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

Depressed


paulwwww

Recommended Posts

paulwwww Newbie

I found out I was a Celiac about a half a year ago. It was nice finally figuring out what was going on. My energy dropped to zero although I continued to eat like crazy. My doctor had me taking Celexa (antidepressant) prior to being diagnosed with celiac disease. Once I was diagnosed I figured I probably wouldn't need Celexa anymore, plus I did not like the mild side effects. Things seem to get gradually better as I became gluten-free however in the last month or two I have had no desire to do anything. Of course this is killing me in my high pressure job and active family life. I generally have a lot of ambition but now can't seem to motivate.

I was considering St. Johns Wort as a possible solution. Any advice would be greatly appreciated.

PW


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



Celiac.com Sponsor (A8-M):



MySuicidalTurtle Enthusiast

For me, I found therapy to be good. I did it for many months after diagnosis and go back when I feel I need it. It helped me out a lot and they can prescribe something if you need medication or someting alternitive if you want.

pwalasik Newbie

Hi PW,

First of all, remember you have been through a lot, medically speaking, and feeling good/ motivated may take awhile physically & emotionally. Maybe you should try going back on your medication. Possibly a combined med/ therapy, may prove to be most effective. I am sorry you are having a problem with motivation. Maybe it is unrealed to celiac... my daughter has celiac disease and an undiagnosed blood sugar level problem. I really have to watch her sugar spikes and dips. I try to equal the amount of protein versus carbs/ sugar..etc. If I don't, it's like dealing with Jekel vs Hyde. Good Luck and please post on this message board when you need support. You ARE going through a tough time and we are here to help.. Good Luck

ianm Apprentice

Welcome aboard. Six months may not be enough time for you to really be fully healthy. Are you lacking in energy or is it just motivation? I have a very demanding job also and once I started to get healthy for the first time in 36 years I found that I wasn't as motivated in some areas as I was before. I had more energy than ever had before but for me it was a case of wanting to do the things that my disease just wouldn't allow me to do. I never had any problems with serious depression requireing medication so I can't be of much help there. There are a lot of great people in this group and a lot of good information. It is going to take some more time and things will get better.

Ianm

Canadian Karen Community Regular

Hi PW,

I have struggled with mild to moderate depression for many years. I have been on anti-depressants for about 10 years now. I have absolutely no qualms about taking them. The way I look at it, my body doesn't produce enough seratonin which requires me to take medication to correct that, the EXACT same way that I take thyroid medication because my body doesn't produce enough iodine. I don't see any difference between the two.

Also, have you ever heard of SAD (Seasonal Affective Disorder)? I am prone to that. From November to February is brutal for me, and then in March I start to pull myself out of the rut. Even Christmas is not great for me, my husband calls me Scrooge (Bah Humbug!!!). Christmas carols make me cry, etc..... :( I find that the more light I expose myself to, the more it alleviates it.......

I think you should re-consider your decision to go off the medication. Or perhaps be pre-emptive, and take the meds only from November to March when the liklihood of the depression is highest.....

Also, have you had your thyroid checked? The reason I found out about my hypothryoidism was because I went to the doctor with the "post-wedding blues", feeling very depressed (a few months after my wedding), and a thyroid test revealed my hypothyroidism. Depression is a symptom of thyroid disease.....

Good Luck, and hope your spirits pick up soon! :)

Karen

plantime Contributor

Your need for the antidepressant could very well be unrelated to celiac disease. I need Lexapro to help me cope with the changing hormones that come with menopause. I have weaned off of it, and I feel the loss of it! Try using sunshine to cope with depression. If you are just not motivated to work, maybe you need a new job? Or an added challenge, to spice it up a bit?

mommida Enthusiast

New studies say, exercise was better than drugs for depression. AS little as 10 minutes a day. Go back to the doctor before you stop taking any antidepressant. Have you made sure that prescription was being taken for best results? i.e. empty stomache, with food, best time of day? What is the length of time the drug is in your system?

Just a few things to think about.

Laura


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



Celiac.com Sponsor (A8-M):



lovegrov Collaborator

I know people with mild to moderate depression who say St. John's Wort is great. I'm nopt sure studies really support it, but it might be worth a try. If you're taking any other medications, you need to make sure the St. John's won't cause problems. Remeber, I am not a doctor or medical person. Please look into this carefully yourself.

Exercise is indeed ALWAYS a good suggestion but there are some types of depression and some situations you can't just exercise your way out of.

richard

Guest BellyTimber

Hi, your story sounds like mine except I'm not a family man & I've been bumping along somehow without antidepressants.

I tried St Johns Wort several years ago and, having been prewarned about possible effects on the eyes, decided after a little while that it didn't suit my eyes. I think that's the main thing to "watch" out for with that remedy.

If you have the space, explore having a lightbox. Some people need to switch it on the evening, some in the morning, some people find it helps a lot, others not much or not at all. Do you have a support group for SAD or light box users?

When I can I walk around with my spectacles off (windows & specs get in the way) - the sunlight can get to the areas somewhere near the eyes that regulate this sort of thing - be sure to not look anywhere near the sun though!

Depression can be a symptom of this condition, can be a reaction to discovering we have the condition, a reaction to the people we have to deal with because of the condition (doctors?), and stem from other things ... (quite likely all of these at the same time).

I am at crunch point and probably need to do some baking this weekend (an unusual activity for me), for me that is an initiative issue.

This forum is the right place to raise that anyway.

All the very best,

Michael

:)

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,553
    • Most Online (within 30 mins)
      7,748

    Jennifer CCC
    Newest Member
    Jennifer CCC
    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.