The sound of steel chains clanking against wood, the feel of a breeze across my face on a sunny day, the sounds of carnival music and children laughing, the fear in the pit of my stomach as we slowly climb the first big hill of a new coaster that I’ve never been on before. Deep down inside, I know we’re safe, but, a horrifying thought, “There is the rare and odd case of a malfunction, like the one I heard of that shot a car of screaming patrons off the tracks and into a billboard sign killing everyone……or was that an urban myth?” “Oh my God, were at the top!” I can see the whole park and half the city from here. We creak up to the tippy top and just begin to crest where I see for the first time just how sharp and steep the trip down will be. Yikes!
This is a how I feel with my plans to hopefully rejoin the work force. I am slowly creaking up the big hill, more than halfway to the top. Most of the time, I am sure it is the correct direction, but that it must be slow, like the car creeping up the tracked hill. Counseling first, volunteer work next, then career counseling and finally the time will be to knock on doors of potential employment situations that will be best suited for me. That day will come when I crest the hill, tipping, and I take the literal plunge. A fleeting thought, “Oh my God, will my car break away from the steady, but fast guidance of the rigid tracks as I fly off and crash and burn!”
Truth is, I don’t know what its like on the other side of that hill, this is a new coaster ride. I do know that chances are infinitely slim that I will fly off the track, because the track I am on is a steady one. It is a well thought out, well advised, researched, prepared for and worked for track, most important is that it is a Higher Powered track and I have faith. I know that the ride will be exhilarating and rewarding. I also know that I will be frightened, but really, really happy too. I love roller coaster rides. Then there is the moment of the fleeting thoughts, “Maybe I shouldn’t do this?! What if….? What if….? And…..What if?!”
Someone shot down my greatest accomplishments in my life on my resume in the space of 60 seconds because they are not suitable to be on a resume. You will be prejudiced against, red flags will be set off with this word and that word. That goes right in line with old paranoia’s that I have worked years to grow out of. Self constructed prisons of, “What will they think?” and, “Who will take me seriously?” I have not had a conventional life, both my failures and my triumphs are controversial to some. Can’t talk about MS, can’t talk about the blog, can’t talk about 26 years clean and sober and all the accomplishments I’ve had with organizing successful events. I wonder if it is okay to list success in drinking events instead. I will not hide my entire life from anyone. I bring all of me or none at all. I said that in college and I wrote honestly and I received nothing but the greatest respect from my teachers and my class mates and one A after another on all my written papers. I said then, “I bring all of myself or nothing.” I will not live a pretend life of safety that was never my real life. My life has been a roller coaster ride that I am not ashamed of. Some of it does belong on a resume. Because I earned it. If someone will prejudice me for that, than why do I want to work for anyone who thinks like that.
The real question ought to be, “Why is Vitamin D a problem right now?” Because when I was a child and into my twenties, it wasn’t an issue. I’m 55, so I am referring to the 60’s, 70’s and 80’s. Back then, I sported a dark brown tan every summer and in my twenties I kept it up year round using tanning booths in the winter. In my childhood, we didn’t talk about sun screen. Babies wore sun hats, mother’s kept them covered, toddlers ran around with tans. My brother and I have olive toned skin and many remarked to our mother about our beautiful dark tans. People who had very pale skin, were cautious when in the sun, but still out in the sun, they were the only ones I saw using salves to protect themselves from burning aside from life guards with bright white stripes of sun block on their noses. We all suffered a sunburn sometimes. I don’t recommend them, they’re not fun, but for most of us, they weren’t the end of the world either.
Its true, too much sun could damage skin and for a few, cause skin cancer. But, I feel we’ve gone way too far in the other direction, where we get no sun anymore. Especially in the north where sun is limited to begin with. In the summer we slather the highest SPF lotions we can find, lest the sun touch our skin. All my life, I’ve met only 2 people with skin cancer (mild cases). And, before you get all up in arms, be rest assured that I am not disputing that skin cancer is real, and maybe its only a coincidence that I’ve only met two people. I am only suggesting moderation and balance. For most people, some sun is not just good, but needed. Sun light is needed to produce vitamin D. It can be had through supplements too, which is what I do. I take 10,000 IUs of Vitamin D3 per day in the form of drops. Fair skinned Dr. Wahls takes 6,000 IUs in the winter along with short visits in a tanning bed and decreases to 4,000 IUs in the summer, whereas she is an avid Gardner and rides her bike to and from work most days.
