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Where You From?


Guest DawterAod

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LJCurly9 Newbie

I'm from Rensselaer, Indiana...however, I'm currently a student at Butler University in Indianapolis.


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  • Replies 117
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Guest talsop

Evansville, Indiana

yllehs91 Apprentice

Southern TX...anyone from around the same area e-mail me! i'd really like to know someone near me that's going through the same thing...bcuz there are NO support groups where i am that i can find. (nearest is 2 hours away from me--corpus) and it'd be cool to meet people (if there are any besides me) that live close to me.

aim: ScoutNBoys1991

  • 1 month later...
Guest Bsecen

Hi everyone!!! I am from Orlando, Fl . :( Any relatives??? E-mail me!

Tiffany

minibabe Contributor
:D Hi, I was just recently diagnosed and I am from New York.....I live on Long Island. I am so glad that I found a message board.
pemmy Newbie

I'm from Glasgow in Scotland. I appear to be the only Celt on the board.

Great to hear about all the different places we come from. :)

  • 1 month later...
joe2008 Newbie

Downtown L.A.


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VegasCeliacBuckeye Collaborator

I live in Vegas.

Born in the U.K.

Raised in Dayton, Oh.

College at Ohio State (Columbus)

Graduate school in San Diego

Whew!

Vyse Newbie

Iowa here :)

Guest Viola

I'm in British Columbia, Canada. In the West Kootenay area, which is the southern part of the province. Only about four hours north of Spokan Washington.

Guest Leidenschaft

Hi all, this thread is very similar to our thread on Open Original Shared Link which asked to modify our signatures so that at a glance we could all know (on each and every post) where the other is from. Please have a glance through that thread! :)

Thanks!

sparkle2085 Newbie

Connecticut

  • 2 weeks later...
gabrielle Contributor
:D Amishtown, Pennsylvania
  • 2 weeks later...
Kels18 Newbie

Pittsburgh, Pennsylvania :rolleyes:

  • 4 weeks later...
teeta Newbie

INDIANA ( i thought if i did it in caps it might sound like more fun....... i dont think it worked)

jams Explorer

I'm from between Milwaukee & Madison Wisconsin!!

Guest GFLisa0405

Im from southeast michigan (halfway between detroit and ann arbor) tho i go to Central michigan in mt. pleasant

jenvan Collaborator

Hey! Shout out to the few from Indiana. I am in Indianapolis--the Ripple, for anyone who knows what that means :D

stef-the-kicking-cuty Enthusiast

Wow :o ! A lot of celiacs from PA here. Guys, we should meat. Maybe we could make a thread where we decide when and where we meat.

Oh, by the way, we're (my husband and I) moving. As of May 1st we will live in the Township (I first thought it's a municipality) of wheatfield :lol: .

kings-kid Newbie

Canada

wickedclown Newbie

brown city michigan..what what..throwin it up for the MI juggalos

  • 2 weeks later...
Guest Doct.Giggles

:P

I'm from Altmonte Springs, Florida!

Guest Doct.Giggles

:D I am from Altamonte Springs, Florida!!!!! :D

-Tiffany

  • 1 month later...
DragonQueen Explorer

Las Vegas, Nevada :lol:

selagirl Newbie

Im from Jerusalem, Israel :rolleyes:

