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

My Brother


JerryK

Recommended Posts

JerryK Community Regular

So my IDENTICAL twin brother, has for a year and a half now, refused to hear me when I tell him about gluten sensitivity. I've given him the whole speil...told him about the big D, the aches, the pains, the depression, the blurred vision all going away when I went gluten-free.

Recently brother was diagnosed with fibromyalgia! He's on Lyrica for pain and has had a couple cortisone shots in his neck.

Now, I've pretty much made gluten-free my lifestyle, and I do it pretty much without even really thinking much about it. I will admit that I fall off the wagon now and then and have been known to eat half a cookie and get away with it. Recently I had a severe backslide and ate a whole carton of glutenated orange chicken.

Man did it taste good! But the next day I was anxious, depressed and I too suddenly had FIBROMYALGIA!!

The problem. I cannot convince my brother that the link between fibro and gluten is real. I cannot convince him that his psychic symptoms are exacerbated by gluten intake. He thinks it's all a "load" no pun intended.

So...does anyone have any links to any hard research showing the gluten/fibro link in all it's glory. I need some real hard data to push in his face, because I'm tired of hearing him whine.


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



Celiac.com Sponsor (A8-M):



RiceGuy Collaborator

I'm sure I'm not the only one who can identify with your situation. It truly is exasperating to watch someone suffer, all the while refusing to listen to reason. You can hand them all the best info on the planet, showing them how easy it would be for them to just TRY the recommendations. We both know that once they TRY gluten-free, they'll likely not need any further proof.

...And I'm also sure I speak for many when I say: "Oh, how I wish I knew long ago what I know now"

Anyway, here's a link to some articles on the relationship between fibro and Celiac:

https://www.celiac.com/categories/Celiac-Di...Celiac-Disease/

I hope you get through to your brother.

Phyllis28 Apprentice

I also hope you get through to you brother.

If you have not already done so suggest a gluten free trail run of one or two weeks. You might even include a little bribery and supply the food for a trail run.

Another option, which includes bribery, would be to take him on vacation where you control the food. Camping for a week out of easy reach of a store might work.

JerryK Community Regular

Funny, because today I've been pounding on him, trying to wear him down. He was telling me today he was feeling kinda crappy...coincidentally he had a large subway sandwich for dinner last night.

I was able to list his symptoms for him. :P Which he found quite shocking.

tarnalberry Community Regular

there isn't much research that I've seen that suggests a link, and I look up fibro research on pubmed often. there's correlation between fibro and irritable bowel syndrome, but take that inference as far as you want, the research doesn't take it any farther. quite frankly, if he's wanting hard evidence, you're not going to find any to give him.

I might suggest another approach.

perhaps saying, "hey, we've got the same genes, and while some things are different, some are the same. I worry about you not feeling better. will you try this with me, just to humor me? try it, for two weeks, without cheating? come over and I'll cook for you; we'll have leftovers that you can have for lunch, and I'll set you up with good breakfasts and snacks. just for one month, humor me, see if it makes no difference. if there's nothing, no change, after that time, I won't say another word about it. but I can worry a little less that you're insides are being damaged like mine were."

if he says no, remember that he is an adult. he is your brother. just as you want him to respect your decision not to eat gluten, you should respect his decision to eat it, no matter what either of you think about your respective decisions.

trying to wear him down is awfully likely to just make him put his back up and get stubborn about it. I mean, if someone pokes you over and over again in the arm, and doesn't stop, do you start to approve of it?

RiceGuy Collaborator
there isn't much research that I've seen that suggests a link, and I look up fibro research on pubmed often. there's correlation between fibro and irritable bowel syndrome, but take that inference as far as you want, the research doesn't take it any farther.

I'll suggest looking at the articles I linked to in my previous post.

JerryK Community Regular

My mental health professional, who knows my story well, now agrees that my condition does indeed

appear to be exacerbated by gluten ingestion.

I related to him the fact that my brother has been diagnosed with Fibromyalgia and the first thing out of

my docs mouth was "well you know Fibromyalgia has been linked to gluten..right?"

Regardless, when you eat gluten and feel like curling up into a ball for two days, this is an indication that "perhaps I shouldn't eat that". Slowly getting thru to my brother I hope...

