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

Had Great Success


wowzer

Recommended Posts

wowzer Community Regular

I finally tried making an old favorite molasses cookie recipe gluten free. The taste came pretty close, but the texture was a little different.

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



GRUMP 1 Contributor

Oh my, Can you PLEASE share? I have tried this numerous times and have not been able to get them right yet. I am using the Betty Crocker recipe and then changing the flour to Bob's red mill All Purpose gluten-free Baking Flour. They taste good but they are about as flat as paper. Good and chewy but just flat............ HELP........

Link to comment
Share on other sites
wowzer Community Regular

Molasses Drop Cookies

1 cup of raisins or dry cranberries plumped (pour boiling water and let them soak for 5 minutes then drain) (I used cranberries)

1/2 cup chopped nuts

2 cups flour (I used 1 cup white rice, 2/3 cup potato starch and 1/3 cup garbanzo bean flour)

1 teaspoon baking soda

1/4 teaspoon salt

1/8 teaspoon ginger

1/2 teaspoon cloves (I didn't have any so didn't add it)

1/2 teaspoon cinnamon

1/4 cup brown sugar packed

1/2 cup + 2 Tablespoons butter or margarine (I used butter)

1 egg

1/2 cup dark molasses

1/2 cup buttermilk

Grease baking sheets. Preheat oven to 400. Plump raisins or cranberries. Combine dry ingredients, set aside. Cream butter and brown sugar. Beat in egg until fluffy. Beat in molasses until satiny. Stir in flour mixture and buttermilk alternately in 2 or 3 portions, beginning and ending with flour mixture. Stir in raisins or cranberries and nuts. Drop by heaping teaspoons onto prepared cookie sheet. Bake about 10 minutes or until delicately browned. Remove at once from sheet to cooling rack. When cool, store in jar or box with tight-fitting cover with sheet of waxed paper between layers. 3 dozen

This is more of a cake like cookie. It is the molasses cookie I grew up eating. I did put the batter in the fridge between batches. I hope you like it. Good luck and let me know.

Link to comment
Share on other sites
GRUMP 1 Contributor

Sounds interesting, I have never had them with raisins, dry cranberries, chopped nuts, or buttermilk in them. Mother always made them out of the Betty Crocker cookbook and that is what I have been trying to do but using Bob's red mill All Purpose gluten-free Baking Flour instead of wheat flour. But as I said before they just never turn out right. So when I get back on my feet ( have been down for 2 days now ) I am going to give this one a try. Thank you so much for sharing.

Grump

Link to comment
Share on other sites
wowzer Community Regular

I'm pretty new to this, I just went gluten free the beginning of the year. I've tried some of the gluten free recipes for cookies also. I grew up with that recipe, but know the kind you are talking about. I was born in Canada, but have been in the U.S. since I was 8 years old. I am one that likes to just follow a recipe, but got brave on that one. I think it is the best cookies that I have baked so far. I have had great luck baking muffins with the Fearns brown rice baking mix too. I still haven't found any bread that has thrilled me. I hope that you get back on your feet soon. Wendy

Link to comment
Share on other sites
  • 2 weeks later...
wowzer Community Regular

I tried making these cookies again. I only used a 1/2 cup of butter and they turned out so much better. I even taste tested them on my Mom and she said they tasted the same.

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
      121,069
    • Most Online (within 30 mins)
      7,748

    angie78
    Newest Member
    angie78
    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

