Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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 Celiac.com!
    eNewsletter
    Donate

New Here, Feeling Miserable


SarahRN482

Recommended Posts

SarahRN482 Newbie

Hi everyone. I found this site during a desperate web search for resources on gluten allergies/sensitivities. I am in need of answers and reassurance that I'm not losing my mind! 

 

My name is Sarah, I'm a 30 year old married mommy of 2. I work full time as a Registered Nurse on a cardiac intensive care unit. My life is busy busy busy and always hectic to say the least!

 

Last fall, I started having a lot of digestion issues, but I chalked it up to poor eating and stress. I've have intermittent bouts of nausea/dry heaving, mostly in the mornings, for years. For a long time, I thought I had gall bladder issues, but I've had that route checked out at least 3 times, and nothing ever comes back abnormal (ie: no gall stones, sludge, inflammation, etc.). October of last year, I started breaking out in hives for no apparent reason. I had made no changes in my diet, no new skin products, no new laundry products, nothing. I just woke up one morning itching like crazy, looked on my stomach, and I was covered in hives. That went on for about 2 weeks, just random hive outbreaks that I couldn't get rid of with anything OTC, so I went to my primary doctor. They thought it could be a reaction an antihypertensive medication that I was on (ACE inhibitor), but I had literally been on that medication for over 10 years. They changed my meds around, gave me Rx strength antihistamines, and told me to continue taking Zyrtec everyday. The hives cleared up and I didn't have any problems until after the start of the new year. 

 

Since January, I have had constant diarrhea. Within 30-60 minutes of eating, I am nauseous and in the bathroom. I started to notice it was a lot worse after I would eat things with bread, like sandwiches, and especially pizza. Pizza is the absolute WORST. I have taken enough Immodium in the past 3 months to clog a person up for a year, yet I was still having diarrhea. The end of February/beginning of March, I broke out in another rash that started on my legs and spread to my arms. The itching was so intense, I literally did not sleep for days on end because I could not stop scratching. I tried everything I could think of, including the Rx antihistamines I had been given in October, and they didn't even help. I scratched my skin until I had sores on my legs and arms, it was awful. I got in with my doc after a week of going crazy from itching, and she referred me to a dermatologist. The dermatologist said she was pretty sure I have follicular eczema, gave me Rx strength hydrocortizone cream and lotion, and told me to up my Zyrtec to 2x daily. Finally, after several days, I started to get relief from the skin issues. 

 

However, the GI issues have still remained. I generally feel miserable all the time. My gut hurts continuously. I feel bloated and swollen all the time. I'm gassy all the time. I have horrible indigestion and acid reflux (I'm on Prilosec and Zantac). I'm tired of being tired and feeling like crap (ha!) all the time.

 

2 weeks ago, I decided to go gluten-free. I just completely cut all gluten out of my diet. Within the first week, I felt 1000 times better, and actually lost 4.5 lbs in 5 days (which is good, I need to lose weight). Like a fool, after a week, my kids talked me into ordering pizza one night, and I ate a piece of it. Laziness on my part for not making myself something "clean". Within an hour, I was in the bathroom with the worst stomach cramps and diarrhea. I was nauseous all night after that. I vowed then that I was never eating gluten again! Bold statement, I know. Fast forward to tonight, a week later, and I stupidly did it again. And once again, within an hour of eating, I was in the bathroom. And I am so nauseous and dry heaving, I had to run to the store to buy Tums and I grabbed some Probiotics to see if that would help too. I am currently in misery and it's my own stupid fault! I guess I just needed to be absolutely sure.

 

I know this is long, I'm trying to wrap up...hang with me!

 

My biggest issue is trying to figure out how to approach this subject with my doctor. I love my doctor, I trust her opinion, we have a great relationship. But I sometimes feel like she must think I'm a hypochondriac with all of the health issues I've had at such a young age. I really, truly, deep down think that a lot of my issues may stem from this issue with Gluten. I'm going to call her office tomorrow and see if I can get an appointment with her soon to discuss all this and see if she will refer me to a GI specialist. I guess I have to start somewhere.

