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

Advice Please


Sheloveshim

Recommended Posts

Sheloveshim Newbie

Hi

I posted a few weeks ago about my tests not being negative and not positive. Well I started eating gluten again for the last 3 weeks after being off for 3 weeks. My symptoms returned but differnrnt instead of having 2 to3 times aday D now I can go 3 or 4 days without going to te bathroom, my hair is falling out in clumps, my legs and arms falling asleep (tingling) also my scalp tingles, bloating, irritable , forgetfulness , tired, I also have a twitch (might be stress) about two hours after I eat I feel drunk and my eyes can't focus. So I went to the dr the first time to get my blood results month ago or so and she said I wasn't neg or positive and to not eat gluten if it made me feel better, we'll I wanted a more positive answer so I am eating a sandwhich or toast at least once day so I can get retested which I went in expecting her to retest and she told me no and that if it hurt don't do it that's all I told her my symptoms and I was worried that I might have damaged stuff by eating gluten for basically all my life and I want to make sure she told me that celiac doesn't cause other issues in your body just tummy problems and to simply stop eating it. When she ran my tests she mentioned my liver enzymes being high 76 normal is 65 (I have not drank in atleast 3 years and I don't take Tylenol or any pain meds) I mentioned to her that three years ago when my son was born my husband made me get life insurance and I had to do blood work well they mentioned my enzymes high too I don't remember how high. She said again I am fine but the mentioned one test I don't know what it was but the number was 1.1 and in order for it to be positive has to be above 7 . I said ok the only thing I want to know is why is my hair falling out she mentioned I am nursing my 4 month old and 2 1/2 year old with my first baby I had normal hair loss but this is crazy blading spots. She said that I might be different in vitiamns and minerals but they can't test for it . After I ended up crying because I don't want to leave my two babies if there was something wrong and nobody caught it (my parents passed when I was 18 ) the dr reffered my to a gastologist she mentioned that the dr would yell at her for this Refferal. Now I feel like a crazy balding lady who is going to this gastro dr for nothing. Now what do I do? What's the best stuff to eat? Should I keep a food diary? I am also lactose intolerant which came on suddenly after birth of my first so I avoid also since they both react to milk in my milk. I don't know should I bother going? Or just stop eating gluten

Thank you for reading my confusing novel

Also my husband is navy and we are moving in a few months with a possible year +/- deployment with no family around to help so I want to figure what wrong or suffer till he returns

Thank you again


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



Celiac.com Sponsor (A8-M):



Skysmom03 Newbie

First of all, I am sure you will be fine if you do indeed have Celiac. Secondly, she is a bit misleading because it can cause other issues ( cancer, neurological problems, kidney issues, bone brittleness)which is why people should always have an endoscopy when Celiac comes into question. But with that being said, you will be okay.... You just have to make sure you stick with the diet and make sure you have regular bloodwork done to check for vitamin deficiencies and other issues).

Try not to worry... That can cause hair loss as well.

mushroom Proficient

I would definitely accept the gastro referral, keep eating the gluten, tell lhim you were gluten lite or free when you were tested previously and ask him to test you again with a full celiac panel. Be sure also to tell him about your lactose intolerance and that of your babies also when you drink milk. Be sure to tell him about your liver enzymes and take a copy of those results if you can or ask the doc to send them (if you are military your chart may follow you around??) Make it clear that you want a definite diagnosis because if you should end up with an overseas assignment that could complicate things for you. Stress that the prior testing was not accurate because you were not eating gluten. This is what a full celiac panel looks like:

  • tTG (anti-tissue transglutaminase)-IgA
  • EMA (anti-endomysial antibodies)-IgA
  • DGP (deamidated gliadin peptide)-IgA and IgG
  • Total serum IgA

They need to do all these tests; the last is important to make sure you produce normal quantities of IgA.

As the previous poster said, celiac can do much more damage than just to your intestines - to your nervous system, to your joints, to your brain, to your skin - and it can affect your whole body through lack of absorption of essential nutrients which are necessary for all functions in the body. So you need to be sure that your levels of Vit. D, B12, iron/ferritin, magnesium, zinc have been tested, and also your thyroid function. And yes, a food and symptom log is always helpful.

By the way, child birth is often the trigger for the onset of celiac disease.

