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

Confused And Overwhelmed


hmseyer21

Recommended Posts

hmseyer21 Rookie

I'm going to give you a bit of history and basically beg for advice, I am so overwhelmed.

In 2002, I was diagnosed with hypothyroidism. I was 24 years old. My family doctor put me on synthroid and antidepressants. The antidepressants made me crazy, so I took them only for about 4 months. I felt a little better but would have bouts of depression and gained about 10 pounds pretty quickly. I started off very healthy at about 135.

My levels were managed on the high end on about 75 mcg for a couple of years.

In 2005, I got pregnant with my first child. I started seeing an endocrinologist and he kept my levels on the lower end of normal and I felt okay. Better than before, but still not too great. I also began using generic levothyroxine around this time. I was really sick during the first trimester, but got a little better once I hit the second. I went full term, but my child was born with several birth defects(heart, spine, hearing loss, and eye issues) My levels were kept normal during the pregnancy and genetic tests were ran to see if they could diagnose him with a syndrome, but nothing came back.

My levels were a little up and down after the pregnancy, but got under control pretty quickly.

In 2007, I got pregnant with my second child and had a miscarriage at 10 weeks. I was completely devastated and began to research natural ways of living. I didn't know what else to do but to try to be as healthy as possible.

Over the next six months, my son was getting stomach viruses every few weeks and was failing to thrive. He was referred to a gastroenterologist. He suggested that my son may have celiac disease because he had a lot of symptoms. They did bloodwork, a stool sample, and an endoscopy. His tests were all negative and he was diagnosed with lactose intolerance. During this time of testing, I became pregnant again. After reading about celiac disease and before getting my son's tests results, I removed gluten from my diet because I was afraid I had it too and that may have caused my miscarriage. After the tests for my son came back negative, I assumed I didn't have it, mainly because it was soooo hard to be so sick and try to adopt a gluten free diet at the same time. During this time, my OBGYN ran some tests and found out I have a genetic blood clotting disorder called mthfr. I was told this could have been the cause of the birth defects in my first child because with this disorder, the body doesn't absord folic acid and other B vitamins properly. So I began taking a ton of folic acid, blood thinner shots, and B6 and B12. My son was born without any problems.

About 4 months after this pregnancy, my thyroid levels became extremely hyper. I had never experienced these symptoms and it was extrememly hard to cope with. After a couple of months of dealing with this, I decided to stop taking my thyroid medicine. I was in an extreme state of desperation with two young children and the extreme symptoms of hyper made me think maybe my thyroid was working again.

WRONG! In December of 2008, after two months of no levothyroxine my TSH was 219, my T3 was 50(low), and my Free t4(low) was 49, Oops, guess that was a really bad decision. So I began taking levothyroxine again and my levels seemed to be mostly normal after a few adjustments.

In August 2009, I became pregnant again. Another healthy baby was born in April 2010. But I started going through the hyper to hypo trainreck again. This past summer I was taking 137 mcg and started feeling the extreme symptoms of hyper again. It was awful again and I had trouble coping. So after getting tested, I was right, and they lowered my dose to 112. Two months later, I began feeling hypo, rechecked, and my TSH was at 13. So instead of putting me in between at 125, my annoying endocrinologist would not listen to me and put me on 150.

Last month, week after going on the dosage f 150, I started seeing a new doctor who tested me for a lot of things, including hashimotos. She said it sounded like I have all the symptoms, and suggested I start eating a gluten free diet to see how my body responds. So two weeks ago, I followed her advice and started eating gluten free. Last week, I got a call saying I was low in vitamin D levels, and that my bloodwork suggest that I have hashimotos. My antithyroid peroxidase was 440 and apparently normal is below 35. My Free T3 was also on the low normal end, but total t3 was normal. She didn't recheck TSH or T4 since I had just changed my dose a week before.

This past week, I began feeling extremely hyperthyroid again, and I am having trouble coping with the symptoms. So I am now taking my 112 dosage until I can see my current physician to put me on 125. I'd rather be hypo, hyper symptoms make me feel crazy.

