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

Hashimotos, Celiac And Now Muscle Pain!


glutenfreegirl

Recommended Posts

glutenfreegirl Enthusiast

Hope I am posting this in the right area...I apologize in advance if I have not done so...

Ok so first I got the dx of celiac and hashimotos at the same time....now I am in such pain with both digestive bloat, rumbling ever time I eat and now major back muscle and joint pain!!!

Look I have a pretty good pain threshold...I delivered 2 big babys oh natural ..so I can tolerate a lot of pain!! Lol ..but this constant muscle and digestive upset is so frustrating, my body aches unless I am moving constantly the minute I sit for a few minutes I get stiff, saw my GP the other day he wants me to take a probiotic and pill for gas relief (he said my stomach and abdomin where full of gas )and let him know if I do not feel better in 2 weeks.... I came across. Book yesterday after watching a PBS special :rolleyes:

Called eat to live by dr Joel fuhrman I have been reading since and it sounds pretty hopeful can anyone help me here on their thoughts or if they are familiar with his book and plan..he claims he can heal autominun issues, and leaky gut etc via diet, dha and high probiotics....I was thinking of seeing him for an apt he is not far from me....I am worrying that now another auto immune issues isnmoving in via the muscle pain...this needs to stop I have been gluten-free for 6 months now I have more joint and muscle pain now than before,.....sorry for the rant I send you all big hugs.....


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



Celiac.com Sponsor (A8-M):



viviendoparajesus Apprentice

i have been gluten free for a year and i have had more muscle pain than before I went gluten-free, so I can relate to what you are going through.

i have not heard of dr joel fuhrman's book but it sounds like he does some of the same things as dr datis kharrazian (one of his books is - why do i still have thyroid symptoms) he talks a lot about the role of gluten in hashimoto's disease. he focuses on glutathione, emulsified vitamin d, diet changes. i think he also talks some about dha and probiotics.

it would be worthwhile to make an appointment and find out what the cost and treatment would be like.

cahill Collaborator

.he claims he can heal autominun issues, and leaky gut etc via diet, dha and high probiotics....I was thinking of seeing him for an apt he is not far from me....I am worrying that now another auto immune issues isnmoving in via the muscle pain...this needs to stop I have been gluten-free for 6 months now I have more joint and muscle pain now than before,.....sorry for the rant I send you all big hugs.....

BIG ((HUG)) to you too :)

Is he saying he can CURE autoimmune diseases or is he saying that he can heal the damage from the autoimmune diseases??

txplowgirl Enthusiast

Hi Glutenfreegirl, I haven't read the book but I have Fibromyalgia, Rhuematoid arthritis and i'm gluten free. The muscle and joint pain that I had did not ease up until I got rid of all gluten, dairy, soy and the nightshade vegetables. Nightshades cause swelling and pain in the muscles and joints also. Nightshades are tomatoes, potatoes, all bell peppers and eggplant including tobasco sauce. Maybe if you get rid of all those that might help.

glutenfreegirl Enthusiast

Thank you alll...

Txplowgirl, I will give that a try, I have been making a Lot of potatoes lately.....

glutenfreegirl Enthusiast

BIG ((HUG)) to you too :)

Is he saying he can CURE autoimmune diseases or is he saying that he can heal the damage from the autoimmune diseases??

That is a good question I will reread and let you know.....

Debbie B in MD Explorer

I definitely vote for eliminating the nightshades. This made a really big difference for me. Potatoes, formerly one of most favotrite foods, is the biggest culprit. I really do not miss them. Feeling better is so much better than something that tastes good. I too am eliminating soy and go very, very easy on the corn. Best of luck to you.


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



Celiac.com Sponsor (A8-M):



GFinDC Veteran

Hi,

When I used to get gassed up like the Goodyear blimp I would take Altoids peppermints. The peppermint helps to relax the stomach and get the gas out. Helps you burp basically. I don't think it is good to take them all the time though. It is better to eliminate the foods from your diet that are causing the upset in the first place. You can check my signature for the list of foods I eliminated to get better. You also might get some relief by taking a Bentaine HCL before eating a couple times a week. and also taking pro-biotics and reducing or eliminating sugar from your diet.

  • 2 months later...
kennedymoore Rookie

i have been gluten free for a year and i have had more muscle pain than before I went gluten-free, so I can relate to what you are going through.

i have not heard of dr joel fuhrman's book but it sounds like he does some of the same things as dr datis kharrazian (one of his books is - why do i still have thyroid symptoms) he talks a lot about the role of gluten in hashimoto's disease. he focuses on glutathione, emulsified vitamin d, diet changes. i think he also talks some about dha and probiotics.

it would be worthwhile to make an appointment and find out what the cost and treatment would be like.

I am responding to your comment about Dr. Datis Kharrazian book. I read it and found it helpful. On my own I started a non-soy based vitamin D3 (Premier Research Labs D3 Serum) I take 5000 ius daily. It is in an olive oil base. I increased my vitamin C, tremendously, started taking LIPH to raise glutathione and SOD levels, I also take the Oxicell gluatathione and adrenal creams, and omega 3s. All of that turned my health around. I still have hair loss I don't know what to think or say about that.

