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

Does Anyone With Celiac Disease Hear Their Pulse?


jackay

Recommended Posts

jackay Enthusiast

I would like to know if anyone else with gluten intolerance hears their pulse (vascular/pulsitile tinnitus)?

I have been hearing my pulse for about four years. It started after a long spell with severe headaches. The pain caused my blood pressure to spike which started the noise. It sounds like a clock ticking in my head and is very annoying. I do have my headaches somewhat under control and my blood pressure is now normal. For a while about a year ago the pulsing noise went away but has come back. I am hoping that being off gluten for a while will stop it.


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



Celiac.com Sponsor (A8-M):



jerseyangel Proficient

Yes, I have it and it's very annoying. It seems to have started when I woke up with vertigo a few years ago. I also have blood pressure issues, but it's under control with a combination of diet and medication. That doesn't seem to have any bearing on it for me.

I also have allergies and chronic allergic rhinitis--I always feel that if my ear would just "pop", I would get relief. I've had cardiac testing to rule out anything there, and am currently seeing an ENT specialist. He prescribed Nasacort AQ, which does seem to help if I take it religiously (which I don't always). The ENT also suggested Afrin, but just for three days before bed. (people with high blood pressure need to speak with their doctors before using a decongestant)

One interesting thing was that the ENT told me that he does see these sorts of problems more often with his Celiac patients.

Wolicki Enthusiast

I have it too but I have low blood pressure :huh:

codetalker Contributor

I've experienced that when I would eat too much salt or when I would let work get to me and my blood pressure would spike (similar to what you mentioned in your post).

In my case at least, gluten probably wasn't a factor. However, if you are on a gluten-free diet, your celiac-related symptoms/problems should subside. That should reduce stress levels which in turn should reduce blood pressure.

Have you tried activities like swimming or jogging? Repetitive, mind-numbing exercise is good for reducing stress.

mushroom Proficient

I have it too, but it usually only bothers me at night. My head is too "busy" during the day, and I have tinnitus in one ear also. But I have had it for so long now it doesn't really get to me. When I have pressure from gas I can "hear" my whole body throbbing and pulsing :huh: I do take hypertensive medications which control my blood pressure; I remember the first time a took a beta blocker it had such a profound effect--my whole body was quiet and still; I thought I had died!! :lol: Wish that effect had lasted--it was so restful and calm. :)

nascentes morimur Newbie

I have it too, not sure what causes it..think most of your 'quirks' you could attribute to Celiac

brigala Explorer

I didn't know that wasn't normal. My husband says he can't hear his pulse. I often hear my pulse if it's not being drowned out by a louder noise. I only really find it annoying when I'm trying to get to sleep at night. It's worse when I lay on my side but doesn't go away in any position. It doesn't happen ALL the time, but most of the time.

I have no idea when it started. I think maybe it's always been like that.

For the record, my blood pressure is on the low end of normal. Before I went gluten-free it was below normal. Doctors always said it was "great" but when it would get down to like 92 over 55 I really didn't feel good. It doesn't do that any more, thank goodness, and I feel much better and it's now within a realistic normal range.

-Elizabeth


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



Celiac.com Sponsor (A8-M):



jackay Enthusiast

I have tried swimming but am sensitive to the chemicals in the water and break out in hives. It was hard giving it up but I feel for the time being it is the thing to do. My doctor is hoping I can get over this sensitivity and eventually go back to swimming. I cannot jog because I have bad feet. Walking isn't a problem for my feet if I don't walk for too long. I do not hear my pulse when I walk or when driving. The car and traffic noises mask it. I usually hear my pulse when doing anything else including watching tv. I did find that crocheting calms me down and brings the pulse noise to a tolerable level.

My doctor has me taking the amino acid L-Theanine which sometimes quiets it down. If it is going to work, I can notice it almost right away. Unfortunately, it doesn't always help. I have tried both 100 mg and 200 mg. Lately I am getting no more relief from 200 mg than 100 so I am sticking with 100.

I am also taking a Vitamin B5B6 complex which is supppose to support the production of adrenal hormones. My doctor also feels my adrenal glands are creating havoc. (Tests have confirmed this.) One tablet provides 5000% of each. The first time I took it, I crashed. I cut down to about 1/8 of a tablet and built up from that. I do feel more relaxed and my pulse is not nearly as loud as it use to be. I am now taking 1/4 of a tablet. I was up to 3/8 but my sleep, which is very little, seemed affected.

I have tried other supplements for my adrenal stress and they have all made it worse. I am hoping that getting off gluten will bring adrenal relief.

I realize this noise is associatd with anxiety but I don't think that is the only issue. Some nights it has been so loud and annoying yet I have been able to get some decent sleep. Other nights, it is quieted down and I lay awake the whole night hearing it. It definitely makes me anxious so it is a vicious circle. It is so frustrating :(

Nancym Enthusiast

That can be a symptom of thyroid issues. When I was hyperthyroid I heard my heart beating at night. Very unsettling.

jackay Enthusiast

I had my thyroid checked a few months ago and that was normal. Also, most recent bloodwork for parathyroid was almost all normal. One calcium test was a little low but is continuing to get closer to the normal range.

