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

New,positive Biopsy Lots Of Dammage


Gcbec

Recommended Posts

Gcbec Newbie

Ok here I got, Hello my name is Cindy. I am 36 and was just told yesterday that I have celiac disease. This has been going on for several years really, I also have Lupus Hypothyroid, SVT, and a blood clotting disorder oh yeah and anemia. It really started 7 years ago when my daughter was born 3 months premature, I had blood clot in my lung then a few months later I had ischemic colitis which they say was from another blood clot. I continued to have problems on and off severe pain diareaha nassua vomiting. in 2002 I had intusseseption had emergency surgery. They said this was so rare they have no Idea what caused it, nor did they find out. well 12/04 I again had intussesception went to different hospital and they ran more tests. My blood work came back positive for Celiac but they said it could be from lupus causing a false positive. So they did endoscopy and biopsy and came back positive, again they said could be from lupus so wanted to wait 1 month. I waited 6 months because I started to feel better, I was having occasional cramps and diareaha mostly through the nights. I get fevers night sweets and I am always always tired. I went and had biopsy endoscopy done last week and it came back positive for celiac, the dr said it looks like it progressed much more than they would have expected. They said there was lots of imflamation throughout and there were several areas of concern and they are still waiting on those biopsy to come back. I had a cousin that died from this 2 years ago, has anyone had a biopsy endoscopy or any kind of cancer that might be able to help me further? I am really scared because they are sending me to Manhatten to meet another specialist. They keep telling me they are very concerned. Please help me find information and experiences from people that might have been through this. How could this have gotten so bad in 6 months and could the problems from all these years been the cause?


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



Celiac.com Sponsor (A8-M):



Jnkmnky Collaborator

Are you on the gluten free diet yet?

KaitiUSA Enthusiast

The only thing that will heal damage is the diet. That will reverse damage and you need to get on it right away. The other things you have are linked with untreated celiac.

This site will help you out tremendously.

Gcbec Newbie
Are you on the gluten free diet yet?

<{POST_SNAPBACK}>

No Dr just told me yesterday. I have been in denial for some time, didnt expect this at all. She said I should start imediatly. I dont know where to start, she set up appointment with nutrisionist on tuesday.

KaitiUSA Enthusiast
No Dr just told me yesterday.  I have been in denial for some time, didnt expect this at all.  She said I should start imediatly.  I dont know where to start, she set up appointment with nutrisionist on tuesday.

<{POST_SNAPBACK}>

Many nutritionists know nothing about celiac. You need to do alot of research on this yourself and this site will help with everything you need to know. You are also going to have to look at makeups you wear and products like that. Did you know 6 months ago you had celiac too? You said it progressed alot more then they would have expected...so that made me think you knew about this before.

Anyway, you need to be gluten free right away because having gluten will lead to other serious and life threatening things.

Jnkmnky Collaborator

Are you in the U.S.? There are many great stores you can go to to get the food you need. WholeFoods, Henry's, Boney's, Wild Oats, Trader Joe's...on-line ordering. Here are two sites with great bread products.

Open Original Shared Link

Open Original Shared Link

All of their products are tasty and will help make your transition smooth and enjoyable. There's no reason to live life eating food that makes this diet difficult. There are lots of great food suggestions in the parents of kids with Celiac section. Post Fruity and Cocoa Pebbles are gluten free. Tinkyada pastas are the best. Classico sauces *even the alfredo* are all gluten free. Velveeta cheese is gluten free. Look around this site for good foods that will make this diet doable. Order your breads right away. It may take a week for them to be delivered.

Jnkmnky Collaborator

You may want to avoid dairy products for a few months while your villi heal. You're probably lactose intolerant right now. That may change as your villi heal. Rice milk is an excellent alternative. Soy causes problems in some people.


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



Celiac.com Sponsor (A8-M):



Guest zipy

Hi there,

I was just diagnosed as well...and it was triggered by having my second child. I don't know about all the untreated problems, but I hope that you start the diet soon and that you start to feel better as well. This board has tons of information to help you.

Good luck,

Erin

tarnalberry Community Regular

Welcome to the board, though I'm sorry you went through so much getting here.

