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Learning Curve


thumper

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thumper Apprentice

Sense I have been gluten free sinse Feb. 6, 2008 which I realize is only 3 weeks I have been on a mission to learn as much as possible about celiac as fast as possilbe.. Maybe it is just because I was so very sick for over 13 yrs before getting a right diagnoses and maybe I have my expectations too high. I truly thought that by this time I would be feeling good as new and I am so frustrated because It seems all I have learned is that I also can't tolerate milk (dairy products) and I didn't have the chicken pox I have Dermatitis Herpetifomis and I have to learn about that as well.

I am getting overwhelmed with my symptoms and stupidity all I did today was lay on the couch feeling awful, stupid, itchy, crabby, frustrated and my bottom is sore from all the trips to the bath room. Oh I forgot crying most of my day away..

I swear that I know nothing more than I did 3 weeks ago am I just stupid, am I reading the wrong book, The gluten-free bible by Jax Peters Lowell ?? I've spent all my money on gluten free food that I can't afford another book at this time and I am not finished with her book yet.

And what the f*** do you use in recipes that call for milk when you can't have it ??

I have no one in my house to talk to about all this so I feel all alone in it I know there are those who have been living with this for many years, how did you all do it ?? How do you learn faster and when do you start to feel better ???

Thumper


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Jestgar Rising Star

Well, you're just as stupid as all of us were when we first started this adventure. It really does get better, it's just that there's so much to learn at the beginning.

I use almond milk in place of dairy. There are also soy and rice substitutes for milk. You can find non-dairy subs for cheese and yogurt as well, but I don't like any of them so I mostly do without and cheat with cheese occasionally.

Check out your local library to see if they have gluten-free books you can read.

And hang in there, it does get better.

Ursa Major Collaborator

Thumper, I wished I could come over and help you out. You are having the 'diet blues' right now, and everything seems impossible. But you will get better, be patient. It takes a LOT longer than three weeks to feel 'good as new'. It took you years to get really sick, and it will take at least a year to be really well.

Instead of 'real' milk, people here use a variety of products. I use rice milk (not rice dream, it has barley malt). Others use soy milk (I don't really recommend that, soy is another thing many people with celiac disease can't tolerate, and it isn't healthy), while there are those that use almond milk.

I use rice milk on cereal, in cooking and baking, and it works just fine and tastes okay (I don't drink it straight).

You are NOT stupid. All this is overwhelming, especially if you don't have the support you need. You will get the hang of it, really, you will. It all takes time, it is a whole new life style.

The gluten-free bible is okay, but not the best book out there. But you can get all the info you need right here in the forum, just ask questions.

Pretty much all you need to know about dh is, that you need to be on a gluten-free diet, and shouldn't eat a lot of iodine. Because the only real valid treatment for dh is the gluten-free diet, everything else is a bandaid solution that doesn't solve the underlying issue.

Worriedtodeath Enthusiast

It does get easier. It's also a great idea to stick with just basic fruits/veggies/plain meat for the first month or so while you figure out the whole gluten free thing. The gluten free products like cookies and such can be hard on your stomach at first. maybe sticking with simple foods that are naturally gluten free will help you feel better quicker.

HTH

Stacie

sickchick Community Regular

You're just frustrated. I am on the same path as you and I was sick for 11 and just went Dairy & Soy free Dec 1st. I actually have been sick so long I knew it wasn't going to be a quick recovery.

I really keep things basic for myself right now. I drink Almond Milk too and it's really yummy! :)

I found some brown rice breakfast cereal that is pretty good, very basic, I don't eat very much just because I feel better when I don't. My body digests food so retarded (yup I am wheat-tarded ) ;) I just wait until evenings and I only have one meal.

Good luck and don't be hard on yourself.

