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

Help! Excruciating Muscle Pain And Stiffness


Guest BERNESES

Recommended Posts

Guest BERNESES

Hi Everyone- My back neck and jaw are so tight I could practically scream. I've tried all the home remedies (ice, heath, baths, arnica, OTC pain stuff) and the muscle relaxants my doctor gave me when I had a ski accident this winter and nothing is helping. And I'm having weird muscle spasms in my feet and legs. Could this be a vitamin deficiency? i take cal mag and I've been feeling really good otherwise. It's scaring me. Thanks, Beverly


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



Celiac.com Sponsor (A8-M):



Guest nini

when I get this type of pain and stiffness, I usually just want to crawl into a hole somewhere and sleep... but I hurt to bad to sleep!

Yes it could be a vit. issue... look into potassium, or eat some bananas! that usually helps me feel better. That and taking loads of tylenol and packing myself in ice packs.

mommida Enthusiast

Make sure you do not have a fever. If you do, seek medical help. If you are still feeling worse or can not find relief, go to the doctor. Try putting your head forward, chin to chest. If that causes more pain, go to the emergency with or without a fever. (It would be significant pain.)

Laura

jenvan Collaborator

Laura had a good idea, make sure you don't have a fever too--that the pain isn't a sign of acute illness. Could it be fibromyalgia pain? I have it and sometimes my pain is really horrible. Donna, another woman who deals with Fibro gets muscle spasms too, possibly like your describing. We both use heat to treat the soreness. I use a heating pad about 5 nights a week .

A year a half ago I suffered from incredible neck, upper back pain and tightness. It came on fairly suddenly, with noticeable injury. So much so I had trouble moving my neck without using my hands to help. I tried acupunture, meds, chiropractor, possible surgery... and nothing helped. It eventually went away (praise God!) and I attribute it to changing jobs. At my previous job I spent a lot of time with my neck bent and back hunched over. I think that may have been the culprit. I also had burning in my muscles. If that is a possibility, make sure your work station is ergonomic. ( I can give you more info ) Try and stretch and take frequent breaks during work too.

You might want to ck this link out and read about Fibromyalgia as a possibility and see if it might relate to you. Many people with Fibro also have TMJ (jaw) type problems too. Open Original Shared Link If interested, you could also read these recent posts on Fibro. https://www.celiac.com/index.php?s...t=0entry46260

Hope you start to feel better soon !!

jaimek Enthusiast

I think I have this. How do you get tested for it?

jenvan Collaborator

Jamie-

Its my understanding that there is really no test for Fibro... just a diagnosis based on how you meet a certain number of criteria. Such as pain for a certain period of time and in certain areas. Go here and it gives you those criteria and pictures of the points. Open Original Shared Link

If you have a doctor that is familiar with Fibro, they could help you diagnosis for sure, rule out other possibilites. What are your symptoms like?

mommida Enthusiast

I had viral meningitis that was turning bacterial before I made it to the hospital. That was about 4 years ago. I was also misdiagnosed when I went into the doctor's office, and 6 hours later had a seizure in the middle of the night. Your odds of having meningitis are about 1 in 250,000. Most adults with viral meningitis do not receive medical treatment. The fatality rate for bacterial meningitis is 1 in 10.

This not to diagnose, but to let you know- seek medical treatment when you have an unexplained onset of symptoms and are experiencing pain. In my case I was misdiagnosed and had to wait longer for relief.

Laura


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



Celiac.com Sponsor (A8-M):



mela14 Enthusiast

My fibro came about after a terrible viral infection (Parvo Virus) 8 years ago. I have not been the same since and now have to deal with daily pain. There are times when it flares up and gets worse......like a flu, cold, bacterial infection, stress or just being run down by over doing it. Mornings are usually the worst. I also now get sick a lot as my immune system changed after that illness.

going gluten free has helped as I now know when it is a virus or gluten contamination. Before I would l think I had a virus ALL the time. At least now there is a break between periods of being ill. I also notice that when I accidentaly ingest gluten I actually feel sick with muscle pain...and it cold actually pass for a virus if I didn't know better.

tammy Community Regular

I found a website that might shed some light on managing multiple health symptoms:

DR. MAJID ALI

He is located in NY, NY and Denville NJ.

