Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×

  • 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 Celiac.com!
    eNewsletter
    Donate

Gf Restaurant Chains

Karen(England)

Recommended Posts

Lisa Mentor
Lisa
Posted
It would be a place to start...

even better would be a list online that gets updated with new information!

I have the Triumph Dining Guide and it is very helpful when I leave town. If you would like to PM me the city where you daughter lives - I can send you come recommendations and contact numbers.

Link to comment
Share on other sites
Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):

Celiac.com Sponsor (A8-M):


  • Replies 70
  • Created
  • Last Reply
bellabrit7 Rookie
bellabrit7
Posted

celiac3270

would you mind sending me the list also?? that would be greatly appreciated!

Thanks so much

bellabrit7@yahoo.com

Link to comment
Share on other sites
PeggyV Apprentice
PeggyV
Posted

I would really appreciate the list also. Thanks in advance.

Peggy

peggyvesper@sbcglobal.net

Link to comment
Share on other sites
  • 3 weeks later...
rajawali Newbie
rajawali
Posted
Hey,

Actually, if you give me your e-mail address, I can send you a list of about 240. It's an adobe file compiled by another online support group.

Or I could just list a few off of the top of my head, but I only know about 10 offhand... McDs, outback, TGIF, PF changs, etc.

-----------------------------------------------------

celiac3270,

You must have received tons of requests for your list, and I am one of them.

I would greatly appreciate receiving your list. I got into too many accidents since I was diagnosed.

My email address is: dsugeng@cox.net

Thanks a million.

Darmo

Link to comment
Share on other sites
Lisa Mentor
Lisa
Posted

FYI - this is a pretty old thread. celiac3270 is a busy student, but with hopes he will find this thread again.

Lists of gluten free restaurant items change frequently. I would suggest you call or e-mailing the restaurants and get a current listing. Most can be found by using the "www. ( ).com.

Chilli's

Wendy's

McD's

Chick-fil-A

Outback

P.F. Changs

Cabarras ....and others have menus on line.

Link to comment
Share on other sites
Lulu Magoo Newbie
Lulu Magoo
Posted

I was wondfing if you would possibly send me the information on the gluten free list. I have just been recently diagnosed and it would help me out tons!

lindsay.nickol@gmail.com

Hey,

Actually, if you give me your e-mail address, I can send you a list of about 240. It's an adobe file compiled by another online support group.

Or I could just list a few off of the top of my head, but I only know about 10 offhand... McDs, outback, TGIF, PF changs, etc.

Link to comment
Share on other sites
Lisa Mentor
Lisa
Posted
I was wondfing if you would possibly send me the information on the gluten free list. I have just been recently diagnosed and it would help me out tons!

lindsay.nickol@gmail.com

Lulu Magoo,

The post that you responded to is two years old. It would not be a current list. I understand that it is difficult in early diagnosis. Please don't rely on dated information. Things change rapidly, especially in the restaurant business.

If you would like current information, it would be best to contact the Company or Restaurant directly.

Many have web sites that you can access.

There are many thread here on this site that have current information. Take time to read through some of them. I am sure that you will find them helpful.

Link to comment
Share on other sites
Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):

Celiac.com Sponsor (A8-M):


BARLEY MISSING Newbie
BARLEY MISSING
Posted

I WOULD VERY MUCH APPRECIATE A COPY OF THE RESTAURANTS ALSO AND HERE IS ONE THAT IN CASE IT IS NOT ON YOUR LIST IS IN CONNECTICUT AT FOXWOODS IT IS CALLED THE CEASARS STEAKHOUSE FAIRLY PRICY BUT EXCELLENT FOOD NO BAD REVIEWS HERE THANKS

RIVERGIRLJ7@HOTMAIL.COM

Link to comment
Share on other sites
Lisa Mentor
Lisa
Posted

Sigh....what to do? :(

Link to comment
Share on other sites
  • 6 months later...
jeffandmeg007 Newbie
jeffandmeg007
Posted

I too would love this list. It would be of great help.

email jpfeiler@austin.rr.com

Link to comment
Share on other sites
  • 2 weeks later...
beaglemania Rookie
beaglemania
Posted

Could you please send me the list too???

horsegal1139@bellsouth.net

~Thank you sooo much!! ~

Link to comment
Share on other sites
Lisa Mentor
Lisa
Posted

This thread was begun in 2005. Any information provided in 2005 would certainly not be guaranteed/accurate.

Link to comment
Share on other sites
goyanks720 Newbie
goyanks720
Posted
Hey,

Actually, if you give me your e-mail address, I can send you a list of about 240. It's an adobe file compiled by another online support group.

Or I could just list a few off of the top of my head, but I only know about 10 offhand... McDs, outback, TGIF, PF changs, etc.

I would LOVE to get copy of your list if it wouldn't be too much of a hassle. I am newly diagnosed and am having a really hard time adjusting. Thanks so much. Pat - My mail is: goyanks720@yahoo.com

Link to comment
Share on other sites
Sue C Rookie
Sue C
Posted

I am new to the gluten free life and would appreciate a copy of the list as well.

sue0321@gmail.com

Link to comment
Share on other sites
pixiegirl Enthusiast
pixiegirl
Posted

I really need this list and ASAP. If someone has it can they send it to me? My daughter is going on vacation with her dad and he doesn't get gluten-free very well.

