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Dr. Green @ Celiac Disease Center, Columbia University


farofa

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farofa Rookie

Hi,

Has anyone on this forum had the good fortune (or bad ;)) to see Peter Green or any of his associates at Columbia? How did you feel about the experience? Has it been helpful to you? Any feedback would be greatly appreciated.

Alex


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penguin Community Regular

I haven't seen him, but my GI doc and his PA have :)

Based on their impressive knowledge of celiac and gluten intolerance, I would say it would be worth looking in to. I know that's where my GI doc gets most of his research info.

eLaurie Rookie

I'm hoping to learn this week that my sister (a family Nurse Practitioner) can go with me to their symposium/forum in November. If she can't go, I can't afford lodging alone, so am praying she can.

The symposium is for physicians and researchers, but the clinical forum is open to patients. If you're interested, don't let the symposium fees scare you away. You'll want the "clinical forum" no credit hours option described in the second link. NOTE ...fees increase by $100 after August 1.

Open Original Shared Link

Open Original Shared Link

bklynceliac Apprentice

I have an appointment with Susie Lee on Monday. She also has a practice in Fort Washington which might be easier to get into, and I know she accepts a lot more types of insurance than Dr. Green. Having already seen a few reported experts that were anything but, I'm very hopeful. I'll let you know how it goes.

bklyn Enthusiast

I was at the Celiac Center last week and I had an endoscopy and capsule endoscopy. I have seen Dr. Suzie Lee in the past, but I'm having stomach problems so I decided to go back to her. All my tests were good, my Ttg was negative, my villi have returned to normal. She did these tests to be sure that Celiac was under control. No real answer to my stomach aches, but at least I was relieved to hear I'm responding well to the diet.

jayhawkmom Enthusiast

I will be seeing him speak at Stanford in September! =)

Open Original Shared Link

I wish I could see him as a patient.

par18 Apprentice
Hi,

Has anyone on this forum had the good fortune (or bad ;)) to see Peter Green or any of his associates at Columbia? How did you feel about the experience? Has it been helpful to you? Any feedback would be greatly appreciated.

Alex

Hi Alex,

I have not seen Dr. Green but I did have the good fortune to attend a talk given by Dr. Fasano from the University of Maryland. The talk was presented at the University of Virginia medical center about a month ago. Dr. Fasano talked about the background of Celiac Disease and how it came to be diagnosed during the grain shortages of WWII. He also talked about the ongoing research projects from his group and the group at Stanford University. He listed the main research centers in the U.S. including the one at Columbia. It was nice to meet someone who is devoting most of his career to the search for and possible cure of this condition. He answered as many questions as he could and his delivery with a little humor allowed all of those that attended the opportunity to laugh at some of the things that are sometimes overlooked in the medical community. Anyway it was well worth the drive to meet him and see what someone with his knowledge is doing. I would probably see him again if the opportunity comes.

Tom


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Jean-Luc Rookie
I was at the Celiac Center last week and I had an endoscopy and capsule endoscopy. I have seen Dr. Suzie Lee in the past, but I'm having stomach problems so I decided to go back to her. All my tests were good, my Ttg was negative, my villi have returned to normal. She did these tests to be sure that Celiac was under control. No real answer to my stomach aches, but at least I was relieved to hear I'm responding well to the diet.

bklyn,

could you forward me her contact information?

Thanks,

Picard

bklyn Enthusiast

Picard,

Celiac Disease Center at Columbia University

Susie K. Lee, MD

Assistant Professor of Medicine

(212) 342-4508

180 Fort Washington Ave.

Suite 956, New York, N.Y. 10032

farofa Rookie

Open Original Shared Link

This link is for the bios of the staff at the Columbia Celiac Center.

I actually had an appointment with Susie Lee some months ago but my endo and my gp convinced me to see a GI — who was good but not too interested in celiac sprue. I'm glad to hear she's a good doctor.

  • 2 weeks later...
Jean-Luc Rookie
Picard,

Celiac Disease Center at Columbia University

Susie K. Lee, MD

Assistant Professor of Medicine

(212) 342-4508

180 Fort Washington Ave.

Suite 956, New York, N.Y. 10032

Thank you.

  • 2 months later...
KerriAnne Rookie

My GI doc is Dr. Jeffrey Stein ~ also at Columbia Health Center, but not officially in the Celiac Disease Center. I did see Dr. Susie Lee after 1 year on the gluten-free diet. I'm a grad student at Columbia so it was convenient enough for me to go see her. Dr. Stein recommended I see her since they have so many on-going studies, though since I had already improved on the diet my meeting with her was kind of uneventful. Anyhow, she is very nice, but I also highly recommend Dr. Stein.

