Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Tingling, Buzzing And Twitching


cristiana

Recommended Posts

cristiana Veteran

Hello All

 

Well it is nearly two years now since my gastro symptoms started, although I think I could say that before that I had tingling in my fingers, buzzing on the back of my legs, twitching in my face, for about six months - minor but annoying.  I was then diagnosed with celiac disease in the Spring of 2013. My blood iron and B12 levels were very low so I took supplements, plus magnesium and cod liver oil and all this nerve stuff faded, with a few blips en route.  

 

Odd thing some of this tingling and buzzing has started up again over the last three weeks although the twitching hasn't (yet!).    I am as strict as I can be with avoiding gluten.  The only thing that is happening at the moment is I am going through a raft of tests for other conditions and I do feel a bit edgy about them at times.  Do you think anxiety in itself can reignite old nerve problems?  Is there anyone out there who gets this nerve stuff come back from time to time?  

 

In case of interest, I have had some MRIs on my brain and spine since DX which were all entirely normal.

 

Thanks.


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



Celiac.com Sponsor (A8-M):



icelandgirl Proficient

Hi Cristiana,

I think that stress and anxiety can bring out our physical ailments or make the existing ones worse. That's been my experience at least.

I have also had tingling in my feet, toes and fingers. I always wonder if it has something to do with my thyroid because that thing is having issues.

Have you had your b12 and ferritin levels checked recently? If not it might be worth having them checked.

In the meantime, take good care of yourself...a nice Epsom salt bath with a good book is my favorite. Or go for a nice walk or just whatever feels good to you.

It does feel, to me at least, that there is always something.

(((Hugs)))

cristiana Veteran

Do you know, Icelandgirl, there is always something!  I think I shall change my user name to alwayssomething.   Just back from hospital tests on Friday, looking forward to a bit of a breather until the next blood tests, and then this buzz in my face starts up again!  And in my legs! I am thinking I will go private to get my iron and B12 checked again.  My nutritionalist told me when my B12 level wasn't improving much with supplements that she was surprised I wasn't offered an injection just to get me started back on the right track.  I have lapsed with the sublinguals so perhaps it is time to take them again, religiously.  Thank you for your tip about the bath with Epsom salts, that sounds a really good idea too.

icelandgirl Proficient

If you do that I shall change mine to alwayssomethingtoo. Because that's what it feels like! I do think getting the levels checked is a smart idea. If they're low you know that supplementing can help. I get very annoyed with my tingling when it becomes pronounced...it can be hard to ignore.

janpell Apprentice

Do you get all over tingling? Do you have inflammation that may be compressing nerves in that area? When my knee swells I get tingling down my leg because I think my nerves are compressed. I hate it so much. I find if I eat too many sweets (had a prune binge over a couple of days) and noticed an eye twitch during this time. I am staying away from fruit all day and so far so good - I don't really eat sugar but over indulge in some natural sweets at times and get bothered by even that. I have no idea where any of this comes from but my own conclusions what is happening with me.

cristiana Veteran

janpell... hi.  Not all over tingling.  The ball of my left foot, around the ankle; sometimes in the toes (left and right); sometimes up the back of my left calf; a spot on my right calf; I sometimes wake up feeling my fingers have gone to sleep (I do have a DX for carpel tunnel and ulnar compression but some days are definitely worse than others) and the odd twitch and buzz on my face.   I took a good dose of magnesium the other day and the facial twitching ended overnight. Maybe it is partly inflammation, not sure?  I think malabsoption might also be the cuprit - and as icelandgirl says - stress.  One phenomenon I have noticed is since around DX if I get pins and needles, say, after kneeling for a while or sitting in a bad position, it takes much longer to recover.  I asked a clinical neurologist about this and he says after having had all these deficiencies our nerves start to complain.   I am beginning to think that my gut can't have healed as well as I'd hoped if my nerves are still complaining!  

  • 3 weeks later...
MomBTired Newbie

Read about small fiber neuropathy. My son has the automatic one. His neuromuscular doctor told us that many people who have celiac end up with this form of neuropathy.

 

Open Original Shared Link


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



Celiac.com Sponsor (A8-M):



cristiana Veteran

Hi MomB - thanks for sharing.  Apart from all the other things I mention, I have noticed that for about a year now I have found it really painful on one side of my body if I wear tight clothing.  I thought it might be shingles without the rash - a line along my chest to my spine on the left, it has really hurt to the point of it feeling almost like a burning sensation.  I had the same thing on my left hip round to my spine.  If I wear tight waistband or bra I still feel bruised there.   It is a pain which gets worse as the day goes on, I don't have it at night but at night I wear loose pyjamas.   I wish I knew what it was caused by - celiac, shingles.  All I know is I didn't have it pre-diagnosis!

  • 1 month later...
cristiana Veteran

Back on this topic, again.  I am thinking about going back to my doctor as I do think I have small fibre neuropathy symptoms returning to the levels I had at DX -   MomBTired's posted link has really made me think.   I guess I could have blood sugar issues but I am not so sure.  In recent months I have stopped supplementing and the tingles and buzzes have got worse.  However, in the last couple of weeks this has prompted me to go back on magnesium, B12 and other B vitamins and I believe I am already feeling the benefit.

