Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Undiagnosed With Questions


dani nero

Recommended Posts

dani nero Community Regular

Hello everyone,

I've had amenorrhea (absence of menstrual cycles) since I was 12, and I've been taking birth-control pills to regulate my periods since 16, as the doctor's conclusion was that I had a hormonal imbalance. I'm 33 now.

I've always been constipated (sometimes diarrhea but not as often as constipation) and always overweight, even as a little child. I never had any abdominal problems other than the constipation and bloating, but I never felt any pain.

I went to doctors so many times complaining about being depressed, suffered severe mood-swings & anxiety, tired and constipated, and I even told them that I ate healthy and exercised, but they always smirked at me and linked my problems to my weight. They told me that nothing was wrong with me, to go home and start eating vegetables and cut down on pasta. A gynecologist even told me that there was no need for me to get periods at all, so even the birth-control treatment was needless!

I started reading a lot about hormonal conditions because I wasn't satisfied with the treatments I got from doctors, and I falsely came to the conclusion that I had PMDD (advanced state of PMS), so I went to yet another gynecologist and explained all my issues to him. All he did was prescribe a different type of birth-control pill and gave me anti-depressants, which only made things worse.

I however read on a PMDD website that a good natural treatment for PMDD was to cut gluten, sugar, lactose, salt, caffeine and salt from my diet, so I did that. That's when I started feeling better, but still not all the time (since I had no clue I had to be 100% strict! I still ate processed foods and ready-made sauces which I had no clue contained gluten).

As I was visiting family this summer, they all tried talking me out of gluten-free eating because they felt bad that I couldn't enjoy all that food they were eating. They told me it was all bulls$#& and silly because no doctor actually told me to stop eating gluten. I was almost convinced since I wasn't really feeling so good anyway, but I went online a see if any websites confirmed it was all a myth.

That's when I found that amenorrhea is a symptom of celiac disease. I always thought that my digestive issues were caused by my hormonal imbalance, and not the other way around. I dismissed celiac disease before because the doctors told me I had a hormonal imbalance. I didn't know doctors could be so stupid.

I also discovered that my gluten-free diet wasn't effective while reading about celiac disease. I had no clue I was still eating so much "hidden" gluten.

Discovering I might have celiac disease made so much sense, because whenever I exercised, I would feel weaker after.. and people are supposed to feel stronger after working out, but I would have such awful muscle weakness (not pain) that pushing on the bicycle paddle was harder than the previous day, until it would be too difficult, so I'd stop working out until the next week (where my strength would be back). It also made sense because I don't have hair or acne on my face or any faulty reproductive features which could be caused by hormonal problems.

Now I'm watching every last ingredient if I buy any ready-made good or sauce, and I even try to avoid anything in a jar or a can. I'm sticking to only fresh stuff and keeping check on all the hidden gluten in flavorings and whatever. Even my weight has been going down, but I have a few questions that I'm hoping you guys can help me with, since there is no way I'm going to a god-forsaken doctor anymore.

1. How do I know what kind of supplements I need? My teeth are slightly transparent and decayed but I don't have any serious bone or dental problems. My nails tend to bend even when they're short.

2. I sometimes get dandruff and itchy scalp. Will this be treated by dieting? I'm currently using VICHY shampoo which I hope is gluten-free (they're not answering my emails).

3. Since I don't get any immediate symptoms (like cramps or sore throat) after eating gluten, how do I know I've made a mistake before it's too late? All I feel is constipation, bloating and anxiety.

Thank you anyone who reads this. I appreciate any help and pointers, specially since I don't know anyone else who knows about this. My entire family cares less about ingesting gluten even though I've told them it's hereditary. Not a single doctor I've met ever thought twice about helping me since to them being overweight pretty much sums it all up for them. My weight has been going down on it's and I pretty much eat the same amounts as I always have.


