224 petitions

Update posted 17 hours ago

Petition to Canadian Ministers of Health, Justice, Amnesty International

Save Canadian Inuit Children: Every year in Canada about 30 Canadian Inuit young people die by suicide. These deaths are entirely preventable. Please take immediately the necessary action to bring these rates to close to zero.

See us at, and on Youtube HeyZorgzilla, Inukulu, and DizzyandSockless, and Piujuq Inuit Art Studios.  Help saves the lives of 30 Canadian Inuit young people this year.  Give Canadian Inuit young people and their families hope.  Please. Thank you, Qujannamiik, Merci. .For more information on heavy metal toxicities, and how it may contribute to ill health, and suicides see this research by Rice and his co-workers: No wonder so many of us Inuit are ill.  Too bad we cannot go to the Health Centers, and be tested for  heavy metals, and then if found positive, have them removed from our bodies (yes, there is scientific and proven way of doing that). For the test for mercury a small piece of hair is put in an envelope and sent to Doctors Data's lab in the US. It costs about $80.00. That's all, and then you'll know if you have to much mercury in your body and brain.  It's not that complicated or difficult.  It just seems that the powers that be are for whatever reason not motivated to provide funding for this, or to do it.  Let's motivate them, shall we?   Please sign our petition.  Together we can do this. We are not powerless.

Piujuq Inuit Art Studios
4,573 supporters
Update posted 1 week ago

Petition to Health Minister Petitpas Taylor, Prime Minister Justin Trudeau, Public Health Agency of Canada, Lyme Letters Campaign, CanLyme

Ticking Lyme Bomb in Canada. YOU are at RISK. Sign now!

