Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

New And Need Advice


fryzway

Recommended Posts

fryzway Newbie

I went to my Gastro yesterday for a follow up. I have been having severe burning in my stomach and throat. I always feel hungry but can never eat a lot at one sitting anymore. Seems better in the morning before I start to eat for the day. I have no diarrhea or stomach PAIN per-say. I have not lost any weight, I actually am gaining weight! I had a biopsy and my lower intestine showed "blunting of the villi" and my blood work was negative for H Pylori and Celiac disease accept for 1 blood test, he didn't say which, was right on the negative mark. Which he called a "weak positive". Anyway, he gave me Cerefate to try for my Reflux, gerd, gastritis that I have. I also take Prilosec 2x day. He said if that didn't help my burning and false hunger pains that I could then switch to the Gluten-Free diet and see if it helps me. I have no family history on either side of celiac disease. I am a 26yr old male in overall good health. It is hard to say if I have any malnutrition bc he didn't do any blood work for that. So, I called him today and suggested he run a genetic test to see if I even hold a gene for celiac and if he could run blood work for vitamin and nutrient deficiencies as well as anemia. I am constantly tired and grouchy but I've been this way for a yr now. I have sever panic attacks also but I am also under the care of a Endo for very very Low Testosterone, which could cause most of my issues. My question to all of you who do have this, what was it like on a daily basis for you before you got your diagnosis and also was it a 100% YES from the Gastro that this is what you have. From what I was also told celiac is severely under diagnosed bc it is tricky to diagnose and just bc someone test negative for it doesn't mean they don't have it. Also, I was told there can be weak and false positive and negative test results. He said the Gluten free diet could actually do harm if you don't really need to be on it and it's very bland and expensive. HELP !!!


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



Dixiebell Contributor

Welcome to the forum fryzway.

A lot of people here, including myself, my daughter and my son had negative tests but tried gluten-free anyway and have gotten better. My son's symptoms are what led us to look for celiac. He had severe constipation, tummy aches, headaches, unexplained rashes, various types of BM's, he missed a lot of school and he is a foot shorter than his class at school. My symptoms were depression, anxiety, joint and bone pain, headaches, tired all the time (at my worst, I was taking three naps a day), once in a while I would have tummy problems, I even had to quit my part-time job. My daughter, she is 20, was vomiting and had D with blood and had to go to the ER three times because of dehydration. If she eats any gluten she will get sick three days later everytime. She made the mistake with Doritos the other day.

Eating gluten-free will not harm you. It is a little difficult at first but it is like learning anything new, it takes time. The food that I cook and eat is very good and not bland at all. And it only gets expensive if you try to buy all the gluten-free replacements. It is best to start with fresh meats and veggies.

About the genetic testing, most Dr.s only know about the two most common but other countries have found more than that. The testing for vitamin levels is good to do.

Takala Enthusiast

I am self diagnosed, based on my (many) symptoms AND various medical tests, which unfortunately the neurologist I had at the time could not and would not admit to withholding some of said test results because she had already labeled me a head case/MS/fibro and was ignoring what I told her about how I responded to a grain free diet. Alas I had not been "thin" since I was a small child (and then I was very thin) so of course how could I possibly be celiac or gluten intolerant.

I did not go on to seek an "official" diagnosis from any gastro, because by then I was completely and totally fed up that anyone who was having this many neurological problems could be repeatedly blown off by so many different doctors. I merely went back to the PCP and told them don't send anyone to this neuro because of what happened, and btw, I'm not eating gluten anymore, and you've noticed how many of my symptoms are resolving.

I was having severe bouts of ataxia (dizziness) and balance problems, loss of sensation and burning and twitching in my feet, legs, shoulders, hands, plus kidney problems, gall bladder symptoms, and arthritis flares, besides the heartburn and problems with eating anything with fat in it. Oh, and my vision was really messed up. Bone loss. Dry mouth/eyes. Brain fog. Asthma. Ob- gyn problems. There's more, but let's not write a novel here.

That being said, I am completely puzzled by your test result of blunted villi not resulting in a definite diagnosis of celiac disease. That is supposed to be The Final Word.

