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

New And Looking For Input.


solarpower

Recommended Posts

solarpower Rookie

Hi all, I have been visiting this forum for months and finally decided to join. First off I am self diagnosed. After discussing my issues with a number of people (my chiropractor and celiac friends) I was told to try going gluten free. I had almost immediate improvements. Here is my story;

Almost a decade ago I started having acid reflux symptoms. When the reflux continued to get worse I sought medical help. I was immediately prescribed acid reducers. Medication provided almost no relief. I continued visiting doctors over the years and none were willing to help beyond giving me reflux medication. I have tried almost every reflux medication there is and none helped me. As the years progressed my symptoms got worse and worse. When I had finally gotten to a point were I was "regurgitating" almost everything I ate, frequent shortness of breath, dizziness, muscle and joint pain I gave up. I was severly depressed, contemplating suicide and out of work. When some concerned friends with celiac asked what my symptoms where they insisted I avoid gluten for a while and see how I felt. Within days of going gluten free I had vast improvements. My reflux all but disappeared, my muscle and joint pain dissipated. I started feeling happier and more alert. I did this for several months until I started feeling tired all the time. I setup a visit with a gastroenterologist. The doctor wanted me to go back on gluten before issuing me the test. I tried it for 3 days before having to quit. I suffered more intense and immediate symptoms so I decided it wasn't worth it. I still experience general tiredness but have improved that with B12 supplements. I have been managing my condition fairly well for the last few months but now I am experiencing considerable weakness. I have a physical job and find myself sore and weak constantly. I'm not sure what to do to regain my strength. I try to get a healthy amount of protein, I take vitamins and probiotics. I haven't been able to get my strength back. Any ideas?

PS

here are the symptoms I have when I eat gluten:

vomiting, muscle and joint pain, brain fog, chills, flu symptoms, non-localized pain (mostly my left side) with arm twitching, sore jaw (painful chewing), trouble speaking clearly, and a scary "feeling like I'm dying" sensation (probably all in my head)


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



Celiac.com Sponsor (A8-M):



RiceGuy Collaborator

What kind of vitamin B12 are you taking? What vitamins are you taking, and what are the dosages?

How are your fingernails? The condition of the nails often helps to identify possible nutritional deficiencies. The skin around the nails can also be a good indicator.

Do your eyes adjust to different lighting easily, or does it take more time than for most people you know?

This might seem like a strange question, but have you noticed any change in the frequency of yawning?

solarpower Rookie

Riceguy- Thanks for the reply.

The B12 I'm taking is a methylcobalamin @ 1000mcg, I usually take one 3 times a day. The vitamin I currently use is by a company called Nature's Way, The product is Alive! Once Daily Men's Ultra Potency. As far as my fingernails go they seem pretty healthy although they don't seem to grow as fast as I remember. I can't say much about my skin since I work with my hands and they tend to get covered in various things (soldering flux, salt water, several types of cleaners). My eyes do take a little bit to adjust for light and dark extremes but I believe its normal. Since I experience weakness and tiredness I do yawn throughout the day. Although the tiredness has dropped off quite a bit since I started taking the B12. Being a guy I tend to ignore my body, so its difficult to say with any certainty exactly what has changed with the exception of the extreme symptoms i.e. the weakness, fatigue and soreness.

GF Lover Rising Star

This might seem like a strange question, but have you noticed any change in the frequency of yawning?

I'm curious about the yawning, I yawn constantly, like I need a deep breath but can't get it.

I hope I'm not hijacking this thread.

kittty Contributor

I had a sore jaw for years too. My dentist said it was TMJ, and took my wisdom teeth out to try and fix it. It didn't stop the pain or stiffness though. Very probably a gluten reaction. Like you I've had lots of different symptoms, and every now and then someone will mention something in this forum and it'll be another "AHA!" moment where I can link another issue from my past back to gluten.

How long have you been gluten free? Maybe you haven't reached your point of full healing yet.

RiceGuy Collaborator

Riceguy- Thanks for the reply.

The B12 I'm taking is a methylcobalamin @ 1000mcg, I usually take one 3 times a day. The vitamin I currently use is by a company called Nature's Way, The product is Alive! Once Daily Men's Ultra Potency. As far as my fingernails go they seem pretty healthy although they don't seem to grow as fast as I remember. I can't say much about my skin since I work with my hands and they tend to get covered in various things (soldering flux, salt water, several types of cleaners). My eyes do take a little bit to adjust for light and dark extremes but I believe its normal. Since I experience weakness and tiredness I do yawn throughout the day. Although the tiredness has dropped off quite a bit since I started taking the B12. Being a guy I tend to ignore my body, so its difficult to say with any certainty exactly what has changed with the exception of the extreme symptoms i.e. the weakness, fatigue and soreness.