It is a fact that lack of Vitamin D has been linked to autoimmune diseases and other equally surprising conditions:
“A lack of vitamin D has also been linked to some other conditions such as cancer, asthma, type-II diabetes, high blood pressure, depression, Alzheimer’s and autoimmune diseases like multiple sclerosis, Crohn’s and type-I diabetes.” – https://www.vitamindcouncil.org/about-vitamin-d/what-is-vitamin-d/
Yes, we had these diseases then too, but not to the outrageous degree that they are now prevalent in our society these days. When I was a child, I met one person who had MS. In my twenties, I knew another. Two people in two decades. The last two decades the opposite has been true, autoimmune diseases of all sorts are cropping up everywhere in cooler climate industrialized nations. Interesting though is the fact that I knew two people my entire life who had skin cancer, the kind they can remove. That is not to say that it doesn’t exist, that it shouldn’t be a prudent concern, especially for those with fair skin, who are most susceptible to damage. The darker your skin is the more melanin you produce, which is the skins natural defense against the sun that, paradoxically, is produced when the skin is exposed to sun light.
Melanin gives the skin its pigment. The darker your skin is the better protected you are from the sun. This is the reason why warmer climates have darker skinned people. A natural occurrence to the environment. My grandparents are from Southern Italy, hence the olive tone to my skin and gives me a decreased chance of sun burns. I can burn. I need to be cautious the first one or two times out in the sun and use sun block. Once a tan begins to build, I don’t burn anymore. A tan is the skin producing melanin in response to the sun for protection.
I am not an expert, but I have left three addresses from both sides below. I suggest that you take the time to read up. It is important to say that Vitamin D is not the only reason for the sharp increase in autoimmune conditions, there are other factors, which is why Vitamin D is only one of the components of the Protocol, but it is definitely a factor.
When I tackle something, I have learned through the years of my life to bring all of myself or nothing. I am an open book. Following the Wahls Protocol and how I am defeating MS is no different. My goals for this blog have been:
- To help keep myself motivated and accountable
- To provide a detailed record of one person’s healing
- To inspire others
- To give a truthful account, good and bad
- To share helpful information and shortcuts that I have learned
- To give a realistic account that does show how hard, yet how doubly rewarding this has been and is
- To prove that its all worth it
At this time, as I have written in the past few blogs, I am rehabilitating in preparation for the workforce. I will have a job that fully utilizes all that I have to offer. Too be successful, I have had to look at some tough to swallow truths about myself. I have written about these as I deal with them. Is it wise to publicly speak of a crippling past fear of success, of horrible wreckage at the hands of MS, of darker issues that I have worked very hard to successfully overcome, thereby preparing me for a one hundred percent commitment to the Wahls Protocol?
Fear….what if a future employer reads about these issues and discriminates and I lose the opportunity for this job or that? Here’s my answer to that…..I bring all of myself or nothing. That includes any future job on my horizon. My learned skills, my experiences, and my wisdom comes with me. I once lived in a self constructed prison, terrified that the world would know where I’ve been and what I’ve done and that secretly, deep down inside, I knew you knew that I was worthless. It has taken me a long time to overcome that. Today, I have so much to give, so much I want to learn, and so much to share. Because of the Wahls Protocol, my body is finally catching up to my ambition and drive to help others. My mind is out of the fog, awake and hungry to learn more.
I had a friend in the early 90’s who had Progressive MS. She was diagnosed when she was 18. She managed to complete her degree in education, but was never able to realize her potential in her chosen career. By 26, just as I met her, she lost her right to drive, her husband left her for someone else and she then had to let go of her position as the primary caregiver for their three year old son. She was athletic, she went to the gym five days a week. A tiny, muscular thing. She strained as she forced her spastic legs to walk, her hands shook uncontrollably and the day she messed herself, but then calmly gave us direction to help her, all of us embarrassed for her, whilst she stayed calmer then us all. I think often of her courage and dignity in the face of all that ugliness.
