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

Your art and relationship to art on gluten


Spherical Bird

Recommended Posts

Spherical Bird Contributor

Hi everyone ! 

It's been a while that I wanted to post this topic because I'm very curious about the artistic practice or tastes of other intolerants...

The idea came to me as I discovered migraine induced art. Which seems to have touched something very personal in me... (I think this is has something to do with the loneliness that these intolerances have implied in my own life) I've always felt very isolated from others, so when I discovered about migraine art, it really comforted me in the idea that I am not alone with these struggles and pains...

And this might sound like the strangest thing ever, but I also personally found out I had some problems with food thanks to my own art. It began with stories about disabled characters (and that, without precisely being able to determine if they were disabled in the first place or not) but I also always had an obsession for gooey textures, and a lot of sympathy for tired characters, and eventually, texts that were talking a lot about curious physical sensations and exhaustion. Contemplation...

So obviously, I have been wondering if anyone have had a similar experiences. Weither it's through their art taste or very own art pieces...

Not that I consider that this necessarly impact our tastes in terms of characters/stories/art but I always tend to think that our minds get to be attracted or inspired by topics and things that can help us later on... Like a sort of intuition...

But maybe I'm just having too much expectations here ! And maybe I'm being a little bit weird...Who knows. Either way, I'm curious, feel free to share anyway 

Again, to anyone I haven't talked to yet, I'm French, so I apologize for the typos. Feel free to correct me ! 

  • Spherical Bird changed the title to Your art and relationship to art on gluten

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



Celiac.com Sponsor (A8-M):



Scott Adams Grand Master

This is an interesting concept, and it may be the first time it's been brought up here.

I've sensed a certain anti-establishment sentiment among many with celiac disease, and although I'm not very artistic, I did play guitar in a punk rock band in the early 80's. I've often wondered what attracted me so much to punk music, and perhaps part of this was the feeling of being a misfit due to various health symptoms?

Spherical Bird Contributor
10 hours ago, Scott Adams said:

This is an interesting concept, and it may be the first time it's been brought up here.

I've sensed a certain anti-establishment sentiment among many with celiac disease, and although I'm not very artistic, I did play guitar in a punk rock band in the early 80's. I've often wondered what attracted me so much to punk music, and perhaps part of this was the feeling of being a misfit due to various health symptoms?

That makes sense ! At least, I can see the correlation here ! And I can agree with the anti-establishement sentiment too. I've often had a very similar feeling when talking to people with all sort of digestive issues too... And without much surprise, I usually get along very well with people who suffers from these things too. And it does show up in their tastes too !

I guess it all boils down to the fact that it can simply be very difficult for all of us to feel at ease in societies that often (cheerfully) advertise things or foods that aren't meant for all of us...

I mean, I know I often felt very bitter at marketing for similar reasons. Often left  to wonder why would anyone would show me a poster of someone delighted by an hamburger... when all it inspired me was... Puking (sorry) haha

I'm usually very careful about foods that are sold in such cheerful ways now... Same goes with art/musics that are too "happy" (it often feels suspicious to me)

Scott Adams Grand Master

After hearing of artists who had many different health issues, including mental issues, for example Vincent van Gogh, I sometimes wonder if they had celiac disease or gluten sensitivity? Of course there is no way to know for sure, but I'll admit that I look through this lens now at many things, art included.

I.M.Celiac Apprentice
On 4/2/2022 at 2:34 PM, Scott Adams said:

After hearing of artists who had many different health issues, including mental issues, for example Vincent van Gogh, I sometimes wonder if they had celiac disease or gluten sensitivity? Of course there is no way to know for sure, but I'll admit that I look through this lens now at many things, art included.

I wonder this as well. Especially after learning about gluten ataxia and my own decreased anxiety +neuro issues after quitting gluten. 
Guess someone would have to genetically study Van Gogh’s nephew’s children to see if they have the Celiac gene? 

  • 2 weeks later...
Spherical Bird Contributor
On 4/6/2022 at 4:17 AM, I.M.Celiac said:

I wonder this as well. Especially after learning about gluten ataxia and my own decreased anxiety +neuro issues after quitting gluten. 
Guess someone would have to genetically study Van Gogh’s nephew’s children to see if they have the Celiac gene? 

