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New To Forum/dealing With Celiac And Ra


JamieSims

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JamieSims Newbie

I've been reading thru some of the links here and am gratified that there's lots of support for the gluten and lactose intolerant as well as advice for the different ways to cope. Thanx to everyone for advice given: past, present and hopefully future as well. I'll be reading for a long while. :D

Going gluten, lactose, yeast and wheat free is helping to ease a number of my symptoms considerably. Goodbye stomach agony. But I am now finding that I am increasingly dealing with rheumatoid arthritic symptoms. Due to the lack of support from my doctors (due to negative tests and told to destress), and finding that going 'celiac' as it were helped significantly, I have had to go about guessing and estimating my condition on my own. As alot of you would know I suspect. :angry:

The considerable fatigue and pain in my elbows and hands which I am experiencing I try try to remedy with my partner's assistance using a type of primitive lymphatic massage. Intense pain has me resorting to drastic measures such as stopping the blood flow in my elbows or hands for a few seconds. This has helped. :ph34r:

The thing is I have gone as far as I can on my own and I am falling behind in my job. I'm an apprentice techie. I may even lose my job if this keeps up. I need both my hands (all my joints actually) and my brains. I am loathe to ask a medical specialist considering the past treatment I have received. My naturopath has me on a new course of drops, as well as now committing to my new 'life diet' (food and high grade vitamin supplements), as it were.

Are any of you dealing with rheumatoid arthritis? Do you have pain in the glands in your neck which sets off that 'dirty high'?. When I am having a decent or full attack I am literally ghosting thru the day and feel like I'm on some sort of dirty drug high and can easily sleep 11 hours a night at least 4 times a week. I have resorted to strong pain medications at this point which does provide relief, but I am aware that my intestines are in a bad state and so is my immune system. So I keep the pain killers to a bare minimum.

I am going forward on the premise that RA is celiac related via leaky gut syndrome. Remedy the holes, repair the intestines, hopefully bye bye RA. But in the meantime is there something else I can try.

I apologise for the long winded letter, but would be grateful for your views, tips, or just even sharing your story with me. Thank you. :blink:


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chasbari Apprentice

I was dealing with severe RA before I was ever diagnosed with celiac. My rheumatologist wanted to put me on Dmards and antiinflammatory drugs. I resisted. When finally DX'ed with celiac I first tried the standard gluten-free diet which made me feel less worse but not necessarily that much better. I used to have two or more hours of gel time in the mornings and had a hard time getting out of a chair much less walking at any time throughout the day. Hand weakness was very bad. Long story short I went Paleo with the diet being careful to follow recommendations for anti-inflammatory diet guidelines as well avoiding all night shades, beans, peas, other legumes and peanuts. No potatoes, tomatoes or eggplant and peppers. My RA has been melting away and my numbers prior to diagnosis were extremely high... any titer over 17 is considered positive for RA and mine was in the 800+ range. Since going strict paleo I now have zero gel time in the morning and I can think straight and have much better energy throughout the day. The only supplement I take is a CAL/MAG/ZINC Vit D because of bone density issues. A year ago it was dangerous for me to even try to do anything involving gripping a tool for fear that something would go airborne and imperil someone nearby. Now I work with steel and welding and fabricating with no problem. Good luck.

CS

YoloGx Rookie

I have not been diagnosed with RA however I have had severe joint inflammation and pain as has my partner. He in fact gets so bad he can't even go out for walks, he has so much pain in his joints plus his skin becomes very painful.

However the following remedies have helped both him and me.

I agree with Chasbari, going on a diet without grains or sugars is very helpful. For us, we have also been helped by making and using the 24 hour home made yogurt suggested in the Specific Carbohydrate Diet (SCD)--of which there is a thread on celiac.com. After fermenting it for 24 hours all the lactose is removed and yet you get the benefit of high doses of probiotics. We use a plain Greek yogurt as a starter. For those that still can't handle that, there is a similar probiotic soured cabbage juice you might be interested in.

We recently went on a combined paleo and SCD but now are OK with an addition of some brown rice, however it took ten months to get here. I started a thread that I call "Back to the Basics" taking the middle path--in case you are interested.

