Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Still Not Better


Worriedwife

Recommended Posts

Worriedwife Apprentice

My husband was diagnosed about 2 1/2 months ago. We have cleaned out the house, and we're pretty sure we've gotten rid of everything that had gluten in it. We also replaced all of our plastic utensils, strainers and bought a new toaster. I have stopped eating gluten as well, so that there is no chance of cross-contamination. Lastly, we have also gone through all of our soaps, shampoos and personal items for possible sources.

My concern is that my husband shows almost no signs of improvement. His symptoms are general joint and muscle pain, that had previously been diagnosed as fibromialgia. I'm just wondering how long it normally takes for these types of symptoms to go away.

Don't get me wrong, I'm happy that he has been diagnosed, and I do a lot of research on this for him, but I'm concerned. I would like to see him not be in pain anymore. Any ideas on how long we might have to wait? Thanks!


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



Celiac.com Sponsor (A8-M):



CarlaB Enthusiast

Has he seen any improvement at all? Which symptoms?

How was he diagnosed?

It varies from person to person how long it takes to get better. If some symptoms improve and others don't, he could have a second condition.

AndreaB Contributor

I second Carla's response.

Worriedwife Apprentice

It doesn't seem like any of his muscle or joint pain has eased up at all. He doesn't seem to have any other symptoms.

Our regular doctor (who's pretty good) ordered the blood tests for him. I'm not sure why it occurred to him to do it. All three tests came back positive. We have an appointment with the GI doctor tomorrow. I'm sure he's going to want to do further tests, and I'm going to try to talk him into an endoscopy rather than a colonoscopy.

I guess we'll just have to wait and see.

AndreaB Contributor

Keep us posted if you will.

The muscle/joint pain can be from something other than gluten so if it doesn't get better then further testing from an alernative/integrative doctor would be something I'd suggest.

CarlaB Enthusiast

After 2 1/2 months, an endoscopy has a high probability of coming out negative even if he has celiac. You might have to just go on the blood work for the celiac diagnosis.

I'd definately tell the GI that you've not seen any improvement.

Worriedwife Apprentice

So, we went to the GI. We were very disappointed. First of all, the office staff seemed stupid and rude. The, the doctor wasn't very interested in helping us. He said that the blood work wasn't really conclusive. The only way to really check, the "gold standard" was to have a biopsy done. When my husband said he wasn't very happy about having to "gluten" himself for the test, the doctor said it wasn't a problem at all. Since he had been eating gluten for so many years, a few more weeks certainly wasn't going to help. Then the doctor told us that since he wasn't showing any digestive symptoms, he could probably going on eating gluten for the rest of his life and not really have any significant problems.

Needless to say, we were less than impressed with this doctor. Unfortunately, this is the only GI group in town. At this point, we've decided to continue going gluten free, and see what happens. If we want to get another opinion, we're going to have to go up to Phoenix. If anyone know of a good doctor in that area, I would appreciate some reccommendations.

Maybe out primary care doctor can find out if something else is causing the joint and muscle pain. If he was smart enough to test for celiac, maybe he as some other ideas.

Thanks for the words of support, this site was a great find!


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



Celiac.com Sponsor (A8-M):



Karen B. Explorer

Have you checked for a local Celiac group? They might know a more supportive GI doc in a nearby town?

https://www.celiac.com/st_main.html?p_catid...-41107060117.a6

Two things come to my mind...

1. I take turmeric and fish oil every day for achy joints and it's made a big difference for me. I've been able to stop taking aspirin since I started this.

2. I had gradually weaned myself off of most sugar and all high fructose corn syrup, not because I had to but because it seemed like it was healthier. Recently, my co-workers got sneaky for my birthday and bought me a beautiful gluten-free birthday cake (lavendar and white with all the trimming) and I had a big slab of it. WOW! I felt like I was in sugar shock the rest of the week and all of my joints started aching and my muscles felt like I'd been beaten or something. I had no idea that sugar would have that effect on me. It's been 2 weeks and I finally feel like I might be getting back to normal.

I don't know how much sugar your hubby eats, but some of the gluten-free goods are loaded with it. Just a thought.

Lillian Newbie
So, we went to the GI. We were very disappointed. First of all, the office staff seemed stupid and rude. The, the doctor wasn't very interested in helping us. He said that the blood work wasn't really conclusive. The only way to really check, the "gold standard" was to have a biopsy done. When my husband said he wasn't very happy about having to "gluten" himself for the test, the doctor said it wasn't a problem at all. Since he had been eating gluten for so many years, a few more weeks certainly wasn't going to help. Then the doctor told us that since he wasn't showing any digestive symptoms, he could probably going on eating gluten for the rest of his life and not really have any significant problems.

Needless to say, we were less than impressed with this doctor. Unfortunately, this is the only GI group in town. At this point, we've decided to continue going gluten free, and see what happens. If we want to get another opinion, we're going to have to go up to Phoenix. If anyone know of a good doctor in that area, I would appreciate some reccommendations.