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    • cristiana
      @Colleen H   I am just curious,  when you were tested for coeliac disease, did the doctors find out if you had any deficiencies? Sometimes muscle pain can be caused by certain deficiencies, for example, magnesium, vitamin D, calcium, and potassium.   Might be worth looking into having some more tests.  Pins and needles can be neuropathy, again caused by deficiencies, such as iron and B12,  which can be reversed if these deficiencies are addressed. In the UK where I live we are usually only tested for iron, B12 and vitamin D deficiencies at diagnosis.   I was very iron anemic and supplementation made a big difference.  B12 was low normal, but in other countries the UK's low normal would be considered a deficiency.  My vitamin D was low normal, and I've been supplementing ever since (when I remember to take it!) My pins and needles definitely started to improve when my known deficiencies were addressed.  My nutritionist also gave me a broad spectrum supplement which really helped, because I suspect I wasn't just deficient in what I mention above but in many other vitamins and minerals.  But a word of warning, don't take iron unless blood tests reveal you actually need it, and if you are taking it your levels must be regularly monitored because too much can make you ill.  (And if you are currently taking iron, that might actually be making your stomach sore - it did mine, so my GP changed my iron supplementation to a gentler form, ferrous gluconate). Lastly, have you been trying to take anything to lessen the pain in your gut?  I get a sore stomach periodically, usually when I've had too much rich food, or when I have had to take an aspirin or certain antibiotics, or after glutening.  When this happens, I take for just a few days a small daily dose of OTC omeprazole.  I also follow a reflux or gastritis diet. There are lots online but the common denominators to these diets is you need to cut out caffeine, alcohol, rich, spicy, acidic food etc and eat small regularly spaced meals.   When I get a sore stomach, I also find it helpful to drink lots of water.  I also find hot water with a few slices of ginger very soothing to sip, or camomile tea.  A wedge pillow at night is good for reflux. Also,  best not to eat a meal 2-3 hours before going to bed. If the stomach pain is getting worse, though, it would be wise to see the doctor again. I hope some of this helps. Cristiana    
    • Me,Sue
      I was diagnosed with coeliac disease a couple of years ago [ish]. I love my food and a variety of food, so it's been hard, as it is with everyone. I try and ensure everything I eat doesn't contain gluten, but occasionally I think something must have got through that has gluten in. Mainly I know because I have to dash to the loo, but recently I have noticed that I feel nauseous after possibly being glutened. I think the thing that I have got better at is knowing what to do when I feel wiped out after a gluten 'episode'. I drink loads of water, and have just started drinking peppermint tea. I also have rehydration powders to drink. I don't feel like eating much, but eventually feel like I need to eat. Gluten free flapjacks, or gluten free cereal, or a small gluten free kids meal are my go to. I am retired, so luckily I can rest, sometimes even going to bed when nothing else works. So I feel that I am getting better at knowing how to try and get back on track. I am also trying to stick to a simpler menu and eat mostly at home so that I can be more confident about what I am eating. THANKS TO THOSE WHO REPLIED ABOUT THE NAUSEA .
    • Francis M
      Thanks. Since the back and forth and promises of review and general stalling went on for more than six months, the credit company will no longer investigate. They have a cutoff of maybe six months.
    • Scott Adams
      Is this the same restaurant? https://www.facebook.com/TheHappyTartFallsChurch/ Is it too late to take this up with your credit card company? Normally you have a few months to do a chargeback with them. It seems very odd that they are taking this approach with someone who is likely to be a regular customer--not a good business-minded way of handling things!
    • Scott Adams
      Many people with celiac disease, especially those who are in the 0-2 year range of their recovery, have additional food intolerance issues which could be temporary. To figure this out you may need to keep a food diary and do an elimination diet over a few months. Some common food intolerance issues are dairy/casein, eggs, corn, oats, and soy. The good news is that after your gut heals (for most people who are 100% gluten-free this will take several months to two years) you may be able to slowly add some these items back into your diet after the damaged villi heal. This article may be helpful: The most common nutrient deficiencies associated with celiac disease that may lead to testing for the condition include iron, vitamin D, folate (vitamin B9), vitamin B12, calcium, zinc, and magnesium.  Unfortunately many doctors, including my own doctor at the time, don't do extensive follow up testing for a broad range of nutrient deficiencies, nor recommend that those just diagnosed with celiac disease take a broad spectrum vitamin/mineral supplement, which would greatly benefit most, if not all, newly diagnosed celiacs. Because of this it took me decades to overcome a few long-standing issues I had that were associated with gluten ataxia, for example numbness and tingling in my feet, and muscle knots--especially in my shoulders an neck. Only long term extensive supplementation has helped me to resolve these issues.        
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