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

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
      131,543
    • Most Online (within 30 mins)
      7,748

    yfuvhg
    Newest Member
    yfuvhg
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Beverage
      I had a very rough month after diagnosis. No exaggeration, lost so much inflammatory weight, I looked like a bag of bones, underneath i had been literally starving to death. I did start feeling noticeably better after a month of very strict control of my kitchen and home. What are you eating for breakfast and lunch? I ignored my doc and ate oats, yes they were gluten free, but some brands are at the higher end of gluten free. Lots of celics can eat Bob's Red Mill gluten-free oats, but not me. I can now eat them, but they have to be grown and processed according to the "purity protocol" methods. I mail order them, Montana Gluten-Free brand. A food and symptoms and activities log can be helpful in tracking down issues. You might be totally aware, but I have to mention about the risk of airborne gluten. As the doc that diagnosed me warned . . Remember eyes, ears, nose, and mouth all lead to your stomach and intestines.  Are you getting any cross contamination? Airborne gluten? Any pets eating gluten (they eat it, lick themselves, you pet them...)? Any house remodeling? We live in an older home, always fixing something. I've gotten glutened from the dust from cutting into plaster walls, possibly also plywood (glues). The suggestions by many here on vitamin supplements also really helped me. I had some lingering allergies and asthma, which are now 99% gone. I was taking Albuterol inhaler every hour just to breathe, but thiamine in form of benfotiamine kicked that down to 1-2 times a day within a few days of starting it. Also, since cutting out inflammatory seed oils (canola, sunflower, grapeseed, etc) and cooking with real olive oil, avocado oil, ghee, and coconut oil, I have noticed even greater improvement overall and haven't used the inhaler in months! It takes time to weed out everything in your life that contains gluten, and it takes awhile to heal and rebuild your health. At first it's mentally exhausting, overwhelming, even obsessive, but it gets better and second nature.
    • Jsingh
      Hi,  I care for my seven year old daughter with Celiac. After watching her for months, I have figured out that she has problem with two kinds of fats- animal fat and cooking oils. It basically makes her intestine sore enough that she feels spasms when she is upset. It only happens on days when she has eaten more fat than her usual every day diet. (Her usual diet has chia seeds, flaxseeds, and avocado/ pumpkin seeds for fat and an occasional chicken breast.) I stopped using cooking oils last year, and when I reintroduced eggs and dairy, both of which I had held off for a few months thinking it was an issue of the protein like some Celiac patients habe mentioned to be the case, she has reacted in the same fashion as she does with excess fats. So now I wonder if her reaction to dairy and eggs is not really because of protein but fat.   I don't really have a question, just wondering if anyone finds this familiar and if it gets better with time.  Thank you. 
    • Chanda Richard
      Hello, My name is Chanda and you are not the only one that gose through the same things. I have found that what's easiest for me is finding a few meals each week that last. I have such severe reactions to gluten that it shuts my entire body down. I struggle everyday with i can't eat enough it feels like, when I eat more I lose more weight. Make sure that you look at medication, vitamins and shampoo and conditioner also. They have different things that are less expensive at Walmart. 
    • petitojou
      Thank you so much! I saw some tips around the forum to make a food diary and now that I know that the community also struggles with corn, egg and soy, the puzzle pieces came together! Just yesterday I tried eating eggs and yes, he’s guilty and charged. Those there are my 3 combo nausea troublemakers. I’m going to adjust my diet ☺️ Also thank you for the information about MCAS! I’m from South America and little it’s talked about it in here. It’s honestly such a game changer now for treatment and recovery. I know I’m free from SIBO and Candida since I’ve been tested for it, but I’m still going to make a endoscopy to test for H. Pylori and Eosinophilic esophagitis (EoE). Thank you again!! Have a blessed weekend 🤍
    • knitty kitty
      Yes, I, too, have osteoporosis from years of malabsorption, too.  Thiamine and magnesium are what keep the calcium in place in the bones.  If one is low in magnesium, boron, selenium, zinc, copper, and other trace minerals, ones bone heath can suffer.  We need more than just calcium and Vitamin D for strong bones.  Riboflavin B 2, Folate B 9 and Pyridoxine B 6 also contribute to bone formation and strength.   Have you had your thyroid checked?  The thyroid is important to bone health as well.  The thyroid uses lots of thiamine, so a poorly functioning thyroid will affect bone heath.  
×
×
  • 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.