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

Diagnosing Celiac Disease - Questions


garlit

Recommended Posts

garlit Newbie

I am starting to wonder whether I may have celiac disease. I have had lower back pain, neck and knee joint painf or years (I am 40 and otherwise healthy). 2 years ago I suddenly became very ill after a bout of what I believe was food poisoning. Doctors test showed nothing but symptoms are as follows. Sacroilitis, lower back pain, neck pain, stomach tenderness but only when palpated, thyroid issues, low energy, rashes and a few other things. After researching on the web whether I figured that maybe I am gluten intolerant. I suggested this to my doctor who said she didn't think so.

I have been on a gluten free diet for 3 weeks now and have seen a little improvement.

My question is does this sound like gluten intolerance because I don't have upset stomach, cramping etc.?

If so, how can I get tested for it?

Also, when you go gluten-free, how long does it take for results?

Thanks

Jane


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



Celiac.com Sponsor (A8-M):



Nancym Enthusiast

Do you feel stiff and sore while in bed at night? Does it get better when you get up and walk around or after you get up in the morning?

It can take people quite awhile to feel better after starting gluten free. Are you sure you're not getting hidden gluten? You might want to try an elimination diet and see if perhaps there is something else bugging you. For me, dairy, and all grains seem to be a problem. I try especially hard to avoid gluten containing ones, next would be corn. I am still eating rice bran, but not whole rice.

I suggested this to my doctor who said she didn't think so

Doctors are about 10 years out-of-date on celiac disease. If they didn't perform a blood test and endosocopy on you, then they can't rule it out.

garlit Newbie

YES! my si joints and hips start hurting often when I get into bed and then during the night. Doesn't always keep me awake but for sure when I wake up in the morning, I feel very stiff and almost fragile (like one wrong move will trigger horrible pain).

I've been on an elimination diet for 3 weeks and was actually starting to feel better when I suddenly took a turn for the worse again end of last week.

Do you know if there is gluten in flax seeds as I take them ground up daily?

Thanks for your reply.

It's nice to know I may not be out of my mind.

PeggyV Apprentice
YES! my si joints and hips start hurting often when I get into bed and then during the night. Doesn't always keep me awake but for sure when I wake up in the morning, I feel very stiff and almost fragile (like one wrong move will trigger horrible pain).

I've been on an elimination diet for 3 weeks and was actually starting to feel better when I suddenly took a turn for the worse again end of last week.

Do you know if there is gluten in flax seeds as I take them ground up daily?

Thanks for your reply.

It's nice to know I may not be out of my mind.

I believe flax seed is fine. I use it all of the time.

Good Luck

Lisa Mentor

Jane:

I had been diagnosed with IBS for many, many years and in the last three years prior to being diagnosed with Celiac, I too has chronic back pain. On three occasions, I was in bed for a week when my back "went out". I have not had a back issue since gluten free.

You have options here. You can try the diet and be totally gluten free and see what you dietary response is. This may take up to a months time to see improvements. For me I saw gradual recovery over a six month period. For all my neurogical symptoms to wain, it took almost two years and still not 100%, but close.

Secondly, you can return to a gluten diet for one months time and request some blood work done. But it is not always accurate. Your best indicator is dietary response. But, it requires you to be totally gluten free.

Hope this was helpful.

Nancym Enthusiast
YES! my si joints and hips start hurting often when I get into bed and then during the night. Doesn't always keep me awake but for sure when I wake up in the morning, I feel very stiff and almost fragile (like one wrong move will trigger horrible pain).

I've been on an elimination diet for 3 weeks and was actually starting to feel better when I suddenly took a turn for the worse again end of last week.

Do you know if there is gluten in flax seeds as I take them ground up daily?

Thanks for your reply.

It's nice to know I may not be out of my mind.

You might have ankylosing spondylitis. I have that. It is an autoimmune disease that sometimes leads to fusing of joints in the spine/hips (but often not). The classic symptoms are pain in the SI joint, stiffness in bed that gets better when you move around, and pain in many tendons and joints. I had a lot of pain in the ribs... oddly enough. It comes in flares.

This is something you should see a rhuematologist about right away, you want to get identified early because it can lead to serious issues down the road. It can affect the lungs, heart, eyes and also the intestines. Are you male or female? Women generally have a MUCH easier time with the disease... but not always.

There's a great support web site at Open Original Shared Link

Since I've gone gluten/dairy free and gotten on some meds for the AS my own symptoms are VASTLY better. The kickas site has a lot of people doing a No-Starch diet that seems to help many of them. I eat very little starch too, I find I just seem healthier without too much starch or sugar in my diet.

Anyway, get thee to a good rhuematologist. You might want to contact the Ankylosing Spondylitis association to get the name of one or see if the kickas.org people can refer you to one in your area. It isn't always an easy disease to diagnose, most people with AS have a gene called HLA B27 but sometimes they don't.

