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

gluten-free A Cruel Joke On Me?!


Cath724

Recommended Posts

Cath724 Apprentice

Hi all,

It's only been a week and a half that I've been gluten-free, but I'm really finding my symptoms very ironic--I was one of the "lucky ones" who was largely symptom-free before, but as soon I stopped ingesting gluten, I've gotten every symptom on the list! GI "issues," limbs keep falling asleep, fatigue, irritability, edema, ataxia, lactose intolerance, dry eyes, itchy skin, and the list goes on! I've read of the gluten withdrawal, but can anyone relate to my situation? Is it possible I'm already more sensitve and am unknowingly ingesting gluten somewhere, or is this normal for the silent type of celiac disease? It seems odd to NOW have all the symptoms that gluten causes...

Thanks (again!)


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



Celiac.com Sponsor (A8-M):



ShayFL Enthusiast

I felt worse before I felt better. So it is possible that it is withdrawal/detox symptoms. But also keep in mind that if you ate gluten regularly, that removing it all from your diet is a major change and your body will need to "figure" out the "new deal".

Also, what have you replaced the gluten with? Corn? Rice? It is possible that you increased another grain that you are sensitive too that is causing these symptoms.

It takes some sleuthing to find out the foods that bother you. I am a WIP myself. :)

cruelshoes Enthusiast

It is not uncommon to get worse before you get better. There can be a detox effect in a lot of people. Also, gluten has an opiate effect in the brain, and it can definitely cause withdrawl symptoms. Unfortunately, too, many find that their reactions to gluten get stronger the longer they are gluten free. I am one of those. Before I was DX, I would not notice a single gluten intake because I was sick all the time. But now that I am feeling well, if I get into the smallest crumb of gluten I get violently ill.

Have you rid yourself of as much gluten as is humanly possible? Checked all your meds, lotions, cosmetics? Do you use a shared kitchen? Have you replaced your toaster, wooden spoons, collander, etc.? Have you replaced all the condiments that are prone to double dipping - butter, PB&J, Mayo, etc? We all make mistakes in the beginning, and it is possible you are not being as gluten-free as you think you are. That's not an insult, we all have to work the steep learning curve of the gluten-free diet.

Cath724 Apprentice

Thanks for the advice. And I certainly don't take the questions on gluten as an insult, because I'm about as amateur as they come right now! Rather than get completely overwhelmed all at once, I've been trying to have a positive attitude about the whole situation and do a little research everyday (I'm on my second book, and reading these forums). To answer your questions, I've not eaten anything that either wasn't labeled gluten-free, or that I called the company first to confirm. My first and foremost obstacle will be eating the right foods, not just gluten-free ones--- I'm having a challenge getting my protein because I'm a vegetarian and all of the pseudo-meats (veg.burgers, sausages, etc.) where I live contain wheat, so I'm depending on AdvantEdge protein shakes right now to supplement. Basically, the high carbs and lower protein is likely why I feel so sluggish, on top of the withdrawal.

Thanks again! Any advice is always appreciated

purple Community Regular
Thanks for the advice. And I certainly don't take the questions on gluten as an insult, because I'm about as amateur as they come right now! Rather than get completely overwhelmed all at once, I've been trying to have a positive attitude about the whole situation and do a little research everyday (I'm on my second book, and reading these forums). To answer your questions, I've not eaten anything that either wasn't labeled gluten-free, or that I called the company first to confirm. My first and foremost obstacle will be eating the right foods, not just gluten-free ones--- I'm having a challenge getting my protein because I'm a vegetarian and all of the pseudo-meats (veg.burgers, sausages, etc.) where I live contain wheat, so I'm depending on AdvantEdge protein shakes right now to supplement. Basically, the high carbs and lower protein is likely why I feel so sluggish, on top of the withdrawal.

Thanks again! Any advice is always appreciated

We were looking for a protein snack last night. Popcorn has 6 grams of fiber and 6 grams of protein in 1/4 cup (I assume that is prepopping). I buy Natural Value, organic and pop it in unrefined coconut oil with no added butter and a dash of salt. Cook it in more oil if its too dry the first time. Its a healthy snack.

ericjourney Newbie

Cath--

Keep up the good work on finding wheat-free vegetarian alternatives. I like brown rice protein shakes, available at most health food stores. I recommend running it through the blender to dissolve well though.

