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

Hashbrown Pizza Crust


angel-jd1

Recommended Posts

angel-jd1 Community Regular

:rolleyes: I am not sure who recommended this, but I am pretty sure it was someone on this board. I tried it tonight and it was so GOOD!! Just wanted to say thanks!!

-Jessica :rolleyes:

For those who have no clue what I'm talking about.....you can make a pizza crust out of hashbrowns.

I used a pie plate, thinly sliced hashbrowns

Pour some hashbrowns into a lightly Pam'ed pie plate/pizza pan.

Defrost Hashbrowns and press onto the sides of the dish.

I added some garlic powder and oregano and basil to the hashbrowns.

Bake for about 20 min at 350...or until slightly brown and crispy.

Top with pizza sauce, toppings(meat, veggies) and cheese bake for another 10-12 min. and you now have a great quick pizza!! YUM!! :D


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



Celiac.com Sponsor (A8-M):



wildones Apprentice

I posted about hash brown crust like you described for quiche, but have not tried it for pizza- it sounds yummy ! I will have to try it soon. My kids are probably more upset about not having pizza than any other food. We have tried gluten free pizza crusts (from the mixes) and have not liked them.

Lorraine

  • 2 weeks later...
khyricat Rookie

sounds yummy- I use potatoes and or onions sliced thin as a crust for quiches and other things like that.. hadn't thought of pizza... but had been debating trying it in a lasagna recipe... layers and all..

angel-jd1 Community Regular

I made this again the other day. Made a Ham and pineapple pizza was SOOOO good.

I used regular sauce, but then also added a little bbq sauce (sweet baby ray's) for some extra kick. It was AWESOME!!!

-Jessica :rolleyes:

MySuicidalTurtle Enthusiast

Do you buy frozen hashbrowns or make them from home? If you buy them whih brand do you get?

Kristina

angel-jd1 Community Regular

I use Ore-Ida Hashbrowns..the thinly sliced NOT the country style(chunky). Mr. Dell's is another gluten-free brand that you could use, and I have used before.

-Jessica

MySuicidalTurtle Enthusiast

I just made this and it was okay. I think next time I will cook the hashbrowns longer and use less sauce but it's still yummie!


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



Celiac.com Sponsor (A8-M):



  • 2 weeks later...
Lima Newbie

Pardon my ignorance: I'm Australian. We have something here called hash browns, but they don't sound much like what you're talking about. Could you please elaborate on what they are? Thanks!

I'm new to celiac disease and this board. Thank goodness for this and other internet resources; I'd still be following a lot of bad advice without them. You people are very supportive and encouraging, and I've learnt a lot from you already.

Just a little about me: I'm 47, supposedly asymptomatic (though I've run a bit of a gamut over the years, I now realise), though definitely coeliac, with blood results over the top and biopsy showing 'severe' damage. Been gluten-free a month now, and loving it - mostly. Still having the odd foggy brained day, but oboy, is this what normal digestion feels like?

My biggest problem is not boring my friends & family, as I'm still excited to realise all the things I CAN eat. They're very patient, but it's not of great moment to them the way it is for me when I find I can adapt another recipe or find a great tasting substitute. Successes so far: home made gluten-free pasta and crepes. Failure: scones (I think you call them biscuits?) which absolutely failed to rise. They made good soft crumbs, though. Dubious: bread, the formula for which I made up as I went. It rose fine and looked fabulous but tasted to me like dry cake. My partner, on the other hand, had no idea it was gluten-free and ate it quite happily, so I guess it was my expectations that made it a dubious success, not the thing itself.

Thanks for being here!

Lindy M

South Australia

angel-jd1 Community Regular

Hashbrowns are potatoes thinly sliced. They are usually fried as a side dish.

