioxx-death-and-awards-253-million.html. Accessed 7 April 2019.

[4] National Vaccine Information Center. “A Guide to Reforming Vaccine Policy and Law.” http://www.nvic.org. Web. 26 Sept. 2018, https://www.nvic.org/Vaccine-Laws/state-vaccine-requirements/Reforming-Vaccine-Policy—Law-Guide.aspx. Accessed 7 April 2019.

[5] Centers for Disease Control and Prevention, Immunization Schedules, Table 1. Recommended Adult Immunization Schedule for ages 19 years or older, United States, 2019. Web. 5 Feb. 2019, https://www.cdc.gov/vaccines/schedules/hcp/imz/adult.html. Accessed 7 April 2019.

[6] Robert F. Kennedy, Jr. “Vaccines and the Liberal Mind.” Children’s Health Defense. www.ChildrensHealthDefense.org. Web. 14 June 2018, https://childrenshealthdefense.org/news/vaccines-and-the-liberal-mind/. Accessed 7 April 2019.

[7] Moskowitz, Richard, Vaccines – A Reappraisal. New York, New York: Skyhorse Publishing, 2017. 31-42. Print.

[8] Imus, Deirdre.  “Toxic Vaccine Ingredients:  The Devil is in the Details.”  www.ChildrensHealthDefense.org. Web. 6 March 2018, https://childrenshealthdefense.org/news/toxic-vaccine-ingredients-the-devils-in-the-details/. Accessed 7 April 2019.

[9] Ibid

[10] National Vaccine Information Center. “New Human Fetal Cell Lines Available for Vaccine Production.”  http://www.nvic.org. Web. 15 Jan. 2018, https://www.nvic.org/nvic-vaccine-news/january-2018/new-human-fetal-cell-lines-for-vaccine-production.aspx. Accessed 7 April 2019.

[11] Miller, Neil Z., Miller’s Review of Critical Vaccine Studies: 400 Important Scientific Papers Summarized for Parents and Researchers, Santa Fe, New Mexico: New Altantean Press, 2016. Print.

[12] Moskowitz, Richard, Vaccines – A Reappraisal. New York, New York: Skyhorse Publishing, 2017. Print.

[13] Handley, J.B., How to End the Autism Epidemic. White River Junction, Vermont: Chelsea Green Publishing, 2018. Print.

_____________________

This says it all:

iu

 

 

 

 

 

Cancer Crusaders: Canine Patients Advancing Better Therapies

https://www.vetmed.wisc.edu/cancer-crusaders/

Cancer Crusaders

How today’s canine patients help to advance better cancer therapies for pets and people

Rossi, a seven-year-old Alaskan Malamute, visits UW Veterinary Care for treatment as part of an oncology clinical trial

Rex, a five-year-old Cane Corso weighing in at 100 pounds, had a summer to remember in 2018.

Swimming in Lake Michigan, enjoying walks in the woods, dipping his feet into a nearby creek, and relishing adventure after adventure. All the while adapting to life on three legs.

“Me and Rex had probably the best summer of our lives once he got his leg amputated,” says owner Trevor Smithson. “We did so many fun things together.”

Rex’s left hind leg was amputated in July due to osteosarcoma, a type of bone cancer, and he began chemotherapy soon after. A few months later, it was discovered that Rex’s cancer had spread to his lungs. In the new year, cancerous tumors were found in two of Rex’s other legs.

Rex, a five-year-old Cane Corso battling osteosarcoma

Rex and Smithson have faced each diagnosis with a brave spirit and a goodwill that may one day help other patients — both dogs and people — facing similar situations. As part of Rex’s treatment regimen, he has taken part in several clinical studies — investigational trials of novel, potentially more effective treatment options with applications in veterinary and human medicine.

The UW School of Veterinary Medicine (SVM) is an early and national leader in this field of research, known as comparative oncology, studying naturally occurring cancers in pets as models for human disease. The goal is to advance new cancer therapies and diagnostics that could benefit animals and people. The decoding of the canine genome in 2005 spurred a larger effort among researchers to apply a comparative, “one medicine” approach to better understand, diagnose, and treat diseases with a genetic basis, such as cancer.

“The answer to cancer may be walking beside us,” notes David Vail, professor and Barbara A. Suran Chair in Comparative Oncology at the SVM.

