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

Joint Pain With Many Other Symptoms


tbritt

Recommended Posts

tbritt Rookie

Hi all. I posted here about two weeks ago.

I have been in EXTREME pain in my neck and shoulder for six months along with nausea, general ickiness, gas and tiredness. Strangely, I took antibiotics and I felt better for a time, but upon stopping the antibiotics, the pain returned. I did a second round of antibiotics and the pain returned again. I apparently had mononucleosis this year some time, too. (Which could have triggered this all.) Physical therapy didn't help. Months of being on anti-inflammatory drugs didn't help. Antibiotics seemed to help... but only while I was taking them. And I KNOW how bad antibiotics are for you, so I didn't want to be on them except they seemed to help.

I was desperate to find an answer why nothing was working for this pain.

I have always been sickly.

Age 7 - Anemic

Age 13 - Dizzy spells

Age 16 - Hypoglycemia

Age 17 - Eczema/Psoriasis/rashes/hives/etc

Age 18 - Ulcers/Reflux

Age 21 - Epilepsy

(You get the picture. Depression, etc.)

About four weeks ago, I had a dream about changing my diet. I started to read about food allergies and for some reason decided I would try going gluten free. That was three weeks ago.

It has been the only thing that has helped. I feel better than I have in six months. It no longer feels like something is attacking my neck and shoulder. The swelling has gone down. I am feeling much better. The pain is manageable, not all the way better, but enough that I am VERY excited. I can sleep again at night. I was even able to go for a hike last weekend! I don't have gas anymore. I would have never guess that was related.

After less than a week on the diet, I got a blood test screening for elevated IgA. It came back normal. Should I go off the gluten free for a while and get proper testing or just forget about getting a diagnosis and leave the gluten out of my diet?

The doctor (a new rheumatologist I am seeing) diagnosed me as "gluten intolerant" and he seems to think that getting rid of gluten isn't a bad thing. He suggested I might go back on it and get the other tests if I wanted, or I could save a lot of time and energy by just going gluten free for a while and seeing if I'm better.

He had a theory that the antibiotics killed all the bacteria in my large intestine (which caused less irritation there) which caused the antibodies in my blood to be lowered while I was taking it. It's an interesting theory. Basically, he thinks the antibiotics were helping the malfunction that was going on in the intestine, thus causing less irritation in my joint while I was taking it. As I stopped the antibiotic, I got worse again. Maybe that's another reason the IgA was normal?

Thoughts, ideas, anything?


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

It is really up to you whether you want or need a formal diagnosis. It sounds like your rhuemy is a good one who has realized that gluten is a toxin for you. If you feel you need a celiac diagnosis then do go ahead and do a challenge but be forwarned your body may really not like the challenge and you may still have a false negative on the biopsy.

srall Contributor

I had chronic neck and shoulder pain that finally went away when I went gluten free. I always thought it was a muscle that was knotted up but now I realize it was arthritis/joint pain. I'm also self diagnosed, and the thought of getting a formal diagnosis sends me into a panic. My SIL is an allergist and she's very insistent that I get a formal diagnosis, but my mother's GI tells her that the best way to determine if you are intolerant to something is to do an elimination diet. (Mom is gluten free also) There are good arguments on both sides.

I take a probiotic everyday as part of my recovery. If I were you I'd expect to stay gluten free my entire life, unless you decide to do the formal testing. But just remember that even if you don't get diagnosed celiacs doesn't mean you should be on gluten. My brother had testing done several years ago, including a blood test that was negative, so his doctor and he took it as clearance to eat gluten. And years later he's still suffering.

srall Contributor

Isn't it interesting how answers come to us in dreams? I find that very interesting.

tbritt Rookie

I had chronic neck and shoulder pain that finally went away when I went gluten free. I always thought it was a muscle that was knotted up but now I realize it was arthritis/joint pain.