GottaSki Mentor

When a doctor is being both dismissive and relaying FALSE information in is time for a new doctor. Celiac Disease has over 300 symptoms - many of which are not GI related. Unfortunately many doctors are neither trained nor have experience with Celiac. It sounds like you may be switching doctors very soon - so for now move onto the GI and hold off on switching primary.

Are you still consuming gluten since you reintroduced it for more bloodwork? (Good plan BTW). It would be best if you can remain on gluten until you see the GI.

I suggest you ask to speak with the GIs nurse and let them know you would like a full celiac panel based on your sypmtoms - preferably before your appt so that the GI can review them with you rather than waiting for a second appt. If asked tell them that your primary refused to run said panel.

Next prepare for your upcoming GI appt. Write down all your symptoms prior to removing gluten, improvements along with new symptoms. It is unfortunate, but you do need to arm yourself with knowledge of symptoms and know ALL the proper tests to ask for - you can not assume even the GI will be up to date with regard to testing or treating celiac.

Hang in there - I understand completely what it is like to be dismissed by doctors - ask as many questions as you like - a lot of folks here can help.

AandGsmomma Apprentice

Im sorry your doctor is giving ypu the run around. You can get a vitamin panel run to see of you are deficent in anything. Also, my liver enzymes were always high, I was told I had fatty liver disease and that I would probably need a transplant in 30 years. I went off gluten amd with in weeks my cholesterol, triglicerides, and liver enzymes dropped. Good luck, I hope the GI is better than the primary.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,859
    • Most Online (within 30 mins)
      7,748

