When I first connected with Debbie Lambert about her experience with gadolinium toxicity, I had to google ‘gadolinium’. When I read that gadolinium is the substance they inject you when you get an ‘MRI with contrast’ and that it can cause toxicity, I immediately started to search my memory.
I can recall at least one occasion of getting an MRI with contrast -- I remember the warm sensation it caused in my body, and the technicians telling me to drink lots of water to flush the chemical out of my body.
After intervie...
When I first connected with Debbie Lambert about her experience with gadolinium toxicity, I had to google ‘gadolinium’. When I read that gadolinium is the substance they inject you when you get an ‘MRI with contrast’ and that it can cause toxicity, I immediately started to search my memory.
I can recall at least one occasion of getting an MRI with contrast -- I remember the warm sensation it caused in my body, and the technicians telling me to drink lots of water to flush the chemical out of my body.
After interviewing Debbie about her experiences living with the disabling chronic symptoms, and learning the facts about gadolinium toxicity, like the black box warning the FDA now requires, and the admission by the manufacturer that gadolinium accumulates in the body, I’m shocked that I’d never heard about this widespread problem. I guess that’s a testament to the medical industries ability to hide, ignore and deny medical errors.
As Debbie recounts, she was experiencing severe pain and it was determined it was emanating from her pancreas. Debbit was sent for a routine MRI with contrast to be able to get a better image of her troubled pancreas. The MRI technician did not ask for Debbie’s consent to be injected with gadolinium or inform Debbie about any potential harms from the invasive procedure. Debbie was hooked up to an IV and the gadolinium started to flow into her veins.
It was during Debbie’s 3rd MRI with contrast when things went horribly wrong and Debbie felt like she was being fried from the inside out. Debbie told the MRI technician immediately, but Debbie’s symptoms were dismissed and she was told to drink lots of water.
But water wasn’t going to cure the damage done to Debbie’s organs. Water wasn’t going to stop the pain. Water wasn’t going to stop her from being disabled.
Debbie does share what has helped - but not cured - her battle with gadolinium toxicity, and she shares about the community of survivors advocating and creating awareness about this problem so that others can make informed decisions about having the procedure.
If you’ve had an MRI with contrast, or are concerned about the potential harm from gadolinium toxicity, you’ll want to hear what Debbie has learned about the medical system, the legal system, and your body’s systems when they are exposed to this rare earth metal.
Connect with Debbie Lambert on twitter: @DebbieLambert
On Facebook - Living With Gadolinium: https://m.facebook.com/livingwithgadadmin/…
Info about MRIs and Gadolinium Toxicity:
ttp://Mridye.com
Amazon e-book by Dr. Catriona Walsh: Contrasts: More Than Meets The MRI
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I am always looking for guests to share their medical error experiences so we help bring awareness and make patients safer.
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Scott Simpson:
Counsellor + Patient Advocate + (former) Triathlete
I am a counsellor, patient advocate, and - before I became sick and disabled - a passionate triathlete. Work hard. Train hard. Rest hard.
I have been living with HIV since 1998. I was the first person living with HIV to compete at the triathlon world championships.
Thanks to research and access to medications, HIV is not a problem in my life.
I have been living with ME (myalgic encephalomyelitis) since 2012, and thanks in part to medical error, it is a big problem in my life.
Counseling / Research
I first became aware of the ubiquitousness of medical error during a decade of community based research working with the HIV Prevention Lab at Ryerson University, where I co-authored two research papers on a counseling intervention for people living with HIV, here and here.
Patient participants would often report varying degrees of medical neglect, error and harms as part of their counseling sessions.
Patient Advocacy
I am co-founder of the ME patient advocacy non-profit Millions Missing Canada, and on the Executive Committee of the Interdisciplinary Canadian Collaborative Myalgic Encephalomyelitis Research Network.
I am also a patient advisor for Health Quality Ontario’s Patient and Family Advisory Council, and member of Patients for Patient Safety Canada.
Medical Error Interviews podcast and vidcast emerged to give voice to victims, witnesses and participants in this hidden epidemic so we can create change toward a safer health care system.
My golden retriever Gladys is a constant source of love and joy. I hope to be well enough again one day to race triathlons again. Or even shovel the snow off the sidewalk.