That year a new drug, the first ever, was introduced. Copaxone. I watched her face light up with a renewed hope, only to see it fall just a few days later when she was told that the drug could do nothing for her as she was Progressive. Well Joanne, I just want to say to you, I have relapsing remitting MS and I have been on Copaxone for ten years. I started the drug when I had 20 lesions and now I have double that. I too lost my ability to drive, lost my ability to work, had incontinent bowels and had to give up primary care of my children. So, my dear friend, you missed nothing. She died a few years later, bedridden. When I was diagnosed with MS in 2004, I immediately thought of Joanne. Terrified, having watched what it did to her. If she had been given the knowledge that I have been given, she would’ve jumped on that band wagon in a heartbeat. She was far more disciplined than I am. If she’d known that Dr. Swank had published his 30 year trial on MS and diet with astounding results around the same time as the release of Copaxone, she’d be here telling me about the new exploits of her now adult son.
That’s why I have a responsibility to share my experience, strength and hope and that includes the dark stuff. So anyone afflicted with not just MS, but other autoimmune conditions, can have a chance to take control of their own health again or even better, prevent themselves from ever developing one of these diseases. This is my personal journey, and like all journey’s, though they may be the same road, each will be its own.
My success is in memory of Joanne.
Picture from Pexels: https://www.pexels.com/photo/adult-background-beach-blue-296282/
Below is the information to see Living Proof in Calgary, where and when:
Landmark Cinemas Canada is hosting screenings of Matt Embry’s documentary Living Proof February 03-05!
Saturday Feb. 03, 2018 1 p.m.
Sunday Feb. 04, 2018 1 p.m.
Monday Feb. 05, 2018 7 p.m.
Surrey – Landmark Cinemas 12 Guilford
GTA – Landmark Cinemas 24 Whitby
Ottawa – Landmark Cinemas 24 Kanata
Calgary – Landmark Cinemas 16 Country Hills
Edmonton – Landmark Cinemas 9 City Centre
Available soon @ https://www.landmarkcinemas.com/film-info/living-proof
Off to see the Social Worker tomorrow!
I have my appointment with her tomorrow at 9 am. Our discussion will be about my intent to go back to work, the possible fall outs, the logistical nightmare with not one but two disability programs in the US and Canada, the need to assess skills against disability I still have, and fears associated with past disasters as a result of unexpected attacks throwing monkey wrenches reocurring again in my life. From there I will have appointments with Occupational Therapists and the MS Psychologist.
When I am done with this phase of my rehabilitation, then I will contact Champions, which is a career counseling program specifically for the disabled. I have a tricky resume and a past full of black holes. Examples:
- I have 64 college credits in business and writing with a high GPA, but I can’t get my transcripts due to a government bankruptcy I was forced to declare at that time due to, you guessed it, MS.
- I sold credit cards for MBNA for three years and was one of that telesales center’s best sales performers and sales coaches. But, MBNA sold out to Bank of America, so I have no reference that I can give an employer.
- I spearheaded grassroots, non profit events from the ground up over 15 years, all successes, all unpaid. The college degree was to back up my experience with a bachelors in business and a minor in writing. The plan was to be a professional events planner.
- I have seven years experience as a Mental Health Technician. Two years as an Aid at a State Hospital and trained in Crisis Intervention with five years experience on an Acute Mental Health Unit at a community hospital. But, a long time ago, 1980-1982 and 1989-1994, a. shows my age (55), which can discriminate myself from getting the first interview and back then, you didn’t have to have a degree or certificate for these positions. I was hired for the five year position based on my two years experience at the state hospital.
- Then there’s the years disabled. How do I deal with that with an interviewer and on my resume. Tough one, of which I am not alone. I am assuming that Champions Career Counseling is familiar with this conundrum.
You see the issues, I have a lot of honed skills, but not much proof on paper, although testing will help and once I am hired, my actions will show over time what I am capable of. But, ….to get there. Well, I guess that’s where my Higher Power comes in. I’ll do the foot work, the rest is not mine to control.
Most important to see is that I am on a vista that has a far ranging future. I do not anticipate a future MS attack, not on this lifestyle. Can I gauge that by my own experience, no, its only been ten months. I can, however, gauge it by the many others I’ve talked with and listened to online and in person, who have followed this lifestyle and kept their autoimmune illnesses at bay and in check for years and for some decades. I know this works. Once upon a time, I couldn’t predict what could happen with this illness, now, I feel confident to say, I can.
Wish me luck as I move out into this phase of my journey to health!