How long did it take to get 100 percent better? I feel I am around 85 percent better. It used to feel like something was attacking my body. Now it just feels like there is some tendon and muscle pain. (Before it had gotten to the nerve and was just unbearable.) I really thought I was dying. (And on the days I didn't think I was dying, I wished I was because the pain was so much I couldn't handle it.)

How long have you been gluten free? Have you found you've had to give up anything else?

I so badly want miss alcohol and chocolate but have been trying to be really good about not. I had some wine and some dark chocolate last week (both were supposed to be gluten free) but I wonder if they slowed my progress. I don't know if they had hidden gluten or if I have a problem with the chocolate or the wine. I might have to cry if I have to give up dairy, chocolate, and alcohol altogether. I haven't eliminated dairy yet.

srall Contributor

How long did it take to get 100 percent better? I feel I am around 85 percent better. It used to feel like something was attacking my body. Now it just feels like there is some tendon and muscle pain. (Before it had gotten to the nerve and was just unbearable.) I really thought I was dying. (And on the days I didn't think I was dying, I wished I was because the pain was so much I couldn't handle it.)

How long have you been gluten free? Have you found you've had to give up anything else?

I so badly want miss alcohol and chocolate but have been trying to be really good about not. I had some wine and some dark chocolate last week (both were supposed to be gluten free) but I wonder if they slowed my progress. I don't know if they had hidden gluten or if I have a problem with the chocolate or the wine. I might have to cry if I have to give up dairy, chocolate, and alcohol altogether. I haven't eliminated dairy yet.

First off I've been gluten free since March/April of this year.

You know, I had so much weirdness going on during my detox that it might have been months before I realized that "Hey, my neck hasn't bothered me in awhile." I have to be honest here though, I still have joint pain. I don't know if it's my body healing or if some gluten is sneaking in. My neck is sort of bothering me today...don't know if I cranked it in yoga. I just don't know. I trust that as I continue to devote myself to this diet, that I'll continue to improve, but I think I have arthritis that I'll have to manage forever. Somedays are pain free, some days are awful. I KNOW FOR A FACT that gluten/dairy/soy in my diet contributed to chronic pain for years. The fact that I have pain free days is enough for me to keep going.

I think my back is slightly screwed up too as a result of adjusting my body to carry the pain. Does that make sense?

I have also dealt with pinched nerves as a result of this. The summer my daughter was 3 I was flat on my back on powerful pain killers. I couldn't even lift a grocery bag for 6 weeks. We were trying to have another baby and it was heartbreaking to put that on hold. (never had another baby...thank you gluten). I wish I could have figured this all out 10 years ago. I'm just thankful I'm not like my mom who realized at age 67 that she's gluten intolerant.

Keep going...feel better. I believe you will.

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. - cristiana replied to sha1091a's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      2

      Issues before diagnosis

    2. - chrisinpa commented on Scott Adams's article in Skin Problems and Celiac Disease
      2

      Celiac Disease and Skin Disorders: Exploring a Genetic Connection

    3. - knitty kitty replied to xxnonamexx's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      3

      My journey is it gluten or fiber?

    4. - trents replied to sha1091a's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      2

      Issues before diagnosis

    5. - trents commented on Jefferson Adams's article in Other Diseases and Disorders Associated with Celiac Disease
      6

