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Rethinking Thin : The New Science of Weight Loss - and the Myths and Realities of Dieting

Rethinking Thin

Rethinking Thin: The New Science of Weight Loss–and the Myths and Realities of Dieting by Gina Kolata presents a clear-headed analysis of the research in the field of obesity and weight loss instead of the common beliefs.

They are far from the same.

Through a thorough analysis and painstaking interviews Ms. Kolata shows how diets do not work and that every person has a different set point for their weight. And most of us are not going to meet the Hollywood ideal.

She follows a group of volunteers who sign up for a University of Pennsylvania study of a restricted calorie diet vs. the Atkin’s diet. Each diet is then paired with a variant of behavior modification therapy. This study lasted two years and followed people through weight loss, weight loss plateaus, and the almost inevitable weight gain once the diet was over. The findings of the very rigorous study - and several others - blew all of the “common sense” ideas surrounding weight loss out of the water.

People are not fat because they eat too much and exercise too little. Those who are predisposed to be skinny have bodies that work to become skinny, and those who are prone to be heavy, will have bodies that work to be heavy. As a matter of fact, hunger, that most basic of drives, works very differently among those who are obese and those who are not.

In the obese, it seems that restricting diet makes that person obsess on food due to the reaction of the endocrine system. There are a number of chemicals that govern hunger and if the triggers or receptors are not working just right, that person will eat more - or less - than their body actually needs. They will physically suffer if they do not eat. (Yes, some suffer if they do eat as well.) In the most severe cases, leptin can be given to those who do not make enough of it. However, there is a subset of patients who can receive all the leptin in the world and they will never know they are satiated because their brain does not receive that signal.

It seems that the endocrine system is intricately linked into the way in which we process food as fuel. Those who tend to be skinny will turn more into muscle, and those with a tendency to be fat, turn food into fat. It doesn’t seem to matter much (One weakness of the book is that Ms. Kolata does not go into the increasing use of endocrine disrupting substances in our environment which may contribute to the problem.)

Now, some say we are fatter than we have ever been. I - and Ms. Kolata - beg to differ. Look at the paintings of the great masters. Those men and women would be considered obese under current standards. As a matter of fact, prior to the turn of the 20th century, women were not considered beautiful if they did not have something spilling out of their corsets! What happened? Today we have Photoshopped models representing an impossible ideal of thinness and beauty instead of real people.

Now, wouldn’t you think that the research that could point to the real reasons people fail to keep weight off would be welcomed by the scientific community? Nope. The scientific community, as usual, went back to the days of Copernicus and Galileo with aspersions as to the veracity and methodology of the studies showing that weight had other causes - or that it was not, in isolation, a factor in younger time of death.

“If you are on he political right, obesity is indicative of moral failure,” he says, “If you are on the left, it means rampaging global capitalism. - - Eric Oliver, a political scientist at the University of Chicago, an obesity researcher, p. 195

This sums up the problem with obesity research nicely. It has been politicized. Completely and thoroughly politicized. Nobody wants to hear the simple truth that weight - like height - is a matter of genetics, not environment, or will power.

This book also goes into the discrimination against those who are overweight. People are turned down for jobs, unable to build families, and even denied necessary medical treatment because of their weight. Several stories are of men and, especially, women, who when trying to find treatment for disease were turned away because they were heavy. There are several known diseases in women especially (PCOS, anyone?) that can contribute to obesity.

This book needs to be read by health care practitioners, patients, and society as a whole so that the myth that will power can bring about weight loss can be crushed. There is so much talk about the “ownership society” in insurance and health care that it concerns me that this myth pervades so much of the literature.

If someone is overweight or obese, should they have to pay a premium for health insurance in the same way many push that smokers should? If the conclusions of this book - and the majority of scientific research - are followed, no, they should not. It is no more within the person’s control than any other genetic feature.

Where does this book fall down? It does not give mention to co-morbidities that can exist in the overweight and obese that may actually be contributing to weight problems. One of the favorites these days is the risk of asthma with obesity. Is that an accurate portrayal? Isn’t it more likely that due to asthma someone becomes less active and then gains weight? Correlation is not causation and there is a dangerous tendency to make causation out of correlations in the field of obesity research. Of course, there are drugs that can cause obesity as well. Some of them have a greater benefit than the treatment of obesity does for a certain population of patients. That is something only an individual and their doctor can decide.

So, please, the next time you feel like telling that “fatty” that they should close their mouth, think about the fact that weight is in your genes, not your mind.

