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

Rheumatoid Arthritis


cgilsing

Recommended Posts

cgilsing Enthusiast

My mom went to the doctor this morning and they suspect that she has RA. :( We are now waiting on the blood test results. Several people in our family have celiac disease (mom included), but we have no experience with RA. I know people with celiac disease are more likely to develop RA. She is 61 years old. Right now it is in her fingers and wrists. Does anyone have experience with this? What kind of prognosis is there for a woman her age, with her symptoms? What kind of treatment options are there? Thanks in advance!


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



Celiac.com Sponsor (A8-M):



ENF Enthusiast
My mom went to the doctor this morning and they suspect that she has RA. :( We are now waiting on the blood test results. Several people in our family have celiac disease (mom included), but we have no experience with RA. I know people with celiac disease are more likely to develop RA. She is 61 years old. Right now it is in her fingers and wrists. Does anyone have experience with this? What kind of prognosis is there for a woman her age, with her symptoms? What kind of treatment options are there? Thanks in advance!

I'm going to be speaking with someone soon who has had a very bad case of RA for almost 40 years, and will try to ask him about it. I do not know if he has celiac. My mother-in-law also has it, but it's not as severe.

In the meantime, I have a question: Has she been following the Celiac diet and if so, for how long?

cgilsing Enthusiast

no, she hasn't been following a strict diet. I have tried to convince her to do it, but she still cheats. She cooks with rice flour, and tries to avoid it at home, but especially when she eats out....she cheats...

ravenwoodglass Mentor
no, she hasn't been following a strict diet. I have tried to convince her to do it, but she still cheats. She cooks with rice flour, and tries to avoid it at home, but especially when she eats out....she cheats...

I could be wrong but I think the answer is right there.

I had severe arthritis with joint damage and pain that the pills they gave me didn't touch. I had a lot of indications and symptoms of RA but was not forming the rheumatoid factor that is usually found with it. That is looked for in a blood test. Celiac was for me the cause and my arthritis has now been in remission for almost 5 years. The joint damage is permanent and that won't reverse but I now have full function and no pain after progressive damage for over 10 years.

Your Mom, as I am sure you know, is not doing herself any favors by cheating, for one thing there is a withdrawl aspect to gluten and if someone keeps cheating they never get fully through the withdrawl and they never stop forming the antibody reaction that causes so many other problems I hope she becomes stricter in her diet soon. It is very hard to watch someone do this to themselves and I wish I had some good advice to get her to stop but that is a decision she has to make for herself.

MaryJones2 Enthusiast

I agree with ravenswood. I had all the symptoms of RA except the factor. I even got a round of methotrexate because my Dr didn't want to wait for the rheumatoid factor to be positive. For me, it was gluten all along. If I even get a little bit through cross contamination my joints burn and my hands and feet go numb and stop working for 5 days. Even now I have a few joints that are permanently damaged. Having to avoid gluten should be a minor inconvience in life. Developing RA isn't... See if you can get your mom to not cheat for 1 full month. My guess is she'll stop when she realizes how much better she feels.

lonewolf Collaborator

I had the same thing several years ago. All the symptoms of RA, but no rheumatoid factor. I have psoriasis, so I was diagnosed with Psoriatic Arthritis.

I just have to chime in that being gluten-free might not be enough. I need to be dairy-free and soy-free too. If I eat much soy or dairy at all (cheese or butter, never would drink milk) my joints start to ache. Just something to think about. And, at first, I also eliminated all red meat, poultry, nightshade vegetables, peanuts, and most legumes. After a year I was completely better and I only get joint pain if I eat the "big three".

nikki-uk Enthusiast
I had the same thing several years ago. All the symptoms of RA, but no rheumatoid factor. I have psoriasis, so I was diagnosed with Psoriatic Arthritis.

My hubby also.

His arthritis is alot better since his celiac disease dx and going gluten-free. Unfortunately quite alot of joints were damaged before then.

