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

Questions From An Scd Newbie


marthamom

Recommended Posts

marthamom Newbie

Hello Everyone,

This is only my second time posting on the forum, so sorry if I'm not doing it right!

I was diagnosed with celiac in September 2008 (positive blood tests and biopsy) and have been gluten free since then. My gastro symptoms have really not gotten noticeably better at all, so I've decided to try SCD to see if things improve. I just have a couple of questions for all of you SCD pros out there:

1. I was so excited to try my SCD yogurt this morning when it was ready and was a bit surprised at how tart it was---so much so that i'm having trouble eatng it. Anyone else experience this? Any way to make it less tart without adding a lot of stuff? Also, it was a little runnier than I'm used to with yogurt. I made this batch with 2% milk--would using whole milk or 1/2 and 1/2 help?

2. I take a daily medication for anxiety, and I'm wondering if I need to be concerned about starch that might be in it--I'm taking Freeda multivitamin and calcium, and I know those are ok, but wondering about this one.....

3. After doing the intro diet for a few days, how long should I be taking to introduce other "legal" foods? I've read Breaking the Vicious Cycle, but it's not entirely clear.....I don't want to jump into certain foods too soon...

4. I was diagnosed last month with osteopenia--this isn't specifically related to SCD, but does anyone know if I should be taken a calcium supplement that also has magnesium (I think I've read something about needing magnesium for maximum absorption...is it enough if there is magnesium in my multi)?

Thanks so much for any advice!!


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



Celiac.com Sponsor (A8-M):



Lisa Mentor

Hi marthamom and welcome. You can find more information on the SCD diet here: https://www.celiac.com/gluten-free/index.ph...c=54285&hl=

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      130,251
    • Most Online (within 30 mins)
      7,748

    Janet Lima
    Newest Member
    Janet Lima
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Wheatwacked
      Vitamin D deficiency can contribute to rib pain. Chest pain stemming from the ribs ccould be costochondritis, which involves inflammation of the cartilage connecting the ribs to the breastbone. This pain can range from mild to severe, potentially mimicking heart attack symptoms, and is often worsened by breathing or movement. Other potential causes include muscle strain, rib fractures, or even referred pain from other conditions.  It will also help to chose vegetables low in omega 6.
    • Scott Adams
      Great question! Even if some individuals with celiac disease don’t experience immediate villi damage from occasional cross-contamination, it’s still strongly recommended to maintain strict avoidance of gluten. The immune response triggered by gluten can vary between individuals, and even small amounts may cause systemic inflammation or other symptoms, even if intestinal damage isn’t immediately detectable. Additionally, repeated exposure—even at low levels—could lead to cumulative harm over time. Strict avoidance of cross-contamination remains the safest approach to prevent long-term complications and ensure overall health. Everyone’s sensitivity differs, so working with a healthcare provider to tailor precautions is ideal.
    • Zuma888
    • knitty kitty
      You have one gene for Celiac.  You have a second autoimmune disease, Hashimoto's thyroiditis, which is frequently found at a higher rate with Celiac.  HLA genes carry autoimmune disease genes like Celiac and Hashimoto's and diabetes and others.   You have Celiac symptoms of reacting after gluten.  You said "I am however still suffering from the effects of the gluten challenge (food sensitivities, slight brain fog, weird stool, fatigue, swollen thyroid, bodyaches)."  And your anti-thyroid antibodies increase after gluten exposure.  While tTg IgA does not directly attack the thyroid, gluten exposure does trigger the  immune system to produce antibodies against the thyroid in genetically predisposed individuals.  You did not eat sufficient gluten (10 grams of gluten per day for two weeks minimum) to raise the autoimmune antibodies to the point they can be measured in the blood, so your blood tests may well be inaccurate.  You could choose to continue the gluten challenge of 10 grams a day for at least two weeks and get retested.   At the very least, you know that gluten is harmful to your thyroid, and because you are genetically predisposed to Celiac disease, a strict gluten free diet would be beneficial for your overall health.  
    • Zuma888
      Thanks @Scott Adams! I guess my question now is: do the celiacs who can get away with regular contamination without villi damage as you mentioned have to be strict about cross-contamination ? 
×
×
  • Create New...