Oh... don't forget to mention that you got the arthritis symptoms after getting food poisoning. That could be something like Ritter's Syndrome, which is another form of spondylitis.

garlit Newbie

Hi there,

I had a test for AS (the HLA B37 you mentioned) two years ago and it was negative. They also did an mri on my si joints which came back negative. So as far as my rheumatologist is concerned, I don't have it. However, I have done a lot of reading about it as I certainly exhibit a lot of the symptoms. My problem is that if you have a doctor that doesn't agree with you or is willing to go down a different path, then you're out of luck. I'm in the process of trying to get another GP but it is very hard here in Ontario as so few doctors are accepting new patients. Thanks for your input though - I think it's certainly worth pursuing.

Jane


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



Celiac.com Sponsor (A8-M):



Nancym Enthusiast

There are a bunch of spondyarthropathies (ones that cause fusing). You really need a better rhuemy. There's at least one sort that is connected to food poisoning.

You can definintely have a lot of the pain and stuff and not have fusing. And of course you can be B27 negative and have it. Your doctor isn't staying current on diagnosis. My rhuemy (I lucked out with him, he's excellent) says women usually don't fuse and their symptoms exhibit more like fibromyalgia. I notice my tendons tend to have problems, I've had TMJ, a sore tendon in my forearm and problems with one in my foot.

Seriously, you need to find a support group online and find a good doctor... if you can, I know Canadians have a hard time with it.

Ack! It's Reiter's syndrome, not ritter's.

Here's an online reference: Open Original Shared Link

Another symptom I haven't had in ages: Muscle spasms. God, I'm getting so I am forgetting how miserable I felt. This is good!

My advice to you would be to cut out gluten and dairy products if you can. Dr. Fine from Enterolab has ankylosing spondylitis and recommends quite a restricted diet, one I would have a very hard time following. But I suppose it depends on how miserable I was.

If you're willing to go outside your medical system I think you can get tested by Enterolab for gluten/casein (dairy) sensitivities. The url is Open Original Shared Link

garlit Newbie

Thanks, I just read the link you posted and it's an interesting read - yes, I need to find another rheumatologist. Actually, my doctor just phoned today with test results from knee xrays I had done on Monday. Both knees show arthritis on both sides, plus under the kneecap as well and minimal joint space and osteophytes. From reading online, it seems that arthritis can also be caused by food allergies...I shouldn't really have knee problems - I'm 40, average weight and in good shape. Oh well...I'm going shopping for some gluten free and dairy free foods!

Roger Slemmer Newbie

I have a friend, a young mother, Mary, who is nursing her baby. The baby has GI symptoms - frequent diarrhea and slow growth rate. The baby is only nursing - not any solid food. Mary has asked me if it is possible for gluten to affect her child through her milk. I didn't think so and that is what I told her. But say Mary is Celiac and passing antibodies to her baby? Mary is asymptomatic unless it is only causing her to have depression, anxiety or emotional - psychological symptoms. I have suggested she try getting the blood test. Has anyone heard of this being possible?

I would appreciate any input on this.

Roger Slemmer

Nancym Enthusiast

Rodger, you should start a new thread, probably in the Parenting section. Otherwise probably people won't see your question here.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,855
    • Most Online (within 30 mins)
      7,748