I'm not suggesting that every case of Psoriatic Arthritis or RA will be cured by being gluten-free - but your Mum owes it to herself that she's as careful as possible with the diet - if only to see if her discomfort improves.

If her symptoms still continue there are alot of drugs docs can throw at RA, usually starting with NSAIDS (Non Steroidal Anti Inflammatories) to DMARDS (e.g Methotrexate, Sulphasalazine) which are 'Disease Modifying' drugs and slow down the progression of any damage caused by arthritis.

I am hoping though that your Mum will feel better just by being stricter with the diet - Good Luck :)


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



Celiac.com Sponsor (A8-M):



Ann1231 Enthusiast

I WISH gluten free would cure my RA! I do have a high ra factor. Gluten free helps me feel better and my flares aren't as bad, but I still have them.

I'm 44, was diagnosed January of 2005. I was extremely strict vegan diet, no grains at all for 10 months, couldn't get out of bed, couldn't feed myself, couldn't hold a cup of water. I tried homeopathy, massage, etc, to no avail. I'm now on methotrexate, plaquinil, folic acid, prednisone when I need it and I've needed it for the last two months or so. I'm functioning now. I have very good days and I have not so good days. I do NOT have joint damage though!! I think that's because I went on the meds. The meds aren't always fun. I'm up at 3:15am because of nausea from the methotrexate but I can sit up, I can type, I made myself a cup of tea and can drink it all by myself so the nausea is a minor, albeit uncomfortable, trade off.

Ann

rock on Apprentice
I agree with ravenswood. I had all the symptoms of RA except the factor. I even got a round of methotrexate because my Dr didn't want to wait for the rheumatoid factor to be positive. For me, it was gluten all along. If I even get a little bit through cross contamination my joints burn and my hands and feet go numb and stop working for 5 days. Even now I have a few joints that are permanently damaged. Having to avoid gluten should be a minor inconvience in life. Developing RA isn't... See if you can get your mom to not cheat for 1 full month. My guess is she'll stop when she realizes how much better she feels.

Hi Janet,

I was just wondering how long you were on the diet before you realized that the diet was working for you. Were you officially dx with Celiac?

My husband was diagnosed with psoriatic arthritis. He, like you, has no RA factor...but because he has minor psoriasis, it's been diagnosed as psoriatic arthritis. We've been wondering if perhaps it's just arthritis related to gluten sensitivity and that he also happens to have psoriasis. His nephew is a textbook case of an infant with Celiac...he would've died if they hadn't dx'd him in time. My husband's bloodwork for celiac came back negative, but he's been on the diet for about 7 weeks now & has been feeling some improvements in mood, psoriasis & up & down with the arthritis. We believe that's got to be an indicator that he's got a problem with gluten.

What really interested me in your post is that you said that your joints burn...his do too! He said that the burning has gotten better over this time on the gluten-free diet, so we are hopeful that it will continue.

Glad to hear that you've found the source of your problem!

Best,

R.O.

lonewolf Collaborator
I WISH gluten free would cure my RA! I do have a high ra factor. Gluten free helps me feel better and my flares aren't as bad, but I still have them.

I'm 44, was diagnosed January of 2005. I was extremely strict vegan diet, no grains at all for 10 months, couldn't get out of bed, couldn't feed myself, couldn't hold a cup of water. I tried homeopathy, massage, etc, to no avail. I'm now on methotrexate, plaquinil, folic acid, prednisone when I need it and I've needed it for the last two months or so. I'm functioning now. I have very good days and I have not so good days. I do NOT have joint damage though!! I think that's because I went on the meds. The meds aren't always fun. I'm up at 3:15am because of nausea from the methotrexate but I can sit up, I can type, I made myself a cup of tea and can drink it all by myself so the nausea is a minor, albeit uncomfortable, trade off.

Ann

Have you tried eliminating soy? I know I wouldn't have gotten better if I had only eliminated gluten. For me it was (and still is) gluten, dairy and soy.