Making Ketchup - Includes Canning (Hot Water Method)

I went to the county farmer’s market today for the first time. I bought a bushel of Roma tomatoes from a stall that I couldn’t find again for a good 1/2 hour! The sad part? This is not a large Farmer’s Market. (My sense of direction is notorious.)

I did make quite a haul:

sony 110 sony 141

I even decided to get a second bushel of ketchup. This inspired me to make ketchup.

(Graphics Intensive) (Continued)

UGH! More Ways To Substitute Corn - Gelatin

Vegetarian Capsules: Biorefining Of Corn Brings Gelatin Production Into The 21st Century

Wonderful. Just wonderful. As if dealing with cornstarch is not enough for the corn allergic. There are plans on making it nigh unto impossible to get non-corn gelatin in pills.

Guess what? The argument they give us corn allergics about cornstarch not containing any corn proteins does not hold for gelatin since gelatin is a protein!

Corn is the most subsidized of all crops. It ends up everywhere. I believe The Omnivore’s Dilemma: A Natural History of Four Meals (on my to read list), had a chemical analysis done and found corn molecules in his hair! Do you realize how much corn has to be ingested for that to happen? Do you know how much corn that you are exposed to and you don’t even know about it?

Let’s not even discuss the increasing pressure for monoculture agriculture that happens as they find new uses for corn. Is it really good agricultural practice to grow corn all the time? (Hint: The answer is no.)

How I Converted The Cake Recipe From June 24, 2007

I started with the basic:

Two-Egg Cake (One-Bowl) Method, Culinary Arts Institute Encyclopedic Cookbook: New Revised Edition, Ed. by Ruth Berlzheimer, 1968. pg. 687.Two-Egg Cake (One-Bowl) Method, Culinary Arts Institute Encyclopedic Cookbook: New Revised Edition, Ed. by Ruth Berlzheimer, 1968. pg. 687.

This recipe is a very basic 2 egg cake. Here are the basic ingredients:

  • 2 1/4 cups sifted cake flour
  • 1 1/2 cups sugar
  • 3 teaspoons baking powder
  • 1 teaspoon salt
  • 1/2 cup soft shortening
  • 1 cup milk
  • 1 1/2 teaspoons flavoring
  • 2 eggs

Ok, for me the allergens include baking powder, milk, and soft shortening (depending on what is used).

 

Ok, first, the baking powder - it has cornstarch. I’m allergic to corn, so I minimize my exposure. (It is impossible to completely avoid cornstarch due to its extensive use within our economy. I’ll post on that another day, though.) So, I usually make some up by either making 2 parts starch, 1 part baking soda. You are supposed to use cream of tartar, but I often forget and, honestly, it hasn’t messed up any of my baking yet. There are lots of recipes for substituting baking powder out there.

Next, the milk. Believe it or not, in most cases you have a one to one replacement with any liquid when baking quick breads or cakes. So, I just substitute apple juice or cider. (If you wanted an orange flavor, you could use orange juice, lemon uses lemon juice, etc.).

Now, according to The King Arthur Flour 200th Anniversary Cookbook by Brinna B. Sands you don’t necessarily need to use any oils or shortening in quick breads or cakes if you will eat them immediately. Since I used the 6 apples, they were equivalent to any shortening I may have used. If you were making the cake plain, you can just use any oil or shortening you like.

Of course, sometimes conversions don’t work, but when you succeed, it can be a very sweet success!

Apple Cider Spice Cake

This cake is corn-free and milk-free.

The Apple Cider Spice CakeWe Couldn't Wait

The Cake:

Pre-heat oven at 350 degrees.

  • Take 6 small apples, peel and slice them. Put the slices in a food processor.
  • Put 2 eggs in the food processor - without the shell, please. (I’ve seen it done!)
  • Put 1 Tbs. cinnamon in the food processor.
  • Put 1 1/2 cups sugar in the food processor.
  • Dash salt on the stuff in the food processor.

Start the food processor.

  • Slowly add 1 cup apple cider to the food processor.

While the food processor is doing its thing, measure into a mixing bowl:

  • 2 1/2 cups flour (I use a combination of 1/2 whole wheat and 1/2 white flour King Arthur Organic Artisan flour)
  • 3 Tsp. Corn-free Baking Powder from Miss Roben’s Kitchen.

Stop the food processor. Pour the mixture from the food processor onto the dry ingredients. Mix well.

 

Pour into a bundt cake pan and bake between 35 and 45 minutes - or until a knife, when inserted, comes out clean.

*Cake recipe modified from Two-Egg Cake (One-Bowl) Method, Culinary Arts Institute Encyclopedic Cookbook: New Revised Edition, Ed. by Ruth Berlzheimer, 1968. pg. 687.