Change is not easy. It usually means the adoption of foreign ideas and concepts along with emotional and physical adaptations that take reasonable time to accept and implement. I often refer to my experience of quitting smoking because it parallel’s well with what and why I am doing the Wahls Protocol. My father was a jazz musician who played accordion. He was a product of a time when most people were smoking. Born in 1933, he began smoking at the age of nine. I grew up watching him chain smoke non filter Camels. He went through four packs a day, not an exaggeration. His two fingers that held the cigarette had permanent tobacco stains. You could hear the sound of him opening and closing his Zippo lighter every ten minutes, “Ka-ching”. Most people had ashtrays in their homes, even if they didn’t smoke, for guests who did. Smoking was expected and allowed almost everywhere. My father said often that it was his right to smoke. Even when it was killing him with Emphysema, he died at age 62 in 1996. A painful, long drawn out twenty-five year illness, the last fifteen in particular…..just like his father before him, who passed at age 60 from the same thing. I heard stories of my grandfather in the hospital under an oxygen tent, lifting his tent off so he could smoke his cigarettes in his hospital room. We think of that now and we think how ridiculous that was.
My mother who also was a heavy smoker, managed to quit in the seventies. As young children in the sixties, my brother and I had candies in the shape of white cigarettes in a “pack” box. We held the cigarette candies between our fingers like we saw our parents and pretended we were smoking, sucking in and blowing out imaginary smoke, then we’d tap our cigarettes on the edge of the imaginary ashtray. So, its no surprise that I started smoking when I was eleven in 1973. Marlboro’s, I loved Marlboro’s. They were apart of my identity. I always had a pack of red and white Marlboro’s with me everywhere I went. The first time I experienced a public restaurant that had a “No smoking” sign in the window was in 1983. It was a Ben and Jerry’s ice cream shop in Western Massachusetts. I’d never heard of them and I was incensed that I couldn’t smoke inside. That was unheard of, “Who do they think they are?”, I exclaimed. I refused to go in and waited outside while my friends had their ice creams. Fast forward to 1992, the hospital I worked in went no smoking on July 4th, Independence Day, now that was maddening. I spent the last three years freely smoking cigarettes out on the floor at the nurses desk. In the mean time, my father, long on oxygen, was getting sicker and sicker. At night when I slept, my feet were cold, and I felt bad in the morning. It became obvious that I had to do something about my smoking and I was furious about it.
It took me the next three years, stopping and starting before I finally quit for good in 1996, not long after my father’s death. That year, we lost five close friends and my father to smoking related illnesses, lung cancer, Emphysema and throat cancer. Five of us, together, supported each other to quit. Three of us stayed stopped. After my diagnosis’ of MS and a compression on my spinal cord that would result in an immanent surgery, I picked cigarettes up again after nine years of not smoking in 2004. I thought, I’ll just smoke for a short time, just to get through this. Feeling like an idiot buying cigarettes at the store the first time and lighting up at home, to have my 14 year old son catch me, calling me, “Puffer!” It was no longer acceptable to be a smoker anymore and I was very embarrassed to be seen smoking and even more embarrassed to smell like a smoker and it had become horribly expensive too.
I couldn’t smoke for a short time, my habit came back full force, only this time it was harder to quit. Cigarettes were different. They had more addictive chemicals added to them, they burned faster too. It seemed no sooner had I lit up, that the cigarette had a long ash already. I spent the next five years starting and stopping till I finally became willing to go to any lengths and stopped for good. This time around though, it took a whole year to be rid of the obsession to smoke as compared to the first time I quit in 1996, just one month for the obsessive cravings to dissipate then.
Suffice it say, that profiteers will do anything to make money. Fillers, chemicals, sugars, and whatever else, inundate our food source, like the increase in addictive fillers in cigarettes. Commercials assault our senses with melted cheese pizza’s, snacks and sweets beckoning us to be hungry, setting off cravings. Illness is rampant these days in a day and age when it should be the opposite. There have been no cures for much of anything in decades. How is that, when we eradicated polio, mumps, scarlet fever, and other childhood illnesses in the 50’s and 60’s. My father is deaf in one ear from his bout with polio. We have drugs that cost tens of thousands of dollars that only manage symptoms and poorly so. That then, need other drugs to combat the side effects, one leading to the next, leading to the next. If you replace all this with cigarettes, it is no less insane and just as outrageous. And like cigarettes, it is just as hard to change eating habits in a culture that, largely, still accepts this as the norm.
