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

Looking For A Celiac Dr. Around The Toronto, ON Area


LuBelle

Recommended Posts

LuBelle Newbie

Hello all,

I am new to this forum and live in Ontario, Canada.

I have chronic Lyme disease...but have also been dx with many of the conditions typically seen w/celiac disease..osteopenia, anemia, depression, chronic fatigue, IBS, fibromyalgia, bloating and sometimes abdominal tenderness after eating certain foods.

A fellow chronic Lyme patient, found out she has celiac and suggested I look into it also..as she has greatly improved since going gluten -free...

I have been doing some research and reading on the tests etc..and want to see a G.I. specialist who really knows their stuff on celiac..It took me 13 years, until I was accurately dx with Lyme disease...I do not wish to go on anohter merry-go-round ride of many Dr.'s to determine whether I am either gluten sensitive or have celiac disease...

Can anyone recommend a Dr. in or around the Toronto area?

and...Does anyone have an experience seeing Dr. Ralph Warren who use to be on the board of the Candian Celiac Association??

Many thanks!!

LuBelle

  • 2 weeks later...

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



Celiac.com Sponsor (A8-M):



Reba32 Rookie

I don't personally know of any Celiac specific GIs in the GTA, (I was living in the US when I was diagnosed) but your best bet is to contact the CCA or the Toronto chapter info@torontoceliac.org and then ask your GP for a referral.

I do know that the tests are NOT covered by OHIP, and the wait is crazy long, a friend of mine waited 4 or 5 months for an appointment, which by that time it was moot because her eejit GP already had her on a gluten free diet! (her doctor did not know that she had to be eating gluten in order to be properly diagnosed by biopsy and blood test!) I think the biopsy costs $100 here. Which is absolutely f*@%ing crazy AFAIC because the province could save themselves sooooooooo much money by properly diagnosing Celiac disease rather than continuing to misdiagnose it as IBS and treat its symptoms and just make people sicker.

ElseB Contributor

The biopsy is covered by OHIP, the blood test is not. Unless you have it done at a hospital lab. My GI works out of Toronto General, and I had the blood test done at the hospital lab, so I didn't have to pay for the blood test. I won't recommend my GI though - great at diagnosing, but horrible at explaining things.

adab8ca Enthusiast

Hi

I am from Burlington Ontario...My celiac was diagnosed by accident by a neurologist who, even after seeing the SKY HIGH antibodies I had insisted it wasn't celiac. Unfortunately, as far as I can tell, in Canada we do not seem to have these Celiac hospitals or centers that I see in the US. The GI I saw basically said " yeah, you have Celiac. See a dietician" and rushed me out the door.

My GP does not have a TON of experience with celiac but she did the right things (i had a bone density scan, vitamins checked etc, checked my total IgA) and last summer, even with Vit D supplementation, my Vit D levels were dropping hugely. However, they are coming back nicely.

Can you ask your Dr. for the tests? There are celiac panels. If this comes back positive, you can get a biopsy that OHIP will pay for (blood testing they don't for some reason. Like this is elective blood work...sheesh). Also ask for Iron, B12, full blood panel. My iron, Vit D and B12 were all very low "normal".

Then I would suggest giving the gluten-free diet a try, regarless of results. A really good try, like 6 months. In this instance, a dietician may be your best bet. I dealt with one here in Burlington that has a brother that has celiac and she herself does not eat gluten, so she had lots of tips etc...

Good luck! I hope you get some answers soon. Unfortunately, you may need to take the bull by the horns with your doctor and get some testing done.

(interestingly, when I had all these low normal levels in my blood work, the dietician looked at my bloodwork and said I was the worst celiac she had ever seen. i LOOKED anemic and sick...Dr's missed it for the most part and only paid attention when my TTG antibodies were off the charts)

Ada

adab8ca Enthusiast

Which is absolutely f*@%ing crazy AFAIC because the province could save themselves sooooooooo much money by properly diagnosing Celiac disease rather than continuing to misdiagnose it as IBS and treat its symptoms and just make people sicker.

ElseB Contributor

The GI I saw basically said " yeah, you have Celiac. See a dietician" and rushed me out the door.

