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Bronkobux - Is Catching Up To Me!


Lisa

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Lisa Mentor

Happy Birthday Chris, I hope you celebrate and raise a little bit of $ell in Vegas!


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CarlaB Enthusiast

Happy Birthday, Chris!

jerseyangel Proficient

Happy Birthday, Bronco :D

happygirl Collaborator

Happy Birthday Chris! (even if you are a buckeye....)

kaylabobayla Rookie

happy birthday

:D

mouse Enthusiast

HAPPY BIRTHDAY Chris (again). His girlfriend is taking him out to a very special dinner tonight.

My husband and I are having dinner with Chris and his girlfriend in LV on March 4th. I always love to see him.

2Boys4Me Enthusiast

Happy Birthday!


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VegasCeliacBuckeye Collaborator

Thanks for the thoughts everyone!

Tiffany (the gluten-free) took me out to Joes Prime Steak and Stone Crab last night. It was a bit pricey, but Good Lord is the food good!

We started out with some Florida Stone Crab Claws - if you havent had these, they are wonderful and tender! Joe's breaks them up so its easy to get to the meat!

Then we had a delicious chooped salad with tomatoes and blue cheese!

For my entree, I had the Bone In Filet Mignon (WOW) We also shared some sauteed spinach with garlic and "Daddy's Potatoes". "Daddys Potatoes" are not on the menu and you have to ask your wiater about them. In a nutshell, they are layers of hash brown potaotes with cheese, bacon, scallions and sour cream.

I talked to a manager and the chef before ordering. Everything was perfect.

We also shared a bottle of sparkling Italian Rose wine.

Perfect birthday, perfect dinner...

:)

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    • Samanthaeileen1
      thank you RMJ! That is very helpful advice. Good to know we aren’t crazy if we don’t do the endoscopy. We are going to try the gluten free and see how symptoms and levels improve.    thank you Wheatwacked (love the username lol) that is also reassuring. Thankfully she has an amazing and experienced pediatrician. And yesss I forgot to mention the poop! She has the weirdest poop issues.    How long did it take y'all to start seeing improvement in symptoms? 
    • Wheatwacked
      My son was diagnosed when he was weaned in 1976 after several endoscopies.  Given your two year old's symptoms and your family history and your pediatrition advocating for the dx, I would agree.  Whether an endoscopy is positive or negative is irrelevant.   That may happen even with endoscopy.  Pick your doctors with that in mind. In the end you save the potential trauma of the endoscopy for your baby.   Mine also had really nasty poop.  His doctor started him on Nutramigen Infant because at the time it was the only product that was hypo allergenic and had complete nutrition. The improvement was immediate.
    • RMJ
      So her tissue transglutaminase antibody is almost 4x the upper end of the normal range - likely a real result. The other things you can do besides an endoscopy would be: 1.  Genetic testing.  Unfortunately a large proportion of the population has genes permissive for celiac disease, but only a small proportion of those with the genes have it. With family history it is likely she has the genes. 2.  Try a gluten free diet and see if the symptoms go away AND the antibody levels return to normal. (This is what I would do). Endoscopies aren’t always accurate in patients as young as your daughter. Unfortunately, without an endoscopy, some doctor later in her life may question whether she really has celiac disease or not, and you’ll need to be a fierce mama bear to defend the diagnosis! Be sure you have a good written record of her current pediatrician’s diagnosis. Doing a gluten challenge for an endoscopy later in life could cause a very uncomfortable level of symptoms.   Having yourself, your husband and your son tested would be a great idea.  
    • Samanthaeileen1
      here are the lab ranges.  Normal ranges for tissue transglutaminase are: <15.0 Antibody not detected > or = 15.0 Antibody detected normal for endomysial antibody is < 1.5. So she is barely positive but still positive. 
    • JoJo0611
      I have been diagnosed with coeliacs disease today after endoscopy, bloods and CT scan. I have also been diagnosed with Mesenteric Panniculitis today. Both of which I believe are autoimmune diseases. I have been told I will need a dexa scan and a repeat CT scan in 6 months. I had not even heard of Mesenteric Panniculitis till today. I don’t know much about it? Has anyone else got both of these. 
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