Past clinical studies in oncology at the SVM have yielded new immunotherapy drugs in research first led by Greg MacEwen, one of the school’s founding faculty members; chemotherapy and radiotherapy treatments with better effectiveness and less toxicity; and revolutionary new technologies. For example, successful clinical trials in pet dogs with nasal tumors at UW Veterinary Care in the early 2000s, shepherded by Professor Lisa Forrest, led to widespread use of TomoTherapy in human medicine. This state-of-the-art radiation machine built into a CT scanner, developed at UW–Madison, allows for precise delivery of radiation therapy to attack tumors while sparing healthy tissue. More than 500 TomoTherapy units are now installed in human hospitals worldwide and the SVM remains one of only two veterinary medical hospitals in the world to offer this technology.

Conquering Cancer Together

An important goal of comparative oncology clinical trials is to raise the current standard of cancer care. In veterinary and human medicine, recurrence and metastasis (the spread of cancer) for aggressive tumors is “a very real problem,” says Vail. “We have such a long way to go both in physician-based and veterinarian-based oncology.”

“For some very aggressive cancers, we truly don’t have a good standard of care or the standard of care available fails our patients in that we’re not achieving high cure rates,” he adds. “Having the opportunity to use and apply this one medicine approach more globally in all species will allow us to help humans with cancer, while also helping our veterinary patients. It’s a huge need that we are working to move forward.”

Cancer by the numbersDogs and people not only share similar cancer rates — about one in four dogs and one in three people will develop cancer in their lifetime — but naturally occurring tumors in dogs and other companion animals often share almost identical characteristics to human cancers in terms of biological behavior, therapeutic response, metastasis, and more.

What sets dogs apart, as those who have loved and lost a canine companion know all too well, is their shorter lifespan, which also speeds the cellular clock. Cancers tend to develop, spread, and grow faster in dogs.

“You talk about one dog year equals seven people years; the same holds true for cancers,” says Vail. “Things progress quicker and occur at an earlier age. Chronologically, everything is compressed.”

This abbreviated timeline, while heartbreaking for an affected dog’s family, means that oncologists can determine much more quickly whether a cancer treatment works or doesn’t work. This is an important advantage of clinical trials in client-owned pets, potentially accelerating the development of better cancer therapies more rapidly and less expensively.

At Great Cost

According to Vail, it currently takes an average of 10 to 15 years and a cost of approximately $1.5 billion per drug to develop a new FDA-approved oncology medicine. Some cancer drugs can cost human patients more than $100,000 for a year’s treatment. Contributing to this toll in time and money is the high number of drug candidates that fail in human clinical trials. Only about five percent of oncology therapies make it from first-in-human clinical studies to final drug approval.

“Where we feel comparative oncology can really help is by including companion species in this preclinical work, as they may better recapitulate the human condition than artificial rodent models,” says Vail.

While important for studying cancer biology, the mouse models of cancer that are often used in medical research — immunosuppressed, with tumors that have been implanted — lack many characteristics of human cancers. Thus, there is a disconnect between the number of anti-cancer therapeutics that work in mouse models versus in human patients, says Mark Albertini, an associate professor of medicine at UW–Madison and chief of oncology at the William S. Middleton Memorial Veterans Hospital.

“In contrast, many human clinical trials have benefited from the translational dog model,” he says.

Successful clinical trials in dogs with nasal tumors at UW Veterinary Care, shepherded by Professor Lisa Forrest, led to widespread use of TomoTherapy in human medicine

Cancer arising in dogs naturally,

“is genetically closer to the human condition, where each person is genetically distinct and their cancers are the same,” adds Jacques Galipeau, the Don and Marilyn Anderson Professor in Oncology and associate dean for therapeutics development at the UW School of Medicine and Public Health. In laboratory rodent models, all mice are genetically identical, he explains. “Though you can treat 100 mice, it is more like treating a single mouse a hundred times. Treating cancer in dogs is a more robust, reality-based test of innovative treatments.”

Moreover, Galipeau says, researchers can deploy novel cancer treatments in client-owned animals at a rate that far outpaces the regulatory, pharmaceutical, and cost constraints of human studies. (Clinical trials in companion animals must meet their own strict criteria and are rigorously executed. All studies conducted at the SVM are reviewed and approved by the school’s Animal Care and Use committee to assure minimal risk to the patient and to guarantee that animal welfare requirements of the National Institutes of Health and Food and Drug Administration are met.)

