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

Struggling With Anger At Doctors


greenbeanie

Recommended Posts

greenbeanie Enthusiast

I have an appointment in a few days with a new doctor who seems willing to finally test me for celiac, after 37 years of increasing symptoms. I'm glad to have finally found someone who seems willing to take my concerns seriously, but I've had such bad experiences in that past that I don't know what I'll do if she turns out to be another doctor who won't listen. I've prepared everything I can think of to bring to the appointment - a chronological list of the many symptoms that have worsened over the years, factsheets from multiple prominent celiac research centers, scholarly article abstracts, etc. Any suggestions for what else I can say or do to get her to listen? 

 

My symptoms are way too many to list briefly, but here are the most bothersome ones:

  • Horrible, itchy rashes since age 6, often over large areas of my body.They ooze yellow/clear fluid and bleed when I scratch. I was told it was eczema, then stress, then contact dermatitis. But no creams, relaxation techniques, or perfume-and-dye free detergents/soaps/shampoos have helped.
  • Diarrhea 4-6 times per day since early teens, along with nausea after meals and extreme fatigue. Doctor did one stool test for parasites (negative) and concluded I was fine. When there was no improvement after a year, I went back several more times. Doctor reminded me of "The Boy Who Cried Wolf" and said that if I kept coming back with the same complaint, she wasn't going to be able to believe anything I told her. She said I was lucky to have such a fast metabolism that I could eat whatever I wanted and never gain weight. On the fifth or sixth visit, she essentially threatened me by saying that if I came back complaining of diarrhea again, she'd make me get a colonoscopy that would be "extremely unpleasant" and would involve "shoving something up my butt". She also implied that my parents would be upset at having to pay for the procedure when she knew there was nothing wrong with me. I didn't go to a doctor for years after that.

  • Awful insomnia for the last 20+ years. Sleep study ruled out obvious causes, through my brain waves showed very little deep sleep waves (which they couldn't explain). Medications did not help.

  • Terrible SI joint pain that did not respond to physical therapy, acupuncture, massage, or cortisone shots.

  • Increasingly bizarre neurological symptoms - walking into doorframes, falling down stairs, hand cramps, trouble with buttons and coordination, forgetting names of people I've known for decades. Neurologists found nothing wrong and said it was from stress.

  • Internal shaking for the last five years, extreme nausea much of the time, and soaking several shirts and blankets per night with sweat. Repeated negative tests for diabetes and thyroid problems. Again, I was told it was from stress. When I pointed out that it's just as bad on vacation, or at times of my life when everything is going perfectly well, doctors said that stress can come from good things too, and that even being happy with my job is a form of stress! No matter what I say, I can't win. Previous doctor wouldn't test me for celiac because she said that I would have died in childhood if I'd had untreated celiac (which I know isn't accurate), and the most I insisted that something was really wrong, the more convinced she became that I was irrational.

  • Clear response to a 12-day strict gluten-free trial - exhaustion for the first few days, then felt better than I ever have in my life, then became violently ill upon reintroducing gluten.

This last bit is what got a new doctor to finally agree to meet with me to talk about celiac testing. I feel awful but I've continued eating some gluten every day since then because I really need accurate test results. I simply can't handle larger amounts, but I'm worried that I'm not eating enough for it to show up, and that my doctor will stop pursuing this if tests are negative.

 

Obviously, I'm going to stop eating gluten immediately once the tests are over (regardless of the results), but a diagnosis is crucial because my daughter is having similar symptoms, and her own doctor keeps telling us she's just an anxious child and won't test her either. So there is a lot riding on this appointment, and I'm getting more and more nervous as it gets closer. Any advice would be most appreciated! Sorry this is so long.

 

 


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



Celiac.com Sponsor (A8-M):



Celiac Mindwarp Community Regular

Hi greeniebeanie

I am so sorry to hear you have had such a terrible time with doctors. No one deserves to be treated like that. Sadly, this is a very familiar story. Many of us have been told we are stressed, making it up etc.

It sounds as if you are doing exactly the right things. There is a list around of the FULL list of tests to request.

The fact you had such a positive response to the gluten-free diet speaks volumes, as does your suffering back on. You may be referred for a biopsy, and will need to carry on on gluten for that too.

Your symptoms sound like a good possibility of celiac or non celiac gluten intolerance.

Stick around, ask questions, rant, we are here

stanleymonkey Explorer

Some doctors are clueless and quite happy to blame the patient

We had annoying experiences when my now 4 yr old was younger

Me:she has green diarrhea up to 20 times a day it is so toxic it burns her skin off

Doc: stop giving her juice

Me: she has never had juice

Doc: then it's toddler diarrhea

Me: she's lost 20% of her body weight in 1 week

Doc: see your ped about the toddler diarrhea !!!

