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

My Story


andrew1273278

Recommended Posts

andrew1273278 Newbie

Hi all,

 

I figured I needed to start here so I could comfortably share my issues in a place of understanding and similar feeling people. My doctor and my family are understanding but I believe they still have a lot to learn about gluten intolerance. I believe I have gluten ataxia, which is a gluten intolerance with neurological issues. My doctor agrees that I have a gluten intolerance, but doesn't link my social anxiety - that never goes away - to this. Let me start at the beginning. 

 

I'm normal. I love carbs, but especially love pizza, brownies, cookies and anything to do with wheat. I've always been overweight in the waist/stomach area. This was normal when I was growing up. What my family and friends didn't understand was my extreme lethargy after eating almost anything. I mean, in America, we are saturated in wheat. Everything is wheat. I can/could barely ever catch a break from being sleepy. But when I would eat those foods that are JUST wheat, like pasta, that's it. I am passed the hell out. 

 

And looking back at the past year, I've had to overcome such a struggle that wasn't even about being ridiculously sleepy all the time. I had lactose intolerance, I've developed intestinal issues which is another ungodly issue to have to deal with, especially while being at work, where bathroom time is limited. I get a very flushed, hot face after eating anything with a sprinkle of wheat. And though I typically resorted to caffeine, I remember a particular day last year at work when it was very busy. I was tired and BAM - anxiety hit. And I had absolutely no clue what was going on. I was on a register and I was cashing out a customer and had to have a supervisor come in and save me. I ended up crying into the arms of a coworker who helped me contact my parents for a ride, all while I was extremely confused and dizzy as hell. 

 

This would have been over quickly if I knew what was going on, but for months and months and months I dealt with it as if it were an ear infection, sinus, and then a cold. I had no clue what I was dealing with and neither did my primary doctor. I would go through weeks of confusion, easily getting paranoid, angry, confused, fearful, lethargic. Finally, I made sense of it about 6 months later online while searching out my symptoms. I was dealing with anxiety. So, for months and months after that I tried new medicines which helped a bit, but it took me about 6 more months to discover gluten sensitivity through work while talking to customers. 

 

I work at Whole Foods and it is common for people to get anxious and confused, tired and hot when they have gluten issues. After going gluten free, I think my anxiety has gotten a lot better, and I can even say that my other unrelated issues like psoriasis are clearing up, too. But sometimes I cheat on my diet and here's what happens: I feel like someone knocked me out. My face swells and I have troubles breathing. And then I can sleep for hours, no matter the time of day. 

 

So, I am actually putting this out there for my friends, family and others to see all in one shot what I was going through. There are times where I was mean, tired, confused, unfriendly, paranoid, sick, etc. This is why and I finally have figured it out. And all is clear, and I hope that others with this issue can figure it out and treat themselves to a healthy alternative diet. 


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



Celiac.com Sponsor (A8-M):



bartfull Rising Star

Welcome, Andrew!

 

So I take it you never got tested for celiac? Your symptoms could be from celiac or from non-celiac gluten intolerance, and based on the fact that you feel better gluten-free, it sure sounds like one or the other.

 

The difference is though, that if you have celiac, not only do you feel lousy when you "cheat" on the diet, but you are doing realdamage to your body. If that is the case you need to be REALLY strict. Read the Newbie 101 thread in the coping section to help you get started. Then come back and ask as many questions as come to mind. We're glad to help. :)

nvsmom Community Regular

Welcome!  :)

 

That's impressive that you figured out your gluten intolerance and have started to take action already. I hope your days of cheating are behind you though, because regardless of whether it's celiac disease or NCGI, you're hurting yourself when you eat that stuff... but you know that already, right? 

 

I wish you good health and success with switching to a gluten-free life.

GFinDC Veteran

Hi Andrew,

 

Welcome to the forum! :)

 

It sounds like you are on the right track going gluten-free.  If you want to know about celiac disease you can find plenty of information reading this forum.

 

If you want to know for sure if you have celiac disease you would need to get blood drawn for antibodie tests.  But that doesn't work unless you are eating gluten for 6 to 6 weeks before the blood draw.  Some doctors suggest 3 months to be sure.

 

There is a genetic component celiac disease.  You can be tested for those genes at any time.

eers03 Explorer

Welcome to the forum.  If you are reacting to rare gluten consumption as you stated, you need to never consume it again.  Ever.  There is research out there that makes gluten to a celiac look like poison to a normal person.  Congrats on your determination and open-mindedness to listen/learn/apply what you figured out.  Right on!