As for the diet - start at the easy places, but start now. Until you get a handle on what you can and can't have in the processed food world, stick with naturally gluten free whole foods. Whole fruits and vegetables are gluten free. Fresh, unprocessed meats are fine (though check the labels, of course, to verify that, for instance, you don't pick up ground beef that has wheat added to it). Plain nuts and beans/lentils are also fine. Unseasoned rice and corn are fine as well. Add some olive oil and plain spices (McCormick is a safe and common brand), and you have a wide variety of meals that you can make to get you through the days/weeks of navigating the diet.

Gcbec Newbie
Welcome to the board, though I'm sorry you went through so much getting here.

As for the diet - start at the easy places, but start now.  Until you get a handle on what you can and can't have in the processed food world, stick with naturally gluten free whole foods.  Whole fruits and vegetables are gluten free.  Fresh, unprocessed meats are fine (though check the labels, of course, to verify that, for instance, you don't pick up ground beef that has wheat added to it).  Plain nuts and beans/lentils are also fine.  Unseasoned rice and corn are fine as well.  Add some olive oil and plain spices (McCormick is a safe and common brand), and you have a wide variety of meals that you can make to get you through the days/weeks of navigating the diet.

<{POST_SNAPBACK}>

Thankyou all so much for the information. I am gonna start the diet as soon as I can. I still am left wondering if anyone here has had lots of dammage and besides diet was anything else done? And has anyone here ever moved on to late stages like cancer? I am going to a specialist in NYC Dr Peter Greene so hopefully that will help. Thanks again and I know how important diet is now just got to face up to it.

Guest zipy

Hi again,

I'm the first diagnosed celiac in my family. My grandfather passed away almost 10 years ago of colon cancer and had always been lactose intollerant, my uncle has had parts of his colon removed because of cancer, he's always had digestive problems as well. I'm not in his shoes and I can't make him get tested for gluten intollerance, but I'm highly suspect, there are too many coincidences. So, for me at least, I can say that I think there is probably a link between gluten and cancer in the family. I'll keep a positive vibe for you while you're going through all your tests.

~Erin ;)

Canadian Karen Community Regular

Hi Cindy! Welcome to the board!!

Well, now that you know that definitely you have celiac, you can start firstly by getting gluten free immediately. The second most important thing you can do is think positively. There are people on this board who literally were knocking on death's door before they finally got the celiac diagnosis and have worked their way back to a healthy active life.

Celiac can be devastating to your body. It can be so debilitating that you literally are convinced that you are dying. I know, I've been there. In fact, if it wasn't for all the knowledgeable, supportive people here in this forum and the invaluable advice and encouragement they have given me, I am afraid to think where I would have been by now..... I at one point was convinced that due to years of damage done due to celiac, that I was past the point of no return. After I finally grasped the enormity of the situation (being celiac, that is), I gave this disease the respect it deserves and smartened up and started taking this diet really seriously. I learned many things that I was doing wrong i.e. exposing myself to cross-contamination (like using the same toaster as the rest of my family), not checking medications properly (I was using Gax-X Chewable Tablets like candy for the gas not realizing they contained gluten), wasn't careful enough with my shampoos, make-up etc. (I now use Pantene stuff now as the hair products I previously used contained gluten).....

Celiac often needs a "trigger" to kick in and the birth of your daughter 3 months premature sure is one heck of a trigger! I know, I have twin boys who were born at 31 weeks gestation and were 3 lbs. 12 oz. each. I also know the stresses that go along with the NICU and all of the ups and downs of good days and bad days that your preemie has. The good thing now is that now you know, YOU CAN TAKE CONTROL AND DO SOMETHING ABOUT IT!!! You have the power to change your life and change the way you live and eat. Think of it as your body is yelling at you, telling you THIS STUFF IS NOT WHAT I NEED!!!!!

Any support, encouragement or answers you need, you will find here. There are a bunch of really great people on this board who have been down this road and will help you go down it also..... Anything you need to know, just post away. If you are having a not so great day, let us know and you will get all the encouragement you need. Just remember, you had the strength to weather the storm of the NICU and all of the stresses of having a preemie, you can weather this storm also!! ;)

Hugs and welcome!