Change is hard, but I want my life back and for that, I’ll learn to eat healthy, untainted whole foods, that unfortunately includes wheat products. There is nothing wrong with wheat, the problem is what we’ve done to it in the last one hundred years that is the problem. Watch, “What’s with Wheat” on Netflix to learn what I am referring too. All I know, is ever since I stopped eating sugar, gluten, dairy and began eating six to nine cups of fresh, mostly organic vegetables everyday, I’m healing at a profound rate. Just like smoking, a few people had to make an unpopular stand against it. So, thank you Ben and Jerry’s and anyone else who had that courage.
Matt Embry’s documentary Living Proof is an example of standing up to several such Leviathans, one of which is the MS Society, which has long been tainted by pharmaceutical companies. This is the letter put out by the US MS Society in reference to Matt’s documentary:
Below is a message that was sent to all the National Multiple Sclerosis self-help groups in the United States of America about our award winning documentary ‘Living Proof’:
As you are aware, filmmaker Matt Embry is promoting his film around the United States. At this time, we ask that you please refrain from promoting via your Self-Help group.
The National MS Society is a trusted and reliable source of information and resources for people affected by multiple sclerosis. We continue to be here as a supportive partner for each person affected by MS. The Society has not yet reviewed the film and therefore not promoting it. The National MS Society only promotes or endorses content – information, sources, video, film, etc. – after a thorough review of the material, including scientific or clinical review where needed. We only endorse content that is aligned with our strategic plan, including our research strategy that engages leading MS experts around the globe.
Please continue to connect with me with any questions on promoting any third party events. Also, please don’t hesitate to contact me with any questions or concerns. I appreciate your dedication, commitment, and support to the MS community and this request.
Enjoy your day!
Christy A Bomba, MPA CTRS
Manager, Program Implementation and Engagement
National MS Society
Includer, Arranger, Woo, Positivity, Communication
JOIN THE MOVEMENT®
Consider a gift to the Society (and get a tax benefit!) Learn more about the ways you can give.
1-800-344-4867 (Information and Referral)”
Note: to see the comments to this click on Matt Embry’s name. Well worth the time to read.
After premiering to sold-out crowds and standing ovations at the Toronto International Film Festival, LIVING PROOF will hit theatres across the United States and Canada beginning February 1, 2018. Take a stand for patients, take control of autoimmune disease. Visit www.SeeLivingProof.com to find a screening near you.
Living Proof is a documentary featuring Matt Embry’s successful example of having MS while experiencing a normal, healthy life due to diet, exercise and supplements. The documentary is also an expose on pharmaceutical companies and the MS Society. I saw the documentary twice when it debuted here in Calgary at the film festival. It was excellent and won best Alberta feature. All three of its Calgary showings sold out.
I copied Matt Embry’s Facebook announcement with the comments because there are answers in the comments to questions asked. I thought it easiest to copy and paste, less chance of mistaken information.
Great news! ‘Living Proof’ will be available to watch in February 2018 to people in the USA via Theatrical on Demand. Sign up with Gathr Films and help bring ‘Living Proof’ to your community. It will cost you nothing to captain a screening and start sharing hope.
I have my neurology appointment tomorrow. I’ve not seen my Neurologist since just before I began the Protocol. My last visit with him was an emergency visit because of an attack I was having and after three visits to the emergency room with excruciating back pain and a bad fall, I realized I was having an attack. My walking had deteriorated significantly and really had been getting progressively worse year after year. I had walked with a cane for four years, but now I needed a walker, even at times in my own home. The Doctor told me to take only half a dose of steroids. He was worried about what it may do to my bones where I have three fusions in my neck. I asked him for muscle relaxers. For me to ask for that, things are bad. I’m not big on taking drugs if I can help it. I chose to not fill the steroids script and took a half dose of muscle relaxers at the prescribed times. On day two of this, I was slurring my speech, sleeping hours during the day and drooling on myself. I said, “F@#k this!”, and started working towards what I knew was the answer all along having been introduced to the Wahls Protocol two years before. I saw the wheel chair and the motorized scooter looming ahead.