Also, a friend of mine has HIGHLY recommended Dr. Fasano in MD. Her brother & sister both have Celiac, and the whole family has a lot of respect for him.

  • 2 weeks later...
bookie124 Newbie

I saw Dr. Lee -- I thought she was a flake and told me a number of inconsistent things and was also rather unresponsive to any phone calls

the only thing of value I got out of my visit was to use prometheus labs for blood testing...

i.e. the best thing to do to get comparable and reliable blood test results to test one's gradual remission of celiac disease is to do the following:

go to your trusted PCP and ask to have MULTIPLE vials of blood taken (as many as you can muster -- maybe 6 or 7). At that point ask your PCP to freeze all but one of the vials and send that unfrozen vial to prometheus for their celiac disease serology test. Given that even their tests change but are at least performed with care unlike at Quest (they are very unreliable in my experience, they use the least expensive test kits as it's not their liability and they are publically traded), Prometheus is the only useful place to attempt to relate serology changes. Every 3 or so months, you'll want to get the celiac disease serology test repeated on two vials of blood (one new one and one of the frozen ones, especially if they claim they changed their serology testing methodology in the slightest way).

Hopefully you guys will have better luck than me

  • 1 year later...
wakefield Apprentice

I see this thread is 2 years old but I was wondering if any of you had any new information about Dr Green, Dr Lee and how you are doing. I am 2 months into my diagnosis and this week started with numbness in 3 toes of my left foot and some pain up my leg. In reading I see different opinions about B12, levels, amount etc. Any advice is appreciated.

darlindeb25 Collaborator

I have not been a patient of Dr. Green's, but I have attended many of his talks, met him in person many times, even helped him with a book signing at our vendor fair. He knows his stuff, and he is a very down to earth person. He is a very busy doctor though, and takes a long time to see him.

As for your numb toes and such, you should see a neurologist, that is their speciality.

givenupgluten Explorer

I have an appointment with Dr. Green tomorrow actually...I just happened upon this thread! I have waited about 5 months for my first appointment with him, so hopefully it's worth it. From all the wonderful reviews and advice I've heard, I think it will be. I'm hopeful at least...I'll fill you all in once get back.

Gemini Experienced
I have an appointment with Dr. Green tomorrow actually...I just happened upon this thread! I have waited about 5 months for my first appointment with him, so hopefully it's worth it. From all the wonderful reviews and advice I've heard, I think it will be. I'm hopeful at least...I'll fill you all in once get back.

I would be very interested in hearing what you think of Dr. Green, after your appointment. I just finished reading his book on Celiac Disease and have to admit it was very impressive. He dispels many of the myths that are rampant with people regarding Celiac Disease, one of which is about DH and how people think it can be caused by touching gluten. There is so much misinformation about the disease and with so many having a hard time with it all, it's important to learn the truth so you'll make better choices and have an easier time with maintaining the lifestyle.

I also like the fact that he believes patients regarding their suffering and inability to get help from other doctors. He also seems to back up the strong connection between Celiac and many other autoimmune problems. I don't think he's the type of doctor to tell you it's all in your head! Good luck to you!

givenupgluten Explorer

FABULOUS APPOINTMENT! I went to see Dr. Green yesterday afternoon, and what an experience it was. I hate going to see doctors re: this issue, b/c I feel like I have so much unwarranted anxiety about it and discomfort, that surely nobody is going to believe me or help me through it. The last dr. I saw was nice enough, but insisted that after my celiac blood panel came back negative, that there was no way I could have the disease, so the biopsy was out of the question. In the meantime (while waiting on my appt to arrive with dr. green) I decided to try a gluten free diet out for myself. It has helped, although I still do have enormous trouble with anxiety triggering symptoms (traveling, etc) - but in general, my day to day symptoms are gone.

