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

Face Numbness


whattodo

Recommended Posts

whattodo Enthusiast

hi i was just wandering if anyone else gets face numbness. I get it on the left side of my face and it comes and goes. There is no drooping or loss of movement.

I was just wandering if this is a sign of nerve damage or vitamin deficiency?

Anyone?


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



Celiac.com Sponsor (A8-M):



Fiddle-Faddle Community Regular

YES!!!

I had this on one side of my face. Doctor said on the phone that it was probably Bell's Palsy, but I kept insisting that there was no paralysis or dropping. (Sound familiar?) My thyroid meds were too high, and when they were dropped down, the numbness went away, but then it came back later (more mildly, though), and my thyroid levels were fine.

But since going off gluten, I haven't noticed a problem. I did see a rheumatologist about 6 months after going off gluten, who tested me for lupus. The tests were negative, and he said to stay off gluten (like I was really going to start eating it again???? :blink: )

Right before going off gluten, I got a terrible rash on my arms that I now suspect was DH. I wonder if my immune system was attacking my skin, both in the numb cheek and the arm rash?

Anyway, welcome to the club!

jerseyangel Proficient

I have facial numbness primarily on the left side. It's gotten much better since going gluten-free.

Before I was diagnosed, I also had numbness and an altered feeling in my arm, and both of these along with tingling in my legs. At that point, the facial numbness was constant and was accompanied by tingling and frequent feelings of intense heat.

I would say it took about 4 months on the gluten-free diet for most of these symptoms to begin to subside.

In my case, I'm sure it was caused by vitamin/mineral deficiencies. I was also severly anemic.

whattodo Enthusiast

Thanks for the response, in a funny way its comforting to know that is could be due to gluten. I am waiting for my blood results to see if i am a celiac. Do you think if taking vitamins would slightly help? Is so which one?

TrillumHunter Enthusiast

I had numbness in my face and soles of my feet. I also had the electric tingling in my arms. That was how a neurologist figured out I had super low b12. I started on shots and it got much better. I didn't realize how many numb places I had. :blink: Unfortunately she didnt figure out I had celiac disease. :angry: I had to wait five more years for that. I am hoping once my small intestines heal I can stop the shots.

Monica

Canadian Karen Community Regular

It also happened to me. I remember once in my early 20's, I was at work and all of a sudden the whole right side of my face went numb. Again, no drooping though. Again, I was told it was Bell's Palsy.......

Fiddle-Faddle Community Regular
Thanks for the response, in a funny way its comforting to know that is could be due to gluten. I am waiting for my blood results to see if i am a celiac. Do you think if taking vitamins would slightly help? Is so which one?

Well, there are a lot of variables.

If you ARE celiac or gluten-intolerant, then you need to be gluten-free so that your intestines can heal enough for you to actually be able to absorb the vitamins,and that could take weeks to months or longer, depending on whther or not you have damaged villi, and how extensive the damage, etc.

But are you relying on a blood test for your answer, on dietary response, or a combination of both?

Were you eating gluten (4-5 slice of bread or equivalent ) for several months prior to having blood drawn for the test? If not, your test will likely come up as a false negative, but don't count on your doctor to know that....BTW, what clued your doctor into checking you for celiac in the first place (maybe your doc is one of the good ones )??


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



Celiac.com Sponsor (A8-M):



whattodo Enthusiast
Well, there are a lot of variables.

If you ARE celiac or gluten-intolerant, then you need to be gluten-free so that your intestines can heal enough for you to actually be able to absorb the vitamins,and that could take weeks to months or longer, depending on whther or not you have damaged villi, and how extensive the damage, etc.

But are you relying on a blood test for your answer, on dietary response, or a combination of both?

Were you eating gluten (4-5 slice of bread or equivalent ) for several months prior to having blood drawn for the test? If not, your test will likely come up as a false negative, but don't count on your doctor to know that....BTW, what clued your doctor into checking you for celiac in the first place (maybe your doc is one of the good ones )??

I was experiencing stomach pain in the upper left side of my stomach 7 months ago. After a CT Scan i was diagnosed with diverticular disease in the transverse colon. After researching diverticular i realised that was not the problem. I was experiencing a constant dull pain. I did however change my diet to chicken, fish and vegetables. Along with fruit. So yes I was reletavely gluten free but i did eat things like oats, brown bread etc. This could be why i still have the pain. I went to my doc and told him i wanted to see a specialist. On seeing the specialist this week he said it must be 1 of 2 things. either ibs or Celiac. Like i said i have given blood and waiting for that response. I think whatever the outcome i will still continue with this diet and i love the fresh food etc. I do however want to know if this pain will subside and i can live a happy life????????