Karen

Guest BERNESES

Just wanted to say welcome Cindy- you came to the right place. Here's a link that has been enormously helpful to me in finding gluten free food if you don't have a health food or Whole Foods store near you. It's:

Open Original Shared Link

You want to click on the upper right folder that says April 2005. This list has really helped me but still READ LABELS. i would also suggest reading "Wheat Free, Worry Free" by Danna Korn (spelling?) ASAP. It's enormously helpful. We're glad you're here. Beverly

Ignatia Newbie

There is so much information on the internet that you may find out more here than what a "nutritionist" can tell you. My experience with them has also been that they haven't a clue.

While you are learning about the diet, simplify. Eat just a few things that you are positive are gluten free. I had to start cooking all my own foods; we rarely go out anymore. Keep it simple for awhile until you can start adding foods you know to be safe. You will be surprised how fast you feel better.

My mother is crippled by arthritis and osteoporosis, in a wheelchair for the rest of her life. Her father and four brothers all died of colon cancer. I feel so good on the diet that I don't think I will have to deal with any of those problems. Mom eats my same diet, because I do all the cooking and even she feels better.

We have been on it for 5 years now. Neither of us takes much medication any longer and before the diet, we were both a walking drug store.

Please educate yourself. Make sure you are not ingesting gluten. Don't dwell on "gluten free". Do dwell on all the great foods you still can eat. Gradually you will find recipes and products you can eat. Read labels. Miracles will happen in your life and health.

Ignatia Newbie

[You were curious about damage that some of us suffered. I spent my whole life with dreadful allergies, gas, bloating, constipation, cramps, fatigue, aching joints and many other complaints from my early teen years. I am 62 now.

When my doctor did a colonoscopy, he told me that diet had nothing to do with my SEVERE ULCERATIVE COLITIS! I was bleeding to death. I got no relief from his prescriptions and ended up back in the hospital twice for a week each time from "unknown illnesses." My daughter finally figured out what was wrong with me. My doctor had tested me for Celiac (because I looked Irish and am) but it came back negative, which is common; therefore his announcement of diet not being cause.

My daughter told me to stop eating gluten. A friend of hers was a Celiac. From that moment, I haven't touched gluten in 5 years. Within 24 hours I felt better, more energy. Within 2-3 weeks, I stopped taking acid reflux meds; didn't need them. My joints quit hurting, I lost 30 pounds (not from lack of food, just the diet), I have energy, my allergies are less and I feel great. After a year, I noticed my bleeding had stopped. Asked for another colonoscopy. The gastro doc was amazed that I was totally healed because of the diet.

We probably all have damage done from years of not being on the diet. But, you can heal. Just give it a chance. My mother in her wheelchair is healing and feeling better. Just wish it could help her walk again. Gluten intolerance, I am sure, is the reason she is crippled with osteoporosis. Your colon is so torn up by gluten that it cant absorb calcium and other nutrients needed to avoid other diseases. Get off the gluten and you'll feel great.

Susan in Texas

thomas3000 Rookie

Hi susan,

I loved your post!! It's amazing what the body can do once the stressors are taken off. Just let everyone know, I'm not celiac, but am gluten intolerant. My family has a history of depression, anxiety disorder, strong tobacco addiction..These are all signs of gluten sensitivity. My aunt and uncle both suffer from panic disorder and are currently taking meds for it. If they miss the underlying factor here(gluten), I'm afraid of the health consequences they will have in the future. I told both of them to stop eating gluten, but they won't listen. We're english, dutch, irish, swedish, scottish, scandinavian. Does it get any clearer than that? I also suffered from panic, ptsd, depression, but have found the genetic link. My symptoms are fading away thank the lord, it's been a tough struggle, but I thank god he made me stubborn enough not to see conventional docs and find my own answers. I found out that 6 percent of people get correctly diagnosed accurately. My doc focuses beyond symptoms and finds root causes to illnesses. I didn't correlate my mental symptoms with my diet, but I'm living proof that living gluten free will "cure" depression and anxiety disorders.. I hate the FDA and the AMA for profiting on illness, unless they just don't know the truth behind this hidden epidemic...Would they even accept it?? Who knows...