Ann1231 Enthusiast
Have you tried eliminating soy? I know I wouldn't have gotten better if I had only eliminated gluten. For me it was (and still is) gluten, dairy and soy.

I've never really used soy for anything. I've avoided dairy for about 10 years as well. I basically eat a paleo diet, fruits, non-starchy vegetables and a little lean meat...I often don't eat meat

thank you for the thought though!

Yellow Rose Explorer

I have had RA for 28 years now. I have the genetic marker for RA. However, gluten seems to be the thing that set it off to begin with. After going gluten free for 7 months I have improved. I still have swelling and pain but started eleminating other foods like milk, nightshades, soy, corn, and rice. When I started 7 months ago I could barely walk to the bathroom and back. I couldn't lift anything and mostly sat as still as I could. Now I am working, have stamina, and am starting to exercise. I still have pain but it is getting better each day. Eleminating the other things that were causing swelling and pain has really helped. It is amazing to me that food does so much harm to our bodies. Your mom will have to figure out for herself how much pain she wants to be in. It is not an easy life change.

Yellow Rose

  • 4 months later...
mushroom Proficient
I had the same thing several years ago. All the symptoms of RA, but no rheumatoid factor. I have psoriasis, so I was diagnosed with Psoriatic Arthritis.

I just have to chime in that being gluten-free might not be enough. I need to be dairy-free and soy-free too. If I eat much soy or dairy at all (cheese or butter, never would drink milk) my joints start to ache. Just something to think about. And, at first, I also eliminated all red meat, poultry, nightshade vegetables, peanuts, and most legumes. After a year I was completely better and I only get joint pain if I eat the "big three".

Hi All:

I have been going through and re-reading the threads on rheumatoid and psoriatic arthritis, and would like to revive this one for a moment. Please bear with me and help me if you can.

I have psoriatic arthritis (diagnosed four years ago, negative RA factor) and have been through all the pharmaceutical treatments and became intolerant of them all, including NSAIDS which cause kidney failure in me (I am very sensitive to meds and often have perverse reactions). My last one was plaquenil which really flared up my psoriasis for three years but it worked for the arthritis--no joint damage. But, oh, all the side effects with I think hair loss being the worst. I thought I was going to end up bald. Anyway, then the plaquenil turned on me and gave me mouth ulcers, progressively swollen ankles overflowing my shoes and, to make matters worse, my arthritis was breaking through it. So I cut it out. I had no idea about the gluten connection at that point.

Went gluten free to try to alleviate the life-long bloating and gassiness, insomnia, palpitations, and sure enough it worked. Went gluten free Nov. 07, quit the plaquenil Aug. 07. Started reading these forums and read about the gluten connection to psoriatic arthritis--what a shock! By December my arthritis was in remission and the psoriasis calming down. Oh boy, was I hopeful. However, since Feb my arthritis has come roaring back--welll not exactly roaring, but burning wrists (one wrist joint really swollen but not hot), left hand totally stiff in the mornings, takes an hour or two to get it moving, weakness in the legs, fatigue, stiff shoulders and neck, all the old familiars except so far no toe or finger involvement. I have no meds to take to alleviate this (except a I have an approval for leflunomide which has side effects worse than the others I have tried and is the last option other than footing the bill myself for Remicade which is available here and has its own really bad side effects.)

I have eliminated all gluten, and no, I would never even think of cheating! Don't even wear any makeup at the moment until I can get back to the U.S. and try some Essential Minerals.

About 12 years ago in the U.S. I tested sensitive to corn and soy, and stopped eating those in the U.S. However, here (in New Zealand) I have been able to tolerate our non-GM corn and have recently eaten a fresh tender ear of corn with absolutely no gas or bloating as formerly with corn. I do dairy light, i.e., cheese, sour cream and yogurt only, having figured out the lactose intolerance bit 18 years ago. And I take some Lactaid Fast Acting with me for emergency situations when I am out.

