Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Gluten Guy From Tallahassee Fl


CeliacMe

Recommended Posts

CeliacMe Rookie

There is a brave man, known as "gluten guy" to the students at FSU's School of Hospitality Management. I would like to thank you for all that you have done to educate the resturants about gluten-free through your bravery. I bet you are a big part of the reason why chain resturants are offering gluten-free menus. If you are out there, Thank You.

  • 3 months later...

Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



floridanative Community Regular

I too am in need of 'the gluten guy of Tallahassee's' help. I've never heard of him before reading this post but my Mother is getting tested for Celiac next week and if she has it, I need to point her in the direction of help down in FL. If no one knows 'the gluten guy' from Tall., do any of you know if there is a support group for Celiacs there? Or even in Panama City, FL?

  • 1 year later...
Guest KG in FL
I too am in need of 'the gluten guy of Tallahassee's' help. I've never heard of him before reading this post but my Mother is getting tested for Celiac next week and if she has it, I need to point her in the direction of help down in FL. If no one knows 'the gluten guy' from Tall., do any of you know if there is a support group for Celiacs there? Or even in Panama City, FL?

Hey floridanative, I am in Destin, FL. I've been hoping there would be anyone close to me posting but there hasn't yet. I know there are celiacs right around me by the new availability and sale of gluten-free products at the supermarkets and a the healthfood stores here. I don't know of glutenguy, but my son (not celiac) will be starting school at FSU soon so I'll be there a lot. Is there a group there? Hey, and I am a FL native too!!

floridanative Community Regular

Hi KG - as far as I know there still is not a group in Tall. The woman who ran one previously apparently moved. Very few people in town are dx'd with Celiac as far as we can tell. We rarely eat out when in Tall. but if we do, we go to Bonefish or Carrabas which at least offer decent gluten-free menus. Sorry not t be of more help but since you're in Destin, do you know of any places to eat in Orange Beach, FL? We're going down for a few days before heading to New Orleans, and we're hoping not to cook every dinner in the condo while at the beach.

ReneCox Contributor

im 19 and have lived in Tallahassee, FL my whole life. Ive never heard of gluten guy but I would def. like to meet him! The only places I eat out are at outback, bonefish, and Teds Montana Grill.

  • 6 months later...
GFinNC Newbie
im 19 and have lived in Tallahassee, FL my whole life. Ive never heard of gluten guy but I would def. like to meet him! The only places I eat out are at outback, bonefish, and Teds Montana Grill.

Where do you shop for gluten-free food? Do regular grocery stores (Albertson's and Publix) have gluten-free food? I've been spoiled with Whole Foods....

  • 3 months later...
Jeff Swartz Newbie

I am also a celaic in Tallahassee.I am 56 years old. I have found no group meeting in Tallahassee, but might be interested in helping one get started.

After fighting for almost 25 years and in failing health [before the dx if celiac], I was finally fired from state work about a year ago.I was a Professional Geologist. I would love to hear from other Celiacs in this area.

Jeff Swartz


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



  • 1 month later...
RockHammer Rookie

Anouncing an orginizational meeting for a Celiac Support Group for the Tallahassee "Area. Next Saturday April 26, 2008 at 2 PM at the office of Dr John Ness 616 Universal Dr, Tallahassee FL.

From downtown Tallahassee go north on Monroe St. Turn Left on Universal Drive (at chik-fl-a). On Right Side at end of street. for info email jswartz.pg@gmail.com.

SEE YOU THERE

RH :D

  • 2 weeks later...
jparsick84 Rookie

Eating out in Tally:

* La Fiesta (on Appalachee Parkway) is safe for those with only Celiac. Stick to the corn stuff (chips, tortillas, etc). Ask if anything is breaded before you order it, they're up front with you. Tell them you're allergic to wheat, and that nothing you are served must have touched anything wheat. I've never had any problems there, and they do Happy Hour almost every night of the week, so even if you just want to go for drinks and chips/salsa, it's a great place to go.

That's the only non-chain restaurant I've been willing to try, but if you're looking for some GREAT Mexican food, it's the place to go. :)

RockHammer Rookie
Anouncing an orginizational meeting for a Celiac Support Group for the Tallahassee "Area. Next Saturday April 26, 2008 at 2 PM at the office of Dr John Ness 616 Universal Dr, Tallahassee FL.

