Blog

  • Dear Gluten Dude: I’m newly diagnosed…when does it get better??

    Dear Gluten Dude: I’m newly diagnosed…when does it get better??

    Sorry for the delay in posts to the Daily Digest folks. Running two businesses, family, knee surgery and LIFE has gotten the best of me lately. I promise to do better moving forward.

    Anyway…here’s an email I received:

    Hi Gluten Dude,

    I was diagnosed with Celiac this summer, a week before my 24th birthday. It was supposed to be my “golden birthday”, turning 24 on the 24th. Instead, it was essentially another day of people cracking jokes at my expense – “oh I added extra gluten to my burrito today” and crap like that.

    I’m struggling with how to find a balance in my social life. I want to still see people, but I feel like they get tired of me talking about CD constantly. I also live in a very small community with very limited resources, and I feel like my world is just shrinking smaller and smaller. I already struggle with anxiety and depression. My husband tries so hard to understand what I am going through but he has no context in his own life.

    I guess I’m asking, when does it get better? When do I get to not live in fear of food? I know my life is changed forever, but everyone, my family included, seems to think this is just a phase. How do I get my bearings back?

    Thank you.

    Just a phenomenal email. I think most of us have been in dark places at some point with our disease. I’ll share how I got out of mine and hopefully you all can pipe in and share your journeys as well. You’ll not only be helping this lovely person, but I’m sure many more as well.

    First, I’d like you to read my five-part series on How to Go Gluten-Free. It touches on my experiences after diagnosis and gives specific advice on how to handle the transition. I think the two most important factors in the transition are your attitude and your support system.

    Without acceptance that this is your new journey, it will be tough to get over that hump.

    Without the desire to WANT to feel better, gluten-free will always be a challenge.

    And without those closest to you getting on board, you will always have that tension in your life. A tension that will make it even more difficult for your body to heal. I’m a huge believer that stress plays a vital role in our physical well-being. Life itself is stressful enough. Try not to surround yourself with people who make it more so.

    I have a whole section my GlutenDude.com blog about dealing with relationships (https://glutendude.com/category/relationships). Please pick the most applicable posts and send the links to your husband and your family so they know that this is not just a phase. This is your life. And celiac disease does not define you. It’s just now a part of who you are.

    I wish you the best and please keep in touch with me.

    GD

    And I’m damned if I do and I’m damned if I don’t
    So here’s to drinks in the dark at the end of my road
    And I’m ready to suffer and I’m ready to hope
    It’s a shot in the dark aimed right at my throat

    – Shake it Out, Florence + the Machine

  • Struggling with Celiac? 41 Ways to Live a Better Life.

    Struggling with Celiac? 41 Ways to Live a Better Life.

    Just diagnosed with celiac and struggling with how to cope on your new journey? Eating gluten-free but still feeling like crap? Worried about what the future will bring? We’ve all been there. That’s the main reason I started this blog in 2011. Because I wasn’t feeling better. I wasn’t happy with my celiac life. I had to make a change.

    Thankfully I did and never looked back. But it’s not just me. Many of us in the celiac community have come to terms with how to cope best with our disease.

    I asked the celiac community the following question: What advice would you give to the newly diagnosed or those who are struggling? Not necessarily what foods to avoid because anybody can look that up. But what have YOU learned from living with celiac disease that you wish you knew when you were first diagnosed?

    Here is some of the spot-on advice they offered:

