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

Very Discouraged


mm&j

Recommended Posts

mm&j Apprentice

It is Sept. 9th. I know I got some gluten, (very little) at the middle to end of July so that is over 6 weeks ago and I am still experiencing numerous symptoms. There seem to be a string of things that happen to me. I'll try to put it briefly...first intestinal problems, then the skin rash on elbows and behind knees, followed by extreme fatique, almost like I have been drugged, flu-like symptoms, cold sores all over my mouth and tonque, now I am experiencing extreme bone pain and achiness and so depressed after more than a month of this that I am so irritable that I can't stand myself and don't know how my family can. Each symptom lasts at least a week, some overlap, but it is always this seemingly never-ending chain of symptoms. Does anyone else experience anything else like this. I was diagnosed a year and 1/2 ago and probably been gluten-free for over a year with the exception of the accidental times that cause so much distress. Thanks for your time.

mm&j (Susie)


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



Celiac.com Sponsor (A8-M):



mm&j Apprentice

Can I add that I am so depressed and feel so hopeless that I am in tears every day? :(

ShayFL Enthusiast

I have heard that some people respond violently when glutened. You may be one of them.

The best you can do is cut out the dairy for a month or so. Eat simple foods cooked at home: meats, eggs, veggies, fruits, safe nuts & seeds and go easy on the grains (even gluten-free ones) and processed foods. Stick to whole foods.

Drink lots of water.

Get plenty of rest so your body can repair itself.

Get some sunshine.

Consider "Intestive" or "Sea Cure" to speed healing.

mymagicalchild Apprentice
Can I add that I am so depressed and feel so hopeless that I am in tears every day? :(

Yes, you may add that thought, but "hopeless" is not good, MM&J. Not good at all. Which you already know.

I'm confident one of the experts on this website is all set to give you some great advice and comfort. Your physical symptoms sound like a combination of problems, but your despair sounds like it comes from a woman with the world on her shoulders and she knows she doesn't have the strength to carry it.

Are you on extra-virgin coconut oil, 3 tablespoons throughout each day? Try googling "coconut oil and candida" to see if there's any "light at the end of the tunnel" for you there. Candida goes hand-in-hand with Celiac disease and it has serious side effects.

I'm just a fellow-sufferer out here feeling really bad for you. My advice: You, Girl, need a vacation! You need to be taking care of YOURSELF or you won't be able to take care of anything or anyone else.

I would have a really good cry and then I'd head for the ocean. Someplace where I could hear the surf all night long. No cell phone. No email.

Get family members or friends to take over that "world" for awhile and go to your healing place. Go find your hope!

GlutenGuy36 Contributor
It is Sept. 9th. I know I got some gluten, (very little) at the middle to end of July so that is over 6 weeks ago and I am still experiencing numerous symptoms. There seem to be a string of things that happen to me. I'll try to put it briefly...first intestinal problems, then the skin rash on elbows and behind knees, followed by extreme fatique, almost like I have been drugged, flu-like symptoms, cold sores all over my mouth and tonque, now I am experiencing extreme bone pain and achiness and so depressed after more than a month of this that I am so irritable that I can't stand myself and don't know how my family can. Each symptom lasts at least a week, some overlap, but it is always this seemingly never-ending chain of symptoms. Does anyone else experience anything else like this. I was diagnosed a year and 1/2 ago and probably been gluten-free for over a year with the exception of the accidental times that cause so much distress. Thanks for your time.

mm&j (Susie)

Yes The same thing happens to me. I have all kinds of symptoms that far exceed the intestinal issues. Depressed where I cry at night and I am a guy. Skin rash, achy joints and bones, hurt from head to toe, my head feels like its heavy on one side of my face, and those are just a few. I was diagnosed on july 14th and been on gluten-free diet ever since. I'm sure that I am still getting some in my diet somewhere. I am to the point of just going vegan for a while till I figure it all out. Cross contimination and where gluten hides. A lot of days I feel like there is no hope.

mftnchn Explorer

It IS really hard at first to find all the sources of gluten. Personal care products and kitchen pans and utensils need to be considered. Is your household gluten free?