And yes, I too felt worse before I felt better. Before diagnosis I ate gluten all the time, and I was just generally sick all the time. But now that I'm gluten-free and my intestines have had time to heal, I have a much stronger reaction to even a small amount of gluten contamination.

You're on the road to recovery. Stick with it.

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. - tiffanygosci posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      Aldi Pueblo Lindo Yellow Corn Tortillas

    2. - tiffanygosci replied to tiffanygosci's topic in Coping with Celiac Disease
      9

      New Celiac Mama in My 30s

    3. - trents replied to tiffanygosci's topic in Coping with Celiac Disease
      9

      New Celiac Mama in My 30s

    4. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      9

      New Celiac Mama in My 30s

    5. - cristiana replied to Jhona's topic in Introduce Yourself / Share Stuff
      38

      Does anyone here also have Afib


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,974
    • Most Online (within 30 mins)
      7,748

    LRB
    Newest Member
    LRB
    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

    • tiffanygosci
      Another annoying thing about trying to figure this Celiac life out is reading all of the labels and considering every choice. I shop at Aldi every week and have been for years. I was just officially diagnosed Celiac a couple weeks ago this October after my endoscopy. I've been encouraged by my local Aldi in that they have a lot of gluten free products and clearly labeled foods. I usually buy Milagro corn tortillas because they are cheap and are certified. However, I bought a package of Aldi's Pueblo Lindo Yellow Corn Tortillas without looking too closely (I was assuming they were fine... assuming never gets us anywhere good lol) it doesn't list any wheat products and doesn't say it was processed in a facility with wheat. It has a label that it's lactose free (hello, what?? When has dairy ever been in a tortilla?) Just, ugh. If they can add that label then why can't they just say something is gluten free or not? I did eat some of the tortillas and didn't notice any symptoms but I'm just not sure if it's safe. So I'll probably have to let my family eat them and stick with Milagro. There is way too much uncertainty with this but I guess you just have to stick with the clearly labeled products? I am still learning!
    • tiffanygosci
      Thank you all for sharing your experiences! And I am very thankful for that Thanksgiving article, Scott! I will look into it more as I plan my little dinner to bring with on the Holiday I'm also glad a lot of research has been done for Celiac. There's still a lot to learn and discover. And everyone has different symptoms. For me, I get a bad headache right away after eating gluten. Reoccurring migraines and visual disturbances were actually what got my PCP to order a Celiac Panel. I'm glad he did! I feel like when the inflammation hits my body it targets my head, gut, and lower back. I'm still figuring things out but that's what I've noticed after eating gluten! I have been eating gluten-free for almost two months now and haven't had such severe symptoms. I ate a couple accidents along the way but I'm doing a lot better
    • trents
      @Mari, did you read that second article that Scott linked? It is the most recently date one. "Researchers comparing rates of headaches, including migraines, among celiac patients and a healthy control group showed that celiac subjects experienced higher rates of headaches than control subjects, with the greatest rates of migraines found in celiac women.  Additionally, celiacs had higher rates of migraine than control subjects, especially in women. In fact, four out of five women with celiac disease suffered from migraines, and without aura nearly three-quarters of the time."
    • Mari
      As far as I know and I have made severalonline searches, celiac disease disease has not been recognized as a cause of migraines or any eye problems. What I wrote must have been confusing.
    • cristiana
      Interesting, when I suffered for a few months with ectopics I noticed that carbohydrates would cause indigestion and bloating in my stomach, then that would lead to my heart skipping beats, and I could feel it in my throat, it was very unsettling.  My last serious bout of this was after eating a Muller Rice Pudding for breakfast.   I happened to be wearing a 48 hour halter at the time and cardiology picked it up, but they weren't worried about what they saw. There was some British doctor who'd made some videos on the Vagus nerve that I remember watching at the time which made sense of what I was experiencing, there did seem to be some sort of connection.
×
×
  • 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.