 

If you made it this far, thanks for reading my story, and any insight anyone can give me is greatly appreciated. I just want to feel good and I'm hoping that this is a step in the right direction!

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



EmiPark210 Contributor

Welcome to the forum and you've come to the right place for questions about gluten intolerance! 

 

It sounds like your symptoms are lining up strongly enough with gluten consumption to warrant a test. The unfortunate news is you have to continue eating gluten throughout testing for celiac to maintain antibody levels and damage in the small intestine. So if you're considering getting testing done, don't cut it out completely. You can cut it down to half a piece of bread or a gluten dessert (cookie, cracker, brownie, something of that size) every other day if the symptoms are disturbing your life. There are people on this forum who can tell you what types of blood tests to request, and what to look for as the first step. Usually your primary care doctor can order the tests but they might refer you to the GI depending on the availability of testing in your area (urban is a usually easier than rural). 

A diagnosis will certainly help with the slip ups because, if it is celiac disease, then it can mess up your body completely to continue to eat gluten. And this whole thing can just turn itself on at any moment so you're totally justified in wanting to get information after a year of issues (aka not a hypochondriac).

 

For future steps, if your blood tests come back positive, then you'll definitely get referred to a GI to do an endoscopy to biopsy your small intestine to confirm the diagnosis. If it comes back positive, you should definitely get your kids tested (this is genetically linked) and encourage all 1st degree relatives (siblings, parents) to also get tested. If your tests come back negative even with a full gluten challenge, you might still be "non-celiac's gluten intolerant." Even if all tests come back negative, your body is more accurate. If cutting out gluten makes you feel better, then do it. The testing just helps with insurance and as a way to make sure you stick to it and have everyone who provides you with food stick to it. 

 

Let us know if you have any other questions!

Link to comment
Share on other sites
gfreemarketingguru Rookie

Sounds like you've figured out your own problem, like a huge number of people with gluten issues. Your reactions scream gluten intolerance or likely celiac. It is no secret that the medical community is far behind in diagnosis of celiac. It can be important to know if you are gluten-intolerant or have celiac disease...however you need to have gluten in your system to test accurately for celiac, so call your doctor ASAP, tell her your find & get blood test immediately. Dont worry about what your doctor might think...celiac is one of those diseases that requires you to be your own advocate. I discovered my baby's celiac after 2 months of misdiagnosis by gi docs thanks to this website & it saved his life!

Link to comment
Share on other sites
beachbirdie Contributor

Hi Sarah, and welcome to the forum!

 

You have come to the right place for information and friendly support!  Hopefully your doctor will move quickly to get you tested.

 

This forum is full of people who have struggled for YEARS with misdiagnoses before finally figuring out celiac was the cause of their problems.  Your short gluten-free trial has already told you a lot, you feel better when you do not eat it!

 

But please, as EmiPark said, keep eating gluten while you are in the midst of testing.  You won't produce antibodies if you are not eating gluten, and the antibody level can drop quickly when you stop.

 

Keep us posted how things go with your doc, and keep asking questions!  Be sure she tests for these things:

 

Total Serum IgA

Deamidated Gliadin Peptides - (2 tests... DGP IgA and DGP IgG)

Endomysial Antibodies (anti-EMA)

Tissue Transglutaminase antibodies (IgA is usual version, I'd ask for IgG too)

 

 

 

 

Link to comment
Share on other sites
sisterlynr Explorer

Welcome.  You have found a great site.  I too have suffered for too long w/o a diagnosis.  I had an aunt that died at the age of 38 with Celiac colon cancer, never diagnosed or thought of until her daughter was diagnosed with Celiac.  In addition 3 of my aunt's siblings died from colon cancer the oldest being 64.  None of them had the skin rash.  My cousin was diagnosed 6 years ago via EGD biopsy and she did have the rash on her scalp.  

