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

Mayo Appt


Sharonmarie

Recommended Posts

Sharonmarie Rookie

There is a Celiac Clinic at the Rochester Mn. Mayo. Clinic!

I am so happy to have discovered this!

I have an appointment there tomorrow. June 25 2013 .

Wish me luck!


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



Celiac.com Sponsor (A8-M):



bartfull Rising Star

I have known many people who went to the Mayo Clinic in Rochester. Believe me, you are putting yourself in VERY good hands. Let us know how it turns out. :)

1desperateladysaved Proficient

Have a productive time!

Sharonmarie Rookie

I have known many people who went to the Mayo Clinic in Rochester. Believe me, you are putting yourself in VERY good hands. Let us know how it turns out. :)

Thank You so much. I was diagnosed ten years ago with Celiac. And I have been on a very strict gluten free diet since then.

But. My condition steadily gets worse.

I am cautiously hopeful.

Sharonmarie Rookie

I am so sad to say I was totally disappointed. The ( cealic Doctor ). Was tunnel visioned!

I can not understand why I would require another upper endoscopy when I have been diagnosed with celiac disease. My numbers are very high from the blood tests they did.....

My complaint right now is that my feet,legs and arms are so extremely painful right now.

Also the backs of my thighs and every part of my feet are so sensitive to everything that they rest on.

The Doctor exclaimed that it is a nerve problem and has nothing to do with celiac disease! She can't help me!

Right now I feel like there is no help.

Thanks for listening.

kareng Grand Master

I am so sad to say I was totally disappointed. The ( cealic Doctor ). Was tunnel visioned!

I can not understand why I would require another upper endoscopy when I have been diagnosed with celiac disease. My numbers are very high from the blood tests they did.....

My complaint right now is that my feet,legs and arms are so extremely painful right now.

Also the backs of my thighs and every part of my feet are so sensitive to everything that they rest on.

The Doctor exclaimed that it is a nerve problem and has nothing to do with celiac disease! She can't help me!

Right now I feel like there is no help.

Thanks for listening.

 

 

If your Celiac antibodies are still high, 10 years later, they will want to do another endoscopy to see how big a mess it is in there.  They will also want you to really tighten up your diet.

 

If I miss understood what you wrote, and your antibodies are fine, then I don't see a reason for another endo unless you told them you were having GI issues.  IF your antibodies have been fine  for 10 years, then he may be right that your other issues have nothing to do with Celiac.  Every illness we get isn't related to Celiac.  Maybe you should see a neurologist or maybe an ortho doctor about the leg & feet pain.

Sharonmarie Rookie

If your Celiac antibodies are still high, 10 years later, they will want to do another endoscopy to see how big a mess it is in there.  They will also want you to really tighten up your diet.

 

If I miss understood what you wrote, and your antibodies are fine, then I don't see a reason for another endo unless you told them you were having GI issues.  IF your antibodies have been fine  for 10 years, then he may be right that your other issues have nothing to do with Celiac.  Every illness we get isn't related to Celiac.  Maybe you should see a neurologist or maybe an ortho doctor about the leg & feet pain.

My IgA was 103.0 . That was why my general Dr. Referred me to the Celiac Dr. Even though my complaint was about the pain and discomfort through my entire body.

Pain in arms and legs. I did not complain about digestive issues.

I feel like they see me as $$$ signs.

I just love your quote about this party LOL

I shall make the best of it. :)

Sorry for my negativity.


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



Celiac.com Sponsor (A8-M):



frieze Community Regular

My IgA was 103.0 . That was why my general Dr. Referred me to the Celiac Dr. Even though my complaint was about the pain and discomfort through my entire body.

Pain in arms and legs. I did not complain about digestive issues.

I feel like they see me as $$$ signs.

I just love your quote about this party LOL

I shall make the best of it. :)

Sorry for my negativity.

was that your total IgA? if so, that is WNL, I think. 

  • 4 weeks later...
Sharonmarie Rookie

was that your total IgA? if so, that is WNL, I think.

What is WNL ?
frieze Community Regular

With in Normal Limits.....

What is WNL ?

AlwaysLearning Collaborator

Sharonmarie.

Get yourself tested for vitamin deficiencies. They go hand in hand with the malabsorption problems that come with gluten allergies and some of what you are describing with the leg pain is a symptom of B12 deficiency, I think. Either that or vitamin D.

Sharonmarie Rookie

Thank you for your reply. The Celiac Doctor advised I go off all supplements. Which I have done. I feel very depressed and alone. I think there is no help for Celiac Disease. Only perhaps for the side effects. So I will continue on the gluten free diet and.... Take pills for restless leg syndrome and for depression, and accept this condition for what it is.

AlwaysLearning Collaborator

I have to ask, did the celiac doctor who told you to stop taking supplements run any tests for deficiencies before telling you to stop taking them? 

Granted, I'm generally anti-pill and would advise getting tested before advising taking them, but if you're having issues, I'd at least look into it further.

ravenwoodglass Mentor

Thank you for your reply. The Celiac Doctor advised I go off all supplements. Which I have done. I feel very depressed and alone. I think there is no help for Celiac Disease. Only perhaps for the side effects. So I will continue on the gluten free diet and.... Take pills for restless leg syndrome and for depression, and accept this condition for what it is.

