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

*obligatory help with my results post* :)


summer94

Recommended Posts

summer94 Newbie

OK, 

Bare with me!

I am 39 years old, officially dx with fibro, cfs, mthfr 677, chronic low d and am very high risk for other AI like lupus, sjorgens, RA etc (sister has 9 major AI so far)

Back in April I was dx with hashimoto's and told I need to go on a gluten-free diet. I begrudgingly did. Well, I did the AI protocol diet. VERY much to my surprise, the only thing I reacted to was gluten. I did NOT want to believe it, because bread. So I took it away, brought it back, a few times. Each time reacting with swollen hands, sleepiness, body aches, bloating and the feeling of an alien trying to claw it's way out of my gut. 

So fast forward, I've been gluten-free for about 7 months, feel awesome. Fibro/cfs symptoms pretty much gone. Then I accidently got some gluten (was given a regular hamburger bun without my knowledge), I thought my gut was literally going to explode out the front of me the next day, it was awful.

So that got me thinking, maybe I'm celiac. But also, maybe my middle son is also. Both of us are thin. Like THIN. I know I had malabsorption issues as a kid. I was 14, freshman in hs and weighed 63lbs (I'm not short either). Gained 30lbs that year thanks to finally going through puberty (was the last in my class). My middle son now is 14 1/2, only 5'1 and 90lbs and hasn't really grown in the last 1 1/2 years. He's just like me. Very thin, very pale, etc. Both of us get nauseous very easily. (Until I went gluten-free, then it went away!) I really feel we both had malabsorption issues. So that got me thinking maybe he has celiac as well, he looks just like me. Oh, we come from a very tall, but very thin family.

So I pulled our 23andme results to see what it said about celiac. I am a DQ8 carrier, my kiddo, he's a dq8 and dq2 carrier :(

So I talk to my dr, well a PA that helped me with the hashi's and said I want to be tested. She thought I was nuts because I'd have to eat gluten. She went ahead and ordered my test and told me to eat a lot of gluten for the next couple of weeks. I did so for a week and a half and my alien gluten baby came back raging. He was pissed!

I did it, took the test and got my results. Neg. ugh. Maybe I didn't eat gluten for long enough?

Should I do another one?? I just feel like having something "official" will get dr's and others to take me serious. I'm getting my son (currently not gluten-free) to the dr next week to talk about testing. He's just not growing. He should be well on his way to being over 6 ft tall (all the men on both husband and my side are 6 ft- 6'7", the women avg around 5'10), yet I'm the second shortest at 5'6. 

Thoughts??

 

CELIAC.webp


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



Celiac.com Sponsor (A8-M):



RMJ Mentor

A week and a half is not long enough for a gluten challenge if you've been gluten free for months.  Eight to twleve weeks is more like it.

CherylS Apprentice

I have the HQ8 gene as well and not the HQ2.  I also tested negative on my celiac panel.  I have AIH and chronic iron deficiency anemia.  I'm getting an EGD with biopsies and a colonoscopy January 8 to see what's going on.  You know yourself best and if you feel this is what is going on, you should push for a diagnosis.

I'm not sure you were eating gluten enough to test positive.

squirmingitch Veteran

You didn't eat gluten long enough.

Open Original Shared Link

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,544
    • 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.