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

Do Neuralogical Symptoms Go Away?


frenchiemama

Recommended Posts

frenchiemama Collaborator

This question is on behalf of my mom. I'm a recently diagnosed celiac (I had raging DH for 2 years and was only diagnosed 3 weeks ago :blink: ) and although my mom hasn't been formally diagnosed yet (she goes in next week) I'm just sure that this is what is wrong with her.

She has been sick for her whole life, getting worse and worse for at least the last 25 years. She has severe migraines, ataxia, vertigo, unexplained seizures, transient numbness in her extremities, severe stomach/intestinal symptoms, etc.

For the last 25 years she has been tested for everything under the sun (except celiac) and been told that she is crazy and needs a shrink instead of a doctor.

My question is, how much of this damage is permanent? It makes me really sad to think that she could have a normal life right now if she had been diagnosed long ago. She can't work and can't drive because of this. Is she going to get better?


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



Celiac.com Sponsor (A8-M):



KaitiUSA Enthusiast

If she is celiac then by going on the diet should help with the symptoms. I can't guarantee anything because everyone is different but she should.

judy05 Apprentice

Frenchiemama,

I was diagnosed at the age of 62, just in time for retirement B) I was like your Mom always sick, people don't believe you and attribute it all to stress,overwork,etc. I suffered with environmental allergies, got allergy shots for 20 years, also had thyroid problems and a lot of headaches, numbness in fingers, migraines, vertigo, you name it I had it. By pure luck I started to have GI symptoms that wouldn't go away and after all those years found a GI doc who listened and began testing me. Although I tested negative for Celiac, my IGA was high,about 75. He suggested a gluten-free diet and I immediately started feeling better. Most of the neurological symptoms lessened or went away completely. When I gave up dairy I felt my head clear up, no more brain fog and even my eyes felt better. I later tested myself at York labs and found I am intolerant to corn, egg whites, cow's milk, yeast and of course wheat. I wasted a lot of years feeling sick but I'm glad to know that it wasn't all in my head. I have days when I feel sorry for myself, that's when I come on here, it helps to know that we aren't alone and others are experiencing the same problems. Tell your Mom that the diet really works, but it takes time, it has been a year and a half for me.

gf4life Enthusiast

I've read a few articles that indicate the neurological problems associated with gluten do not always go away. They can sometimes get better, but not always.

It seems that if the symptoms have just started within a short time before being diagnosed they have a greater chance of being helped by the diet, but the longer you have had the neurological problems the less chance you have of the gluten-free diet helping to relieve those symptoms. Six months or less from onset of symptoms seems to be the common idea in the different articles I've read. Over six months and the symptoms might not go away.

My son and I both have migraines and I had some painful tingling and numbing in my extremities. The migraines we have both had for years and those have not gone away, but the tingling had started a few months before I went gluten-free for good, and that did go away.

I can't say that your mother would not benefit from the diet. If she is Celiac, she should be on the gluten-free diet, regardless of whether it makes all her health problems go away. But sometimes the damage is more permanent...especially when it is neurological.

Open Original Shared Link

https://www.celiac.com/st_prod.html?p_prodi...-11105480250.11

https://www.celiac.com/st_prod.html?p_prodi...-11105480250.11

frenchiemama Collaborator

Thanks everyone for your replies.

I am hopeful that at least *some* of her problems will get better. I guess if nothing else her GI problems should improve and she won't get sick from every single thing she eats anymore. I guess we'll just have to wait and see.

It makes me really angry that so many of those doctors she went to didn't even seem to take her seriously at all. I know that it's not right, but I blame them for her condition. She is only 53 but she seems like a little old lady.

Guest nini

in my case, the seizures have gone away completely, so has the brain fog, but the tingling and numbness in my extremities is still very very present. I'm 2 years gluten-free now and I will be 36 tomorrow. I'm hopeful that the longer I am gluten-free, the better I will feel.

gf4life Enthusiast

There is a really good article in the Winter 2004 Scott Free Newsletter titled- When Gluten Gets On Your Nerves, that basically details all the best parts of these links that I have given you (and also other articles). If you don't already get this newsletter, I highly recommend it. When you get a subscription you will have access to all the old issues online. Just click on the "Newsletter" link in the upper left hanf side of the screen here on the message board and it will give you instructions on how to get it.

God bless,

Mariann

(I am a moderator here on the message board, but I do not get anything out of promoting the newsletter. It is just a really good source of gluten free information about current medical issues regarding Celiac, food related issues and recipes, as well as adds for gluten-free products.)


