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

Am I Making It All Up?


abc

Recommended Posts

abc Rookie

I finally went to the doctor last week to address digestive issues that have plagued me since the birth of my first child (s=who is now 3.5 years). Obviously, I have been able to live with them (or I would have gone in sooner), but lately, they seem to be getting worse. The most prevelant issue is the extraordinary gas I produce (I can't even be in the same room with me at times), and some bloating etc. I'm just lucky that I work part time and am in and out of the office, so no one (well, I don't think) really notices the problem (aside from my husband and mother). Usually, if it is particularly offensive, I at least have my 8 mos old nearby and can suggest that he has a dirty diaper. In the past month, I have been experiencing more cramping and some very loose stools. I've been attributing it to lactose intolerance - but the dr. did blood work for celiac and I am awaiting results. No one in my family has it (or at least has been diagnosed with it), but I do have family members with food intolerances.

As I read more about celiac, I'm becoming convinced I do indeed have the intolerance to gluten. I had infertility issues with my first pregnancy (unexplained) and my second child was born 6 weeks early (unexplained). In the past few years I have been able to eat a lot of food, without gaining weight and keeping quite low body fat (as remarked by the dr). However, I am active (a fitness instructor) and nursing - so a lot of this could be hormones? My husband is beginning to think I am crazy, and at times, I am too. I especially feel this way when I read other's symptoms on these pages that are much much more severe. two people that I know rather well have been diagnosed lately with celiac, and I wonder if I just am hearing so much more about it these days that I have self-diagnosed myself. I have put myself on a gluten-free/dairy free diet (for about 5 days now), but was replacing the dairy with a lot of soy, which I now understand can create some of the symptoms I've been having. I'm cutting soy out now - with hopes of figuring out if gluten is the culprit.

Does anyone have any thoughts? I am awaiting blood test results, but know they can be unreliable.


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



Celiac.com Sponsor (A8-M):



CarlaB Enthusiast

You say you are fitness instructor and a nurse. I would guess that you could have gluten intolerance and your testing might come out negative because you are probably more in touch with your body than many so noticed the changes before damage was done. In my opinion, dietary response will be your best gauge.

Nantzie Collaborator

(Carla - I think she's saying that she's nursing as in breastfeeding.)

The really bad gas was one of the biggest reasons I kept searching for answers and eventually found out about celiac. I also had to use my kids as an excuse for my issues more than once. There was a point where I had no idea what I was going to do when they got potty trained. It got really bad for me. To the point where I couldn't even go anywhere.

My husband also thought I was nuts when I found out about celiac. He spent an hour and a half one night telling me that I was a hypochondriac and that I just wanted people to feel sorry for me. It was really bad. That was October. By Valentine's Day, he bought me a bag full of gluten free stuff from the health food section of the grocery store because he couldn't remember what chocolates were gluten-free. Now, almost a year later, our house is gluten-free, and if he cooks, he has me check the ingredients to make sure everything is gluten-free.

For some reason, it's really common for the people around us to freak out about this. I have no idea why. It just happens. I've written the above story dozens of times it seems. I think this is the third or fourth time this week alone. I've long since gotten over it. A bag of gluten-free baking mixes for Valentine's Day will do that to a girl... :wub: I retell it because sometimes you just have to know that there's hope for something like that.

Congratulations to you for standing up for your health. A lot of people would just eat antacids for the next 20 years. (Many of which have gluten btw.)

There are all sorts of people here. Some officially diagnosed, some who had negative tests but responded well to going gluten-free, some who just figured it out on their own and didn't go for a diagnosis. There are celiacs and there are gluten intolerant people. No matter where we fall on the diagnostic scale, we all seem to be dealing with the same condition. There are people who just have problems with gluten, and there are people who have problems with many foods. There are also people who suspected gluten and then found through really paying attention to what they were eating that it was something else causing their symptoms; dairy, soy, egg, etc. So wherever you end up in the mix of things, you're welcome here.

:)

Nancy

CarlaB Enthusiast
(Carla - I think she's saying that she's nursing as in breastfeeding.)

LOL Still, dietary response will tell everything!

Nooner Newbie
LOL Still, dietary response will tell everything!

I agree, listen to your body. It will tell you what it wants. I had a negative blood test for celiac, but I know that gluten and a few other foods make me miserable. It takes time, but you will find what works for you.

~Li

abc Rookie

Thank you both for your responses - turns out my IgG is elevated so they are referrring me in for the biopsy. My gut (hah) is telling me I am indeed needing to be gluten free. For now, however, I'm eating it up to make sure my results come out.

Turns out it seems to in fact exist in my family, now that I;ve brought it up. Just, no one has been diagnosed - so perhaps I'm helping others too! (and my husband doesn't think I'm so crazy anymore:))

Guhlia Rising Star

Glad to hear your husband is coming around. Sometimes that's the hardest part of the disease, getting others to understand and support you. Even if your biopsy shows no villous atrophy, I would still go gluten free. At least see how you feel. It may take a few weeks, sometimes even months, for you to start feeling better, so give it time.