 

I've had gut issues and rashes for many years.  When I broke out in Feb of 2012 with a severe rash. . . I started searching for an answer and I found it.  This was one of the first sites that I was able to see 'real' people with pictures of their rashes.  There is a area out here that addresses Dermatitis Herpetiformis, in depth.  It will really help you to connect with members.  My blood tests were negative but that didn't stop me.  My cousin's blood test were negative too.  She became so iron deficient that she required infusions to recover.  She was told to notify all of her blood relatives by her GI.  She cannot get one bit cross contaminated without what you have described happening to her.  Good luck, hang in there and there is a resolution.  Gluten free, forever!

Link to comment
Share on other sites
1desperateladysaved Proficient

I wonder if you might have water weight.  Oh, high blood pressure probably so!    My water wieight is due to adrenal gland not being able to make cortisol. My adrenals had given out.   At any rate I saw an osteopathic doctor a few days back which is trained in Functional Medicine.  The nurse practiitioner and doctor gave me an herbal mix to support the adrenals.  I am sure my adrenal glands have kicked back on.  I woke up during the night and felt them going.  Wow!  They expect that I will lose weight, and I wonder if it will be dramatic.  I once lost 30 lbs in a week, so I know what it can mean.  Whatever your problems end up to be work on improving your diet and healing your illness from the roots.  I hope you will be able to slow down a little.  I know that is tough with a job and little ones.

 

You can tell if your adrenals are taxed by orthostatic blood pressure.  As I understand if you pressure goes down when you stand, your adrenals are having trouble.

 

Diana

Link to comment
Share on other sites
GFinDC Veteran

HI,

 

If I were you I'd print out this thread and show it to your doctor.  You wrote a pretty darn good description of your symptoms and how gluten affected them.  So let your doctor know so the can start from the same information.

 

DH (dermatitis herpetiformis) is a skin rash that only people with celiac disease get.  They test for it by taking a biopsy sample of the skin next (not in) a lesion and check it for IgA antibodies.  Some people with DH find that limiting or removing iodine from the diet while they are flaring helps resolve symptoms faster.  A dermatologist cna take a biopsy for DH.  If you have DH, then you have celiac disease, regardless of any other test results being positive or negative. Check the dermatitis herpetiformis section of the forum for more info.

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      121,090
    • Most Online (within 30 mins)
      7,748