I am actually beginning to like no cheese on my pizza! hahaha

lovelove

sickchick

gottaBGfree Newbie

It will get better! Having been sick/misdiagnosed for 10 years, it is taking me a while too! I am so thankful that I can think (by that I mean that the brain fog has lifted) and believe me the day will soon come that you spend much less time in the bathroom! Now, I'm gaining weight and actually having to monitor my calories and what I eat because I'm actually gaining weight!! I never thought I would have that problem.

If you are reading about celiac, you know that the depression and "blues" are par for the course. I am now learning where in the realtively small town that I live in I can eat out safely. Not being able to go out to eat or even have a few drinks was a major bummer for me. If you are really depressed to the point that you are crying and having a miserable time, maybe you should talk to your dr about that. There are mild antidepressants that can help you get through this if needed, and no you will not be the first person with celica who has had to go there!! learning that you have to live gluten free and dairy free in your case, is much like dealing with loosing someone that you love. I thought I was crazy when i was feeling so sad when I was first diagnosed. It was like I was trying to cope with the loss of a family member...then I logged onto this site and realized that it is something that almost all of us have delt with! Hang in there, I promise better days are headed your way!! :)

CeliacMom2008 Enthusiast

I don't have advice, just kind words...hang in there. You may not have support at home, but you have it here. A previous poster is right - you don't need to spend money on books. Just hang out around here and ask lots of questions. We're new to the Celiac family (Dec. '07) too, but I can tell you I've stopped crying (mostly) and am doing much better. When you need a boost or a friend, just start typing. Someone will be here to help pick you up and share a smile! :D


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sickchick Community Regular
It was like I was trying to cope with the loss of a family member...then I logged onto this site and realized that it is something that almost all of us have delt with! Hang in there, I promise better days are headed your way!! :)

It took me a year of mourning the person I was before I got sick.

but since I actually can reverse what's happened to my body I am letting nothing stand in my way!

Be well B)

happygirl Collaborator

It will get better!

Also, once you heal, you may be able to tolerate dairy products. Its not necessarily a long-term problem.

"Lactose intolerance may be a transitional problem until the villi heal." Open Original Shared Link

Hang in there.

YoloGx Rookie
It will get better!

Also, once you heal, you may be able to tolerate dairy products. Its not necessarily a long-term problem.

"Lactose intolerance may be a transitional problem until the villi heal." Open Original Shared Link

Hang in there.

I sympathize with your situation. It just isn't easy giving things up. I think in part this is why so many people who are sensitive to gluten just choose to ignore their complaints. I think this is also why my mother put me back on gluten when I was four years old even though I had previously been hospitalized and almost died from being introduced to grains when I was 4 months old. My constant ill health then was mocked rather than understood as being dietary related. There is so much attachment in this country to a "standard" American diet and fear of being different in that arena. People use comfort food to feel safe after all.

However its way worth it in improved health and a better, longer life in all kinds of ways to give up the gluten. I was sick all my life until I figured out slowly what was what. Even now I am still learning and am so greatfull for this forum. One of the last steps for me was learning about avoiding all the hidden glutens, like in your old wooden utensils and cutting boards and any iron pots or pans you might have or things with old baked in food stuck in the pyrex etc. Plus cross contamination issues...

For me I can't tolerate almond milk and rice milk usually has beta carotene in it which I am also allergic too. So when I want milk I either use coconut milk or plain non fat organic yogurt that I thin down.

As far as the books go, later on when you can afford it look at one of those online book sellers. You can usually get used books for a lot less.

Herbs that could help against the depression might be skullcap, melissa, rosemary and lavender tea. My brother swears that using St. Johns Wort helps. That plus exercise and sauna as much as you can even if its just going out for a walk.

I also find the detox herbs a big help--dandelion and burdock (this will help with the skin big time) and maybe yellow dock or Oregon grape root every other week. Pao de Arco also helps maintain good flora and elimination. Plus marshmallow root and/or slippery elm caps will help soothe and heal the lining of the intestines. You see its all these accumulated toxins that are making you feel bad. That plus the unhealed lining of the intestines allowing leaky gut to make a lot of your food a little dangerous for you until you have healed more although you still have to eat. That is why eating a more paleo diet of vegetables, meat and some fruit is usually better to begin with and whenever you feel low or out of sorts anyway--despite all inner programming about processed food and sweets etc. being comfort food. For us they really are not given the boomerang effect!