*Updated: May 10, 2018 We have set up a national not-for-profit organization - LymeHope:   Lyme disease is one of the fastest spreading infectious diseases in the world. According to a 2017 national Canadian benchmark survey, 4 MILLION Canadians report that they, or someone they know in Canada, has been diagnosed with Lyme disease.  Yet people are still being told "no Lyme here" and being denied proper assessment of symptoms, diagnosis and adequate treatment.  This is unacceptable. Please sign this petition asking the Canadian Government to reject the current Action Plan (Framework) for Lyme disease and FIX IT.   The Framework must recognize the seriousness of this disease for all of us.  Time is ticking. Canada’s current Plan is GROSSLY inadequate.  You could be the next BITE. Lyme Disease is carried by ticks, which are migrating all across Canada at an alarming speed.  Canadian scientists predict that by the year 2020, 80% of the population in Eastern Canada (including Manitoba) will be living in a tick-populated area. [1] Ticks are rapidly spreading in the West as well. The Lyme bacteria can also be passed from pregnant mother to her child in the womb [2] and there are concerns this infection may be sexually transmitted.[3]  Babesia, a Lyme Co-Infection, has been found to be in the U.S. blood supply.[4] According to the Centre for Disease Control (CDC), there are more than 300,000 NEW cases of Lyme in the US every year most of which occur within 400 miles of the Canadian border.  The numbers in Canada are also growing FAST.[1] In 2014 Bill 442 was passed, requiring the Canadian Government to create a Lyme Action Plan (Framework).  The final Framework was released in May, 2017.  This Framework fails to take real action, has minimal funding, and fails to protect Canadians from Lyme.   We need you to sign this petition to demand this Framework be rejected in its current form. All Canadians are at risk.  All it takes is a walk in the grass, a hike on a trail, a day of gardening or golf and for our kids - playing outside in the schoolyard or in a park.  Your pets can bring ticks into your house. Who would think that a tick the size of a poppy seed you may never notice, has the impact of a bomb going off in your body and your life? In this video, you will meet Nicole Bottles, a 24 year old from Victoria B.C., who explains her 9-year battle with Lyme disease from her wheelchair.  She was just 15 years old in Grade 10, when her life as she knew it changed forever. Nicole highlights the problem we are all going to face.  A tick explosion is underway.  Canada is currently NOT equipped to prevent, educate, diagnose or treat people who get infected.  Nicole saw countless specialists and endured endless testing including the flawed Canadian test for Lyme.  She was forced to leave the country to receive proper diagnosis, testing and treatment. Canadian families are currently paying out of pocket for treatment.  Lyme patients report spending tens of thousands of dollars on necessary care, placing families in financial jeopardy. Nicole’s family and friends all pitched in tens of thousands of dollars to cover some of her costs.   Who will pay for your care if you need it? Nicole’s hope for ALL Canadians is that the Action Plan for Lyme would be the “catalyst for change”.  Nicole and thousands of other Lyme sufferers across Canada are devastated to see that this Framework has NO EFFECTIVE ACTION at all. The Framework is a violation of Public Health’s mandate, Bill 442 and possibly the Canadian Charter of Rights and Freedoms (s. 7) granting all Canadians the right to life, liberty and security of the person.   Please sign this petition asking the Canadian Government to reject the current Federal Framework for Lyme disease and FIX IT.   The Plan must recognize the seriousness of this disease for all of us.  Time is ticking. Canada has NO good plan.  You could be the next BITE.   #TickingLymeBomb   SIGN THE PETITION, ADD YOUR COMMENT, AND SHARE WIDELY    Please ALSO send an email to your federal MP – click here to find your MP based on your postal code: Let him or her know you are concerned about Lyme disease and the issues raised in this Petition, and that the Federal Framework is inadequate to protect you and other Canadians.   Below is the history of this Petition and all the updates since this Petition was first Launched in February 2017.   UPDATES: [May 2018 UPDATES: On May 7th, LymeHope, CanLyme and the G. Magnotta Foundation co-hosted a federal MP Round Table educational event on Lyme Disease across Canada.  Over 40 MPs or their staffers were in attendance.] [DECEMBER 11, 2017 UPDATES: In October, 2017, Anne Kingston from Maclean’s Magazine published an article featuring our work through LymeHope over the last few months.  You can read the online version here: and pick up a hard copy on newsstands now (with Justin Trudeau on the cover).  LymeHope has incorporated as a Canadian national-not-for profit organization, and we held our first public educational event in Oakville, Ontario on November 3, 2017.  Sue Faber, RN, co-founder of LymeHope spoke about pregnancy and congenital Lyme disease – watch her presentation here: Sue Faber and Jennifer Kravis, co-founders of LymeHope, met with the then Federal Health Minister Jane Philpott in August 2017, and delivered 4 bound volumes of research on the topic of pregnancy and transmission of Lyme disease through pregnancy.  This was also addressed in testimony to the House of Commons Standing Committee of Health in June, 2017.  