Gastro: I see she's dairy free? Good dairy can cause issues in a lot of children. You just Ned to be more diligent.

Me: she has an anaphylactic allergy to milk, she has never touched any since she was 9 months old!

Doc: guess its just functional constipation then, and reflux give her Zantac

Me: what dosage ?

Doc: I don't know ask the pharmacists

If you aren't happy with your doc and no one will help with testing, I would just go gluten free unless you need an official diagnosis of medical insurance or school etc.

We ignored our ignorant gastro, and now have a happy healthy 4 yr old

1desperateladysaved Proficient

Sorry to hear you have suffered like this.  I hope that your new doc will show you respect and try to get to the root of your problem.  I want you to get definitive answers that will help you to be delivered from the weight of your burden.

 

Hi Greenbeanie,

 

I like bringing a list of questions to the doctor.  That way, I don't forget anything.  I hope you will get a test of your nutrient levels.  I shook every day of my life until I took Magnesium supplement a few days.  I always thought I was nervous!  I had Undiagnosed celiac for at least 30 years, so I understand the grief of the loss of years.  I hope one day you will appreciate feeling well again. 

 

Doctors can only be human and will make mistakes, even big ones. They are only as good as their training and their use of it.  I think they generally care for people and I hope they will learn to put celiac in their minds as a possibility.  Meanwhile, I am glad for the forum, books,  and the interned.which are helping many people discover their health problems are rooted in celiac.  Even those like me that didn't have a family history!

 

Once you know you have a problem, you can make a great difference in your health.  That is a freeing feeling. 

 

Diana

ravenwoodglass Mentor

You poor thing. I know what you're going through as I went through the same. If your new doctor refuses to test you ask for a referral to a GI doctor. Some are getting better at diagnosing us. If one wants to do a colonoscopy INSIST they also do an endoscopy to look for celiac. Another route to diagnosis might be to look for a dermatologist who is knowledgeable about dermatitis herpeformis so the skin next to your lesions can be biopsied. A diagnosis of DH is a diagnosis of celiac. Do make sure that they are looking for DH though as the lab needs to know that is what is suspected. I had the same itchy oozing rash for most of my life and know how miserable it is.

I wish you good luck.

This is a link to the NIH website for DH. Bring a copy with you to the derm if you go to one.

 

Open Original Shared Link

greenbeanie Enthusiast

Thank you all so much for your kind words. I will definitely bring a list of questions, and a list of tests to request. Surely the new doctor will at least be willing to refer me to a dermatologist, so that might be another route to a diagnosis. (I've never actually seen a dermatologist about the rash since I was a little kid - my last few primary care doctors haven't been willing to refer me for anything. But I have a well-documented history of unexplained rashes for 30+ years, so hopefully the new doctor will at least listen to reason about that!) I will also push hard for a referral to a GI doctor, regardless of what blood tests show.

 

Diana, thanks for the magnesium suggestion! I took some yesterday and again today, and it does help with the shaking! This is amazing! My diet is already high in magnesium (lots of leafy greens, cashews, and buckwheat), so I never would have thought of this as a potential deficiency. It's hard to believe that just two days' worth of vitamins could really make much difference, so perhaps it's just a placebo effect...but anyhow, I'll definitely keep it up for a while and see. I had three years of infertility treatments before conceiving my daughter, and they started me on a high-quality prescription prenatal vitamin at the beginning of that time. I always felt great on it, and many of my long-standing health problems were much better during pregnancy. I wonder if that's why. 

Deaminated Marcus Apprentice

I have a lot of medical issue also.

I think it's best to go there goal oriented.

Your goal is to get tested for Celiac so just tell her a few of the classic symptoms she can understand.

Don't expect the doctor to understand so much, just the basics.

 

This line you wrote is convincing:

 

"Clear response to a 12-day strict gluten-free trial - exhaustion for the first few days, then felt better than I ever have in my life, then became violently ill upon reintroducing gluten."

 

Then give her a list of the celiac blood tests that you want done as listed in this forum.

Be sure to be eating gluten before the blood test.

 

Then decide if you want an endoscopy based on the blood test results.

 

Once that issue is figured out, if you still like this doctor, then go back to discuss another other medical problem.

Step by step is the way to go.

 

Good luck.