Meanwhile, I have found for both of me and Graeme that the periodic use of a detox herbal mash really helps with joint issues and general well being. We combine dandelion root, yellow dock root and licorice root which we lightly boil for 30 minutes to make a pungent brew. I sometimes add cleavers which is a powerful lymphatic drain as well as good for the kidneys--but Graeme for whatever reason does not tolerate it.

Dandelion root is very good clearing toxins from the liver and the kidneys; yellow dock is a good systemic purifier as well as purifies and strengthens the intestines. Licorice root is an adaptogen that helps the effectiveness of the other two herbs; it also helps raise the blood pressure (you may or may not need this); and it is a good glandular in case you need help there too (Graeme has a low thyroid for instance and a tendency towards low adrenal function so it helps against that). Even just taking the dandelion root by itself should help if you find the other herbs not to your taste. Don't take any of the above detox herbs however if you get diarrhea since they do mildly help activate the release of bile and thus peristalsis.

I also suggest detoxing in other ways--saunas, mud packs (like with Indian Healing Clay on the hands and feet for 20 minutes) and exercise--swimming being one of the best to help with the lymphs and/or one of those rebounders. Graeme uses one of those simple small home stair master like pedal devices that have a dial resistance. Daily walks of course also help.

In addition, I have recently discovered that olive leaf tea or extract (obviously avoid any tinctures made with alcohol in order to avoid gluten) has really helped immensely with both my neck and low back and elbow pain. I also now sleep like a log rather than go through this whole rigamarole with nightly leg and foot pain. Initially I had a Herxheimer effect which means I felt much worse the first 3 days taking the olive leaf; however apparently that is a good sign indicating it is working. After that my body adjusted. Nevertheless I suggest you start slow and work your way up to a larger dose as needed if you decide to try it.

And yes, continue with lots and lots of vegetables! Am concerned though that you might not be getting enough protein. I have found chicken to be the easiest meat to digest. Some people swear by fish. Some combination thereof might be worth trying. Like you we are avoiding beans for the time being. Try taking plant enzymes by Now or some such equivalent with your meals--it may help with protein (esp. meat) digestion.

I also eat a lot of sunflower seeds since I can't digest nuts. Graeme in turn can't tolerate sunflower seeds but does well with sesame seeds which he grinds and makes into tahini (he still has to use just small amounts of it however). I don't know what your situation is but it might be worth a try. For some they need to soak seeds or nuts overnight first before eating.

Hope at least some of these suggestions help!

