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

Could Use Your Opinions


ali11

Recommended Posts

ali11 Newbie

(I am a 20 yr old female) For more than 5 months now, I have been nauseous most every morning. I have to force myself to eat something, and usually the only thing I can tolerate and get down is something really sweet, like a dessert, which I know is not healthy but it's all I can handle. Lately, even just looking at food or thinking about what to eat in the morning makes me gag. By lunch time, the nausea is gone, but I have no appetite. I'll force myself to eat little meals so again, I'm eating something. Then by dinner time, things are normal and I'm very hungry. Not every time, but often when I eat out at restaurants I have diarrhea after. And my stools have been orange in color for about 5 months too. I also have suffered from fatigue for over 2 years. Lately I have been getting headaches a lot and occasionally will have numbness in my feet and toes, as well as pins and needles in my hands and fingers. Finally, I have had bad knee problems for almost a year now, and they are not healing near as fast as they should. My muscles are also really weak in my legs too. I'm wondering if I do have celiac disease, if it could be prolonging my recovery from the knee pain and also causing the rest of these symptoms. For anyone who has personal experience, I would really appreciate your input. Thank you.


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



Celiac.com Sponsor (A8-M):



wschmucks Contributor

It sure sounds like you have Celiac. Get to a good GI pronto and demand a Celiac panel blood test. The pins and needles is a big tip off, I had the same thing too-- my finger or foot would get totally numb for a few hrs (soo wierd!). Take it really seriously though, you need to get tested. Also an idea for breakfast-- do you think maybe you could do a protein shake? or some sweet flavored yogurt? Chocolate covered almonds? Try to get snack throughout the day if you cant eat. I had the same problem.

mommida Enthusiast

I recently had my gallbladder taken out after having the worst nausia of my life. That is after 5+ years gluten free. Hashimoto's for 15 years. Recent diagnoses of Pernicious anemia too. The pins and needles pain is most likely from a vitamin B12 deficiency. Get to the doctor pronto and try and get this figured out. You should get a refferal to a gastro.

Start putting together a timeline of symptoms and a food journal. That could help the doctor realize how serious your case is and how you need care.

:)

ali11 Newbie

Thank you so much for the replies, sorry it took me so long to respond. I have been trying to be more aware of symptoms after eating, and I've noticed that whenever I eat bread, for instance, I have bad stomach pain after. The nausea in the mornings has also been getting worse, the last week or so I am nauseous and gagging upon waking before I even think of eating breakfast. I'm going to try to get in to see my doctor as soon as possible.

Mskedi Newbie

Hopefully you'll figure out what's going on soon.

I don't know how bad your nausea is, but when mine is annoying, but not quite debilitating, I can usually down a small fruit smoothie made with yogurt, soy milk, and frozen berries & fruits. I think the fact that it's not solid and it's cold helps it stay down. Several months ago when I had a particularly bad reaction to an accidental glutening, that's all I could eat for about a week. (I also got some chewable vitamins to suck on in an attempt to get SOME, albeit minimal, nutrition).

I don't know if that will work for you, but I thought I'd throw it out there.

Megs613 Newbie

I would get in to see a GI or at least demand a Celiac panel. I've had terrible nausea and sometimes mine would go on all day, worst in the morning though. I'd have occasional diarrhea too. My blood test panel was positive, scope was negative....enterolab showed gluten intolerance and that I carry one of the celiac genes and one of gluten sentivity genes.

I've been on gluten for 6 weeks, and most days it is better, but I still have bad days here in there and mornings are always the worst. Sucking on a peppermint really helps me too.

ali11 Newbie

Thanks for the advice. I finally went in to see my GP today, because I needed a referral from her first, and the first thing she said after I told her my symptoms was "it sounds like celiac disease". She said there's also a chance it could be the beginning stages of colitis as well. I made an appointment with a GI, but it isn't for a week and half. My doctor told me to try to avoid fatty foods and dairy, and she wants me to come in for a blood test on Monday. For the most part I should continue to eat how I have been, even if it causes pain, because if I don't it could skew the results of the test, right?


