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

Hugging


Di2011

Recommended Posts

Di2011 Enthusiast

I live in Australia. It seems that here hugging is a pretty normal/acceptable kind of physical response to meeting friends/family. It is family dependent but I wonder if hugging is or is not a normal response within other cultures?


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



Celiac.com Sponsor (A8-M):



Bubba's Mom Enthusiast

I live in Australia. It seems that here hugging is a pretty normal/acceptable kind of physical response to meeting friends/family. It is family dependent but I wonder if hugging is or is not a normal response within other cultures?

I'm in USA. It kind of depends on the family here? We weren't huggers in my family.

Before I married my husband we went to a family reunion of his family. They were huggers. It was so odd to me to have strangers come up to me and nearly squeeze my breath out! :blink: I never did get used to that in all of the years I've been in the family. :lol:

dilettantesteph Collaborator

My husband's family is Norwegian and they are super huggers. My family, not so much.

IrishHeart Veteran

USA --Boston Bred.

My family and friends---we're all a bunch of molesters! :lol:

Overly-enthusiastic even.

(Irish, Italian, Armenian, giant mixed bag of people....)

I hug freely. But only if I know it's okay with someone. (I respect boundaries) I always told my Dad, "you give good hug." :)

He said "right back atcha!"

Long good byes at family gatherings involved multiple group huggings.

And hubs, well, he gives the big, all encompassing bear hug.

But he learned it from me.

love2travel Mentor

It is very normal where I live in Canada. Half my family hugs like crazy; half stand stiffly and look as though they are being tortured. I am a hugger but as a very private person only hug those I know very well. Having said that, the odd time I hug spontaneously if I am moved to do it emotionally (i.e. if someone is terminally ill).

pricklypear1971 Community Regular

I don't like hugging. It's reserved only for specific people at specific times but I'm weird that way.

Half my family hugs and kisses left and right and they always laugh at my expression and explain I have to do it.

It's about personal space for me. I don't like to be touched.

And yes, I'm from the U.S.. Southern U.S.

Oddly enough it's the New Yorkers that always want to kiss and hug and touch. :) aside from my family (who are definitely southern).

Adalaide Mentor

My family aren't really huggers. I grew up in Pennsylvania with a very close family, we just didn't hug. The exception is my grammy who is a hugger. Not like all the time, but with hellos and goodbyes. I live in Utah now and lots of people here are huggers. My best friend is a super hugger which took some real getting used to. Still though, the only people I'll let near me are her, my family back east and my husband. Anyone else gets in my bubble and things get pretty awkward pretty quick. I just like people a whole lot more when they are at least arm's length away from me.


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



Celiac.com Sponsor (A8-M):



  • 2 weeks later...
vella Newbie

I come from a family of non-huggers, but I'm entirely opposite......I like ya, I hug. :)

The culture I come from are very warm and friendly people....Big sloppy kisses too.

Archived

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

  • 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. - trents replied to Ginger38's topic in Related Issues & Disorders
      1

      Shingles - Could It Be Related to Gluten/ Celiac

    2. - Ginger38 posted a topic in Related Issues & Disorders
      1

      Shingles - Could It Be Related to Gluten/ Celiac

    3. - Russ H commented on Scott Adams's article in Latest Research
      5

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

    4. - Russ H posted a topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      0

      Coeliac UK Research Conference 2025

    5. - Rejoicephd replied to Rejoicephd's topic in Related Issues & Disorders
      5

      Basic metabolic panel results - more flags


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,376
    • Most Online (within 30 mins)
      7,748

    Citydweller
    Newest Member
    Citydweller
    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

    • trents
      I don't know of a connection. Lots of people who don't have celiac disease/gluten issues get shingles.
    • Ginger38
      I’m 43, just newly diagnosed with a horrible case of shingles last week . They are all over my face , around my eye, ear , all in my scalp. Lymph nodes are a mess. Ear is a mess. My eye is hurting and sensitive. Pain has been a 10/10+ daily. Taking Motrin and Tylenol around the clock. I AM MISERABLE. The pain is unrelenting. I just want to cry.   But Developing shingles has me a bit concerned about my immune system which also has me wondering about celiac and if there’s a connection to celiac / gluten and shingles; particularly since I haven't been 💯 gluten free because of all the confusing test results and doctors advice etc., is there a connection here? I’ve never had shingles and the gluten/ celiac  roller coaster has been ongoing for a while but I’ve had gluten off and on the last year bc of all the confusion  
    • Russ H
      There were some interesting talks, particularly Prof Ludvig Stollid's talk on therapeutics for coeliac disease.    https://www.youtube.com/playlist?list=PLRcl2mPE0WdigRtJPvylUJbkCx263KF_t
    • Rejoicephd
      Thank you @trents for letting me know you experience something similar thanks @knitty kitty for your response and resources.  I will be following up with my doctor about these results and I’ll read the articles you sent. Thanks - I really appreciate you all.
    • knitty kitty
      You're right, doctors usually only test Vitamin D and B12.  Both are really important, but they're not good indicators of deficiencies in the other B vitamins.  Our bodies are able to store Vitamin B12 and Vitamin D in the liver for up to a year or longer.  The other B vitamins can only be stored for much shorter periods of time.  Pyridoxine B 6 can be stored for several months, but the others only a month or two at the longest.  Thiamine stores can be depleted in as little as three days.  There's no correlation between B12 levels and the other B vitamins' levels.  Blood tests can't measure the amount of vitamins stored inside cells where they are used.  There's disagreement as to what optimal vitamin levels are.  The Recommended Daily Allowance is based on the minimum daily amount needed to prevent disease set back in the forties when people ate a totally different diet and gruesome experiments were done on people.  Folate  requirements had to be updated in the nineties after spina bifida increased and synthetic folic acid was mandated to be added to grain products.  Vitamin D requirements have been updated only in the past few years.   Doctors aren't required to take as many hours of nutritional education as in the past.  They're educated in learning institutions funded by pharmaceutical corporations.  Natural substances like vitamins can't be patented, so there's more money to be made prescribing pharmaceuticals than vitamins.   Also, look into the Autoimmune Protocol Diet, developed by Dr. Sarah Ballantyne, a Celiac herself.  Her book The Paleo Approach has been most helpful to me.  You're very welcome.  I'm glad I can help you around some stumbling blocks while on this journey.    Keep me posted on your progress!  Best wishes! P.S.  interesting reading: Thiamine, gastrointestinal beriberi and acetylcholine signaling https://pmc.ncbi.nlm.nih.gov/articles/PMC12014454/
×
×
  • 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.