Susan

Link to comment
Share on other sites
kevsmom Contributor
kevsmom
Posted
This thread was begun in 2005. Any information provided in 2005 would certainly not be guaranteed/accurate.

Thanks for bringing this up. I was about to wish celiac3270 welcome back. We haven't heard from him in a while.

Link to comment
Share on other sites
  • 2 months later...
mushroom Proficient
mushroom
Posted

Hi:

I was quite excited to read about celiac3270's list, but then understand it is out of date and he hasn't been around for a while. If there is anyone who has a copy of his list, could you please send it to justneroli@hotmail.com. I would be most appreciative. While it may be out of date, it is a good starting point. I am coming back to U.S. (Lake Tahoe/Reno) area for first time since being gluten free. Understand I can shop at Trader Joe's and Costco (have always loved Amy's foods), but am a bit nervous about transplanting myself for a couple of months. Also, if anyone has info on Reno/Carson City restaurants, I would love that :wub:

Thanks a bunch if you can help.

Neroli

Link to comment
Share on other sites
happygirl Collaborator
happygirl
Posted
Open Original Shared Link may be a more up to date alternative.
Link to comment
Share on other sites
Lisa Mentor
Lisa
Posted
Open Original Shared Link may be a more up to date alternative.

I have the 2006-07 version and I have used it quite a bit. I plan on getting the latest addition and I highly recommend it.

Link to comment
Share on other sites
lmvrbaby Newbie
lmvrbaby
Posted

Hi celiac3270, I just got back from a trip and know of only a couple of places that had gluten free on the menu or spoke to the managers before ordering. We are planning another trip for next year and would love to have more than a couple of choices, so can I get a copy as well of the resturants? Thanks.

lmvrbaby@yahoo.com :rolleyes:

Link to comment
Share on other sites
mushroom Proficient
mushroom
Posted
I have the 2006-07 version and I have used it quite a bit. I plan on getting the latest addition and I highly recommend it.

Thank you so much, Momma Goose and HappyGirl. That sounds like an indispensable little book. It's on its way.

Neroli

Link to comment
Share on other sites

Archived

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

Go to topic listing
  • Celiac.com Sponsor (A19):


  • Member Statistics

    • Total Members
      121,224
    • Most Online (within 30 mins)
      7,748
    Suzi374
    Newest Member
    Suzi374
    Joined
  • Celiac.com Sponsor (A20):

  • Forum Statistics

    • Total Topics
      120.3k
    • Total Posts
      1m
  • Celiac.com Sponsor (A22):



  • Celiac.com Sponsor (A21):


  • Upcoming Events

  • Posts

    • Suzi374
      Lots of tests

      By Suzi374 · Posted

      And I’m anaemic, however I’m also female and vegetarian. I had an iron trans a couple of years ago however it’s starting to dwindle and taking supplements doesn’t seem to work. I can’t seem to absorb it. 
    • Suzi374
      Lots of tests

      By Suzi374 · Posted

      Hi, I attended a neurologist appt last Tuesday, which I nearly cancelled, due to ongoing numbness and tingling in toes to mid foot. One of the first things he asked was ‘are you celiac’. I’m not. He thought all reflexes were ok but at the last minute decided on nerve conduction tests which were low normal. He was a little confused as he felt they should be better and tried a new set of probs, all the time, giving me multiple shocks which were not enjoyable lol. Anyway, he’s now ordered tests for myeloma, and all the vitaminy things that so many of you mention on here, also tests looking for autoimmune responses. I already have Hashimotos. Interestingly, to me, but maybe someone out there can relate or knows more than i do, although I was a nurse, but ED not ‘weird symptoms’  nurse. Anyway back to the interesting thing, I took duramine in 2013 to lose weight which caused a massive panic attack when I stopped taking it and half my hair fell out. I only took it for a week but it was horrible and I regret it. It triggered ongoing panic attacks which are horrendous. So I feel like I’m a bit crazy. Then in 2020 I had this sudden onset of horrible pain when trying to eat a cinnamon roll. It continued and I lost around 20 kgs. I had two gastroscopes and a colonoscopy and they were all normal. I scored a barium swallow and CT angiogram. All normal. The pain subsided a little but I was left with reflux and an awful feeling that I couldn’t get air when I ate some foods. This was not anxiety.  The anxiety was separate and I still maintain this. This was something to do with eating. It was like the air was thick but I wasn’t short of breath. I just had the sensation I was, then it triggered anxiety. Anyway, I had other weird things- couldn’t bend knees to shave legs in shower lol. Knees felt stiff and swollen but they weren’t. Knee WOUld swell up randomly but mri showed minimal issues. A bit of a meniscus degeneration but insignificant. Then the buzzing sensations in my head, the feeling like someone was stabbing me with something sharp. So now, I pre empted his tests, although I don’t think I’m celiac because it should have come up on gastroscopy, I’ve gone off gluten. Since Tuesday last week so 9 days. Since then I don’t appear to be as constipated, I realised I got through today without a nap and I’m not tired, maybe it’s just today and not related but I get very tired normally and sleep straight after work often, I can bend my knees and shave my legs lol, the buzzing vibrating has gone from my head, I had to call and ambulance as my heart decided we were off on a run, but we weren’t running and I’ve been a bit twitchy at bed time when trying to sleep, reflux is improving, I did get the weird suffocating feeling a bit when eating today but not as bad normall. Tingling and numbness still present and I felt like it moved up my legs a bit today but I’m a bit jittery. So I don’t know if it’s celiac disease or a gluten intolerance but I think, and it may be wishful thinking because my symptoms do make life a bit challenging, but maybe I’m feeling better. I don’t feel as cloudy. My thinking feels crisper. Like there’s no buzzing and I’m not fighting to break through the cloudiness now. I hope so much that this may help me feel a bit better moving forward. It would be a miracle as I really have struggled to work and parent and keep the house clean and I’m always anxious and exhausted.  If you get this far, please tell me if you you can relate to any of the above. Oh and tonsils out 5 years ago but before that antibiotics multiple times a year, sometimes intramuscular because they were so bad.  Op was meant to take 30 mins, it took 1.5 hours due to size of them. 
    • Peace lily
      Would like to gain weight