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

Thanks for the advice. I finally went in to see my GP today, because I needed a referral from her first, and the first thing she said after I told her my symptoms was "it sounds like celiac disease". She said there's also a chance it could be the beginning stages of colitis as well. I made an appointment with a GI, but it isn't for a week and half. My doctor told me to try to avoid fatty foods and dairy, and she wants me to come in for a blood test on Monday. For the most part I should continue to eat how I have been, even if it causes pain, because if I don't it could skew the results of the test, right?

Yes you do need to stay on the gluten until your blood and endo (if your having one)testing is finished. As soon as that is done go ahead and get on the a trial of the diet. You don't have to wait for the test results.

newgfcali Rookie

You might try chewing on a little ginger in the morning if you can. It might help to soothe your stomach.

kareng Grand Master

I hurt my knee a year ago skiing. Not bad enough to be treated but annoying. Wouldn't completely go away. After being gluten-free for 2 weeks, it really got better. Still hurts a little when I do a lot but almost gone.

Also, the scent of lemon is good for nausea. Suck on a lemon drop or sniff some lemon juice.

ali11 Newbie

I hurt my knee a year ago skiing. Not bad enough to be treated but annoying. Wouldn't completely go away. After being gluten-free for 2 weeks, it really got better. Still hurts a little when I do a lot but almost gone.

Also, the scent of lemon is good for nausea. Suck on a lemon drop or sniff some lemon juice.

That's really encouraging to hear. I talked to my physical therapist yesterday about the possibility of me having celiac disease, and she said it could definitely be contributing to my pain. She seemed kind of relieved, honestly, because she's been treating me on and off since July 2009, and I'm still in lots of pain. So I don't know, I don't have the blood test results yet or anything, but it would be kind of amazing if that's why my knees haven't gotten better.

I just can't wait until I see the GI and hopefully find out an answer.

Pac Apprentice

That's really encouraging to hear. I talked to my physical therapist yesterday about the possibility of me having celiac disease, and she said it could definitely be contributing to my pain. She seemed kind of relieved, honestly, because she's been treating me on and off since July 2009, and I'm still in lots of pain. So I don't know, I don't have the blood test results yet or anything, but it would be kind of amazing if that's why my knees haven't gotten better.

I just can't wait until I see the GI and hopefully find out an answer.

Adding a bit of hope for your knee:

I hurted a tendon at the back of my tight about six years ago. It looked like it's never gonna heal. I tried everything, ointments, letting it rest with no exercise for months. Every time I got back to the gym, no matter how slow I started, the injury was back within a week. Last spring, after only a few weeks of gluten free diet, it healed. It didn't just get better, it was gone - no trace of pain, no movement restriction, as if nothing was ever wrong with my leg. :)

Black Sheep Apprentice

I also have found that ginger is very good for nausea. Ali, if you don't like to eat fresh ginger, you can always slice some up and make a tea out of it, even add peppermint, which is also good for nausea. I can't stand peppermint, so I substitute spearmint leaves. Not sure if the spearmint helps or not, but it sure is tasty! :P Another good way to take ginger, if you don't like the tea, is in capsule form. It's also quicker and easier than making tea.

That's very encouraging, what I'm reading about knee problems vanishing after going g.f.! I have an old (minor)knee injury as well, from slipping in a spilled drink at a grocery store and falling smack on my kneecap. It flares up if I climb more than a few stairs, so I'm hoping being g.f. will help this annoying problem.

Keep us posted on how you're doing, Ali. This is a great place to come for empathy and understanding, as well as advice!

ali11 Newbie

I saw the GI's PA today (they asked if I was ok with it and I said yes). He was really nice and took the time to make sure he understood all my symptoms. The blood tests I had done came back normal, but with my allergies, asthma, and being prone to sinus infections, I guess there's a good chance of a false negative. So two weeks from today I'm having both an endoscopy and a colonoscopy done. Yikes. And in the meantime, I'm going to start going gluten-free. I really hope this helps. It's so great to hear these stories about knee and leg pain getting better too. I really hope that this can help my pain. It's been almost a year now that I've been going through it, and all of the doctors say that I shouldn't still be in pain, but none of them no what to do to help me. If being gluten-free can fix both my stomach and knee problems, it will be well worth the sacrifice.