I've also read about ataxia and I've been wondering too. Strangely, I remember having excellent visual memory while suffering from it, but also very poor movement coordination for everyday tasks, except maybe for dancing or artistic activities which were the things I could learn with more ease... since art didn't follow as much logic as other things in my mind (I mean, when you practice them alone at least, they can be as chaotic as you want them to be)

From what I've understood and also experienced, it does require much more conscious efforts to learn when you have ataxia. So you're kind of forced to mimic more... And damn, I definitely felt this... While also wondering why did "artsy" things felt easier to do while in this state too (maybe they're more impulsion-based than logical) all of this raises so many questions... 

But yes, the neurological implications of it all often made me question the whole artistic process too ! That and the cliché of the "tortured" or "damned" artist too... 

knitty kitty Grand Master

When I've had ataxia, I've been very uncoordinated and awkward trying to do everyday tasks, too, but I've found that doing something involving muscle movement memory is much more successful.

Dancing would involve muscle movement memory, as would knitting. 

I knit really plain socks when I have ataxia, instead of the delicate lace knitting I love to do.  My brain can't translate the lace pattern chart/instructions into the stitches needed to make the lace.  The first time this happened I was truly a "tortured artist"!

There's a rhythm to plain knitting and my fingers remember what to do.  It's comforting, the feeling I can still be productive, even if I don't feel well physically or if I feel isolated because those around me don't understand what it feels like.  And my toes stay warm!  

Perhaps it's easier to do "artsy" stuff with ataxia because our inhibitions are lower and art is a form of nonverbal communication, like painting, dancing and knitting.

 

 

 


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



Celiac.com Sponsor (A8-M):



Spherical Bird Contributor
3 hours ago, knitty kitty said:

When I've had ataxia, I've been very uncoordinated and awkward trying to do everyday tasks, too, but I've found that doing something involving muscle movement memory is much more successful.

Dancing would involve muscle movement memory, as would knitting. 

I knit really plain socks when I have ataxia, instead of the delicate lace knitting I love to do.  My brain can't translate the lace pattern chart/instructions into the stitches needed to make the lace.  The first time this happened I was truly a "tortured artist"!

There's a rhythm to plain knitting and my fingers remember what to do.  It's comforting, the feeling I can still be productive, even if I don't feel well physically or if I feel isolated because those around me don't understand what it feels like.  And my toes stay warm!  

Perhaps it's easier to do "artsy" stuff with ataxia because our inhibitions are lower and art is a form of nonverbal communication, like painting, dancing and knitting.

 

 

 

I think this is a very good guess about the link between ataxia and arts ! There's resolutely something related to inhibitions too. And muscle memory. 

All of this remind me of the fact that a lot of people used to tell me I was very good when it comes to draw facial expressions. But I remember it would frustrate me sooo much to hear this ! Because this aside, I felt like I was really unable to communicate in more normal ways...

  • 1 year later...
Spherical Bird Contributor

It's been a while but thanks everyone for your answers ! They're interesting (and yes, I'm pushing this topic up again because who knows, maybe we have some more tortured artists around who feel like outcasts) ; )

You're not alone !

I'd be interested to read more answers !

Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!

Register a new account

Sign in

Already have an account? Sign in here.

Sign In Now
  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - knitty kitty replied to Jmartes71's topic in Related Issues & Disorders
      14

      My only proof

    2. - Jmartes71 replied to Jmartes71's topic in Related Issues & Disorders
      14

      My only proof

    3. - marion wheaton posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      Are Lindt chocolate balls gluten free?

    4. - Dorothy O. commented on Scott Adams's article in Latest Research
      7

      Study Estimates the Costs of Delayed Celiac Disease Diagnosis (+Video)

    5. - JoJo0611 replied to JoJo0611's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      4

      CT with contrast.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,405
    • Most Online (within 30 mins)
      7,748

    Kbradway
    Newest Member
    Kbradway
    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

    • 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 
    • marion wheaton
      Wondering if anyone knows whether Lindt chocolate balls are gluten free. The Lindt Canadian website says yes but the Lindt USA website says no. The information is a bit confusing.
    • JoJo0611
      I didn’t know there were different types of CT. I’m not sure which I had. It just said CT scan with contrast. 
    • Scott Adams
×
×
  • 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.