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

Foood..going To A Ren Faire


123glldd

Recommended Posts

123glldd Collaborator

We're hoping to get to the local Renaissance Faire this weekend but we'd be spending quite a while there. What do you recommend we do for food? trail mixy type stuff isn't going to cut it..we'll be walking around a lot and probably will be dying for food. Real good food....any thoughts? Most gluten free stuff is frozen and i'm not eating much variety at the moment and re-introducing stuff one thing at a time.


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



Celiac.com Sponsor (A8-M):



srall Contributor

Our's has turkey legs so my daughter and I get that. I think our meal last weekend was a huge turkey leg and dill pickles. But honestly that was the only thing there we felt like we could eat. I'd pack nuts and cut up veggies I guess? Oh...there are caramel apples, but we can't do dairy or corn syrup so those are off the table for us, but perhaps okay for you?

Typically what I do is eat a huge meal before I go. We're seeing a baseball game tonight and I just ate a huge dinner (at 4pm) so I can hopefully get through the game without too much hunger. I'll pack nuts and veggies. So, that's one thing I've learned to do over the past couple of years.

Oh, and back to the Ren Fest. At our's we can leave and reenter so perhaps food in a cooler left in the car, where you can leave the fair, have a safe meal (rice and beans, or soup in a thermos...gluten free sandwich) and then re-enter.

rosetapper23 Explorer

When I've gone in the past, I've eaten the fruit (served usually in half a cantaloupe) as well as the frozen desserts (again, fruit-based ones).

bartfull Rising Star

I used to go to King Richard's Faire on Cape Cod. I LOVED it! We went every year. The jousting matches were my favorite part. ("KILL, KILL, HATE, HATE, MURDER, MURDER, MUTILATE!!")

But they would not let anyone bring in food from outside at all. I don't know if they've changed their policy though. It's been years since I've been.

cap6 Enthusiast

I throw in a tote bag things like tuna & crackers or cheese, nuts, fruit or even a sandwich. I have a small thermos (snack size) that is good for (very mild for me!) chili or other warm food. I also have a leter from my doctor that states I have celiac and must eat gluten-free in case I am ever stopped but have only needed it once.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,034
    • Most Online (within 30 mins)
      7,748

    CE1963
    Newest Member
    CE1963
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Jmartes71
      Thankyou so much for your words.Its a hard battle when a supposed well known hospital whose celiac " specialist " has down played me because my colon looks fine and put it in my medical and so pcp doesn't take seriously. In their eyes we all carry that gene.Im having alot of bad days trying to be positive because of it.
    • Scott Adams
      Your experience is both shocking and critically important for the community to hear, underscoring the terrifying reality that cross-contamination can extend into the most unexpected and invasive medical devices. It is absolutely devastating that you had to endure six months of sickness and ultimately sustain permanent vision loss because a doctor dismissed your legitimate, life-altering condition. Your relentless research and advocacy, from discovering the gluten in MMA acrylic to finding a compassionate prosthodontist, is a testament to your strength in a system that often fails celiac patients. While the scientific and medical consensus is that gluten cannot be absorbed through the skin or eyes (as the molecules are too large to pass through these barriers), your story highlights a terrifying gray area: what about a substance *permanently implanted inside the body*, where it could potentially shed microparticles or cause a localized immune reaction? Your powerful warning about acrylic lenses and the drastic difference with the silicone alternative is invaluable information. Thank you for sharing your harrowing journey and the specific, severe neurological symptoms you endure; it is a stark reminder that celiac is a systemic disease, and your advocacy is undoubtedly saving others from similar trauma.
    • Scott Adams
      Those are driving distance from me--I will try to check them out, thanks for sharing!
    • Scott Adams
      I am so sorry you're going through this bad experience--it's difficult when your own lived reality of cause and effect is dismissed by the very professionals meant to help you. You are absolutely right—your violent physical reactions are not "what you think," but undeniable data points, and it's a form of medical gaslighting to be told otherwise, especially when you have a positive HLA-DQ2 gene and a clear clinical picture. Since your current "celiac specialist" is not addressing the core issue or your related conditions like SIBO and chronic fatigue, it may be time for a strategic pivot. Instead of trying to "reprove" your celiac disease to unwilling ears, consider seeking out a new gastroenterologist or functional medicine doctor, and frame the conversation around managing the complications of a confirmed gluten-free diet for celiac disease. Go in and say, "I have celiac disease, am strictly gluten-free, but I am still suffering from these specific complications: SIBO, chronic fatigue, dermatological issues, and high blood pressure linked to pain. I need a partner to help me address these related conditions." This shifts the focus from a debate about your diagnosis to a collaborative plan for your current suffering, which is the help you truly need and deserve to work toward bouncing back.
    • NanCel
      Hello, no I had to have them re done and then used a liner over the top.  Many dentists are not aware of the celiac effects.  Best of luck.   There is other material, yet, very expensive.
×
×
  • 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.