Fiddle-Faddle Community Regular

I wish I knew enough to give you an answer!

I do know, however, that IBS is a list of symptoms, not a disease. Those symptoms just happen to be identical to those of celiac. Many here (myself included) believe that IBS is a "trash bin" diagnosis, when the doctor has no idea what is CAUSING the symptoms, but gives you an official "diagnosis" of IBS and meds that may or may not mask those symptoms, but certainly won't address the cause.

At least, your doctor knows enough to consider celiac! (I am amazed how many don't)

Have you stopped eating gluten at this point, or are you waiting for the results of the blood work before you do so?

You don't need blood work or a doctor's permission to do so, as I'm sure you are aware; I was just trying to figure out if you still had the pain because you are still eating gluten, or if you still have the pain in spite of being off gluten, in which case, it might be a question of waiting long enough for your intestines to heal, or it might be caused by something other than gluten.

Sorry to be so long-winded!

whattodo Enthusiast
I wish I knew enough to give you an answer!

I do know, however, that IBS is a list of symptoms, not a disease. Those symptoms just happen to be identical to those of celiac. Many here (myself included) believe that IBS is a "trash bin" diagnosis, when the doctor has no idea what is CAUSING the symptoms, but gives you an official "diagnosis" of IBS and meds that may or may not mask those symptoms, but certainly won't address the cause.

At least, your doctor knows enough to consider celiac! (I am amazed how many don't)

Have you stopped eating gluten at this point, or are you waiting for the results of the blood work before you do so?

You don't need blood work or a doctor's permission to do so, as I'm sure you are aware; I was just trying to figure out if you still had the pain because you are still eating gluten, or if you still have the pain in spite of being off gluten, in which case, it might be a question of waiting long enough for your intestines to heal, or it might be caused by something other than gluten.

Sorry to be so long-winded!

For the last 2 days i have now eaten a gluten free diet. I am not waiting for results as this diet is not far from one i need to follow to keep my diverticular in order. Its healthy anyway......

The pain is still there but going to persist. I have a appointment to see a dietician next week which will help me with foods i can eat. Does celiac mean that the whole intestine is affected, i am just wandering how long it will take to clear up?

Fiddle-Faddle Community Regular

I sure hope that the dieticians in the UK know more than most in the states! Most here don't seem to know that Corn Flakes and Rice Krispies are not gluten-free, or that barley malt and soy sauce are on the no-no list! And I do believe that in the UK, wheat starch is officially considered gluten-free, but here in the states it's a total No-No.

Two days doesn't seem long by the standards of most here. I DID feel much better (no more cramping or bloating!)starting about 2 days in, but I probably had far less damage than you. It did take 2 full weeks til I stopped craving bread (hadn't found the good recipes at that point, and the store-bought gluten-free bread tastes like styrofoam to me)!

Most here report that it takes weeks or months to feel better.

Hang in there!!!!

With celiac, your immune system can attack anything: the whole intestinal system, your skin, your brain, your thyroid, your pancreas. Nothing is safe...

AndreaB Contributor

Definately make sure you have all your vitamin levels tested. B12 deficiency could cause tingling.....don't know if it does in the face though.

Another thing to consider if all your other tests come up with nothing and this hasn't resolved is to have testing done for lyme. I know Igenix in the US is the lab to use. Bells Palsy can be a sign of lyme but doesn't necessarily mean that is what you have. Just keep it in your mind if symptoms don't resolve, unless you want to run testing along with other tests. Most labs aren't reliable so if you go for lyme testing search out a lyme board in the UK to find out which lab is reliable.

whitball Explorer

I used to have numbness of my chin, lips and the left side of my face. In addition, my tongue used to twitch. I have not had this since I went gluten-free in February 2006. What are the symptoms of low b12?