    • From day one, your illness will be trivialized. From the doctors who diagnose you, who can make it seem that going gluten free is the easiest thing in the world, to anyone you speak to who tell you “there are so many gluten free things on menus now, there’s never been a better time to do it” (like it was a choice), to the waiters that roll their eyes at you. Rise above it.
    • It is surprising and alarming how many food professionals have absolutely no idea what they are putting in to their food.
    • Some symptoms will lift immediately. For me, the migraines (which I didn’t realize were related until after they stopped), the extreme bloating and pain ceased very quickly. Others will take awhile. Be gentle. Know that your body will take a while to recover and that is OK.
    • A lot of people go “Gluten Free” for weight and diet reasons. You very well could gain weight. I personally have been severely underweight for a long time. I gained 7.5 kilograms (16.5 pounds) when I stopped eating gluten. Roughly 15% of my body weight. Even though I was now eating a lot less, my body had not been absorbing what I had been eating. Weight gain was a very unexpected side effect!
    • There will be a break down of some or many of your relationships. This illness can be debilitating and socially ostracizing. Either you will tire of the people who tell you how they eat gluten free for “health reasons” and its SOOOO easy, or they will tire of you, because you are now a “burden” at social engagements.
    • You will spend a lot of time apologizing for your illness. Over time you will stop doing this, but particularly in the beginning you will feel like a burden. Sometimes its easier not to eat than it is to “cause a fuss”. If any one makes you feel like this – it’s easier to remove them from your life than it was to remove gluten so feel free to do that.
    • Research has indicated that there are significantly higher levels of depression and anxiety among those with Celiac Disease, in particular young adults. Celiac disease is 24 hours a day, with no end in sight. Most days it is OK, and you get used to it, but you cannot switch it off, you are constantly in a state of high alert, because anything that you put in your mouth can make you sick. More knowledge and awareness and comfort will lesson this, but it will never go away. Do not let it consume you.
    • Check the ingredients of EVERYTHING. Gluten is a filler and hides in the most unexpected places. Some recent places that I have found it – Oral Contraceptive pill, Cold and Flu Tablets, and other medicines. Again – ignorance from medical professionals mean that you can and will still be prescribed tablets that contain gluten. Always always always double check.
    • You WILL start to feel better. Your eyes will become clearer, the fog that you felt in your mind will lift, the migraines will end, the pain will end, any nutritional deficiencies you had will even out.
    • There is something empowering about knowing that you don’t have to take medication, and you can (to a large extent) control this illness.
    • While you will lose some relationships, you will gain others. You will gain a new appreciation for people who have a basic respect and thoughtfulness for you, and the little things will become big things.
    • There will be some long days, and hard weeks that turn into months, but you will discover a strength you didn’t realize you had, and instead of feeling isolated, and isolating yourself, you will search deep into your own soul and the values of those around you, and surround yourself with people who make you feel exactly how you should – that celiac can suck, but it is not your fault, you are not a burden and you are not alone.
    • Knowledge is POWER especially with this disease. I was diagnosed 6 years ago and I can say with 100% certainty that it does in fact get easier and better every single day.
    • Attitude is everything in this journey and there’s no other way to say it. Keep your chin up, don’t apologize for having a disease that is out of your control and find new foods you enjoy that are also healthy for you.
    • Stay away from the processed foods as much as possible. Fresh fruits and vegetables, meats, cheeses, wine, etc. are all gluten free and fantastic! Keep it simple and learn to enjoy whole foods.
    • You will link so many different problems to Celiac that arise. Issues that you thought were separate and just how your body works… good chance they’re part of the effects of the disease. I thought Celiac was mostly my dermatitis herpetiformus… turns out it’s linked with fatigue, nerve and mood issues, insomnia, cramping, bloating, etc.
    • It’s a learning curve. Take it slowly and build on your knowledge base. You will make mistakes, and they will be painful. You learn from them though and move forward until it’s second nature.
    • It is so important to be your own advocate. If you think something is wrong, FIGHT for your doctors to hear you. I was almost not diagnosed because of my doctors. If your doctor isn’t listening to you, it’s time to find a new doctor.
    • Life goes on, but gluten stays behind – You are going to feel angry, frustrated, and nervous after finding out you now can’t eat some of your favorite foods, and while you may think “life as you knew it is over,” you need to change your mindset and focus on what you CAN eat verses what you no longer can. It will make a huge difference.
    • It takes TIME – Nothing comes easy or fast, and you’ll realize that with this diagnosis. Patience is probably the hardest part because you just want to feel better NOW. Take it one step at a time, and know that things will start to become second-nature to you quicker than you thought!
    • If you don’t love cooking, learn to love it. Start experimenting with different ways to prepare foods that are very tasty to you. Also, don’t take any food for granted. I made a lot of mistakes along the way eating foods that would normally be gluten-free but were not. Above all, be kind to yourself when you mess up and get sick. It happens to all of us.