    • Fluka66
      Thank you again for your reply and comments which I have read carefully as I appreciate any input at this stage. I'm tending to listen to what my body wants me to do, having been in agony for many years any respite has been welcome and avoiding all wheat and lactose has thankfully brought this.  When in pain before I was seen by a number of gynacologists as I had 22 fibroids and had an operation 13 years ago to shrink them . However the pain remained and intensified to the point over the years where I began passing out. I was in and out of a&e during covid when waiting rooms where empty. My present diet is the only thing that's given me any hope for the future. As I say I had never heard of celiac disease before starting so I guess had this not come up in a conversation I would just have carried on. It was the swollen lymph node that sent me to a boots pharmacist who immediately sent me to a&e where a Dr asked questions prescribed antibiotics and then back to my GP. I'm now waiting for my hospital appointment . Hope this answers your question. I found out more about the disease because I googled something I wouldn't normally do, it did shed light on the disease but I also read some things that this disease can do. On good days I actually hope I haven't got this but on further investigation my mother's side of the family all Celtic have had various problems 're stomach pain my poor grandmother cried in pain as did her sister whilst two of her brother's survived WW2 but died from ulcers put down to stress of fighting.  Wishing you well with your recovery.  Many thanks  
    • knitty kitty
      Welcome to the forum, @Nacina, What supplements is your son taking?
    • knitty kitty
      @BluegrassCeliac, I'm agreeing.  It's a good thing taking magnesium. And B vitamins. Magnesium and Thiamine work together.  If you supplement the B vitamins which include Thiamine, but don't have sufficient magnesium, Thiamine won't work well.  If you take Magnesium, but not Thiamine, magnesium won't work as well by itself. Hydrochlorothiazide HCTZ is a sulfonamide drug, a sulfa drug.  So are proton pump inhibitors PPIs, and SSRIs. High dose Thiamine is used to resolve cytokine storms.  High dose Thiamine was used in patients having cytokine storms in Covid infections.  Magnesium supplementation also improves cytokine storms, and was also used during Covid. How's your Vitamin D? References: Thiamine and magnesium deficiencies: keys to disease https://pubmed.ncbi.nlm.nih.gov/25542071/ Hiding in Plain Sight: Modern Thiamine Deficiency https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8533683/ The Effect of a High-Dose Vitamin B Multivitamin Supplement on the Relationship between Brain Metabolism and Blood Biomarkers of Oxidative Stress: A Randomized Control Trial https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6316433/ High‐dose Vitamin B6 supplementation reduces anxiety and strengthens visual surround suppression https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9787829/ Repurposing Treatment of Wernicke-Korsakoff Syndrome for Th-17 Cell Immune Storm Syndrome and Neurological Symptoms in COVID-19: Thiamine Efficacy and Safety, In-Vitro Evidence and Pharmacokinetic Profile https://pubmed.ncbi.nlm.nih.gov/33737877/ Higher Intake of Dietary Magnesium Is Inversely Associated With COVID-19 Severity and Symptoms in Hospitalized Patients: A Cross-Sectional Study https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9132593/ Magnesium and Vitamin D Deficiency as a Potential Cause of Immune Dysfunction, Cytokine Storm and Disseminated Intravascular Coagulation in covid-19 patients https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7861592/ Sulfonamide Hypersensitivity https://pubmed.ncbi.nlm.nih.gov/31495421/
    • BluegrassCeliac
      Hi,   Not saying Thiamine (B1) couldn't be an issue as well, but Mg was definitely the cause of my problems. It's the only thing that worked. I supplemented with B vitamins, but that didn't change anything, in fact they made me sick. Mg stopped all my muscle pain (HCTZ) within a few months and fixed all the intestinal problems HCTZ caused as well. Mom has an allergy to some sulfa drugs (IgG Celiac too), but I don't think I've ever taken them. Mg boosted my energy as well. It solved a lot of problems. I take 1000mg MgO a day with no problems. I boost absorption with Vitamin D. Some people can't take MgO,  like mom, she takes Mg Glycinate. It's one of those things that someone has try and find the right form for themselves. Everyone's different. Mg deficiency can cause anxiety and is a treatment for it. A pharmacist gave me a list of drugs years ago that cause Mg deficiency: PPIs, H2 bockers, HCTZ, some beta blockers (metoprolol which I've taken -- horrible side effects), some anti-anxiety meds too were on it. I posted because I saw he was an IgG celiac. He's the first one I've seen in 20 years, other than my family. We're rare. All the celiacs I've met are IgA. Finding healthcare is a nightmare. Just trying to help. B  
    • Scott Adams
      It sounds like you've been through a lot with your son's health journey, and it's understandable that you're seeking answers and solutions. Given the complexity of his symptoms and medical history, it might be beneficial to explore a few avenues: Encourage your son to keep a detailed journal of his symptoms, including when they occur, their severity, any triggers or patterns, and how they impact his daily life. This information can be valuable during medical consultations and may help identify correlations or trends. Consider seeking opinions from specialized medical centers or academic hospitals that have multidisciplinary teams specializing in gastrointestinal disorders, especially those related to Celiac disease and Eosinophilic Esophagitis (EOE). These centers often have experts who deal with complex cases and can offer a comprehensive evaluation. Since you've already explored alternative medicine with a nutrition response doctor and a gut detox diet, you may want to consider consulting a functional medicine practitioner. They take a holistic approach to health, looking at underlying causes and imbalances that may contribute to symptoms. Given his low vitamin D levels and other nutritional markers, a thorough nutritional assessment by a registered dietitian or nutritionist specializing in gastrointestinal health could provide insights into any deficiencies or dietary adjustments that might help alleviate symptoms. In addition to routine tests, consider asking about more specialized tests that may not be part of standard screenings. These could include comprehensive stool analyses, food intolerance testing, allergy panels, or advanced imaging studies to assess gut health.
×
×
  • Create New...