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

One Sided Headache/pressure?


Nen

Recommended Posts

Nen Explorer

I am normally not a headache person, but lately I've kind of become one.

For the past 6 months on and off I will get a dull headache/and or head pressure mainly focused on the right side of my head (behind the eye, around to the back right side of my head down my neck even into my shoulder), and it drives me nuts. Sometimes even my lymph node gets inflamed on that side, and I get ear pain too on the one side with it. Thankfully its not *bad* pain, more just there when it happens and it is annoying.

This is on top of my pretty much constant sinus issues (pressure and clear drainage) that I've had long before this head crap started. Pain killers pretty much don't help which is odd to me. I wonder if it isn't a nerve or neurological type thing.

Does anyone with Celiac get this sort of stuff? I've been experimenting and trying allergy meds and sinus drainage meds and keeping notes, also have been to the docs twice where of course they don't really do anything to help but push more meds. I do have good days where it isn't there, but it comes and goes. Next step is going to be an elimination diet as its the one thing I haven't yet tried that I could do to experiment.


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



Celiac.com Sponsor (A8-M):



AMom2010 Explorer

I get the same headaches, and have been considering gall bladder dysfunction might be the cause. Not too uncommon for people with gluten intolerance from what I understand. Several close relatives have had gall bladders removed. Google "gallbladder headache" and see if yor symptoms match too!

Roda Rising Star

I have had headaches like you describe for years, going back as far as teenager(the pain though was not into my neck and shoulder, that has developed in the last several years). Last year they were becoming worse and more frequent, so at my hubsband's insistance, I brought it up to my doctor. To her she said they sounded like a mixture between a migraine and tension headache. If I start having the slightest pressure behind my eye I usually can take 3 200 mg ibuprofen and can catch it before it gets bad. If I let it go and it gets any worse, then they last for about 3-4 days and nothing helps. I try not to take much ibuprofen or NSAIDS anymore since I had an ulcer about 1 1/2 years ago. It is healed, but I try to be careful. I also noticed when I get that knotted feeling at the base of my neck and into my muscle behind my shoulder, if I apply a heat patch, or bengay patch, it helps loosen up the tense muscles and it helps the headache. I did and do this as my first approach now and it does help with the headache. I will still take ibuprofen when necessary. My biggest trigger I have noticed recently is the position of my head at night when I sleep. If I sleep with my head on anything but the flat matress, it will trigger one.

My doctor gave me a prescription for verapimil to see if it would help my raynaud's symptoms. She also said it might help the headaches too. I haven't used it hardly at all, but if my raynaud's symptoms get bad this year I may try it.

domesticactivist Collaborator

You might want to see an osteopath and look into possible nerve, muscular, or bone alignment issues.

Nen Explorer

Thanks for the replies, I didn't realize you could get headaches with gall bladder issues, I'll have to look into that.

Also thanks for the suggestion about the pillow, I will have to try sleeping without a pillow and see what that does. I do have Raynauds as well.

I figure if this doesn't get any better maybe try a chiropractor, sometimes they seem more "on the ball" than a regular doctor would.

Archived

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

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,228
    • Most Online (within 30 mins)
      7,748

    CindyNR
    Newest Member
    CindyNR
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • xxnonamexx
      I noticed eating gluten-free or CGF foods have higher sugar and sodium some. No added sugar protein bars I found better with plant fiber. I wanted to know what are you go to besides whole fruits/veggies that you find are healthy for you where you can feel eating normal without hurting yourself or health. I was looking into subscription based like Thrift to see if there is something that is healthier CGF that can make me feel normal. Thanks
    • Jmartes71
      Thankyou because I met up with K B with well known bay area hospital once and she said she knows I don't like to take meds, I said thats incorrect, I have issues.Thats the one that said I was deemed " unruly " when she admitted I was celiac when I asked why am I going through this.
    • cristiana
    • trents
      Cristiana, that sounds like a great approach and I will be looking forward to the results. I am in the same boat as you. I don't experience overt symptoms with minor, cross contamination level exposures so I sometimes will indulge in those "processed on equipment that also processes wheat . . ." or items that don't specifically claim to be gluten free but do not list gluten containing grains in their ingredient list. But I always wonder if I am still experiencing sub acute inflammatory reactions. I haven't had any celiac antibody blood work done since my diagnosis almost 25 years ago so I don't really have any data to go by.   
    • cristiana
      I've been reflecting on this further. The lowest TTG I've ever managed was 4.5 (normal lab reading under 10).  Since then it has gone up to 10.   I am not happy with that.  I can only explain this by the fact that I am eating out more these days and that's where I'm being 'glutened', but such small amounts that I only occasionally react. I know some of it is also to do with eating products labelled 'may contain gluten' by mistake - which in the UK means it probably does! It stands to reason that as I am a coeliac any trace of gluten will cause a response in the gut.  My villi are healed and look healthy, but those lymphocytes are present because of the occasional trace amounts of gluten sneaking into my diet.   I am going to try not to eat out now until my next blood test in the autumn and read labels properly to avoid the may contain gluten products, and will then report back to see if it has helped!
×
×
  • 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.