    • So many different symptoms with this disease, and sometimes, no matter how hard you try to do everything right, in the end, it is your acceptance that maybe you won’t have perfect health with this disease which will help you the most.
    • My contribution is to give yourself permission to grieve – the loss of your life as you now know it, the uphill battle with friends and family to come (“No, Grandma, I can’t use the same tub of butter”), the radical changes coming your way (no more picking up Chinese takeout when you’re too tired to cook). If you try to repress it at the beginning, you’ll wind up standing in the middle of the grocery store, bawling your eyes out because you’ve just read a label and realized you can’t have one of your favorite foods anymore. But it’s just as important to move on from grieving – the radical changes coming your way DO include feeling better, knowing who your true friends are, and learning about lots of delicious food you might not ever have looked into (quinoa, anyone?)
    • It may feel like your entire life revolves around food and eating safely. It may actually be true. Those with other illnesses/diseases have a heightened awareness about what makes them ill. Paying close attention to what you eat is no different. Think of it as saving your own life…your new mission.
    • Advanced planning is part of your life now (as much as food is). Being spontaneous may be difficult but being healthy and having quality of life is so much better. Take a few minutes to pre-plan and everything else will fall into place.
    • ALWAYS HAVE SAFE FOOD WITH YOU!!! Always. If there’s an emergency you need to be able to eat safely.
    • Learn how to say “thanks, but no thanks” to the well-meaning person who insisted they made you a special gluten-free dish for the potluck. If you know they understand cross-contamination, it’s one thing, but for me the risk of getting glutened is so great.
    • My advice is prepare for peer pressure. I don’t mean stress about it. Just prepare yourself. Plan what you are going to do or say at the next company potluck when a coworker wants you to try his or her dish and even though they say its gluten-free, you watched three other people cross-contaminate the dish with the wrong spoon. Be ready for the next family dinner when Aunt Sally insinuates that a little gluten won’t hurt anybody. From interactions to people close to you to complete strangers, have a plan. Write a list of things you can say. Keep your reasons short, polite, and to the point.
    • LEARN TO COOK! You just have to. It’s not that bad. And yes, you have the time.
    • Know that a lot of the time you will feel like it’s unfair. It is unfair that there are people who can be carefree and just walk into any restaurant and eat and you can’t. But try to remember there are people who have it way worse than you. You can cure your body with just food!
    • At the risk of sounding like I am trying to get on Gluten Dude’s good side…the first thing I tell anyone newly diagnosed is GO TO THE GLUTEN DUDE website and meet your people!! I have told GD this but this website was a huge blessing and source of strength to me. The people here are amazing and made my life so much better. (Dude note: I have a good side?)
    • There’s a withdrawal. And it sucks. I’m pretty sure it feels just like going off sugar or caffeine. I felt restless, confused, I ate twice as much as usual for a week and never felt satisfied. Still, cold turkey is the way to go. “Easing” into the gluten-free lifestyle is only delaying the time you will feel better.
    • You will find there are a lot of people spreading rumors, selling dubious products and tests, and just plain nonsensical “information” out there. You need to have a good dose of common sense, a basic understanding of anatomy, a basic understanding of cooking, and the ability to look for reliable scientific or medical information. Don’t believe someone with a slick website calling themself a “gluten free XYZ” or a “doctor of gluten” or some other made up credential.
    • While it isn’t a great thing to have this disease, having it will open your eyes as to what really is and isn’t good for you, as well as teach you to be your own advocate and how to take care of you.
    • You’ll learn how to become a good advocate for yourself. It’s hard – it’s not something that comes naturally to many of us! But it’ll get easier, and know that looking out for your health isn’t being unreasonable, overly demanding, or “too needy.”
    • Socializing will be trickier for a while, but don’t let your world shrink down out of fear. Sharing food is a central part of a LOT of our social moments, and it’s going to take a while for you, your family and friends to figure out a new way of navigating these times.
    • Grocery stores become grief stores. So much of what is sold is completely and forever off limits. Know this, and be ready for the weirdest bouts of grocery store tears. Once when the grocery store was out of my crackers, I wept, openly. This will happen, and its ok. After a while the tear portion of the program will taper off, and the angry section will open its doors. Losing so much food is bound to fire up the emotions. It’s normal and you are totally allowed to express your feelings.
    • Traveling by air and finding food either in the airport or on the plane is usually impossible. Carry your own, and more than you’d think is necessary. Supplement with chips, fresh fruits, and nuts, bought at the airport.
    • Upon diagnosis, I cried, not because of the loss of all those foods I loved – I cried from sheer relief of finally knowing what my “enemy” was. The enemy had ravaged my body and nearly killed me. Focus on how good it’s going to feel to feel good!
    • Stand firm in your goal to become healthy. The enemy has been exposed and it is gluten! Now go fight for your health, and stop spending so much energy on the memory of those foods that robbed you of that health!
    • And finally, never forget your sense of humor! Gluten Dude is an excellent example to us all. Keep pushing forward, never give up, and laugh at yourself and the tough things in life every chance you get.