Dr. Green discussed in detail my history and parent's history (my mother has celiac...so we also discussed her symptoms, diagnosis, etc). Frankly, I was pretty sure he was going to get on to me for going gluten free before having a biopsy. He was wonderful though...He offered up many suggestions before I could even suggest them myself (and I had a LARGE list). He wanted me to get a blood panel test AGAIN, and stated that a negative blood test result did not mean i did not have the disease. He also handed me the genetic testing packet right then and there, which is something I had also been very interested in doing. He recommended a potential medication that may help with my anxiety issues, so that I could really see if the gluten free diet was working - without the nervous stomach (which he mentioned is a very common ibs component of celiac). He wrote out a step by step list as to what we should do first, and next, and so on. He provided alternatives for almost every step, and made it clear that it was about my comfort and well being. We took care of alot during one meeting, and it was the first time I felt like I had an actual doctor/patient relationship - especially for New York. I find it very hard here to get real, personal care in this city...but he provided just that. I was very impressed and felt like he was truly invested in helping me get to the root of my issues. He was extremely thorough....SO i would definitely recommend anyone to see him!

Gemini Experienced
FABULOUS APPOINTMENT! I went to see Dr. Green yesterday afternoon, and what an experience it was. I hate going to see doctors re: this issue, b/c I feel like I have so much unwarranted anxiety about it and discomfort, that surely nobody is going to believe me or help me through it. The last dr. I saw was nice enough, but insisted that after my celiac blood panel came back negative, that there was no way I could have the disease, so the biopsy was out of the question. In the meantime (while waiting on my appt to arrive with dr. green) I decided to try a gluten free diet out for myself. It has helped, although I still do have enormous trouble with anxiety triggering symptoms (traveling, etc) - but in general, my day to day symptoms are gone.

Dr. Green discussed in detail my history and parent's history (my mother has celiac...so we also discussed her symptoms, diagnosis, etc). Frankly, I was pretty sure he was going to get on to me for going gluten free before having a biopsy. He was wonderful though...He offered up many suggestions before I could even suggest them myself (and I had a LARGE list). He wanted me to get a blood panel test AGAIN, and stated that a negative blood test result did not mean i did not have the disease. He also handed me the genetic testing packet right then and there, which is something I had also been very interested in doing. He recommended a potential medication that may help with my anxiety issues, so that I could really see if the gluten free diet was working - without the nervous stomach (which he mentioned is a very common ibs component of celiac). He wrote out a step by step list as to what we should do first, and next, and so on. He provided alternatives for almost every step, and made it clear that it was about my comfort and well being. We took care of alot during one meeting, and it was the first time I felt like I had an actual doctor/patient relationship - especially for New York. I find it very hard here to get real, personal care in this city...but he provided just that. I was very impressed and felt like he was truly invested in helping me get to the root of my issues. He was extremely thorough....SO i would definitely recommend anyone to see him!

You know, after reading this, I think I have doctor envy! :P

The nervous stomach issue may just be the unhealed gut reaction. My stomach was nauseous and felt like butterflies for awhile, even after going gluten-free. It took a little while to resolve, about 6 months, but it was all due to Celiac. I am not one to take an anti-anything med so decided to wait it out and all my symptoms have resolved with the gluten-free diet.

I would recommend that everyone read Dr. Green's book because he set straight some issues that I see thrown around this forum that people get bad advice for. People need the correct information or they will struggle with this lifestyle.

I am surprised there is any big question as to whether or not you have celiac disease. If your mother has it, then your odds are so high, if you present with symptoms, it should be pretty much a no-brainer. My family all have "in your face" symptoms, the Celiac gene is on BOTH sides of my family yet everyone else but my sister and I will not hear that they have celiac disease. No wonder there is a host of autoimmune problems in my family.

I wish you luck and am thrilled you found a doctor that actually listens and didn't treat you like an ass for doing a trial diet. I wish I had heard about this guy years ago and maybe it wouldn't have taken 20 years for me to be diagnosed.

givenupgluten Explorer
You know, after reading this, I think I have doctor envy! :P

The nervous stomach issue may just be the unhealed gut reaction. My stomach was nauseous and felt like butterflies for awhile, even after going gluten-free. It took a little while to resolve, about 6 months, but it was all due to Celiac. I am not one to take an anti-anything med so decided to wait it out and all my symptoms have resolved with the gluten-free diet.

I would recommend that everyone read Dr. Green's book because he set straight some issues that I see thrown around this forum that people get bad advice for. People need the correct information or they will struggle with this lifestyle.

I am surprised there is any big question as to whether or not you have celiac disease. If your mother has it, then your odds are so high, if you present with symptoms, it should be pretty much a no-brainer. My family all have "in your face" symptoms, the Celiac gene is on BOTH sides of my family yet everyone else but my sister and I will not hear that they have celiac disease. No wonder there is a host of autoimmune problems in my family.

