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Long Island Doc?

blondebombshell

By blondebombshell
in Doctors

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blondebombshell Collaborator
blondebombshell
Posted

just wondering who y'all went to.

thanks. :rolleyes:

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Silly Yak Pete Rookie
Silly Yak Pete
Posted

Dr Gautum Reddyin Valley Stream NY on Sunrise Highway. He also has a office in Middle Village Queens. I have been going to him for 8 years for GERD and he diagnosed me right away 3 years ago for my Celiac Disease when I first started to having the really bad gluten reactions.

Puddy Explorer
Puddy
Posted

Dr. Corina Serer in Massapequa. Seems to be very knowledgeable. Had no GI symptoms, but was anemic and had osteoporosis. She put 2 and 2 together and sent me for endoscopy and bloodwork. Good luck finding a doc you like.

  • 2 weeks later...
de caps Contributor
de caps
Posted
Dr. Corina Serer in Massapequa. Seems to be very knowledgeable. Had no GI symptoms, but was anemic and had osteoporosis. She put 2 and 2 together and sent me for endoscopy and bloodwork. Good luck finding a doc you like.

I have been seeing Dr. Serer for 3 years now. In the beginning I really liked her. Now she seems to busy. She likes to blame every GI symptom on Celiac when it could be something else. I'm now looking for a second opinion out of this practice. I also saw Dr. Pearlman in this group, he hasn't got a clue about Celiac. He said I was "cured" because my blood work is now normal. Go figure.

darlindeb25 Collaborator
darlindeb25
Posted

There must be some doctors with celiac knowledge at Stony Brook. Our celiac support group was saying there is talk that Stony Brook is thinking about starting up a Celiac Center like Columbia University has. Wouldn't that be wonderful? I can't help you with a doctor though. My doctor has no problem believing I am celiac, but he has very little knowledge about celiac. For now, it seems the best doctors are at Columbia, but there is a waiting list to be seen, that isn't good!

blondebombshell Collaborator
blondebombshell
Posted
  • Author

i saw dr. kohlrosser/lobo in babylon and they were clueless. they told me that the endo came back negative and that i cant have a gluten allergy/celiac. that being gluten free is expensive and tough.

WTH you know?

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    • Mari
      New Celiac Mama in My 30s

      By Mari · Posted

      There is much helpful 'truth' posted on this forum. Truths about Celiac Disease are based on scientific research and people's experience. Celiac disease is inherited. There are 2 main Celiac 'genes' but they are variations of one gene called HLa - DQ What is inherited when a person inherits one or both of the DQ2 or the DQ8 is a predisposition to develop celiac disease after exposure to a environmental trigger. These 2 versions of the DQ gene are useful in diagnosing  celiac disease but there are about 25 other genes that are known to influence celiac disease so this food intolerance is a multigenic autoimmune disease. So with so many genes involved and each person inheriting a different array of these other genes one person's symptoms may be different than another's symptoms.  so many of these other genes.  I don't think that much research on these other genes as yet. So first I wrote something that seem to tie together celiac disease and migraines.  Then you posted that you had migraines and since you went gluten free they only come back when you are glutened. Then Scott showed an article that reported no connection between migraines and celiac disease, Then Trents wrote that it was possible that celiacs had more migraines  and some believed there was a causal effect. You are each telling the truth as you know it or experienced it.   
    • tiffanygosci
      Aldi Pueblo Lindo Yellow Corn Tortillas

      By tiffanygosci · Posted

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    • tiffanygosci
      New Celiac Mama in My 30s

      By tiffanygosci · Posted

      Thank you all for sharing your experiences! And I am very thankful for that Thanksgiving article, Scott! I will look into it more as I plan my little dinner to bring with on the Holiday I'm also glad a lot of research has been done for Celiac. There's still a lot to learn and discover. And everyone has different symptoms. For me, I get a bad headache right away after eating gluten. Reoccurring migraines and visual disturbances were actually what got my PCP to order a Celiac Panel. I'm glad he did! I feel like when the inflammation hits my body it targets my head, gut, and lower back. I'm still figuring things out but that's what I've noticed after eating gluten! I have been eating gluten-free for almost two months now and haven't had such severe symptoms. I ate a couple accidents along the way but I'm doing a lot better
    • trents
      New Celiac Mama in My 30s

      By trents · Posted

      @Mari, did you read that second article that Scott linked? It is the most recently date one. "Researchers comparing rates of headaches, including migraines, among celiac patients and a healthy control group showed that celiac subjects experienced higher rates of headaches than control subjects, with the greatest rates of migraines found in celiac women.  Additionally, celiacs had higher rates of migraine than control subjects, especially in women. In fact, four out of five women with celiac disease suffered from migraines, and without aura nearly three-quarters of the time."
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      New Celiac Mama in My 30s

      By Mari · Posted

      As far as I know and I have made severalonline searches, celiac disease disease has not been recognized as a cause of migraines or any eye problems. What I wrote must have been confusing.
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