ravenwoodglass Mentor

I saw the GI's PA today (they asked if I was ok with it and I said yes). He was really nice and took the time to make sure he understood all my symptoms. The blood tests I had done came back normal, but with my allergies, asthma, and being prone to sinus infections, I guess there's a good chance of a false negative. So two weeks from today I'm having both an endoscopy and a colonoscopy done. Yikes. And in the meantime, I'm going to start going gluten-free. I really hope this helps. It's so great to hear these stories about knee and leg pain getting better too. I really hope that this can help my pain. It's been almost a year now that I've been going through it, and all of the doctors say that I shouldn't still be in pain, but none of them no what to do to help me. If being gluten-free can fix both my stomach and knee problems, it will be well worth the sacrifice.

Do not go gluten free until after the endo is done. You need to be actively eating gluten for the endo to have any chance of being accurate. Wait until the endo is done and then go gluten free that day.

ali11 Newbie

Do not go gluten free until after the endo is done. You need to be actively eating gluten for the endo to have any chance of being accurate. Wait until the endo is done and then go gluten free that day.

Yeah, I realized that was probably not a good idea. What if I tried going gluten-free for 3 days to see how it goes, and then start eating gluten again until the procedures. That way I would be off for 3 days and back on for 10 days. Would that be ok?

ravenwoodglass Mentor

Yeah, I realized that was probably not a good idea. What if I tried going gluten-free for 3 days to see how it goes, and then start eating gluten again until the procedures. That way I would be off for 3 days and back on for 10 days. Would that be ok?

I would just stay with the gluten. It is not a long time to go and you can use the time to 'study' up and prepare the house, go through your toiletries etc. There is a chance if you eliminate it even for just a couple days that your reaction when you add it back will be worse than it is now. IMHO you should just hang in there.

sa1937 Community Regular

Ali, I would agree with ravenwoodglass. Stay on gluten until the bitter end. My endo/biopsy was on April 9 and I continued eating gluten through April 8 (unpleasant as it was and oh so tempting to cut it off a bit early). I have no idea what the biopsy will show, but yesterday (only 3 days gluten free), I felt amazingly well. That has continued through today.

At this point in time for me, I don't give a squat what the biopsy shows. I only know I was desperate to feel better and actually had very low expectations for feeling so much better so soon. I was hoping I'd feel better in two to three weeks. Crossing my fingers that it stays that way. I know this is a strange disease and everyone reacts so differently.

Wishing you well!!! biggrin.gif

  • 2 weeks later...
ali11 Newbie

Ok, I had my endoscopy/colonoscopy yesterday. I took your advice and kept eating gluten all the way through. The doctor who did the procedures has never seen me, but he said they took a lot of biopsies. I have to wait until May 3rd to follow up with my doctor though (who has also never seen me, just his PA) and get the results. The nurse said they found some gastritis and that my colon was spasming, which is probably why I remember being in a lot of pain at one point during the colonoscopy, but that's all she saw on the report. I told her I was just going to start going gluten-free now, and she said that's a good idea. When she was putting the IV in before the procedures, the tourniquet turned my arm really red and she asked if I was being tested for celiac disease, because I "fit the bill". So I guess I just have to wait the 9 days to see what the doctor says, but at the very least I think I must be gluten intolerant if I have bad stomach pains after eating gluten and no stomach pains when I don't.

skates79 Newbie

Ok, I had my endoscopy/colonoscopy yesterday. I took your advice and kept eating gluten all the way through. The doctor who did the procedures has never seen me, but he said they took a lot of biopsies. I have to wait until May 3rd to follow up with my doctor though (who has also never seen me, just his PA) and get the results. The nurse said they found some gastritis and that my colon was spasming, which is probably why I remember being in a lot of pain at one point during the colonoscopy, but that's all she saw on the report. I told her I was just going to start going gluten-free now, and she said that's a good idea. When she was putting the IV in before the procedures, the tourniquet turned my arm really red and she asked if I was being tested for celiac disease, because I "fit the bill". So I guess I just have to wait the 9 days to see what the doctor says, but at the very least I think I must be gluten intolerant if I have bad stomach pains after eating gluten and no stomach pains when I don't.

