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

"internal Shaking" And Hand Trembling


flutterby

Recommended Posts

flutterby Apprentice

Hey folks,

I started introducing gluten again after the doctor said I could 'cheat' a little before my blood tests. Like everyone else, what this made me realize is that even with negative tests I will remain gluten-free!

Anyway, I was wondering if anyone else has experienced the following sensation after getting glutened. I refer to it as 'internal shaking' because it feels like my body is shaking all over, but there aren't any visible signs. After an hour or so, my hands start to tremble and my fingers twitch. It is usually accompanied by disorientation, concentration problems. Sometimes my fingers start to tingle.

When I was younger we thought this was hypoglycemia. It got better when I stopped eating "high carb" breakfasts (i.e. wheat, cereal, etc). So now I realize it must be a gluten or wheat reaction!


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



Celiac.com Sponsor (A8-M):



Looking for answers Contributor

There have been people on that have mentioned this. You may want to search, but I've read about it several times. Never experienced it myself though.

gf-soph Apprentice

Hey folks,

I started introducing gluten again after the doctor said I could 'cheat' a little before my blood tests. Like everyone else, what this made me realize is that even with negative tests I will remain gluten-free!

Anyway, I was wondering if anyone else has experienced the following sensation after getting glutened. I refer to it as 'internal shaking' because it feels like my body is shaking all over, but there aren't any visible signs. After an hour or so, my hands start to tremble and my fingers twitch. It is usually accompanied by disorientation, concentration problems. Sometimes my fingers start to tingle.

When I was younger we thought this was hypoglycemia. It got better when I stopped eating "high carb" breakfasts (i.e. wheat, cereal, etc). So now I realize it must be a gluten or wheat reaction!

I've had something similar, but for me it's not a direct gluten reaction. I had it for a while when I wasn't eating regularly enough, but was gluten free. At one point my drs medicated me for insulin resistance with metformin, but it made it so much worse. I discontinued it pretty quickly, and my insulin resistance was extremely mild. It may be that the gluten is throwing your blood sugar off?

I think I've also had that sensation when my B12 was too low. For me, glutening can make my B12 levels crash. I have no idea how, but i've seen it twice that I got glutened and my B12 levels crashed by several hundered points in a week or two. Might be worth getting those levels checked if you haven't already.

Also, if the blood tests you're mentioned are the gluten antibody tests, you need to be eating a LOT of gluten, not a little. If you aren't eating several serves of gluten a day for at least several weeks, possibly months, they could come back as a false negative.

There are plenty of other posts about this if you need some guidlines.

Sophie

flutterby Apprentice

Also, if the blood tests you're mentioned are the gluten antibody tests, you need to be eating a LOT of gluten, not a little. If you aren't eating several serves of gluten a day for at least several weeks, possibly months, they could come back as a false negative.

There are plenty of other posts about this if you need some guidlines.

Sophie

Thanks, Sophie. Basically, at this point, eating a lot of gluten for weeks or months isn't really an option. I'm not willing to be miserable just to get a positive diagnosis. I've already noticed some symptoms like problem with short term memory ... something I REALLY don't want to mess with. I brought this up with my doctor and he said we'll do the tests, but that they're not the only indicator he uses for a diagnosis, in part because he thinks that reintroducing gluten completely would probably be a bad idea for my health. He's basically THE celiac expert in the country where I live so we'll see what happens.

I think he's more concerned with ruling out that it's not something else besides celiac than getting a positive celiac test. That's more my concern, too.

I had never heard of the B12 thing ... interesting! I did have my bloodsugar levels tested a few years ago. The doctor said my levels weren't "enough to be considered hypoglycemic" but I should follow a hypoglycemic diet. Go figure. I always knew that it wasn't just SUGAR like they use in the test but sugar combined with wheat that made me get that way.

  • 3 years later...
across Contributor

I realize this is an old thread, but I just want to say that I get this, too! It's a terrible feeling! I had it last night. I was trying to figure out how I could have gotten glutened, and the only thing I could come up with is that we just had a whole bunch of drywall work done in our house, and there is a lot of drywall dust around (which apparently contains gluten).

 

It feels like my body is trembling and weak, and when it gets really bad, it even feels like my brain is trembling (hard to explain exactly what that feels like, but it is scary). I didn't get any sleep last night because of it.

 

If you're still around, were you ever able to figure anything else out about this?

