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

Elias, RA and Plaquenil


Alexia N

Recommended Posts

Alexia N Newbie

I was diagnosed two years ago with celiac and my doctor advised me to take Intravenous iron and three months after I got pains in my joins.  After blood test we concluded that I got a second autoimmune disease RA. Two years now I don’t take any medicines. I did fasting only with water several times, starting with 3 days max to 5. I was fasting every 2 months about. My diet was very careful. Eating organic salads, green juicing, avocados, nuts, little chicken and very rare red meat. Avoiding everything with gluten. Situation was not bad but fasting is quite hard.. and maybe not a very good idea to do it so often. Now I follow a vegan, plant base diet, avoiding many fruits (due to fructose). The situation remains stable but not eliminated. The pains in my joins are the same. I came to the point where I am thinking to start Plaquenil and I would like to know if anybody has the same symptoms and Plaquenil is ok for celiac?


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



Celiac.com Sponsor (A8-M):



GFinDC Veteran

Hi, I haven't tried Planquil.   But I  did have joint pain in my shoulders and hips.  It went away after I stopped eating nightshades.  Nightshades are potatoes, tomatoes, peppers and eggplant.  Nightshades have alkaloid chemicals in them that some people can't process.  So they build up and cause joint pain.  So, I'm not sure if it would help you to stop all nightshades but maybe it would.  If you try eliminating nightshades keep at it for a couple months.  It can take that long for symptoms to go away.

Welcome to the forum! :)

Alexia N Newbie
19 minutes ago, GFinDC said:

Hi, I haven't tried Planquil.   But I  did have joint pain in my shoulders and hips.  It went away after I stopped eating nightshades.  Nightshades are potatoes, tomatoes, peppers and eggplant.  Nightshades have alkaloid chemicals in them that some people can't process.  So they build up and cause joint pain.  So, I'm not sure if it would help you to stop all nightshades but maybe it would.  If you try eliminating nightshades keep at it for a couple months.  It can take that long for symptoms to go away.

Welcome to the forum! :)

Thank you very much for the suggestion, I did it already but unfortunately it did not worked. 

cyclinglady Grand Master

I do not have RA, but my mother does.  She is on hydroxychloroquine and is doing well.  

You sound like me attempting to treat without drugs.  I also fast, but only intermittent (12 to 16 hours).  It helps my blood sugar and gives my GI tract much needed breaks.  Longer fasts?  Not much research has been done, especially on women, so I am wary.  

In addition to celiac disease, I have Hashimoto’s and Autoimmune Gastritis.  I do take a thyroid replacement, but since being gluten free, my thyroid is no longer enlarged and my nodules are gone.  Unfortunately, my thyroid function was permanently damaged.  I am trying to avoid a 4th AI. I am guessing that it will be RA since my mother and my paternal grandmother had/have it.  

As much as I resist taking medications (I have Mast Cell issues that cause reactions that are usually triggered by insects or medications), if I develop RA, I may be required to take a medication.  Quality of life is important to me.  My grandmother was bedridden as a result of RA and I would not want that to occur.     Hydroxychloroquine has been around for a long time.  It is reasonably safe.  Unfortunately, with this pandemic, my mother has reported shortages in her area.  

Your Vegan diet is your choice, but do you not think it is odd that this diet requires you to supplement with Vitamin B-12 (fortified foods or supplements)?    Could our ancestors have survived on a Vegan (not vegetarian) diet?  I am just curious. 

I hope you figure it out.  

GFinDC Veteran
10 hours ago, Alexia N said:

Thank you very much for the suggestion, I did it already but unfortunately it did not worked. 

Bummer, but it's good you tried.  I hope you find a treatment that helps.

Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!

Register a new account

Sign in

Already have an account? Sign in here.

Sign In Now

  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,025
    • Most Online (within 30 mins)
      7,748

    Amari Love
    Newest Member
    Amari Love
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      Your experience is both shocking and critically important for the community to hear, underscoring the terrifying reality that cross-contamination can extend into the most unexpected and invasive medical devices. It is absolutely devastating that you had to endure six months of sickness and ultimately sustain permanent vision loss because a doctor dismissed your legitimate, life-altering condition. Your relentless research and advocacy, from discovering the gluten in MMA acrylic to finding a compassionate prosthodontist, is a testament to your strength in a system that often fails celiac patients. While the scientific and medical consensus is that gluten cannot be absorbed through the skin or eyes (as the molecules are too large to pass through these barriers), your story highlights a terrifying gray area: what about a substance *permanently implanted inside the body*, where it could potentially shed microparticles or cause a localized immune reaction? Your powerful warning about acrylic lenses and the drastic difference with the silicone alternative is invaluable information. Thank you for sharing your harrowing journey and the specific, severe neurological symptoms you endure; it is a stark reminder that celiac is a systemic disease, and your advocacy is undoubtedly saving others from similar trauma.
    • Scott Adams
      Those are driving distance from me--I will try to check them out, thanks for sharing!
    • Scott Adams
      I am so sorry you're going through this bad experience--it's difficult when your own lived reality of cause and effect is dismissed by the very professionals meant to help you. You are absolutely right—your violent physical reactions are not "what you think," but undeniable data points, and it's a form of medical gaslighting to be told otherwise, especially when you have a positive HLA-DQ2 gene and a clear clinical picture. Since your current "celiac specialist" is not addressing the core issue or your related conditions like SIBO and chronic fatigue, it may be time for a strategic pivot. Instead of trying to "reprove" your celiac disease to unwilling ears, consider seeking out a new gastroenterologist or functional medicine doctor, and frame the conversation around managing the complications of a confirmed gluten-free diet for celiac disease. Go in and say, "I have celiac disease, am strictly gluten-free, but I am still suffering from these specific complications: SIBO, chronic fatigue, dermatological issues, and high blood pressure linked to pain. I need a partner to help me address these related conditions." This shifts the focus from a debate about your diagnosis to a collaborative plan for your current suffering, which is the help you truly need and deserve to work toward bouncing back.
    • NanCel
      Hello, no I had to have them re done and then used a liner over the top.  Many dentists are not aware of the celiac effects.  Best of luck.   There is other material, yet, very expensive.
    • sleuth
      He is not just a psychiatrist.  He is also a neuroscientist.  And yes, I have already read those studies.   I agree with benfotiamine.  This is short term while glutened/inflammation occurs.  As I had already mentioned, these symptoms no longer exist when this phase passes.  And yes, I know that celiac is a disease of malnutrition.  We are working with a naturopath.
×
×
  • 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.