Hopefully my stomach will repair itself by eliminating gluten and the pulsing will go away. I know I'm not absorbing all my nutrients so it could possibly be some deficiency.

SGWhiskers Collaborator

add one more to that list. Low blood pressure here. I notice it more when I'm having a fibro flare or a migraine. It has become intermittant the longer I'n gluten-free.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      128,336
    • Most Online (within 30 mins)
      7,748

    jojocle
    Newest Member
    jojocle
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.1k
    • Total Posts
      70.8k

  • Celiac.com Sponsor (A22):




  • Who's Online (See full list)


  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • knitty kitty
      Hello, @Itsabit, Your journey sounds very similar to mine.   I'm very concerned about your diet since you say you don't eat a lot of meat, which is the main source of B vitamins.  Nutritional deficiencies go along with Celiac Disease.  Blood tests are not accurate measurements of deficiency states.  The body robs stored vitamins from organs to circulate in the bloodstream to supply the brain and heart.  You can have deficiency symptoms before blood levels change. I have a hypersensitivity to sulfites, so much so that I had to switch my toothpaste to one that doesn't contain Sodium Lauryl Sulfate.  SLS can cause oral irritation as a side effect, too.   My mouth would burn and I avoided certain foods.  Dapsone contains sulfites, as do antibiotics.  Treatment with sulfites can precipitate a Thiamine deficiency disorder because sulfites cut thiamine in two making it useless. https://pubmed.ncbi.nlm.nih.gov/35506963/ https://pmc.ncbi.nlm.nih.gov/articles/PMC10506142/ I have an allergy to nickel, also.  Zinc helps keep other metals in balance in the body.  Zinc is also terribly important to skin health and oral health. https://pubmed.ncbi.nlm.nih.gov/8445075/ https://pmc.ncbi.nlm.nih.gov/articles/PMC11274920/ https://pubmed.ncbi.nlm.nih.gov/1977254/ Thiamine (Vitamin B 1) deficiency disorder symptoms and altered thiamine metabolism can occur after radiation or chemo.   Thiamine and Niacin B 3 are important in nerve conduction.  When I was very malnourished, I had paresthesia that made me feel itchy all over, and made my dermatitis herpetiformis extremely unbearable.  The form of Niacin that causes flushing, Nicotinic Acid (not the same as nicotine in cigarettes) is beneficial because the flushing helps open the small capillaries in the skin which allows the antibodies to be cleared and disposed.  Pellagra can occur in Celiac Disease.   I had it, and my doctor didn't properly diagnose it, either.   I had a rash around my neck, Casal's Necklace, along with a blistering rash on my arms and any skin exposed to the sun.   https://pubmed.ncbi.nlm.nih.gov/8445075/ https://cgp.iiarjournals.org/content/10/4/169 https://pmc.ncbi.nlm.nih.gov/articles/PMC11722086/ https://pmc.ncbi.nlm.nih.gov/articles/PMC6780714/ https://pmc.ncbi.nlm.nih.gov/articles/PMC10229844/ https://pubmed.ncbi.nlm.nih.gov/1977254/ You should be checked for more than just B12 deficiency.  The eight B vitamins work together, and we need more of them when we're trying to heal.  They are water soluble, so the body can easily excrete them if not needed. Have you had your Vitamin D level checked?  Vitamin D regulates the immune system and lowers inflammation.   I hope you can find some benefit from my experiences.  Keep us posted on your progress.  
    • knitty kitty
      Hello, @Jack Common, I know how frustrating health mysteries can be. Perhaps you're having a reaction to the medication you were given for the giardiasis you mentioned in another post. The giardiasis infection would account for the high Igg results.  Have you been reinfected? The site I've linked below has lots of information about the long term consequences of being treated with a medication frequently prescribed for giardiasis infection.   https://hormonesmatter.com/metronidazole-toxicity-doctor-denial/ https://hormonesmatter.com/?s=metronidazole https://pmc.ncbi.nlm.nih.gov/articles/PMC3870550/ Please let us know if your symptoms may be due to this reaction to the prescription for giardiasis. Best wishes.
    • knitty kitty
      Hello, @Jack Common, I know how frustrating health mysteries can be. Perhaps you're having a reaction to the medication you were given for the giardiasis. The giardiasis infection would account for the high Igg results.  Have you been reinfected? The site I've linked below has lots of information about the long term consequences of being treated with a medication frequently prescribed for giardiasis infection.   https://hormonesmatter.com/metronidazole-toxicity-doctor-denial/ https://hormonesmatter.com/?s=metronidazole https://pmc.ncbi.nlm.nih.gov/articles/PMC3870550/ Please let us know if your symptoms may be due to this reaction to the prescription for giardiasis. Best wishes.
    • Itsabit
    • Itsabit
×
×
  • Create New...