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,546
    • Most Online (within 30 mins)
      7,748

    KimberlyAnne76
    Newest Member
    KimberlyAnne76
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Beverage
      I had a very rough month after diagnosis. No exaggeration, lost so much inflammatory weight, I looked like a bag of bones, underneath i had been literally starving to death. I did start feeling noticeably better after a month of very strict control of my kitchen and home. What are you eating for breakfast and lunch? I ignored my doc and ate oats, yes they were gluten free, but some brands are at the higher end of gluten free. Lots of celics can eat Bob's Red Mill gluten-free oats, but not me. I can now eat them, but they have to be grown and processed according to the "purity protocol" methods. I mail order them, Montana Gluten-Free brand. A food and symptoms and activities log can be helpful in tracking down issues. You might be totally aware, but I have to mention about the risk of airborne gluten. As the doc that diagnosed me warned . . Remember eyes, ears, nose, and mouth all lead to your stomach and intestines.  Are you getting any cross contamination? Airborne gluten? Any pets eating gluten (they eat it, lick themselves, you pet them...)? Any house remodeling? We live in an older home, always fixing something. I've gotten glutened from the dust from cutting into plaster walls, possibly also plywood (glues). The suggestions by many here on vitamin supplements also really helped me. I had some lingering allergies and asthma, which are now 99% gone. I was taking Albuterol inhaler every hour just to breathe, but thiamine in form of benfotiamine kicked that down to 1-2 times a day within a few days of starting it. Also, since cutting out inflammatory seed oils (canola, sunflower, grapeseed, etc) and cooking with real olive oil, avocado oil, ghee, and coconut oil, I have noticed even greater improvement overall and haven't used the inhaler in months! It takes time to weed out everything in your life that contains gluten, and it takes awhile to heal and rebuild your health. At first it's mentally exhausting, overwhelming, even obsessive, but it gets better and second nature.
    • Jsingh
      Hi,  I care for my seven year old daughter with Celiac. After watching her for months, I have figured out that she has problem with two kinds of fats- animal fat and cooking oils. It basically makes her intestine sore enough that she feels spasms when she is upset. It only happens on days when she has eaten more fat than her usual every day diet. (Her usual diet has chia seeds, flaxseeds, and avocado/ pumpkin seeds for fat and an occasional chicken breast.) I stopped using cooking oils last year, and when I reintroduced eggs and dairy, both of which I had held off for a few months thinking it was an issue of the protein like some Celiac patients habe mentioned to be the case, she has reacted in the same fashion as she does with excess fats. So now I wonder if her reaction to dairy and eggs is not really because of protein but fat.   I don't really have a question, just wondering if anyone finds this familiar and if it gets better with time.  Thank you. 
    • Chanda Richard
      Hello, My name is Chanda and you are not the only one that gose through the same things. I have found that what's easiest for me is finding a few meals each week that last. I have such severe reactions to gluten that it shuts my entire body down. I struggle everyday with i can't eat enough it feels like, when I eat more I lose more weight. Make sure that you look at medication, vitamins and shampoo and conditioner also. They have different things that are less expensive at Walmart. 
    • petitojou
      Thank you so much! I saw some tips around the forum to make a food diary and now that I know that the community also struggles with corn, egg and soy, the puzzle pieces came together! Just yesterday I tried eating eggs and yes, he’s guilty and charged. Those there are my 3 combo nausea troublemakers. I’m going to adjust my diet ☺️ Also thank you for the information about MCAS! I’m from South America and little it’s talked about it in here. It’s honestly such a game changer now for treatment and recovery. I know I’m free from SIBO and Candida since I’ve been tested for it, but I’m still going to make a endoscopy to test for H. Pylori and Eosinophilic esophagitis (EoE). Thank you again!! Have a blessed weekend 🤍
    • knitty kitty
      Yes, I, too, have osteoporosis from years of malabsorption, too.  Thiamine and magnesium are what keep the calcium in place in the bones.  If one is low in magnesium, boron, selenium, zinc, copper, and other trace minerals, ones bone heath can suffer.  We need more than just calcium and Vitamin D for strong bones.  Riboflavin B 2, Folate B 9 and Pyridoxine B 6 also contribute to bone formation and strength.   Have you had your thyroid checked?  The thyroid is important to bone health as well.  The thyroid uses lots of thiamine, so a poorly functioning thyroid will affect bone heath.  
×
×
  • 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.