I wish you luck and am thrilled you found a doctor that actually listens and didn't treat you like an ass for doing a trial diet. I wish I had heard about this guy years ago and maybe it wouldn't have taken 20 years for me to be diagnosed.

Well thank you for the support ! It was a really good experience. I even mentioned that my mother was diagnosed so long ago, that at that point, they were telling people that after going gluten-free if your symptoms ceased, then you could introduce gluten back into your diet. He seemed very concerned, giving examples, and ultimately encouraging me to explain it to her as he explained it to me - that this was NOT correct. He was genuinley interested in her health as well. He just seems to truly care for people dealing with celiac and related issues.

It's good to know (although not good you had to experience it) that other people have had the anxiety issues as well. I'm not one to take meds if I don't have to...mostly b/c i have had very back luck with them in the past. I haven't made a decision as to whether or not I'll take it yet - but it's an option I suppose. I like to research things like that before I make any decisions.

It's also a relief to hear that your nervous stomach symptoms DID go away! That gives me lots of hope!

Gemini Experienced
Well thank you for the support ! It was a really good experience. I even mentioned that my mother was diagnosed so long ago, that at that point, they were telling people that after going gluten-free if your symptoms ceased, then you could introduce gluten back into your diet. He seemed very concerned, giving examples, and ultimately encouraging me to explain it to her as he explained it to me - that this was NOT correct. He was genuinley interested in her health as well. He just seems to truly care for people dealing with celiac and related issues.

It's good to know (although not good you had to experience it) that other people have had the anxiety issues as well. I'm not one to take meds if I don't have to...mostly b/c i have had very back luck with them in the past. I haven't made a decision as to whether or not I'll take it yet - but it's an option I suppose. I like to research things like that before I make any decisions.

It's also a relief to hear that your nervous stomach symptoms DID go away! That gives me lots of hope!

If you follow a strict gluten-free diet, your anxiety issues will most likely resolve. Having celiac disease really screws up both body and mind....I am a totally different person than I was pre-diagnosis. You may want to try just going gluten-free and if that doesn't do the trick within a set amount of time, then consider meds....but make sure they are gluten-free! I think for many that everyday stresses become impossible to deal with if you are vitamin starved and are not processing your food correctly. You don't realize how bad things have gotten because it happens slowly over time and you sort of adjust to it. You keep compensating until you crash. I hit the point where I really wasn't eating all that much food because my stomach was so messed up...not good when you are underweight to begin with. I can not tell you the difference now that I have been gluten-free for 3 years! How many people do you know that have zero GI issues? My stomach has never felt so good.

It must be so nice to have a doctor that knows so much about celiac disease and doesn't look at you like you have 3 heads when you go into symptoms. I was treated badly by a number of doctors so do not have a very high opinion of the medical profession. When I read Dr. Green's book, I realized this man was different

because his information was correct and his desire to help people get diagnosed was apparent.

Good luck with talking to your mother about it. My family won't even discuss their medical issues with me anymore because they are so steeped in denial

and think they'll die without bread. It has affected our relationship but that's their problem. I feel so good now I just don't care......some people would rather be on meds and have health issues than do the work to be healthy. Dumb!

  • 1 year later...
lucia Enthusiast

FABULOUS APPOINTMENT! I went to see Dr. Green yesterday afternoon, and what an experience it was. I hate going to see doctors re: this issue, b/c I feel like I have so much unwarranted anxiety about it and discomfort, that surely nobody is going to believe me or help me through it. The last dr. I saw was nice enough, but insisted that after my celiac blood panel came back negative, that there was no way I could have the disease, so the biopsy was out of the question. In the meantime (while waiting on my appt to arrive with dr. green) I decided to try a gluten free diet out for myself. It has helped, although I still do have enormous trouble with anxiety triggering symptoms (traveling, etc) - but in general, my day to day symptoms are gone.

Dr. Green discussed in detail my history and parent's history (my mother has celiac...so we also discussed her symptoms, diagnosis, etc). Frankly, I was pretty sure he was going to get on to me for going gluten free before having a biopsy. He was wonderful though...He offered up many suggestions before I could even suggest them myself (and I had a LARGE list). He wanted me to get a blood panel test AGAIN, and stated that a negative blood test result did not mean i did not have the disease. He also handed me the genetic testing packet right then and there, which is something I had also been very interested in doing. He recommended a potential medication that may help with my anxiety issues, so that I could really see if the gluten free diet was working - without the nervous stomach (which he mentioned is a very common ibs component of celiac). He wrote out a step by step list as to what we should do first, and next, and so on. He provided alternatives for almost every step, and made it clear that it was about my comfort and well being. We took care of alot during one meeting, and it was the first time I felt like I had an actual doctor/patient relationship - especially for New York. I find it very hard here to get real, personal care in this city...but he provided just that. I was very impressed and felt like he was truly invested in helping me get to the root of my issues. He was extremely thorough....SO i would definitely recommend anyone to see him!