    Tara M
    Newest Member
    Tara M
    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
    • Jillian83
      Hi, I was recently diagnosed with Celiac and dermatitis herpetiformis after years of suffering without answers. I lost my mind. I lost my job. I lost so much time. I lost Me. Conventional doctors are opulent come near me and the one who did sat across the room, misdiagnosed me, pumped me full of steroids which collapsed my entire hip for 6 months. So without answers I began my holistic journey. Fast forward a couple of years and still struggling with a mysterious whole body itchy, crawling “skin hell”, perfect teeth now deteriorating, thick hair now thinning rapidly and no more than a day or 2 at most relief….An acquaintance opened up a functional medicine practice. Cash only, I found a way. Within a month tests clearly showing my off the charts gluten allergy/sensitivity as well as the depletion of vital nutrients due to leaky gut and intestinal damage. dermatitis herpetiformis was more than likely what I was experiencing with my skin. I was happy. I thought this is easy, eat healthy Whole Foods, follow the diet restrictions and I finally get to heal and feel confident and like myself again very soon! 😔 Supplements are very pricey but I got them and began my healing. Which leads to the other major issue: not working, stay at home Mom of young kids, entirely financially dependent on my man of 7 plus years. He’s never been supportive of anything I’ve ever done or been thru. He controls everything. I’m not given much money ever at a time and when he does leave money it’s only enough to possibly get gas. His excuse is that I’ll spend it on other things. So my “allowance” is inconsistent and has conditions. He withholds money from me as punishment for anything he wants. Since being diagnosed, he’s gained a new control tactic to use as punishment. He now is in control of when I get to eat. He asked for proof of my diagnosis and diet bc he said I made it up just to be able to eat expensive organic foods. Then after I sent him my file from my doctor he then said she wasn’t a real doctor. 😡. I go days upon days starving, sometimes breaking down and eating things I shouldn’t bc I’m so sick then I pay horribly while he gets annoyed and angry bc I’m not keeping up with all the duties I’m supposed to be doing. His abuse turns full on when I’m down and it’s in these desperate times when I need his support and care the most that I’m punished with silence, being starved, ignored, belittled. He will create more of a mess just bc I’m unable to get up and clean so that when I am better, I’m so overwhelmed with chores to catch up that the stress causes me to go right back into a flare from hell and the cycle repeats. I’m punished for being sick. I’m belittled for starving and asking for healthy clean water. I’m purposely left out of his life. He won’t even tell me he’s going to the grocery or to get dinner bc he doesn’t want me to ask him for anything. I have no one. I have nothing. Im not better. My supplements ran out and I desperately need Vitamin D3 and a methylated B complex at the very minimal just to function….he stares at me blankly…no, a slight smirk, no words. He’s happiest when im miserable and I am miserable.  this is so long and im condensing as much as I can but this situation is so complicated and disgusting. And it’s currently my life. The “IT” girl, the healthy, beautiful, perfect skin, perfect teeth, thick and curly locks for days, creative and talented IT girl….now I won’t even leave this house bc Im ashamed of what this has dont to my body, my skin. Im disgusted. The stress is keeping me from healing and I think he knows that and that’s why he continues to keep me in that state. He doesn’t want me confident or successful. He doesn’t want me healed and healthy bc then how would he put the blame of all his problems on me? This journey has been hell and I’ve been in Hell before. I’ve been killed by an ex, I’ve been raped, robbed, held hostage, abused beyond nightmares but the cruelty I’ve experienced from him bc of this disease is the coldest I’ve ever experienced. I’ve wanted to give up. Starving and in tears, desperate…I found a local food pantry in our small town so I reached out just saying I had Celiac and was on hard times. This woman is blessing me daily with prepared gluten free meals, donations, educational info, people who know this disease and how they manage life and the blessings just keep coming. But it’s overwhelming and I feel like I don’t deserve it at all. He just glared and I know he’s going to sabotage it somehow. I don’t even know what to do anymore. I’m so broken and just want peace and healing. 
    • cristiana
      @Colleen H   I am just curious,  when you were tested for coeliac disease, did the doctors find out if you had any deficiencies? Sometimes muscle pain can be caused by certain deficiencies, for example, magnesium, vitamin D, calcium, and potassium.   Might be worth looking into having some more tests.  Pins and needles can be neuropathy, again caused by deficiencies, such as iron and B12,  which can be reversed if these deficiencies are addressed. In the UK where I live we are usually only tested for iron, B12 and vitamin D deficiencies at diagnosis.   I was very iron anemic and supplementation made a big difference.  B12 was low normal, but in other countries the UK's low normal would be considered a deficiency.  My vitamin D was low normal, and I've been supplementing ever since (when I remember to take it!) My pins and needles definitely started to improve when my known deficiencies were addressed.  My nutritionist also gave me a broad spectrum supplement which really helped, because I suspect I wasn't just deficient in what I mention above but in many other vitamins and minerals.  But a word of warning, don't take iron unless blood tests reveal you actually need it, and if you are taking it your levels must be regularly monitored because too much can make you ill.  (And if you are currently taking iron, that might actually be making your stomach sore - it did mine, so my GP changed my iron supplementation to a gentler form, ferrous gluconate). Lastly, have you been trying to take anything to lessen the pain in your gut?  I get a sore stomach periodically, usually when I've had too much rich food, or when I have had to take an aspirin or certain antibiotics, or after glutening.  When this happens, I take for just a few days a small daily dose of OTC omeprazole.  I also follow a reflux or gastritis diet. There are lots online but the common denominators to these diets is you need to cut out caffeine, alcohol, rich, spicy, acidic food etc and eat small regularly spaced meals.   When I get a sore stomach, I also find it helpful to drink lots of water.  I also find hot water with a few slices of ginger very soothing to sip, or camomile tea.  A wedge pillow at night is good for reflux. Also,  best not to eat a meal 2-3 hours before going to bed. If the stomach pain is getting worse, though, it would be wise to see the doctor again. I hope some of this helps. Cristiana    
    • Me,Sue
      I was diagnosed with coeliac disease a couple of years ago [ish]. I love my food and a variety of food, so it's been hard, as it is with everyone. I try and ensure everything I eat doesn't contain gluten, but occasionally I think something must have got through that has gluten in. Mainly I know because I have to dash to the loo, but recently I have noticed that I feel nauseous after possibly being glutened. I think the thing that I have got better at is knowing what to do when I feel wiped out after a gluten 'episode'. I drink loads of water, and have just started drinking peppermint tea. I also have rehydration powders to drink. I don't feel like eating much, but eventually feel like I need to eat. Gluten free flapjacks, or gluten free cereal, or a small gluten free kids meal are my go to. I am retired, so luckily I can rest, sometimes even going to bed when nothing else works. So I feel that I am getting better at knowing how to try and get back on track. I am also trying to stick to a simpler menu and eat mostly at home so that I can be more confident about what I am eating. THANKS TO THOSE WHO REPLIED ABOUT THE NAUSEA .
    • Francis M
      Thanks. Since the back and forth and promises of review and general stalling went on for more than six months, the credit company will no longer investigate. They have a cutoff of maybe six months.
×
×
  • 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.