Jump to content
  • You are not alone. Join Celiac.com for trusted gluten-free answers and forum support.



  • Celiac.com Sponsor (A1):
    Celiac.com Sponsor (A1-M):

Testing Questions


wacky~jackie

Recommended Posts

wacky~jackie Rookie

Hi all! First I just want you to know that I have found this message board very informative.

Here's a short bio. Older sister diagnosed by positive blood tests and positive biopsy. She recommended that I be tested as I have many symptoms (bloating, joint pain, thyroid, depression, gall bladder, headaches - just to name a few!!). After much research I decided to ask my doctor to do blood tests. She really listened to what I had researched and my symptoms and ordered blood tests. After waiting almost 2 weeks for the results (which I didn't expect such a long wait.) they came back negative (IGG of 4 and IGA of 5, iron ok, B12 ok) but she only did those four tests.

My question is should I have her do further testing based on some of the posts I have read? Should I keep the appointment that I have scheduled with a GI and request a biopsy? Or do I just go gluten-free?

In the past I was on the Atkins diet and felt 100% better - which I now believe is because my gluten consumptions was definitely dramatically reduced (although probably not 100% gluten free). I'm ready to cut-out gluten completely to feel better but I don't want to do a gluten challenge for more tests so I just keep eating like I always have. I feel like I'm in limbo!!

Any suggestions?


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



Celiac.com Sponsor (A8-M):



plantime Contributor

It is your choice what to do next. Your bloodwork was negative, but that could mean that there just is not enough damage to show up. You can still get the biopsy if you want to. You say you felt better on the Atkins diet, so I recommend you try the gluten-free diet for 6 weeks. A doctor's diagnosis is not needed to eat gluten-free, so if you feel better on a gluten-free diet, there is no reason why you can't remain on it. The dietary response is a test in and of itself.

AndreaB Contributor

If you can swing the money I would recommend Enterolab. They can catch the intolerance before it hits the blood as they test stool. Open Original Shared Link for more info.

mle-ii Explorer

I too noticed how much my symptoms improved when doing Atkins, I didn't make the link to gluten until I found out I had Lymphocytic Colitis and found that others with my disease had improvement with going gluten free. I had Enterolab test me and found that I had gluten sensitivity as well as the genes.

wacky~jackie Rookie
I too noticed how much my symptoms improved when doing Atkins, I didn't make the link to gluten until I found out I had Lymphocytic Colitis and found that others with my disease had improvement with going gluten free. I had Enterolab test me and found that I had gluten sensitivity as well as the genes.

It was amazing. I only ate when I was hungry. No more cravings. I had no bloating and my knees and back felt 100% better. I ended up going off it after some complications from my gall bladder removal and the hospital put me on a clear liquid diet (all sugar!!! which is a major no-no on Atkins) I tried to go back on it when I started gaining the weight back but I haven't had much success because it's too strict. At least on a gluten-free diet I can try corn, potatoes and rice and I can have fruit - none of that is allowed on Atkins. So I think I'll be able to stick to gluten-free pretty easily, especially if I feel better. I guess I was hoping for a definite positive diagnosis. I figured that I could stay away from the bread and stuff easier if I knew it would damage my intestine. I'm worried that I'll be more apt to cheat without the diagnosis. :(

Archived

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

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      134,148
    • Most Online (within 30 mins)
      10,442

    depoe84
    Newest Member
    depoe84
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.7k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • transplantwest
      Psyllium can't sit for more than a minute in the water or it is like drinking sludge. Swallowed fairly soon means it's more like an flavorless undermixed protein smoothie. Chlorophyll ( or two tbsp) really helps the taste, makes it minty. Taking Psyllium and Chlorophyll separately rather than together at first helps determine if there's intolerance to either. Also starting the Psyllium in small doses, starting with 1/2 to 1 teaspoon to tolerate the fiber change. 
    • DanMc
      BuddhaBar, I came across this thread while searching online for celiac insomnia (having also scared myself stupid by finding out about fatal insomnia) and it did bring me some piece of mind as it so closely matches my own experience. I know this thread is old now, I hope you're doing well, and thanks for posting your experience.
    • cristiana
      That's great news, @HelloFlowersGoodbyeFlour.  And you might find that if you do have asthma, keeping your reflux under control may help, if my experience is anything to go by.  
    • trents
    • HelloFlowersGoodbyeFlour
      Quick update I ended going to a clinic they heard me wheezing and gave me a steroid shot I’m feeling much better now and I’m planing on getting reevaluated for asthma as the clinic doctor is thinking it might be that based on how I reacted to the steroid. But he couldn’t diagnose.  thanks again to everyone that applied (still seeing the gastrointestinal doctor too!) 
×
×
  • Create New...