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



Celiac.com Sponsor (A8-M):



  • 1 month later...
citygirl114 Newbie

Brain fog is one of my worst symptoms... :blink:

I have been gluten free for about 5 mnths now and it is not improving. I work in the financial industry and find it extremely upsetting when I notice I have made errors. I have recently gone on short term disability due to the pain & fog I have been experiencing. The forgetfulness is getting out of control. Left a frying pan on the stove the other day and forgot to turn the burner off.... this is so stressful I feel as if I am losing it big time....going back to the doctors today to see if he has any suggestions..... anyone have an suggestions.....

:(

judy05 Apprentice

Have you tried going dairy or even casein free? It took me a few months to realize that dairy and sometimes soy were causing a lot of problems. I did a York test and found that I am intolerant of corn, egg whites, cow's milk, yeast, and of course wheat. Maybe you have other intolerances along with gluten. Oddly my test did not show intolerances to barley, rye and oats! I haven't tried any of them yet, but did have a bad reaction to oatmeal before I took the tests.

My biggest problem is my GI doc. He told me that I needed to go gluten-free when I first saw him and my IGA was elevated. After he tested me for the gene, was neg for celiac disease he now tells me that I can eat wheat and drink milk. He says I am using the gluten-free diet as a "placebo"! I think he is schizophrenic! He was the only one to help me, after many years of trying to find out what was wrong with me. After this I won't be needing him anymore.

citygirl114 Newbie

Hi Judy

I havent tried the dairy free as I hardly ever consume any dairy products. I do take calcium though...not sure what casein is?????

Saw my doc today he said the brain fog is just because I am not feeling well...I think I should put him in a canoe and send him out to sea!!!!

Guest Eloisa

Casien is milk. Brain fog is part of being Celiac since you don't absorb what you consume well. You can remove the dairy but sometimes not even that makes the fog go away.

marycubs Rookie

Penny -

If your doctor hasn't checked your thyroid out yet, have that tested. A friend of mine had hypothyroid (low) and the forgetfulness, brain fog was very noticeable.

Mary

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      130,407
    • Most Online (within 30 mins)
      7,748