Now, from what I have been reading, and I really don't want to hear this you probably realize, I am beginning to suspect that I must cut out all traces of dairy and soy if I am going to recover. I never actively seek soy but I am not always 100% vigilant to make sure some doesn't sneak in. Anyway, with no meds to treat me and arthritis getting worse, psoriasis getting better, is there anything else I can do? Hubby has been supportive and gone gluten free too, but might baulk at the rest.

Sorry, this is rather long, but I would like your opinion(s) on this, though it's probably obvious. Thanks for reading.

Neroli

MaryJones2 Enthusiast

Soy causes inflammation in my body and stiffens me up nicely. Dairy has about the same effect. Gluten gives me the RA-type burning joint pain. I can feel the effects of any form of soy(soybean oil, letichens, etc.). Unfortunately, I think you should consider cutting out both. My husband didn't care about eliminating soy and doesn't eat a lot of dairy. We keep cheese in the fridge so he can add as necessary.

One thing that helps is practicing yoga 2-3 times per week. I particularly like Iyengar yoga because it is slower and you hold poses longer than other forms. It's great for chronic pain. I would recommend taking classes until you understand proper form because you can seriously hurt yourself. For home based yoga, I really like Rodney Yee's Yoga Burn and Alison Nolans Yoga Wisdom series (Tight hips/back and neck pain).

I also did the Open Original Shared Link a few years ago and found it very helpful in opening up my joints. I saw Rolfing featured on Oprah recently.

Taking a magnesium supplement every day and making sure you get potassium will also help. There is an old folk remedy of taking 1 teaspoon of apple cider vinegar every morning to alleviate joint pain. Some of the older people around here say it works but you have to do it for a few months.

mushroom Proficient
Soy causes inflammation in my body and stiffens me up nicely. Dairy has about the same effect. Gluten gives me the RA-type burning joint pain. I can feel the effects of any form of soy(soybean oil, letichens, etc.). Unfortunately, I think you should consider cutting out both. My husband didn't care about eliminating soy and doesn't eat a lot of dairy. We keep cheese in the fridge so he can add as necessary.

One thing that helps is practicing yoga 2-3 times per week. I particularly like Iyengar yoga because it is slower and you hold poses longer than other forms. It's great for chronic pain. I would recommend taking classes until you understand proper form because you can seriously hurt yourself. For home based yoga, I really like Rodney Yee's Yoga Burn and Alison Nolans Yoga Wisdom series (Tight hips/back and neck pain).

I also did the Open Original Shared Link a few years ago and found it very helpful in opening up my joints. I saw Rolfing featured on Oprah recently.

Taking a magnesium supplement every day and making sure you get potassium will also help. There is an old folk remedy of taking 1 teaspoon of apple cider vinegar every morning to alleviate joint pain. Some of the older people around here say it works but you have to do it for a few months.

Thank you for your response Janet. As you realize, it confirms my latest thinking. I think I will start by eliminating soy and see if that helps. If no relief I will move on to complete dairy although I really haven't been eating a lot lately--occasional cheese. Cut out the breakfast yogurt. I will follow your advice on the magnesium and I do take potassium. Maybe also try the apple cider vinegar since I threw out all my malt vinegar, the favourite of New Zealand cooks.

I have had two really bad experiences with yoga when I had other interfering injuries and have always felt a little leary about it since. The one exercise which used to work for me in CA was exercising in a physio pool--water walking and styrofoam water resistant weight training. It has been impossible to replicate down here, but I have a fresh line on perhaps a pool that might help at a rest home, and I think I can get some pool time at Parafed through the arthritis foundation. Now that I am seeing some light at the end of the tunnel (that is not a train coming) I feel a little more positive about pursuing these options. Now if I can just make these weak legs carry me up the stairs to bed!

Neroli

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,962
    • Most Online (within 30 mins)
      7,748

    AlissaW
    Newest Member
    AlissaW
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • 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.