-Jessica

j9n Contributor

I saw a recipe on Foodtv where someone ( I can not remember which show) made a crust using pasta but I bet it would work with shredded potatoes (hashbrowns). this is assuming you can have dairy. Basically make a mixture of hasbrowns, shredded cheese and eggs in a oven ready fry pan. Fry it until it the bottom is crispy then put under the broiler until the top is crispy. I bet it would make an awesome pizza crust. I am going to try it this weekend. Very high calorie though I am sure!

  • 1 year later...
angel-jd1 Community Regular

I think I need to go buy some hashbrowns........I had forgotten about this recipe ha

-Jessica :rolleyes:

VegasCeliacBuckeye Collaborator

Lima,

Americans have about 5000 versions of cooked/fried potatoes -- its no wonder people get them confused -- even Americans have differing opinions betweem hash browns, home fries, potatoes o brien, etc.

When you grate a potato on a cheese grater, the "pieces" are hash browns (well, they become hash browns with some oil, salt and pepper...)

Hope this helps,

Bronco

lpellegr Collaborator

If you can find frozen hashbrown potato patties (like McD's hash browns) they make very good mini-pizzas with even less work. When I was newly diagnosed and feeding my family english muffin pizzas, this was my version of dinner, and everyone pouted when I wouldn't share. :lol:

Lister Rising Star

"Ore-Ida Hashbrowns" yay another person with no problems with ore-ida now i can try my frys that have been in the freezer hmm i bet good in chili

i love the idea for the pizza i have to try it sometime after i start eating dairy again

queenofhearts Explorer

Hi Lindy! I'm a mad baker myself so one of the first things I did after my endoscopy (even before the official diagnosis) was to head straight for the kitchen & start experimenting with different flours. Do you know about xanthan gum? It replaces gluten in recipes to help bind the starches, aid rising & keep the crumble factor down. You just need to use a little bit, so don't freak out when you see the price. It goes far. Also, run out and get some sorghum flour to use in the bread-- it REALLY helps with the moistness. Bette Hagman & Annalise Roberts have great baking books that will help a lot. I've made both biscuits/scones & yeast bread with enough success that my family ate them with gusto... actually the biscuits were gobbled up in no time, just like the old wheat ones! Now if only all those flours weren't so doggone pricey!

Happy Baking,

Leah

DingoGirl Enthusiast
Hi Lindy! I'm a mad baker myself so one of the first things I did after my endoscopy (even before the official diagnosis) was to head straight for the kitchen & start experimenting with different flours. Do you know about xanthan gum? It replaces gluten in recipes to help bind the starches, aid rising & keep the crumble factor down. You just need to use a little bit, so don't freak out when you see the price. It goes far. Also, run out and get some sorghum flour to use in the bread-- it REALLY helps with the moistness. Bette Hagman & Annalise Roberts have great baking books that will help a lot. I've made both biscuits/scones & yeast bread with enough success that my family ate them with gusto... actually the biscuits were gobbled up in no time, just like the old wheat ones! Now if only all those flours weren't so doggone pricey!

Happy Baking,

Leah

Leah - would you mind posting your biscuit recipe? I would be SO happy to have good biscuits.....with honey and butter.... :( Oh the pain of not having fluffy biscuits.....

TCA Contributor
Leah - would you mind posting your biscuit recipe? I would be SO happy to have good biscuits.....with honey and butter.... :( Oh the pain of not having fluffy biscuits.....

Have you tried th Cause You're Special brand?MMMMMMMMMMMMMMMMMMMMM

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. - catnapt posted a topic in Related Issues & Disorders
      0

      anyone here diagnosed with a PARAthyroid disorder? (NOT the thyroid) the calcium controlling glands

    2. - catnapt replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      how much gluten do I need to eat before blood tests?