    Ripken
    Newest Member
    Ripken
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Pablohoyasaxa
      I feel your pain. Grain and gluten intolerant. Hang in there. This forum is very helpful
    • ElisaL
      IDK how common it is but it does happen. I'm celiac, allergic, and intolerant to the fiber in grains. (Fodmaps) So not only do I get sick from cross contamination, also gluten free wheat statch/fiber, and beauty products with wheat will get me. While I don't stop breathing the full body hives and short breath are not fun. Then once I make through that me and the bathroom become reacquaint. Sigh if I didn't feel so much better with the restrictions on my diet I'd feel sorry for myself. Least it makes for some good jokes about how the gremlin that lives in my gut really hates wheat. 
    • Wends
      Hi Dora77. “Questions I Need Help With” “1. Is it realistically safe to eat food my mom cooks…” YES - you wouldn’t be here if it wasn’t for your mother. Trust she still knows how to take the best care of you in her own way. Mishaps and cross contamination may happen - will happen on occasion, in fact - that’s life. But for the bulk of it as long as you’re aware of cc and try to avoid it for the most part, don’t sweat the small stuff! See the gluten free diet as a process. Own the process, Do Not let the process own you! “2. Do I need to worry about touching doorknobs, fridge handles, light switches, etc. that family members touched after eating gluten? What about public places like bus handles or school desks? Or like if i went to the gym, I would be touching stuff all the time, so there will be small amounts of gluten and those would get transferred on my phone if I touch my phone while in the gym. But I want to knos if it would be enough to do damage.” NO - this is OCD brain at its best! Hijacking your thoughts and justifying it because of the very real fear of gluten contamination. That’s OCD all over. Like a devil in the driving seat. Fears that are based on some kind of reality are hard to argue with. Boss it back! Recognise this for what it is. OCD using fear of gluten as its excuse to keep you entrapped. Own the OCD in this scenario, don’t let it own you. Normal cleanliness rules apply. Washing your hands before you handle food you’re putting in your mouth is fine. Washing after the gym is normal. Once daily cleansing wipe of your phone etc. Even if you did go rubbing your hands all over surfaces and licking them there might be a trace exposure to gluten possible. But I’m guessing you don’t usually do that sort of thing. Even if you inadvertently were to ingest trace gluten - it won’t be enough to do damage, no. It takes weeks to months of at least a few hundred milligrams of gliadin daily for the innate immune system followed by the adaptive immune system in coeliac disease to kick in and start producing antibodies and cause villous atrophy. “3. Is an endoscopy (without biopsy) enough to tell if my intestines are healed? I’d pay privately if it could help and if i dont get a refferal. Or do i need a biopsy?” Only biopsy, as the gold standard of diagnosis, can tell for certain if villi have recovered. Having said that video capsule etc. can give an indication of any inflammation. “4. Could my job (powder coating, sandblasting, etc.) expose me to gluten or damage my intestines through air/dust?” Assuming your employer provides all necessary PPE - appropriate mask and overalls etc. All you can do is take the precautions that are advised according to risk assessments and regulations of the relevant industry governing bodies? (I don’t know what this would be in the USA. Sorry. But there’s safety and governing regs in the UK for this sort of thing. Assuming it would be very similar over the pond in fairness). “5. Do I need certified gluten-free toothpaste, hand soap, shampoo, or moisturizer? (For example: Vaseline and Colgate don’t contain gluten ingredients but say they can’t guarantee it’s gluten-free.)” This comes down to personal threshold of gluten tolerance. People that are highly sensitive may need certified products. Especially those with dermatitis herpetiformis - the skin manifestation of gluten sensitivity. Listen to your body on this one. “6. Is spices like pepper with “may contain traces of gluten” safe if no gluten ingredients are listed? Or does everything need to be labeled gluten-free?” This one is easy - when following a strict gluten free diet, avoid products that say May contain traces of gluten. But it does not have to be labelled gluten free. There are many foods naturally gluten free. Having said that, there is nuance and personal tolerance threshold. If you’re super sensitive “may contain gluten” labelling is a godsend. But this kind of labelling is more aimed at informing customers with type 1 food hypersensitivity/ allergy reactions. The company is basically legally covering themselves, because there may be a risk of cross contamination. Not to be confused that it means there is cross contamination. In addition to products being labelled gluten free. Many products that are labelled can still contain gluten by the way - in fact any processed products labelled gluten free can still contain the allowable level of gluten (up to 20 parts per million according to Codex). A study was done not too long ago that showed gluten free processed products such as cereals, breads, flours etc. can and some are in fact contaminated and have above the legal allowable amount of gluten in them. While most gluten free products are fine for most celiac patients and tolerated, highly sensitive patients fail to heal fully if relying on processed gluten free products. The trace gluten exposure adds up for someone eating a typical western diet of gluten free cereal for breakfast, gluten free sandwich for lunch, gluten free pasta or pizza for dinner for example day after day, week after week. This is why, at least in the beginning after diagnosis, the gluten free diet should be one of whole real food - food that does not require a label. Meats, oily fish, eggs, beans, natural gluten free complex carbohydrates and vegetables according to custom and taste. Limit fruit as fructose worsens leaky gut and has been hypothetically linked to increased OCD and ADHD - Professor Richard Johnson published study on this recently. “7. Is continuing to only eat my own food the better choice, or could I eventually go back to eating what my mom cooks if she’s careful?” NO and YES. What you listed as your current, limited diet is nutrient poor. Correct it as soon as possible for your own sake and future health! Ditto what others have replied regarding vitamin and minerals that are lacking in malabsorption syndromes like celiacs and need replenishing. Gluten free products are not fortified. You were likely healthier, dare I say it, on a gluten containing diet for this reason. Your brain , and gut for healing and maintenance, needs lots of nourishment from omega 3s, B complex vitamins, folate, B12, iron, selenium etc. Meats, fish, natural fats that come with, do not fear - the brain is made of fat. Limit sugar, seed oils, and high glycemic cereals