      Celiac Disease Patients Face Higher Risk of Systemic Lupus

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

    • Total Members
      132,693
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • cristiana
      I agree, it so often overlooked! I live in the UK and I have often wondered why doctors are so reluctant to at least exclude it - my thoughts are perhaps the particular tests are expensive for the NHS, so therefore saved for people with 'obvious' symptoms.  I was diagnosed in 2013 and was told immediately that my parents, sibling and children should be checked.  My parents' GP to this day has not put forward my father for testing, and my mother was never tested in her lifetime, despite the fact that they both have some interesting symptoms/family history that reflect they might have coeliac disease (Dad - extreme bloating, and his Mum clearly had autoimmune issues, albeit undiagnosed as such; Mum - osteoporosis, anxiety).  I am now my father' legal guardian and suspecting my parents may have forgotten to ask their GP for a test (which is entirely possible!) I put it to his last GP that he ought to be tested.  He looked at Dad's blood results and purely because he was not anemic said he wasn't a coeliac.  Hopefully as the awareness of Coeliac Disease spreads among the general public, people will be able to advocate for themselves.  It is hard because in the UK the NHS is very stretched, but the fallout from not being diagnosed in a timely fashion will only cost the NHS more money. Interestingly, a complete aside, I met someone recently whose son was diagnosed (I think she said he was 8).  At a recent birthday party with 8 guests, 4 boys out of the 8 had received diagnosis of Coeliac Disease, which is an astounding statistic  As far as I know, though, they had all had obvious gastric symptoms leading to their NHS diagnosis.  In my own case I had  acute onset anxiety, hypnopompic hallucinations (vivid hallucinations upon waking),  odd liver function, anxiety, headaches, ulcers and low iron but it wasn't until the gastric symptoms hit me that a GP thought to do coeliac testing, and my numbers were through the roof.  As @trents says, by the grace of God I was diagnosed, and the diet has pretty much dealt with most of those symptoms.  I have much to be grateful for. Cristiana
    • knitty kitty
      @xxnonamexx, There's labeling on those Trubar gluten free high fiber protein bars that say: "Manufactured in a facility that also processes peanuts, milk, soy, fish, WHEAT, sesame, and other tree nuts." You may want to avoid products made in shared facilities.   If you are trying to add more fiber to your diet to ease constipation, considering eating more leafy green vegetables and cruciferous vegetables.  Not only are these high in fiber, they also are good sources of magnesium.  Many newly diagnosed are low in magnesium and B vitamins and suffer with constipation.  Thiamine Vitamin B1 and magnesium work together.  Thiamine in the form Benfotiamine has been shown to improve intestinal health.  Thiamine and magnesium are important to gastrointestinal health and function.  
    • trents
      Welcome to celiac.com @sha1091a! Your experience is a very common one. Celiac disease is one the most underdiagnosed and misdiagnosed medical conditions out there. The reasons are numerous. One key one is that its symptoms mimic so many other diseases. Another is ignorance on the part of the medical community with regard to the range of symptoms that celiac disease can produce. Clinicians often are only looking for classic GI symptoms and are unaware of the many other subsystems in the body that can be damaged before classic GI symptoms manifest, if ever they do. Many celiacs are of the "silent" variety and have few if any GI symptoms while all along, damage is being done to their bodies. In my case, the original symptoms were elevated liver enzymes which I endured for 13 years before I was diagnosed with celiac disease. By the grace of God my liver was not destroyed. It is common for the onset of the disease to happen 10 years before you ever get a diagnosis. Thankfully, that is slowly changing as there has developed more awareness on the part of both the medical community and the public in the past 20 years or so. Blessings!
    • knitty kitty
      @EndlessSummer, You said you had an allergy to trees.  People with Birch Allergy can react to green beans (in the legume family) and other vegetables, as well as some fruits.  Look into Oral Allergy Syndrome which can occur at a higher rate in Celiac Disease.   Switching to a low histamine diet for a while can give your body time to rid itself of the extra histamine the body makes with Celiac disease and histamine consumed in the diet.   Vitamin C and the eight B vitamins are needed to help the body clear histamine.   Have you been checked for nutritional deficiencies?
    • sha1091a
      I found out the age of 68 that I am a celiac. When I was 16, I had my gallbladder removed when I was 24 I was put on a medication because I was told I had fibromyalgia.   going to Doctor’s over many years, not one of them thought to check me out for celiac disease. I am aware that it only started being tested by bloodwork I believe in the late 90s, but still I’m kind of confused why my gallbladder my joint pain flatulent that I complained of constantly was totally ignored. Is it not something that is taught to our medical system? It wasn’t a Doctor Who asked for the test to be done. I asked for it because of something I had read and my test came back positive. My number was quite high.Are there other people out here that had this kind of problems and they were ignored? 
×
×
  • 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.