So now after all these years, I find out I most likely have hashimotos. I know nothing about this and I honestly hate chagning my diet so drastically. I will be honest and say I despise having to be gluten free and alter my lifestyle so much. I feel like emotionally if I could get back on track, I wouldn't be so overwhelmed, but I am so confused at what to do. I don't feel any better so far, I really feel worse to be honest. I want to eat bread, but I won't because if it is truly causing me to be sick, it isn't worth it. Anyone have advice to help me understand what is going on? I am so overwhelmed today and I just want to be happy. I have a fantastic life and a ,wonderful family, it grieves my soul that these health issues are preventing me from enjoying my blessings. :(


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



Celiac.com Sponsor (A8-M):



eatmeat4good Enthusiast

Gluten can make you have a lot of the symptoms you have that cause you to say you had trouble coping. It can cause depression, anxiety, weight gain, messed up metabolism and Hashimoto's. You are likely experiencing withdrawal from gluten. I have Hashimoto's and DH (Dermatitis Herpetiformis) the skin form of Celiac, and a lot of neurological problems directly related to gluten. I only know this because they went away when I went gluten free. Although it is inconvenient to have to be gluten free, if you can stay hopeful, you may find that many things you never thought could get better actually do. Gluten interferes with so many things in the body and the way it metabolizes...and in the brain as well. I no longer have anxiety or depression at all unless I get glutened. I thought they were related to Hashimoto's but they seem to be directly gluten related. It is amazing that you have a Dr. smart enough to recommend that you try being gluten free. That is truly something to be thankful for. You may be surprised at what this does for your health and sense of well-being. There is no slice of bread worth the price of gluten to your body. Hang in there. I can't help but be excited for you because you are probably going to be feeling some wonderful benefits to being gluten free. Once the gluten withdrawal blues leave you that is. Gluten acts like an opiate and tells your brain you need more, more, more, of the very substance that is harming you. You will be fine if you can get through this without giving in. It is a big cahllenge and always difficult to change behavior and especially tastes we have developed, but you sound very committed to doing this so you can be the best mom you can be to your children. I admire you for what you have been through and you have the strength to get through this too. Good luck. Hope you will post about your symptoms that resolve after being gluten free for a time.

pricklypear1971 Community Regular

Also add a good multivitamin. Gluten and Hashi people are low on lots of things and a multi helps. Vitamin/ mineral supplements help balance things out. Make sure you get mild exercise 3x a week, too.

hmseyer21 Rookie

Thank you so much. Just encouragement that things can get better as you've experienced gives me more motivation to keep going. Do you know how long withdrawals usually last? l

Gluten can make you have a lot of the symptoms you have that cause you to say you had trouble coping. It can cause depression, anxiety, weight gain, messed up metabolism and Hashimoto's. You are likely experiencing withdrawal from gluten. I have Hashimoto's and DH (Dermatitis Herpetiformis) the skin form of Celiac, and a lot of neurological problems directly related to gluten. I only know this because they went away when I went gluten free. Although it is inconvenient to have to be gluten free, if you can stay hopeful, you may find that many things you never thought could get better actually do. Gluten interferes with so many things in the body and the way it metabolizes...and in the brain as well. I no longer have anxiety or depression at all unless I get glutened. I thought they were related to Hashimoto's but they seem to be directly gluten related. It is amazing that you have a Dr. smart enough to recommend that you try being gluten free. That is truly something to be thankful for. You may be surprised at what this does for your health and sense of well-being. There is no slice of bread worth the price of gluten to your body. Hang in there. I can't help but be excited for you because you are probably going to be feeling some wonderful benefits to being gluten free. Once the gluten withdrawal blues leave you that is. Gluten acts like an opiate and tells your brain you need more, more, more, of the very substance that is harming you. You will be fine if you can get through this without giving in. It is a big cahllenge and always difficult to change behavior and especially tastes we have developed, but you sound very committed to doing this so you can be the best mom you can be to your children. I admire you for what you have been through and you have the strength to get through this too. Good luck. Hope you will post about your symptoms that resolve after being gluten free for a time.

pricklypear1971 Community Regular

Depends. I was a raging lunatic for a week.

Had to give up milk Thursday (lower iodine for DH) and that is driving me nuts. Gluten was easy in comparison.

hmseyer21 Rookie

We eat minimal dairy since we are all lactose intolerant but to give up all dairy would be tough. :( I have a feeling it might be causing some issues too. I have craved dairy since going Gluten-Free. One thing at a time I guess. I have tried total elimination before and only made it 3 days. I decided that I could do gluten first then work on the rest. Thanks again. I have a feeling I will be on here often since you all understand.