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,174
    • Most Online (within 30 mins)
      7,748

    jaxie
    Newest Member
    jaxie
    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

    • Jane878
      By the time I was 5 I had my first auto0immune disorder, Migraine headaches, with auras to blind me, and vomiting, sensitivity to light and sound. I was 5 years old, and my stepfather would have pizza night, milling his own flour, making thick cheesy gluten pizza, that I would eat and the next day, I would have serious migraines, and my mother & stepfather did nothing about my medical problems. When I was 17 in my first year at college, I was diagnosed with my 2nd known auto-immune disorder, Meniere's disease. I was a elite athlete, a swimmer, and soccer player. And once again my parents didn't think anything of understanding why I had a disorder only older people get. Now after my mother passed from Alzheimer's disease she also suffered with living with gluten. She had a rash for 30 years that nobody could diagnose. She was itchy for 45 years total. My brother had a encapsulated virus explodes in his spleen and when this happened his entire intestines were covered with adhesions, scar tissue and he almost lost his life. He has 5 daughters, and when I finally was diagnosed after being pregnant and my body went into a cytokine storm, I lost my chance to have children, I ended up having Hashimoto's disease, Degenerative Disc disease, and my body started to shut down during my first trimester. I am 6ft tall and got down to 119lbs. My husband and I went to a special immunologist in Terrace, California. They took 17 vials of blood as we flew there for a day and returned home that evening. In 3 weeks, we had the answer, I have Celiac disease. Once this was known, only my father and husband made efforts to change their way of feeding me. At the family cabin, my stepfather & mother were more worried that I would ruin Thanksgiving Dinner. It wasn't until one of my cousins was diagnosed with Celiac disease. They finally looked into getting Gluten Free flour and taking measures to limit "gluten" in meals. He did nothing but ask for me to pay for my own food and wi-fi when I came to the cabin to stay after our house burned down. When he informed my mother, they proceeding to get into a physical fight and she ended up with a black eye. The is just more trauma for me. Sam had no interest in telling the truth about what he wanted. He lied to my mother that he had asked my husband if I could pay for "food" when he asked Geoffrey if I had money to pay for my wi-fi. My mother hates when he spends so much time on the computer so he lied and said I could pay for my own food. I will remind you I weighed 119lbs at this time. (At 6ft) that is a very sick looking person. Neither parent was worried about my weight, they just fought about how cheap my stepfather was. As my mother was diagnosed with Alzheimer's disease in 2014. He had her sign over the will to a trust and added his children. He had no testimonial capacity at the time, so she signed without proper papers. Making this Trust null and void. When I gave my brother my childhood home, my mother stated I would be getting an equal part of inheritance to the house on Race. It currently worth 2.0 million $. I got nothing, and my stepfather has since disowned me b/c of my claim and he knows that my mother would never have left it uneven between my biological brother and myself. She sat me and my husband down, as we lived at the Race Street house and treated and took care of it as our own. My brother took over b/c he was going through a horrific divorce and needed a home so he could get a better custody deal with his soon to be ex-wife who was a Assist DA for Denver. She used the girls against him, and he & I were the primary caregivers. We, Judd and I spent the most time with them pre the divorce. Once Judd moved into the house, he threw all of my mother, grandmother and my family heirlooms out to the Goodwill. Nobody told my mother about this as she was going through cancer treatment and had Alzheimer's disease in her mother and her sister. My stepfather and biological brother took advantage of this matter, as I called a "family council" that my brother just never could make it to at the last moment. All of the furnishing, kitchen ware, everything was in the house my brother just moved into. He had had 2 weddings, I chose to elope b/c my stepfather ruined my brother's first wedding by talking about his relationship with my brother in front of my dad and his entire family, insulting him and having my grandfather leave the ceremony. It was a disaster. My stepfather just plays dumb and blames my father for the slight. I was the only child not to have a wedding. So, my mother and stepfather never had to pay for a thing. My mother had had an agreement with my father he'd pay for college and all medical issues with their kids, myself and Judd. So truly my mother never had to pay for anything big for me in her entire life. I am looking for anyone that has had a similar story, where they grew up in a household that had a baker that regularly milled flour and ate gluten. What happened to you? DId you suffer from different auto-immune diseases b/c of living with a baker using "gluten" Please let me know. I have been looking into legal ways to get my stepfather to give me what my mother had promised, and he erased. Thank you for listening to my story. Jane Donnelly  
    • trents
      Possibly gluten withdrawal. Lot's of info on the internet about it. Somewhat controversial but apparently gluten plugs into the same neuro sensors as opiates do and some people get a similar type withdrawal as they do when quitting opiates. Another issue is that gluten-free facsimile flours are not fortified with vitamins and minerals as is wheat flour (in the U.S. at least) so when the switch is made to gluten-free facsimile foods, especially if a lot of processed gluten-free foods are being used as substitutes, vitamin and mineral deficiencies can result. There is also the possibility that she has picked up a virus or some but that is totally unrelated to going gluten-free.
    • Sheila mellors
      I asked about the new fruit and nut one and the Dietician said yes I could eat it safely. Hooe this helps
    • Heatherisle
      Daughter has started gluten free diet this week as per gastroenterologists suggestion. However says she feels more tired and like she’s been hit by a train. I suggested it could be the change to gluten free or just stress from the endoscopy last week catching up with her. Just wondering if feeling more tired is a normal reaction at this stage. I suppose it’s possible some gluten might have been present without realising. Have tried to reassure her it’s not going to resolve symptoms overnight
    • DAR girl
      Looking for help sourcing gluten-free products that do not contain potato or corn derived ingredients. I have other autoimmune conditions (Psoriatic Arthritis and Sjogrens) so I’m looking for prepared foods as I have fatigue and cannot devote a lot of time to baking my own treats. 
×
×
  • Create New...