I got "you have celiac, look it up on the internet!" Then she sent me to a dietician who kept suggesting foods that contain gluten!

adab8ca Enthusiast

I got "you have celiac, look it up on the internet!" Then she sent me to a dietician who kept suggesting foods that contain gluten!

In a standard sense, the basics are pretty simple...I cannot imagine a dietician or Dr that can't even give you the basics (ie fruit! vegetables! meat!). The newbies can't possibly know this but I bet most people HERE could give better food advice than we are getting from professionals. I think they need to get away from REPLACEMENTS for the foods and start simple...

***gently steps off of soapbox and apologizes for hijacking thread***


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



Celiac.com Sponsor (A8-M):



chrissygirlca Apprentice

okay my doctor used to tell me it was just stress or that i had a virus. He only made me do the endoscopy after i forced him too. He even went as far as to tell me that there is a condition for people who always think there are things wrong with them. For years ive been complaining about stomach problems pains anxiety depression headaches dizziness no energy. Now im sensetive to 1049745974945 foods because of it. I was also told that nutritionist in toronto well vaughan(gta) where i am are only availble for people with diabetes. So im supper skinny self concious about my weight can eat almost nothing not sure what to eat and my only option is to pay some nutritionist 200 for the first visit and 100 for each visit after that or some crazy amount like that in order to get the care i need to be healthy. How do i even know this naturo path or nutritionist is going to help me when doctors have been feeding me bs all my life. Id rather pay money buy the text books they read and learn everything myself. Im scared of taking supplements even because i dont know if the ingredients are going to make me sick. I just wanna feel better and have my life back. So much for free health care.

chrissygirlca Apprentice

In a standard sense, the basics are pretty simple...I cannot imagine a dietician or Dr that can't even give you the basics (ie fruit! vegetables! meat!). The newbies can't possibly know this but I bet most people HERE could give better food advice than we are getting from professionals. I think they need to get away from REPLACEMENTS for the foods and start simple...

***gently steps off of soapbox and apologizes for hijacking thread***

i agree this site came up with every search i would find and now i just type celiac before each search and it usually brings this up or i search in the form i get more information out of reading than my doctor would give me. My stomach doctor after he diagnosed me and i told him i cant even eat gravy or sauce anymore he told me it doesn't have wheat. When i asked my family doctor if i really should be changing my pots and pans he said i should not be too concerned about that but here i read i should be! You people save my life i dont know what i would do without this site id be like 20lbs without you people.

Reba32 Rookie

The biopsy is covered by OHIP, the blood test is not. Unless you have it done at a hospital lab. My GI works out of Toronto General, and I had the blood test done at the hospital lab, so I didn't have to pay for the blood test. I won't recommend my GI though - great at diagnosing, but horrible at explaining things.

Well then how come everyone I've spoken to recently (like in the past few months) has told me that they can't get the biopsy because they don't have the money to pay for it, and OHIP doesn't cover? Plus, from what I was told by one friend, only one blood test was covered by OHIP, the other is not covered.

A lot of conflicting info out there apparently! I am glad now that I got my dx down in the States, and although I did have to pay for it, my insurance paid 80% of the cost of all tests. The GI doc was a git though, arrogant so-and-so!

I haven't heard much good about the nutritionists/dietitians in this province either that people have been going to or been sent to by their GPs. (or in the US either, it's no better there I assure you!). Even "nutritionists" who claim to be on a gluten free diet themselves have told friends/acquaintances that some forms of wheat are ok, like spelt or duram. I tell them to run as fast as they can away from that "nutritionist" before they kill them with their diet suggestions! Seriously, one nutritionist told my friend that barley and rye were ok in moderation! ugh...gotta wonder what school that one went to.

Reba32 Rookie

in case anyone in Ontario has missed this group on Facebook

Open Original Shared Link

If any politicians come to your door asking for their vote, ask them why Celiac testing is not covered by OHIP :)

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,904
    • Most Online (within 30 mins)
      7,748

    AnneSN
    Newest Member
    AnneSN
    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

