When I discovered this on YouTube, I sobbed as a happy young boy’s health disintegrated before my eyes because of Lyme and co-infections—and no appropriate treatment. I weep when I see it today.
Shame on the Canadian health system. He had to travel to the US for treatment. Not that it was easy to find a doctor here, either.
How many more victims of the Lyme controversy could make a video like this? How many more have lost their childhoods?
If he had been diagnosed and treated early, this video would never have been made.
Jean-Luc, I think of you often. You are my hero. Your courage has sustained me many a day. I haven’t found the rest of your story online, but I hope the treatment you finally got has brought you to remission.
That’s the little portable pump for my IV drugs. Then there were the pills. More pills. Harsh meds that made me sicker so I could get better. I can’t believe I made it through all that. When it could have been avoided…
It’s 2016, and I’m finally climbing out of the Lyme hell I fell into blindly four-and-a-half years ago. If only I’d known more, sooner.
Maybe I can help someone, somewhere, by offering a few things I was shocked to learn. Frankly, it is damned hard to pick just 10 things. But here goes: Continue reading
I’m always a little stunned when I track this blog and am reminded that people from all over the world visit. So many of us are on the lookout for information.
Today I’m thinking about Canadians because lots of my traffic at the moment is coming from my neighbors to the north, who’ve been checking out my post from several years ago on how Lyme was affecting my brain at the time. Looks like some of you are sharing the link on Facebook. Thank you!
Like others around the globe, many Canadians are having a tough time getting good treatment. Health officials just don’t get it (sound familiar?).
The nonprofit Canadian Lyme Disease Foundation says: Continue reading
It’s not just places in the U.S. where people are told, “No lyme here.”
In this video posted on YouTube from Australia’s “Today Tonight” (aired 13 February 2012), a government health official says people with lyme in Australia most likely got infected elsewhere.
Patients interviewed say otherwise.
Note: For those not familiar with lyme at its worst, I must warn you that the interviews are graphic examples of the suffering inflicted by persistent lyme disease.
See another “Today Tonight” lyme report about a 3-year-old infected with lyme here.
And here’s research on coinfections in Australia.
For more information on lyme down under, visit the Lyme Disease Association of Australia.
If you haven’t seen the compelling and award-winning lyme documentary “Under our Skin” by Open Eye Pictures, check out the trailer above from YouTube. It doesn’t seem to be streaming for free any more but see below for info on how to buy it or arrange a screening in your area.
Through interviews with people living the nightmare of chronic lyme as well as the doctors and researchers deeply committed to helping them recover, you’ll learn about this hidden epidemic.
It’s all here, from the shameful treatment of many patients by some in the medical establishment who deny the very existence of persistent lyme to the inaccuracies of testing and the impacts of this insidious illness on individuals and families.
You’ll also hear success stories from people who found health again thanks to lyme literate doctors. If enough people see this film, maybe we can attain the long overdue public awareness and action this health crisis deserves.
To buy the DVD, find out about screenings in your community, or to sign up to host a screening, visit www.underourskin.com.
UPDATE: The sequel, an Academy Award runner up, is now available! PLEASE SHARE ON SOCIAL MEDIA AND EMAIL. We need this information to reach beyond those already impacted.