Sue Faber’s testimony is here: Jennifer’s testimony on the realities Canadians with Lyme disease are facing is here: Given the volume of compelling research clearly indicating a risk to pregnant women and babies, as well as clear warnings on the websites of the March of Dimes (“If you get Lyme disease during your pregnancy, it may cause problems for your baby including certain birth defects and stillbirth”) and the Centres for Diseases Control (“Lyme disease acquired during pregnancy may lead to infection of the placenta and stillbirth”), we were quite shocked to see this recent response by the current Health Minister Ginette Petitpas-Taylor to concerns raised by the Health Committee, in which she states: “there is little evidence to suggest that the agent of Lyme disease can be transmitted sexually, prenatally, perinatally or through blood transfusions”, and “there is no conclusive evidence to suggest Lyme disease can be transmitted though other means than a direct bite.”  The full letter may be found on MP Len Webber’s website here:  We have requested a meeting with Health Minister Petitpas-Taylor but have not yet received a response. [SEPTEMBER 17, 2017 UPDATE: Jennifer Kravis, representing LymeHope, along with 11 other Lyme patient/advocates from across Canada, were invited to Ottawa to a Round Table discussion with Public Health Agency of Canada to get an update on the rollout of the Framework.  Video update here: [AUGUST 28, 2017 UPDATE: Sue Faber and Jennifer Kravis, co-founders of LymeHope, met with then Health Minister Jane Philpott on August 22, 2017 and delivered over 2,700 personal Lyme Letters and 50,000 Petition signatures with over 13,000 personal comments.  Video Update here:] On August 28, 2017, there was a federal Cabinet shuffle.  Minister Philpott was moved to a newly created portfolio – Indigenous Services – which includes responsibility for the delivery of health care services to Indigenous populations.  We plan to follow up with Minister Philpott in her new role as there is much work to be done to educate and protect Indigenous communities, many of whom live in high risk areas for Lyme disease.  Minister Ginette Petitpas Taylor was appointed as the new health Minister and we are following up with her. [JULY 23rd UPDATE : We have great news - after 3 trips to Ottawa, numerous meetings with MPs and senators, and 6 months of continued phone calls and emails to Minister Philpott's office requesting a meeting - we have finally been invited to Ottawa in August to meet the Minister and deliver the personal Lyme Letters.  We need even more Lyme Letters!  Please send yours to by AUGUST 15TH and please let us know if we have your permission to keep a copy of your letter for purposes of sharing with the media and other MPs. You can follow our journey on Facebook at and on ] [JUNE 10th UPDATE: The House of Commons Standing Committee of Health had a 2 day study into the concerns about the Lyme Framework on June 6th / 8th.  We (Jennifer Kravis and Sue Faber) were both called to testify as witnesses – our testimony can be watched here: and here:  The Committee wrote a letter of recommendation to the Federal Health Minister but we have not been given a copy.  Please continue writing your MP to let him or her know you are very concerned and the issues raised in this Petition need to be addressed urgently.  Also consider writing to ALL the members of the Health Committee to express your concerns and ask them to take action including (1) directing research into immediate better testing, congenital and sexual transmission, and (2) the establishment of an oversight committee with equal representation from public health, members of the Canadian Lyme Science Alliance, Clinicians specialising in treating chronic Lyme and patients and advocates.  Committee Members: Bill Casey (lib) Cumberland-Colchester, NS (Chair), Len Webber (pc) Calgary-Confederation, AB (Vice Chair), Don Davies (ndp) Vancouver Kingsway, BC (Vice Chair), Ramez Ayoub (lib) Thérèse-De Blainville, QC, Colin Carrie (pc), Oshawa, ON, Doug Eyolfson (lib) (an MD), Charleswood — St. James — Assiniboia — Headingley, MB, Rachel Harder (pc) Lethbridge, AB, Darshan Singh Kang (lib), Calgary Skyview, AB, John Oliver (lib), Oakville, ON, Sonia Sidhu (lib), Brampton South, ON] [JUNE 8th UPDATE: Federal Health Minister Jane Philpott announced the release of the final Framework on May 30th, as well as $4 million in funding (spread over 5 years).  The final Framework DOES NOT address in any meaningful way ANY of the serious issues raised in this Petition (see the Update on this Petition: the Final Framework has NOT been fixed. Please continue to sign and share until Canadians are adequately protected.] [APRIL 29th UPDATE: Minister Philpott, despite numerous requests, has not agreed to talk to or meet with us despite almost 40,000 signatures and over 10,400 comments.  Sue Faber and Jennifer Kravis are headed to Ottawa on May 2nd for the second time to raise these Canadian voices to Members of Parliament.  Follow their journey here: [MARCH 9TH UPDATE: Yesterday (March 8, 2017) Public Health Agency of Canada (PHAC) stopped accepting public feedback.  PHAC received notice of over 36,000 signatures before their cut-off date.  This Petition will continue until the original goal, to have the Health Minister reject the Framework, is met.] [MARCH 9TH UPDATE: The MP Round Table was held in Ottawa on Monday March 6th.  We continue to suggest that concerned Canadians write their MPs via the MP Letter link on to ask him or her to encourage Minister Philpott to reject the draft Framework. ] [FEBRUARY 7, 2017: The draft Framework is released, and this Petition was launched shortly after in protest.]    This petition will go to:  Prime Minister Justin Trudeau Federal Health Minister Ginette Petitpas Taylor (who replaced Jane Philpott in September 2017) Public Health Agency of Canada   A copy of the petition will be sent to: Lyme Letters Campaign CanLyme, Canada’s National Lyme Advocacy Group   For More Information: On Lyme Disease & Co-Infections: and On the Lyme Letters Campaign: Public Health Agency of Canada Framework:   References:  [1] Patrick A. Leighton, Jules K. Koffi, Yann Pelcat, L. Robbin Lindsay, Nicholas H. Ogden. Predicting the speed of tick invasion: an empirical model of range expansion for the Lyme disease vector Ixodes scapularis in Canada.Journal of Applied Ecology, 2012;;jsessionid=BDF9CD369FD70D6E8CA8FF16A4AA5015.f04t01 [2] Annals of Internal Medicine: PubMed: [3] [4]  