“Our canine clientele can benefit from ethically sound, FDA-compliant clinical trials of therapeutic innovations far quicker and more cheaply than is achievable in humans,” Galipeau notes. “Lessons learned in dogs subsequently inform the best path to pursue in equivalent studies in people — hence the ‘comparative therapeutics’ angle.”

This bidirectional flow of new technologies and therapies is critical for veterinarians such as Vail. “Yes, we’re informing human clinical trials, but at the end of the day we are veterinarians and it’s really important to ensure that our veterinary patients are benefiting as well,” he says.

A Chance to Help Children

Osteosarcoma, a highly aggressive and painful bone cancer, has long been a poster child for the potential of comparative oncology, according to Vail. This disease affects both dogs and people and shares the same metastatic pattern and genetic profile between the two species.

In humans, osteosarcoma tends to occur in children, preteens, and teenagers.

“It is a devastating disease,” Vail says. Only about 800 cases are diagnosed annually in North America, which has led to the disease being understudied in human medicine, he says. “It’s essentially been orphaned because there are so few patients.”

In dogs, however, the disease is far more common, often affecting the long bones of large breed dogs. More than 20,000 new cases are seen each year in North America. Despite therapy (limb amputation plus chemotherapy), most dogs succumb to the disease within a year of diagnosis due to cancer spreading to other parts of the body.

Gus, a 9-year-old Rhodesian Ridgeback mix who recently completed treatment for osteosarcoma, is participating in an oncology clinical trial at UW Veterinary Care

The large number of patients seen in veterinary medicine allows researchers to evaluate new therapeutics in a way that wouldn’t be possible by studying humans alone.

“Median survival for a dog with standard of care therapy is one year and median time to progression in kids, when the disease starts to worsen or spread, is about five years,” Vail explains. “So we get information that much quicker.”

SVM oncologists are working to uncover osteosarcoma’s underlying causes and develop more effective therapies. The school is one of several sites, for example, now investigating a new approach to stimulate the body’s own immune system to attack any remaining tumor cells in osteosarcoma patients. This clinical trial is sponsored by the Morris Animal Foundation and the National Cancer Institute as part of an innovative 5/5/5 initiative to test five drugs, in five years, for approximately $5 million.

Dogs participating in the trial receive a vaccine made from the bacteria Listeria monocytogenes, which has been genetically modified to express a tumor protein found in many cancer cells, including canine bone cancer cells. When injected into the bloodstream, this modified Listeria stimulates the immune system to attack cells expressing the specific tumor protein. The goal is to delay or prevent the spread of cancer following removal of the primary bone cancer tumor and chemotherapy.

Veterinarians Serving Veterans

The SVM has also just launched a four-year trial of a new immunotherapy treatment for malignant melanoma. A common skin cancer in humans and a common oral cancer in dogs, melanoma frequently spreads within the body, resulting in poor survival rates once it reaches distant sites.

This investigational drug will be tested in dogs with melanoma at UW Veterinary Care and in a related study of human melanoma patients. The project is led by Albertini, who in addition to his roles at the Veterans Hospital and UW Health directs the Comprehensive Melanoma Clinic at the UW Carbone Cancer Center. He and Vail have worked collaboratively for several years to identify new melanoma treatments. This latest study is funded by the Department of Veterans Affairs; veterans who have served in the Middle East experience sunlight exposure and melanoma at rates higher than the general population.

With the treatments and novel therapeutics that we look at, the types of things that work in the dog tend to work in people, and the types of things that work in people tend to work in dogs.”

David Vail, professor and Barbara A. Suran Chair in Comparative Oncology

“This is the first Veterans Administration-funded companion animal trial,” says Vail. “We see a lot of malignant melanoma in canine populations — in our clinic, almost daily — and this granting agency recognized the value of the comparative approach.”

The study involves injecting an immune stimulant directly into melanoma tumors to turn the cancerous tumor, while still in the body, into its own anti-cancer vaccine. The treatment may allow patients with melanoma to live longer or even be cured.

“We know that in a tumor developing in a person or dog, it’s no longer presenting as foreign to the immune system, otherwise the immune system would do the job it’s supposed to do,” Vail explains. “We’re trying to trick it back and make the tumor immunogenic again, provoking an immune response.”

MRI and CT scans of dogs who have received the treatment show promising preliminary results. “The tumor becomes very quiet after immunotherapy, with fewer cancer cells dividing,” says Vail. “Importantly, the lymph node, which is kind of the immune fort that gets turned on to attack the tumor and send in anti-cancer cells, becomes more active.”