 

I have also found the following link helpful and I realise, in reading it, I need to go back to trying to get more calcium in my diet, too.  Posting all this in case it is of help to anyone else.

 

Open Original Shared Link

icelandgirl Proficient

That was a good read Cristiana. I wonder sometimes if I'm getting the right nutrients. Besides cutting out gluten and soy, I'm very dairy light. I don't know if I get enough calcium or magnesium or any of the B's. So much of the gluten food I used to eat was fortified with all of this. If you look at the breads, cereals, pastas that contains gluten they have a lot of vitamins and minerals. Most of the gluten free ones don't. So...how do we know if we're getting enough? I don't know. Thanks for sharing that...lots to think about.

cristiana Veteran

I don't understand why gluten-free alternatives aren't fortified in the way that mainstay stuff is, such as bread and cereals, here in the UK.   I am sure we need the vitamins more than the average person!

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      127,950
    • Most Online (within 30 mins)
      7,748

    Malik
    Newest Member
    Malik
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121k
    • Total Posts
      70.5k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • cookiesyum
      The easiest way to remember the difference between the cholesterol types is HDL;   H=healthy equals healthy (omega 3, 7, limit 6 & 9 MCFA'S =Medium Chain Fatty Acids. 3= coconut oil, 7= sunflower oil, avocado. The higher your HDL the healthier you are & less likely to experience strokes, clogged arteries Etc. You can even use cold expeller pressed coconut oil on your skin and that is the best kind of coconut oil to eat as well. You want your HDL much higher than your LDL, it will help you stay healthy.   LDL;    L=Lousy. Meat fats, processed fats.  The higher your LDL is the more likely you will have strokes, clogged artery is, heart disease, fatty liver.   Then there's lipids... they are the culprit to be blamed for many heart attacks and things like that they are very small round particles that transport fats. You can have a low overall cholesterol reading and most of it be healthy cholesterol and have a ton of lipids and there's nothing you can do to change the lipid count. High number of lipids is very dangerous.   I'm going on statins is extremely dangerous if you ask me it's just completely my opinion, because I have seen so many of my elderly friends bleed to death internally because of the statins. I mean you wouldn't take all the oil and grease out of your car or a motorcycle and then try to drive it that way would you? You see that's what statins do they remove all of your bodies fats and it doesn't matter whether it's healthy fats or a lousy fats. It removes all of them and then your body can't function properly. You have to have fats to keep your skin supple and to stay warm. Your body also needs fats to digest & process certain nutrients, amino acids & vitamins.   Your brain is composed of fat so is that something you really want to remove with a pill every morning and night?   The thing about statins is that they also make the blood vessels and capillaries permeable. So this is how my friends who were on cardiac medication for a long time and statins ended up bleeding internally to death.   If you want to make sure that your heart is healthy, take odorless garlic at night and magnesium, vitamin K & calcium.     
    • pdm1981
      It's also a symptom of EPI.
    • Wheatwacked
      Yes.  Proportionately a small piece to a toddler is like a whole slice to an adult.  This is an important clue.  She was doing well, accidentally ate gluten and later the old behavior returned. I remember reading posts here of people reacting to a kiss from someone who had just eaten gluten. Recent research indicates that 40% of first degree relatives of someone with Celiac have undiagnosed Celiac Disease.  Father, mother, siblings.  There is a whole list of symtoms of "silent celiac".  Here is an article of symptoms possibly mistaken for other causes than Celiac Disease.  When I finally stopped gluten at 63 years old, I counted 19 things that improved, including lifelong mouthbreathing.  I never smelled bad things, so I as a kid, I learned to respond to the other kid's response in order to not seem weird. I really recommend you pursue testing for all the family if you can, and the whole family following GFD.  It is difficult at first, but the benefits will be worth it.  
    • Visionaerie
      I get these but where we are, they are called chicken potstickers. I would obviously suggest that it is the ginger in the product that is causing a stimulative digestive effect! So you might want to do what I do, just cook one of them with the rest of your meal so you don't have the same effect. I love the Feel Good products but they are on the expensive side. (I also drink Reed's ginger brew so in general, ginger is a friend of mine..when delivered at the right dose). Hope this helps and have a warm healthy week!
    • ognam
      Has anyone had Steatorrhea (oily/fatty poop) as a temporary glutening symptom or should I be concerned I've introduced chronic gluten somewhere (like in meds)? I haven't gotten Steatorrhea since before I went gluten free. However, I moved in the past few weeks and haven't been as careful - I've eaten at restauraunts with cross contamination but only experienced minor symptoms like headache. The past week, I ate only gluten free food at home except I went to Red Robin and got fries (told them gluten-free; allergy). The next day I had Steatorrhea and the day after that.   I know it's a symptom of malabsorption so I was wondering if it was the kind of thing that could be caused by one event or if it was due to a more chronic issue. Of course I will speak to a GI but I recently moved and need to find one.   Thank you for any info
×
×
  • Create New...