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
      131,979
    • Most Online (within 30 mins)
      7,748

    volivier
    Newest Member
    volivier
    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

    • trents
      @Riley, on this forum we sometimes get reports from people with similar experiences as you. That is, their celiac disease seems to go into remission. Typically, that doesn't last. At age 18 you are at your physical-biological peek in life where your body is stronger than it will ever be and it is able to fight well against many threats and abuses. As Wheatwacked pointed out, absence of symptoms is not always a reliable indicator that no damage is being done to the body. I was one of those "silent" celiacs with no symptoms, or at least very minor symptoms, whose body was being slowly damaged for many years before the damage became pronounced enough to warrant investigation, leading to a diagnosis. By that time I had suffered significant bone demineralization and now I suffer with back and neck problems. Please, if you choose to continue consuming gluten, which I do not recommend, at least get tested regularly so that you won't get caught in the silent celiac trap down the road like I did. You really do not outgrow celiac disease. It is baked into the genes. Once the genes get triggered, as far as we know, they are turned on for good. Social rejection is something most celiacs struggle with. Being compliant with the gluten free diet places restrictions on what we can eat and where we can eat. Our friends usually try to work with us at first but then it gets to be a drag and we begin to get left out. We often lose some friends in the process but we also find out who really are our true friends. I think the hardest hits come at those times when friends spontaneously say, "Hey, let's go get some burgers and fries" and you know you can't safely do that. One way to cope in these situations is to have some ready made gluten-free meals packed in the fridge that you can take with you on the spot and still join them but eat safely. Most "real" friends will get used to this and so will you. Perhaps this little video will be helpful to you.  
    • Wheatwacked
      @Riley., Welcome to the forum.   It was once believed that Celiac Disease was only a childhood disease and it can be outgrown.  That was before 1951, before gluten was discovered to be cause of Celiac Disease, also called Infantilism.  Back then Cileac Disease was thought to be only a gastro intestinal disease, once you  "outgrew" the colicky phase, you were cured. You were so lucky to be diagnosed at 5 years old so your developing years were normal.  Gluten can affect multiple systems.  The nervous system, your intellegence. The muscules, skeleton. It can cause neurological issues like brain fog, anxiety, and peripheral neuropathy.  It can cause joint pain, muscle weakness, and skin rashes. Epilepsy is 1.8 times more prevalent in patients with celiac disease, compared to the general population. Because through malabsorption and food avoidances, it causes vitamin D and numerouus other essential nutrient deficiencies, it allows allergies, infections, poor growth, stuffy sinuses and eustacian tubes. There is even a catagory of celiac disease called "Silent Celiac".  Any symptoms are explained away as this, that or the other thing. Gluten is one of the most addictive substances we consume.  Activating the Opiod receptors in our cells, it can numb us to the damage that it, and other foods are causing.  It has become socially acceptable to eat foods that make us feel sick.  "There's a pill for that".   It is generally accepted that n fact you are weird if you don't. The hardest part is that if you don't eat gluten you will feel great and think why not.  But slowly it will effect you, you'll be diagnosed with real diseases that you don't have. You'll be more susseptable to other autoimmune diseases.  As you read through the posts here, notice how many are finally dianosed, after years of suffering at older ages.  Is it worth it? I think not. Perhaps this book will help:  Here is a list of possible symptoms:   
    • Riley.
      Hi! Im Riley, 18 years old and have been diagnosed for 13 years.. the testing started bc I stopped growing and didn’t gain any weight and was really small and thin for my age.  I got diagnosed when I was 5 and have been living gluten free since, in elementary and middle school it was hard for me and I kept contaminating myself bc I wanted to fit in with my friends so so badly. I ate gluten secretly at school and mostly regretted it 30 minutes later.  I’ve had symptoms like diarrhea, nausea, headaches, stomachaches, threw up a lot and was really emotional.  In 2022 I really started working on myself and tried to stay gluten free and if I did eat gluten I wouldn’t tell anyone and suffer in silence.  Last year in July I begged my mom to let me „cheat“ one day bc I just wanted to fit in… I ate a lot of different stuff, all the stuff I missed out on in my childhood like nuggets, pizza and all that.. I didn’t have symptoms that day and was doing really fine My mom and I wanted to test how far we can go and said we would test it for 12 weeks to get my blood taken after to see if I’m doing good or if symptoms start showing  As a now 18 year old girl who finally gained a normal weight and doesn’t get symptoms I’m to scared to get tested/my blood taken cuz I finally found comfort in food and it got so much easier for me and my family.  A year and 4 months later i still didn’t get any symptoms and have been eating gluten daily.  I’m scared to get tested/my blood taken cuz what if I’m actually not fine and have to go back to eating gluten free. Any tips to get over that fear and „suck it up“ cuz I know I could seriously damage my body… sorry if I seem like a idiot here… just don’t really know what to do :,)
    • 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!
×
×
  • 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.