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

Am I In The Right Place?


justlisa

Recommended Posts

justlisa Apprentice

Tired...sick...scared...

I'm just going to list what's wrong with me:

In 2004, I suffered from hives...lasted about a year or so... The docs couldn't find the cause. I used benadryl but, when that didn't work I would be put on steroids... The hives disappeared one day and have never returned.

I noticed "aches and pains" (mostly when I really pushed myself) and fatigue...but I just pushed through it.

Please note that I only add the two items above in hindsight (as I only now wish to see if there could be a connection).

In 2007, I started experiencing a pain in the bottom of my foot...trouble walking on it. It would come and go.

Around the same time period I started experiencing "pressure", "anxiety"...whatever you want to call it...and was diagnosed with high blood pressure.

The pain in my foot as sporadic and "livable" up to that point...but then started having pains elsewhere. Blood test for rheumatoid factor was positive. Referred to a rheumatologist. For about 4 or 5 years, I have been on enbrel then humira...along with steroid courses. I've not seen any real relief for this... I would always question the rheumatoid arthritis dx because I didn't seem to have the same symptoms as I read associated with RA...but I was told that " not everyone's the same".

Also, during this time I started having heart palpitations and was put on atenolol.

Approx a year ago, my rheumatologist noticed something in my gait and referred me to a neuro. She did an mri and determined (using a previous mri) that my cerebellum had "shrunk some". That i have "cerebellar ataxia". I was told my condition was progressive would worsen.

My condition has "worsened". I have great difficulty walking unaided (by walls, furnishings, people, etc). I seem to do okay driving locally...at "city speeds" but, have a lot of discomfort (and no longer do it) on highways (vertigo, etc). I, also, experience occasional tremors in my left arm...along with significant "weakness" in my limbs...

I can't tell you how many times (every time I go) I've cried in the doctors' office...

At my GP's office today I asked about gluten intolerance/celiac. My GP chuckled (can I just say how THAT made me feel?!) but said we'd draw some blood and test but he highly doubted my symptoms were caused by celiac because I would have abdominal paim, vomiting, diarrhea, etc). I don't have those symptoms...true...but I've always had "issues" (bloating, discomfort, irregularity, etc, etc).

I started gluten-free today...don't know if it will help...what can it hurt?

Oh and...I am a 44 yr old mom (who can't carry the laundry up and down the stairs).

Any advice is welcome.


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



Celiac.com Sponsor (A8-M):



Teri Lou Apprentice

So sorry to hear how poorly you are feeling. Can definitely sympathize with you as I have lupus, and went through a lot of the same things you are. I also suggested a gluten intolerance to the dr and was pooh poohed by the MD, however started gluten free anyway and it made a HUGE difference in how I felt. Then accidentally got glutened and developed DH rash which was tested and so ended up with the Celiac diagnosis through the back door so to speak. IF your testing comes back negative I would recommend trying gluten free it shouldn't hurt anything but might make a huge difference for you. I know it did for me. I honestly never thought I would feel this good again.

Good luck. Hang in there and post here if you need support :)

beachbirdie Contributor

Tired...sick...scared...

I can't tell you how many times (every time I go) I've cried in the doctors' office...

At my GP's office today I asked about gluten intolerance/celiac. My GP chuckled (can I just say how THAT made me feel?!) but said we'd draw some blood and test but he highly doubted my symptoms were caused by celiac because I would have abdominal paim, vomiting, diarrhea, etc). I don't have those symptoms...true...but I've always had "issues" (bloating, discomfort, irregularity, etc, etc).

I started gluten-free today...don't know if it will help...what can it hurt?

Oh and...I am a 44 yr old mom (who can't carry the laundry up and down the stairs).

Any advice is welcome.

