Living Proof in Early February in Calgary

Below is the information to see Living Proof in Calgary, where and when:

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MS Hope

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

TICKETS
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!

 

Bonne Sante

If nothing changes, nothing changes

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

Phone: 989-2xx-xxx4
Fax: 989-3xx-xxx3

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.

 

Bonne Sante

Important update for Living Proof Documentary

Matt Embry
Matt Embry Hello everyone, we are currently holding screenings in cities across the United States in February. We need everyone’s help now to spread the word within your community about this screening and to reserve tickets for showings. If you would like to set up a screening in your city you can sign up to be a captain now free of charge. Please follow this link to see which cities are showing the film on which date and help us in the fight against MS! https://gathr.us/films/living-proof
The above is a message from Matt Embry (the producer of the film). As you can imagine, it takes a break to get a national screening of anything. A small project such as this with minimal backing must be that much harder. As many people as possible should be given the opportunity to at least know that there is an answer for autoimmune illnesses and this documentary does an excellent job of showing that. It is part biography and part expose. It does focus primarily on MS, however it is a fact that most of the methods shown in the documentary apply to any autoimmune conditions. It is important to support it so that maybe with enough push, after its public screenings that I hope many of you will either attend if one is captained in your city in the US or volunteer to captain a screening in your city in the US, it will be picked up by a major network like Netflix, where far more people can watch it. I was lucky to live in Calgary where it premiered three sold out shows at the Calgary Film Festival. I saw two showings with two different sets of friends. It deserves our best effort to help it be seen.
Disclaimer: The second paragraph is my opinion, I don’t have inside information. After looking at the On Demand theater site, its common sense to me that this will need as many voices and as much footwork as possible for it to have the best chance.
Bonne Sante

Living Proof Documentary soon available to view in the US

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.

Matt Embry
7 hrs · 

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.

Bring Living Proof to your city!
GATHR.US
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Ravinder Minhas
Ravinder Minhas Iowa City buy your ticket here for Feb 7, 2018 https://gathr.us/screening/22142

Help bring Living Proof to Iowa City, IA on Wednesday,…
GATHR.US
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Tessa Rushton
Tessa Rushton Thank you for producing this Ravinder! The story needs to be told! I too am living proof 😊

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Michelle Peloso Pasqualotto
Michelle Peloso Pasqualotto And when do we in Victoria get to see it?

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Matt Embry
Matt Embry We will be announcing the Canadian theatrical plan very soon.

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Alina Floch
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Sidia Di Benedetto
Sidia Di Benedetto What about Melbourne Victoria Australia

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Amy Lepinski Egan
Amy Lepinski Egan Is the DVD for sale yet?

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Diane Wilson
Diane Wilson Is there any other way to get the movie ? we have horrible internet and can’t stream – as we live in a rural area

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PMayfield Anaya
PMayfield Anaya will it ever be on Netflix or Amazon?

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Sapna Bedi
Sapna Bedi How about the UK? Xx

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Amy Penszynski
Amy Penszynski I can’t wait!

Gobble Gobble

Note: At the end of this blog is an update from Direct-MS about the documentary Living Proof and new MS research. Be sure to click to the whole blog article and scroll down to read their letter.

Alright, I’m in a slightly better mood today. What I mean by that is that I was frustrated with having to leave level III. I’m worried about back tracking and I am worried about gaining weight. The point of all of this is not about losing weight, however it has been a side effect, a nice side effect. I lost weight when I was on levels I and II also, so I don’t know what I’m worried about. The cost is relatively the same for all levels, it is the lack of flexibility for level III that is the biggest problem. The last two weeks of the month is a financially lean time for me. It requires me to be very creative with what I have on hand. The problem with level III is that the food list is very limited. If I run out of this or that, it leaves me without enough nutrients to keep me out of the Ketosis flu, not pleasant. If I have something I shouldn’t then it kicks me out of Ketosis causing me to readjust again when I get back in ketosis, again the ketosis flu, not pleasant. I have been mostly in ketosis, but I am tired half the time, which means not enough nutrients. This is why I made the decision, for now to go back to level II. If I don’t get the right combination of foods because I simply don’t have them, I won’t be sick and I won’t be tired. Then, when really down with money, I can get by with what is on hand with less consequences. When I am in a better position financially, I’ll definitely revisit level III. And if I find that I regress at all in my healing, then I’ll get right back on level III and figure out a way to make it happen.

Today was the United State’s Thanksgiving Day. Always a weird day for me here in Canada. It is my favorite holiday, because its simply about dinner with family and being grateful for each other. That’s how it is in my family, I realize coming from Massachusetts where the pilgrims landed that its about that and then we can add the politics and controversy. But, I am going to keep it very small, it was simply a wonderful day with my family and I miss that and I miss them.

I had an email from Direct-MS today. I will copy and paste here the whole letter, its not super long and has a lot of information of interest to those of us with MS and their families.

The letter:

We would like to thank you for your continued support and to let you know what has been happening with DIRECT- MS over the past year.

 This year our main focus has been on supporting my son’s production of a documentary which examines the challenges of living with MS, and various issues regarding multiple sclerosis therapies, from drugs to diet to CCSVI. The documentary, called Living Proof, was shown at the Toronto and Calgary International Film Festivals and was very well received. It will be publicly available early in 2018 and we will let everyone know how to access it.