    Nicole K
    Newest Member
    Nicole K
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Denise I
      I am looking to find a Celiac Dietician who is affiliated with the Celiac Disease Foundation who I can set up an appointment with.  Can you possibly give some guidance on this?  Thank you!
    • Posterboy
      Nacina, Knitty Kitty has given you good advice. But I would say/add find a Fat Soluble B-1 like Benfotiamine for best results.  The kind found in most Multivitamins have a very low absorption rate. This article shows how taking a Fat Soluble B-1 can effectively help absorption by 6x to7x times. https://www.naturalmedicinejournal.com/journal/thiamine-deficiency-and-diabetic-polyneuropathy quoting from the article.... "The group ingesting benfotiamine had maximum plasma thiamine levels that were 6.7 times higher than the group ingesting thiamine mononitrate.32" Also, frequency is much more important than amount when it comes to B-Vitamin. These are best taken with meals because they provide the fat for better absorption. You will know your B-Vitamin is working properly when your urine becomes bright yellow all the time. This may take two or three months to achieve this.......maybe even longer depending on how low he/you are. The Yellow color is from excess Riboflavin bypassing the Kidneys....... Don't stop them until when 2x a day with meals they start producing a bright yellow urine with in 2 or 3 hours after the ingesting the B-Complex...... You will be able to see the color of your urine change as the hours go by and bounce back up after you take them in the evening. When this happens quickly......you are now bypassing all the Riboflavin that is in the supplement. The body won't absorb more than it needs! This can be taken as a "proxy" for your other B-Vitamin levels (if taken a B-Complex) ...... at least at a quick and dirty level......this will only be so for the B-1 Thiamine levels if you are taking the Fat Soluble forms with the Magnesium as Knitty Kitty mentioned. Magnesium is a Co-Factor is a Co-factor for both Thiamine and Vitamin D and your sons levels won't improve unless he also takes Magnesium with his Thiamine and B-Complex. You will notice his energy levels really pick up.  His sleeping will improve and his muscle cramps will get better from the Magnesium! Here is nice blog post that can help you Thiamine and it's many benefits. I hope this is helpful but it is not medical advice God speed on your son's continued journey I used to be him. There is hope! 2 Tim 2:7 “Consider what I say; and the Lord give thee understanding in all things” this included. Posterboy by the grace of God,  
    • trents
      I'll answer your second question first. The single best antibody test for monitoring celiac blood antibody levels is the tTG-IGA and it is very cost effective. For this reason, it is the most popular and often the only test ordered by physicians when checking for celiac disease. There are some people who actually do have celiac disease who will score negatives on this test anyway because of anomalies in their immune system but your wife is not one of them. So for her, the tTG-IGA should be sufficient. It is highly sensitive and highly specific for celiac disease. If your wife gets serious about eating gluten free and stays on a gluten free diet for the duration, she should experience healing in her villous lining, normalization in her antibody numbers and avoid reaching a celiac health crisis tipping point. I am attaching an article that will provide guidance for getting serious about gluten free living. It really is an advantage if all wheat products are taken out of the house and other household members adopt gluten free eating in order to avoid cross contamination and mistakes.  
    • Anmol
      Thanks this is helpful. Couple of follow -ups- that critical point till it stays silent is age dependent or dependent on continuing to eat gluten. In other words if she is on gluten-free diet can she stay on silent celiac disease forever?    what are the most cost effective yet efficient test to track the inflammation/antibodies and see if gluten-free is working . 
    • trents
      Welcome to the community forum, @Anmol! There are a number of blood antibody tests that can be administered when diagnosing celiac disease and it is normal that not all of them will be positive. Three out of four that were run for you were positive. It looks pretty conclusive that you have celiac disease. Many physicians will only run the tTG-IGA test so I applaud your doctor for being so thorough. Note, the Immunoglobulin A is not a test for celiac disease per se but a measure of total IGA antibody levels in your blood. If this number is low it can cause false negatives in the individual IGA-based celiac antibody tests. There are many celiacs who are asymptomatic when consuming gluten, at least until damage to the villous lining of the small bowel progresses to a certain critical point. I was one of them. We call them "silent" celiacs".  Unfortunately, being asymptomatic does not equate to no damage being done to the villous lining of the small bowel. No, the fact that your wife is asymptomatic should not be viewed as a license to not practice strict gluten free eating. She is damaging her health by doing so and the continuing high antibody test scores are proof of that. The antibodies are produced by inflammation in the small bowel lining and over time this inflammation destroys the villous lining. Continuing to disregard this will catch up to her. While it may be true that a little gluten does less harm to the villous lining than a lot, why would you even want to tolerate any harm at all to it? Being a "silent" celiac is both a blessing and a curse. It's a blessing in the sense of being able to endure some cross contamination in social settings without embarrassing repercussions. It's a curse in that it slows down the learning curve of avoiding foods where gluten is not an obvious ingredient, yet still may be doing damage to the villous lining of the small bowel. GliadinX is helpful to many celiacs in avoiding illness from cross contamination when eating out but it is not effective when consuming larger amounts of gluten. It was never intended for that purpose. Eating out is the number one sabotager of gluten free eating. You have no control of how food is prepared and handled in restaurant kitchens.  
×
×
  • Create New...