I dared him to go off of wheat for two weeks and then eat a big gob. He will be a believer after that.


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



Celiac.com Sponsor (A8-M):



Mom23boys Contributor
Funny, because today I've been pounding on him, trying to wear him down. He was telling me today he was feeling kinda crappy...coincidentally he had a large subway sandwich for dinner last night.

I was able to list his symptoms for him. :P Which he found quite shocking.

Good start!

We are trying to convince hubby's sister. I think you have to just keep presenting the info and those little "mind reading" stunts like you just did.

tarnalberry Community Regular

I should have been more careful in my wording - there aren't studies that I've seen that show any sort of causal relationship. The sources sited on the article above offer plenty of tantalizing evidence that the two conditions may be related. But saying "I see this here" and "I see this there", doesn't mean that here and there are connected. It doesn't mean they're not either, but a dyed-in-the-wool skeptic is probably not going to take that as evidence, so I skipped it.

For your brother's sake, though, Jerry, I hope I'm wrong and he won't ignore it.

AliB Enthusiast

A friend in the village has Fibro., as does my husband. I went to see my friend after I stopped gluten as I had seen people's comments on the forum that their Fibro got better when they went gluten-free. She said that interestingly, she actually went gluten-free for a three month period back last year and her Fibro was so much better. Unfortunately she visited her doctor and because she had lost weight and looked a bit on the thin side, he asked what she was doing and when she told him he sternly advised her to re-introduce the Gluten, which she did.

Now, she not only has the Fibro back with a vengeance, but a very persistent and tiring cough that has been with her since December. We had a chat and she said that she may try going back on to the gluten-free again. I did point out that it can take a lot longer than 3 months for the body to sort itself out and perhaps she needs to keep it going longer to give her body a decent chance to heal - I left her thinking about it.

My husband has been doing gluten-free with me since Jan. He still gets tiredness and fatigue at times, but he doesn't seem to be in quite so much pain, so it does look as if it may be benefitting him. He does occasionally allow a bit of gluten to pass through so that might have delayed his progress somewhat but one thing he has really noticed is that he is much more alert and able to concentrate. His 'nerves' are a lot better and he doesn't jump like he used to, and he generally seems to be sleeping better.

Your brother might notice a little difference after a week or two but it may take longer for any real benefit to be noticed. Obviously, in order for it to work properly and to give it a good trial, he would have to be extremely disciplined and careful not to consume any gluten at all. Some seem to think that if they just cut out the main stuff that will do, then when it doesn't work they can discount it, not realising they were still getting gluten, and haven't given it a proper trial at all!

Perhaps there are some out there who could post and give you their personal experiences and you could show your brother how it has helped them.

Worriedwife Apprentice

Another consideration is weight gain. If your brother is at all concerned about his weight, taking the Lyrica could be a problem. It definitely increases the appetite, and if he's eating things he shouldn't be it will only make things worse.

My husband is just stopping this medicine because it hasn't really seemed to help the fibro, and he's gained at least 20 pounds in the last six months.

RiceGuy Collaborator

Well, only you know how you're brother might take it, but seems this thread is quite compelling IMO.

curlyfries Contributor

I don't know if one month gluten free will be enough for him to see a difference in his fibromyalgia. It's been over 2 months for me and there's been no change as yet. However, there is a big difference with other issues :D . Hopefully he will see a difference in other ways that will motivate him to stick with it---provided you can get him to try it.

I would like to hear from others as to how long it took their symptoms to improve ( or not) and to what extent. I'm still holding on to hope for myself :P

Lisa

Jestgar Rising Star
Open Original Shared Link
Ursa Major Collaborator

I was on 50 - 100mg of codeine contin (depending on how bad the pain was) twice a day for five years (it's slow release and lasts for 12 hours) for the terrible fibro pain.

I was very ill from May to October of 2005, with unrelenting watery D and awful stomach cramps after trying a bowel cleanse, which apparently was the last straw and put me over the edge. My backache was getting worse every day, I could hardly move. My doctor told me to eat crackers and drink rice soup, which made it worse, of course.