The Topping:

  • 1 cup sugar
  • 1 cup apple cider

Heat over a low flame until it gets to a syrupy consistency. This means that when you stick a clean spoon in, a nice layer of stickiness remains on the spoon. It will bubble for anywhere from 5 to 10 minutes before this is true.

 

Putting It Together:

Pour the syrup into the center and spoon over the sides. It will fill up the center at first. Next, take a knife and slice from the center into the cake every 1/2 inch or so. This allows the syrup to more easily seep into the cake.

Give it about 30 minutes and it is ready to eat.

How Doctors Think (Audiobook)

How Doctors Think

Those who suffer from troublesome, hard-to-define or rare illness know much of what is in this book, but this book would be invaluable to someone newly navigating a diagnosis. Groopman demystifies doctors - something long overdue. Guess what, they are just like us.

Doctors have preconceived notions borne of their own education and experience that sometimes interfere with proper diagnosis. Hoofbeats don’t always mean horses, sometimes there really are zebras, as the saying goes. Too often doctors stop testing.

Groopman opens the book with a tale of a woman who many in the allergy community can identify. She had been diagnosed as having psychological problems (anorexia among them) and IBS. Well, she was celiac. It took 10 years to get this diagnosis from a new doctor - everyone else figured her to be properly diagnosed. Everyone assumed that she was lying when she said she was eating and throwing up despite not wanting to. If you aren’t aware, a common effect of a food allergy is gastrointestinal distress. (That’s the nice way of saying it is coming from both ends. Think food poisoning except you are also having other histamine reactions - maybe hives, maybe swelling, maybe blood pressure drops.)

I felt for this woman. I recognized this woman. I admired this woman for continuing on when she knew that her doctors were wrong. Now, here is the thing. This woman was educated. Probably upper middle class and had access to the proper education and materials to know what to ask at the doctor’s office to get him to probe a little further. Or, as in her case, to try yet another specialist.

Some physicians call this diagnosis shopping, but I think that is rather wrongheaded. Diagnosis shopping is the continued visiting of physician after physician in hopes of getting a certain diagnosis. I don’t know anyone without hypochondria that would do that.

Here is the thing, if my doctor can’t help me and I know something is wrong, why wouldn’t I continue going to new people in search of answers? I would do that for gardening, cooking, books to read, etc. Why on earth should medicine be any different? Yes, doctors are the “experts” in medicine. But, in reality, they are really the monopoly holders on medical information. Their training is in interpreting symptoms for the purpose of diagnostics and treatment. If the treatment is not working, it is time to move on.

Since I live with a rare food allergy (corn) and difficult drug allergy (ingested alcohol), I’m used to having to deal with recalcitrant physicians who think they know better than I do. I can’t count the number of times I have had physicians tell me what happened to me was not possible - despite having a confirmed diagnosis from a well-respected allergist.

That is what makes Groopman’s book so refreshing. He doesn’t say to defer to the doctor. Rather, he says that you, as patient, are an equal partner in treatment and if a given doctor is not the right fit for you, move on. I know I have done this. Of course, my criteria for different types of doctors are different. I usually spend an inordinate amount of time training a new primary care physician.

Currently, I like my PCP, but I don’t think he fully understands the ramifications of the severity of my allergies - he was shocked that I take Claritin-D 24 hour every single day. And, ocassionally, I will take a Benadryl if things get really, really out of hand. (I always care an epi pen.) Of course, he is not an allergist, nor a radiologist (a.k.a. paranoid doctor), so I don’t expect him to have the heightened awareness.

Of course, I could have an unreasonable expectation because my previous PCP was very aware of the problems of allergy due to her son being highly allergic to the world. She often worked with the pharmacy to come up with the right drug. I would drive over an hour to see her. I was not a happy person when she retired.

So, though I know some physicians will take umbrage with what Groopman suggests in the role of patient as a partner in treatment - and even diagnostics - that is a correct statement in my mind.

The real problem with his hypothesis is that there is just too much information. No one person, not even a librarian, can keep up with all of the research in a single field.

Disclaimer: I am a trained librarian and I still find new studies on corn all the time. Some I should have seen years ago by their publication date. But there is just too much to keep up with.

I would recommend this book to all newly diagnosed patients - those of us entering the world of medical care recipients for whatever reason - and their families. Even for the seasoned and cynical veterans there are hidden gems, such as the doctor, himself, finding too many conflicting opinions. Or that the much vaunted academic expert is not as useful as the day-to-day practitioner.