Three weeks after that I started this blog to help me stay on track and be accountable. I considered naming the blog “F@#k this!”, but thought that might detract from what it is actually about without an explanation in the title. So, Defeating MS – My Journey became the title, it says it all. As many of you know, I’m off the walker, then the cane. My mobility has improved back to what it was five years ago and gets a little better everyday, I’ve lost 34 lbs and my cognitive damage has improved dramatically as well. So, I’m going to see my Neurologist, who hasn’t seen me since all of this occurred. He’s been a good Doctor for me. I’ve had support. They know what I am doing and he sent the scripts and paperwork I needed to do Wahls electrical stimulation and physical therapy for my leg. He could’ve said no or charged me money for the paperwork. I have no resentment with him. The system, though, is too inundated with medication as the only resort for autoimmune illnesses. Someone debated with me not long ago, who is in the medical field, she argued the tired defenses that you can’t truly test if the Wahls Protocol works because you don’t know if their sticking to it and even if you do tell people, they won’t do what’s good for them. I agreed, that’s true in regards to the second point, but maybe 25% of them would if they at least knew that this exists and that it works. People need to at least know that this is an option and it comes with no ill side effects. And in answer to the first point, Wahls has suggested that they record their progress. Wahls Warriors she calls them. They are filming, writing, and blogging. Living proof they are. No its not a double blind study which costs millions to do. Right now the backing isn’t exactly there, but the testing is happening. Dr. Wahls is a published research MD aside from her Protocol, Autoimmune Wellness AIP are in the midst of research testing as is Dr. Jelinek of Overcoming MS OMS in Australia. Whether the pharmaceutical companies like it or not, it is coming.
Alright, back to my Neurologist. I keep side tracking the original thought. I have no idea what his reaction to any of this will be. I stopped my Copaxone about a month ago, they know that. Will it be indifference? Will it be interest? Might he be excited about my progress in the other, unexpected direction? Will he try to talk me into going back on Copaxone? No clue! I have a had an MRI confirming the attack. It showed two new lesions in my back, the year before, lesions were developing in my mid back. Scariest is the conversation I need to have with him in regards to seeking support and therapy to become ready to try working full time. I want to try this in five months, I understand full well, it may not be possible for me to ever work full time because of fatigue. While fatigue has diminished greatly, it is still around and must be factored in. My hope is that it will continue to get better. Then there’s the fact that I am 55 years old. Glass half full: I have at least ten years I could work, glass half empty: I am 55 and have MS, Wahls or no Wahls, like it or not, it is a major factor. I am confident I could work a little part time job. I have been considering doing this right now to help offset costs of the diet. This diet with supplements is costing me $500 to $600 a month. Ordinarily, $300 is what I spend on groceries and household a month. It’s a heavy amount on a small fixed income with no other source of income.
I am of this belief: Nothing is impossible if it is meant to be and you work hard for it. How do I know its meant to be? Well, the healing for one. I feel like I’ve been in some ways, frozen in time, unable to move forward. I feel free to once again work for future goals like school or work or non profit work. I have hope, when once I didn’t.
I am no longer a powerless victim of this disease.
Hello all, I have spent the last three hours trying to figure out a reason that Dr. Wahls Tedx Iowa city talk, “Minding your Mitochondria” would have this disclaimer on it from Ted:
“This talk, which features health advice based on a personal narrative, has been flagged as potentially outside TED’s curatorial guidelines. Viewer discretion advised.”
This is what I did to find the answer to the reason for the disclaimer:
- I read their curatorial guidelines, all of them and could find nothing about her talk that was outside their guidelines. Now keep in mind this is where human error can be wrong, I’m no expert on anything, I could be inaccurately reading that information. Therefore, I always suggest that anyone read and research for themselves.
- I thought maybe the Tedxiowacity was the problem, maybe all of their talks are flagged. So, I went to their website, but found that the site was only for that one event, November 11, 2011. No answers here.
- I looked into the Ted sites, there are many, I only looked at the main Ted website and the Tedmed website. I really didn’t find anything helpful here except this, I was curious to see the partners for Tedmed, I found three of their partners are large pharmaceutical companies. Does this have anything to do with the disclaimer? I don’t know. But, it does make me trust them less.
- I looked up what is the difference between a Ted talk and a Tedx talk. Tedx means that it is was filmed at an independent Tedx event.
- Next, I examine the disclaimers: reading the disclaimer that is splashed across the screen in “evil” blood read, it says: “This talk, which was filmed at an independent Tedx event, falls outside Teds curatorial guidelines, see more below.” and then the more below is as stated above: “This talk, which features health advice based on a personal narrative, has been flagged as potentially outside TED’s curatorial guidelines. Viewer discretion advised.”
I like words, actually I love words and I especially love the art of persuasion, in examining these disclaimers, this is what I glean from them.
- “This talk” denotes that the problem they are identifying is the talk itself, not who organized it.