SVM researchers are collaborating with oncologists at the Carbone Cancer Center to develop novel ways of using advanced medical imaging to determine which patients are benefiting from immunotherapy and which are not — an emerging need as more and more immunotherapies are deployed across cancer types. “That’s important because these drugs are very expensive and they do have side effects,” Vail says.

Gaining Momentum

Writing in The Veterinary Journal, Vail and coauthor Douglas Thamm of Colorado State University note that “a new era of clinical trial awareness, brought on by new consortia and cooperative groups, is beginning.”

The Comparative Oncology Program at the National Cancer Institute and the Comparative Oncology Trials Consortium, of which the SVM is a founding member, are among the initiatives that have emerged to bring researchers together and provide needed resources.

In 2015, a national workshop hosted by the Institute of Medicine’s National Cancer Policy Forum served to build momentum among scientists, veterinarians, physicians, and the general public toward greater integration of pet clinical trials into translational cancer research.

Last year, the Open Philanthropic Project awarded a $6 million grant for the largest clinical study conducted to date for canine cancer. This five-year trial, being performed at the SVM and two other institutions, will test a novel vaccine strategy for the prevention, rather than the treatment, of many types of cancer in dogs — a potential paradigm shift in veterinary and human medicine.

Trevor Smithson and his dog Rex

Most recently, the V Foundation for Cancer Research launched a grant-making program to accelerate comparative oncology research through grants to five top veterinary schools, including the UW School of Veterinary Medicine, paired with five leading human cancer centers. As part of this effort, the SVM has partnered with the UW Carbone Cancer Center to form the Comparative Oncology Working Group, together conducting studies and clinical trials aimed at more efficient cancer prevention, diagnosis, and treatments for pets and people.

Vail says the thousands of pets and pet owners that take part in the school’s oncology clinical studies are critical partners in advancing this work, “helping to push the envelope as far as what can be done to prevent and treat cancer in the future.”

“Our clients come to us demanding high-quality care and access to novel therapeutics and novel technologies,” he says. “They’re highly motivated.”

For Smithson, who has logged countless miles driving from Chicago to the University of Illinois, Ohio State University, and then to UW to allow Rex to participate in oncology clinical trials, the novel therapies have offered optimism in Rex’s battle with cancer. “It’s always good to have a little hope blown into your sails,” he says.

The decision to enroll in the trials hasn’t always been easy for Smithson, who says Rex’s quality of life has guided his decisions. “If Rex didn’t want to live, we wouldn’t have even considered it.”

“I talked to him quite a little bit about this, even before he had his leg amputation, and said ‘If you want to live and you want to fight, I’ll fight with you. And if you don’t want to do it, I’m not going to make you.’ Because there’s no point in doing all this if he’s not happy,” Smithson adds. “But he still finds it in him to wag his tail, eat his food, and chew on his toys. As much as he’s been through, it hasn’t hampered his spirit one bit.”

Meghan Lepisto

Editor’s note: We regret to share that Rex, featured in this article, passed away in March following a courageous battle with cancer.

Categories: Medical Sciences News, On Call, Research News, School News, UW Veterinary Care News.

 

Teenage Lyme Disease Patient & TickTracker App Inventor Honored by U.S. Government for Groundbreaking Lyme Disease Advocacy

https://www.globenewswire.com/news-release/2019/02/25/1741823/0/en/Teenage-Lyme-Disease-Patient-and-TickTracker-App-Inventor-Honored-by-U-S-Government-for-Groundbreaking-Lyme-Disease-Advocacy.html

Teenage Lyme Disease Patient and TickTracker App Inventor Honored by U.S. Government for Groundbreaking Lyme Disease Advocacy

14-year-old Olivia Goodreau youngest ever to participate in Department of Commerce –The Opportunity Project

Denver, Colo., Feb. 25, 2019 (GLOBE NEWSWIRE) — 14-year-old Lyme disease patient, advocate and technology pioneer Olivia Goodreau will be in Washington D.C. February 27 – March 1 to be honored for her groundbreaking TickTracker App, which works to gather data and alert the world to tick sightings in an effort to decrease the number of Lyme and tick-borne disease cases. Selected for The Opportunity Project’s 14-week TOP Health Sprint (TOP), Olivia became the youngest inventor ever to participate in the program which is conducted by the Department of Commerce.

