Category Archives: Voices on Lyme

People provide their independent input on the Lyme controversy … none are CanLyme approved or not.

Recent in: Voices on Lyme

Latest Lyme disease risk map for Nova Scotia

Lyme disease carrying species of ticks, Ixodes scapularis, have been in Nova Scotia for decades There is no part of the province where you are risk free.  This latest risk map … shows areas of greatest risk, moderate risk and lower risk.  Because the ticks are transported by birds such as robins, wrens, finches and other birds there is the Continues →

Watch Mount Allison University Lyme Research Network announcement partnering with the Canadian Lyme Disease Foundation

May 5th, 2017 One of the pillars within the mission statement of the Canadian Lyme Disease Foundation is promoting research. We are pleased to announce our partnership with Mount Allison University in assisting their Lyme Disease Research Network with funding. Developing a broad capacity within Canadian universities to cope with what the government of Canada has admitted is a coming Continues →

Mount Allison University and Canadian Lyme Disease Foundation announce partnership in research.

Mount A researchers uniting expertise against Lyme disease May 5th, 2017 CumberlandNewsNow.com Fourteen researchers have come together to form the Lyme Research Network to provide a co-ordinated way to respond to the research needs of the Lyme community, to develop research that looks at the issue from new perspectives, and to share findings. The researchers represent a variety of disciplines Continues →

Listen to AM 740 radio interview with CanLyme president Jim Wilson

Zoomer AM 740 radio interview with CanLyme president Jim Wilson  May 1st, 2017 Lyme disease a serious and growing concern.  Government and medical leadership refuse to allow experts who disagree with their policies to be at the table… very dangerous for the Canadian public. Listen now, go here and scroll down to hear CanLyme interview.  

PGA Champion Jimmy Walker diagnosed with Lyme Disease

Published: Wednesday, April 19, 2017 | 2:24 p.m. PGA Champion Jimmy Walker said he has felt fatigued since around Thanksgiving. After a long PGA Tour season, his first major championship title at Baltusrol and a scintillating Ryder Cup win at Hazeltine, most might think the late-year fatigue was normal. But lasting this long? Walker knew something wasn’t right. On Wednesday Continues →

June 3rd, Ottawa: We Need To Continue To Be VOCAL

We Need To Continue To Be VOCAL The Federal Framework on Lyme Disease Conference held in Ottawa in May of 2016 allowed for people suffering with Lyme disease to finally come together. Because of the opportunity, the idea of VOCAL was formed. VOCAL – Voices of Canadians About Lyme – is a cross-Canada Lyme awareness initiative whereby each province will Continues →

MP Ramsey says local Lyme disease sufferers feel betrayed by federal response

Brian Cross, Windsor Star MP Tracey Ramsey implored Canada’s health minister to scrap the draft framework on Lyme disease on Tuesday, describing how sufferers of the debilitating tick-borne illness are heartbroken by the government’s “status quo” approach. “There was hope that something would come out of this that would change the way Lyme disease is treated in Canada, and unfortunately this fails to Continues →

LymeHope Moms Bring Voices to the Hill

(04/12/2017) Ottawa, ON-Tens of thousands of Canadians, whose lives have been devastated by Lyme disease, are having their voices heard on Parliament Hill. Two Canadian moms, Jennifer Kravis and Sue Faber, who have both been diagnosed with Lyme disease, are delivering more than 10,000 petition comments and personal letters written by men, women and children.  These Canadians are literally pleading Continues →

Ottawa: Canadian politicians, scientists, physicians, and advocates unite in request of Minister Philpott to insist upon an ethical process

[CanLyme Note: No disease in history has ever been so massaged and manipulated behind closed doors as Lyme disease (borreliosis)  Is profit the motive? Keeping people sick and on pills for every symptom seems to be the approved Canadian policy while they refuse to transparently look at better tests that are available, and they refuse to allow potentially curative treatments.] View Continues →

Yet another United States state enacts a law to protect doctors who treat Lyme disease appropriately.

Unanimous legislative approval for bill on Lyme Disease treatment March 22nd, 2017 by O. Kay Henderson The Iowa legislature has voted to let Iowa doctors prescribe more aggressive treatment for Lyme Disease than is currently allowed by the state’s Board of Medicine, but the state’s medical community opposes the move. According to Representative Sandy Salmon of Janesville, the state Board Continues →

Mothers of children with Lyme are targeted by Infectious Disease doctors… Research concludes: not one single accusation of child abuse is valid

[CanLyme Note:  This same unethical and sinister practice goes on across Canada with many Canadian mothers of children with Lyme disease having been accused by infectious disease doctors of abusing their children because they seek effective treatment for their children. Most investigations are triggered by the parent taking the child to one of our Children’s hospitals where they wrongly thought Continues →