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

Update And Venting


SunnyDyRain

Recommended Posts

SunnyDyRain Enthusiast

Hey all, I've been away for a while. Life has been crazy I went on a cruise earlier this month (didn't get glutened once... Yes Carnival Cruises are safe! )

Now I'm back and back to doctors in force. I went to my GP and she ran alot of tests. I am low on folic acid, and what I concider low on B12 (will be calling her about that tomorrow). My Celiac tests came back negitive so I'm adhering to the diet! (Gold star for me!)

However she sent me to a Gastro and a Derm. The Gastro is worried about my continued D even though I am on the diet and testing "clean" for gluten. I have to have a colonosopy on Wednesday :( She is testing me for some sort of colitis that is common in people with auto immune diseases. Bah! She is not doing a endoscopy and or making me do a gluten challenge... thank god!

The Dermatologst was looking into my hair loss, but now he is worried about Vitamin C deficency due to hair loss and rough skin.

So as my doctor ruled out celiac, seems like the specialists are finding ways to blame it on celiac 14 months after I stopped eating gluten.

I just sort of feel frustrated, I say "celiac disease" and they blame that for all my problems. I'm really feeling as if none of them are really looking outside of the Celiac box.

I really am much more than a "Celiac Pacient"!!

Oh, today the Derm asked what sort of medications I was taking for Celiac Disease... i almost laughed until I realized he was prolly a med student and it's not nice to laugh at med students as they are really just learning.

Ok that's the end of rant.. i welcome comments and ideas!


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

I am glad you had a good safe cruise but it is too bad you are still struggling with issues. The only thing that struck me was the note in your sig that said you are lactose intolerant. Could you be casien intolerant and not lactose? Casien is in a lot of 'nondairy' items and in many dairy replacement cheeses and that sort of thing. Casien intolerance is pretty common with us and that would be the first thing I would look for along with an intolerance to soy, also common with us. You may have already eliminated these as issues but figured I would mention them as both could cause continued GI distress even when gluten-free.

RiceGuy Collaborator

Well, all I can add is that I think you're right about the B12 deficiency, since you mentioned the hair and skin problems. You can't overdose on B12, so I say go ahead.

pele Rookie
Oh, today the Derm asked what sort of medications I was taking for Celiac Disease... i almost laughed until I realized he was prolly a med student and it's not nice to laugh at med students as they are really just learning.

I was chatting with a Chiropractor/acquaintance recently and mentioned celiac disease. She, too, asked me about the meds. I saw her a few days later and she had obviously looked it up and was embarrassed. I'm happy she is better educated now!

Is your colonoscopy to check for microscopic colitis? I was just reading Dr. Fine's essay on enterolab and he says 4% of celiacs have it, and it is a major reason for continued D.

sickchick Community Regular

I am off of EVERYTHING (including vinegar, soy lecithin, soy, nightshades, carageenan, potatoes)

and I am still struggling with chronic 'D'

I actually ordered Dr Fine's Microscopic Colitis stool test but it's been sitting on my table for like a MONTH! :lol::ph34r: I am so bad I need to DO IT and send it in already... trying to psych myself into doing it HAHAHA

Good luck to you.

Oh and for my gi trouble I eat psyllium every day. Metamucil plus Calcium. I get the pills.

lovelove

SunnyDyRain Enthusiast

Hey everyone, I had a colonoscopy yesterday.... my colon looks stunning (got the pictures to prove it!) however... i have inflamation and an ulcer in my ileum!

From what i have read does that mean Crohns Disease? :(

Anyone have any experince with this?

I have to wait until the end of the month for the follow up, but this wait is killing me! I'm so worried about this!

Jestgar Rising Star

I don't think one ulcer is worrisome.

I wanted to tell you that when I stopped eating soy, my hair stopped falling out, and finally, after cutting back to only vegetables and meat, my bowel movements are somewhat normal. You may need to investigate other foods (sorry :( )


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



Celiac.com Sponsor (A8-M):



gfpaperdoll Rookie

yes, be careful about getting labeled with something like Crohn's. A friend of mine was misdiagnosed with Crohn's for years - she really had celiac disease - DQ8 & DQ2 & positive thru Enterolab. she said her "Crohn's" was gone at day 5 of the gluten-free diet...

Are you eating any gluten-free grains? That could be a problem for you, also dairy & soy. Look into the SCD diet... I would totally be looking at your diet as the cause of your problems? Are you eating a lot of white potatoes? eggs? nuts? just a few of the common problems... I would cut back to no processed foods.

also, are you sure you are totally gluten-free including skin cream, & all personal care products? Do you live in a house that is gluten-free? Are you on any meds or vitamins that you have not checked?

Hope you are better soon.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,947
    • Most Online (within 30 mins)
      7,748

    Sinch23
    Newest Member
    Sinch23
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • 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
    • DebJ14
×
×
  • 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.