AndreaB Contributor

The following site has b12 information.

http://www.nlm.nih.gov/medlineplus/ency/article/000574.htm

whattodo Enthusiast
The following site has b12 information.

http://www.nlm.nih.gov/medlineplus/ency/article/000574.htm

May be a silly question but would this show up in a full blood count test? I have had this 7 months ago and was normal

AndreaB Contributor
May be a silly question but would this show up in a full blood count test? I have had this 7 months ago and was normal

I'm not sure about that but my assumption has been that you always have to ask for vitamin levels to be checked.

whattodo Enthusiast

For everyone who has has facial numbness, how long did they have it concecitavely. I have had mine for about 4 days now and not sure if i need to go back to the doctors. This is not the first time i have had it neither. I have had it once before about 2 months ago. I have my blood results coming back in 7 weeks but cant help but feel slightly uneasy that i need to wait that long to do anything about it. I do have a MRI scan on friday but hopefully that will be fine.

whattodo Enthusiast
I have facial numbness primarily on the left side. It's gotten much better since going gluten-free.

Before I was diagnosed, I also had numbness and an altered feeling in my arm, and both of these along with tingling in my legs. At that point, the facial numbness was constant and was accompanied by tingling and frequent feelings of intense heat.

I would say it took about 4 months on the gluten-free diet for most of these symptoms to begin to subside.

In my case, I'm sure it was caused by vitamin/mineral deficiencies. I was also severly anemic.

Jerseyangel did you ever feel like you were about to have a stroke with the numb face. This seems to be a big worry with me.

jerseyangel Proficient
Jerseyangel did you ever feel like you were about to have a stroke with the numb face. This seems to be a big worry with me.

It's really interesting that you should ask me that. Yes--one evening, on a Friday, I did get worried enough to call my doctor. This was about a week into the diet--and the numbness and tingling just got much worse, sort of all of a sudden.

Since it was pronounced on the left side, I panicked and actually thought about going to the emergency room. My husband thought I should call the doctor first, and I'm glad I did. Just speaking with her brought my anxiety level down.

I really think that it peaked at that point, and then slowly began to subside--it took a while, though.

Calikat4 Rookie

I completely forgot about this -- I used to get face numbness ALL the time (pre diagnosis). Then, one day when I had to get an IV due to dehydration (yikes, the things that happened before my appropriate diagnosis!) I had the numbness again and was told that the 2 were possibly related.

  • 6 years later...
Suzy12345 Newbie

hi i was just wandering if anyone else gets face numbness. I get it on the left side of my face and it comes and goes. There is no drooping or loss of movement.

I was just wandering if this is a sign of nerve damage or vitamin deficiency?

Anyone?

I could cry reading this post 

YES !!!!!!!!!!     I have started to find some answers

I started to loss the feeling in my face about 2 years ago ,and like most people the left side

I have seen heaps of Neurologist  and no one could figure out what was wrong and why  

 I had a lap band done a year ago and that natural cut out a lot if gluten based foods from my diet.over the last 6 months my face numbness has lessoned very slowly but it has got better and better .  I had my band lossend and started to eat things like bread again and that is when i notice the worse stomach pains and my face numbness return with the worse pain ever.

i have had my testing done and changed my diet and if i slip with gluten my face numbness tells me about my mistake before my tummy 

i also have head fog so bad that i had to change jobs 

i can't wait to see my neuro again and tell me ,  

finding other people with the same makes me feel i am not insane , not imagined the systems. which i am sure some Doctors thought i was nuts or just saying it for attention

OMG 

i am so happy right now 

thank you all for sharing your stories 

I am only one week into Gluten Free and already i can start to see light at the end of the tunnel    

Celiac Mindwarp Community Regular

Hi Suzy

Welcome to the forum :)

So glad these posts have helped you.

Just to let you know this is an old thread, and the original posters may not be about. Hopefully there will be some new ones to chip in their experiences.

Do ask lots of questions. Most of us have made it through the gluten free transition and can help out if you have any wobbles. Great you are already getting improvements.

  • 2 years later...
JKS1221 Newbie

My numbness isn't in my face, it's around my waist. However I have had numbness in my face and my whole left side, but the numbness in my waist is constant. Does anyone suffer with this?

  • 3 years later...
Clarice Sage Newbie
On 4/28/2007 at 1:11 PM, whattodo said:

hi i was just wandering if anyone else gets face numbness. I get it on the left side of my face and it comes and goes. There is no drooping or loss of movement.

I was just wandering if this is a sign of nerve damage or vitamin deficiency?

 

Anyone?

I had numbness on the left hand side of my face and earache - quit all wheat products and gmo products. If I touch a non-organic diet it comes back immediately. This has nothing to do with gluten. We are being poisoned by glysophate and all the rest. Go organic if you can.

Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!

Register a new account

Sign in

Already have an account? Sign in here.

