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

How Long Have I Been A Celiac, And How Much Damage Have I Done?


S-J-L

Recommended Posts

S-J-L Apprentice

Hi,

I was always a healthy weight up until 12, then i became unbelievably skinny, except i didnt notice this at the time and put it down to puberty lol. However i have been quite badly constipated since 7or 8. I was really anemic at about 15 and had headaches and tiredness all the time. At 16 i started to have heart problems (fast, irregular) and was put on medication. One doctor said i was so thin that my heart was strained, another didnt know, and another said it was just a random thing that some people get.

I have also suffered depression off and on since 12, and am on medication. When i came to uni, in my first year i got so exhausted that i ended up in a&e alot, dropped a paper and thought about not coming back. I went to a dietician cos i was concerned about my weight, and she analysed my diet as being good, and was put on 'fortisip', a high calorie drink which they usually give to the dying people that cant eat lol. This, plus my normal diet didnt put any weight on me, and that was the end of it for awhile. Last year my immune system was so low, i had the flu bad twice. My tiredness got worse and still is, i have such a foggy head and when im tired it feels like im guna faint. I lost another 4kg, (5'8 and 103pounds) so went to another doctor who sent me to a GI specialist who did all these tests on me, including celiacs.

I just found out afew weeks ago that:

t-transglutaminase is 164

antiendomysial is positive

I had my biopsy a week ago and im waiting for results.

When do you think my celiac (if i have it) started?

Also how much damage has been done?

Thanks, Sarah.


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

Hi Sarah, It is very hard to tell when exactly your celiac was triggered but it sounds like it has affected you since 7 or 8. Many of us start out with C as our bodies response to the drop in absorption, trying to draw everything out it can I guess. Many of the other things you mention are also likely celiac related and as such should resolve. No matter how much damage was done you stand a real good chance of complete recovery. Most do, although it can take time.

You should get some sublingual B12 as soon as you can, that will help with your energy levels. Also get a good multiple that is gluten-free.

The easiest way to heal fastest is to eat whole, unprocessed foods for a bit. Fresh fruit and veggies, rice, potatoes, meats, eggs, nuts etc. I would strongly advise you to drop dairy for at least a couple months also. You can add in processed stuff like Lay's chips, specialty gluten-free baked goods etc after you have healed a bit. You want to check the gluten statis of everything that goes into or onto your body also.

You have come to a great place for info and support, read as much as you can and ask any question you need to. Be sure also to check out the links on the home page for some good additional information. Do be sure that all your first degree relatives get tested, whether they think they have symptoms or not. Celiac can be really sneaky and disguise itself as arthritis, mood disorders, gallbladder and liver problems, skin disorders and much more.

S-J-L Apprentice

OK, thanks, good to know. Any other opinions?

gfp Enthusiast
OK, thanks, good to know. Any other opinions?

ravenwood already said most of it....

Search the forums a bit, ask more questions and ... biopsies can be false negative because of the way they are sampled.

Going gluten-free is quite a change, its hard at first like learning to ride a bike but once you actually make it habit it's actually quite easy.

Search this forum for cross contamination (CC) and hidden gluten ... get back to basics and get healthy.

If you are in shared accomadation this will almost certainly prove the hardest problem ... as others tend to be careless ..

S-J-L Apprentice

Thanks, im flatting and cooking separate from my flat mates anyway cos ive been trying to put on weight lol

gfp Enthusiast
Thanks, im flatting and cooking separate from my flat mates anyway cos ive been trying to put on weight lol

Even so you do share pans and utensils....or a dishwasher or dishcloth, towels etc.

Ursa Major Collaborator

Sarah, have you eliminated gluten from your diet yet? Since you have had your biopsy done, there is no point in waiting for the results before doing so. As gfp said, false negatives with biopsies are fairly common, and a negative biopsy cannot rule out celiac disease.

Your blood work was positive. Along with a positive diet response that would prove celiac disease, even without a biopsy.

Make sure you get a new toaster, as you absolutely cannot clean a toaster well enough to be safe. The same goes for plastic colanders that have been used for wheat pasta, wooden cooking spoons and cutting boards and scratched non-stick pots and pans. All of those need replacing I am afraid.

Also, you will need to replace any personal care products (shampoo, conditioner, lipstick, soap, lotion etc.) that contain gluten. Look for things like wheat germ oil and barley extract. In addition I know that where you are (I assume you are in Britain somewhere because of saying 'flat' instead of apartment, but of course, you might be in Australia) people with celiac disease are told that wheat starch is safe. But many people with celiac disease react badly to it, and I advise you not to eat anything with wheat starch, no matter what anybody says.

Depression is a VERY common symptom with celiac disease and might clear up on the gluten-free diet. So, you may be able to wean off your medication after starting the diet! Many people (especially doctors it seems) are unaware of the fact that gluten will not just affect the digestive system, but the brain and the nervous system as well. In fact, it can affect any body system, and the damaged villi is just one of many possible symptoms.

The same goes for your heart. You may not need that medication any more, either. You do need to be checked for nutritional deficiencies. Low potassium, low magnesium or low vitamin B12 could be causing your heart problems, as could low ferritin (iron) levels and low vitamin D! All of those deficiencies are very common in celiac disease.


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



Celiac.com Sponsor (A8-M):



S-J-L Apprentice

Can makeup affect you even though it just goes on your face??

Ursa Major Collaborator
Can makeup affect you even though it just goes on your face??

Some of us (me included) will get a rash (I get psoriasis and terrible itching) when anything containing gluten gets on my skin.

But will you ever touch your face during the day? Will you remember to wash your hands with soap every time afterwards, to make sure you don't eat anything after touching your gluten containing makeup? Do you ever lick your fingers, poke around in your teeth etc.? If you have anything with gluten on your hands and forget to wash them before touching your lips or food you eat, you will gluten yourself.

So, while you may not be somebody who obviously reacts to gluten applied to the skin, why take the risk? I feel much safer knowing that I don't have to worry about it, because everything I use is gluten-free.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,964
    • Most Online (within 30 mins)
      7,748

    Cbear
    Newest Member
    Cbear
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • 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.