If you can influence your library, make them add this to their collection. I believe it is that valuable.

The next book I’d like to see from this area of publishing? How to find medical information and research and how to present to my doctor. Hrm… that might make a good post.

On Curses

Now, I don’t really believe in curses, but there are times it feels like there might be a curse or evil spirits surrounding me. Like this past Friday.

Now, I know that the idea of curses is ridiculous, but I do know a number of others in the blogosphere have been discussing the idea of being under curses. I know that at one point during my study of religious history and culture I noticed a pattern in almost every tradition when dealing with curses and evil spirits:

  • Bells or other percussion instruments, prayer, or chanting;
  • Incense or smudge;
  • Salt, holy water, or anointing oil - interchangeable.

These three elements seem to be in every tradition. It doesn’t seem to matter where the tradition has come from, there is some piece of the above elements within them.

 

Now, there are some other traditions that I have run across that almost have a comical tendency to them when seen through modern eyes - do not take this as an aspersion to those who believe, but it does seem odd to think wearing one’s underwear inside out will repel the evil eye according to a Hungarian grandmother I knew once.

Some cultures believe that when you enter a home for the first time, you need to go through with one or all of the elements of repulsion as you walk through the house.

Now, if you think you are really under attack, you need to anoint all your windows, doors, and vents with salt, holy water, or anointed oil. This is to prevent the evil from returning, or, if already in place, from pulling in new energy.

But, in reality, for me, it is faith in Jesus Christ and the Salvation He brought that overrides the power of any curse - real or imagined. This isn’t to say that faith is never tested, or that I never “lose” faith. Rather, it is the knowledge that ultimately, whatever happens, He is, and always will be, with me.

Popcorn at Live Theater?

If I believed in curses, I think I would think I am under one.  There is a community theater known as the Starlight Theater.  I like to support local artists and thought it would be fun to see one of their productions.  It never occurred to me that there would be popcorn there as I regularly shop at the nearby Kohl’s department store and had not run across it before.

As my husband and I started to walk in to go to the performance, I saw the popcorn popper first and froze. 

“Popcorn?” 

My husband looked at me as he was saying: “I don’t think they had it before…”

“We can’t go.”

As we were leaving he put his arm around me, “I’m sorry.”

Once we got to the car we decided to go to the local comic book store first and hang out.  After buying a couple of graphic novels and putting the new P.S. 238 (author’s blog link) PS238 graphic novels on order, we headed towards Border’s Bookstore. 

We spent the rest of the evening at Border’s reading.

My husband pointed out that they were doing Disney’s High School Musical and the popcorn might be an aberration due to it being a kid’s production.  I don’t think so.  I think they have discovered the wonders of the money made from concessions.  It just makes me sad.

How much more of the world is going to be cut off from me because popcorn can kill me?

Well, now I know the community theater is off limits - and Kohl’s when they are performing.

I Got Corned…

In the Avoiding Corn Forum, we have an expression “got corned” to describe what happens when one of us gets exposed to corn. Well, I got corned trying to take my dog to the veterinarian.

SMR had to go to the vet for a follow-up to his surgery. I was supposed to meet my husband and when we walked into the vet’s office I could not identify the smell. This is a very bad sign. He sent me outside within seconds. I stood outside the vet’s door waiting to know what was happening. Someone had just popped popcorn. (My understanding is that microwave popcorn fumes are not very good for animal lungs - let alone in a surgery, so I never thought I would run into this at the veterinarian’s!)

I went home feeling like nothing ever goes right. Yet another place that is no longer ’safe’. I then felt my upper lip going numb. I sat in my car with the garage door open and the car off. Tears started to come from my eyes because I was terrified. I didn’t know what to do. I felt somewhat disoriented by what had happened.

My husband, of course, panicked when he found me sitting in the car in the garage. This just scares me. It really doesn’t help when he starts over reacting. I really need him to be calm and caring, but he gets scared and loud. Now, considering what happened between Christmas and New Year’s, I can’t blame him for panicking. (I’m thinking that there was cross-contamination with corn oil since every other treatment for this uses corn oil - including items from the same manufacturer.)

So, I did not want to go to any ER - not after that event. I took a Benadryl and immediately remembered that every physician I know calls it the “over-the-counter” sleeping pill. It always knocks me out. Well, currently, I have to take another two medications at exacting times, relying on my husband for this is out of the question as by Thursdays he is almost as useless as he is on Fridays. (Too tired to move or think, in other words.) Luckily, my phone rang around the time I needed to take the medications in question. I then immediately went back to sleep.