Olivia will travel to Washington D.C. to participate in the Census Bureau’s TOP Demo Day, Friday, March 1. The event will showcase 20+ new innovative tech tools to more than 15 governmental agencies searching for effective ways to solve some of the world’s most critical challenges. Olivia’s TickTracker App was also selected by the Department of Health and Human Services as one of the most impactful technological creations coming out of the TOP Health Sprint. This recognition has garnered Olivia an invitation to present at the TOP Health Showcase at the Eisenhower Executive Office Building on the White House grounds Thursday, February 28 at the request of the Presidential Innovation Fellows and Department of Health and Human Services. Olivia will also meet with a growing list of Congressional members and top scientists on Wednesday, February 27 as a part of her three-day visit.

Olivia’s schedule for this unique media opportunity includes:

  • February 27
    • Congressional Visits to Multiple Members of the U.S. Congress
    • 2:30 – 4:30 p.m. (Press Invited and Credentials Needed)
  • February 28
    • White House Grounds Presentation (Not a Press Event)
    • 9:00 a.m. Artificial Intelligence and Open Data Innovation for Health
    • 3:00 p.m. Lafayette Building – VA – TOP Health: Together, Futurecasting Next Steps
    • (Press Invited and Credentials Need)
  • March 1
    • U.S. Census Bureau
    • Noon–3:3:30 pm The Opportunity Project (TOP) Demo Day at Suitland, Maryland
    • 3:30 – 5:00 p.m. Office Location – (Press Invited and Credentials Needed)

Olivia’s Story
Stricken with Lyme disease after a tick bite while on a family vacation to Missouri in the second grade, doctors struggled to find out what was wrong with Olivia since she did not present the common bulls-eye rash. After being seen by 51 different physicians, she was finally diagnosed with Lyme disease. Currently, she takes over 80 medications daily and several IVIG treatments monthly causing her to not only miss out on school, but a normal life of a 14-year-old girl. This experience prompted her to start the LivLyme Foundation where she devotes countless hours to the cause through supporting research, organizing fundraising events, and developing a life-saving app called TickTracker. Olivia has been honored by prominent research universities for her work, presented before federal officials and agencies, helped pass critical state legislation, raised more than $1 million to fund Lyme disease research, and continues to offer grants to treat under-insured children and young adults affected by Lyme.

Olivia’s Technological Solution -TickTracker App

  • In an effort to help curb new cases of Lyme disease, Olivia launched the TickTracker app which went live on the Apple and Google Play stores in February 2018.
  • Olivia recognized the need for technology to play a role in tick sightings and prevention, which she hopes will ultimately help to find a cure for the disease.
  • TickTracker helps combat tick transmitted infections and disease by showing real time and historic tick activity data on an interactive map through reported sightings and bites. The app also educates users on tick prevention and safety.
  • TickTracker uses a patent pending algorithm to coordinate multiple tick activity data sources into a simple and user-friendly map view. https://ticktracker.com/

Why Olivia’s Important Work Matters

  • Olivia has raised more than $1 million in two years, has given medical assistance grants to 31 kids ages 5-21 in 28 different states who are stricken with the disease, and has given four research grants to top scientists at Stanford, John Hopkins, and the University of New Haven.
  • She has received 260+ grant applications for medical assistance from kids in 48 different states and the numbers of grant applications continue to increase.
  • According to the Tick-Borne Disease Working Group’s 2018 report to Congress, over the past 25 years, reports of Lyme disease have increased steadily with estimated annual cases numbering approximating 300,000.
  • The report goes on to say, “the number of U.S. counties now considered to be of high incidence for Lyme disease has increased by more than 300% in the Northeastern states and by approximately 250% in the North-Central states.”
  • Most often transmitted by tick bites, Lyme disease has been found in all 50 US states and in more than 60 other countries, which is why public awareness of its symptoms and possible contraction is so critical.
  • Not only are these numbers staggering, the U.S. is not fully prepared for the explosive increase in the tick population.
  • With the discovery of the Asian Longhorn Tick in 2017, health officials are concerned about the case numbers increasing. This particular tick, which can also be found on pets, livestock, and wildlife, can reproduce without mating. Swarms of ticks can attack in numbers of 1,000 or more on one animal or person.
  • For more information on ticks, prevention and the LivLyme Foundation, visit: https://livlymefoundation.org/

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Jeff Howard
Gomez Howard Group
303-513-1628
jeff@gomezhowardgroup.com