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

Omg...i Might Be On To Something


Rachel--24

Recommended Posts

confused Community Regular

I had an lightbulb moment at 2 am this morning. My body hates citric acid. Remember how i got sick from the spaghetti. Well yesterday i had some iced tea that has citric acid and i felt a little off but still able to clean and cook lol. Well then my stomach was cramping and my head hurt at midnight.

I guess i need to stay away from it. I still kinda feel out of it this morning. I guess just one more thing to add to my list lol

I only got to page 7 last night. The talk about corn is kinda boring lol. I need to get to the good stuff like metals and stuff lol

paula


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



Celiac.com Sponsor (A8-M):



  • Replies 33.4k
  • Created
  • Last Reply
mftnchn Explorer

Kassandra, my prayers are with you too!

Sherry

dlp252 Apprentice

Paula, I think the metals issue came after the corn, histamines, and probably about two or three more "issues", lol. Keep reading!

Green12 Enthusiast

Thinking about Kassandra :wub: :wub:

AndreaB Contributor
I think they just do a leg block with a light sedation, but I can't imagine being awake for 90 minutes while they cut my bones, so I may ask for the "forget everything" drug. One of those things really messes me up though, but I think it might be worth it to not hear the sawing. :lol:

What about ear plugs? I did have something done on my toes a long time ago. I don't remember them sawing bones though. Mine was toenails that grew from the inside of my toe. Seems like that problem came back a little but it doesn't hurt nearly as much as it did.

I had an lightbulb moment at 2 am this morning. My body hates citric acid. Remember how i got sick from the spaghetti. Well yesterday i had some iced tea that has citric acid and i felt a little off but still able to clean and cook lol. Well then my stomach was cramping and my head hurt at midnight.

I only got to page 7 last night. The talk about corn is kinda boring lol. I need to get to the good stuff like metals and stuff lol

Isn't citric acid on the moldy side?

MSG isn't too far into the thread. I had run across that within the first 90 pages. That was stuff I had started commenting on.

dlp252 Apprentice

Ear plugs might work...I'll bring some, lol! They're soft foam, so shouldn't be objectionable to them.

Guest tamedandfoxed
Katy,

Dont give up...hang in there. You'll get this figured out.

Is the Dr. "guessing" about the infection?? Have you had any tests run??

I've had several labs... they run a culture and about a week later (4 times now) the culture grows this strepticochous bacteria.. the logical treatment being antibiotics. but antibiotics have done nothing but give me candida. so they put me on this other drug which is a really old anti-depressant that for some reason they've seen good results with..but the side effects have made me brain foggy, depressed and really anxious / easily agitated. i.e. NOT FUN and it hasn't helped anything...

i feel disengaged from everything..


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



Celiac.com Sponsor (A8-M):



confused Community Regular
Ear plugs might work...I'll bring some, lol! They're soft foam, so shouldn't be objectionable to them.

What about an ipod or mp3 player or even an old celiac disease player with head phones.

paula

aprilh Apprentice

Paula,

Citric acid is now derived from fungus. That's probably why your body doesn't like it. It would feed any candida issues that you might have. That might be a good one to avoid. I think Moldlady talked about it back on the candida thread???

Kassandra,

OH NO! :( That's all you need!

Does anyone know if it was from Iron IV's or IV abx?

aprilh Apprentice

Lisa,

About Zeolite....I was all into trying it and then I started researching it and found all of these websites saying DON"T take liquid form?? Have you read any of that? Some websites were really adamant about it. Something about the liquid form not being known if the structure is still in tact as it is in a mineral (powdered) form.

I guess I need to do some more reading. I know there are always somebody saying something bad about a natural product. I guess I just don't know enough about this stuff to judge either way.

It sounds like its working wonders for you - so maybe I'll just take a chance to try it!

April

confused Community Regular

April.

That all makes sense. I might have to dig up that old thread and see what it says. I have lived in denial about the candida isue long enough now lol.

The one thing i dont get is why can i drink beer that hs yeast and feel fine. But i cant have citric acid without feeling like death. I just dont understand lol.

Im guessing i better not even try cheese even with these enzymes. Im ao upset about this.

Whatever you find out about the zeolite please post here. Im thinking of trying it, but so afraid to try anything anymore.

paula

Rachel--24 Collaborator

I believe citric acid is from aspergillus specifically. Maybe you're sensitive to aspergillus??

Damn...I wish I could I could have a beer and feel fine!!

OK...I need supplement help!

I need calcium citrate....without any Vit. D added in. Just plain calcium....NO excipients and no other unnecessary junk. I just need calcium....is that too much to ask?? :rolleyes:

I cant find anything. :(

confused Community Regular
I believe citric acid is from aspergillus specifically. Maybe you're sensitive to aspergillus??