From downtown Tallahassee go north on Monroe St. Turn Left on Universal Drive (at chik-fl-a). On Right Side at end of street. for info email jswartz.pg@gmail.com.

SEE YOU THERE

RH :D

The next meeting of the still un-named Celiac Support Group serving Tallytown and Enviirons will meet Tuesday May 20 2008 again at the office of Dr John Ness. I hope to see you there.

To join or for info please contact Rockhammer, or email at jswartz.pg@gmail.com.

RH

  • 3 weeks later...
katifer Apprentice

i was in John Ness' office today (the 20th of May) and he told me that "Rock Hammer" died recently of a heart attack--absolutely horrible. and there isnt anyone in Tallahassee who is taking over the support group right now.

  • 4 weeks later...
Celiac#8 Newbie
i was in John Ness' office today (the 20th of May) and he told me that "Rock Hammer" died recently of a heart attack--absolutely horrible. and there isnt anyone in Tallahassee who is taking over the support group right now.

WOW! Did not see that coming when I started to post on here. I was going to ask if you all were still meeting in Tallahassee. That is awful. I just happened across Rock Hammer's posts on the web and was thrilled to see someone trying to get a group together. I'm sorry for your loss to all who knew him.

If there is still going to be a group, I am interested in meeting with you all.

My regards,

Celiac#8

mrsgarner_ela@yahoo.com

jparsick84 Rookie

Yes, I think there's still interest. It may be hard to rustle up people during the summer, but I know of at least 5 Celiac students at FSU, so maybe we should plan a date once the students come back to town?

And if anyone just wants to get together for dinner one night this summer, PLEASE contact me! (I'm dying for some Outback...)

~ Jennifer :)

taylor- Rookie
Anouncing an orginizational meeting for a Celiac Support Group for the Tallahassee "Area. Next Saturday April 26, 2008 at 2 PM at the office of Dr John Ness 616 Universal Dr, Tallahassee FL.

From downtown Tallahassee go north on Monroe St. Turn Left on Universal Drive (at chik-fl-a). On Right Side at end of street. for info email jswartz.pg@gmail.com.

SEE YOU THERE

RH :D

Hey guys! so we are officially having a meeting tomorrow! 6:30, at Dr. John Ness' office (directions above) PLEASE come if you can, because we are going to try and make some definite plans for a monthly meeting. thanks so much! if you have any questions send me a message and ill try and check before tomorrow to respond!

  • 3 weeks later...
deb18 Newbie

I would be interested in something here. Let me know. deb

  • 2 weeks later...
katifer Apprentice

hey just want to update real quick there is a support being led Fall 2008 by a woman named Beverly

Beverly Vichich

bevnurse1@earthlink.net

next meeting 6:30pm Dr. John Ness' office waiting room

  • 1 month later...
rebkin Newbie

If we can help you all with any information regarding living gluten free, or setting up a group - please contact us at: birminghamceliac@hotmail.com, or at our blog site: birminghamceliac.spaces.live.com

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,554
    • Most Online (within 30 mins)
      7,748