    And finally, here is my biggest piece of advice. Live Your Life. Do not let celiac hold you back. It’s a bump in the road, but it’s a bump that is manageable. I promise.

    Yes, you’ve got some serious adjustments to make.

    Yes, your body will take some time to heal.

    Yes, you will lose a little bit of freedom and spontaneity in your life.

    But you know what? You’re getting your health back and that’s what matters.

    There is an unbelievable amount of fear-mongering online. “You can’t have this” and “you should stay away from that”. Some of it is accurate. Some of it is complete BS. Stick with the facts.

    Do not live your life afraid to do things simply because of GLUTEN. No matter what people say, it’s NOT everywhere and you CAN lead a normal life (with a few adjustments).

    Take precautions. Educate yourself. Use common sense. And if in doubt, do without.

  • No…Wendy’s is NOT safe for people with celiac disease

    No…Wendy’s is NOT safe for people with celiac disease

    The Nima Sensor influencers have gone nuts. It’s amazing what people will do for money.

    The latest example: This woman whose every other post is testing shitty fast food with the Nima Sensor and then celebrating that she can eat whatever she just tested. And then eats it.

    She just did this with Wendy’s fries.

    It doesn’t matter to her that:

    • Wendy’s actually says their fries are not GF.
    • It only tests a miniscule amount.
    • It’s not 100% accurate.

    When there is money to be made, damn the celiac community.

    Here is my response to her post:

    And you can see I wasn’t alone in my feelings.

    It’s a shame.

    But in today’s me-first world, nothing surprises me anymore

  • Does anyone out there have celiac AND tourette syndrome?

    Does anyone out there have celiac AND tourette syndrome?

    I have had a long and sordid health history, going way, way back.

    Here’s a brief summary from childhood til now: warts, rheumatoid arthritis, acne, back pain, bladder cancer, celiac disease, pulmonary embolisms, covid 4 times, dupuytren’s contracture, osteoarthritis, melanoma and cracked teeth.

    You can read all about it here: https://glutendude.com/does-celiac-disease-cause-other-health-issues/

    Yes I’m convinced they are mostly connected to celiac.
    No I have no proof.

    But one thing I did not mention that I’ve had since childhood is Tourette Syndrome. Sometimes very controllable. Other times…not so much.

    My parents completely ignored it. Thanks mom and dad.

    I’m nowhere near childhood and I still unfortunately deal with it.

    If you have both celiac and tourette, I would love to hear from you.

  • My sh*t don’t stink. Literally. And now neither will yours.

    My sh*t don’t stink. Literally. And now neither will yours.

    Warning #1: This article contains some serious journalism. If you are not into someone uncovering the facts with big words that make me sound important, stop reading now.

    Warning #2: Warning #1 is a lie. This article talks about poop. Proceed at your own discretion.

    Funny story…about 20 years ago, I was visiting my mom (RIP) with my family and had to use the facilities. Yes…number two. There was only one bathroom. I did my business. When I got out, my then nine year old nephew went it. And came right back out and said “IT SMELLS NOT GOOD IN THERE.” We still giggle about it to this day.

    If there was only a product that could make my poops smell like roses?

    WELL…THERE IS (watch the video).

    I initially came across that video a few years ago and thought, as hysterical as it was, there was no way it was a real product. And if it was a real product, there was no way it works.

    Well guess what Mrs. Dude brought home a few weeks ago?

    Yeah…I was skeptical. As a celiac, let’s just say I can make a bathroom unusable for a day every once in awhile. It ain’t fun being me at times…or living with me. So I figured, what have I got to lose.

    I should have read the instructions though. Instead of spraying the toilet, I thought I was supposed to spray it up my butt. You don’t need to teach me that lesson more than once.

    Yes…I’m just kidding.

    Anyway, no need to go deep into details here (you’re welcome). I sprayed. I pooped. It worked. Amazingly well. Like really amazingly well. Like “I’m bringing it with me when I travel” well.

    Like I said…serious journalism here at the Daily Digest.

  • Breathe Scott…everything is gonna work out

    Breathe Scott…everything is gonna work out

    For those of you who follow me on Facebook, bless your little hearts, you may have seen this post last week.

    But I also wanted to share it with you, my wonderful app family.

    This may be a bit of a rambling post, so bear with me.

