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

How Long Does It Take To Start Feeling Better (And Other Questions)


gh0st

Recommended Posts

gh0st Newbie

Hi guys. I was looking for an intro section but it isn't available as far as I can tell. 

 

I've been sick for the past year trying to figure out what is wrong with me. My primary told me there was nothing more he could do for me after him giving me the run around for 2-3 months. He took a few tests but then started giving me antidepressants, saying I was just depressed and anxious.

 

To shorten the story I took an endoscopy and everything came out negative and I was sent to an infectious disease doctor who tested for a variety of things and celiac came back strong positive. I went off gluten immediately and felt great within 3 days. 

 

My symptoms are need for immediate evacuation of bowels to painful bm to no pain. I don't really get D or C. I do however get mucus in my stool every so often. (maybe 1-2 times a week). It really hits me more in the energy, mood, and foggy head feeling. I also feel a burning in my bowels and feel like I have a constant fever. I almost every night have 37.1 to 37.4C temp. Very lowgrade fever. And you might say this isn't a fever but im always at night around 36.5 (when I wasnt sick).

 

Anyway the digestion specialist wanted me back on gluten so he could perform another endoscopy. So I asked him how much to eat and he said normally. So I had cookies and pies, and sandwiches/burgers. I felt like crap that whole week. 

 

Results came back positive for celiac and the biopsy was positive.

 

Now I am recovering but I find that it is taking much longer and feel as if at times I'm not progressing at all. I even started throwing up the first few days.

 

I guess my question is how do I find out my sensitivity? Is there a test? Also I've been eating mainly raw stuff except for peanut butter which seems like a good processed choice because it is really just a blend of peanuts and oil.

 

Is the mucus thing a normal thing for recovering celiacs? I also seem to have very thick spit that sinks in water then pops back up. Just very thick spit.

 

Sorry for all the questions but I've been really bummed last few weeks and really have been thinking my time here might be short. I know this is a crappy way to live, but I decided to just live my life, fight through it, and leave the rest up to the universe to sort out.

 

I will be traveling in a few days to europe to see my baby doll, because I feel like she helps me a lot through this. I will be flying on virgin and they have a gluten free meal. Should I consider this celiac safe?

 

Thanks for being an ear, and listening to my psychotic ramble :)

 

 


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



Celiac.com Sponsor (A8-M):



GF Lover Rising Star

Hi Gh0st and welcome to the Forum.  We love psychotic rambles :D

 

First off, there is no range of sensitivity with Celiac however there may be a range of the severity of symptoms.  Celiac is an Autoimmune Disease so if you ingest gluten, you will have an autoimmune reaction causing a myriad of symptoms.  ANY amount of gluten will cause this reaction so you must be 100% gluten free.  The mucus in your stool is most likely from Malabsorption which is common in Celiac Disease.  As you begin to heal this will most likely improve.  Your body is damaged from the disease and will take a lot of time to recover.  Try to eat only whole foods for the first few months.  Some people also remove Dairy for awhile as it can be difficult to digest with damaged villi.  You may also want to get your Nutrition levels checked by blood test to see it you are deficient and need to supplement.  This is also common with Celiac.  Try not to eat out for a few months as the risk of cross contamination is great and you will need to learn the skills to do this successfully.  You should read the Newbie 101 thread to find out what changes you may need to make in your kitchen to be safe.  You should also check any medications or suppliments for gluten.  Check your shampoo if you get it in your mouth.   Recovery takes time.  Some symptoms may clear up relatively quickly, a couple weeks to months.  Others may take up to a year. 

 

I hope I have answered some of your questions.  Have a great trip. Your recovery will depend on your faithfulness to a 100% gluten free diet. 

 

Colleen

nvsmom Community Regular

Welcome to the board.  :)

 

Ditto everything Colleen said: healing can take quite a while. Some symptoms improve immediately, others feel worse for a few weeks if they experience withdrawal, and others find recovery is not steady with symptoms that backslide sometime in the first year... And those gluten challenges can take quite a toll on people; it may take a few months to recover.  :(

 

If possible, bring your own food on the flight. Their gluten-free meal might be gluten-free but make sure there is no chance of contamination before eating it... basically, make sure it came as a sealed meal and you are the one to open it. I tend to bring my own food just to be safe; I'd hate to get sick while travelling.

 

Hope you feel well soon.

Greebo115 Rookie

Ditto what the others have said - but another reason you must take back-up food for the flight: I ordered gluten free (it might have even been on a Virgin flight), and it got left behind, so they offered me a VEGETARIAN meal - like that was ANY good to me at ALL - arghhh! (pasta and veggies slathered in sauce, with a cake for dessert)

gh0st Newbie

Thanks guys I appreciate it.

