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

Celiac Blood Panel Done On My Mother


Fire Fairy

Recommended Posts

Fire Fairy Enthusiast

Okay I have Celiac disease and I think there is a great likleyhood my mother does as well. To be honest listing all the things that have gone wrong with her health since I've been alive (39 years) is like writing a poster for Celiac symptoms and complication. Most recently she went in to have cataract surgery in November and either during or immediately after surgery (unknown or at least unacknowledged at the time) she had a mild stroke. We found out about the stroke after she went to her new DO in March for weakness. She is finding it difficult to stand/walk and is often very dizzy. The DO first noticed she had a small mass in her right breast which became her immediate focus. It was a very tiny cancer and the Dr's alternated between saying it was malignant and benign but either way they insisted it must come out immediately. They also assured her this had nothing to do with the weakness. They did a lumpectomy and sent her in for an MRI of the brain to make sure the weakness wasn't brain cancer. MRI came back showing she had had a stroke a few months earlier. Now before we could do anything else including physical therapy and X-ray therapy for the affected breast she developed shingles! She was finally allowed after another two weeks to begin X-ray therapy. The oncologists are panicd because she has been getting the lowest doses possible and she is getting weaker and Mom is telling them she wont survive the treatments. The Oncologist suggested she could have an unusual case of a rare autoimmune disease called Myastenia Gravis. It usually shows itself through weakness in the eyes and her eyes look fine. So Monday the oncologist insisted her DO has to get her in to a Neurologist now! He also sent her for another MRI. We went to her DO yesterday and after a bit of poo pooing the oncologists panic the results arrived at the DO's office. There is new damage to my mom's brain. It is not a stroke but they don't have any idea what it is! The DO ordered full bloodwork (including a celiac panel at my insistence) and told us to come back in 2 weeks and by then she will have found mom a neurologist. Now when Mom went for her X-ray therapy the nurse at the oncologist said that would never do and she now has another appointment to talk to the Oncologist today.

 

All this to ask two things 1) The DO said that the results of the Celiac panel could come back false positive because mom is immune compromised by the X-ray therapy. Is that true?

2) Anyone have any thoughts on my mom's situation? Mom is getting very tired of not knowing what is wrong and she used to a sitter, she sat with mostly dementia patients, she's getting rather scared and so am I. Right now she is mentally on the ball it is physically she is falling apart but with it being brain damage.....she also going crazy not being able to do anything. Her arms and more so her legs are so weak she can't hardly get to the bathroom and it's only a couple feet away.  

 

They should get the blood work back today but I don't know if they will call us with the results or not.


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



Celiac.com Sponsor (A8-M):



pricklypear1971 Community Regular

I know you're scared, and I'm sorry your family is going through this.

Considering what may be at stake, will your mother try gluten-free now? There's no reason not to. As we all know, it can't hurt...but may help tremendously.

greenbeanie Enthusiast

Unfortunately I don't have answers to your questions, but I hope they figure out what's wrong soon. It sounds like you're being a great advocate for her healthcare. My mother has had leukemia for almost 20 years and has been through three rounds of treatment that left her weak for several years each time, in addition to having strange unexplained neurological and muscular problems (like only being able to walk backwards) that left her in a wheelchair for a while. I know how scary it is when even the doctors have no idea what's going on. 

 

Given the urgency of the situation, and your own celiac diagnosis, it seems like it would make sense to try having her go gluten-free immediately, without even waiting for further test results. It may be totally unrelated, and I know it's not generally advisable to go gluten-free before all testing is complete, but it sounds like you don't have any time to lose. If there's even a tiny possibility that gluten might be causing or exacerbating her problems, it surely can't hurt to try. I imagine your mother must be willing to try just about anything right now, so hopefully she'd go along with the suggestion.

 

...The reply above was just added as I was writing this - so I second pricklypear's suggestion!

Fire Fairy Enthusiast

She is willing to try it even after her DO told us both that "Going gluten-free when you don't have Celiac Disease can cause serious health issues." :blink: I have no idea what she was talking about but I tried not to roll my eyes. Now I just need to tear apart the kitchen and go through all her meds and lotions etc. She has a lot of prescriptions. If there any data base to check for gluten in prescription drugs?  

pricklypear1971 Community Regular

She is willing to try it even after her DO told us both that "Going gluten-free when you don't have Celiac Disease can cause serious health issues." :blink: I have no idea what she was talking about but I tried not to roll my eyes. Now I just need to tear apart the kitchen and go through all her meds and lotions etc. She has a lot of prescriptions. If there any data base to check for gluten in prescription drugs?

Yes. Open Original Shared Link

Fire Fairy Enthusiast

thank you :D

pricklypear1971 Community Regular

thank you :D

Whatever you need, just ask. You're going through a tremendous amount of stress right now.


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



Celiac.com Sponsor (A8-M):



powerofpositivethinking Community Regular

sending you positive thoughts!!!  glad that you pushed for the celiac panel for your Mom :)  I know you have the next appointment scheduled, but is there any way you can get the results earlier since you all need some answers?  I hope so!

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      130,681
    • Most Online (within 30 mins)
      7,748

    emmajag
    Newest Member
    emmajag
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):




  • Who's Online (See full list)


  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Rebeccaj
      Hello , I would like to know what happens to people living or working in a industry or living with people that are non celiac or allergy Pron or anaphylaxis.    what are the symptoms and have you reached neurological symptoms during Airbourne exposure or hours later. persistent just ptsd related or unknown as its usually only high inflammation in the body when consumed with Vegas nerve symptoms of ingested or neuroglial of ingestion of inhalation accidently as my doctor has given me the ok to work but then my boss has let me go for a focal seizure as  Allery or ptsd unsure  any Insite of what someone else has gone through I was diagnosed when I was 27 so gluten free for the rest of my life but my family are not . ?
    • Beverage
      I strongly agree with others about processed gluten free foods, like breads and pasta, being bad for us. Read the labels, full of this starch and that starch, seed oils that are inflammatory, etc. Before you were celiac, you probably wouldn't even touch something with those ingredients. I do much better with whole foods, meat, veggies, a little fruit. I made 90% myself, make extra and freeze it for future meals. Cutting out processed gluten free food and eating mostly real whoke food helped me feel much better. And definitely benfotiamine!
    • knitty kitty
      Please be sure to try Benfotiamine or Thiamine Hydrochloride.  The form Thiamine Mononitrate is not absorbed nor utilized well.  Benfotiamine is much more bioavailable.  Perhaps Thiamine Mononitrate was in your previous B Complex supplements, explaining why they didn't work for you.   All the B vitamins work together.  Thiamine needs the other B vitamins to make enzymes and ATP, so you will need to take them.  Taking them in individual supplements is fine.  I've done the same.  Just remember you need all eight.   Let me know how it's going for you!
    • Zuma888
      Thanks! This makes a lot of sense.
    • Zuma888
      Thanks! I am currently trying B1 out on its own. I tried many brands of B-complex and they always make me feel nauseous and tired. I think I may have to try taking each B vitamin on its own.
×
×
  • Create New...