Bea

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    • marion wheaton
      Thanks for responding. I researched further and Lindt Lindor chocolate balls do contain barely malt powder which contains gluten. I was surprised at all of the conflicting information I found when I checked online.
    • trents
      @BlessedinBoston, it is possible that in Canada the product in question is formulated differently than in the USA or at least processed in in a facility that precludes cross contamination. I assume from your user name that you are in the USA. And it is also possible that the product meets the FDA requirement of not more than 20ppm of gluten but you are a super sensitive celiac for whom that standard is insufficient. 
    • BlessedinBoston
      No,Lindt is not gluten free no matter what they say on their website. I found out the hard way when I was newly diagnosed in 2000. At that time the Lindt truffles were just becoming popular and were only sold in small specialty shops at the mall. You couldn't buy them in any stores like today and I was obsessed with them 😁. Took me a while to get around to checking them and was heartbroken when I saw they were absolutely not gluten free 😔. Felt the same when I realized Twizzlers weren't either. Took me a while to get my diet on order after being diagnosed. I was diagnosed with small bowel non Hodgkins lymphoma at the same time. So it was a very stressful time to say the least. Hope this helps 😁.
    • knitty kitty
      @Jmartes71, I understand your frustration and anger.  I've been in a similar situation where no doctor took me seriously, accused me of making things up, and eventually sent me home to suffer alone.   My doctors did not recognize nutritional deficiencies.  Doctors are trained in medical learning institutions that are funded by pharmaceutical companies.  They are taught which medications cover up which symptoms.  Doctors are required to take twenty  hours of nutritional education in seven years of medical training.  (They can earn nine hours in Nutrition by taking a three day weekend seminar.)  They are taught nutritional deficiencies are passe' and don't happen in our well fed Western society any more.  In Celiac Disease, the autoimmune response and inflammation affects the absorption of ALL the essential vitamins and minerals.  Correcting nutritional deficiencies caused by malabsorption is essential!  I begged my doctor to check my Vitamin D level, which he did only after making sure my insurance would cover it.  When my Vitamin D came back extremely low, my doctor was very surprised, but refused to test for further nutritional deficiencies because he "couldn't make money prescribing vitamins.". I believe it was beyond his knowledge, so he blamed me for making stuff up, and stormed out of the exam room.  I had studied Nutrition before earning a degree in Microbiology.  I switched because I was curious what vitamins from our food were doing in our bodies.  Vitamins are substances that our bodies cannot manufacture, so we must ingest them every day.  Without them, our bodies cannot manufacture life sustaining enzymes and we sicken and die.   At home alone, I could feel myself dying.  It's an unnerving feeling, to say the least, and, so, with nothing left to lose, I relied in my education in nutrition.  My symptoms of Thiamine deficiency were the worst, so I began taking high dose Thiamine.  I had health improvement within an hour.  It was magical.  I continued taking high dose thiamine with a B Complex, magnesium. and other essential nutrients.  The health improvements continued for months.  High doses of thiamine are required to correct a thiamine deficiency because thiamine affects every cell and mitochondria in our bodies.    A twenty percent increase in dietary thiamine causes an eighty percent increase in brain function.  The cerebellum of the brain is most affected.  The cerebellum controls things we don't have to consciously have to think about, like digestion, balance, breathing, blood pressure, heart rate, hormone regulation, and many more.  Thiamine is absorbed from the digestive tract and sent to the most important organs like the brain and the heart.  This leaves the digestive tract depleted of Thiamine and symptoms of Gastrointestinal Beriberi, a thiamine deficiency localized in the digestive system, begin to appear.  Symptoms of Gastrointestinal Beriberi include anxiety, depression, chronic fatigue, headaches, Gerd, acid reflux, gas, slow stomach emptying, gastroparesis, bloating, diarrhea and/or constipation, incontinence, abdominal pain, IBS,  SIBO, POTS, high blood pressure, heart rate changes like tachycardia, difficulty swallowing, Barrett's Esophagus, peripheral neuropathy, and more. Doctors are only taught about thiamine deficiency in alcoholism and look for the classic triad of symptoms (changes in gait, mental function, and nystagmus) but fail to realize that gastrointestinal symptoms can precede these symptoms by months.  All three classic triad of symptoms only appear in fifteen percent of patients, with most patients being diagnosed with thiamine deficiency post mortem.  I had all three but swore I didn't drink, so I was dismissed as "crazy" and sent home to die basically.   Yes, I understand how frustrating no answers from doctors can be.  I took OTC Thiamine Hydrochloride, and later thiamine in the forms TTFD (tetrahydrofurfuryl disulfide) and Benfotiamine to correct my thiamine deficiency.  I also took magnesium, needed by thiamine to make those life sustaining enzymes.  Thiamine interacts with each of the other B vitamins, so the other B vitamins must be supplemented as well.  Thiamine is safe and nontoxic even in high doses.   A doctor can administer high dose thiamine by IV along with the other B vitamins.  Again, Thiamine is safe and nontoxic even in high doses.  Thiamine should be given if only to rule Gastrointestinal Beriberi out as a cause of your symptoms.  If no improvement, no harm is done. Share the following link with your doctors.  Section Three is especially informative.  They need to be expand their knowledge about Thiamine and nutrition in Celiac Disease.  Ask for an Erythrocyte Transketolace Activity test for thiamine deficiency.  This test is more reliable than a blood test. Thiamine, gastrointestinal beriberi and acetylcholine signaling.  https://pmc.ncbi.nlm.nih.gov/articles/PMC12014454/ Best wishes!
    • Jmartes71
      I have been diagnosed with celiac in 1994, in remission not eating wheat and other foods not to consume  my household eats wheat.I have diagnosed sibo, hernia ibs, high blood pressure, menopause, chronic fatigue just to name a few oh yes and Barrett's esophagus which i forgot, I currently have bumps in back of my throat, one Dr stated we all have bumps in the back of our throat.Im in pain.Standford specialist really dismissed me and now im really in limbo and trying to get properly cared for.I found a new gi and new pcp but its still a mess and medical is making it look like im a disability chaser when Im actively not well I look and feel horrible and its adding anxiety and depression more so.Im angery my condition is affecting me and its being down played 
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