Damn...I wish I could I could have a beer and feel fine!!

OK...I need supplement help!

I need calcium citrate....without any Vit. D added in. Just plain calcium....NO excipients and no other unnecessary junk. I just need calcium....is that too much to ask?? :rolleyes:

I cant find anything. :(

I bet you hit the nail on the head with that assumption. That is one of the molds they found in the boiler room when i was so sick in the kitchen. I bet that is the mold that hates my body. Is there a test to test for that lol.

paula

AndreaB Contributor
I need calcium citrate....without any Vit. D added in. Just plain calcium....NO excipients and no other unnecessary junk. I just need calcium....is that too much to ask?? :rolleyes:

I cant find anything. :(

Yep, too much to ask. They like to put everything into everything. :angry: I had to get more supp's with the stearates. Can't be avoided and I need them for the amalgam removal for one.

mftnchn Explorer

Quick drive by, I'll write an email update later for my LLMD appointment.

Biggest change is that I have to go on the SCD diet. The tests show that I cannot handle disaccharides at all. My LLMD thinks this will make quite a bit of difference in how I feel.

Also he wants my 25 Vit D levels at 80, so I'm to take 10,000 a day and they'll do another blood draw in 2-3 weeks.

Sherry

confusedks Enthusiast

I'm back. Man that was rough! I started breaking out in hives and welts all over my body. Had horrible back and knee pain out of nowhere while infusing at the Dr's office, but I thought it was Lyme related so I didn't say anything.

I called the Dr, after I drove myself home, lol, and he said to take benadryl, lay down and call him back in 2 hours. Within 20 minutes I was having difficulty breathing. My face and eyes were swelling quickly. So we called the dr back and I was gasping for air as I was talking to him. He said to go right to the nearest ER.

We went, and they gave me all kinds of stuff to stop the reaction. Including steroids. :( But it was a life and death situation, so there wasn't much to say. They gave me oxygen and breathing treatments to open my lungs. Put all kinds of heart monitors on. Gave me pain meds.

They then decided because of the Lyme, etc. that since my body was so weak, I could continue reacting for a while, so they wanted to observe me overnight.

I'm still in a lot of pain. I talked to Dr H yesterday and he was concerned that they gave me steroids, but obviously there wasn't anything we could do about it. They infused Rocephin last night and that went fine.

It had to have been a reaction to the Iron IV, but it's strange because I've had 12 other Iron IV's and no reaction. So the problem is, now they don't want to give it to me again, but I'm still really iron deficient. My Hematologist said no more IV's, and he wants to follow up with me next week.

My concern is that I am so anemic, and I can't do iron IV's now. He said he might admit me back into the hospital to have another one, and have them observe me.

AndreaB Contributor

Kassandra,

Could it be the IV abx that threw things off with the iron IV.

That sounds like a scary ordeal, I'm glad you're ok.

jerseyangel Proficient

Kassandra,

I'm so sorry---that must have been very frightening for you. Take care, I'm sending good, positive thoughts and a hug your way :)

mftnchn Explorer

Kassandra, so good to hear from you, and ditto to Andrea's question.

Sherry

dlp252 Apprentice

Gosh Kassandra, that is absolutely FRIGHTENING!!!!

confusedks Enthusiast

There's no known interaction between the Iron and Rocephin. I will have to talk to the Hematologist on Tuesday and see what he wants to do.

It is possible to develop allergic reactions to anything and any given moment. People eat peanuts their whole life, then suddenly stop breathing one day....so it was definitely the iron. The thing that is so bizarre is that I had one on Monday and had NO problems at all! Then yesterday had a severe reaction. So who really knows? :P

jerseyangel Proficient
It is possible to develop allergic reactions to anything and any given moment.

Very true--allergies can appear at any time and can come and go throughout life.

So scary....

Green12 Enthusiast
I need calcium citrate....without any Vit. D added in. Just plain calcium....NO excipients and no other unnecessary junk. I just need calcium....is that too much to ask?? :rolleyes:

I cant find anything. :(

Did you look into Pure Encapsulations Rachel?

Biggest change is that I have to go on the SCD diet. The tests show that I cannot handle disaccharides at all. My LLMD thinks this will make quite a bit of difference in how I feel.

Oh wow Sherry, that's an interesting development. I hope the diet will make a difference for you.

I started breaking out in hives and welts all over my body. Had horrible back and knee pain out of nowhere while infusing at the Dr's office, but I thought it was Lyme related so I didn't say anything.

.My face and eyes were swelling quickly. So we called the dr back and I was gasping for air as I was talking to him. He said to go right to the nearest ER.