    • Xravith
      Yes, you are right. Indeed, I’ve been feeling anemic since the beginning of this week, and today I felt horrible during a lecture at the university, I was trembling a lot and felt all my body incredibly heavy, so I had to come back home. I’ll do a blood test tomorrow, but I’m just worried about the possibility of it coming back negative. I’ve been eating two cookies in the morning as my only source of gluten over the past two weeks—could that affect the final result?
    • trents
      Welcome to the forum, @Judy M! Yes, he definitely needs to continue eating gluten until the day of the endoscopy. Not sure why the GI doc advised otherwise but it was a bum steer.  Celiac disease has a genetic component but also an "epigenetic" component. Let me explain. There are two main genes that have been identified as providing the "potential" to develop "active" celiac disease. We know them as HLA-DQ 2.5 (aka, HLA-DQ 2) and HLA-DQ8. Without one or both of these genes it is highly unlikely that a person will develop celiac disease at some point in their life. About 40% of the general population carry one or both of these two genes but only about 1% of the population develops active celiac disease. Thus, possessing the genetic potential for celiac disease is far less than deterministic. Most who have the potential never develop the disease. In order for the potential to develop celiac disease to turn into active celiac disease, some triggering stress event or events must "turn on" the latent genes. This triggering stress event can be a viral infection, some other medical event, or even prolonged psychological/emotional trauma. This part of the equation is difficult to quantify but this is the epigenetic dimension of the disease. Epigenetics has to do with the influence that environmental factors and things not coded into the DNA itself have to do in "turning on" susceptible genes. And this is why celiac disease can develop at any stage of life. Celiac disease is an autoimmune condition (not a food allergy) that causes inflammation in the lining of the small bowel. The ingestion of gluten causes the body to attack the cells of this lining which, over time, damages and destroys them, impairing the body's ability to absorb nutrients since this is the part of the intestinal track responsible for nutrient absorption and also causing numerous other food sensitivities such as dairy/lactose intolerance. There is another gluten-related disorder known as NCGS (Non Celiac Gluten Sensitivity or just, "gluten sensitivity") that is not autoimmune in nature and which does not damage the small bowel lining. However, NCGS shares many of the same symptoms with celiac disease such as gas, bloating, and diarrhea. It is also much more common than celiac disease. There is no test for NCGS so, because they share common symptoms, celiac disease must first be ruled out through formal testing for celiac disease. This is where your husband is right now. It should also be said that some experts believe NCGS can transition into celiac disease. I hope this helps.
    • Judy M
      My husband has had lactose intolerance for his entire life (he's 68 yo).  So, he's used to gastro issues. But for the past year he's been experiencing bouts of diarrhea that last for hours.  He finally went to his gastroenterologist ... several blood tests ruled out other maladies, but his celiac results are suspect.  He is scheduled for an endoscopy and colonoscopy in 2 weeks.  He was told to eat "gluten free" until the tests!!!  I, and he know nothing about this "diet" much less how to navigate his in daily life!! The more I read, the more my head is spinning.  So I guess I have 2 questions.  First, I read on this website that prior to testing, eat gluten so as not to compromise the testing!  Is that true? His primary care doctor told him to eat gluten free prior to testing!  I'm so confused.  Second, I read that celiac disease is genetic or caused by other ways such as surgery.  No family history but Gall bladder removal 7 years ago, maybe?  But how in God's name does something like this crop up and now is so awful he can't go a day without worrying.  He still works in Manhattan and considers himself lucky if he gets there without incident!  Advice from those who know would be appreciated!!!!!!!!!!!!
    • Scott Adams
      You've done an excellent job of meticulously tracking the rash's unpredictable behavior, from its symmetrical spread and stubborn scabbing to the potential triggers you've identified, like the asthma medication and dietary changes. It's particularly telling that the rash seems to flare with wheat consumption, even though your initial blood test was negative—as you've noted, being off wheat before a test can sometimes lead to a false negative, and your description of the other symptoms—joint pain, brain fog, stomach issues—is very compelling. The symmetry of the rash is a crucial detail that often points toward an internal cause, such as an autoimmune response or a systemic reaction, rather than just an external irritant like a plant or mites. I hope your doctor tomorrow takes the time to listen carefully to all of this evidence you've gathered and works with you to find some real answers and effective relief. Don't be discouraged if the rash fluctuates; your detailed history is the most valuable tool you have for getting an accurate diagnosis.
    • Scott Adams
      In this case the beer is excellent, but for those who are super sensitive it is likely better to go the full gluten-free beer route. Lakefront Brewery (another sponsor!) has good gluten-free beer made without any gluten ingredients.
×
×
  • 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.