 

I have one more question. I constantly feel like I have a fever even when I don't. But my temperature seems to be fluctuating a lot. Sometimes from 95.9 to 99.3. Is it possible I might have something else as well or am I being a hypochondriac, and need to wait this out?

Gemini Experienced

The gluten-free meals on Virgin are very safe.  I fly that airline a lot and have never, ever gotten sick and I am very sensitive.  They serve the food allergy people first so your food doesn't get mixed in with the gluten eaters.  The flight attendants seem to be very knowledgeable about Celiac also.  They seem to get it right every time with me so I trust them.

BelleVie Enthusiast

It definitely takes time, and it is worth being absolutely rigid about the diet in the beginning to make sure you are doing everything right. I'm now almost three months in to 100% gluten free, and it's only in the past couple of weeks that I've started feeling consistently okay. It takes time, but you'll get there. 

 

About your fever, have you been to the doctor to check for a regular infection or anything of that nature? Several times in the past, I've had a low grade infection that creeps up on me over time, and one day I realize that I feel awful and that I am feverish. Though I don't care to take them, sometimes a round of antibiotics really helps. I had an infection a few days ago, took some antibiotics, and have a lot more energy today than normal. 

 

Hope you feel better soon! 


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



Celiac.com Sponsor (A8-M):



gh0st Newbie

I haven't gone to the doctor to check for an infection but the fevers almost always start after i eat dinner (which is my biggest meal of the day), and always low grade. Sometimes within an hour I get drops from 99 to 97. It just seems like a huge drop, and I always get cold from the drop. As I'm writing this I have a 98.8F temperature and I feel like I'm burning up.

 

I'm heading out to europe (croatia) tomorrow and I'm wondering if I should see a doctor over there or will it be a waste of time.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,930
    • Most Online (within 30 mins)
      7,748

    Mhp
    Newest Member
    Mhp
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • AnnaNZ
      I forgot to mention my suspicion of the high amount of glyphosate allowed to be used on wheat in USA and NZ and Australia. My weight was 69kg mid-2023, I went down to 60kg in March 2024 and now hover around 63kg (just after winter here in NZ) - wheat-free and very low alcohol consumption.
    • AnnaNZ
      Hi Jess Thanks so much for your response and apologies for the long delay in answering. I think I must have been waiting for something to happen before I replied and unfortunately it fell off the radar... I have had an upper endoscopy and colonoscopy in the meantime (which revealed 'minor' issues only). Yes I do think histamine intolerance is one of the problems. I have been lowering my histamine intake and feeling a lot better. And I do think it is the liver which is giving the pain. I am currently taking zinc (I have had three low zinc tests now), magnesium, B complex, vitamin E and a calcium/Vitamin C mix. I consciously think about getting vitamin D outside. (Maybe I should have my vitamin D re-tested now...) I am still 100% gluten-free. My current thoughts on the cause of the problems is some, if not all, of the following: Genetically low zinc uptake, lack of vitamin D, wine drinking (alcohol/sulphites), covid, immune depletion, gastroparesis, dysbiosis, leaky gut, inability to process certain foods I am so much better than late 2023 so feel very positive 🙂    
    • lehum
      Hi and thank you very much for your detailed response! I am so glad that the protocol worked so well for you and helped you to get your health back on track. I've heard of it helping other people too. One question I have is how did you maintain your weight on this diet? I really rely on nuts and rice to keep me at a steady weight because I tend to lose weight quickly and am having a hard time envisioning how to make it work, especially when not being able to eat things like nuts and avocados. In case you have any input, woud be great to hear it! Friendly greetings.
    • Hmart
      I was not taking any medications previous to this. I was a healthy 49 yo with some mild stomach discomfort. I noticed the onset of tinnitus earlier this year and I had Covid at the end of June. My first ‘flare-up’ with these symptoms was in August and I was eating gluten like normal. I had another flare-up in September and then got an upper endo at the end of September that showed possible celiac. My blood test came a week later. While I didn’t stop eating gluten before I had the blood test, I had cut back on food and gluten both. I had a flare-up with this symptoms after one week of gluten free but wasn’t being crazy careful. Then I had another flare-up this week. I think it might have been caused by Trader Joe’s baked tofu which I didn’t realize had wheat. But I don’t know if these flare-ups are caused by gluten or if there’s something else going on. I am food journaling and tracking all symptoms. I have lost 7 pounds in the last 10 days. 
    • trents
      Welcome to the forum, @Hmart! There are other medical conditions besides celiac disease that can cause villous atrophy as well as some medications and for some people, the dairy protein casein. So, your question is a valid one. Especially in view of the fact that your antibody testing was negative, though there are also some seronegative celiacs. So, do you get reactions every time you consume gluten? If you were to purposely consume a slice of bread would you be certain to develop the symptoms you describe?
×
×
  • 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.