Maybe out primary care doctor can find out if something else is causing the joint and muscle pain. If he was smart enough to test for celiac, maybe he as some other ideas.

Thanks for the words of support, this site was a great find!

Hi worriedwife, You sound like you have true concerns about your husband's comfort and that's great to know. My husband is extremely suppoprtive also and often eats gluten free food with me. Don't get discouraged. I was diagnosed about 2 years and it's still and will always be a daily battle/getting informed/becoming my own advocate sort of lifestyle. Thank G-d there are things we can do. One of them would be to go to a 'Vitamin Shoppe' vitamin place where all their own brand stuff is gluten free- my nutrionist from Rush Hospital in Chicago told me that. Perhaps he can get on some calcium/magnesium daily vitamins, glucosamine-chonondrite, fish oils and daily vitamins. Don't forget that while being on glutens and our villi being flat we've lost a lot of nutrients- so now that he is gluten free as much as possible, he'll need to begin to replenish all those nutrients. I found that advil, tylenol and all those gave me gastritis-redness in the stomach lining as shown on my last biopsy in April- which showed I was 'cured' but of course this is an autoimmune condition that I'll have the rest of my life. So again, don't get discouraged- talk to people in the 'Vitamin Shoppe' and go from there. I know- boy do I know- food is so much more expensive now, and there is no pill to cure this. So my new motto is-pay now or pay later. Invest in those vitamins and he'll feel a big difference. Hope this helps for now. Lillian

Worriedwife Apprentice

He does take a daily vitamin and fish oil each day. He also takes extra iron, as the doctor says he's a bit anemic. He tried the glucosamin/chondroitin, but it did not agree with him at all. I think it was mostly the chondroitin, but he's not really interested in trying again.

He's not much of a sugar eater. He's always been very concious of what he eats, and has been doing the cooking for us for the last 20 years. We don't eat red meat or poultry, only fish. Of course, lots of fruit and veggies with nuts thrown in for extra protien

I've not heard of using tumeric for joint pain before. I'm not sure that we have any in the house, especially as I don't do any of the cooking. Do you just use it in cooking, or take some other way?

happygirl Collaborator

worriedwife,

I am sorry that your husband is still having problems. I wish that there was an easy answer....but it could still be related to gluten, or it could be another issue, or both.

Just a note, to confirm what you already know. The nutritionist that works at University of Maryland's Celiac Center (with a leading Celiac researcher, Dr. Alessio Fasano) recently spoke at a support group meeting and said that even eating gluten free for one week can begin to alter the results of a biopsy.

I definitely would find a support group to contact, and find someone who is willing to find the cause of your husbands pain. It would be worth having the Celiac blood panel re-run, to see if he is still reacting to gluten (i.e., if his numbers haven't come down, then it indicates it is at least part of the problem)

Best of luck.

natalie Apprentice

Hi,

My daughter was diagnosed 1 1/2 years ago. We were just at a pediatrician appointment last week. She still seems " slow" compared to her brother, she just can't keep up. I asked the doc about this. He said it can take up to 3 years to heal muscle wasting completely and get the vitamins back into her body. I was shocked.

Does your hubby seem a little better? You may want to see your doc for any additional testing.

Good Luck

Natalie

blueeyedmanda Community Regular

It does vary person to person. I know my stomach symptoms went away fairly quickly but my other symptoms lingered a bit longer.

WorkNsurf Rookie

my stomach problems persisted for many months after not eating gluten. vegetable enzymes before meals and some Primadophilus definatly helped the system to break down food. papaya is a good fruit if available, it is full of natural enzymes.

Karen B. Explorer
----snip----

I've not heard of using tumeric for joint pain before. I'm not sure that we have any in the house, especially as I don't do any of the cooking. Do you just use it in cooking, or take some other way?

I get the turmeric in capsules at Whole Foods. I do eat curries and use mustard, but it's not enough to make a difference and it's not everyday. The capsules make it much easier. Also, my Mom found that Capsaicin (sp?) helped her joint pain.

Sometimes one thing will help and not another so it's good to have several things to try. I wanted to get off aspirin for my stomach's sake and everything else has side effects too. I've not seen any side effects from the turmeric but it takes a few weeks to kick in.

  • 3 weeks later...
crosstalk Newbie

Your husband may have another food intolerance(s). My symptoms show up about four hours after I eat something I am intolerant to. I honestly think that the wheat intolerance can bring about other intolerances esp. if you have been diagnosed after eating wheat for a lifetime. I suspect that this is the norm rather than the exception.

