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Eating Out gluten-free In Glasgow, Scotland


KCG91

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KCG91 Enthusiast

Hey,

 

Just after my diagnosis I began emailing around my favourite restaurants here in the West End of Glasgow asking them whether they could still accommodate me. I thought it might be useful to post their replies (I asked about gluten free options and the steps the kitchen takes to prevent CC) to help anyone else in the area (and maybe save them a little legwork :)) I'll update the post when I've tried the ones whose answers I liked :) 

The Oran Mor, Byres Road:

"Dear Katie,
Thank you for taking the time to write to us to inform us of your recent diagnosis. Please rest assured that our chefs here at Òran Mór can cater for all kinds of dietary restrictions. Should you wish to make a reservation in the future please mention that you suffer from Coeliac Disease, we shall make note of it in our diaries so that your server & our kitchen is aware of it on the night.
We very much look forward to welcoming you again soon.
Kind Regards"
 
The Richmond Brasserie, Gibson Street:
"Hi Katie
 
Thank you for getting in touch- we're glad to hear you like The Richmond so much and would love to try and accommodate your new dietary requirements.
 
As I'm sure you've noticed, we're quite a small place and there isn't much demand for gluten free products so we don't routinely have them, but if you gave us a little bit of notice we'd be more than happy to get them in for you (gluten free bread, pasta etc). Otherwise, our chefs are very flexible and so we could modify most of our dishes to suit your needs. 
 
In terms of cross contamination, the chef has said that he would do everything he could in terms of making sure utensils, the preparation area, the grill etc are thoroughly cleaned before preparing your food, and using fresh butter and things to avoid the spread of crumbs (again, it would be ideal if you were able to call ahead, so that the kitchen could have utensils etc ready, otherwise your food might take a little longer to prepare than usual). However, we only have one fryer and wouldn't really be able to change the oil during service which would obviously rule out fried foods for you. 
 
I hope this is of some use to you, don't hesitate to get back in touch if you have any further questions."

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KCG91 Enthusiast

(Also, fellow Glaswegians, please do add your experiences!) 

love2travel Mentor

No recommendations but just a note to say I LOVE SCOTLAND!!!! My husband and I have been there six times and my sister lived in Glasgow so she was sort of a temporary foreign Glaswegian! :-)

KCG91 Enthusiast

No recommendations but just a note to say I LOVE SCOTLAND!!!! My husband and I have been there six times and my sister lived in Glasgow so she was sort of a temporary foreign Glaswegian! :-)

Aha good to hear! I love it here. Sadly the national dish ;) of deep friend Mars Bars is off limits now. 

love2travel Mentor

Aha good to hear! I love it here. Sadly the national dish ;) of deep friend Mars Bars is off limits now.

I know...sigh...
KCG91 Enthusiast

An update! Last night my Dad and I went for dinner at the Oran Mor on Byres Road. I was really impressed with both the food and the amount of effort the waitress went to to make absolutely sure of everything for me. As well as telling the chefs that I was Coeliac and checking that the dish I'd ordered (Thai vegetable curry) was gluten free she checked for any other food intolerances. All of this was done with a smile and nothing was too much trouble. It was a great evening and today I feel good.

I've also had a reply to my standard email from Wudon on Great Western Road:
Hi Katie

I am not sure if you had received an email from me already regarding 
your enquiry as my internet has been playing up.

Just incase you haven't received my reply. We can amend our dishes to 
suit your allergy. We use Tamari soy that is wheat and gluten free and 
we can swap the noodle dishes i.e ramen or udon to a Ho fun noodle 
that is made of rice.

So there should still be plenty of options for you as long as you ask 
a member of staff before ordering and we will help you choose the 
dishes that we can amend to suit you.

Kind regards
Jennie

  • 2 weeks later...
KCG91 Enthusiast

More updates... Ironically I seem to be eating out more than usual since I've been diagnosed :/ This was not the plan!!

I had an impromptu lunch at the Hillhead Bookclub on Byres Road on Thursday. Usually I wouldn't go somewhere without checking first but ... Anyway, I asked the waitress if the soup was gluten free (it was, and I watched her asking the chef about it) Then when a different staff member brought the soup out he made a point of it being 'the gluten free soup without bread' - they hadn't needed reminding. And I feel fine! 

My Mum took me to the Richmond last weekend. The waiting staff were attentive and careful and the chef was happy to alter a dish for me - they do a really good mushroom arancini so instead of the arancini I just had the risotto before it was friend. 

Finally, as the secretary of a sports club at Uni it falls to me to organise our Christmas dinner night out. We are going to the Griffin, on Bath Street and this was the manager's reply to my email: 

"Hi Katie,

Yes we have catered for Coeliacs and nut allergy sufferers previously.

Would it be possible for you to call me, Robert,  on 0141 331 5170 to discuss your potential booking?

There's various menu changes in December and I want to nail exactly what your looking for.

Kind Regards Robert
ps No dancing on the bar!!!!" 


