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

I'm New... Could I Be Celiac?


DaisyJane

Recommended Posts

DaisyJane Newbie

Hi guys,

I know you must get many many questions like this, but I guess I'm just looking for reassurance at this point. Please bear with me while I tell my story...

I don't know if this is relevant but when I was little I had problems with balance, lack of coordination, weak muscle tone (I didn't walk until I was 2 and a half). I recall some of these issues being linked to celiac so thought I'd mention it.

Besides the above, I was never a terribly healthy child I don't think, but I don't recall having overt health problems until I was around 14 or 15. I had been through a few years of intense stress and depression at that point (family/school problems), and I'd also just started restricting my diet too. I did a junk-food version of low carb when I was about 13, eating various processed low-carb products, many of which I believe contain isolated gluten (wheat protein minus the starch, to bump up protein content and reduce carbs presumably). Looking back, it was after this diet that my digestive problems really became noticeable. I went off low-carb but gained a newfound interest in healthy eating, cutting out all sugar, processed foods, dairy products, and meat (at least, I thought this was healthy at the time). I just seemed to feel worse. Eventually I was having mood swings, fatigue and bloating on a daily basis, so I knew something must be up.

A friend suggested I might have candida so I limited my diet further, cutting out all fruit, starchy vegetables, and later, gluten. I lost tons of weight and was thin for the first time in my life (aged 15). My periods also stopped. I went to doctors, but they weren't much help, making me feel hypochondriac and suggesting my diet was too limited (they were probably right about that). I remember them carrying out a blood test for celiac antibodies and it came back negative, but I don't think I was eating gluten at that point, except maybe in tiny amounts (I think I ate some oats back then, and Rice Dream which I didn't realise had barley). I never really got well either.

After a year or so, I got sick of the restricted diet and despite being thinner, I didn't feel healthier at all. I began to add foods back, and it was like a slippery slope. Soon I was bingeing on sweets, white bread, biscuits, LOTS of gluteny things and SUGAR. I was unstoppable. I probably gained about 50 pounds very, very fast. I was a real mess at that time too; it's not surprising, given that I was starving myself during the day and bingeing on non-foods at night. A few months after this began I managed to get my eating back under control and give up the junk foods and the awful bingeing, but by then I was suffering severe adrenal fatigue, not sleeping, absolutely unable to lose weight despite returning to my strict diet and I also thought I might have PCOS as I was growing facial hair (that scared the crap out of me).

Fast forward to today (I'm 20). Overall I'm healthier and stronger now, and I feel my hormone imbalances and sugar addiction are more under control. However, I'm still not functioning at my best. I suspect I might have low thyroid and/or adrenal issues (tho I've been tested for hypothyroid a few times and it always comes back "normal", grr!), I have bouts of depression/fatigue/just not feeling *right*, and I feel ill eating dairy, soya, gluten and pretty much all restaurant food. Since I've never been diagnosed celiac, I make excuses to eat gluten sometimes because I adore wholegrain rye breads and oatmeal - I even tried the gluten free oats last week - BUT I suffer immediately afterwards with horrible digestion, depression ranging from a mild feeling of anxiety to extreme despair/feeling mentally f'ed up, headaches, insane hunger pangs/urges to binge (I've binged on dry rolled oats before, ew), random foot cramping, fatigue, etc. I'm sure I'm forgetting something. Anyway, DO YOU THINK I MIGHT HAVE CELIAC???? And, is it worth getting a formal test? I'm not sure I could cope, judging by my gluten reactions. I'd be a total mess. Is it really worth getting an official diagnosis?

Thanks for your help :wub:


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



Celiac.com Sponsor (A8-M):



nu-to-no-glu Apprentice

You'll probably get varied responses to your question about getting a formal diagnosis. Having been through the ringer trying to get one myself, I could suggest that you just cut out gluten and dairy for at least 2 weeks and see how you feel. From experience, it does take a little while for those "strange" symptoms to dissapear,but they do (I still have many, but not like I was...exhausted just to get up and take a shower-and now only 1 1/2 months into the gluten-free lifestyle). I have suffered from childhood like you,and now in my late 20s, it seems logical that it will take quite a while to undo the damage of so many years!

It sounds likely that you could have Celiac. If you do some research there is loads of info on thyroidand adrenal connections to the disease...and there are manyon here that believe they have yeast (candida) overgrowth as a result of undiagnosed celiac.

I think you could get a blood test, if you think it will help you stay on track, but loads of us have tested negative that still have the disease. So, it's not a definite. You should definitely poke around on the forums, I have learned loads from all of the helpful people here and I was like you, fed up, exhausted, and looking for answers! I found a lot of stories that I related. I usually think that our suspicions can lead us to the answers, sometimes it just makes sense! Welcome and good luck!

DaisyJane Newbie

Thanks for replying Nu. Believe me, I have already scoured these forums - they have proven very helpful indeed. Actually I am doing gluten & casein free now, and have been for a couple of weeks - or at least, what I THOUGHT was gluten-free/CF free. Since I had an obvious reaction to "gluten free" oats, I am having to go back to square one. I also think corn bothers me all of a sudden. I've been eating gluten free corn flakes and have had gluten-like symptoms such as brain fog, depression, constipation, feeling generally insane, and ravenous hunger leading to bingeing on the offending food. I feel I've been going round in circles for years with these food issues. GRRR! I think I'll do a strict diet of rice, fish and fruit for a couple of weeks. I'd do vegetables but they look repulsive to me right now. :(

I am feeling really fed up at the moment....

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.