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



Celiac.com Sponsor (A8-M):



kareng Grand Master

Just to address the chewing gum and ketchup issue. I don't chew gum but I haven't heard of any with gluten. I would think sugar free gum would be OK. In the US, i haven't seen any ketchup with gluten.

Have you had yourself tested for anemia, iron, ferritin, B12, calcium, magnesium, vitamin D? Severe vitamin deficiencies are a result of the intestinal damage. You can't absorb the nutrients.

I assume through all this they are watching your thyroid?

Not every pain or problem is related directly or indirectly to gluten. Your back might just hurt because you lifted something wrong. Alot of things, like bad fingernails, can be related to the vitamin deficiencies caused by celiac. They can also be related to thyroid, dry air, etc.

Make sure you are not deficient and supplement what you are lacking.

dani nero Community Regular

Just to address the chewing gum and ketchup issue. I don't chew gum but I haven't heard of any with gluten. I would think sugar free gum would be OK. In the US, i haven't seen any ketchup with gluten.

Have you had yourself tested for anemia, iron, ferritin, B12, calcium, magnesium, vitamin D? Severe vitamin deficiencies are a result of the intestinal damage. You can't absorb the nutrients.

I assume through all this they are watching your thyroid?

Not every pain or problem is related directly or indirectly to gluten. Your back might just hurt because you lifted something wrong. Alot of things, like bad fingernails, can be related to the vitamin deficiencies caused by celiac. They can also be related to thyroid, dry air, etc.

Make sure you are not deficient and supplement what you are lacking.

Thanks kareng. I'll get myself tested when I get back to Sweden. I'm currently on a trip in the middle-east. The chewing-gum and ketchup are local brands. The gum contained dexterin and the ketchup some type of flavoring. I did a thyroid check a few years ago because I was gaining unexplained weight (which turned out to be due the anti-depressant paroxatin). They said my thyroid was not under-active.. but I'm not sure if that has anything to do with celiac disease symptoms.

kareng Grand Master

Thanks kareng. I'll get myself tested when I get back to Sweden. I'm currently on a trip in the middle-east. The chewing-gum and ketchup are local brands. The gum contained dexterin and the ketchup some type of flavoring. I did a thyroid check a few years ago because I was gaining unexplained weight (which turned out to be due the anti-depressant paroxatin). They said my thyroid was not under-active.. but I'm not sure if that has anything to do with celiac disease symptoms.

Who knows in the middle-east? I didn't even know they had ketchup!

IN the US. dextrin and flavorings are considered safe.

dani nero Community Regular

I've been reading some other posts and some new questioned have come up! I would appreciate your input and advice.

Can Dermatitis Herpetiformis appear on a single finger? I was getting a rash where the skin broke and got flaky together with tiny blisters. It both itched and burns (specially at night). I went to a doctor and he told me it was allergies from dish soap, and gave me cortisone cream for it. The rash went away when I started using gloves when washing dishes, and the cream was quite effective if it showed up again. This rash only appears on my right middle finger and the back of my left hand but milder. A few weeks ago I got a red flaky patch on the bikini line as well but it didn't have blisters. It was very itchy and a little inflamed though. They've both gone now that I've gotten off gluten 100%. I'm starting to think it might be a mistake not to get myself diagnosed now.

I'm trying to figure out which one of my parents has celiac, even though they're not taking me seriously. My mother is very short and skinny, can suffer from constipation, and has a red rash patch (small and flaky but no blisters) on both her knees. She doesn't have diabetes and I don't know about her thyroid.

My dad on the other hand has diabetes, thyroid problems, constipation, and suffers severe mood swings like me (I used to think he was bipolar because he'd be calm for months then become overactive and irritable the next months). But he's quite tall and his bone structure is wide. Is it possible that both my parents have celiac?

dani nero Community Regular

Hello forum dwellers,

I've sadly not gotten any responses to my questions, but I know that the forum is large and it's hard to give every last poster your attention. I've luckily read around and found answers to most of my questions as well so no worries:-)

Nevertheless I'm still having stomach aches. I just never had them before, or maybe I just didn't notice them, or maybe they're just placebo.. I don't know, but I've been getting them often since getting off the gluten. The constipation is gone on it's own for the first time in my life but I don't know why I'm getting stomach aches. Like when I sit or lie down on it, it hurts. I didn't stop the lactose yet because I'm on trip in the middle east and the yogurt dishes or dishes that are eaten with yogurt are made really often. Could the lactose be causing the ache? My stools are kindof loose as well (sorry for the grossness). Will continuing to eat lactose prohibit my intestines from healing as well? I'm going home in a week.