eatmeat4good Enthusiast

Withdrawal got me for a bit longer...like probably 3 weeks...but it's because I refused to give up dairy. Even though I read that it is usually a problem, without wheat I felt that cheese and corn tortilla's were the only foods left on earth...so I had problems until I realized that yes, I too, could not eat dairy. I still did it. Cottage cheese and yogurt...but after enough experimentation, I realized that gluten was NOT my only problem...and I had to give up iodine foods too due to the DH....but once I got rid of them all....recovery went pretty fast...Withdrawal was bad...but once I learned to live with cravings....I was ok... Casein and gluten tend to be opiates for the brain in some people. That is why you often see gluten and casein free diets for children with Autism spectrum disorders....I wonder if it should be the diet for a lot more of us...like those of us who deal with depression and anxiety symptoms too. You are the only one who can tell if dairy is a problem for you....if it is only gluten though...some people have withdrawal symptoms for longer periods of time and some are ok after a couple of weeks. However, it all comes raging back even with trace gluten or cross contamination. Hope this isn't the case for you but it certainly is for me.

I wish I'd learned of this thing called gluten years ago...don't you wonder?


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



Celiac.com Sponsor (A8-M):



pricklypear1971 Community Regular

Funny you mention it... I read about it in connection with Hashis but the description didn't sound like me.

I see incomplete descriptions of celiac/gluten problems everywhere. It boggles my mind.

I can't understand how something that effects 1 in 133 people is not routinely screened for. Especially in vulnerable populations. Having Hashis puts me at roughly 30% chance. Geez. They worry about my cholesterol, risk of diabetes, breast cancer BUT NOT ONE SCREENED ME FOR CELIAC.

I cry BS on that one!

hmseyer21 Rookie

I hear you on the cheese and corn tortillas!!! I have Mexican for half my diet the past two weeks. I honestly have not gotten to the point of getting super serious about cross contamination. That is overwhelming to even think about. I know I will eventually have to, but I'm doing this in baby steps. I may have accidentally cross contaminated in the past two weeks but I felt better the first two days, then i have gotten worse since. I feel like an alien has taken over my body, I have felt this way in the past too and I know my thyroid is causing it.

I keep wondering if gluten caused my thyroid issues or is just related. I wonder if hashis came on after years of thyroid problems or if I developed it because of gluten.

Kind of like trying to figure out if the chicken or egg came

first.

I have never had a severe allergic reaction but I know I am probably gluten sensitive. I don't mind cutting out gluten so much honestly it's worrying about cross contamination that I feel overwhelmed with right now.

Do you think I should glutenate and be tested or just keep on trucking with the diet? I am just hoping I will be able to stop thinking so much about how to eat. I am still eating food that is good it's just the psychological aspect of it all.

I think it's crazy too how many doctors do not take these things seriously. It took me a while and many years of suffering but I am definitely thankful to have found one who knows what she is talking about. I have my follow up appointment in 3 weeks. I wish it were tomorrow!

hmseyer21 Rookie

Oh and I don't have DH but I do have keratosis pilaris. Do you know if that's related? It seemed to be better for 2 days but now is worse. Do you think that is because of withdrawal?

eatmeat4good Enthusiast

I've seen posts in the archives here that keratosis pilaris cleared up on the gluten free diet...but I don't know how it is related...only that there are many skin conditions associated with gluten and Celiac...not just DH. Although cross contamination and trace gluten are overwhelming to think about that might be why you cleared up for the first days of your diet and then reacted. Many people get better when they go gluten free then become hypersensitive to cross contamination as your body rebels against that which has been poisoning it for so long. You might have to pay close attention to traces of gluten in order make any progress. I know it sucks...it did for me too. But it is very common for people to have just as serious a reaction to trace gluten as if they had eaten a sandwich or slice of pizza. It is maddening. I didn't want to have to be obsessed about food or trace gluten either...but the more vigilant I got the more recovery I experienced. It is a learning process to be sure. Be patient with yourself but keep your mind focused on being more vigilant about eliminating all sources of gluten so you can get maximum benefit to the diet. I hate to say it..but it is imperative and it might be the reason you are feeling yucky. It has taken me a full year to learn to be really good at avoiding all sources of gluten. That's why I say be patient with yourself. My first gluten free meal eating out...I ordered Kebabs and rice at a Mediterranean restaurant...only to find that 3/4 of the way through the meal...my rice was a pilaf with little vermicelli threads of pasta all through it. It didn't occur to me that rice might have gluten. I laugh about that now....as I won't eat out and read packages thrice before consuming the product...but I was very pleased with my decision to go gluten free....until the first dinner was over and I was completely glutened and a complete failure at being gluten free....but still it was part of my learning process. I too wonder if I had learned of gluten or Celiac sooner if I might have avoided the hashimoto's disease. I really do not know which is worse...thyroid symptoms?...or glutening symptoms...they are both awful...