GlutenGalAZ Enthusiast

Thumper:

In the beginning for me I just wanted to start to feel better so I was eating a lot of salads, white corn tortillas (Mission) things that were from the grocery store that I knew were safe while I did research on what I could eat. It is very hard in the beginning with understanding everything and knowing what to look for and hidden gluten. It has been almost a year for me trying to be gluten free, I have messed up a lot during the last year getting frustrated and missing food but it finally hit me that I NEED to do this to feel better and for my family. That in order to not have the run to the bathroom episodes and stomach torture pains I needed to stick to this and not have off diet dinners once in a while.

If your stomach is hurting try a heating pad. Sometimes it helps and sometimes it doesn't. Also Epson Salt baths.

I did A LOT of research online. I bought one gluten free book and then a couple of cookbooks on amazon (read a lot of reviews and even got one for kids/busy adults -- has easy things to cook). I found the internet and this website a lot more understandable than books. I don't have a Henry's or Whole Foods where I live but a health food store in town that helps me with questions about cooking products.

Try to ask questions at the specialty stores. I haven't had luck at regular grocery stores, when I would ask if they carried a product (that I later found) they would look at me with a blank face. You will find a lot of foods that you can eat at the grocery store where you don't always have to go spend a lot of money on expensive gluten free foods at specialty stores.

One of my favorite dinners to make is spaghetti you can use Classico sauce, meat and gluten free noodles.

A lot of websites will have a frequently asked question page and some will have lists of all of their gluten free items (like Hormel and Frito Lays) and some sites will just have a statement about it. Some fast food places and restaurants have started having allergy lists/gluten free lists as well. You still have to be careful though of CC.

Here are a couple of websites:

Open Original Shared Link (Basics/Hints, Avoid and Samples of what to eat)

Open Original Shared Link (if you click on the gluten free diet there is a grains/flours glossary)

Open Original Shared Link (cooking pointers)

Open Original Shared Link (left side of the screen will have different lists to click on)

Best of luck. Things will start to improve, it takes a while for your body to start healing :)

scotty Explorer

'wishiwasbackonthebayou-rollinwithsomecajunqueen'

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flourgirl Apprentice

Hi Thumper. No, it isn't much fun in the beginning. I really thought I would magically feel better quickly, at least I strongly hoped I would. Emotionally I was great, at first, except for being desperately ill. I was just so grateful to not have cancer or something that would require surgery, or nasty drugs or chemo. But, as time dragged on and healing came so slowly I got seriously depressed. I know I'm not myself yet, my moods swing up and down and sideways....but the pendulum is slowing down. Overall I AM doing better, and each day brings better health closer.

You really don't have to buy a lot of books. I did buy books, partly because I LOVE books, almost any books. I like having a reference that I can return to (and I have dragged books to my Dr.s office to back up my thoughts about my treatment). I have reread lots of things because there is just SO MUCH info. to absorb and remember. After a while it'll just become a way of life, and not feel so foreign.

Hope your healing comes quickly and that you can feel better soon. You'll be all right. There are many caring people here to listen and share.

Flourgirl

susieg-1 Apprentice

hang in there kid time will help heal also epsom salt baths, jason's skin andbath products sold at wegmans are great for your sensitive skin. buy new toaster, one new fry pan with spatula, new dishwasher safe pot holder and label everyting gluten-free in kitchen with colored stickers, 8 months gluten-free and still get occasional symptoms :D

sparkles Contributor

When I first went gluten-free, I was so overwhelmed by the diet that I just ate hamburger, lettuce with a lemon squeezed on top and baked potato with all the butter I wanted. I added fresh veggies and fruit after a few weeks and when I was ready about 4 months later, I started reading labels and eating foods labeled gluten-free. For me it was too overwhelming to spend hours in the grocery store reading labels, I just went with what was the easiest. I think that it helped my gut heal faster by limiting the kinds of foods that I ate. It does get easier and cheaper especially when you realize that a lot of the gluten-free foods are really high in fat and the taste is not worth the calories. There are a few I like but I really stick to the main stream foods that label their products. Make it easy on yourself. You will go through a grieving process.... but giving up gluten is the best thing that you can do for yourself.