I'm also wondering why getting diagnosed is very important.

UKGail Rookie

Hi Dani

Doctors like getting you diagnosed as they think that celiacs need to be very strict about the diet to avoid further health problems. They currently think that people with non-celiac gluten sensitivity may not need to be quite as strict, and may even have a level of tolerance to ingesting small amounts of gluten. However I haven't managed to find any research to back this up, and many of us think that doctors are simply missing many celiac cases because of problems with the testing (or simply not testing when they ought to). Given the wide range of symptoms experienced by diagnosed celiacs (from near-death to completely silent)you could argue that if you have observed any form of gluten sensitivity, strict avoidance is less risky.

A formal diagnosis also helps other family members get tested, as medical guidelines encourage the testing of first degree relatives. Celiac disease is strongly heritable, and one day you may need to have your children tested. A diagnosis also helps to stop other family members thinking you are simply odd to avoid gluten for no reason validated by a doctor!

As for the ongoing stomach aches etc - well, it just takes time to heal. Until you do, it may continue to hurt for a while.

Continuing to consume lactose won't help you heal. Lactase to digest the lactose is produced in the tips of the villi. If these are damaged by celiac, you won't be able to digest it. I don't know if consuming it will actually set you back in healing, but I personally feel it is likely, albeit not the same extent as gluten ingestion. I tried some hard cheese for the first time yesterday (after 5 months gluten free), and it just gave me stomach ache, gurgling and bloating. Not as bad as a gluten reaction, but not helpful either. I'm going to continue to avoid it for a bit longer. I agree it is tough for you though, if you are trying to eat while travelling, and dairy is in most of the local food. I hope you enjoy your trip despite your discomfort. It is a fascinating area of the world.


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



Celiac.com Sponsor (A8-M):



mushroom Proficient

I was lactose intolerant for milk, ice cream, cream and frozen yogurt (not really yogurt), but was able to tolerate yogurt, cheese and sour cream without any problem. This is because these products have cultures and enzymes which digest the lactose for you and are mostly lactose free. I believe it is probably not worth spoiling your trip over not consuming a little yogurt - you can find out whether or not it bothers you when you get home, but do avoid the full lactose products like milk, etc.

dani nero Community Regular

Thanks for your help! <3

researchmomma Contributor

Dani, watch out for ketchup in the MIddle East. Only eat it if it is from a packet. They add water and other stuff to "stretch" the Ketchup in my experience. It tastes bad when they do this. We follow this rule anywhere outside the US to be honest but I really noticed the weird ketchup in the Middle East.

dani nero Community Regular

Dani, watch out for ketchup in the MIddle East. Only eat it if it is from a packet. They add water and other stuff to "stretch" the Ketchup in my experience. It tastes bad when they do this. We follow this rule anywhere outside the US to be honest but I really noticed the weird ketchup in the Middle East.