And I agree with the above posts that something that effects 1 in 133 of the entire population should be screened for on a regular basis. Yet we beg Dr.'s for an answer to our seemingly mysterious symptoms, medical problems and mental health problems, only to find out years into the disease process that it was wheat all along. Every single bread loaf should carry a warning label....if the damned cigarette companies have to label their product as being scientifically potentially harmful to your health, then why doesn't Bread and Pasta have to carry a warning label that the contents could be damaging to 1/133 of the population???? It is unbelievable really.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,546
    • Most Online (within 30 mins)
      7,748

    KimberlyAnne76
    Newest Member
    KimberlyAnne76
    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

    • Scott Adams
      Your post demonstrates the profound frustration and isolation that so many in the Celiac community feel, and I want to thank you for channeling that experience into advocacy. The medical gaslighting you endured for decades is an unacceptable and, sadly, a common story, and the fact that you now have to "school" your own GI specialist speaks volumes about the critical lack of consistent and updated education. Your idea to make Celiac Disease a reportable condition to public health authorities is a compelling and strategic one. This single action would force the system to formally acknowledge the prevalence and seriousness of the disease, creating a concrete dataset that could drive better research funding, shape medical school curricula, and validate the patient experience in a way that individual stories alone often cannot. It is an uphill battle, but contacting representatives, as you have done with Adam Gray, is exactly how change begins. By framing it as a public health necessity—a matter of patient safety and protection from misdiagnosis and neglect—you are building a powerful case. Your voice and your perseverance, forged through thirty years of struggle, are exactly what this community needs to ensure that no one else has to fight so hard just to be believed and properly cared for.
    • Scott Adams
      I had no idea there is a "Louisville" in Colorado!😉 I thought it was a typo because I always think of the Kentucky city--but good luck!
    • Scott Adams
      Navigating medication safety with Celiac disease can be incredibly stressful, especially when dealing with asthma and severe allergies on top of it. While I don't have personal experience with the HealthA2Z brand of cetirizine, your caution is absolutely warranted. The inactive ingredients in pills, known as excipients, are often where gluten can be hidden, and since the FDA does not require gluten-free labeling for prescription or over-the-counter drugs, the manufacturer's word is essential. The fact that you cannot get a clear answer from Allegiant Health is a significant red flag; a company that is confident its product is gluten-free will typically have a customer service protocol to answer that exact question. In situations like this, the safest course of action is to consider this product "guilty until proven innocent" and avoid it. A better alternative would be to ask your pharmacist or doctor to help you identify a major national brand of cetirizine (like Zyrtec) whose manufacturer has a verified, publicly stated gluten-free policy for that specific medication. It's not worth the risk to your health when reliable, verifiable options are almost certainly available to you. You can search this site for USA prescriptions medications, but will need to know the manufacturer/maker if there is more than one, especially if you use a generic version of the medication: To see the ingredients you will need to click on the correct version of the medication and maker in the results, then scroll down to "Ingredients and Appearance" and click it, and then look at "Inactive Ingredients," as any gluten ingredients would likely appear there, rather than in the Active Ingredients area. https://dailymed.nlm.nih.gov/dailymed/   
    • Scott Adams
      What you're describing is indeed familiar to many in the Celiac community, especially in the early stages of healing. When the intestinal villi are damaged from Celiac disease, they struggle to properly digest and absorb fats, a condition known as bile acid malabsorption. This can cause exactly the kind of cramping and spasms you're seeing, as undigested fats can irritate the sensitive gut lining. It is highly plausible that her reactions to dairy and eggs are linked to their higher fat content rather than the proteins, especially since she tolerates lean chicken breast. The great news is that for many, this does improve with time. As her gut continues to heal on a strict gluten-free diet, her ability to produce the necessary enzymes and bile to break down fats should gradually return, allowing her to slowly tolerate a wider variety of foods. It's a slow process of healing, but your careful approach of focusing on low-fat, nutrient-dense foods like seeds and avocado is providing her system the best possible environment to recover. Many people with celiac disease, especially those who are in the 0-2 year range of their recovery, have additional food intolerance issues which could be temporary. To figure this out you may need to keep a food diary and do an elimination diet over a few months. Some common food intolerance issues are dairy/casein, eggs, corn, oats, and soy. The good news is that after your gut heals (for most people who are 100% gluten-free this will take several months to two years) you may be able to slowly add some these items back into your diet after the damaged villi heal. This article may be helpful: Thank you for sharing your story—it's a valuable insight for other parents navigating similar challenges.
    • 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.
×
×
  • 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.