  • 3 weeks later...
JNBunnie1 Community Regular

I would honestly be a little suspicious about eating all that fish. If he has Celiac disease (and yes, if the blood tests say he does, then he does, there are no false positives) then his immune system is not up to par and he may be very overloaded with mercury. Fish just isn't safe on a regular basis anymore, for a HEALTHY person, I'd say max once a week. I don't know why you don't eat much meat but I would consider rethinking it, and adding back some organic meat. And I would get him a heavy metal test, STAT. His body is trying to heal, he needs protein and vitamins.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,197
    • Most Online (within 30 mins)
      7,748

    Seeeye
    Newest Member
    Seeeye
    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

    • Bev in Milw
      Scott is correct….Thank you for catching that!      Direct link for info  of fillers.    http://www.glutenfreedrugs.com/Excipients.htm Link is on 2nd page  of www.glutenfreedrugs.com   Site was started by a pharmacist (or 2) maybe 15-20 yrs ago with LAST updated in  2017.  This makes it’s Drug List so old that it’s no longer relevant. Companies & contacts, along with suppliers &  sources would need to be referenced, same amount effort  as starting with current data on DailyMed      That being said, Excipient List is still be relevant since major changes to product labeling occurred prior ’17.           List is the dictionary that sources the ‘foreign-to-us’ terms used on pharmaceutical labels, terms we need to rule out gluten.    Note on DailyMed INFO— When you look for a specific drug on DailyMed, notice that nearly all of companies (brands/labels) are flagged as a ‘Repackager’… This would seem to suggest the actual ‘pills’ are being mass produced by a limited number of wholesaler suppliers (esp for older meds out of  patent protection.).      If so, multiple repackager-get  bulk shipments  from same supplier will all  be selling identical meds —same formula/fillers. Others repackager-could be switching suppliers  frequently based on cost, or runs both gluten-free & non- items on same lines.  No way to know  without contacting company.     While some I know have  searched pharmacies chasing a specific brand, long-term  solution is to find (or teach) pharmacy staff who’s willing help.    When I got 1st Rx ~8 years ago, I went to Walgreens & said I needed gluten-free.  Walked  out when pharmacist said  ‘How am I supposed  to know…’  (ar least he as honest… ). Walmart pharmacists down the block were ‘No problem!’—Once, they wouldn’t release my Rx, still waiting on gluten-free status from a new supplier. Re: Timeliness of DailyMed info?   A serendipitous conversation with cousin in Mi was unexpectedly reassuring.  She works in office of Perrigo, major products of OTC meds (was 1st to add gluten-free labels).  I TOTALLY lucked out when I asked about her job: “TODAY I trained a new full-time employee to make entries to Daily Med.’  Task had grown to hours a day, time she needed for tasks that couldn’t be delegated….We can only hope majorities of companies are as  conscientious!   For the Newbies…. SOLE  purpose of  fillers (possible gluten) in meds is to  hold the active ingredients together in a doseable form.  Drugs  given by injection or as IV are always gluten-free!  (Sometimes drs can do antibiotics w/ one-time injection rather than 7-10 days of  pills .) Liquid meds (typically for kids)—still read labels, but  could be an a simpler option for some products…                 
    • Ginger38
      So I recently had allergy testing for IGE antibodies in response to foods. My test results came back positive to corn, white potatoes, egg whites. Tomatoes, almonds and peanuts to name a few.  I have had obvious reactions to a few of these - particularly tomatoes and corn- both GI issues. I don’t really understand all this allergy versus celiac stuff. If the food allergies are mild do I have to avoid these foods entirely? I don’t know what I will eat if I can’t  have corn based gluten free products 
    • Kris2093u4
      Geography makes a difference.  I'm in the West and Trader Joe's gluten-free bread tastes great and is a better price than most gluten-free breads sold elsewhere in my area.  
    • JForman
      We have four children (7-14 yo), and our 7 year old was diagnosed with NCGS (though all Celiac labs were positive, her scope at 4 years old was negative so docs in the US won't call it celiac). We have started her on a Gluten Free diet after 3 years of major digestive issues and ruling out just about everything under the sun. Our home and kitchen and myself are all gluten-free. But I have not asked my husband/her dad or her other siblings to go completely gluten-free with us. They are at home, but not out of the home. This has led to situations when we are eating out where she has to consistently see others eating things she can't have and she has begun to say "Well, I can't have <fill in the blank>...stupid gluten."  How have you supported your gluten-free kiddos in the mental health space of this journey, especially young ones like her. I know it's hard for me as an adult sometimes to miss out, so I can't imagine being 7 and dealing with it! Any tips or ideas to help with this? 
    • Fayeb23
      I’ve recently had bloods test due to fatigue. Iron was found to be low Serum ferritin level 4 ug/L so doctor sent for Coeliac test. Results have come back TTG ABS NUMERICAL > 250.0 U/mL is this a high reading? Am not waiting a Gastroenterology referral but this could take 10 weeks! This is all total new to me, didn’t think for a second I would have coeliac disease. Been advised not to change diet until seen by specialist 
×
×
  • Create New...