Kritter Rookie

Thumper,

I, too, am realatively new to this, and I also found I was really blue (almost depressed) at first and had NO energy at all. I just sat around for days on end. I could have cared less if I did one productive thing all day. I think it was part of the withdrawal that my body was going through coming off of gluten, which had basically been "toxic" to me. Sort of like alcohol is toxic to an alcoholic, and they withdraw when it's removed. Hang in there, because it's worth it and you WILL feel better - even though it's hard to believe that right now. You're not alone, and the people on this sight are so kind - everyone is here to help you!

Oh, one note about Rice Dream. It was mentioned earlier by someone much more experienced and knowledgable than I, that it contains barley malt, so we shouldn't use it. I ran to my fridge and read the label on my Rice Dream, and can't find barley malt anywhere on there. However, I remember that I quit using the VANILLA flavored Rice Dream and switched to the ORIGINAL flavor because I was scared of something in the ingredients - maybe that was it. I'm still new to this, so I'm trying to figure it all out, but it's possible that the different flavors have different ingredients?! I'm learning to read labels every single time I go to the store because apparently these manufacturers can change ingredients on a whim - and what might have been "safe" last week isn't safe anymore this week!

My best to you - you'll be feeling better soon!

Kritter

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    • marion wheaton
      Thanks for responding. I researched further and Lindt Lindor chocolate balls do contain barely malt powder which contains gluten. I was surprised at all of the conflicting information I found when I checked online.
    • trents
      @BlessedinBoston, it is possible that in Canada the product in question is formulated differently than in the USA or at least processed in in a facility that precludes cross contamination. I assume from your user name that you are in the USA. And it is also possible that the product meets the FDA requirement of not more than 20ppm of gluten but you are a super sensitive celiac for whom that standard is insufficient. 
    • BlessedinBoston
      No,Lindt is not gluten free no matter what they say on their website. I found out the hard way when I was newly diagnosed in 2000. At that time the Lindt truffles were just becoming popular and were only sold in small specialty shops at the mall. You couldn't buy them in any stores like today and I was obsessed with them 😁. Took me a while to get around to checking them and was heartbroken when I saw they were absolutely not gluten free 😔. Felt the same when I realized Twizzlers weren't either. Took me a while to get my diet on order after being diagnosed. I was diagnosed with small bowel non Hodgkins lymphoma at the same time. So it was a very stressful time to say the least. Hope this helps 😁.
    • knitty kitty
      @Jmartes71, I understand your frustration and anger.  I've been in a similar situation where no doctor took me seriously, accused me of making things up, and eventually sent me home to suffer alone.   My doctors did not recognize nutritional deficiencies.  Doctors are trained in medical learning institutions that are funded by pharmaceutical companies.  They are taught which medications cover up which symptoms.  Doctors are required to take twenty  hours of nutritional education in seven years of medical training.  (They can earn nine hours in Nutrition by taking a three day weekend seminar.)  They are taught nutritional deficiencies are passe' and don't happen in our well fed Western society any more.  In Celiac Disease, the autoimmune response and inflammation affects the absorption of ALL the essential vitamins and minerals.  Correcting nutritional deficiencies caused by malabsorption is essential!  I begged my doctor to check my Vitamin D level, which he did only after making sure my insurance would cover it.  When my Vitamin D came back extremely low, my doctor was very surprised, but refused to test for further nutritional deficiencies because he "couldn't make money prescribing vitamins.". I believe it was beyond his knowledge, so he blamed me for making stuff up, and stormed out of the exam room.  I had studied Nutrition before earning a degree in Microbiology.  