I don't know what the bleep it is about the false rumor that the gluten free diet is either harmful (altho I do know which dietician with some Celiac org keeps on giving interviews to the press that say this, and she ought to knock it off) or bland, I assume it is coming from people who are passive about their food and merely like to be fed by somebody else and not think about it, or just too busy to cook. No spices are made from wheat, rye, or barley. You would be shocked at what I can eat now that the true culprit has been taken out of my diet. It might be more expensive, but if you compared the cost of a single doctor's appointment and series of lab tests vs. how much more you would spend on food for a year with the gluten free diet, guess which number is economically cheaper ? I won't even go into how many prescriptions for the WRONG THING waste vast amounts of medical money every year, or how prescriptions end up costing a fortune when doctors won't give you a refill without an office visit or the impact of the upcharge to the uninsured making all medical debt rise in the USA.

It may be time for you to go on that gluten free diet option, and see how you feel. You may also need to go soy free and dairy or lactose free at first, those are the two other food intolerance things that tend to go with this. You may be able to add non lactose dairy back in later.

fryzway Newbie

Thanks dixibell. I'm glad I came across this forum. So, if I were just to start with say turkey,chicken, steak, etc... and a cup of veggies and some cottage cheese. I would see a diff in a week or so correct ? Also, could I eat lunch meat from the deli ? I looked at so much stuff and Hidden gluten words that are used on labels and it's all very daunting to say the least. I would almost rather stay how I am than try and keep up with it all. I know that sounds bad but neither me or my wife can make heads or tales of this disease and it's nutritional requirements. Do you have any simple ways for deciphering the labels on all the food or suggestions on what I could buy from my local supermarket ? Also, what can I use on my meats as far as things to flavor them, like ketchup and seasoning ??? Are their any in-expensive books that are like "celiac for dummies" lol !!!

fryzway Newbie

I don't know about the diagnosis. He said since I don't get diarrhea or puke or haven't lost weight and I'm not having any skin reactions he wouldn't say 100 % that this is celiac disease. He is going to check for vitamin/nutrient deficiencies and do gene test to see if I am even capable of having celiac. I never had any problems with my stomach until I got severe anxiety about 13 months ago and I've dealt with anxiety all my life but never this severe. He says that anxiety would have most likely triggered the celiac in my childhood. I have gastritis/gerd as well which are more of the symptoms I am dealing with. I always just feel so hungry and it's off and on, never constant. Celiac is constant correct ? I would love someone to be able to point me to recepies and help me make sense of all the "Hidden" gluten on labels. I wouldn't even know where to start on this journey. I wouldn't mind giving it a shot but it all just seems so overwhelming. I don't like the thought of eating out of a tuper wear container from pre-prepared food. I love going to eat and eating out. It's the convenience of it all that I will miss. I would love to try it and see if I feel better and if I don't then I won't have any regrets.

Kimbalou Enthusiast

Welcome to the forum. First of all, I have to say your DR. is full of BS to say the gluten free diet is expensive and can be harmful, bland, etc. What a load of cr$%! The only really expensive things are pre-packaged foods such as gluten free pasta, frozen dinners, etc. Or if you go to a gluten free bakery the cupcakes will cost about $3!! But you don't have to eat all that processed food at all. (I was diagnosed with a positive blood test and biopsy of my small intestine.)

Sometimes I feel sorry for myself because I can't just grab a cookie, cupcake or cracker...but that's ok because I don't really need those things anyway! The food I need to eat will make me feel better and give me more energy, that's how I choose to look at it. You should just go ahead and try the diet and see if you feel better. If you feel better, then great! You can eat a lot of food on this diet...meat, fish, eggs, cheese, fresh fruit and veggies, rice, potatoes, Rice Chex, Rice cereal,spices, etc. Just search this site for a list of the safe foods. Its really not that hard to avoid wheat, rye and barley. Let us know if you try the diet, it's really not that hard. My dr. told me it would be hard, but at least she didn't say it was expensive and harmful!!

eatmeat4good Enthusiast

You are way smarter than your Dr.

The blunted villi means you have Celiac.