Hi and welcome. You have found a very good place to get support and information. I think it is one of the best on the 'net. There are a lot of people here with a variety of experiences and conditions, people who have struggled for answers sometimes for decades. Glad you found us. I am so sorry you are having such a difficult time and that you have felt so poorly for so long. Forgive me for getting personal, I hardly know you, but {{{{hugs}}}} to you.

Your doc doesn't know much about celiac if he still thinks it always presents with abdominal symptoms. It does not. In fact, (and this is not supported by any literature) from stuff I've been reading, it sounds like more people might actually present with very few of the "classic" symptoms. I'm one of them.

Be careful about how he interprets your tests, and be sure to check up on him to make sure he does the full array of tests. Testing for this disease is NOT that great, and there is about a 20-30% rate of false negatives. Meaning, 20-30% of people who actually have the disease will have negative blood work.

One of the first things you'll want to do is get your lab test results and read them for yourself. Docs too often say "you're fine" when you might not be fine for YOU. If you share the results here, lots of people will pitch in and give you ideas about it.

Now...question...have they given your thyroid a good going over? That can also cause some of the symptoms you have. I had a lot of arthritis-type pain when my thyroid was bonkers, I'm guessing now it was inflammation from the high level of antibodies in my blood. Your foot pain sounds like plantar fasciitis, a VERY common companion to thyroid problems. Make sure they test your thyroid hormones and not just TSH (a pituitary hormone). You need a Free T3 and Free T4.

Hopefully others will be along for you soon!

justlisa Apprentice

Teri, thanks for the understanding and support.

Beachbirdie, I had blood drawn for my TSH, yesterday, as well. I will ask about the others. The problem with the pain is that it "moves" around my body...not in just one place...not just a foot...and it can be flared up for a few days or gone by the end of one.

Thanks for the info...and the hugs...

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,017
    • Most Online (within 30 mins)
      7,748

    Sjcucinotta
    Newest Member
    Sjcucinotta
    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

    • 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.
    • knitty kitty
      Please do more research before you settle on nicotine. Dr. Paul New house is a psychiatrist.  His latest study involves the effect of nicotine patches on Late Life Depression which has reached no long term conclusions about the benefits.   Effects of open-label transdermal nicotine antidepressant augmentation on affective symptoms and executive function in late-life depression https://pubmed.ncbi.nlm.nih.gov/39009312/   I'm approaching the subject from the Microbiologist's point of view which shows nicotine blocks Thiamine B1 uptake and usage:   Chronic Nicotine Exposure In Vivo and In Vitro Inhibits Vitamin B1 (Thiamin) Uptake by Pancreatic Acinar Cells https://pubmed.ncbi.nlm.nih.gov/26633299/   While supplementation with thiamine in the form Benfotiamine can protect from damage done by  nicotine: Benfotiamine attenuates nicotine and uric acid-induced vascular endothelial dysfunction in the rat https://pubmed.ncbi.nlm.nih.gov/18951979/   I suggest you study the beneficial effects of Thiamine (Benfotiamine and TTFD) on the body and mental health done by Dr. Derrick Lonsdale and Dr. Chandler Marrs.  Dr. Lonsdale had studied thiamine over fifty years.   Hiding in Plain Sight: Modern Thiamine Deficiency https://pmc.ncbi.nlm.nih.gov/articles/PMC8533683/ I suggest you read their book Thiamine Deficiency Disease, Dysautonomia, and High Calorie Malnutrition.     Celiac Disease is a disease of malabsorption causing malnutrition.  Thiamine and benfotiamine: Focus on their therapeutic potential https://pmc.ncbi.nlm.nih.gov/articles/PMC10682628/
    • sleuth
      Thanks for your response.  Everything you mentioned he is and has been doing.  Tobacco is not the same as nicotine.  Nicotine, in the form of a patch, does not cause gastrointestinal irritation.  Smoking does. He is not smoking.  Please do your research before stating false information. Dr. Paul Newhouse has been doing research on nicotine the last 40 years at Vanderbilt University Medical Center.  
    • 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.
×
×
  • 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.