    Lesley-Anne
    Newest Member
    Lesley-Anne
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Rogol72
      Some interesting articles regarding the use of Zinc Carnosine to help heal gastric ulcers, gastritis and intestinal permeability. I would consult a medical professional about it's use. https://www.nature.com/articles/ncpgasthep0778 https://www.rupahealth.com/post/clinical-applications-of-zinc-carnosine---evidence-review https://pmc.ncbi.nlm.nih.gov/articles/PMC7146259/ https://www.fallbrookmedicalcenter.com/zinc-l-carnosine-benefits-dosage-and-safety/
    • Jillian83
      He is. Which makes everything even more difficult. I’m not a believer in “staying for the kids” but I have nowhere to go and it’s not just me, it’s me plus my babies. We live in a beautiful place, lots of land in the country and me and the kids love the place we’ve called home for their entire lives. But Im seeing that he’ll never change, that my kids deserve a happy healthy Momma, and that staying in this as is will be the early death of me. Then I look at the scars covering my entire body…this disease and the chronic stress I’ve been enduring for years that tell me I’m no longer beautiful and no one will ever look at me with interest again. I try self care, try to give myself grace so I can just start loving myself enough to gain strength but the slightest sparkle in my eye and skip in my step attracts his wrath and it all comes crashing ten fold. Life is just absolutely railing me from every single direction leaving me wanting to wave that white flag bc I don’t feel like there’s much hope no matter what happens. 
    • trents
    • Jillian83
      Hi, I was recently diagnosed with Celiac and dermatitis herpetiformis after years of suffering without answers. I lost my mind. I lost my job. I lost so much time. I lost Me. Conventional doctors are opulent come near me and the one who did sat across the room, misdiagnosed me, pumped me full of steroids which collapsed my entire hip for 6 months. So without answers I began my holistic journey. Fast forward a couple of years and still struggling with a mysterious whole body itchy, crawling “skin hell”, perfect teeth now deteriorating, thick hair now thinning rapidly and no more than a day or 2 at most relief….An acquaintance opened up a functional medicine practice. Cash only, I found a way. Within a month tests clearly showing my off the charts gluten allergy/sensitivity as well as the depletion of vital nutrients due to leaky gut and intestinal damage. dermatitis herpetiformis was more than likely what I was experiencing with my skin. I was happy. I thought this is easy, eat healthy Whole Foods, follow the diet restrictions and I finally get to heal and feel confident and like myself again very soon! 😔 Supplements are very pricey but I got them and began my healing. Which leads to the other major issue: not working, stay at home Mom of young kids, entirely financially dependent on my man of 7 plus years. He’s never been supportive of anything I’ve ever done or been thru. He controls everything. I’m not given much money ever at a time and when he does leave money it’s only enough to possibly get gas. His excuse is that I’ll spend it on other things. So my “allowance” is inconsistent and has conditions. He withholds money from me as punishment for anything he wants. Since being diagnosed, he’s gained a new control tactic to use as punishment. He now is in control of when I get to eat. He asked for proof of my diagnosis and diet bc he said I made it up just to be able to eat expensive organic foods. Then after I sent him my file from my doctor he then said she wasn’t a real doctor. 😡. I go days upon days starving, sometimes breaking down and eating things I shouldn’t bc I’m so sick then I pay horribly while he gets annoyed and angry bc I’m not keeping up with all the duties I’m supposed to be doing. His abuse turns full on when I’m down and it’s in these desperate times when I need his support and care the most that I’m punished with silence, being starved, ignored, belittled. He will create more of a mess just bc I’m unable to get up and clean so that when I am better, I’m so overwhelmed with chores to catch up that the stress causes me to go right back into a flare from hell and the cycle repeats. I’m punished for being sick. I’m belittled for starving and asking for healthy clean water. I’m purposely left out of his life. He won’t even tell me he’s going to the grocery or to get dinner bc he doesn’t want me to ask him for anything. I have no one. I have nothing. Im not better. My supplements ran out and I desperately need Vitamin D3 and a methylated B complex at the very minimal just to function….he stares at me blankly…no, a slight smirk, no words. He’s happiest when im miserable and I am miserable.  this is so long and im condensing as much as I can but this situation is so complicated and disgusting. And it’s currently my life. The “IT” girl, the healthy, beautiful, perfect skin, perfect teeth, thick and curly locks for days, creative and talented IT girl….now I won’t even leave this house bc Im ashamed of what this has dont to my body, my skin. Im disgusted. The stress is keeping me from healing and I think he knows that and that’s why he continues to keep me in that state. He doesn’t want me confident or successful. He doesn’t want me healed and healthy bc then how would he put the blame of all his problems on me? This journey has been hell and I’ve been in Hell before. I’ve been killed by an ex, I’ve been raped, robbed, held hostage, abused beyond nightmares but the cruelty I’ve experienced from him bc of this disease is the coldest I’ve ever experienced. I’ve wanted to give up. Starving and in tears, desperate…I found a local food pantry in our small town so I reached out just saying I had Celiac and was on hard times. This woman is blessing me daily with prepared gluten free meals, donations, educational info, people who know this disease and how they manage life and the blessings just keep coming. But it’s overwhelming and I feel like I don’t deserve it at all. He just glared and I know he’s going to sabotage it somehow. I don’t even know what to do anymore. I’m so broken and just want peace and healing. 
    • cristiana
      @Colleen H   I am just curious,  when you were tested for coeliac disease, did the doctors find out if you had any deficiencies? Sometimes muscle pain can be caused by certain deficiencies, for example, magnesium, vitamin D, calcium, and potassium.   Might be worth looking into having some more tests.  Pins and needles can be neuropathy, again caused by deficiencies, such as iron and B12,  which can be reversed if these deficiencies are addressed. In the UK where I live we are usually only tested for iron, B12 and vitamin D deficiencies at diagnosis.   I was very iron anemic and supplementation made a big difference.  B12 was low normal, but in other countries the UK's low normal would be considered a deficiency.  My vitamin D was low normal, and I've been supplementing ever since (when I remember to take it!) My pins and needles definitely started to improve when my known deficiencies were addressed.  My nutritionist also gave me a broad spectrum supplement which really helped, because I suspect I wasn't just deficient in what I mention above but in many other vitamins and minerals.  But a word of warning, don't take iron unless blood tests reveal you actually need it, and if you are taking it your levels must be regularly monitored because too much can make you ill.  (And if you are currently taking iron, that might actually be making your stomach sore - it did mine, so my GP changed my iron supplementation to a gentler form, ferrous gluconate). Lastly, have you been trying to take anything to lessen the pain in your gut?  I get a sore stomach periodically, usually when I've had too much rich food, or when I have had to take an aspirin or certain antibiotics, or after glutening.  When this happens, I take for just a few days a small daily dose of OTC omeprazole.  I also follow a reflux or gastritis diet. There are lots online but the common denominators to these diets is you need to cut out caffeine, alcohol, rich, spicy, acidic food etc and eat small regularly spaced meals.   When I get a sore stomach, I also find it helpful to drink lots of water.  I also find hot water with a few slices of ginger very soothing to sip, or camomile tea.  A wedge pillow at night is good for reflux. Also,  best not to eat a meal 2-3 hours before going to bed. If the stomach pain is getting worse, though, it would be wise to see the doctor again. I hope some of this helps. Cristiana    
×
×
  • 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.