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

Pre-diagnosis Anxiety (and A Few Questions)


Guest ~wAvE WeT sAnD~

Recommended Posts

Guest ~wAvE WeT sAnD~

Hello everyone!

I'm a 21- year-old female who has exhibited many of the symptoms of celiac disease for the past five months. I have had an upper GI, countless blood tests (one of which caused me to pass out), a gallbladder untrasound, an X-Ray, and a stool card test (I never got the results on that one!). All of those tests were normal except for the final bloodwork I had done in June showing gluten antibodies. I have an EGD on Aug. 4th, and I'm not looking forward to being sedated while I swallowed a pencil-sized tube. :unsure:

The Gluten-Free diet has helped, though. :) Before I went on the diet, I was constantly vomiting, in an almost reflexive manner, without any warning. I would simply be eating, feel fine, then suddenly become nauseated. Now I can keep food down and am enjoying the new meals.

I have a few questions and appreciate any advice from anyone.

-How long does it take for the fatigue to go away after starting the Gluten-Free diet? Is it a few weeks, months, etc.?

-Have any of you "not felt like yourself" before going on the diet? Did you have depression/anxiety or difficulty sleeping prior to diagnosis?

-Did you exhibit symptoms after a stressful event? (I'm a college student-I became sick before finals week)

-Can a person be healthy their entire lives and suddenly get Celiac's Diseasee as an adult?

I have tons of other questions, but I figured these are the biggest.

Thank you very much.

~Jill


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



Celiac.com Sponsor (A8-M):



Wish Newbie

Hi and welcome to the forum!

I'm another 21 year-old female and was just diagnosed about 1 year ago, so it is definitely possible to be healthy your entire childhood and only begin experiencing symptoms as an adult. To answer your other questions:

-The amount of time it takes for fatigue to disappear on the gluten-free diet varies a lot from person to person. Some people say they feel like a whole new person in just a couple of days, while other people do not begin feeling better for a few weeks or maybe even a few months. For me it took about three weeks for my GI symptoms (reflux, bloating, constipation) to subside and around 2-3 months for the fatigue to go away. One way to make the fatigue go away sooner is to make sure you are eating a balanced diet. You may even want to look into taking a multivitamin because most gluten-free foods are not fortified, and you want to make sure you don't end up with any vitamin/mineral deficiencies that could lead to sleepiness.

-I was totally not myself prior to diagnosis. I was tired all the time (very unusual for me), irritable, and depressed. As I said before, it was a few months before the tiredness went away. However, the irritability and depression went away as soon as I was diagnosed b/c I was so happy that I finally knew what was causing all of my symptoms (and that my symptoms were NOT just all in my head).

-I had my symptoms about 1 year before I was diagnosed with Celiac disease. The symptoms started while I was doing a study abroad program in Germany, which was a ton of fun and very worthwhile, but also quite stressful b/c I was living in a small town that didn't otherwise see a lot of foreigners, so I always felt like people were making judgements about America based on how I acted. When I came back, I experienced some brief symptom relief, but then my symptoms began to come back and were at their worst during finals week of my Fall and Spring terms. So it definitely seems like stress can be a factor!

Okay, I think I answered all of your questions. Please feel free to e-mail me if you have any more. I'm so glad to hear that the gluten-free diet is helping :D !

~Wish

flagbabyds Collaborator

If you are on the gluten-free diet now go back to eating gluten before your endoscopy.

tarnalberry Community Regular
-How long does it take for the fatigue to go away after starting the Gluten-Free diet? Is it a few weeks, months, etc.?

-Have any of you "not felt like yourself" before going on the diet? Did you have depression/anxiety or difficulty sleeping prior to diagnosis?

-Did you exhibit symptoms after a stressful event? (I'm a college student-I became sick before finals week)

-Can a person be healthy their entire lives and suddenly get Celiac's Diseasee as an adult?

Fatigue: It took me a few weeks, but I don't think I'd been gluten-intolerant very long. Turns out, for me, part of the fatigue problem is low testosterone levels, and that is even more important than the gluten-free diet for keeping me from getting tired. (Though they both play a role.) I know some people take MUCH longer to see an improvement in this area, particularly if they had been sick long enough to have vitamin/mineral deficiency problems.

"Not like yourself": Sorta. For me, I discovered it through another condition I had, which makes it pretty hard for me to answer the question - as that condition has much more of a depressive effect than this one for some people.

Stressful event: Do you mean did I first exhibit symptoms after a stressful event? Since my symptoms are relatively mild, and I have other issues, I can't pin down when my symptoms started. It may have been related to a nine-month off and on bout with lung infections (and hence antibiotics and yeast infections) that triggered this problem.

Sudden onset: Yep. That's the idea. You can have the genes for gluten intolerance, but until they're triggered, and expressed, your body doesn't react to gluten. I've heard that stress, infection (particularly yeast), and other things can be the trigger.

Guest ~wAvE WeT sAnD~

Thanks everyone for answering my questions! Wish, I'm glad to hear from someone whose experience was sismilar to mine--I'll email you anytime! I really appreciate your imput--it's hard to describe the more emotional/mental aspects of the condition to my family--but they do understand the physiology of what's going on.

I'll talk to the nutritionalist I'm seeing next week about hormonal levels, namely testosterone. (hahaha he's male---he'll understand. Just kidding!)

Thanks again everyone!!!!

~Jill

gf4life Enthusiast

Hi Jill,

If you are already gluten free, then your biopsy will most likely show negative. The lining of the intestines heals pretty quickly for most people. Only people with very severe damage take longer than a few weeks for the lining to heal to the point of not being considered Celiac during a biopsy.

I felt so much better being gluten-free, but went back on gluten for two months and my biopsy still showed negative. You might want to talk to the doctor about it before going through the procedure for nothing.

God bless,

Mariann

Guest ~wAvE WeT sAnD~

Mariann,

You've made a good point--I read somewhere on this forum that someone's doctor asked them to ingest gluten before the test so the reading was more accurate. Would that help me?

What other condition would I have if antibodies showed up but my test was negative?


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



Celiac.com Sponsor (A8-M):



celiac3270 Collaborator

after having bloodwork done, doctors will want you to stay on gluten so that your biopsy results are accurate. Therefore, I knew I had celiac disease after bloodwork, but stayed on gluten until after the biopsy....if I had gone off gluten, the biopsy may not have shown celiac disease or may have been more borderline....

-celiac3270

gf4life Enthusiast

A positive biopsy will just confirm that the blood tests were correct. Some doctors don't even have you do a biopsy, but most will recommend it. Your doctor should have told you to stay on gluten until the biopsy was done. It can take up to 3-6 months after being gluten free for enough damage to be done in the intestines to show on a biopsy. (according to Dr. Peter Green, one of the top Celiac specialists in the US) Unless you are willing to go back on gluten for a while and postpone the biopsy, it might not even be worth doing. There is always the chance that you had severe damage and have not healed completely, but if you have healed and the biopsy comes back negative, then your doctor is going to say that the blood tests were wrong and you don't have Celiac Disease. Which of course would not be accurate, given that you were gluten free before the biopsy. But most doctors don't seem to realise how much it affects the results.

God bless,

Mariann

Guest ~wAvE WeT sAnD~

I see. I've only been on the diet for a week, will any damage show up in the next two before my endoscopy?

Guest ~wAvE WeT sAnD~

Will any returning symptoms be worse? I was vomiting constantly before I became gluten-free.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,545
    • Most Online (within 30 mins)
      7,748

    Jem68
    Newest Member
    Jem68
    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.