Pharm Newbie

I just recently had 2 positive blood tests for celiac disease. I am waiting on the endoscopy in January. I read as much as I could about the disease & got lots of info & help from a friend who is celiac. I decided to cut out gluten as a test about 3 months ago. I noticed changes for the positive within days, some of which I haven't heard mentioned by others such as; NO MORE- cold feet at night, thick sinus phelgm..esp at night,aches & pains, extremely dry skin, gas/bloating, smelly bowel movements, lack of energy etc. I was amazed by the quick changes for the better & have never gone back. The more I read & the more follow this board, the more I think gluten hurts almost everyone, just to different extents. Many of my realtives have similar symtioms as I did & even many people in general complain of aches/pains/sluggishness etc. Does any else sense that gluten may be a bad thing for everyone & that we are just more sensitive than most or have I gone overboard with this?

ravenwoodglass Mentor
I just recently had 2 positive blood tests for celiac disease. I am waiting on the endoscopy in January.

<{POST_SNAPBACK}>

I agree with the poison for everyone statement. It impacts much more than just the gut. I believe its' most serious impact is on the brain. It seems to occur long before the gut symptoms show up and makes life really miserable. Please be aware the doctor will need for you to poison yourself for a time before the endo. I wonder why they demand it. I ended up so sick from the gluten challange I couldn't even make it to the test! Oh well we all know in the US medicine is money.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,857
    • Most Online (within 30 mins)
      7,748

    LowellFrancis
    Newest Member
    LowellFrancis
    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

