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

7 Months


w8in4dave

Recommended Posts

w8in4dave Community Regular

Ok it has been 7 months since I was Dx'd , My report is that it is going pretty good in fact very good Gluten wise , but I also figured out I am Corn intolerant , around Oct, so 3 months Corn free. Well going Corn Free is alot more of a struggle than gluten-free let me tell ya! but it is doable!But if I get Corn in me it hits me worse than Gluten!  I am still struggling with something , not sure what my problem is yet. I am doing so much better. I have great support from friends and family. And they try so hard. But I really say just let me do it. They want to feed me lol .... I went to a restaurant with a friend I havn't seen since before Christmas. I was telling the waitress I have Celiac and I am also Corn intolerant , my friend right away said, she doesn't have to know your problems. I said, well actually she does, because she can help me figure out what I can and cannot have. And she did. I had to have a plain burger (no bun) and a veggie salad , no dressing. The girl checked every dressing they had and all of them contained corn. Thats why you want to tell your server. :) I am feeling better have some energy back but not enuf. Maby if they can figure out what eles is bothering me, I can feel wayyy better. But untill then I am going to give on a scale of 1-10,  10 being the best 1 the worst, I say most of the time I feel like a 6, once in a while I feel like a 7. So thats the way it's been going. And again I want to thank everyone here. I have gotten some great advice! Great advice!! Thanks everyone!


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



Celiac.com Sponsor (A8-M):



GF Lover Rising Star

Congratulations Wendy, your doing great !

 

Remember it sometimes takes over a year to see improvement in our issues.  I remember last summer I had an AHA moment.  My brain felt like it finally started back up.  It was an amazing feeling to have that fog lifted after so so many years.  

 

Keep doing what your doing, your IMPROVING!  :D

 

Colleen

bartfull Rising Star

Yeah, corn makes things so hard! The worst part for me is finding medications and supplements that don't have corn. I DID find a vitamin I can take, FINALLY! (Lifetime Iron-free Soft Gels. They don't say gluten-free, but I called the company and it was your basic CYA statement, so I started taking them and have had no problems.) I have to get my Tylenol made at a compounding pharmacy though. Very expensive.

 

Wendy, have you checked out the Mast Cell Activation Syndrome thread? Even though corn isn't one of the bad guys with that, I think it explains why so many other foods bother me. Of course there isn't much we can do about it except take anti-histamines and I haven't found any anti-histamines that don't contain corn, but at least it has cut down on my worries about why I still don't feel good.

NoGlutenCooties Contributor

... I think it explains why so many other foods bother me. Of course there isn't much we can do about it except take anti-histamines and I haven't found any anti-histamines that don't contain corn...

 

If you're open to trying natural remedies, this site explains how some foods act as natural anti-histamines:  Open Original Shared Link

NoGlutenCooties Contributor

... I have great support from friends and family. And they try so hard. But I really say just let me do it. They want to feed me lol ....

 

Congratulations on doing so well with the diet and figuring out what works for you and what doesn't!  I can definitely relate to the well-meaning, supportive friends and family who want to help.  That's one thing I'm trying to deal with diplomatically without hurting anyone's feelings.  They don't quite understand that cooking food in a gluten kitchen doesn't mean it will be gluten-free just because the food itself doesn't start out having gluten in it.  I try to explain how easy it is to get cross-contamination but they still think I'm going way overboard and just being overly paranoid.  My sister didn't believe that I could be so sensitive to gluten post-diagnosis given that I didn't have any obvious symptoms before my diagnosis.  Until I got accidentally glutened a couple of weeks ago and the reaction was identical to getting food-poisoning.  She's still skeptical, but I think she's starting to come around.  :)

bartfull Rising Star

If you're open to trying natural remedies, this site explains how some foods act as natural anti-histamines:  Open Original Shared Link

Wow! Thanks SO MUCH! This really confirms that I have MCAS. I had been eating sweet potatoes every single day, usually for both lunch and dinner. I was also eating Udi's chocolate muffins, one a day, for the past three weeks.

 

Well, I am SO SICK OF SWEET POTATOES, so I switched to white rice last week, but still ate a muffin each afternoon. And NOW I am having a psoriasis flare. Looks like the sweet potato was offsetting the chocolate. I'm still so sick of sweet potatoes I can't stand to look at them, but broccoli is on sale this week and if it looks decent (it often doesn't here), I'll be eating that this week. Of course I'm out of muffins right now and don't plan on buying any for a while, but it's nice to know I can eat them once in a while if I balance things with the right veggies.

 

Thanks again. I LOVE this place!!!

1desperateladysaved Proficient

I am looking forward to some of your 9 days which could lie ahead!  I hope.  I saw some of my vast transitional symptoms at 8 months gluten free, so who knows?

 

All of the best.

 

 

D


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



Celiac.com Sponsor (A8-M):



notme Experienced

w8n4, are you still keeping a food journal?  i always go back to my tried and true food journal when something has got me trying to figure out what i'm eating that is bugging me. 

 

congratulations on your 7 months!!  :)

w8in4dave Community Regular

Yeah, corn makes things so hard! The worst part for me is finding medications and supplements that don't have corn. I DID find a vitamin I can take, FINALLY! (Lifetime Iron-free Soft Gels. They don't say gluten-free, but I called the company and it was your basic CYA statement, so I started taking them and have had no problems.) I have to get my Tylenol made at a compounding pharmacy though. Very expensive.

 

Wendy, have you checked out the Mast Cell Activation Syndrome thread? Even though corn isn't one of the bad guys with that, I think it explains why so many other foods bother me. Of course there isn't much we can do about it except take anti-histamines and I haven't found any anti-histamines that don't contain corn, but at least it has cut down on my worries about why I still don't feel good.

No I have not but will :) Antihistamines I quit taking them. Probably why my ears feel so full!! Ughhh

w8in4dave Community Regular

If you're open to trying natural remedies, this site explains how some foods act as natural anti-histamines:  Open Original Shared Link

Thanks! I have added it to my Favorites :) I will read up on it. Cannot hurt thats for sure.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,963
    • Most Online (within 30 mins)
      7,748

    AlissaW
    Newest Member
    AlissaW
    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

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • 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.