      By Peace lily · Posted

      Im still not gaining weight I’m on a gluten free diet . And still having issues with constapation started priobiocs figured it would help been over two weeks . I guess it’s going to be a long road for me .
    • Smith-Ronald
      Lymph nodes

      By Smith-Ronald · Posted

      Enlarged lymph nodes in neck and groin with celiac are not uncommon. They can take time to reduce even after going gluten-free. Monitoring is key.
    • Random.user556
      I think I might be celiac?

      By Random.user556 · Posted

      Hello! I’m sorry in advance for the long post!   Over the past few months I’ve been having a lot of issues with my stomach and have recently been referred to a Gastroenterologist. I’ve had stomach pain and issues since I was a baby. I had bad constipation (still do) and couldn’t tolerate most formula as a baby. When I was around 8 I started experiencing a lot of lower abdominal cramping (just below the belly button) and ended up missing a fair amount of school because of this. It would start about 2 hours after eating breakfast and I’d have lower abdominal cramps and feel nauseous . After a visit to my family doctor it was brushed off as separation anxiety.. or as the doctor put it “I was just a kid who wanted to stay home from school”. This stomach pain persisted all through my elementary and high school years. In fact I still experience it to this day and I’m now 24. Along with this my doctor believes I have a form of disautonomia called POTS (Postural Orthostatic Tachycardia Syndrome). I frequently feel unwell and exhausted. I also experience Raynaud’s phenomena especially during the winter months or when I’m sick. I also can not tolerate heat for the life of me.. although I’m not entirely convinced my symptoms are from POTS. The last few years I’ve also started experiencing frequent chronic sinus infections up to 5 a year most of which I require antibiotics for… Up until two years ago I have never had allergies or sinus problems. Back to my stomach issues… The last year I have been experiencing lots of stomach bloating and discomfort especially at night.. this has led to a few nights of 3am vomiting.. my doctor tested me for H. Pylori which was negative as well as full work ups to test my kidneys, liver, pancreas, gallbladder.. all of which were normal. At this time he also started me on Rabeprazole 20mg twice daily which is a Proton pump inhibitor (PPI) … as he believes it could be GERD. The PPI has not helped at all and I have since been moved down to once daily which I wait for a referral to a Gastroenterologist for an endoscopy as well as an abdominal ultrasound to verify I have no gallstones.. The pain I feel in my abdomen feels very heavy right around my bellybutton and frequently is accompanied by nausea and occasionally I also experience sharp stabbing like pain left of my belly button. I began tracking my symptoms, what I’m eating and bowel habits on an app called “My IBS” which track’s symptoms and flags foods that could be potential triggers.. all of my flagged potential triggers seem to be gluten related foods like pasta and breads. I asked to be tested for Celiac as I have an uncle with it. My doctor only sent for TtG IGA.. no other tests. My results came back negative at “<0.5 U/ml” the reference range being “ <12 U/Ml”. I am aware that total IGA should of been ordered as well but my doctor is confident we have ruled out celiac so I guess I will have to wait for the Gastroenterologist for more testing.. The other red flag for me is I have a rash that shows on both my knees and recently I have developed a similar rash behind both of my ears, on my neck and into my scalp.. there is dozens of small red and skin coloured lesions that sort of? resemble pimples but have a “head” and don’t pop (yes, i know don’t pop your pimples!) they are also itchy and sore.. I have tried washing and scrubbing them with antibacterial soap and body wash to no avail as well as ensuring I rinse my neck thoroughly after a shower, keeping my neck dry, frequently changing pillowcases and even keeping my hair off my neck as much as possible … it doesn’t have any effect on it.  In your experience does this sound like I could be experiencing celiac? I’ve debated going gluten free to see if my symptoms persist or begin to clear up.. any suggestions or help is appreciated! 
×
×
  • Create New...