Were you taking herbal type supplements? Some doctors might be referring to those and not to vitamin supplements. Some of them also have wheat and barley grass and say they are gluten free but we really won't tolerate them.  I can't imagine a doctor telling someone not to take a regular vitamin and mineral tablet.

You may be having celiac related nerve issues. A good neuro who is familiar with celiac could be helpful. However your GI doctor IMHO had a valid request when they wanted to do another endo. If your levels are still up they would want to see what your villi look like.  

You also mention taking medication for restless legs and depression. Have you checked with the maker to make sure they are gluten free? In addition one of the signs that celiac is impacting the brain is depression that is not relieved by antidepressant medication. Being very strict with the diet can help with that kind of depression.

Don't lose hope there is help for celiac disease. The gluten free diet. If your levels are still up it is likely gluten is sneaking in somewhere.  Give us more info on your diet and eating habits, restaurants, other gluten eaters in your home etc. and we may be able to be more helpful.

Sharonmarie Rookie

I have had blood tests for deficancys and been told my numbers are good.

And I went to what they told me was Dietician that specialized with Celiac and showed , not a written list but all the bottles of supplements I was taking. I also took her a month long log of every food I eat and the portion sizes. She said it looked like I was doing everything right.

Then I saw a Celiac Doctor and she told me to go off all supplements. In her own words she said "Gluten Free Diet is a huge fad right now, so all the supplement company's are on the bandwagon. So even though they read Gluten Free , they may not be! "

And I have had three upper endoscopy's and I woke up during one plus after the last one I had to go back for internal bleeding! Celiac Doctor exclaimed "That can not happen".

Well it did happen And I decided I have had enough of her so called expertise!

This is why I have decided to continue the gluten-free diet and make the best of it.

Thank You for your reply.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,983
    • Most Online (within 30 mins)
      7,748

    CRae
    Newest Member
    CRae
    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

    • Mari
      There is much helpful 'truth' posted on this forum. Truths about Celiac Disease are based on scientific research and people's experience. Celiac disease is inherited. There are 2 main Celiac 'genes' but they are variations of one gene called HLa - DQ What is inherited when a person inherits one or both of the DQ2 or the DQ8 is a predisposition to develop celiac disease after exposure to a environmental trigger. These 2 versions of the DQ gene are useful in diagnosing  celiac disease but there are about 25 other genes that are known to influence celiac disease so this food intolerance is a multigenic autoimmune disease. So with so many genes involved and each person inheriting a different array of these other genes one person's symptoms may be different than another's symptoms.  so many of these other genes.  I don't think that much research on these other genes as yet. So first I wrote something that seem to tie together celiac disease and migraines.  Then you posted that you had migraines and since you went gluten free they only come back when you are glutened. Then Scott showed an article that reported no connection between migraines and celiac disease, Then Trents wrote that it was possible that celiacs had more migraines  and some believed there was a causal effect. You are each telling the truth as you know it or experienced it.   
    • tiffanygosci
      Another annoying thing about trying to figure this Celiac life out is reading all of the labels and considering every choice. I shop at Aldi every week and have been for years. I was just officially diagnosed Celiac a couple weeks ago this October after my endoscopy. I've been encouraged by my local Aldi in that they have a lot of gluten free products and clearly labeled foods. I usually buy Milagro corn tortillas because they are cheap and are certified. However, I bought a package of Aldi's Pueblo Lindo Yellow Corn Tortillas without looking too closely (I was assuming they were fine... assuming never gets us anywhere good lol) it doesn't list any wheat products and doesn't say it was processed in a facility with wheat. It has a label that it's lactose free (hello, what?? When has dairy ever been in a tortilla?) Just, ugh. If they can add that label then why can't they just say something is gluten free or not? I did eat some of the tortillas and didn't notice any symptoms but I'm just not sure if it's safe. So I'll probably have to let my family eat them and stick with Milagro. There is way too much uncertainty with this but I guess you just have to stick with the clearly labeled products? I am still learning!
    • tiffanygosci
      Thank you all for sharing your experiences! And I am very thankful for that Thanksgiving article, Scott! I will look into it more as I plan my little dinner to bring with on the Holiday I'm also glad a lot of research has been done for Celiac. There's still a lot to learn and discover. And everyone has different symptoms. For me, I get a bad headache right away after eating gluten. Reoccurring migraines and visual disturbances were actually what got my PCP to order a Celiac Panel. I'm glad he did! I feel like when the inflammation hits my body it targets my head, gut, and lower back. I'm still figuring things out but that's what I've noticed after eating gluten! I have been eating gluten-free for almost two months now and haven't had such severe symptoms. I ate a couple accidents along the way but I'm doing a lot better
    • trents
      @Mari, did you read that second article that Scott linked? It is the most recently date one. "Researchers comparing rates of headaches, including migraines, among celiac patients and a healthy control group showed that celiac subjects experienced higher rates of headaches than control subjects, with the greatest rates of migraines found in celiac women.  Additionally, celiacs had higher rates of migraine than control subjects, especially in women. In fact, four out of five women with celiac disease suffered from migraines, and without aura nearly three-quarters of the time."
    • Mari
      As far as I know and I have made severalonline searches, celiac disease disease has not been recognized as a cause of migraines or any eye problems. What I wrote must have been confusing.
×
×
  • 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.