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 Our Content
    eNewsletter
    Donate

Anyone Else Work In Residential Treatment?


JillianLindsay

Recommended Posts

JillianLindsay Enthusiast

For anyone who works in a group home or other type of residential treatment, you know we don't get paid well at all. You also know one of the small perks of the job is free food while working :)

I work in a residential treatment facility with teenage boys who are struggling with addiction issues. I love my job! I also loved that we didn't have to bring our own lunch or even prepare the meals. Because it's such a large facility, we have a cafeteria type set-up with a large kitchen and employ kitchen staff to prepare meals.

I just got back to work two weeks ago and have been struggling with what to eat and how to communicate what I can and can't have. The staff I've worked with so far have been fantastic. They've let me tour around the kitchen with them reading labels and explaining what is safe and what is not. They are knowledgeable about cross-contamination.

The downside is I've been eating the same foods over and over. They have a lot of people to feed and don't have time to prepare a completely separate meal for me, nor do I expect them to. I just sent an email to the director cc'ing the kitchen (as per the director's request) with links to celiac disease info, gluten-free diet info, and a list of things I can and can't eat. I'm a full-time student and only work there part-time, so it's not like they can just order groceries with me in mind because I don't work enough to justify them changing their system that they have had in place for years.

Does anyone else work in a residential setting? What do you do? Or for anyone out there who has ideas for me, please, advice and suggestions would be much appreciated :)

I make so little money there -- I do it because I love it -- but if I have to start bringing my own food (on top of the gas money I spend because it's a 45-minute commute for me), I won't be able to afford to work there anymore! I don't mind bringing a few things (i.e. margarine, rice bread, gluten-free sauces), but I do mind (and can't afford) packing a day's worth of food when free food is supposed to be a perk of the job. I don't want to leave the only job I've actually loved doing!

Thanks,

Jillian


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



Celiac.com Sponsor (A8-M):



msmini14 Enthusiast

What do they typically serve? Do they have salads? Do they prepare any meat and if so do they season or marinate it?

Remember you can have all fruits and veggies. You could bring something to eat every other day. Bring snacks with you, lets say they have bananas or apples bring some peanut butter to go with it.

JillianLindsay Enthusiast

Yes, there are fresh fruits and salad available at each meal. Lukcily they use Kraft salad dressings, so I can read the labels and feel comfortable using them if they are gluten-free. The meats are marinated, but they let me look at everything they use to season it and check if it's safe.

I like the peanut butter idea, I love pb and apples :)

What do they typically serve? Do they have salads? Do they prepare any meat and if so do they season or marinate it?

Remember you can have all fruits and veggies. You could bring something to eat every other day. Bring snacks with you, lets say they have bananas or apples bring some peanut butter to go with it.

Kim Hopkins Rookie

I worked in residential as a social worker when I was first diagnosed. It was a small setting, so that helped...although it was a lot less heard of back then, so I was asked TONS of questions CONSTANTLY by both the staff and the boys. I remember I did eat a lot of peanut butter (with apples, carrots, celery) - they bought it in individual servings, so I knew it wasn't contaminated. They also kept nuts and raisins on hand for a quick snack. There was always chips, too. Salad was available every day, as was yogurt. They made me a lot of fried eggs and sauteed veggies. I also kept a bag of gluten-free pasta there in case there was nothing else. Corn tortillas might be good to keep on hand - maybe they would buy them if they could use them for some mexican meals. You could use them for a roll up sandwich or quick quesadilla. Maybe they could do baked potatoes more often? You can get pretty creative with the toppings and use the leftovers to make home fries. Ask if they would mind using corn starch to thicken soups and sauces. Hope that helps!

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      130,371
    • Most Online (within 30 mins)
      7,748

    Nipas
    Newest Member
    Nipas
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):




  • Who's Online (See full list)


  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Katerific
      I was diagnosed with microscopic colitis and celiac a couple of years ago.  The GI doctor prescribed a course of budesonide, which moderately helped until I tapered off.    After a lot of ups and downs over the course of 2 years, I am finally in microscopic colitis remission.  Since I am also diabetic, I was started on metformin and Jardiance.  Metformin by itself helped moderately.  I added Jardiance and I was much better.  I stopped the metformin and relapsed and when I added it back, I regained remission.  I think metformin and Jardiance helped my colitis because they reduce inflammation in the gut.  Metformin is known to favorably modulate the gut microbiome and reduce inflammatory cytokines.  Similarly, emerging evidence supports the anti-inflammatory properties of SGLT2 inhibitors like Jardiance.  Once I was on both, the diarrhea stopped completely, even though nothing else ever worked long-term.  There is a Facebook group that can be very informative and helpful.  Look for "Microscopic Colitis and Lymphocytic Colitis Support Group.  You will find that members of the Facebook group identify other pathways to remission of microscopic colitis.
    • knitty kitty
      Hello, @Mrs Wolfe, I crushed three vertebrae moving a chest of drawers.  I take a combination of Thiamine Vitamin B1, Vitamin B12, and Pyridoxine B6.  Together these vitamins have an analgesic effect.  I think it works better than OTC pain relievers.   I also like  "Takeda ALINAMIN EX Plus Vitamin B1 B6 B12 Health Supplementary from Japan 120 Tablets" .   It's all three vitamins together in one pill.  Works wonderfully!
    • knitty kitty
      It's the Potassium Iodide in the HRT pills that is triggering Dermatitis Herpetiformis and the increased IGG levels.   The thyroid is stimulated by the Potassium Iodide, which stimulates immune cells to make more IGG antibodies.   Thiamine Vitamin B1 helps the thyroid function.  I like Benfotiamine and TTFD Thiamax.  
    • Mettedkny
      @Scott Adams Xiromed is one of the generic manufacturers of Progesterone pills.
    • Scott Adams
      The topic has come up in the forum a lot: https://www.celiac.com/search/?q=lymphocytic colitis&quick=1&type=forums_topic and here are discussions with "colitis": https://www.celiac.com/search/?&q=colitis&type=forums_topic&quick=1&search_and_or=and&sortby=relevancy
×
×
  • Create New...