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

My Cookies Crumbled


Cin

Recommended Posts

Cin Rookie

Hello,

I am not much of a baker to begin with but now that I am gluten-free, I feel compelled to find good tasting foods to eat. I just tried making cookies and substituting one to one on the flour with Bette Hagmans gourmet flour mix and adding 1/4 tsp xanthan gum. My cookies tasted great but you had to scoop them with a spoon.(My daughter said they were great over vanilla ice cream.) Any suggestions? As I said, I dont bake and used vegetable spread instead of butter or margarine. Could this change the consistency as well. They were pretty soupy before I put them in the oven.

Thanks Cindy


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



Celiac.com Sponsor (A8-M):



I-am-silly-yak Newbie
Hello,

I am not much of a baker to begin with but now that I am gluten-free, I feel compelled to find good tasting foods to eat. I just tried making cookies and substituting one to one on the flour with Bette Hagmans gourmet flour mix and adding 1/4 tsp xanthan gum. My cookies tasted great but you had to scoop them with a spoon.(My daughter said they were great over vanilla ice cream.) Any suggestions? As I said, I dont bake and used vegetable spread instead of butter or margarine. Could this change the consistency as well. They were pretty soupy before I put them in the oven.

Thanks Cindy

Hi Cindy,

Add a teaspon more baking powder and another 1/4 tsp. of Xanthan Gum. Betty Hagman is great.Try also Carol Fenster's "Gluten Free 101"

silly yak

penguin Community Regular

I would reccommend that you NEVER substitute vegetable spread OR margerine for butter. I'd bet money that it was the vegetable spread, it's not good for baking.

Personally, I don't believe that vegetable spread or margerine is good for anything, but that's just me. :P

Especially doing it gluten-free, butter is important. Butter flavored shortening can be used, however, if you can't have dairy. :)

lonewolf Collaborator

I agree that you need to use real butter or margarine - not vegetable spread. Also, you probably need to use at least 1 tsp. of xanthan gum to help them stick together better. I use at least 1-1/2 tsp. for my cookies and they don't crumble.

jerseyangel Proficient

My money would be on the vegetable spread, too. For cookies, either butter or shortening is best for consistancy.

skoki-mom Explorer

This is no doubt a stupid question, but what is vegetable spread??? I (used to) bake a lot and I've never heard of such a thing. Is it the same as shortening?? I'm all for butter too. Soft margarine never turns out (too much water content) and hard margarine is worse for you health wise than butter. Besides, now that wheat flour is out of the question, I figure I may as well have the butter. Something has to kill you.......

plantime Contributor

Did you use stick spread or bowl spread? Bowl spread is too soft for baking, but you can use stick spread in place of real butter. Using bowl spread would make your cookies runny, not crumbly. If they were too crumbly, then you need to use more xanthan gum. I think the formula is 1/4 tsp gum for each 1 cup flour. Personally, I am allergic to eggs, so I use ground flax instead of eggs and xanthan gum.


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



Celiac.com Sponsor (A8-M):



Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,546
    • Most Online (within 30 mins)
      7,748

    KimberlyAnne76
    Newest Member
    KimberlyAnne76
    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.