I also switched from synthroid (not gluten-free) to Tirosint as my T4 replacement. For anemia my new hematologist wrote me a prescription for EZFe (pronounced easy fee). I am no longer on IV iron therapy. For the first time in my life (47 years) I am not anemic.

I also drink fresh coconut water and take extra virgin coconut oil before each meal.

I hope this helps someone. I am living well with celiac disease, lupus, and hashimotos.

pricklypear1971 Community Regular

I get muscle cramps from gluten.

That said, vitamin deficiencies do it to most people, too.

I'd also try a good digestive enzyme like enzymedica digest gold, along with a good probiotic like pb8. I have mostly neurological and DH symptoms from gluten, but know my digestive system suffers. They both help tremendously.

  • 1 year later...
Rachelcooks Newbie

About a month ago I started the Eat to Live plan that Dr Fuhrman suggests. (eating a predominantly vegan diet rich in the highest nutrient per calorie foods) which means aiming for up to a pound of cooked and a pound of uncooked veggies. At least one serving of beans and nuts and seeds/day and at least 3 fruits. I haven't been super strict with it but the more Ido the more I want to do. It has helped me feel better than ever. I went gluten-free almost 2 years ago. Eliminating gluten helped but I still had a lot of random stomach issues. I eventually removed artificial sweeteners and as many chemicals as possible. Again this helped but I still had some joint swelling (although not serious yet). So far I feel absolutely the best on this diet. Dr fuhrman does not say he can "cure" autoimmune issues but has had some patients with autoimmune issues like lupus and rhuematoid arthritis find a lot of relief and sometimes disappearance of their diseases. If you are interested I suggest his "eat for health" book. I have finally been able to stop taking probiotics and heartburn meds while eating this way. If you do decide to follow his advice be sure to read his book as I think not having his detailed descriptions can lead to a person eating less than optimally and feeling more sick. (I wasn't eating enough beans nuts and seeds when I first started and it just wasn't right). This also has the added benefit of helping to maintain a healthy weight or reach it. So far my joints are less swollen my stomach is a nonissue (finally) and I feel energetic and not hungry. Let me know if you try it and how it goes!

nvsmom Community Regular

I too was diagnosed with Hashimoto's and celiac disease at almost the same time, and I am having lots of joint problems and hypo symptoms too. I think my problem is with the synthroid I'm on, my body seems to not agree with it so I'm hoping to switch to something more natural and get to a proper dose soon.

I've heard that people get many symptoms while their body adjusts to the meds, could that be happening to you? I also had huge flare-ups of symptoms after starting meds to the point where I strongly suspect that I also have Lupus or some other soft connective tissue disorder... But then again, it could be hypo symptoms (arthritic like pain, massive hair loss and deep fatigue, rashes, etc).

Have you been checked for fibro or other AI diseases yet? With Hashi's, you'll probably have a positive ANA test, but there are other tests that can let you know if something else is up.

I'm also pretty sure that synthroid does NOT have gluten as my pharmacy checked with them. They said they can't guarantee that they are gluten-free but they don't add it to their product... they're trying to cover their backsides.

I hope you feel better soon. (hug) You're not alone with continuing problems, so I know how frustrating it can be. Best wishes.

ButterflyChaser Enthusiast

Hi, and first of all big hugs, that muscle/joint pain sucks, really.

I have Hashimoto's and Grave's disease, diagnosed a year ago (hypo-ish for several months, then hyper till last month). Although I tested negative for celiac blood tests, I went on a gluten-free diet because I noticed that wheat etc worsened my symptoms, and made my legs swell and made it hard to even walk. Now when I accidentally "soy" myself, the same happens. You surely know about this, but are you staying away from soy?

Huggenkiss27 Rookie

Sounds like a lot of us have very similar stories! I was diagnosed with celiac and then hashimoto's a few months later. Once I started synthroid I started getting AWFUL joint pain. My doctor was suspecting rhumatoid arithritis, lupus, fibromyalgia, ect. He switched me to Armour and took a lot of blood tests. Once my armour dose was correct the pain pretty much went away and all my blood work came back negative for the other autoimmune disorders (my RA factor was borderline though so hopefully it stays low). Unfortunatly there are so many other things that could be causing the joint pain (meds, other food allergies, other autoimmune problems) and it seems like we all have to sort out what's causing it. Out of curiosity how is your hashimotos being treated? Good luck getting it all figured out!