Yeah I don't eat it anymore. Thanks

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      128,311
    • Most Online (within 30 mins)
      7,748

    SWilson
    Newest Member
    SWilson
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.1k
    • Total Posts
      70.8k

  • Celiac.com Sponsor (A22):




  • Who's Online (See full list)


  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      Welcome to the forum, @Cathijean90! I went 13 years from the first laboratory evidence of celiac disease onset before I was diagnosed. But there were symptoms of celiac disease many years before that like a lot of gas. The first laboratory evidence was a rejected Red Cross blood donation because of elevated liver enzymes. They assume you have hepatitis if your liver enzymes are elevated. But I was checked for all varieties of hepatitis and that wasn't it. Liver enzymes continued to slowly creep up for another 13 years and my PCP tested me for a lot of stuff and it was all negative. He ran out of ideas. By that time, iron stores were dropping as was albumin and total protein. Finally, I took it upon myself to schedule an appointment with a GI doc and the first thing he did was test me for celiac disease. I was positive of course. After three months of gluten free eating the liver enzymes were back in normal range. That was back in about 1992. Your story and mine are more typical than not. I think the average time to diagnosis from the onset of symptoms and initial investigation into causes for symptom is about 10 years. Things are improving as there is more general awareness in the medical community about celiac disease than there used to be years ago. The risk of small bowel lymphoma in the celiac population is 4x that of the general population. That's the bad news is.  The good news is, it's still pretty rare as a whole. Yes, absolutely! You can expect substantial healing even after all these years if you begin to observe a strict gluten free diet. Take heart! But I have one question. What exactly did the paperwork from 15 years ago say about your having celiac disease? Was it a test result? Was it an official diagnosis? Can you share the specifics please? If you have any celiac blood antibody test results could you post them, along with the reference ranges for each test? Did you have an endoscopy/biopsy to confirm the blood test results?
    • Cathijean90
      I’ve just learned that I had been diagnosed with celiac and didn’t even know. I found it on paperwork from 15 years ago. No idea how this was missed by every doctor I’ve seen after the fact. I’m sitting here in tears because I have really awful symptoms that have been pushed off for years onto other medical conditions. My teeth are now ruined from vomiting, I have horrible rashes on my hands, I’ve lost a lot of weight, I’m always in pain, I haven’t had a period in about 8-9 months. I’m so scared. I have children and I saw it can cause cancer, infertility, heart and liver problems😭 I’ve been in my room crying for the last 20minutes praying. This going untreated for so long has me feeling like I’m ruined and it’s going to take me away from my babies. I found this site googling and I don’t know really what has me posting this besides wanting to hear from others that went a long time with symptoms but still didn’t know to quit gluten. I’m quitting today, I won’t touch gluten ever again and I’m making an appointment somewhere to get checked for everything that could be damaged. Is this an automatic sentence for cancer and heart/liver damage after all these symptoms and years? Is there still a good chance that quitting gluten and being proactive from here on out that I’ll be okay? That I could still heal myself and possibly have more children? Has anyone had it left untreated for this amount of time and not had cancer, heart, fertility issues or liver problems that couldn’t be fixed? I’m sure I sound insane but my anxiety is through the roof. I don’t wanna die 😭 I don’t want something taking me from my babies. I’d gladly take anyone’s advice or hear your story of how long you had it before being diagnosed and if you’re still okay? 
    • trents
      Genetic testing cannot be used to diagnose celiac disease but it can be used to rule it out and also to establish the potential to develop celiac disease. About 40% of the general population has the genetic potential to develop celiac disease but only about 1% actually develop it. To develop celiac disease when you have the genetic potential also requires some kind of trigger to turn the latent genes "on", as it were. The trigger can be a lot of things and is the big mystery component of the celiac disease puzzle at this point in time with regard to the state of our knowledge.  Your IGA serum score would seem to indicate you are not IGA deficient and your tTG-IGA score looks to be in the normal range but in the future please include the reference ranges for negative vs. positive because different labs used different reference ranges. There is no industry standard.
    • Scott Adams
      Since nearly 40% of the population have the genes for celiac disease, but only ~1% end up getting it, a genetic test will only tell you that it is possible that you could one day get celiac disease, it would not be able to tell whether you currently have it or not.
    • KDeL
      so much to it.  the genetic testing will help if i don’t have it right? If theres no gene found then I definitely don’t have celiac?  I guess genetic testing, plus ruling out h.pylori, plus gluten challenge will be a good way to confirm yes or no for celiac. 
×
×
  • Create New...