Sign In Now
  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - cristiana replied to Colleen H's topic in Gluten-Free Foods, Products, Shopping & Medications
      16

      Ibuprofen

    2. - Mari replied to KathyR37's topic in Coping with Celiac Disease
      5

      New here

    3. - Colleen H replied to Colleen H's topic in Gluten-Free Foods, Products, Shopping & Medications
      16

      Ibuprofen

    4. - Colleen H posted a topic in Coping with Celiac Disease
      0

      Methylprednisone treatment for inflammation?

    5. - cristiana replied to Colleen H's topic in Gluten-Free Foods, Products, Shopping & Medications
      16

      Ibuprofen


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,879
    • Most Online (within 30 mins)
      7,748

    Peta Dunn
    Newest Member
    Peta Dunn
    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

    • cristiana
      Ferritin levels.  And see what your hemoglobin looks like too, that will tell you if you are anemic?  You can have 'low normal' levels that will not be flagged by blood tests.  I had 'low normal' levels, my lab reading was. c12, just over what was considered normal, but I had small benign lesion on my tongue, and sometimes a sore mouth, and a consultant maxillofacial ordered an iron infusion for me as he felt my levels were too low and if he  raised them to 40, it would help.   Because you are not feeling 100% it might be worth looking at your levels, then discussing with your doctor if they are low normal.  But I stress, don't supplement iron without your levels being monitored, too much is dangerous.
    • Mari
      Hi Katht -  I sympathize with your struggles in following a gluten-free diet and lifestyle. I found out that I had Celiac Disease a few months before I turned 70. I just turned 89 and it has taken me almost 20 years to attain a fairly normal intestinal  function. I also lost a lot of weight, down to 100 lb. down from about 140 lb. What Trents wrote you was very true for me. I am still elimination foods from my diet. One person suggested you keep a food diary and that is a good idea but it is probably best just to do an elimination diet. There are several ne and maybe one for celiacs. I used one for a while and started with plain rice and zucchini and then added back other foods to see if I reacted or not. That helped a great deal but what I did not realise that it would only very small amounts of some foods to cause inflammation in my intestine. Within the last few years I have stopped eating any trace amounts of hot peppers, corn and soy(mostly in supplements) and nuts, (the corn in Tylenol was giving me stomach aches and the nuts were causing foot pains). Starting an elimination diet with white rice is better than brown rice that has some natural toxins. In addition it is very important to drink sufficient plain water. You can find out how much to drink for your height and weight online. I do have difficulty drinking 48 ounces of water but just recently have found an electrolyte supplement that helps me stay well hydrated, Adding the water and electrolytes may reduce muscle cramps and gag spams you wrote about. . Also buy some anti-gluten enzyme capsules to take with meals. I use GliadinX advertised here. These are a lot of things to do at one time as they reflect my 20 years of experience. I hope you do what you can manage to do over time. Good luck and take care.
    • Colleen H
      Yes thyroid was tested.. negative  Iron ...I'm. Not sure ... Would that fall under red blood count?  If so I was ok  Thank you for the detailed response..☺️
    • Colleen H
      Hi all !! Did anyone ever get prescribed methylprednisone steroids for inflammation of stomach and intestines?  Did it work ??  Thank you !! 
    • cristiana
      Hi Colleen Are you supplementing B12/having injections? I have learned recently that sometimes when you start addressing a B12 deficiency, it can temporarily make your symptoms worse.  But it is important not to stop the treatment.  Regarding your problems with anxiety, again that is another symptom of a B12 deficiency.   I didn't know what anxiety was until it hit me like a train several months before gastrointestinal issues began, so I can certainly relate.   Two books which helped me hugely were At Last A Life by Paul David (there is a website you can look up) and The Depression Cure: The Six-Step Programme to Beat Depression Without Drugs by Dr Steve Llardi.  Although his book is aimed at people who have depression, following the principals he sets out was so helpful in lessening my anxiety.  Llardi suggests we need to focus on getting enough: - physical exercise - omega-3 fatty acids - natural sunlight exposure - restorative sleep - social connectedness - meaningful, engaging activity   ... and we should feel a lot better. That is not to stay you must stop taking medication for depression or anxiety if you have been prescribed it, but adopting the changes Dr Llardi sets out in the book should really help. Can I just ask two more questions:  1) you say that you are B12 deficient, did they test your iron levels too?  If not, you really ought to be checked for deficiency and, 2) did they check your thyroid function, as an overactive thyroid can be cause rapid heartbeat and a lot of coeliacs have thyroid issues? Cristiana        
×
×
  • 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.