I slept 12 hours. I woke up this morning ok, but tired.

Can you think of any better reason to have not gotten my blogging done? There are several things I want to write about, but there is so little time in a day. . .

So now, I have to remember to tell the vet that I’m allergic to popcorn whenever I need to take SMR to the vet.

Social Isolation, Chronic Illness, and Invisible Handicaps - Food Allergy

There are some illnesses that create more of a sense of isolation than others. Our society does not deal with disease well. Now, we have gotten better - but we still make assumptions. I suffer from one “hidden” disease I am very open about - severe allergy - and another chronic illness that I don’t share openly because, frankly, it is a private matter. (And those who don’t know what it is, can just keep guessing.) I also have friends who suffer incredible hardships because their handicaps are hidden, some of the type we don’t talk about in mixed company.

Now, why am I so hesitant to share information about one disease when I am so open about another? The biggest reason is that I must share information about my allergies if I don’t want to inadvertently die. Yep, die. I am not being melodramatic; wish I were. The other disease, though incredibly painful, is something I do not have to share with anyone but my closest family and friends - and some in the blogosphere.

Why am I blogging about this today? Well, one reason is that this week is Food Allergy Awareness Week or some such. Now, I am not a big fan of FAAN, but they do a lot of good things for a large portion of Food Allergy Sufferers. They just neglect those of us with inconvenient allergies. Most of us who have been around a long time saw this come about with them finding corporate funding, but that is another rant. One thing they did do right was a sponsor a study on Social Isolation in Food Allergic Children. This, can, of course, be extrapolated to adults. A socially isolated child tends to become a socially isolated adult.

Why are food allergic patients so socially isolated? Food is the central point of much of our culture. And this is not limited to family functions. How many business deals are done over lunch? Do you think it doesn’t hurt someone’s career wouldn’t be hurt if they can’t effectively network because the presence of a given food can cause a reaction? What about the great numbers of people who will not be inconvenienced for another person’s needs?

I can’t go anywhere where there is popcorn. I have to inform all of my co-workers that I can’t be around popcorn. Think about this. The most common snack food around is microwave popcorn - which can be a triple whammy since I’m allergic to soy and milk as well.

The first question I get asked: “What’s in popcorn that you are allergic to?”

My answer: “Popcorn.”

Then the person starts listing all the places that have popcorn. Most people forget gas stations. Think about this, if there isn’t a “Pay Outside” option, I can’t use the gas station to fill up. I can’t go into a Target, some KMarts, etc. Oh, and thank goodness for DVDs. I can’t even go near a movie theatre.

I’m not the only one.

Honestly, personally, I lost a lot of friends - who obviously weren’t real friends - when I was diagnosed with food allergies that precluded me from going out to eat. It is pretty hard to go out to eat when you are allergic to the triumvirate of the North American Diet: Corn, Soy, and Milk. And Italian is out with Olives and Olive Oil being allergens. Oriental foods? Rice is an allergen. How about a movie? Popcorn. But, there are other things that I can do. We can rent a movie and have food in - I’ll host. We can go to a museum. We can see a play, sometimes. Or a concert, sometimes. (There may or may not be popcorn at either.) It did help me find real friends who value me as a person rather seeing only what I cannot do. Some are brave enough to take the cooking challenge, some are not. A running joke is to try and get the Iron Chef or Iron Chef America (especially Alton Brown) folks to try to cook a meal for me - with me scrutinizing every food.

If you are new to food allergies, Alton Brown is an invaluable resource for the science of food. I want his entire video library and keep meaning to get it as a gift from my dear husband.

I was an adult when I had to deal with this - and it nearly knocked me down. I was lucky enough to find a wonderful community of folks, Stilyagi and Pinatariders, among them - not to mention the knitting communities, allergy communities, etc. in real life. I also had several online support groups I could turn to. Of course, some of them I fell away from due to a variety of reasons, but there are some core groups that have always been there. I can’t imagine how much harder it would have been when I was a teenager? I shudder to think.

There is nothing about me that would indicate that I have a handicap that prevents me from breathing - a major life function - without accommodation. Food Allergy is not the only disease like this. What about the person with severe breathing problems that are “under control” as long as they don’t exert themselves? Or the person with a cardiac problem that precludes exertion? Asthma?

Next time someone with a handicapped sticker who looks whole and hearty parks in a handicapped spot, do not assume that you can see their handicap.

Oh, and let’s not forget sexual issues that are handicaps. We don’t talk about Women’s Health at all in this country, and I will discuss that in my next post.

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