    • Rogol72
      Some interesting articles regarding the use of Zinc Carnosine to help heal gastric ulcers, gastritis and intestinal permeability. I would consult a medical professional about it's use. https://www.nature.com/articles/ncpgasthep0778 https://www.rupahealth.com/post/clinical-applications-of-zinc-carnosine---evidence-review https://pmc.ncbi.nlm.nih.gov/articles/PMC7146259/ https://www.fallbrookmedicalcenter.com/zinc-l-carnosine-benefits-dosage-and-safety/
    • Jillian83
      He is. Which makes everything even more difficult. I’m not a believer in “staying for the kids” but I have nowhere to go and it’s not just me, it’s me plus my babies. We live in a beautiful place, lots of land in the country and me and the kids love the place we’ve called home for their entire lives. But Im seeing that he’ll never change, that my kids deserve a happy healthy Momma, and that staying in this as is will be the early death of me. Then I look at the scars covering my entire body…this disease and the chronic stress I’ve been enduring for years that tell me I’m no longer beautiful and no one will ever look at me with interest again. I try self care, try to give myself grace so I can just start loving myself enough to gain strength but the slightest sparkle in my eye and skip in my step attracts his wrath and it all comes crashing ten fold. Life is just absolutely railing me from every single direction leaving me wanting to wave that white flag bc I don’t feel like there’s much hope no matter what happens. 
    • trents
    • Jillian83
      Hi, I was recently diagnosed with Celiac and dermatitis herpetiformis after years of suffering without answers. I lost my mind. I lost my job. I lost so much time. I lost Me. Conventional doctors are opulent come near me and the one who did sat across the room, misdiagnosed me, pumped me full of steroids which collapsed my entire hip for 6 months. So without answers I began my holistic journey. Fast forward a couple of years and still struggling with a mysterious whole body itchy, crawling “skin hell”, perfect teeth now deteriorating, thick hair now thinning rapidly and no more than a day or 2 at most relief….An acquaintance opened up a functional medicine practice. Cash only, I found a way. Within a month tests clearly showing my off the charts gluten allergy/sensitivity as well as the depletion of vital nutrients due to leaky gut and intestinal damage. dermatitis herpetiformis was more than likely what I was experiencing with my skin. I was happy. I thought this is easy, eat healthy Whole Foods, follow the diet restrictions and I finally get to heal and feel confident and like myself again very soon! 😔 Supplements are very pricey but I got them and began my healing. Which leads to the other major issue: not working, stay at home Mom of young kids, entirely financially dependent on my man of 7 plus years. He’s never been supportive of anything I’ve ever done or been thru. He controls everything. I’m not given much money ever at a time and when he does leave money it’s only enough to possibly get gas. His excuse is that I’ll spend it on other things. So my “allowance” is inconsistent and has conditions. He withholds money from me as punishment for anything he wants. Since being diagnosed, he’s gained a new control tactic to use as punishment. He now is in control of when I get to eat. He asked for proof of my diagnosis and diet bc he said I made it up just to be able to eat expensive organic foods. Then after I sent him my file from my doctor he then said she wasn’t a real doctor. 😡. I go days upon days starving, sometimes breaking down and eating things I shouldn’t bc I’m so sick then I pay horribly while he gets annoyed and angry bc I’m not keeping up with all the duties I’m supposed to be doing. His abuse turns full on when I’m down and it’s in these desperate times when I need his support and care the most that I’m punished with silence, being starved, ignored, belittled. He will create more of a mess just bc I’m unable to get up and clean so that when I am better, I’m so overwhelmed with chores to catch up that the stress causes me to go right back into a flare from hell and the cycle repeats. I’m punished for being sick. I’m belittled for starving and asking for healthy clean water. I’m purposely left out of his life. He won’t even tell me he’s going to the grocery or to get dinner bc he doesn’t want me to ask him for anything. I have no one. I have nothing. Im not better. My supplements ran out and I desperately need Vitamin D3 and a methylated B complex at the very minimal just to function….he stares at me blankly…no, a slight smirk, no words. He’s happiest when im miserable and I am miserable.  this is so long and im condensing as much as I can but this situation is so complicated and disgusting. And it’s currently my life. The “IT” girl, the healthy, beautiful, perfect skin, perfect teeth, thick and curly locks for days, creative and talented IT girl….now I won’t even leave this house bc Im ashamed of what this has dont to my body, my skin. Im disgusted. The stress is keeping me from healing and I think he knows that and that’s why he continues to keep me in that state. He doesn’t want me confident or successful. He doesn’t want me healed and healthy bc then how would he put the blame of all his problems on me? This journey has been hell and I’ve been in Hell before. I’ve been killed by an ex, I’ve been raped, robbed, held hostage, abused beyond nightmares but the cruelty I’ve experienced from him bc of this disease is the coldest I’ve ever experienced. I’ve wanted to give up. Starving and in tears, desperate…I found a local food pantry in our small town so I reached out just saying I had Celiac and was on hard times. This woman is blessing me daily with prepared gluten free meals, donations, educational info, people who know this disease and how they manage life and the blessings just keep coming. But it’s overwhelming and I feel like I don’t deserve it at all. He just glared and I know he’s going to sabotage it somehow. I don’t even know what to do anymore. I’m so broken and just want peace and healing. 
    • cristiana
      @Colleen H   I am just curious,  when you were tested for coeliac disease, did the doctors find out if you had any deficiencies? Sometimes muscle pain can be caused by certain deficiencies, for example, magnesium, vitamin D, calcium, and potassium.   Might be worth looking into having some more tests.  Pins and needles can be neuropathy, again caused by deficiencies, such as iron and B12,  which can be reversed if these deficiencies are addressed. In the UK where I live we are usually only tested for iron, B12 and vitamin D deficiencies at diagnosis.   I was very iron anemic and supplementation made a big difference.  B12 was low normal, but in other countries the UK's low normal would be considered a deficiency.  My vitamin D was low normal, and I've been supplementing ever since (when I remember to take it!) My pins and needles definitely started to improve when my known deficiencies were addressed.  My nutritionist also gave me a broad spectrum supplement which really helped, because I suspect I wasn't just deficient in what I mention above but in many other vitamins and minerals.  But a word of warning, don't take iron unless blood tests reveal you actually need it, and if you are taking it your levels must be regularly monitored because too much can make you ill.  (And if you are currently taking iron, that might actually be making your stomach sore - it did mine, so my GP changed my iron supplementation to a gentler form, ferrous gluconate). Lastly, have you been trying to take anything to lessen the pain in your gut?  I get a sore stomach periodically, usually when I've had too much rich food, or when I have had to take an aspirin or certain antibiotics, or after glutening.  When this happens, I take for just a few days a small daily dose of OTC omeprazole.  I also follow a reflux or gastritis diet. There are lots online but the common denominators to these diets is you need to cut out caffeine, alcohol, rich, spicy, acidic food etc and eat small regularly spaced meals.   When I get a sore stomach, I also find it helpful to drink lots of water.  I also find hot water with a few slices of ginger very soothing to sip, or camomile tea.  A wedge pillow at night is good for reflux. Also,  best not to eat a meal 2-3 hours before going to bed. If the stomach pain is getting worse, though, it would be wise to see the doctor again. I hope some of this helps. Cristiana    
×
×
  • 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.