- “…falls outside Teds curatorial guidelines”, as the disclaimer later states, however, they neglect to say how it falls outside Teds curatorial guidelines.
- “See more below.” I thought, ah, here is where it will tell me how it falls outside the guidelines. But no, rather it says, cryptically,
- “has been flagged as potentially outside TED’s curatorial guidelines.” Why did I say “cryptically”, well lets look at the definition of the word “potentially”:
1.possibly but not yet actually:potentially useful information. from Dictionary.comStill nothing definitive
- “Viewer discretion advised.” Under this last ominous warning, I followed the link to TED’s curatorial guidelines and read everything as stated above. Nothing is there that I could see.
All this leaves me with these questions, “Are they trying to discredit Dr. Wahls talk?” and “Why would they do that without a definite stated reason?” The next question that comes to my mind is, “Is their an immoral reason for discrediting her talk?” and “What might that reason be?”
Most of us in our busy, busy lives will not or cannot take the time to truly explore information. At a glance, the disclaimer looks bad and if you don’t know anything about Dr. Wahls work, you might not bother watching, the blood red warning, the viewer discretion, the “potentially” outside our curatorial guidelines and finally, the following talk title, “Debunking the Paleo Diet.” Which sounds like it is directed at Dr. Wahls talk, which it isn’t, but you wouldn’t know that unless you watch both talks. Then, when you get into the most recent comments, you have this guy butting everything: LudwigVanYesBut is his name. “LudwigVanYesBut”, good one.
Oh well, such is life, research everything for yourself, take nothing at face value, check and double check information. I don’t have a definite answer to this, except this, they don’t have a reason. Put up a reasonable reason or take down the disclaimers.
Picture from Dreamtime: https://www.dreamstime.com/stock-photo-post-truth-letters-word-being-buried-sand-image82597046
This is interesting, of course the talk is interesting, its 17 minutes and 46 seconds, brief, powerful and she’s living proof. This was 2011, since then there’s many more living proof individuals walking, get it walking, around out there because of this “controversial” personal narrative. What I found particularly entertaining about this talk are the comments over the years due to a cautionary disclaimer from Ted X across the screen, which you will need to click the x on the warning to remove to watch the talk with out their banner across it. If I am understanding it correctly, and please do correct me if I am ever wrong, Ted X placed the banner in lieu of removing the talk from YouTube, but there was an uproar of disagreement about them doing that, and so, instead they kept it up and splashed this ridiculous banner on it instead.
See for yourself, I would suggest checking out Tedmed’s partners, three of which are pharmaceutical companies. I found this information on Tedmed’s website under the heading, “Partners.” I then googled each of the partners to see what they were. Some were obvious, such as the AMA (American Medical Association), these were the three that are drug companies: Astellas Pharma in Tokyo under Global Partners and under the heading Innovation Partners are Novartis and Regeneron.
Here is Dr. Terry Wahls talk: Minding Your Mitochondria:
Warning: The Tedmed “warning” banners will reappear forcing to again x them out repeatedly. Of course, I encourage you to read their disclaimer and “more”. And I encourage you to then watch the next video they make a point of following Dr. Wahls talk, “Debunking the Palio Diet.” I also encourage you to read the following comments under Dr. Wahls talk and to join this Facebook group: https://www.facebook.com/groups/wahlsprotocol/
It is a closed group, therefore you will need to request permission to join. If you want to know if this works, listen to the members who are serious about adhering to the suggested diet and lifestyle and watch and hear their triumphs against what was once impossible for them.
What is my motive tonight, I’ll be honest, I was tired, long day, lovely dinner for Canadian Thanksgiving. I was looking to put together an easy blog. I have not watched Dr. Terry Wahls famous Tedx talk, Minding your Mitochondria. The plan was to simply put up the link to the talk. I was going to watch it tomorrow. I had no doubt it was good, as I had seen other talks and have seen Dr. Wahls in person here in Calgary. I’d heard of “the Ted talk”. What I did not expect were the disclaimer banners, and the intent to pull the talk, but then the banners went up when an uproar over them pulling this stopped them. I began researching the situation, reading the comments, reading the Tedmed website and exploring their partners. I have not watched the following talk, “Debunking the Palio Diet.” only because I am too tired and must put this to rest and go to bed, but I promise, I will watch it tomorrow. Finally, if you haven’t done so already, read what has happened to me in six short months on the Wahls Protocol under my blog page: Monthly symptom changes. Okay, bed.