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    • marion wheaton
      Thanks for responding. I researched further and Lindt Lindor chocolate balls do contain barely malt powder which contains gluten. I was surprised at all of the conflicting information I found when I checked online.
    • trents
      @BlessedinBoston, it is possible that in Canada the product in question is formulated differently than in the USA or at least processed in in a facility that precludes cross contamination. I assume from your user name that you are in the USA. And it is also possible that the product meets the FDA requirement of not more than 20ppm of gluten but you are a super sensitive celiac for whom that standard is insufficient. 
    • BlessedinBoston
      No,Lindt is not gluten free no matter what they say on their website. I found out the hard way when I was newly diagnosed in 2000. At that time the Lindt truffles were just becoming popular and were only sold in small specialty shops at the mall. You couldn't buy them in any stores like today and I was obsessed with them 😁. Took me a while to get around to checking them and was heartbroken when I saw they were absolutely not gluten free 😔. Felt the same when I realized Twizzlers weren't either. Took me a while to get my diet on order after being diagnosed. I was diagnosed with small bowel non Hodgkins lymphoma at the same time. So it was a very stressful time to say the least. Hope this helps 😁.
    • knitty kitty
      @Jmartes71, I understand your frustration and anger.  I've been in a similar situation where no doctor took me seriously, accused me of making things up, and eventually sent me home to suffer alone.   My doctors did not recognize nutritional deficiencies.  Doctors are trained in medical learning institutions that are funded by pharmaceutical companies.  They are taught which medications cover up which symptoms.  Doctors are required to take twenty  hours of nutritional education in seven years of medical training.  (They can earn nine hours in Nutrition by taking a three day weekend seminar.)  They are taught nutritional deficiencies are passe' and don't happen in our well fed Western society any more.  In Celiac Disease, the autoimmune response and inflammation affects the absorption of ALL the essential vitamins and minerals.  Correcting nutritional deficiencies caused by malabsorption is essential!  I begged my doctor to check my Vitamin D level, which he did only after making sure my insurance would cover it.  When my Vitamin D came back extremely low, my doctor was very surprised, but refused to test for further nutritional deficiencies because he "couldn't make money prescribing vitamins.". I believe it was beyond his knowledge, so he blamed me for making stuff up, and stormed out of the exam room.  I had studied Nutrition before earning a degree in Microbiology.  I switched because I was curious what vitamins from our food were doing in our bodies.  Vitamins are substances that our bodies cannot manufacture, so we must ingest them every day.  Without them, our bodies cannot manufacture life sustaining enzymes and we sicken and die.   At home alone, I could feel myself dying.  It's an unnerving feeling, to say the least, and, so, with nothing left to lose, I relied in my education in nutrition.  My symptoms of Thiamine deficiency were the worst, so I began taking high dose Thiamine.  I had health improvement within an hour.  It was magical.  I continued taking high dose thiamine with a B Complex, magnesium. and other essential nutrients.  The health improvements continued for months.  High doses of thiamine are required to correct a thiamine deficiency because thiamine affects every cell and mitochondria in our bodies.    A twenty percent increase in dietary thiamine causes an eighty percent increase in brain function.  The cerebellum of the brain is most affected.  The cerebellum controls things we don't have to consciously have to think about, like digestion, balance, breathing, blood pressure, heart rate, hormone regulation, and many more.  Thiamine is absorbed from the digestive tract and sent to the most important organs like the brain and the heart.  This leaves the digestive tract depleted of Thiamine and symptoms of Gastrointestinal Beriberi, a thiamine deficiency localized in the digestive system, begin to appear.  Symptoms of Gastrointestinal Beriberi include anxiety, depression, chronic fatigue, headaches, Gerd, acid reflux, gas, slow stomach emptying, gastroparesis, bloating, diarrhea and/or constipation, incontinence, abdominal pain, IBS,  SIBO, POTS, high blood pressure, heart rate changes like tachycardia, difficulty swallowing, Barrett's Esophagus, peripheral neuropathy, and more. Doctors are only taught about thiamine deficiency in alcoholism and look for the classic triad of symptoms (changes in gait, mental function, and nystagmus) but fail to realize that gastrointestinal symptoms can precede these symptoms by months.  All three classic triad of symptoms only appear in fifteen percent of patients, with most patients being diagnosed with thiamine deficiency post mortem.  I had all three but swore I didn't drink, so I was dismissed as "crazy" and sent home to die basically.   Yes, I understand how frustrating no answers from doctors can be.  I took OTC Thiamine Hydrochloride, and later thiamine in the forms TTFD (tetrahydrofurfuryl disulfide) and Benfotiamine to correct my thiamine deficiency.  I also took magnesium, needed by thiamine to make those life sustaining enzymes.  Thiamine interacts with each of the other B vitamins, so the other B vitamins must be supplemented as well.  Thiamine is safe and nontoxic even in high doses.   A doctor can administer high dose thiamine by IV along with the other B vitamins.  Again, Thiamine is safe and nontoxic even in high doses.  Thiamine should be given if only to rule Gastrointestinal Beriberi out as a cause of your symptoms.  If no improvement, no harm is done. Share the following link with your doctors.  Section Three is especially informative.  They need to be expand their knowledge about Thiamine and nutrition in Celiac Disease.  Ask for an Erythrocyte Transketolace Activity test for thiamine deficiency.  This test is more reliable than a blood test. Thiamine, gastrointestinal beriberi and acetylcholine signaling.  https://pmc.ncbi.nlm.nih.gov/articles/PMC12014454/ Best wishes!
    • Jmartes71
      I have been diagnosed with celiac in 1994, in remission not eating wheat and other foods not to consume  my household eats wheat.I have diagnosed sibo, hernia ibs, high blood pressure, menopause, chronic fatigue just to name a few oh yes and Barrett's esophagus which i forgot, I currently have bumps in back of my throat, one Dr stated we all have bumps in the back of our throat.Im in pain.Standford specialist really dismissed me and now im really in limbo and trying to get properly cared for.I found a new gi and new pcp but its still a mess and medical is making it look like im a disability chaser when Im actively not well I look and feel horrible and its adding anxiety and depression more so.Im angery my condition is affecting me and its being down played 
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