Canadians Concerned About Lyme Disease
63,398 supporters
Update posted 1 week ago

Petition to Honourable Adrian Dix, Patient Care Quality Office, Patient Care Quality Office

Help people with bipolar disorder who need clonazepam

(image attribution) --- Dec 2017 update: It has been 10 months since my benzo withdrawal. The withdrawal symptoms only last a few days. I am very unwell. I need clonazepam. Also, my apologies for the anger which can be heard in my April voice below. --- --- Friends/family: please do not mention my doctor's name, because I do not want to implicate him without his consent. Thanks! --- There is a train-wreck coming around the corner, and formal "doctor-talk" isn't working, so I must publicly appeal to the reason of the citizens of this province. The College of Physicians and Surgeons of British Columbia, Canada appears to be working overtime to ban clonazepam. They started with the opioid/benzo problem, got overzealous, and are now reviewing doctors who prescribe clonazepam to people with bipolar disorder. Their efforts include reviewing and threatening their peers (psychiatrists) with revoking their license to practice if they have acted upon their scientifically-backed knowledge that certain people with Bipolar Disorder and/or PTSD, anxiety, CSA, DID, or seizures benefit greatly from clonazepam. Doctors aren't allowed to talk about this, because their "hands are tied." I talked to someone from the Fraser Health Authority, and he said that they know what's going on lately, but guess what... their hands are also tied. He told me that the College just says, "this is the way it is," and so that's the way it is. The College sounds like a high-school bully. Professionals who are in direct contact with patients aren't allowed to express their opinion? Psychiatrists carefully administer and monitor a controlled addition to clonazepam, which has far less damaging side effects than many prescribed medications, including the "orthodox" atypical antipsychotics and neuroleptics that are prescribed to patients with bipolar disorder. The dosages of these brain-damaging drugs may be reduced if the patient is also taking clonazepam (a benzodiazepine brand-named "Klonopin.").If the CPSBC's reckless efforts continue unchecked, it could eventually leave unstable people with bipolar disorder on the streets, without a doctor, smoking pot (as the only relief from mid-brain distress/damage), and without prescription medications that prevent psychosis and dangerous judgment! This would be a great cost, not only to these patients and their doctors, but also to our province and its taxpayers. Clonazepam effectively calms the damaged amygdalae of people with bipolar disorder and/or Post Traumatic Stress Disorder or early childhood trauma, including Child Sexual Abuse (CSA) and associated Dissociative Identity Disorder (DID). It is also used for people suffering with epilepsy. There are no psychiatry-approved substitutes. Without clonazepam, we observe an increase in symptoms of Tourette Syndrome and other over-active panic responses, as well as an increase in trauma-related nightmares and general anxiety and stress.We do not have the credentials nor the time to conduct careful scientific research into this; however, the College does, and they should do so without bias against "controlled addictions" while ignoring the efficacy of the medication.The formal process of intelligent psychiatrists reasoning with the College and submitting streams of paperwork (forms and letters), and of distressed patients filing formal complaints is not working, so we must increase awareness and pressure using social media.The College is fixated on their agenda, without regard for real people who are suffering.Ironically, the CPSBC's self-generated mandate includes this sentence: "The College’s overriding interest is the protection and safety of patients." Please see this public Facebook post to better understand why this matters to me: If I lost my psychiatrist, I would lose my prescription medications, including access to the antipsychotic which is preventing manic psychosis (delusions) and manic loss of judgment. I would need to lie about my clonazepam addiction for another psychiatrist to accept me as his patient, because doctors are not interested in being put under review because someone under their care is addicted to clonazepam. The best way for me to survive without clonazepam is to use medical marijuana, which also calms the damaged amygdalae in my mid-brain, but no psychiatrist in BC would prescribe medical cannabis to someone with bipolar disorder, because, from their accurate scientific perspective, there is not nearly enough research on using cannabis to treat neurological conditions. I am just one person with bipolar disorder. (We are many.) 1. Official link: There are none, because the information is all hidden from the public. It could only be found in Protected "doctor-speak" forms and letters, which, of course, no doctor is allowed to talk about. 20 April: see the update below for the college's official paper on this from June 2016. This is why the supervisor (the College) is not being supervised; hence, the necessity for (and inevitability of!) one or two or 25 disturbed bipolars with enough energy remaining in them to to go emotional in the news media so that the public and the BC Ministry of Health become the supervisors of the evidently over-bloated College that is ironically able to hide under the banner of "We Are Here to Make Sure that This Sort of Crap Doesn't Happen to Patients in BC."

Paul Jubenvill
346 supporters