    Yesterday was a win. Well…a win-win actually.

    A win for everyone who was able to get lifetime access to my app within their budget. I’ve said since day one, I never want money to be the reason someone cannot use the app. If you want the app, regardless, I’ll make it work. 🧡

    But it was a needed win for me too. Let me explain.

    It’s been a long year. I mean a real long year.

    I knew rebuilding the app from scratch would be a challenge. And it was. A labor-intensive, exhilarating, expensive, creative, hair-pulling challenge.

    When it launched early February, the feedback was awesome, but I was spent.

    And though people love the app and it has a 4.8 rating on the app store, the fact is, not enough people were subscribing to support it.

    The economy stinks, the world is on fire and I think people are subscriptioned to death. Yes…I just made that word up. 😁

    I understand it is not an app people will use every day. But when you need it, you really need it.

    So I tried something different this week. Pay what you can for lifetime access.

    And you showed up. In a big way.

    I won’t share the exact numbers, but I will say this: it genuinely changed my outlook on where this is all heading.

    The app is going to be just fine. And so am I.

    Thank you. Seriously. 🧡👊

    This community has carried me more times than you know.

    Scott

  • Celiac Disease is Bulllshit (according to Call Her Daddy)

    Celiac Disease is Bulllshit (according to Call Her Daddy)

    Call Her Daddy: A podcast with over 2 million subscribers.

    Robbie Hoffman: The current ‘it’ comedienne.

    Just called celiac disease NOT REAL.

    Seriously. In 2026.

    Please go to my Facebook, Instagram or TikTok pages to see the video. It ain’t pretty.

  • GF Jules Recipe: Protein Brownies

    GF Jules Recipe: Protein Brownies

    Chocolate…good. Protein…good for you. The perfect combo for a healthy, yummy treat.

    Prep Time: 15 minutes
    Cook Time: 25 minutes
    Servings: 20 brownies

    INGREDIENTS

    • 2 ounces unsweetened chocolate non-dairy = two 100% cacao baking squares — Ghirardelli or Baker’s Unsweetened
    • 1/2 cup chocolate chips dairy or nondairy, like Enjoy Life®
    • 8 Tbs. butter or non-dairy alternative (like Earth Balance® Buttery Sticks)
    • 3/4 cup granulated cane sugar
    • 1/4 cup brown sugar or coconut palm sugar lightly packed
    • 2 tsp. pure vanilla extract
    • 2 large eggs or egg substitute of choice see Vegan Egg Substitutions Post for suggested substitutions
    • 1/4 cup gluten free protein drink like OWYN Cold Brew OR may use brewed black coffee or chocolate milk
    • 2/3 (90) cup (grams) gfJules™ All Purpose Gluten Free Flour
    • 1/2 teaspoon salt

    INSTRUCTIONS

    1. Preheat oven to 350ºF (static).
    2. Arrange a sheet of parchment paper or aluminum foil in an 8 x 8-inch baking pan, pressing to cover the bottom and up the sides. If using aluminum foil, lightly spray with cooking oil. This step will make it easier to remove the brownies from the pan by pulling up on the paper or foil and leaving behind a clean pan.
    3. Prepare a double boiler or a medium-size pan filled with 1 inch of water, with a slightly smaller pan sitting on top of the pan with water. Boil the water in the bottom pan, then cut the flame back to low-medium and add the chocolates and butter to the top pan over the simmering water. Stir and remove from heat when melted.
    4. Add sugars and stir while the mixture is hot.
    5. Add vanilla, eggs and protein drink or coffee, stirring to integrate.
    6. Whisk in gfJules Flour and salt, continuing to stir until all lumps are smooth.
    7. Pour the batter into the prepared pan and bake for 25–30 minutes, or until a toothpick or cake tester inserted in center comes out with only a few wet crumbs (not totally clean, or they’ll be overcooked!).
    8. (As a rule, brownies are much better on the un-done side, as opposed to the overdone side.)
    9. Cool brownies in the pan on a wire rack for 5 minutes. Lift the brownies from the pan by pulling up on the paper or foil.
    10. Completely cool brownies on a wire rack. Cut into squares with a clean plastic knife or pizza cutter and serve.
    11. Yield: approximately 16–20 brownies, depending on size cut.

    Link to full recipe on Jules’ site.