Well, according to the company's website, the Nature's Way Alive! multi has wheat grass listed twice. Although I've read that the grass itself is gluten-free, I'd say contamination is practically guaranteed. The label doesn't claim it's gluten-free either. Anyway, the amount of magnesium is quite small, so I'd recommend a separate magnesium supplement. Some of the symptoms you mention could be due to magnesium deficiency. Magnesium is vital for energy production.

I've had good experience with the multi from NOW Foods called ADAM. It comes in both capsules and tablets, though I believe capsules are generally easier to digest.

If you haven't loaded up on B12 to overcome deficiency, you may still need a lot for awhile. So you might find it helpful to get the 5mg methylcobalamin, and take that for a month or two and see how it goes. I know it helped me quite a bit, and I did eventually switch to the 1mg. I've also found it helpful to take one 30-60 minutes before bedtime, for a deeper, more restful sleep.

As for protein, perhaps the types of protein you are getting can be better optimized, as well as the time you eat them. For instance, animal protein (meat, dairy, eggs) is generally more difficult to digest, and can therefor slow you down. A plant-based protein powder might help you. If you put the powder (along with any other ingredients you want) into a thermos, you could then take it with you, and all you'd need to do is add water. This way, it won't spoil if it doesn't stay cold, unlike making up the drink beforehand. Protein bars might also help, as might plain nuts and seeds. If you eat sandwiches, a nut/seed butter would help boost the protein value. Nut/seed butters also make a good spread for celery and other veggies, which could be eaten as snacks. Smaller meals with snacks in between may help reduce the digestive load while still providing the nutrition you need to keep energized throughout the day.

RiceGuy Collaborator

I'm curious about the yawning, I yawn constantly, like I need a deep breath but can't get it.

I hope I'm not hijacking this thread.

I mentioned it because when my health was at its lowest point (which was after going gluten-free), I never yawned, even though I was always exhausted.

I had a sore jaw for years too. My dentist said it was TMJ, and took my wisdom teeth out to try and fix it. It didn't stop the pain or stiffness though. Very probably a gluten reaction. Like you I've had lots of different symptoms, and every now and then someone will mention something in this forum and it'll be another "AHA!" moment where I can link another issue from my past back to gluten.

How long have you been gluten free? Maybe you haven't reached your point of full healing yet.

Agreed. And BTW, I also had a lot of pain from TMJ, which is now gone thanks to Glucosamine HCL. The one I take also has MSM in it, though I don't know how much that may have helped.


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



Celiac.com Sponsor (A8-M):



solarpower Rookie

Thanks for the info. It is much appreciated. I have only been gluten free for 6-7 months so maybe I still have some recovering to do. Thanks for the heads up on the vitamins Riceguy, I hadn't even considered my multi as a source of possible contamination. I will also try your other suggestions although snacking probably wont work for me with my on the go job. I've lost over 30 pounds since going gluten free and really need to gain some more muscle. It's been extremely frustrating trying to live life lately and only being able to barely make it through a work day just to crash at home for the evening. It makes for a non existent social life. I'll try upping the B12 and pick up a better multi.

solarpower Rookie

UPDATE

I skipped taking the Alive mutli this morning and did not experience the usual intense nausea I normally have every morning. I'm almost certain this must have been the reason! Took 5mg of B12 as well and already notice a difference so far just this half a day. Now to just find a good multivitamin.

RiceGuy Collaborator

So glad that you've gotten a positive response already. The best Men's multi I've found is the one I mentioned. You can check the details for it on the manufacturer's website: Open Original Shared Link

They also make similar products in tablet and softgel form, also under the same name, ADAM.

solarpower Rookie

Started taking the vitamins you recommended Riceguy. I'm anxious for this weakness/fatigue to go as it obviously interferes with work and life in general. I'm still in the process of eliminating hidden gluten sources in my diet. Just found out the sour cream I use has gluten! I imagine my symptoms will start improving once all traces are gone. Anyone know of a source of gluten free recipes, such as a cookbook?

RiceGuy Collaborator

There's quite a number of gluten-free recipes on this site. Here's a link directly to the recipe section: https://www.celiac.com/categories/Gluten%252dFree-Recipes/

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.