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



Celiac.com Sponsor (A8-M):



Ursa Major Collaborator

Just keep in mind that your symptoms could be related to dairy or soy as well. Or gluten, dairy AND soy. Once you've had your biopsy (and I hope that's really soon, so you can try the diet), you ought to go gluten-free, dairy free and soy free for a month, and then try one at a time (two weeks apart to notice delayed reactions) to see which of the three are the culprit. Really, most people with celiac disease can't tolerate dairy, either. And soy is certainly not the health food the food industry wants us to believe it is. Only fermented soy is okay, and even asians use it only as a condiment, no more than two or three tablespoons a day (or was it teaspoons? I don't remember).

I hope you figure it out and get better! But it looks like you're close, so there is definitely hope now.

Kat-Kat Newbie

I wonder what your husband would have done if you ate a bun and fell over with a grand mall seizure. think he would have thought somthing of it then.

My husband read everything I might touch before I see it. Celiacs is more than a stomach pain.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,543
    • Most Online (within 30 mins)
      7,748

    yfuvhg
    Newest Member
    yfuvhg
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Beverage
      I had a very rough month after diagnosis. No exaggeration, lost so much inflammatory weight, I looked like a bag of bones, underneath i had been literally starving to death. I did start feeling noticeably better after a month of very strict control of my kitchen and home. What are you eating for breakfast and lunch? I ignored my doc and ate oats, yes they were gluten free, but some brands are at the higher end of gluten free. Lots of celics can eat Bob's Red Mill gluten-free oats, but not me. I can now eat them, but they have to be grown and processed according to the "purity protocol" methods. I mail order them, Montana Gluten-Free brand. A food and symptoms and activities log can be helpful in tracking down issues. You might be totally aware, but I have to mention about the risk of airborne gluten. As the doc that diagnosed me warned . . Remember eyes, ears, nose, and mouth all lead to your stomach and intestines.  Are you getting any cross contamination? Airborne gluten? Any pets eating gluten (they eat it, lick themselves, you pet them...)? Any house remodeling? We live in an older home, always fixing something. I've gotten glutened from the dust from cutting into plaster walls, possibly also plywood (glues). The suggestions by many here on vitamin supplements also really helped me. I had some lingering allergies and asthma, which are now 99% gone. I was taking Albuterol inhaler every hour just to breathe, but thiamine in form of benfotiamine kicked that down to 1-2 times a day within a few days of starting it. Also, since cutting out inflammatory seed oils (canola, sunflower, grapeseed, etc) and cooking with real olive oil, avocado oil, ghee, and coconut oil, I have noticed even greater improvement overall and haven't used the inhaler in months! It takes time to weed out everything in your life that contains gluten, and it takes awhile to heal and rebuild your health. At first it's mentally exhausting, overwhelming, even obsessive, but it gets better and second nature.
    • Jsingh
      Hi,  I care for my seven year old daughter with Celiac. After watching her for months, I have figured out that she has problem with two kinds of fats- animal fat and cooking oils. It basically makes her intestine sore enough that she feels spasms when she is upset. It only happens on days when she has eaten more fat than her usual every day diet. (Her usual diet has chia seeds, flaxseeds, and avocado/ pumpkin seeds for fat and an occasional chicken breast.) I stopped using cooking oils last year, and when I reintroduced eggs and dairy, both of which I had held off for a few months thinking it was an issue of the protein like some Celiac patients habe mentioned to be the case, she has reacted in the same fashion as she does with excess fats. So now I wonder if her reaction to dairy and eggs is not really because of protein but fat.   I don't really have a question, just wondering if anyone finds this familiar and if it gets better with time.  Thank you. 
    • Chanda Richard
      Hello, My name is Chanda and you are not the only one that gose through the same things. I have found that what's easiest for me is finding a few meals each week that last. I have such severe reactions to gluten that it shuts my entire body down. I struggle everyday with i can't eat enough it feels like, when I eat more I lose more weight. Make sure that you look at medication, vitamins and shampoo and conditioner also. They have different things that are less expensive at Walmart. 
    • petitojou
      Thank you so much! I saw some tips around the forum to make a food diary and now that I know that the community also struggles with corn, egg and soy, the puzzle pieces came together! Just yesterday I tried eating eggs and yes, he’s guilty and charged. Those there are my 3 combo nausea troublemakers. I’m going to adjust my diet ☺️ Also thank you for the information about MCAS! I’m from South America and little it’s talked about it in here. It’s honestly such a game changer now for treatment and recovery. I know I’m free from SIBO and Candida since I’ve been tested for it, but I’m still going to make a endoscopy to test for H. Pylori and Eosinophilic esophagitis (EoE). Thank you again!! Have a blessed weekend 🤍
    • knitty kitty
      Yes, I, too, have osteoporosis from years of malabsorption, too.  Thiamine and magnesium are what keep the calcium in place in the bones.  If one is low in magnesium, boron, selenium, zinc, copper, and other trace minerals, ones bone heath can suffer.  We need more than just calcium and Vitamin D for strong bones.  Riboflavin B 2, Folate B 9 and Pyridoxine B 6 also contribute to bone formation and strength.   Have you had your thyroid checked?  The thyroid is important to bone health as well.  The thyroid uses lots of thiamine, so a poorly functioning thyroid will affect bone heath.  
×
×
  • 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.