The gluten free diet harms no one. It is just food minus Wheat Barley and Rye.

It is not more expensive for me because there is way less eating out.

We found a few gluten free products to make like easier. Like Udi's bread. That tip right there saves you a bunch a money from not trying crappy bread substitutes. We use Udi's bread for a "treat" not making a bunch of sandwiches a day.

Eat mostly meat, fish, fruit, vegetables, and nuts.

Learn to make your own gluten free cookies...

And you will be good.

I agree with the above posts completely.

You should have a diagnosis from what you shared, but you don't have a REAL Dr.

So...Physician....Heal Thyself.

You will feel better without Gluten.

And the best part is there is no such thing as the Gluten Police.

So eat well without gluten and heal.

Being grouchy, tired and having panic attacks went entirely away after I went gluten free. I was grouchy, tired and had anxiety/panic attacks for 7 years. No Dr. ever suggested Celiac even with multiple symptoms. They just do not know. And it is costing people their lives.

Knowledge is Power.

Once you know what gluten does and how to avoid it, you can have your life back. I hope you heal really fast.


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



yorkieluv Newbie

I know how frustrated you are feeling because I was just wanting someone to tell me definitely I did or did not have celiacs. Unfortunately it isn't always that easy because soooo many doctors are ignorant ont the signs and symptoms of celiacs, the proper test to run and how it is treated. I had a gastro doc tell me there was not way I could have celiacs because I didn't have diarrhea everyday. I had initially found out I had a problem with gluten by my primary doctor who really didn't have a clue about how it is treated. She told me I would be able to start eating gluten again in six months(go figure). Anyway I did a ton of research on my own went to a GI doc (prior to this I did the genetic testing because I wanted to know if I even had the gene, which I do I have a double DQ8) who was suppose to be a little up on celiacs but obviously he wasn't. After me informing him of everything I knew and that he didn't he wanted to refer me to a specialists who specializes in celiac. Since it was only a three hour drive my husband and I went afraid we were going to be told information that we knew was wrong but was pleasantly surprised. She was extremely informative and helpful and was going to write a letter to the doc that referred me and tell him a few things. She actually knew him because at one point years ago she taught him in medical school.

You know your body better than anyone and don't give up on finding the correct diagnosis. I would recommend changing doctors especially considering you have "blunted villi" which I was under the impression was from celiacs. The gluten free diet isn't easy in the beginning but it does get much easier. I haven't read anywhere that it's harmful if you don't have celiacs. As for being more expensive I disagree, it has made me eat healthier and eliminating eating out so much. I started feeling better within a couple of weeks so I didn't have any desires to ever eat gluten again.

This forum is awesome so keep looking for support to get through the tough and frustrating times.

Dixiebell Contributor

There is a 'dummies' book and it is very good.

Living Gluten Free for Dummies

sa1937 Community Regular

Are their any in-expensive books that are like "celiac for dummies" lol !!!

Well, actually the answer is YES! Living Gluten-Free for Dummies by Danna Korn is a good one. My DIL bought it for me for Christmas. Another excellent book is Celiac Disease: A Hidden Epidemic by Dr. Peter Green, Director of the Celiac Disease Center at Columbia University. Both of these are excellent resources for a newly diagnosed celiac.

As overwhelming as it seems at first, the diet is really not all that difficult and if you shop the outer edge of the store for veggies, fruit, eggs and plain meats, etc., it's not any more expensive than normal and you won't have to decipher a lot of labels in doing so. And if you check the recipe section on this forum, you'll find a lot of recipes to give you ideas of what to eat. I would also recommend ditching the dairy for now...I am/was lactose intolerant (just testing the waters lately to see how I can tolerate dairy products). You may very well be able to add them in later.

I think there is danger in eating out so I'd avoid it right away until you can get a handle on what you can safely eat. My daughter (also celiac) seems to do well handling the social scene and eating out but she lives in Denver, which is a celiac's haven for gluten-free restaurants.

And welcome! You'll find answers here for any questions you might have so ask away...

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,962
    • Most Online (within 30 mins)
      7,748

    AlissaW
    Newest Member
    AlissaW
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.