  • Dear Gluten Dude: My Celiac Wife Treats Me Like the Enemy

    Dear Gluten Dude: My Celiac Wife Treats Me Like the Enemy

    Did you know that I have a whole section of  Gluten-Free Love Stories on my blog?  Fantastic, heartwarming stories of how celiac/gluten has brought people together.

    But today, we have something quite the opposite. It seems celiac disease is breaking this marriage up.

    Yes, I’m sure there are many underlying issues as well so I am not pinning this on celiac disease, but it’s not helping matters.

    Read on and share your thoughts.

    ——————————————————————–

    Dear Gluten Dude,

    I KNOW guys are dumb but am I really the idiot my pregnant wife w/ celiac disease makes me out to be??

    I bought her groceries at the hour-trip-across-town grocer. On the way, I bought her some lip gloss (gf of course…she even had me watching YouTube about it.) I bought the 30 dollar stuff thinking I’m gonna be a hero and instead I turned out to be the fool.

    Apparently in Sephora (the store where I bought the lip gloss), gluten is in the air by way of perfume. My clothes are then glutened and I go to the grocery store after this. I buy 50 dollars worth of salsa, whole pineapple and cherries.

    I have tried to surprise her before with other things. Not food. It seems there is always some way to call me an idiot. I cook her food and spend hours via bus and train getting her food. I admit I get frustrated but why do I have to be yelled at even for wearing my jacket in the kitchen? She sends me to stores just to make me return it all even if I even wash my hands thoroughly and double tie the bags.

    I read your spousal support article but at what point is it not my fault? I can’t erase gluten from history (can I?).

    I just want to know what should I do? She is driving me crazy. I know she did not ask for CD. But she yells at me for eating gluten…period. She changes the rules everyday. I can’t afford to buy gluten free food for 2 people on what I make. I cook her food with a clean kitchen and wash my hands with dawn to the point of peeling.

    Do you have any advice for me? I fear we will be heading for divorce.

    ——————————————————————–

    A few quick thoughts here. As I said above, it seems to me your marriage issues go beyond celiac disease but I am not wearing my marriage counselor hat today, so I’ll leave that to the experts.

    To you I would say try to be patient. Celiac can affect somebody not only physically, but emotionally too. Add that to being pregnant and there could be a lot going on with her right now.

    I would say to your wife that she needs to ease up on the gluten paranoia a bit. Yes…we need to be incredibly careful. But worrying about perfume on your clothes and then going grocery shopping seems a bit extreme to me. Celiacs don’t live in a plastic bubble. Being paranoid stops us from enjoying life.

    And there is no reason for you to take any heat for eating gluten. You don’t have celiac disease…she does.

    Good luck to the both of you.

  • Dude…why do I feel like crap if I’m eating 100% gluten-free?

    Dude…why do I feel like crap if I’m eating 100% gluten-free?

    The biggest lie in the world of celiac disease is that you’ll feel better immediately once you begin your gluten-free diet. It sure as hell didn’t happen to me and my guess is you also did not have those results. And it did not happen to this 19 year old woman, whose parents are frustrated. Here’s the email:

    “Hi Gluten Dude. My daughter is nineteen and was diagnosed with Celiac Disease five months ago. She was having severe stomach pain and after landing in the hospital, a biopsy came back as celiac. She has gone completely gluten free and the severe stomach pains are gone but she just feels crappy almost every time she eats. They told us it may take up to a year for her to feel completely better because her celiac was on the severe side. I am looking for confirmation this is normal and that there is still hope she will feel better. She is down right now with all the things she can’t eat. It is devastating to she your child feel so left out I just wish she would turn that corner. Any advice would be terrific! Thank you!”

    My advice? Stop eating gluten-free food. Let me explain.

    When I went to the doctor first and I showed him my diary and he says, Have you ever heard of Celiac disease? And I said, no. He goes, well, we’re going to test you for celiac disease. I said, well, okay. So I took a blood test and then I went home and I looked up Celiac disease.

    And of course, the first thing I saw was, you have to be on a gluten free diet for life. And I said, okay, what’s gluten? So I looked at what gluten was, and then I cried in my closet for like, 3 hours.

    No, I’m just kidding. So I did a bunch of research and every website I found said that once you go on a gluten free diet, you’ll feel better almost right away.

    And I mean, I must have checked 100 websites and 98 of them said the same thing. ‘It’s a miracle diet’. ‘It makes your celiac not obviously go away, but you’ll feel better right away.‘

    Those are my expectations going in.

