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What Medication Are You On To Help You Cope With You Coeliac Disease (And Related) Symptoms?

Kim69

By Kim69
in Coping with Celiac Disease

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Kim69 Apprentice
Kim69
Posted

I had undiagnosed depression for about 10 years. And I have been diagnosed with celiac disease for 1 year. I have been on an antidepressant (citalopram) for 2 1/2 years - it really helped me feel normal again.

Since getting diagnosed with celiac disease I have been slowly getting better (ie abdominal pain lessening, no more diarhoea) but I mentioned headaches and neck/shoulder pain to my dr. She suggested I switch to a different AD since it could possibly assist with reducing the pain. So I am on cymbalta

and it really helps me with depression which has been linked to celiac disease. I have been on it 4 weeks now and haven't really noticed much change in pain but it is supposed to help with bone pain, fibromyalgia and lots of other problems. I am interested to see how I go.

As a side note - I think that some people are scared to try an antidepressant because they are afraid of stigma or are afraid it will change their personality or make them dopey. I have had good results and because I believe that my depression is caused by chemical imbalance I am really grateful for the medication.

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K8ling Enthusiast
K8ling
Posted

Loritabs and Zofran for reactions. Lexapro but I have Generalized Anxiety Disorder.

GlutenFreeJess Newbie
GlutenFreeJess
Posted

I also have Hashimotos and Fibromyalgia, and am on Synthroid (for the Hashis) and Neurontin & Naproxen for the fibro. OTC, I take TUMS and Liquid Antacid. I used to be on Prevacid though. I am on some other meds as well b/c I have bipolar disorder and generalized anxiety disorder, but those are the meds I am on to help deal with the associated autoimmune issues that I have with Celiac. And they work wonders :)

T.H. Community Regular
T.H.
Posted

Not on any at the moment, and I'm very grateful. I managed to cut my gluten down to much lower than 20ppm a day, and that took care of the aches and pains issue, as well as my depression. Mine looks like it's all gluten related, thankfully.

But I'll be honest, I'm really worried about medication in the future. My thyroid was getting worse the last I tested, and thyroid problems run in my family. But the last 4-5 times I tried medication, they all made me very ill. The only prescription meds I took made me so sick I ended up in the ER.

Kind of worried that I"ll need meds in the future and have to make the decision over which will make me sicker: medication or no medication. :(

GFinDC Veteran
GFinDC
Posted

Not on any at the moment, and I'm very grateful. I managed to cut my gluten down to much lower than 20ppm a day, and that took care of the aches and pains issue, as well as my depression. Mine looks like it's all gluten related, thankfully.

But I'll be honest, I'm really worried about medication in the future. My thyroid was getting worse the last I tested, and thyroid problems run in my family. But the last 4-5 times I tried medication, they all made me very ill. The only prescription meds I took made me so sick I ended up in the ER.

Kind of worried that I"ll need meds in the future and have to make the decision over which will make me sicker: medication or no medication. :(

Hmm. that's why I haven't had my thyroid removed yet. I am concerned about the meds for it not being gluten-free. There is not guarantee they will make gluten-free thyroid meds available.

I know I feel better when I use iodized salt, so my thyroid is still working at least.

sandrad Newbie
sandrad
Posted

Ive been on nadalol for over a year for my headaches. I take gravol for nausea and liquid antacid for the burning pain i get and ive also been on plenty ppi...right now its been nexium for a couple years

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    • SamAlvi
      High TTG-IgG and Normal TTG-IgA

      By SamAlvi · Posted

      Thanks again for the detailed explanation. Just to clarify, I actually did have my initial tests done while I was still consuming gluten. I stopped eating gluten only after those tests were completed, and it has now been about 70 days since I went gluten-free. I understand the limitations around diagnosing NCGS and the importance of antibody testing and biopsy for celiac disease. Unfortunately, where I live, access to comprehensive testing (including total IgA and endoscopy with biopsy) is limited, which makes things more complicated. Your explanation about small-bowel damage, nutrient absorption, and iron-deficiency anemia still aligns closely with my history, and it’s been very helpful in understanding what may be going on. I don't wanna get Endoscopy and I can't start eating Gluten again because it's hurt really with severe diarrhea.  I appreciate you taking the time to share such detailed and informative guidance. Thank you so much for this detailed and thoughtful response. I really appreciate you pointing out the relationship between anemia and antibody patterns, and how the high DGP IgG still supports celiac disease in my case. A gluten challenge isn’t something I feel safe attempting due to how severe my reactions were, so your suggestion about genetic testing makes a lot of sense. I’ll look into whether HLA testing is available where I live and discuss it with my doctor. I also appreciate you mentioning gastrointestinal beriberi and thiamine deficiency. This isn’t something any of my doctors have discussed with me, and given my symptoms and nutritional history, it’s definitely worth raising with them. I’ll also ask about correcting deficiencies more comprehensively, including B vitamins alongside iron. Thanks again for sharing your knowledge and taking the time to help. I’ll update the forum as I make progress.
    • knitty kitty
      Son's legs shaking

