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

Question About Chemotherapy


libbyann

Recommended Posts

libbyann Rookie

Two years ago, I was on chemotherapy for a kidney problem. I was nauseated and either couldn't eat or ate some strange things during those 3 months. I did eat wheat because sometimes that was the only thing that appealed to me. But as long as I was on chemo, the wheat didn't seem to bother me. (Or maybe I was just too sick to notice!) Once I finished the drugs, I was right back to stomach cramps, diarrhea, constipation, etc. Any comments?

Libby


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



Celiac.com Sponsor (A8-M):



cruelshoes Enthusiast
Two years ago, I was on chemotherapy for a kidney problem. I was nauseated and either couldn't eat or ate some strange things during those 3 months. I did eat wheat because sometimes that was the only thing that appealed to me. But as long as I was on chemo, the wheat didn't seem to bother me. (Or maybe I was just too sick to notice!) Once I finished the drugs, I was right back to stomach cramps, diarrhea, constipation, etc. Any comments?

Libby

I had 2 years of chemo for cancer as a teenager. That was when my symptoms showed up for the first time. Chemotherapy drugs act on fast growing cells and kill them. That's why people lose hair, get mouth sores, etc. Hair and skin cells are fast growing. I'm not a doctor, but I don't think chemo drugs would have any protective effects for people with celiac. In my case, it was quite the opposite! I had to get fed daily through an IV just to stay alive.

Hope your kidney issues are better! Chemo is a drag.

JNBunnie1 Community Regular

Are you diagnosed Celiac?

JennyC Enthusiast

Hmm. I'll start off by saying that I'm not a doctor or a chemotherapy expert. Chemo kills rapidly dividing cells, like hair, blood cells, and cells that line body cavities. Perhaps the immune cells that release the cytokines, which are responsible for the damage caused when a celiac patient eats gluten, are also killed by the chemotherapy. This makes since because chemo patients are more immune compromised due to the decrease in immune cells. So when on chemo and you eat gluten, there are fewer immune cells, fewer cytokines released, less damage occurs, and therefore fewer symptoms result. Just a theory. (I love this stuff. :rolleyes: )

~alex~ Explorer
Perhaps the immune cells that release the cytokines, which are responsible for the damage caused when a celiac patient eats gluten, are also killed by the chemotherapy. This makes since because chemo patients are more immune compromised due to the decrease in immune cells.

That's kind of what I was thinking too. I know that RA and some other autoimmune diseases are sometimes treated with Methotrexate which I think is a chemotherapeutic. So since Celiac is an autimmune diseae maybe chemo was in a way 'treating' your Celiac disease. It reminds me how greatful I am that Celiac doesn't need the kind of harsh treatments that so many other autoimmune diseases do.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,015
    • Most Online (within 30 mins)
      7,748

    Rockette47
    Newest Member
    Rockette47
    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

    • Jmartes71
      Im so frustrated and still getting the run around trying to reprove my celiac disease which my past primary ignored for 25 years.I understand that theres a ray of medical that doctors are limited too but not listening and telling the patient ( me) that im not as sensitive as I think and NOT celiac!Correction Mr white coat its not what I think but for cause and affect and past test that are not sticking in my medical records.I get sick violently with foods consumed, not eating the foods will show Im fabulous. After many blood draws and going through doctors I have the HLA- DQ2 positive which I read in a study that Iran conducted that the severity in celiac is in that gene.Im glutenfree and dealing with related issues which core issue of celiac isn't addressed. My skin, right eye, left leg diagestive issues affected. I have high blood pressure because im in pain.Im waisting my time on trying to reprove that Im celiac which is not a disease I want, but unfortunately have.It  has taken over my life personally and professionally. How do I stop getting medically gaslight and get the help needed to bounce back if I ever do bounce back to normal? I thought I was in good care with " celiac specialist " but in her eyes Im good.Im NOT.Sibo positive, IBS, Chronic Fatigue just to name a few and its all related to what I like to call a ghost disease ( celiac) since doctors don't seem to take it seriously. 
    • trents
      @Martha Mitchell, your reaction to the lens implant with gluten sounds like it could be an allergic reaction rather than a celiac reaction. It is possible for a celiac to be also allergic to gluten as it is a protein component in wheat, barley and rye.
    • JoJo0611
    • Martha Mitchell
      Scott I also have different symptoms than most people. It affects me bad. Stomach ache, headache, nauseous, heart racing, whole body shaking, can't walk then my throat starts to close. It attacks my nervous system. The only thing that saves me is a 1/2 of Xanax...it calms down my nervous system 
    • Martha Mitchell
      Scott Adams. I was dealing with a DR that didn't care about me being celiac. I repeatedly told him that I was celiac and is everything gluten-free. He put an acrylic lens from j&j. I called the company to ask about gluten and was told yes that the acrylic they use has gluten....then they back tracked immediately and stopped talking to me. The Dr didn't care that I was having issues. It took me 6 months and a lot of sickness to get it removed.... which can only happen within 6 months. The Dr that took it out said that it was fused and that's why I lost vision. If they would have removed it right away everything would be fine. He put in a silicone one that was gluten-free and I've had no issues at all in the other eye. Do not do acrylic!
×
×
  • 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.