Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Dr. Green @ Celiac Disease Center, Columbia University


farofa

Recommended Posts

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


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



Celiac.com Sponsor (A8-M):



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


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



Celiac.com Sponsor (A8-M):



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?

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,191
    • Most Online (within 30 mins)
      7,748

    teresa1955
    Newest Member
    teresa1955
    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

    • Ginger38
      So I recently had allergy testing for IGE antibodies in response to foods. My test results came back positive to corn, white potatoes, egg whites. Tomatoes, almonds and peanuts to name a few.  I have had obvious reactions to a few of these - particularly tomatoes and corn- both GI issues. I don’t really understand all this allergy versus celiac stuff. If the food allergies are mild do I have to avoid these foods entirely? I don’t know what I will eat if I can’t  have corn based gluten free products 
    • Kris2093u4
      Geography makes a difference.  I'm in the West and Trader Joe's gluten-free bread tastes great and is a better price than most gluten-free breads sold elsewhere in my area.  
    • JForman
      We have four children (7-14 yo), and our 7 year old was diagnosed with NCGS (though all Celiac labs were positive, her scope at 4 years old was negative so docs in the US won't call it celiac). We have started her on a Gluten Free diet after 3 years of major digestive issues and ruling out just about everything under the sun. Our home and kitchen and myself are all gluten-free. But I have not asked my husband/her dad or her other siblings to go completely gluten-free with us. They are at home, but not out of the home. This has led to situations when we are eating out where she has to consistently see others eating things she can't have and she has begun to say "Well, I can't have <fill in the blank>...stupid gluten."  How have you supported your gluten-free kiddos in the mental health space of this journey, especially young ones like her. I know it's hard for me as an adult sometimes to miss out, so I can't imagine being 7 and dealing with it! Any tips or ideas to help with this? 
    • Jane878
      By the time I was 5 I had my first auto0immune disorder, Migraine headaches, with auras to blind me, and vomiting, sensitivity to light and sound. I was 5 years old, and my stepfather would have pizza night, milling his own flour, making thick cheesy gluten pizza, that I would eat and the next day, I would have serious migraines, and my mother & stepfather did nothing about my medical problems. When I was 17 in my first year at college, I was diagnosed with my 2nd known auto-immune disorder, Meniere's disease. I was a elite athlete, a swimmer, and soccer player. And once again my parents didn't think anything of understanding why I had a disorder only older people get. Now after my mother passed from Alzheimer's disease she also suffered with living with gluten. She had a rash for 30 years that nobody could diagnose. She was itchy for 45 years total. My brother had a encapsulated virus explodes in his spleen and when this happened his entire intestines were covered with adhesions, scar tissue and he almost lost his life. He has 5 daughters, and when I finally was diagnosed after being pregnant and my body went into a cytokine storm, I lost my chance to have children, I ended up having Hashimoto's disease, Degenerative Disc disease, and my body started to shut down during my first trimester. I am 6ft tall and got down to 119lbs. My husband and I went to a special immunologist in Terrace, California. They took 17 vials of blood as we flew there for a day and returned home that evening. In 3 weeks, we had the answer, I have Celiac disease. Once this was known, only my father and husband made efforts to change their way of feeding me. At the family cabin, my stepfather & mother were more worried that I would ruin Thanksgiving Dinner. It wasn't until one of my cousins was diagnosed with Celiac disease. They finally looked into getting Gluten Free flour and taking measures to limit "gluten" in meals. He did nothing but ask for me to pay for my own food and wi-fi when I came to the cabin to stay after our house burned down. When he informed my mother, they proceeding to get into a physical fight and she ended up with a black eye. The is just more trauma for me. Sam had no interest in telling the truth about what he wanted. He lied to my mother that he had asked my husband if I could pay for "food" when he asked Geoffrey if I had money to pay for my wi-fi. My mother hates when he spends so much time on the computer so he lied and said I could pay for my own food. I will remind you I weighed 119lbs at this time. (At 6ft) that is a very sick looking person. Neither parent was worried about my weight, they just fought about how cheap my stepfather was. As my mother was diagnosed with Alzheimer's disease in 2014. He had her sign over the will to a trust and added his children. He had no testimonial capacity at the time, so she signed without proper papers. Making this Trust null and void. When I gave my brother my childhood home, my mother stated I would be getting an equal part of inheritance to the house on Race. It currently worth 2.0 million $. I got nothing, and my stepfather has since disowned me b/c of my claim and he knows that my mother would never have left it uneven between my biological brother and myself. She sat me and my husband down, as we lived at the Race Street house and treated and took care of it as our own. My brother took over b/c he was going through a horrific divorce and needed a home so he could get a better custody deal with his soon to be ex-wife who was a Assist DA for Denver. She used the girls against him, and he & I were the primary caregivers. We, Judd and I spent the most time with them pre the divorce. Once Judd moved into the house, he threw all of my mother, grandmother and my family heirlooms out to the Goodwill. Nobody told my mother about this as she was going through cancer treatment and had Alzheimer's disease in her mother and her sister. My stepfather and biological brother took advantage of this matter, as I called a "family council" that my brother just never could make it to at the last moment. All of the furnishing, kitchen ware, everything was in the house my brother just moved into. He had had 2 weddings, I chose to elope b/c my stepfather ruined my brother's first wedding by talking about his relationship with my brother in front of my dad and his entire family, insulting him and having my grandfather leave the ceremony. It was a disaster. My stepfather just plays dumb and blames my father for the slight. I was the only child not to have a wedding. So, my mother and stepfather never had to pay for a thing. My mother had had an agreement with my father he'd pay for college and all medical issues with their kids, myself and Judd. So truly my mother never had to pay for anything big for me in her entire life. I am looking for anyone that has had a similar story, where they grew up in a household that had a baker that regularly milled flour and ate gluten. What happened to you? DId you suffer from different auto-immune diseases b/c of living with a baker using "gluten" Please let me know. I have been looking into legal ways to get my stepfather to give me what my mother had promised, and he erased. Thank you for listening to my story. Jane Donnelly  
    • trents
      Possibly gluten withdrawal. Lot's of info on the internet about it. Somewhat controversial but apparently gluten plugs into the same neuro sensors as opiates do and some people get a similar type withdrawal as they do when quitting opiates. Another issue is that gluten-free facsimile flours are not fortified with vitamins and minerals as is wheat flour (in the U.S. at least) so when the switch is made to gluten-free facsimile foods, especially if a lot of processed gluten-free foods are being used as substitutes, vitamin and mineral deficiencies can result. There is also the possibility that she has picked up a virus or some but that is totally unrelated to going gluten-free.
×
×
  • Create New...