and fruit like bananas unfortunately as they can cause blood sugar highs and lows that can worsen anxiety in some people. Refined carbohydrates should be limited for the same reason. Fructose and simple sugars in excess feed the unhealthy gut bugs that wreak havoc with anxiety disorders like OCD. White potatoes can be problematic for some, also. It can take six weeks of elimination to see improvements. Note, consult your physician regards insulin adjustment if you reduce carbohydrates in the diet. Dr Bernstein diabetes protocol has worked for thousands. Ketogenic and low carbohydrate diets for mental and neurological conditions have shown improvements. Limited studies have and are being conducted under metabolic psychology and nutritional psychology. In a good proportion of anxiety disorders, mental, and neurological conditions including dementias, the brain is lacking nutrition and usable energy, not a drug. Similar in many autoimmune conditions, including celiacs, the prevailing hypothesis is that gut inflammation and resultant permeability allowing exposure to antigens begets triggering the genetically susceptible immune system response. Modern lifestyle exposure, one of the biggest being the food we choose to eat plays a huge role. Avoid ultra processed products, high in seed oils, refined grains, and sugar. Not just gluten can cause a leaky gut. Fructose, alcohol, egg white lysozyme, emulsifiers, added gums, the list goes on. “8. is cutlery from dishwasher safe if there are stains? Stuff like knives is used for cutting gluten bread or fork for noodles etc. I often see stains which i dont know if it’s gluten or something else but our dish washer doesnt seem to make it completely clean.” If in doubt have your own cutlery set, plate and dishes etc. for your sole use that you handwash yourself. Carry a camping fork/spoon set when out and about if needed. “9. I wash my hands multiple times while preparing food. Do i need to do the same when touching my phone. Like if i touch the fridge handle, I wash my hands then touch the phone. I dont eat while using my phone but i leave it on my bed and pillow and my face could come in contact with where it was.” That’s a classic OCD fear. Nothing to do with gluten as such. OCD brain is using gluten as the excuse here. I personally have the habit of using a cleansing wipe or dust cloth on my phone, nightly, that eases this sort of worry. For example a micro fibre dust cloth will do the trick, keep one on your nightstand? They are antibacterial as particles cling to the cloth. “10. Do i need to clean my phone or laptop if theyve been used by people who eat gluten? Even if no crumbs fall onto my keybaord, i mean because of invisible gluten on their fingers.”  NO. But again these OCD thoughts are hard to argue with. If in doubt, just a quick wipe with a cloth daily should suffice. Normal cleanliness practice. But if you don’t, or forget, don’t sweat the small stuff. “11. Does medication/supplements have to be strictly glutenfree? One company said they couldn‘t guarantee if their probiotics don’t contain traces of gluten.” Better if it is gluten free, yes. “12. I had bought supplements in the past, some of them say glutenfree and some of them dont(like the brand „NOW“ from iherb). I bought them and used them when i wasnt washing my hands so often, are they still safe? As I touched and opened them after touching door knobs, water taps etc. It was like a year ago when i bought those and even though i was eating gluten-free, I never worried about what i touch etc.” Still safe if do not explicitly contain gluten grains / derivatives AND if within the use by and use within dates. “I know this post is long. I’m just extremely overwhelmed. I’m trying to protect myself from long-term health damage, but the OCD is destroying my quality of life, and I honestly don’t know what’s a reasonable level of caution anymore.” Really hope these replies to your questions help. Just remember, in the midst of overwhelming thoughts and darkness under OCD clouded vision, the light and sunshine is always shining above. Take a moment or two when you are able in each day - even if it’s last thing at night - to meditate. Focus on something that you enjoy and appreciate. Or sit in a quiet space and try to relax and tune in to your higher self. Ask for guidance and soothing from your guardian angel. Over time it works but don’t worry if your brain is anxious. Eventually it will quieten down some. Try to focus on a real food, nutrient dense and naturally gluten free diet, this will help your anxiety and future health in the long run. Please eat real food - not cornflakes and sandwiches. Eat a steak, eggs or fish for example. Gluten exposures may happen, but don’t sweat it, dust yourself off so to speak, and carry on with a natural gluten free diet as best you can. Own your OCD don’t let it own you! Similarly, when it comes to a gluten free diet for celiac disease, own the process, don’t let it own you! You’re 18. That’s great. I’ve been managing OCD since childhood (in my 40s now. Many years of research, trial and error so to speak. Diet makes a difference. To quote Doc Brown to teenagers Marty and Jennifer, ‘ …your future hasn’t been written yet. No one’s has. It’s whatever you make it. So make it a good one.’
    • maryannlove
      Unfortunately not going to be able to let you know how Amneal is working because I still have almost 3 month supply of Mylan.  Had annual appointment with endocrinologist last week (though get scripts for blood work more often) and since was on my last refill, she sent new script to pharmacist.  Staying on my Mylan until it's gone.  (I tend to build up a supply because after trying a couple of endocrinologists for my Hashimotos, one finally got my thyroid regulated by my taking only six days a week instead of adjusting the strength which had me constantly up and down.  Will be forever grateful to her.  Apparently high percentage of folks with Celiac also have Hashimotos so all this relevant/helpful on Celiac.com.    
    • KimMS
      Thanks for sharing this! Have you started taking the Amneal? I'm curious how it's going for you. My pharmacy gave me the option of Accord, Macleod or Amneal. I didn't realize that Amneal was formerly Lannett, or I might have chosen that one. However, I did read some anecdotal reports that some people had side effects with Amneal, so I chose Accord. I have been taking it for 3-4 weeks and the past 10 days I have developed extreme fatigue/sluggishness, joint pain and some brain fog. I don't know if it is the new levo med, but nothing else has changed. Has anyone else taken Accord levo? Any issues? It seems to fall into the "no gluten ingredients, but we can't guarantee 100%, but it's likely safe category." I'm wondering if it is worth switching to Amneal or at least getting my thyroid levels checked. If the med is causing my symptoms, I'm guessing it's not because of gluten but maybe the potency is different from Mylan and I need different dosing. Accord was recalled for lower potency, but my pharmacist said the pills I have were not part of that lot.  
×
×
  • Create New...