I know this is an old thread, but I thought you needed positive bloodwork to get an appointment at the Celiac Center?

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    • trents
    • Clear2me
      Thanks for the info. I recently moved to CA from Wyoming and in that western region the Costco and Sam's /Walmart Brands have many nuts and more products that are labeled gluten free. I was told it's because those products are packaged and processed  in different  plants. Some plants can be labeled  gluten free because the plant does not also package gluten products and they know that for example the trucks, containers equipment are not used to handle wheat, barely or Rye. The Walmart butter in the western region says gluten free but not here. Most of The Kirkland and Members Mark brands in CA say they are from Vietnam. That's not the case in Wyoming and Colorado. I've spoken to customer service at the stores here in California. They were not helpful. I check labels every time I go to the store. The stores where I am are a Sh*tshow. The Magalopoly grocery chain Vons/Safeway/Albertsons, etc. are the same. Fishers and Planters brands no longer say gluten free. It could be regional. There are nuts with sugar coatings and fruit and nut mixes at the big chains that are labeled gluten free but I don't want the fruit or sugar.  It's so difficult I am considering moving again. I thought it would be easier to find safe food in a more populated area. It's actually worse.  I was undiagnosed for most of my life but not because I didn't try to figure it out. So I have had all the complications possible. I don't have any spare organs left.  No a little gluten will hurt you. The autoimmune process continues to destroy your organs though you may not feel it. If you are getting a little all the time and as much as we try we probably all are and so the damage is happening. Now the FDA has pretty much abandoned celiacs. There are no requirements for labeling for common allergens on medications. All the generic drugs made outside the US are not regulated for common allergens and the FDA is taking the last gluten free porcine Thyroid med, NP Thyroid, off the market in 2026. I was being glutened by a generic levothyroxin. The insurance wouldn't pay for the gluten free brand any longer because the FDA took them all off their approved formulary. So now I am paying $147 out of pocket for NP Thyroid but shortly I will have no safe choice. Other people with allergies should be aware that these foreign generic pharmaceutical producers are using ground shellfish shell as pill coatings and anti-desicants. The FDA knows this but  now just waits for consumers to complain or die. The take over of Wholefoods by Amazon destroyed a very reliable source of good high quality food for people with allergies and for people who wanted good reliably organic food. Bezos thought  he could make a fortune off people who were paying alot for organic and allergen free food by substituting cheap brands from Thailand. He didn't understand who the customers were who were willing to pay more for that food and why. I went from spending hundreds to nothing because Bezo removed every single trusted brand that I was buying. Now they are closing Whole foods stores across the country. In CA, Mill Valley store (closed July 2025) and the National Blvd. store in West Los Angeles (closed October 2025). The Cupertino store will close.  In recent years I have learned to be careful and trust no one. I have been deleberately glutened in a restaurant that was my favorite (a new employee). The Chef owner was not in the kitchen that night. I've had  a metal scouring pad cut up over my food.The chain offered gluten free dishes but it only takes one crazy who thinks you're a problem as a food fadist. Good thing I always look. Good thing they didn't do that to food going to a child with a busy mom.  I give big tips and apologize for having to ask in restaurants but mental illness seem to be rampant. I've learn the hard way.          I don't buy any processed food that doesn't say gluten free.  I am a life long Catholic. I worked for the Church while at college. I don't go to Church anymore because the men at the top decided Jesus is gluten. The special hosts are gluten less not gluten free. No I can't drink wine after people with gluten in their mouth and a variety of deadly germs. I have been abandoned and excluded by my Church/Family.  Having nearly died several times, safe food is paramount. If your immune system collapses as mine did, you get sepsis. It can kill you very quickly. I spent 5 days unconscious and had to have my appendix and gall bladder removed because they were necrotic. I was 25. They didn't figure out I had celiac till I was 53. No one will take the time to tell you what can happen when your immune system gets overwhelmed from its constant fighting the gluten and just stops. It is miserable that our food is processed so carelessly. Our food in many aspects is not safe. And the merging of all the grocery chains has made it far worse. Its a disaster. Krogers also recently purchased Vitacost where I was getting the products I could no longer get at Whole Foods. Kroger is eliminating those products from Vitacost just a Bezos did from WF. I am looking for reliable and certified sources for nuts. I have lived the worst consequences of the disease and being exposed unknowingly and maliciously. Once I was diagnosed I learned way more than anyone should have to about the food industry.  I don't do gray areas. And now I dont eat out except very rarely.  I have not eaten fast food for 30 years before the celiac diagnosis. Gluten aside..... It's not food and it's not safe.  No one has got our backs. Sharing safe food sources is one thing we can do to try to be safe.        
