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Dr. Green

justme

By justme
in Doctors

Recommended Posts

justme Enthusiast
justme
Posted

does anyone go to Dr. Green? I hear he is THE Dr. to go to. I was curious to know if anyone who does go to him, or any of the doctors at Columbia, use Empire for their insurance. With Dr. Green you pay and then get reimbursed. Has anyone used Empire with him?

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darlindeb25 Collaborator
darlindeb25
Posted

I'm sure they do accept some insurances. Dr. Green was asked by a woman Sunday why he doesn't take medicare and he said he does work with medicare. Just call the office and ask what insurances they participate with or just ask if they take yours.

Guest j_mommy
Guest j_mommy
Posted

Elizabeth on "the View" goes to him. Everything i've heard and read about his has been great! I wish I were closer!!!!

  • 2 weeks later...
Annaem Enthusiast
Annaem
Posted
does anyone go to Dr. Green? I hear he is THE Dr. to go to. I was curious to know if anyone who does go to him, or any of the doctors at Columbia, use Empire for their insurance. With Dr. Green you pay and then get reimbursed. Has anyone used Empire with him?

What is so special about this dr. green does he offer some alternatives i haven't heard before? Have you heard of glutenase?

ENF Enthusiast
ENF
Posted
What is so special about this dr. green does he offer some alternatives i haven't heard before? Have you heard of glutenase?

Dr. Peter H.R. Green is founder and director of the Celiac Disease Center at Columbia University in New York City. From Dr. Green's Book, CELIAC DISEASE - A Hidden Epidemic, "The Celac Disease Center at Columbia University is the only center in the United States that provides comprehensive medical care, including nutrician, for adults and pediatric patients with celiac disease. It's mission is to redefine the future of celiac disease and treatment through continuing advances in biomedical research, patient care, and physician and public education. The center is diagnosing and treating more than two thousand patients annually from around the world."

You do not have to see Dr. Green himself at the Celiac Disease Center - there are several other doctors who work there, who are easier to obtain an appointment with, as well as having more insurance options. This is what I did.

There's no magic bullet yet for Celiac, though - you have to be on the diet to recover.

Glutenase cannot be used by people with Celiac Disease to safely consume gluten, although it probably wouldn't hurt to take it.

Website of the Celiac Disease Center at Columbia University:

Open Original Shared Link

Generic Apprentice
Generic
Posted

I have celiac and I take glutenease EVERYTIME I eat out, as a precaution. I figure it can't hurt. So far I have not gotten sick. I take it as a precaution to cc issues. I realized recently they recommend taking it with one of the companies enzymes as well, so I will be picking up a bottle of that too.

  • 3 months later...
nnewjersey Newbie
nnewjersey
Posted
does anyone go to Dr. Green? I hear he is THE Dr. to go to. I was curious to know if anyone who does go to him, or any of the doctors at Columbia, use Empire for their insurance. With Dr. Green you pay and then get reimbursed. Has anyone used Empire with him?

Hello,

I was wondering what the situation would be if you went to the celiac disease center at columbia university with no insurance? I have none right now and was wondering if reimbursement would occur even with no insurance, if not, what occurs for a person with no insurance? Thank you.

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nnewjersey Newbie
nnewjersey
Posted
Dr. Peter H.R. Green is founder and director of the Celiac Disease Center at Columbia University in New York City. From Dr. Green's Book, CELIAC DISEASE - A Hidden Epidemic, "The Celac Disease Center at Columbia University is the only center in the United States that provides comprehensive medical care, including nutrician, for adults and pediatric patients with celiac disease. It's mission is to redefine the future of celiac disease and treatment through continuing advances in biomedical research, patient care, and physician and public education. The center is diagnosing and treating more than two thousand patients annually from around the world."

You do not have to see Dr. Green himself at the Celiac Disease Center - there are several other doctors who work there, who are easier to obtain an appointment with, as well as having more insurance options. This is what I did.

There's no magic bullet yet for Celiac, though - you have to be on the diet to recover.

Glutenase cannot be used by people with Celiac Disease to safely consume gluten, although it probably wouldn't hurt to take it.

Website of the Celiac Disease Center at Columbia University:

Open Original Shared Link

Hello,

I was wondering what the situation would be if you went to the celiac disease center at columbia university with no insurance? I have none right now and was wondering if reimbursement would occur even with no insurance, if not, what occurs for a person with no insurance? Thank you.

  • 1 month later...
kowkitty Rookie
kowkitty
Posted

I also heard about Dr Green (I live in NYC) but he does not take my insurance and cant afford to go out of network :(

stinks, heard he is great. Anyone know anyone else in NYC who takes Oxford Liberty??

ENF Enthusiast
ENF
Posted
I also heard about Dr Green (I live in NYC) but he does not take my insurance and cant afford to go out of network :(

stinks, heard he is great. Anyone know anyone else in NYC who takes Oxford Liberty??

Have you asked Columbia if any of the doctors at the Celiac Center take Oxford Liberty?

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    • catnapt
      how much gluten do I need to eat before blood tests?

      By catnapt · Posted

      oh that's interesting... it's hard to say for sure but it has *seemed* like oats might be causing me some vague issues in the past few months. It's odd that I never really connect specific symptoms to foods, it's more of an all over feeling of unwellness after  eating them.  If it happens a few times after eating the same foods- I cut back or avoid them. for this reason I avoid dairy and eggs.  So far this has worked well for me.  oh, I have some of Bob's Red Mill Mighty Tasty Hot cereal and I love it! it's hard to find but I will be looking for more.  for the next few weeks I'm going to be concentrating on whole fresh fruits and veggies and beans and nuts and seeds. I'll have to find out if grains are truly necessary in our diet. I buy brown rice pasta but only eat that maybe once a month at most. Never liked quinoa. And all the other exotic sounding grains seem to be time consuming to prepare. Something to look at later. I love beans and to me they provide the heft and calories that make me feel full for a lot longer than a big bowl of broccoli or other veggies. I can't even tolerate the plant milks right now.  I have reached out to the endo for guidance regarding calcium intake - she wants me to consume 1000mgs from food daily and I'm not able to get to more than 600mgs right now.  not supposed to use a supplement until after my next round of testing for hyperparathyroidism.   thanks again- you seem to know quite a bit about celiac.  
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    • SilkieFairy
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