I switched because I was curious what vitamins from our food were doing in our bodies.  Vitamins are substances that our bodies cannot manufacture, so we must ingest them every day.  Without them, our bodies cannot manufacture life sustaining enzymes and we sicken and die.   At home alone, I could feel myself dying.  It's an unnerving feeling, to say the least, and, so, with nothing left to lose, I relied in my education in nutrition.  My symptoms of Thiamine deficiency were the worst, so I began taking high dose Thiamine.  I had health improvement within an hour.  It was magical.  I continued taking high dose thiamine with a B Complex, magnesium. and other essential nutrients.  The health improvements continued for months.  High doses of thiamine are required to correct a thiamine deficiency because thiamine affects every cell and mitochondria in our bodies.    A twenty percent increase in dietary thiamine causes an eighty percent increase in brain function.  The cerebellum of the brain is most affected.  The cerebellum controls things we don't have to consciously have to think about, like digestion, balance, breathing, blood pressure, heart rate, hormone regulation, and many more.  Thiamine is absorbed from the digestive tract and sent to the most important organs like the brain and the heart.  This leaves the digestive tract depleted of Thiamine and symptoms of Gastrointestinal Beriberi, a thiamine deficiency localized in the digestive system, begin to appear.  Symptoms of Gastrointestinal Beriberi include anxiety, depression, chronic fatigue, headaches, Gerd, acid reflux, gas, slow stomach emptying, gastroparesis, bloating, diarrhea and/or constipation, incontinence, abdominal pain, IBS,  SIBO, POTS, high blood pressure, heart rate changes like tachycardia, difficulty swallowing, Barrett's Esophagus, peripheral neuropathy, and more. Doctors are only taught about thiamine deficiency in alcoholism and look for the classic triad of symptoms (changes in gait, mental function, and nystagmus) but fail to realize that gastrointestinal symptoms can precede these symptoms by months.  All three classic triad of symptoms only appear in fifteen percent of patients, with most patients being diagnosed with thiamine deficiency post mortem.  I had all three but swore I didn't drink, so I was dismissed as "crazy" and sent home to die basically.   Yes, I understand how frustrating no answers from doctors can be.  I took OTC Thiamine Hydrochloride, and later thiamine in the forms TTFD (tetrahydrofurfuryl disulfide) and Benfotiamine to correct my thiamine deficiency.  I also took magnesium, needed by thiamine to make those life sustaining enzymes.  Thiamine interacts with each of the other B vitamins, so the other B vitamins must be supplemented as well.  Thiamine is safe and nontoxic even in high doses.   A doctor can administer high dose thiamine by IV along with the other B vitamins.  Again, Thiamine is safe and nontoxic even in high doses.  Thiamine should be given if only to rule Gastrointestinal Beriberi out as a cause of your symptoms.  If no improvement, no harm is done. Share the following link with your doctors.  Section Three is especially informative.  They need to be expand their knowledge about Thiamine and nutrition in Celiac Disease.  Ask for an Erythrocyte Transketolace Activity test for thiamine deficiency.  This test is more reliable than a blood test. Thiamine, gastrointestinal beriberi and acetylcholine signaling.  https://pmc.ncbi.nlm.nih.gov/articles/PMC12014454/ Best wishes!
    • Jmartes71
      I have been diagnosed with celiac in 1994, in remission not eating wheat and other foods not to consume  my household eats wheat.I have diagnosed sibo, hernia ibs, high blood pressure, menopause, chronic fatigue just to name a few oh yes and Barrett's esophagus which i forgot, I currently have bumps in back of my throat, one Dr stated we all have bumps in the back of our throat.Im in pain.Standford specialist really dismissed me and now im really in limbo and trying to get properly cared for.I found a new gi and new pcp but its still a mess and medical is making it look like im a disability chaser when Im actively not well I look and feel horrible and its adding anxiety and depression more so.Im angery my condition is affecting me and its being down played 
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