If you are pretty sure that is not the problem, could be you are one of us who needs to be stricter and remove some other things. Soy, milk, major allergens, grains, nightshades, legumes, etc. It's a lot of work to figure it out and there are lots of ideas on the forum about it.

If things don't improve you might try the intro diet and first stage or so of the SCD diet. If you do that you can add one food at a time and have a pretty good elimination diet plus it might do the trick to help with gut healing.

With villi damage we can't make lactase to digest milk, and also some other enzymes to digest other carbs can be lacking. Even after two years of healing the levels of these are typically lower than normal. So my guess is for some of us, we really lack these and just don't handle carbs very well. That's me for sure...and the SCD is really working for me. Wish I had started a year ago or more.

GFinDC Veteran

I get various symptoms too. Can't sleep for days wich I attribute to my thyroid acting up due to glutening. I am planning to see a doctor for more thyroid tests soon. I guess what I am saying is that if you have an associated condition, then your symptoms can flare in that related condition. For me I tend to get hyperthyroid, but am usually hypothyroid. At least that's how I interpret it.


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



Celiac.com Sponsor (A8-M):



lobita Apprentice

So sorry you're going through this! I got glutened this winter, and to make matters worse, I got the flu at the same time. I was sick for two months straight. But the real kicker was that I was going through a personally stressful time.

They've done recent studies on how stress can make allergic reactions worse (Open Original Shared Link), and I'm sure that that goes for gluten reactions as well.

If you've been really stressed out, take time out for yourself and do something fun.

Also, make sure you're getting enough Vitamin D. I know that I wasn't this winter, and when I started indoor tanning (on a whim), I quickly started to feel better...but the whole tanning thing is not something that I'm saying is good for everybody, it just worked for me.

Good luck!

mstrain Rookie
It is Sept. 9th. I know I got some gluten, (very little) at the middle to end of July so that is over 6 weeks ago and I am still experiencing numerous symptoms. There seem to be a string of things that happen to me. I'll try to put it briefly...first intestinal problems, then the skin rash on elbows and behind knees, followed by extreme fatique, almost like I have been drugged, flu-like symptoms, cold sores all over my mouth and tonque, now I am experiencing extreme bone pain and achiness and so depressed after more than a month of this that I am so irritable that I can't stand myself and don't know how my family can. Each symptom lasts at least a week, some overlap, but it is always this seemingly never-ending chain of symptoms. Does anyone else experience anything else like this. I was diagnosed a year and 1/2 ago and probably been gluten-free for over a year with the exception of the accidental times that cause so much distress. Thanks for your time.

mm&j (Susie)

I could be way off base with this, but perhaps something else is occuring along with your being glutened. My body was aching for weeks - i finally went to my GP and had blood work done - I had both Lyme's disease and parvovirus. According to the blood work my doctor estimates that I've had Lyme's for 3 - 4 months! I just finished a month's worth of antibiotics and feel much better. I see you live in PA - how prevalent is Lyme's where you are?

mftnchn Explorer

Michelle, you could be right. And HOW LUCKY YOU ARE to have caught it this early, even though not early enough to eradicate it before it takes hold in the body.

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - trents replied to SilkieFairy's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      IBS-D vs Celiac

    2. - trents replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      how much gluten do I need to eat before blood tests?

    3. - SilkieFairy posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      IBS-D vs Celiac

    4. - catnapt posted a topic in Related Issues & Disorders
      0

      anyone here diagnosed with a PARAthyroid disorder? (NOT the thyroid) the calcium controlling glands

    5. - catnapt replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      how much gluten do I need to eat before blood tests?