Finally I figured out that gluten was the problem on October first. That Saturday morning I ate one slice of rye bread, and was doubled over with stomach cramps within a couple of minutes, and had to run for the bathroom within ten minutes, as the bread went right through me.

I finally clued in, went to the computer and put in 'celiac disease', and realized I've had all the symptoms for most of my life. Right there I stopped eating gluten.

By the next day the D stopped cold. The day after that my back started getting better. And within two weeks the fibro pain had nearly disappeared, and I was able to stop taking the codeine!

Unfortunately, after three months the pain started returning, as I was finally absorbing nutrients and my other intolerances showed up. After figuring out those, I've been fine pain wise. It is very rare that I have to take painkillers now, and usually means I ate something I shouldn't have.

So, while it may take a month to make a difference, it is also possible that your brother's fibro symptoms could dramatically improve within days, as that happened to me. Because in my case, the fibro appears to have been completely caused by intolerances (which apparently isn't true for everybody).

holiday16 Enthusiast

I haven't come across any research that makes an absolute connection, but I can say from personal experience that I am much better off of it. I was diagnosed after going gluten-free because I didn't want to be diagnosed before then since I knew something else was still going on and I didn't want them to just blame it on FM. With the symptoms that were left I was diagnosed with mild FM. However, I had a gluten exposure a year ago that set it off so bad I could hard walk for a couple days and that was just from cross contamination. I would hate to think how bad it would be if I actually took a bite of something with wheat in! I think if I were examined while on gluten the diagnosis would have been more than just mild.

One other thing to ask your brother would be if he has had his Vitamin D checked. It tends to be low in both people with celiac and people with FM. Probably not a coincidence...

I have to keep getting my levels checked and take a supplement or I have all kinds of problems with sleep etc. He should get it checked either way. Just make sure they check the right one. I've had the wrong one checked twice before and it's a hassle to get it done over.

wowzer Community Regular

Hi Jerry, It sounds like he just doesn't want to admit you are right. I have a little sister that is a diagnosed celiac from a year old. Of course, the doctors then told my parents that she would outgrow it. I think she started eating gluten around 13 years old. Eventually she found out that wasn't true. She has a long list of health problems including fibromyalgia. She cheats all of the time. She has to take painkillers to function. I can't believe that she doesn't get what the real problem is. I remember when I was going through itchy blisters and she told me I could have it. I didn't have her symtoms so thought that I was fine. I did finally figure it out and have been gluten free since January 1, 2007. Even my family doctor agrees that my immune system is doing so much better. I did go in today because I pulled a muscle in my chest and back from coughing. I keep trying to tell my Mom, she keeps getting bad itching. I wonder where my sister and I got this from!!! I do hope that brother believes you.

RiceGuy Collaborator

From all the discussions on this board about fibromyalgia, it sounds like I would've been diagnosed with it if I trusted in doctors enough to go to one. I couldn't even walk for over a year. Heck I could barely move.

Now I have none of those pains. Nothing. I took two supplements - methylcobalamin (B12) and magnesium. First was the B12, which helped, but didn't get me very far. Then I added the magnesium, and was on my feet in two weeks! I don't dare stop taking these. While I can't say it would work for everyone, I know it worked for me.

I can only point out that fibro, as with many diseases, has no known root cause. There are only characteristic symptoms. In contrast, we know what causes Celiac. Plus we know it causes deficiencies which lead to other issues. I think it's no wonder why the far eastern cultures are typically much healthier than the west. They don't consume as much wheat as the western world, nor many of the other things Americans do. Sadly, they are becoming more westernized all the time, and along with it the incidence of many diseases is on the rise.

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Scott Adams replied to Jhona's topic in Introduce Yourself / Share Stuff
      35

      Does anyone here also have Afib

    2. - Jacki Espo replied to CDFAMILY's topic in Related Issues & Disorders
      5

      Covid caused reoccurrence of DH without eating gluten

    3. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      1

      New Celiac Mama in My 30s

    4. - Mari replied to Jmartes71's topic in Coping with Celiac Disease
      2

      My only proof


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,959
    • Most Online (within 30 mins)
      7,748

    jenny44
    Newest Member
    jenny44
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • 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.