 In terms of research, we are currently funding a research project which examines the value of a multi-ingredient supplement for preventing and treating MS in laboratory animals. The first results from this work have been extremely positive and the work will be completed in the first half of 2018. The long-term plan is to organize and fund a Phase I/II clinical trial which tests the effectiveness of the supplement for persons with MS.

 We are currently overhauling our website so that it can be accessed on all platforms from computers to cell phones and is easy to navigate. This work should be completed by year’s end.

Thank you very much for your ongoing and generous support for our efforts which have allowed us to provide persons with MS with reliable, science-based information and to fund highly relevant, research projects. Donating to Direct-MS can be done either through our website by accessing the Donate page under the Home tab or by sending a cheque to Direct-MS, 5119 Brockington Rd NW, Calgary, AB, Canada, T2L 1R7. A receipt for tax purposes will be issued promptly for both Canada and the USA. 95% of all donations goes to charitable purposes. Please do not hesitate to contact us by email (info@direct-ms.org ), phone, or letter if you have any questions.

 All the best, 

 

Ashton Embry

President and Research Director

I looked online in a brief search about this supplement research and could find nothing relevant. However, I do trust this source. They are right here in Calgary and they are above board ethically.

 

Bonne Sante

 

Picture from Pexels: https://www.pexels.com/photo/nature-bird-animal-head-40512/

 

 

Living Proof is now an award winning documentary

“Matt Embry a TV/film producer with MS has a new documentary on his journey with the disease that picked up best Alberta feature at the Calgary International Film Festival.” All three of its screenings were sold out. Which is good news, because this will give the documentary strength behind its progression to a mainstream audience.

Okay, onto my day. I have my first physio tomorrow at 11:30 for an assessment of my atrophied muscles that I will learn to treat with my electric muscle stimulation machine (e-stim). Its been a while to get this important part of the Wahls journey into place.

Note: Symptoms page is updated for last month. As such, tonight’s blog is short and sweet, if not a little disjointed. I promise to write a better one tomorrow. My mid back is screaming at me to stop. So, stop I will.

 

Bonne Sante

Found a new local resource!

We found a wonderful nature store in Calgary called Bowness Health Food. Fairly large store which is mostly supplements. Prices are not too bad, some are high. Need to research pricing online before going and then compare. I don’t mind spending $5 more to support a local store and save on shipping and have local convenience. Its a problem when its $20 more. For example, I was gifted Organika Bone Broth Protein Powder by a friend (Thank You!), which sells at the Bowness Health Food $3.00 less than online at The Canadian Vitamin Shop. On the other hand, a bottle of D3 drops, 500 ml was selling for $36.00, common price is $18 at online sources. I did not have the time to look at all their D3 drop brands today, there may be one at a better price. I did buy a Kombucha drink they had there that came in a small can called Kombucha Wonder Drink Sparkling Fermented Tea that was to die for and sold for just $2.49 8.4 fl. oz or 250 ml. I will go back for more of those. Anyway, love this new found (for me) gem. I am looking forward to exploring more. For one thing, they sell Bulletproof Coffee and Brain Octane Oil. I walked around thinking, “They have everything.” I’m like a kid. Of course I have a budget and must buy the most important elements first, then consider things like Bulletproof Coffee.

Going to see the last showing of Living Proof tonight with friends. I saw it a few days ago with a group. I am accompanying a friend, which then turned to three, maybe four. This is something I want to support. Well done biopic/expose. Should you choose to attend it is showing at the Globe Cinema at 9:30 pm. Tickets are still available online and at the Cinema if they don’t sell out first. https://www.calgaryfilm.com/films/2017/living-proof

Life is good, most especially walking freely without my cane, that’s good.

 

Bonne Sante

 

Picture is the Bowness Health Food logo.

Living Proof Toronto International Film Festival Premier

Matt Embry’s Living Proof documentary premiered tonight to the public at the Toronto International Film Festival (TIFF) scheduled at 6:45 pm Eastern time (4:45 pm Mountain time). Below is an interview with Embry at the TIFF tonight before the documentary aired. I weigh a lot of importance on this documentary because I know first hand what this man has done for MS in terms of others and himself. Matt Embry’s profession is film producer. He has made several documentary’s about others, but this is his first with his own journey with MS and his personal quest to answer the seemingly unanswerable regarding the lack of momentum for a cure for not just ms, but all autoimmune illnesses, within the medical industry and major charities and discusses what is moving in that direction. He has traveled the world to interview pockets of success for managing MS. I am anxious to see this documentary.

I’ve said it before that if it weren’t for Matt and his father Dr. Ashton Embry, I wouldn’t know that the Protocol, which is doing such wonders for me, exists. So, from the bottom of my heart, thank you Matt. I know from the online forums that I frequent for support on my quest, the afflicted and their families all over the world are waiting anxiously to see Living Proof. Embry explains in the interview below that plans are in the works to distribute Living Proof world wide. I am blessed and lucky to be living in the same city as the Embry’s and have my ticket for one of the two showings at the Calgary Film Festival later this month. Click on the link below to see the interview.

Living Proof Interview

 

Bravo! And Bonne Sante!

 

Picture taken from, Toronto International Film Festival show times and to see the Trailer go here: https://www.seelivingproof.com/

Go here for Calgary Film Festival show times: https://www.calgaryfilm.com/films/2017/living-proof