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,322
    • Most Online (within 30 mins)
      7,748

    avery144
    Newest Member
    avery144
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • trents
      Welcome to the celiac.com community, @SilkieFairy! You could also have NCGS (Non Celiac Gluten Sensitivity) as opposed to celiac disease. They share many of the same symptoms, especially the GI ones. There is no test for NCGS. Celiac disease must first be ruled out.
    • trents
      Under the circumstances, your decision to have the testing done on day 14 sounds very reasonable. But I think by now you know for certain that you either have celiac disease or NCGS and either way you absolutely need to eliminate gluten from your diet. I don't think you have to have an official diagnosis of celiac disease to leverage gluten free service in hospitals or institutional care and I'm guessing your physician would be willing to grant you a diagnosis of gluten sensitivity (NCGS) even if your celiac testing comes up negative. Also, you need to be aware that oats (even gluten free oats) is a common cross reactor in the celiac community. Oat protein (avenin) is similar to gluten. You might want to look at some other gluten free hot  breakfast cereal alternatives.
    • SilkieFairy
      After the birth of my daughter nearly 6 years ago, my stools changed. They became thin if they happened to be solid (which was rare) but most of the time it was Bristol #6 (very loose and 6-8x a day). I was on various medications and put it down to that. A few years later I went on this strict "fruit and meat" diet where I just ate meat, fruit, and squash vegetables. I noticed my stools were suddenly formed, if a bit narrow. I knew then that the diarrhea was probably food related not medication related. I tried following the fodmap diet but honestly it was just too complicated, I just lived with pooping 8x a day and wondering how I'd ever get and keep a job once my children were in school.  This past December I got my yearly bloodwork and my triglycerides were high. I looked into Dr. William Davis (wheat belly author) and he recommended going off wheat and other grains. This is the first time in my life I was reading labels to make sure there was no wheat. Within 2 weeks, not only were my stools formed and firm but I was only pooping twice a day, beautiful formed Bristol #4.  Dr. Davis allows some legumes, so I went ahead and added red lentils and beans. Nervous that the diarrhea would come back if I had IBS-D. Not only did it not come back, it just made my stools even bigger and beautiful. Still formed just with a lot more width and bulk. I've also been eating a lot of plant food like tofu, mushrooms, bell peppers, hummus etc which I thought was the cause of my diarrhea before and still, my stools are formed. In January I ran a genetics test because I knew you had to have the genes for celiac. The report came back with  DQ 2.2 plus other markers that I guess are necessary in order for it to be possible to have celiac. Apparently DQ 2.2 is the "rarer" kind but based on my report it's genetically possible for me to have celiac.  I know the next step is to bring gluten back so I can get testing but I am just not wanting to do that. After suffering with diarrhea for years I can't bring myself to do it right now. So that is where I am!   
    • catnapt
      learned I had a high PTH level in 2022 suspected to be due to low vit D  got my vit D level up a bit but still have high PTH   I am 70 yrs old (today in fact) I am looking for someone who also has hyperparathyroidism that might be caused by malabsorption    
    • catnapt
      I am on day 13 of eating gluten  and have decided to have the celiac panel done tomorrow instead of Wed. (and instead of extending it a few more weeks) because I am SO incredibly sick. I have almost no appetite and am not able to consume the required daily intake of calcium to try to keep up with the loss of calcium from the high parathyroid hormone and/or the renal calcium leak.    I have spent the past 15 years working hard to improve my health. I lost 50lbs, got off handfuls of medications, lowered my cholesterol to enviable levels, and in spite of having end stage osteoarthritis in both knees, with a good diet and keeping active I have NO pain in those joints- til now.  Almost all of my joints hurt now I feel like someone has repeatedly punched me all over my torso- even my ribs hurt- I have nausea, gas, bloating, headache, mood swings, irritability, horrid flatulence (afraid to leave the house or be in any enclosed spaces with other people- the smell would knock them off their feet) I was so sure that I wanted a firm diagnosis but now- I'm asking myself is THIS worth it? esp over the past 2 yrs I have been feeling better and better the more I adjusted my diet to exclude highly refined grains and processed foods. I didn't purposely avoid gluten, but it just happened that not eating gluten has made me feel better.   I don't know what I would have to gain by getting a definitive diagnosis. I think possibly the only advantage to a DX would be that I could insist on gluten-free foods in settings where I am unable to have access to foods of my choice (hospital, rehab, nursing home)  and maybe having a medical reason to see a dietician?   please let me know if it's reasonable to just go back to the way I was eating.  Actually I do plan to buy certified gluten-free oats as that is the only grain I consume (and really like) so there will be some minor tweaks I hope and pray that I heal quickly from any possible damage that may have been done from 13 days of eating gluten.    
×
×
  • 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.