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Any Body Near Indianapolis..i Am Newly Diagnosed...


ME AND ME

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ME AND ME Newbie

JUST LOOKING FOR SOMEONE TO TALK TOO....FAMILY DOESNT UNDERSTAND AND MOST OF THE SO CALLED FRIENDS DONT CARE...

DONT REALLY WANT TO WHINE ABOUT IT (BOO HOO..LOL) BUT I FEEL KINDA ALONE WITH ALL THIS...


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Darn210 Enthusiast

Hi ME&ME,

Indy has a local support group. Here is there website:

Open Original Shared Link

Take a look around, there is a lot of good information. They also hold beginner's meetings (schedule is on the site). They meet on the north side (Carmel) in the new Clarion building at 116th and Meridian.

In addition, this forum is also a great place for info.

  • 1 month later...
Momoftwo Newbie
JUST LOOKING FOR SOMEONE TO TALK TOO....FAMILY DOESNT UNDERSTAND AND MOST OF THE SO CALLED FRIENDS DONT CARE...

DONT REALLY WANT TO WHINE ABOUT IT (BOO HOO..LOL) BUT I FEEL KINDA ALONE WITH ALL THIS...

I was recently diagnosed with celiac disease and I feel the same way. Are you in Indianapolis?

  • 11 months later...
shayre Enthusiast

I'm newly diagnosed too. I'm in Indy (Fishers). I just met a neighbor who has it as well. My hubby and I are planning a nice night out tomorrow for our anniversary. We are going downtown to eat and stay at the Conrad, so I've been online trying to research accomodating restaurants. I ran across this board, and I was already a member of celiac.com. Nice to meet you! Always good to stay in touch with local people. Are any of you intolerant of everything? I really don't know how I'll eat anything...or drink anything. I wish now that it was JUST gluten that I had a problem with. Hang in there dude! I wish that I could go back to when I just had to avoid gluten, so if that's all that you have to avoid...PLEASE count your blessings! There are a lot of people on this site who can't eat anything without feeling sick. I know that doesn't help right now, and believe me...I go through my angry phases!!! Just realize that it could always be worse! If you guys want to talk, I will try to stay on here more!

  • 5 months later...
Asianmom Newbie

Hello! I am from the Carmel area and have had Celiac for 12+ years now! I know how frustrating it can be, especially right now, as I am 7 1/2 weeks pregnant and SO sick anyways, and it actually takes me back to the days before being diagnosed with the constant stomach aches, and nausea. UGH! I hope you are able to find some people to reach out to and have talked to them...if not sounds like there are a few of us around here!!! Share your frustrations and vent away! It is hard when people do not understand! Nice to see you on here!

Financialman Newbie

Hello from Southern Indiana. Hang in there. You have lots of friends on this forum who have gone through the same thing. Just stay in touch and keep posting and you will get through this.

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      @klmgarland, My dermatitis herpetiformis didn't clear up until I became meticulous about cross contamination. I cut out gluten-free oats and all gluten-free foods, dairy and gluten-free rice. Additionally, getting the right amount of protein for my body weight helped significantly in my body's healing process ... along with supplementing with enough of all the vitamins and minerals ... especially Zinc and Magnesium. I went from 70kg to 82kg in a year. Protein with each meal 3 times daily, especially eggs at breakfast made the difference. I'm not sure whether iodine was a problem for me, but I can tolerate iodine no problem now. I'm off Dapsone and feel great. Not a sign of an itch. So there is hope. I'm not advocating for the use of Dapsone, but it can bring a huge amount of relief despite it's effect on red blood cells. The itch is so distracting and debilitating. I tried many times to get off it, it wasn't until I implemented the changes above and was consistent that I got off it. Dermatitis Herpetiformis is horrible, I wouldn't wish it on anyone.  
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      Thank you so very much Scott.  Just having someone understand my situation is so very helpful.  If I have one more family member ask me how my little itchy skin thing is going and can't you just take a pill and it will go away and just a little bit of gluten can't hurt you!!!! I think I will scream!!
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      It is difficult to do the detective work of tracking down hidden sources of cross-contamination. The scenarios you described—the kiss, the dish towel, the toaster, the grandbaby's fingers—are all classic ways those with dermatitis herpetiformis might get glutened, and it's a brutal learning curve that the medical world rarely prepares you for. It is difficult to have to deal with such hyper-vigilance. The fact that you have made your entire home environment, from makeup to cleaners, gluten-free is a big achievement, but it's clear the external world and shared spaces remain a minefield. Considering Dapsone is a logical and often necessary step for many with DH to break the cycle of itching and allow the skin to heal while you continue your detective work; it is a powerful tool to give you back your quality of life and sleep. You are not failing; you are fighting an incredibly steep battle. For a more specific direction, connecting with a dedicated celiac support group (online or locally) can be invaluable, as members exchange the most current, real-world tips for avoiding cross-contamination that you simply won't find in a pamphlet. You have already done the hardest part by getting a correct diagnosis. Now, the community can help you navigate the rest. If you have DH you will likely also want to avoid iodine, which is common in seafoods and dairy products, as it can exacerbate symptoms in some people. This article may also be helpful as it offers various ways to relieve the itch:  
    • Scott Adams
      It's very frustrating to be dismissed by medical professionals, especially when you are the one living with the reality of your condition every day. Having to be your own advocate and "fight" for a doctor who will listen is an exhausting burden that no one should have to carry. While that 1998 brochure is a crucial piece of your personal history, it's infuriating that the medical system often requires more contemporary, formal documentation to take a condition seriously. It's a common and deeply unfair situation for those who were diagnosed decades ago, before current record-keeping and testing were standard. You are not alone in this struggle.
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