ali11 - i'm so glad you posted! your symptoms are remarkably similar to mine. i've been sick on and off for years - am 30 now, had my first colonoscopy at 20 with no findings. since september 2009, i've been nauseous everyday, i lost 16lbs., i'm extremely fatigued, and also have been dealing with horrible wrist and arm pain that was diagnosed as tendinitis. your post and everyone's helpful feedback made me go back to my primary and demand further celiac testing, even though my results came back negative. thank you so much!

ali11 Newbie

ali11 - i'm so glad you posted! your symptoms are remarkably similar to mine. i've been sick on and off for years - am 30 now, had my first colonoscopy at 20 with no findings. since september 2009, i've been nauseous everyday, i lost 16lbs., i'm extremely fatigued, and also have been dealing with horrible wrist and arm pain that was diagnosed as tendinitis. your post and everyone's helpful feedback made me go back to my primary and demand further celiac testing, even though my results came back negative. thank you so much!

I'm glad I could help :) Even if you're celiac tests came back negative, you still might be gluten intolerant. That's what I figure for myself, so I started going off gluten while I'm waiting for the biopsy results and I'm already noticing some improvements. I really hope you start feeling better soon!

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

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

      Patiently Waiting to See Results

    2. - trents replied to Leeloff's topic in Gluten-Free Foods, Products, Shopping & Medications
      75

      How Come Gluten Didnt Bother Me In Italy

    3. - Gigi2025 replied to Leeloff's topic in Gluten-Free Foods, Products, Shopping & Medications
      75

      How Come Gluten Didnt Bother Me In Italy

    4. - Rejoicephd replied to JulieRe's topic in Related Issues & Disorders
      7

      Oral thrush question

    5. - catsrlife posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      Patiently Waiting to See Results


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,897
    • Most Online (within 30 mins)
      7,748

    Sgp
    Newest Member
    Sgp
    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