      By knitty kitty · Posted

      Blood tests for thiamine are unreliable.  The nutrients from your food get absorbed into the bloodstream and travel around the body.  So, a steak dinner can falsely raise thiamine blood levels in the following days.  Besides, thiamine is utilized inside cells where stores of thiamine are impossible to measure. A better test to ask for is the Erythrocyte Transketolace Activity test.  But even that test has been questioned as to accuracy.  It is expensive and takes time to do.   Because of the discrepancies with thiamine tests and urgency with correcting thiamine deficiency, the World Health Organization recommends giving thiamine for several weeks and looking for health improvement.  Thiamine is water soluble, safe and nontoxic even in high doses.   Many doctors are not given sufficient education in nutrition and deficiency symptoms, and may not be familiar with how often they occur in Celiac disease.  B12 and Vitamin D can be stored for as long as a year in the liver, so not having deficiencies in these two vitamins is not a good indicator of the status of the other seven water soluble B vitamins.  It is possible to have deficiency symptoms BEFORE there's changes in the blood levels.   Ask your doctor about Benfotiamine, a form of thiamine that is better absorbed than Thiamine Mononitrate.  Thiamine Mononitrate is used in many vitamins because it is shelf-stable, a form of thiamine that won't break down sitting around on a store shelf.  This form is difficult for the body to turn into a usable form.  Only thirty percent is absorbed in the intestine, and less is actually used.   Thiamine interacts with all of the other B vitamins, so they should all be supplemented together.  Magnesium is needed to make life sustaining enzymes with thiamine, so a magnesium supplement should be added if magnesium levels are low.   Thiamine is water soluble, safe and nontoxic even in high doses.  There's no harm in trying.
    • lizzie42
      Son's legs shaking

      By lizzie42 · Posted

      Neither of them were anemic 6 months after the Celiac diagnosis. His other vitamin levels (d, B12) were never low. My daughters levels were normal after the first 6 months. Is the thiamine test just called thiamine? 
    • knitty kitty
      Son's legs shaking

      By knitty kitty · Posted

      Yes, I do think they need a Thiamine supplement at least. Especially since they eat red meat only occasionally. Most fruits and vegetables are not good sources of Thiamine.  Legumes (beans) do contain thiamine.  Fruits and veggies do have some of the other B vitamins, but thiamine B 1 and  Cobalamine B12 are mostly found in meats.  Meat, especially organ meats like liver, are the best sources of Thiamine, B12, and the six other B vitamins and important minerals like iron.   Thiamine has antibacterial and antiviral properties.  Thiamine is important to our immune systems.  We need more thiamine when we're physically ill or injured, when we're under stress emotionally, and when we exercise, especially outside in hot weather.  We need thiamine and other B vitamins like Niacin B 3 to keep our gastrointestinal tract healthy.  We can't store thiamine for very long.  We can get low in thiamine within three days.  Symptoms can appear suddenly when a high carbohydrate diet is consumed.  (Rice and beans are high in carbohydrates.)  A twenty percent increase in dietary thiamine causes an eighty percent increase in brain function, so symptoms can wax and wane depending on what one eats.  The earliest symptoms like fatigue and anxiety are easily contributed to other things or life events and dismissed.   Correcting nutritional deficiencies needs to be done quickly, especially in children, so their growth isn't stunted.  Nutritional deficiencies can affect intelligence.  Vitamin D deficiency can cause short stature and poor bone formation.   Is your son taking anything for the anemia?  Is the anemia caused by B12 or iron deficiency?  
    • lizzie42
      Son's legs shaking

      By lizzie42 · Posted

      Thank you! That's helpful. My kids eat very little processed food. Tons of fruit, vegetables, cheese, eggs and occasional red meat. We do a lot of rice and bean bowls, stir fry, etc.  Do you think with all the fruits and vegetables they need a vitamin supplement? I feel like their diet is pretty healthy and balanced with very limited processed food. The only processed food they eat regularly is a bowl of Cheerios here and there.  Could shaking legs be a symptom of just a one-time gluten exposure? I guess there's no way to know for sure if they're getting absolutely zero exposure because they do go to school a couple times a week. We do homeschool but my son does a shared school 2x a week and my daughter does a morning Pre-K 3 x a week.  At home our entire house is strictly gluten free and it is extremely rare for us to eat out. If we eat at someone else's house I usually just bring their food. When we have play dates we bring all the snacks, etc. I try to be really careful since they're still growing. They also, of course, catch kids viruses all the time so I  want to make sure I know whether they're just sick or they've had gluten. It can be pretty confusing when they're pretty young to even be explaining their symptoms! 
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