    • Mmoc
      Thank you kindly for your response. I have since gotten the other type of bloods done and am awaiting results. 
    • Aretaeus Cappadocia
      I wanted to respond to your post as much for other people who read this later on (I'm not trying to contradict your experience or decisions) > Kirkland Signature Super Extra-Large Peanuts, 2.5 lbs, are labeled "gluten free" in the Calif Costcos I've been in. If they are selling non-gluten-free in your store, I suggest talking to customer service to see if they can get you the gluten-free version (they are tasty) > This past week I bought "Sliced Raw Almonds, Baking Nuts, 5 lbs Item 1495072 Best if used by Jun-10-26 W-261-6-L1A 12:47" at Costco. The package has the standard warning that it was made on machinery that <may> have processed wheat. Based on that alone, I would not eat these. However, I contacted customer service and asked them "are Costco's Sliced Almonds gluten free?" Within a day I got this response:  "This is [xyz] with the Costco Member Service Resolutions Team. I am happy to let you know we got a reply back from our Kirkland Signature team. Here is their response:  This item does not have a risk of cross contamination with gluten, barley or rye." Based on this, I will eat them. Based on experience, I believe they will be fine. Sometimes, for other products, the answer has been "they really do have cross-contamination risk" (eg, Kirkland Signature Dry Roasted Macadamia Nuts, Salted, 1.5 lbs Item 1195303). When they give me that answer I return them for cash. You might reasonably ask, "Why would Costco use that label if they actually are safe?" I can't speak for Costco but I've worked in Corporate America and I've seen this kind of thing first hand and up close. (1) This kind of regulatory label represents risk/cost to the company. What if they are mistaken? In one direction, the cost is loss of maybe 1% of sales (if celiacs don't buy when they would have). In the other direction, the risk is reputational damage and open-ended litigation (bad reviews and celiacs suing them). Expect them to play it safe. (2) There is a team tasked with getting each product out to market quickly and cheaply, and there is also a committee tasked with reviewing the packaging before it is released. If the team chooses the simplest, safest, pre-approved label, this becomes a quick check box. On the other hand, if they choose something else, it has to be carefully scrutinized through a long process. It's more efficient for the team to say there <could> be risk. (3) There is probably some plug and play in production. Some lots of the very same product could be made in a safe facility while others are made in an unsafe facility. Uniform packaging (saying there is risk) for all packages regardless of gluten risk is easier, cheaper, and safer (for Costco). Everything I wrote here is about my Costco experience, but the principles will be true at other vendors, particularly if they have extensive quality control infrastructure. The first hurdle of gluten-free diet is to remove/replace all the labeled gluten ingredients. The second, more difficult hurdle is to remove/replace all the hidden gluten. Each of us have to assess gray zones and make judgement calls knowing there is a penalty for being wrong. One penalty would be getting glutened but the other penalty could be eating an unnecessarily boring or malnourishing diet.
    • trents
      Thanks for the thoughtful reply and links, Wheatwacked. Definitely some food for thought. However, I would point out that your linked articles refer to gliadin in human breast milk, not cow's milk. And although it might seem reasonable to conclude it would work the same way in cows, that is not necessarily the case. Studies seem to indicate otherwise. Studies also indicate the amount of gliadin in human breast milk is miniscule and unlikely to cause reactions:  https://www.glutenfreewatchdog.org/news/gluten-peptides-in-human-breast-milk-implications-for-cows-milk/ I would also point out that Dr. Peter Osborne's doctorate is in chiropractic medicine, though he also has studied and, I believe, holds some sort of certifications in nutritional science. To put it plainly, he is considered by many qualified medical and nutritional professionals to be on the fringe of quackery. But he has a dedicated and rabid following, nonetheless.
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