I have had lyme disease for almost eight years, and have been bedridden for close to six of those years. For a long time I have been gnashing my teeth at the weak response by our Canadian leaders toward the escalating problem of lyme disease and other tick-borne co-infections in this country. So… it is with great excitement that I can finally pass on some wonderful news for Canadians! All Canadians.
June 20th, 2012 is the day that the following groups of people should pay careful attention to MP Elizabeth May’s announcement.
- Those who have lyme disease and are desperately trying to get some help in this country.
- Those who have friends or loved ones who are struggling with lyme disease and tick-borne infections.
- Those who know someone with lyme disease. (BTW, this group is getting larger as lyme disease continues to become more prevalent).
My prediction is that within a few years it will be difficult to find anyone in this country who doesn’t know someone with lyme disease. For now, the 20 million of you that currently meet the above criteria can help to get lyme disease treated seriously in this country (see end of this post for specific instructions on how to help).
Although Elizabeth May is the Green Leader, this bill is aimed at supporting all Canadians with a much-needed, coordinated national strategy to get rid of the massive roadblocks currently preventing quick diagnosis, timely and accurate testing, full treatment and longer term support and care. Excerpts from Elizabeth May’s statement on her web site give a little more context to her decision to offer support to the growing cadre of Canadians who are ill or disabled with lyme disease.
May will introduce a Private Member’s Bill calling for the development of a national strategy to address the challenges of the timely recognition, diagnosis, and treatment of Lyme disease. The bill also calls for funding for provinces and territories to implement the strategy.
“Lyme disease can be devastating. Too many Canadians are now disabled, deprived of the joy of family and friends, of school or work, due to Lyme disease. The public and the medical community need to be educated as to the increasing incidence and range of this disease,†said May…..
“Scientists are warning that a warming climate will expand the geographic range of Lyme disease-carrying ticks further into Canada, so it is imperative that we are proactive,†said May.
[From Elizabeth May, MP]
Details
- On Wed. June 20th, 2012 in Ottawa, Elizabeth May is planning to introduce a private member’s bill relating to Lyme disease. Look for a press conference that day and the reading of the bill by Elizabeth to our federally elected MP’s later the same day.
- The bill is multi-faceted, with detailed timelines that require adherence by the Federal Minister of Health at various stages, including when the conference must be convened, when the health minister would report back to MP’s, timeline for posting new national strategy on the official gov’t website, and many other critical details to ensure that the job is done right!
- CanLyme has been consulted at length by Elizabeth to make sure patient’s interests will be heard.
- Elizabeth is allowed to introduce one private member’s bill in her four year term. She has chosen to help Canadians with Lyme disease get their right to health care back.
How can each one of us help Elizabeth pass this bill?
We ALL need to do the following and ask for friends, & family wherever they live in Canada to do the same to support you and get this National Lyme Strategy Bill passed:
- Find out who your federal MP is. Click here.
- Contact your federal MP and if at all humanly possible set up a face-to-face meeting.
- Tell them your story, and how lyme disease affects you, your family or your friend(s).
- Tell them that you know others across Canada in the same predicament (like me, for instance)
- Tell them that you, your family or friend(s) are being denied the right to health care.
- Ask if you can count on their support to get this bill passed.
- Make sure your MP knows this is not just a ‘Green’ party bill, it is a bill that could affect every single Canadian including themselves, or their loved ones.
- Remind your MP to vote with their conscience as this is a private member’s bill; no party vote needed.
- Contact friends, family, acquaintances, people in your local communities. Let them know how important support is. Ask them to contact their MP.
If you need further information, check out Elizabeth May’s web site. Also, use my contact page to ask for assistance, or to find out how to include your picture in the display of Canadians suffering with lyme disease – this display will be part of Elizabeth May’s press conference scheduled to occur before the bill is introduced in parliament on June 20th.