    3. - Jmartes71 posted a topic in Coping with Celiac Disease
      0

      Curious question

    4. - Amy Barnett posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      Question

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,322
    • Most Online (within 30 mins)
      7,748

    avery144
    Newest Member
    avery144
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • catnapt
      learned I had a high PTH level in 2022 suspected to be due to low vit D  got my vit D level up a bit but still have high PTH   I am 70 yrs old (today in fact) I am looking for someone who also has hyperparathyroidism that might be caused by malabsorption    
    • catnapt
      I am on day 13 of eating gluten  and have decided to have the celiac panel done tomorrow instead of Wed. (and instead of extending it a few more weeks) because I am SO incredibly sick. I have almost no appetite and am not able to consume the required daily intake of calcium to try to keep up with the loss of calcium from the high parathyroid hormone and/or the renal calcium leak.    I have spent the past 15 years working hard to improve my health. I lost 50lbs, got off handfuls of medications, lowered my cholesterol to enviable levels, and in spite of having end stage osteoarthritis in both knees, with a good diet and keeping active I have NO pain in those joints- til now.  Almost all of my joints hurt now I feel like someone has repeatedly punched me all over my torso- even my ribs hurt- I have nausea, gas, bloating, headache, mood swings, irritability, horrid flatulence (afraid to leave the house or be in any enclosed spaces with other people- the smell would knock them off their feet) I was so sure that I wanted a firm diagnosis but now- I'm asking myself is THIS worth it? esp over the past 2 yrs I have been feeling better and better the more I adjusted my diet to exclude highly refined grains and processed foods. I didn't purposely avoid gluten, but it just happened that not eating gluten has made me feel better.   I don't know what I would have to gain by getting a definitive diagnosis. I think possibly the only advantage to a DX would be that I could insist on gluten-free foods in settings where I am unable to have access to foods of my choice (hospital, rehab, nursing home)  and maybe having a medical reason to see a dietician?   please let me know if it's reasonable to just go back to the way I was eating.  Actually I do plan to buy certified gluten-free oats as that is the only grain I consume (and really like) so there will be some minor tweaks I hope and pray that I heal quickly from any possible damage that may have been done from 13 days of eating gluten.    
    • Jmartes71
      So I've been dealing with chasing the name celiac because of my body actively dealing with health issues related to celiac though not eating. Diagnosed in 1994 before foods eliminated from diet. After 25 years with former pcp I googled celiac specialist and she wasn't because of what ive been through. I wanted my results to be sent to my pcp but nothing was sent.I have email copies.I did one zoom call with np with team member from celiac specialist in Nov 2025 and she asked me why I wanted to know why I wanted the celiac diagnosis so bad, I sad I don't, its my life and I need revalidaion because its affecting me.KB stated well it shows you are.I asked then why am I going through all this.I was labeled unruly. Its been a celiac circus and medical has caused anxiety and depression no fault to my own other than being born with bad genetics. How is it legal for medical professionals to gaslight patients that are with an ailment coming for help to be downplayed? KB put in my records that she personally spent 120min with me and I think the zoom call was discussing celiac 80 min ONE ZOOM call.SHE is responsible for not explaining to my pcp about celiac disease am I right?
    • Amy Barnett
      What is the best liquid multivitamin for celiac disease?
    • Jmartes71
      I've noticed with my age and menopause my smell for bread gives me severe migraines and I know this.Its alarming that there are all these fabulous bakeries, sandwich places pizza places popping up in confined areas.Just the other day I suffered a migraine after I got done with my mri when a guy with a brown paper bag walk in front of me and I smelled that fresh dough bread with tuna, I got a migraine when we got home.I hate im that sensitive. Its alarming these places are popping up in airports as well.I just saw on the news that the airport ( can't remember which  one)was going to have a fabulous smelling bakery. Not for sensitive celiacs, this can alter their health during their travel which isn't safe. More awareness really NEEDS to be promoted, so much more than just a food consumption!FYI I did write to Stanislaus to let them know my thoughts on the medical field not knowing much about celiac and how it affects one.I also did message my gi the 3 specialist names that was given on previous post on questions on celiac. I pray its not on deaf door.
×
×
  • 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.