We went, and they gave me all kinds of stuff to stop the reaction. Including steroids.

They then decided because of the Lyme, etc. that since my body was so weak, I could continue reacting for a while, so they wanted to observe me overnight.

I'm still in a lot of pain. I talked to Dr H yesterday and he was concerned that they gave me steroids, but obviously there wasn't anything we could do about it. They infused Rocephin last night and that went fine.

My concern is that I am so anemic, and I can't do iron IV's now. He said he might admit me back into the hospital to have another one, and have them observe me.

Oh Kassandra, I'm so sorry you had to go through this, how very scary :(

That's the ER procedure for anaphylaxis, epi, antihistamines, and steroids, unfortunately :)

I'm keeping you in my thoughs, love and hugs to you.

Keep us posted as you are able.

tabasco32 Apprentice
I've known this girl for awhile and no WAY could she eat pizza before! In fact she couldnt even TOUCH pizza before...and actually I'm not even sure if she could LOOK at pizza without getting sick (or without totally ruining the pizza :P ).

Now she's putting up a picture of a whole pizza that she made....she's TOUCHING it and its not turning to WAX!! :o This is REALLY BIG news!!! :D

AND....she's eating leftovers!! :blink:

I'm not really touching it. Look closely at my HANDS!!! :lol:

tabasco32 Apprentice
Lisa,

About Zeolite....I was all into trying it and then I started researching it and found all of these websites saying DON"T take liquid form?? Have you read any of that? Some websites were really adamant about it. Something about the liquid form not being known if the structure is still in tact as it is in a mineral (powdered) form.

I guess I need to do some more reading. I know there are always somebody saying something bad about a natural product. I guess I just don't know enough about this stuff to judge either way.

It sounds like its working wonders for you - so maybe I'll just take a chance to try it!

April

If that were the case I would be getting sicker and not better. Zeolites cannot harm you in anyway. They are not absorbed by the body and something not absords is not being utilized. They clean the body out. Cleaning the cages of the zeolite does not change the structure.

I don't even know if this Dr. which I heard about before is even a certified biochemist like Rik Dietch. Rik is a very, very intellegent guy. I have asked him many questions with incredible answers.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,118
    • Most Online (within 30 mins)
      7,748

    Cwbtex
    Newest Member
    Cwbtex
    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

    • Colleen H
      I did ... But aren't we going to be vitamin deficienct if we are not eating due to being sick ?? If the food we eat is gluten free and we have other sensitivities , how do we get out of the cycle??  Thank you 
    • Colleen H
      Anyone else get pins and needles. ??? Burning feeling ? Heat makes it so much worse 😔  Winter is here.  I had to lower my thermostat because I couldn't take that hot air feeling 😔  Hopefully it goes away soon     
    • trents
      I assume that you already know that genetic testing for celiac disease cannot be used to confirm a celiac diagnosis. About 40% of the general population has the genetic potential to develop celiac disease but only about 1% actually develop celiac disease. It can be used to rule out celiac disease with a high degree of confidence, however, in the case where the genetic testing is negative for the genes. Until and unless you are actually diagnosed with celiac disease I would not raise this as an issue with family. However, if you are diagnosed with celiac disease through blood antibody testing and/or endoscopy with positive biopsy I would suggest you encourage first degree relatives to also purse testing because there is a significant chance (somewhere betwee 10% and almost 50%, depending on which studies you reference) that they will also have or will develop active celiac disease. Often, there are symptoms are absent or very minor until damage to the small bowel lining or other body systems becomes significant so be prepared that they may blow you off. We call this "silent celiac disease". 
    • trents
      If you were off gluten for two months that would have been long enough to invalidate the celiac blood antibody testing. Many people make the same mistake. They experiment with the gluten free diet before seeking formal testing. Once you remove gluten from the diet the antibodies stop being produced and those that are already in circulation begin to be removed and often drop below detectable levels. To pursue valid testing for celiac disease you would need to resume gluten consumption equivalent to the amount found in 4-6 slices of wheat bread daily for at least two weeks, preferably longer. These are the most recent guidelines for the "gluten challenge". Without formal testing there is no way to distinguish between celiac disease and gluten sensitivity since their symptoms overlap. However, celiac disease is an autoimmune disorder that damages the small bowel lining, not true of gluten sensitivity. There is no test available for gluten sensitivity so celiac disease must first be ruled out. By the way, elevated liver enzymes was what led to my celiac diagnosis almost 25 years ago.
    • trents
      Then it does not seem to me that a gluten-related disorder is at the heart of your problems, unless that is, you have refractory celiac disease. But you did not answer my question about how long you had been eating gluten free before you had the blood antibody test for celiac disease done.
×
×
  • 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.