    So when I got the results in, he says, my God, yeah, you’ve got really bad Celiac, I said, okay, and I went home and went to Wegmans and got some gluten free food and just expected to feel better within a couple of days. And a day went by and a week went by and a month went by and a year went by. And I’m not exaggerating. I had some good days in there, but I felt like crap most of the time, and my frustration level was absolutely through the roof.

    I eventually gave up dairy after a large, rare argument with my lovely wife, Debbie, A-K-A. Mrs. Dude, and that helped a lot, but it wasn’t enough. So I knew I had to make a serious change. So this is almost two years into my diagnosis. I heard about a diet called the Whole 30. It’s 30 days of eating just whole foods so you can have fish, you can have meat, you can have veggies, you can have fruit, you can have water. What you can’t have is alcohol, grains, sauces, coffee. Although I cheated on the coffee eventually. Dairy, obviously gluten. The idea is that you’re cleansing your body for 30 days, allowing it to heal and then maybe reintroducing some normal foods after 30 days and I will tell you this; it was insane how much it helped me.

    So let me go over what I was eating in a normal day pre whole 30 and post Celiac diagnosis. I’d wake up and I’d have coffee with a splendid and some kind of gluten free bar, usually a Kind bar, anything that was gluten free and probably not very healthy. For breakfast, I’d have a bowl of honey chex with almond milk. For lunch, I’d have Brown rice, fish and veggies with a gluten free sauce. For snack, I’d have some other unhealthy gluten free bar, and then for dinner, I’d have gluten free pasta with chicken, et cetera.

    Now to me, I thought that was a pretty healthy day, but then why did I always feel like crap? And why couldn’t I lose any of the weight I put on post diagnosis. Not that I was looking to lose weight, but I wasn’t feeling good about myself. I knew I had to shed some pounds, so I looked at the ingredients of honey nut chex and let me go over the first six ingredients: whole grain corn, cornmeal, sugar, honey, salt, molasses, Brown sugar syrup. And you’re wondering why I wasn’t feeling well.

    Now, after the whole 30, this became my average eating day. Early morning black coffee, no sugar. I dropped the sugar in a splendid for my coffee breakfast. Three eggs with sausage asparagus onion and mushroom lunch, fish and veggies, but with olive oil and spices instead of the rice and the sauces. Snack was almonds or a piece of fruit, and dinner was a piece of chicken or steak with veggies, et cetera. Now, a couple of notes here you note, I’m not exactly starving myself with this new diet. Secondly, I’m not eating gluten free anymore. I’m eating just regular foods, and that was the key to my health in this situation.

    For the nineteen year old woman who is not healing and you out there, if you’re not healing, let me ask you a question. When you were first diagnosed with celiac disease, what’s one of the first things that you did? Now, if you’re like me, you went to the store and cleaned the shelves of all the gluten free items you could find. Your mindset is, well, I can’t give up pizza. Oh, I can have gluten free pizza. Well, I can’t give up pasta. Oh, yes, I can have gluten free pasta. I can’t give up cookies. Yes, they have gluten free cookies. You get the point. The problem is, a large majority of the gluten free food out there is garbage. But many of the gluten free food manufacturers are more than happy to feed us this crap because they know the emotional attachment people have with eating, and they know the intense fear Celiacs have of losing their lifestyle as they know it. And they also know the enormous profit they can make off of us.

    For the most part, let’s face it, big companies don’t give a shit about our health. They give a shit about their profit. I have been to a few Celiac awareness functions over the years, but you know what it is? It’s not so much about celiac awareness, but it’s a gluten free food orgy. It’s table after table of foods that Celiacs should not be putting into their bodies, but because it’s gluten free, hey, it must be good for us, right? Who cares if it’s twice as fattening, three times as expensive?

    And look, I’m not saying you should not be eating treats, and I’m not saying you should never process food again. What I am saying is that if you are not healing, stay away from the gluten free foods, at least for a while. Just give your body rest, even for 30 days. Give your body a rest and see if it makes a difference.

    And if you’re like me, you will not go back to the way you used to eat. There is no reason at all any of us should be walking around in pain and simply accepting that, hey, that’s the life of the celiac.

    So bottom line, if you’re struggling, if you’re not healing, if you’re frustrated, do not accept that that’s just the way it is. Make a change. It could be the whole 30. It could be something else. But do not keep doing what you’re doing if you’re not getting the results. We all deserve to feel good inside.