    • trents
      Welcome to the forum, @catsrlife! Celiac disease can be diagnosed without committing to a full-blown "gluten challenge" if you get a skin biopsy done during an active outbreak of dermatitis herpetiformis, assuming that is what is causing the rash. There is no other known cause for dermatitis herpetiformis so it is definitive for celiac disease. You would need to find a dermatologist who is familiar with doing the biopsy correctly, however. The samples need to be taken next to the pustules, not on them . . . a mistake many dermatologists make when biopsying for dermatitis herpetiformis. 
    • trents
      You state in an earlier post that you don't have celiac disease. Here in this post you state you will "be doing another test". What will this test be looking for? What kind of celiac disease testing have you had done? If you have used a Entero Labs it sounds like you have had stool testing done for celiac disease which is not widely accepted as a valid celiac disease diagnostic testing method. Have you had blood antibody testing for celiac disease done and do you realize that for antibody testing to be valid you must have been eating generous amounts of gluten for a period of weeks/months? 
    • Gigi2025
      No, I've not been diagnosed as celiac.  Despite Entero Labs being relocated to Switzerland/Greece, I'll be doing another test. After eating wheat products in Greece for 4 weeks, there wasn't any reaction.  However, avoiding it here in the states.   Thanks everyone for your responses.  
    • Rejoicephd
      Thank you @JulieRe so much for sharing this extra information. I'm so glad to hear you're feeling better and I hope it keeps moving in that direction. I feel I'm having so many lightbulb moments on this forum just interacting with others who have this condition. I also was diagnosed with gastric reflux maybe about 10 years ago. I was prescribed ranitidine for it several years back, which was working to reduce my gastric reflux symptoms but then the FDA took ranitidine off the shelves so I stopped taking it. I had a lot of ups and downs healthwise in and around that time (I suddenly gained 20 pounds, blood pressure went up, depression got worse, and I was diagnosed with OSA). At the time I attributed my change in symptoms to me taking on a new stressful job and didn't think much else about it. They did give me a replacement gastric reflux drug since ranitidine was off the shelves, but when I went on the CPAP for my OSA, the CPAP seemed to correct the gastric reflux problem so I haven't been on any gastric reflux drug treatment for years although I still do have to use a CPAP for my OSA. Anyway that's a long story but just to say… I always feel like I've had a sensitive stomach and had migraines my whole life (which I'm now attributing to having celiac and not knowing it) but I feel my health took a turn for much worse around 2019-2020 (and this decline started before I caught covid for the first time). So I am now wondering based on what you said, if that ranitidine i took could have contributed to the yeast overgrowth, and that the problem has just been worsening ever since. I have distinctly felt that I am dealing with something more than just stress and battling a more fundamental disease process here. I've basically been in and out of different doctor specialties for the past 5 years trying to figure out what's wrong with me. Finally being diagnosed with celiac one year ago, I thought I finally had THE answer but now as I'm still sick, I think it's one of a few answers and that maybe yeast overgrowth is another answer. For me as well, my vitamin deficiencies have persisted even after I went gluten-free (and my TTG antibody levels came down to measurably below the detectable limit on my last blood test). So this issue of not absorbing vitamins well is also something our cases have in common. I'm now working with a nutritionist and taking lots of vitamins and supplements to try and remedy that issue. I hope that you continue to see improvements in working with your naturopath on this. Keep us posted!
    • catsrlife
      Back at the end of July I got this rash on both of my forearms. It started on my right and continued to the left. It was on the top and side. The rash has bumps that would pop with clear liquid if scratched. They would almost crystalize and scab up. They reminded me of chicken pox. They would scab for weeks and not heal much at all except for the blood clotting. If the scab was scratched off, it would bleed and bleed until it scabbed up again. The skin has lost its pigment where the scabs are. I figured it was probably either the plant I had trimmed around the 15th or some reaction to the magnesium complex I was taking or an allergic reaction to the asthma meds I was on. I stopped the asthma meds and the magnesium. The rash seemed to get better but when I took the asthma meds it flared up again so I went to the urgent care as my doctor was unavailable. The UC doctor said it probably wasn't the meds and asked about my diet. I said I was strict keto. I usually am, but there is a story around this. I feel amazing on keto. When I eat sugar, wheat, and starchy veggies I feel horrible. Blood sugar goes up, IBS type symptoms, brain fog, etc. But I have a horrible addiction to carbs so I blow it sometimes and after Mom died in 2023, I fell off the wagon. No rashes, just weight gain. I finally went back on keto and then around that time had a piece of pizza (or so, it's hard to stop the carb rush.) So I was strict keto, off and on. She ignored that and prescribed some allergy meds. It didn't go away.  What was happening by then was that the rash was now on my upper elbows, both of them, on the back of my arms. It starts with a very itchy bump, spreads around it and sometimes just burns like crazy and other times just itches. Then it started on the sides of my knees on the oustide, a little bit down the sides of the calves. It's not as bad there as it is on my arms even though it comes and goes (and so does wheat in my diet.) I then got three tiny blisters on each hand, 3 on the insdie of my index finger on the right hand and 3 on the inside of middle finger of my left hand. There is still a little scab there even though it was two weeks ago. No more have appeared on the fingers. But right now the back of the arms above my elbows are starting to itch. At some point I started to think mites from the possum that was sneaking into our house but it's been 3 months and they would be dead already. It wouldn't be from humans because I don't go near any humans although I did take an Uber to the doctor and the bus back. Plus, it's symmetrical. It starts on one side and is almost identical on the other.  I did my DNA with Ancestry and MyHeritage. I don't have the HLA-DQ2 or HLA-DQ8. I do have HLA-DQ2.2. I took the blood test but it was negative. Then again, I don't eat wheat every day. I rarely eat it except for lately when I've been preparing for the blood test if I have to take it again. I don't like to. It makes my joints hurt, gives me brain fog, stomach problems, I sleep in the middle of the day, etc. I have a doctor appointment tomorrow. I hope that she will be more serious about this than the UC doctor was.  So I have no idea. With my luck they'll magically disappear before the doctor appointment. That's what happens with everything.
×
×
  • 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.