    Becky 0163
    Newest Member
    Becky 0163
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      Your post demonstrates the profound frustration and isolation that so many in the Celiac community feel, and I want to thank you for channeling that experience into advocacy. The medical gaslighting you endured for decades is an unacceptable and, sadly, a common story, and the fact that you now have to "school" your own GI specialist speaks volumes about the critical lack of consistent and updated education. Your idea to make Celiac Disease a reportable condition to public health authorities is a compelling and strategic one. This single action would force the system to formally acknowledge the prevalence and seriousness of the disease, creating a concrete dataset that could drive better research funding, shape medical school curricula, and validate the patient experience in a way that individual stories alone often cannot. It is an uphill battle, but contacting representatives, as you have done with Adam Gray, is exactly how change begins. By framing it as a public health necessity—a matter of patient safety and protection from misdiagnosis and neglect—you are building a powerful case. Your voice and your perseverance, forged through thirty years of struggle, are exactly what this community needs to ensure that no one else has to fight so hard just to be believed and properly cared for.
    • Scott Adams
      I had no idea there is a "Louisville" in Colorado!😉 I thought it was a typo because I always think of the Kentucky city--but good luck!
    • Scott Adams
      Navigating medication safety with Celiac disease can be incredibly stressful, especially when dealing with asthma and severe allergies on top of it. While I don't have personal experience with the HealthA2Z brand of cetirizine, your caution is absolutely warranted. The inactive ingredients in pills, known as excipients, are often where gluten can be hidden, and since the FDA does not require gluten-free labeling for prescription or over-the-counter drugs, the manufacturer's word is essential. The fact that you cannot get a clear answer from Allegiant Health is a significant red flag; a company that is confident its product is gluten-free will typically have a customer service protocol to answer that exact question. In situations like this, the safest course of action is to consider this product "guilty until proven innocent" and avoid it. A better alternative would be to ask your pharmacist or doctor to help you identify a major national brand of cetirizine (like Zyrtec) whose manufacturer has a verified, publicly stated gluten-free policy for that specific medication. It's not worth the risk to your health when reliable, verifiable options are almost certainly available to you. You can search this site for USA prescriptions medications, but will need to know the manufacturer/maker if there is more than one, especially if you use a generic version of the medication: To see the ingredients you will need to click on the correct version of the medication and maker in the results, then scroll down to "Ingredients and Appearance" and click it, and then look at "Inactive Ingredients," as any gluten ingredients would likely appear there, rather than in the Active Ingredients area. https://dailymed.nlm.nih.gov/dailymed/   
    • Scott Adams
      What you're describing is indeed familiar to many in the Celiac community, especially in the early stages of healing. When the intestinal villi are damaged from Celiac disease, they struggle to properly digest and absorb fats, a condition known as bile acid malabsorption. This can cause exactly the kind of cramping and spasms you're seeing, as undigested fats can irritate the sensitive gut lining. It is highly plausible that her reactions to dairy and eggs are linked to their higher fat content rather than the proteins, especially since she tolerates lean chicken breast. The great news is that for many, this does improve with time. As her gut continues to heal on a strict gluten-free diet, her ability to produce the necessary enzymes and bile to break down fats should gradually return, allowing her to slowly tolerate a wider variety of foods. It's a slow process of healing, but your careful approach of focusing on low-fat, nutrient-dense foods like seeds and avocado is providing her system the best possible environment to recover. 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: Thank you for sharing your story—it's a valuable insight for other parents navigating similar challenges.
    • Beverage
      I had a very rough month after diagnosis. No exaggeration, lost so much inflammatory weight, I looked like a bag of bones, underneath i had been literally starving to death. I did start feeling noticeably better after a month of very strict control of my kitchen and home. What are you eating for breakfast and lunch? I ignored my doc and ate oats, yes they were gluten free, but some brands are at the higher end of gluten free. Lots of celics can eat Bob's Red Mill gluten-free oats, but not me. I can now eat them, but they have to be grown and processed according to the "purity protocol" methods. I mail order them, Montana Gluten-Free brand. A food and symptoms and activities log can be helpful in tracking down issues. You might be totally aware, but I have to mention about the risk of airborne gluten. As the doc that diagnosed me warned . . Remember eyes, ears, nose, and mouth all lead to your stomach and intestines.  Are you getting any cross contamination? Airborne gluten? Any pets eating gluten (they eat it, lick themselves, you pet them...)? Any house remodeling? We live in an older home, always fixing something. I've gotten glutened from the dust from cutting into plaster walls, possibly also plywood (glues). The suggestions by many here on vitamin supplements also really helped me. I had some lingering allergies and asthma, which are now 99% gone. I was taking Albuterol inhaler every hour just to breathe, but thiamine in form of benfotiamine kicked that down to 1-2 times a day within a few days of starting it. Also, since cutting out inflammatory seed oils (canola, sunflower, grapeseed, etc) and cooking with real olive oil, avocado oil, ghee, and coconut oil, I have noticed even greater improvement overall and haven't used the inhaler in months! It takes time to weed out everything in your life that contains gluten, and it takes awhile to heal and rebuild your health. At first it's mentally exhausting, overwhelming, even obsessive, but it gets better and second nature.
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.