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. - knitty kitty replied to hjayne19's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      15

      Insomnia help

    2. - TheDHhurts posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      need help understanding testing result for Naked Nutrition Creatine please

    3. - cristiana replied to hjayne19's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      15

      Insomnia help

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

    • Total Members
      133,106
    • Most Online (within 30 mins)
      7,748

    Maggie1349
    Newest Member
    Maggie1349
    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

    • knitty kitty
      @cristiana,  I react the same way.  Dairy consumption flushes out my digestive system within an hour, too! As casein is digested, it forms casomorphins that bind to opioid receptors in our bodies.  This is similar to digested gluten peptides being able to attach to opioid receptors in our bodies.   We have opioid receptors throughout our bodies including lots in the digestive tract. Casein raises tTg IgA antibodies just like gluten consumption does, which leads to further intestinal damage and continuing inflammation.  No wonder our bodies react to it by pushing the "emergency evacuation" ejection seat button! The mother of my childhood friend was British and introduced me to drinking tea properly with milk or cream.  I miss it so much.  And chocolate ice cream.  Not worth the after effects, though.  I've found taking Omega Three supplements (flaxseed oil, sunflower seed oil, evening primrose oil) helps shake those dairy cravings.   Green leafy veggies like broccoli, kale, and greens (mustard, turnip, collards) are great sources of calcium.  Avoid spinach as it is high in oxalates that block calcium absorption and may cause kidney stones.  Yes, more leafy greens are needed to reach the same amount of calcium in a glass of milk, but the greens have other benefits, like increased dietary fiber and polyphenols that act as antioxidants, reduce inflammation, and promote health.   Exposure to gluten (and casein in those sensitive to it) can cause an increased immune response and inflammation for months afterwards.  The immune cells that make tTg IgA antibodies which are triggered today are going to live for about two years. During that time, inflammation is heightened.  Those immune cells only replicate when triggered.  If those immune cells don't get triggered again for about two years, they die without leaving any descendents programmed to trigger on gluten and casein.  The immune system forgets gluten and casein need to be attacked.  The Celiac genes turn off.  This is remission.   Some people in remission report being able to consume gluten again without consequence.  Another triggering event can turn the Celiac genes on again.   Celiac genes are turned on by a triggering event (physical or emotional stress).  There's some evidence that thiamine insufficiency contributes to the turning on of autoimmune genes.  There is an increased biological need for thiamine when we are physically or emotionally stressed.  Thiamine cannot be stored for more than twenty-one days and may be depleted in as little as three during physical and emotional stresses. Mitochondria without sufficient thiamine become damaged and don't function properly.  This gets relayed to the genes and autoimmune disease genes turn on.  Thiamine and other B vitamins, minerals, and other nutrients are needed to replace the dysfunctional mitochondria and repair the damage to the body.  
    • TheDHhurts
      Hi, I bought Naked Nutrition Creatine. It lists itself as gluten free but is not certified. (It used to be, but they dropped it in the past year or two apparently.) I wrote the company and asked them what testing results they had for creatine and they sent me the attached, which says the test result for gluten is <0.025MCG. I'm used to seeing test results as ppm, so I'm not sure what <0.025MCG means. Can it be converted to ppm easily? I want to confirm that it is safe to use.
    • cristiana
      When I was still recovering my gastroenterologist suggested I bought lactofree product as I was very bloated.  So I bought some from the supermarket and from memory, I drank a nice big glass of milk - and it went right through me literally within an hour or so, if my memory serves correctly.  I came off dairy completely next and it worked like a charm, but started to reintroduce quite gradually it as I missed it! To this day, if I overdo dairy products, they work like a mild laxative.  I've never wanted to give up milk completely as I like it so much, and my mum had osteoporosis and it's an easy way of getting calcium.  But it doesn't really 'sit' well with me.   You may need to experiment a bit as when I was healing certain dairy products were worse than others - I could cope with one brand of Greek yoghurt, but I got extremely and painfully bloated with another brand of live British yoghurt.  
    • wellthatsfun
      i have been strictly gluten free for 7 months. this includes avoiding anything that may contain gluten and making sure surfaces and appliances are clean. i am 18 years old in australia and my tTG-IgA results were 69U/mL, pretty low compared to most people's, for reference. i feel the exact same as before. sure, i was pretty much asymptomatic/silent. the worst i'd get was occasionally bad stools and pitting of the nails/brittle hair since early childhood - and i was diagnosed with low iron and vitamin d which checks out due to easy bruising and such. but those symptoms have remained. maybe i'm jumping the gun, sure. i know it can take years to fully heal. but being over half a year in, i feel that i should be, y'know, healing. i'm nearly at my wits end and wondering if i should have a piece of bread or something to see how i go - to see if i possibly have refractory? my mental health is declining as i feel myself wanting to bang my head against a damn wall out of frustration every day. cravings haven't gotten better. look, i love the stuff i still can have, like salads and such. OH! i haven't lost any weight, which is mind boggling considering i eat very healthily now! i've always been on the chubbier side which is atypical of coeliac. i just don't know what's going on with me. i try to remain hopeful but i'm just so sad all the time. thanks for reading  
    • trents
      @Charlie1946There is a PM (Personal Message) tool built into the forum website that allows you to send a private message to other forum users. Just hover over their name with your mouse cursor and the menu containing that tool will pop up. This is useful if you want to communicate with an individual without everyone else involved in the thread seeing it.  Are you realizing that in my PPI taper down recommendations in an earlier post above, I was responding not to your posts but to @Caligirl57? If you must use a PPI, I certainly would advise taking the lowest dose that is effective for you.  
×
×
  • 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.