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

Usa-Spain student exchange of gluten intolerant kids


Jose Manuel

Recommended Posts

Jose Manuel Newbie

Hello,

First of all, I want to send greetings from Spain and introduce myself. My name is Jose Manuel and I live in Tres Cantos, a nice city 14 miles north of Madrid. My wife is Eva and our three children are: Dario who is 17 years old, Pablo who is 14 years old, and was diagnosed gluten intolerant 12 years ago, and Jaime, 11 years old, and also diagnosed gluten intolerant 2 years ago.

After the introduction, I would like to share the following proposal for those families of this forum who think it would be interesting to make a student exchange.

Every family with a gluten intolerant member knows all the problems that arise finding gluten free diet when we leave home, or when we go out abroad even more so if we go out to a foreign country. We want our son Pablo to study in the USA for the next school year (2016-2017) and we have thought of a student exchange with a family with a gluten intolerant child. That way, our son will live in a celiac aware environment. We would likewise take care of an American gluten intolerant child, whose family is interested in that exchange.

Thanks for your attention. I am at your disposal for any question and those families who want to talk about that proposal and would like further information, can contact us at our email address: Open Original Shared Link

 

Greetings from Spain.

Jose Manuel Garcia Mulas

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



kareng Grand Master

Personally, I would go with one of the established groups. i wouldn't send my teen to a foreign country by himself to stay with strangers I met on the Internet.  At least with the established groups, they do some background checks and give the child someone to call for help if there are issues with the host family.  

Link to comment
Share on other sites
cyclinglady Grand Master

We have hosted kids from Germany and Japan.  I would strongly recommend going through an established student-exchange group.  They screen families for criminal records, etc.  They also cover health and liability insurance.  They work with the high schools as well.  And like Karen said, if it does not work out, the group steps in and resolves the situation.   It is a great experience but you want to make sure your child is safe (and not just safe from gluten).  

The forum has had specific requests from student exchange groups about placing celiac kids into a celiac family in the past.    So we are a resource for then xchange groups.  It is possible for them to find a perfect match!  

Here  is a link to a US government website that mentions some of the top organizations.

Open Original Shared Link

Good Luck! 

Link to comment
Share on other sites
Jose Manuel Newbie

Thank you for your answers and advice.

My purpose is to get in touch with a family interested in hosting my son, while at the same time, we would host theirs. That way, there shouldn’t be any problem. The first thing, of course, would be for the two families to meet and iron out the fine points.

I know that to send my son with an agency would be less problematic. I have already asked for information, but this procedure costs a lot more than I cannot afford: somewhere between 10,000 and 20,000 euros. And with my proposal of exchange, the cost would be much lower, basically the student visa charge, the plane tickets and health insurance.

 

Greetings,

Link to comment
Share on other sites
mommida Enthusiast

Have you looked into 4H student exchange?  4H works with colleges and universities extension.  It is more common for farming communities to be involved with, and does not as much as other organizations.

Good luck.

Link to comment
Share on other sites

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      121,183
    • Most Online (within 30 mins)
      7,748

    Bernadine
    Newest Member
    Bernadine
    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

    • Beverage
      Sounds like you are in the UK. With blood numbers that high, I thought docs in UK would give an official diagnosis without the biopsy. You should ask about that, so you can get support faster.  I'd try to find and print out anything that supports that in your country, get another appointment and take all of it with you. Even in the US now, some docs are doing this, my 19 year old step granddaughter got an official diagnosis here in US with just blood results a few months ago.
    • Beverage
      Is soy sauce in Korea also made from wheat like it usually is in US? I'd be concerned that even if asking about gluten, they would not be aware of or think of some like that. 
    • trents
      That's a good idea. It can at least establish the potential for developing celiac disease and can help people decided between a celiac diagnosis and NCGS (Non Celiac Gluten Sensitivity). And it doesn't require a gluten challenge and can be had without a doctor's prescription.
    • awright24
      I have my endoscopy on Thursday, has anyone had the procedure done with a cough? I don't have a continuous cough, but every now and then throughout the day I have sort of coughing episodes. They are a lot better than they were but I called endoscopy and they said to speak to my gp and my gp got back to me and said I need to ask endoscopy if its ok if I have it done still.  Help!
    • MMH13
      Thank you so much, everyone. For the moment my doctor just has me taking iron but hopefully we can reconnect soon. I'm going to look into genetic testing, too. Great advice all around and I appreciate it--and you can bet I'm going off the PPIs!
×
×
  • Create New...