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

Should I Tell My Old Doctors?


Adelle

Recommended Posts

Adelle Enthusiast

My mom brought up an interesting point.

I've been to 10 doctors (including 1 GI). All of whom missed the diagnosis. She said I should write to them telling them what was wrong with me. Would they be receptive to that? I obviously have to wait until I'm not as MAD as I am now, but at some point, should I tell them that it wasn't in my head, that they dismissed me prematurely.

I'm still unsure. Any thoughts? Thanx.


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



Celiac.com Sponsor (A8-M):



gfp Enthusiast
My mom brought up an interesting point.

I've been to 10 doctors (including 1 GI). All of whom missed the diagnosis. She said I should write to them telling them what was wrong with me. Would they be receptive to that? I obviously have to wait until I'm not as MAD as I am now, but at some point, should I tell them that it wasn't in my head, that they dismissed me prematurely.

I'm still unsure. Any thoughts? Thanx.

It can't hurt so long as you are not hurt by their responses.

Don't expect them to admit mistakes, doctors never do, they bury them....but you might save someone else the same anguish and health problems.

Just don't be upset by their responses or lack of.....

I'd probably add you don't expect an answer and you are just informing them for the benefit of their other patients. That way you won't get nasty lawyers letters back

IrishKelly Contributor
My mom brought up an interesting point.

I've been to 10 doctors (including 1 GI). All of whom missed the diagnosis. She said I should write to them telling them what was wrong with me. Would they be receptive to that? I obviously have to wait until I'm not as MAD as I am now, but at some point, should I tell them that it wasn't in my head, that they dismissed me prematurely.

I'm still unsure. Any thoughts? Thanx.

I've actually been thinking the about doing this myself, especially my GI Dr., only because i would like to save others from this horrible nightmare. The worst part about him was that he said to me, "there is something out there called Celiac's disease but you don't seem to qualify for that, so i'm not going to test you for that"...what an idiot! Anyway, i agree with the fact that if we do, we must inform them that we are letting them know strictly for the future of other patients

Ursa Major Collaborator

I think it would be a good idea to let the doctors know, and to send a brochure as well, that points out why so many people remain undiagnosed. Also, it should have a list with all the possible symptoms of celiac disease, as most doctors will only look for two of them, weight loss and diarrhea. If you don't have those, you 'can't' have it, in their opinion.

I have educated my doctor on celiac disease, and fortunately, she is one of the extremely rare doctors who admits her mistakes (that's why she is still my doctor, I prefer a humble doctor to a knowledgable one).

Nancym Enthusiast

I've always been frustrated because MD's never hear about their mistakes, their patients just leave and they go on very blythely ignorant of their failings. Yes! You should write!

chrissy Collaborator

you know, i really don't see it as a "failing" for a doctor to have missed celiac-----the information just was not readily available. it is only recently that it has been realized that celiac is a common disease and not a rare disease.

kbtoyssni Contributor

I was planning on doing this as well. Just haven't gotten the time to sit down and do it. I had one GI who should have caught it and if I sent him a letter I feel like it might be received as "you're incompetent". Which is true, but not the message I want to send :)

The other doctors I don't expect to recognize celiac. These are doctors like my ob/gyn and psycologists/psychiatrists. The symptoms I had were definitely gluten-related, but I don't expect a therapist to say "you're depressed, let's test for celiac". For these doctors, I'd like to treat it more as an educational things. Sort of a "thank you for helping me, I just found out the root cause and it's really common so maybe more of your patients have it".


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



Celiac.com Sponsor (A8-M):



Ursa Major Collaborator
The other doctors I don't expect to recognize celiac. These are doctors like my ob/gyn and psycologists/psychiatrists. The symptoms I had were definitely gluten-related, but I don't expect a therapist to say "you're depressed, let's test for celiac". For these doctors, I'd like to treat it more as an educational things. Sort of a "thank you for helping me, I just found out the root cause and it's really common so maybe more of your patients have it".

That's a very good point you're making. I am doing the same thing with my chiropractor and therapist. Because the cause of my chronic lower backpain (which was helped, but never quite alleviated by chiropractic) was celiac disease! When I went gluten-free, that pain went away about 80% within a couple of weeks, and only comes back when glutened.

And of course, my therapist treats many patients with depression. If he knows that depression is a possible celiac disease symptom, and one of his depressed patients has gastrointestinal symptoms as well, I imagine that now a light might go on in his head, and he might suggest testing for celiac disease.

And my GP now knows that yes, people with celiac disease can have unexplained weight gain, not just weight loss, thanks to me educating her on that fact. And she also knows now that lectins can cause many problems, as can salicylates.

As for my former doctors, there is no way I can do anything about them, as they're either in Germany, retired or have left the country because in the USA doctors are treated better than in Canada.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,541
    • Most Online (within 30 mins)
      7,748

    Jacqueline Dee
    Newest Member
    Jacqueline Dee
    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

    • petitojou
      Thank you so much! I saw some tips around the forum to make a food diary and now that I know that the community also struggles with corn, egg and soy, the puzzle pieces came together! Just yesterday I tried eating eggs and yes, he’s guilty and charged. Those there are my 3 combo nausea troublemakers. I’m going to adjust my diet ☺️ Also thank you for the information about MCAS! I’m from South America and little it’s talked about it in here. It’s honestly such a game changer now for treatment and recovery. I know I’m free from SIBO and Candida since I’ve been tested for it, but I’m still going to make a endoscopy to test for H. Pylori and Eosinophilic esophagitis (EoE). Thank you again!! Have a blessed weekend 🤍
    • knitty kitty
      Yes, I, too, have osteoporosis from years of malabsorption, too.  Thiamine and magnesium are what keep the calcium in place in the bones.  If one is low in magnesium, boron, selenium, zinc, copper, and other trace minerals, ones bone heath can suffer.  We need more than just calcium and Vitamin D for strong bones.  Riboflavin B 2, Folate B 9 and Pyridoxine B 6 also contribute to bone formation and strength.   Have you had your thyroid checked?  The thyroid is important to bone health as well.  The thyroid uses lots of thiamine, so a poorly functioning thyroid will affect bone heath.  
    • Celiac50
      That sounds so very likely in my case! I will absolutely ask my doctor on my next bone check coming up in March... Thanks a lot! 
    • trents
      Calcium levels as measured in the blood can be quite deceiving as the body will rob calcium from the bones to meet demands for it by other bodily functions. Also, supplementing with calcium can be counterproductive as it tends to raise gut pH and decrease absorption. More often than not, the problem is poor absorption to begin with rather than deficiency of intake amounts in the diet. Calcium needs an acidic environment to be absorbed. This is why so many people on PPIs develop osteoporosis. The PPIs raise gut pH. And some people have high gut PH for other reasons. Low pH equates to a more acidic environment whereas high pH equates to a more basic (less acidic) environment.
    • Celiac50
      Kind thanks for all this valuable information! Since my Folate was/is low and also my Calcium, there IS a chance I am low in B vitamins... My doctor only measured the first two, oh and Zinc as I has twisted her arm and guess what, that was mega low too. So who knows, until I get myself tested properly, what else I am deficient in... I did a hair mineral test recently and it said to avoid All sources of Calcium. But this is confusing for me as my Ca is so low and I have osteoporosis because of this. It is my Adjusted Ca that is on the higher side and shouldn't be. So am not sure why the mineral test showed high Ca (well, it was medium in the test but relative to my lowish Magnesium, also via hair sample, it was high I was told). But anyway, thanks again for the VitB download, I will look into this most certainly!
×
×
  • 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.