He uses a variety of treatments, mainly oxygen therapy and vitamins.

I hope this brightens your day!!

Guest BERNESES

Thanks Everyone- For some reason I never got an email that there were replies to this topic. Luckily, the apin went away. I THINK what happened was I tried to cut down on my anti-anxiety medicine (klonopin- it has VERY bad withdrawal) because the symptoms strted right around then. I returned to my regular dose, am wearing my mouth guard while I sleep and have been taking ibuprofen and Tylenol arthritis (I have arthritis in my neck and back) and finally feel human again. I've also been heating, icing and using arnica gel. I feel much better. Even went surfing for a bit yesterday. thanks Everyone! i am going to check out the info on fibromyalgia though. Beverly

hnc Newbie

The correct doctor to see to check to see if you have fibromyalgia is a rheumatologist. As someone else pointed out, they will diagnose by asking you about your pain and putting pressure on spots on your body called "trigger points." It may make you want to jumpt through the roof for a few seconds, but it pretty clearly defines if you have it. Keep in mind that it is only in the past few years that most doctors accept this as a "real" illness, so if you find one who doesn't, change doctors. Almost all now understand how serious it can be. Good luck!

Guest BERNESES

Thanks- it's probably a good idea considering I have arthritis and I'm 37! Yuck!

skbird Contributor

B -

Glad you're feeling better. Yeah, that klonopin can be nasty - when I was on it (about 6 months) my medical insurance kept changing around (off my parents, onto the county insurance at the time) and they took me off klonopin - COLD TURKEY! Four days of pure hell, then the next month was uncomfortable but not so bad. Have you seen Trainspotting? I felt a lot like the guy in the movie when he was going off heroin.

Still amazed at the idiots in the county health system who let that happen. Unfortunatly, at the time I was not in a good place where I could argue with the wisdom (didn't know it was going to hurt me like that).

Take care

Stephanie

Guest BERNESES

Thanks Stephanie and Everyone- yeah, klonopin ishideous to get off of. My sister couldn't leave the house for a week. I can't believe they made you go off like that- it's actually medically dangerous. You can have a seizure and die! Talk about ignorance. That's obscene!

I am feeling better and don't plan on trying to cut down again anytime soon. Beverly

cdford Contributor

Two things about klonopin.

1- Check with the manufacturer to be certain that it is gluten-free. Some are not.

2- If you need to change this med, come off it slowly. There are what I believe to be better alternatives out there and the only way to determine which is right for you is a discussion with your doc. The change went far more smoothly for me with the doc's help.

Another important note:

The advise in these posts was excellent about checking with a medical professional when you have pain and fever, especially when that pain is in or around the head/neck area. Even a sinus infection gone awry can kill with meningitis if not correctly assessed. My stepsister died having her third child not from the pregnancy but from a sinus infection that seeped into the meninges.

mela14 Enthusiast

That's terrible about your step sister. i am so sorry. :(

  • 10 years later...
etm567 Newbie

I see that this is very old. I kjust wanted to add that I have many problems like this, and they seem to be mostly caused by mineral and vitamin deficiencies. But the whole mineral balance is so incredibly complicated that it can be difficult to pin down.

For example, I have read that a magnesium deficiency can cause a potassium deficiency, and you just can't get enough potassium if you really are low in magnesium.

And then vitamin D is involved as well. And that also becomes very difficult. If you take vitamin D, you can indirectly cause your body to reduce the number of receptors for it, which means you can't use it as much.

And, finally, I have read that the part of the lower intestine that absorbs most minerals is the end of it, just before the large intestine begins. And when you develop SIBO, which many celiacs suffer from, the bad bacteria migrate from the large intestine into the lower part of the small intestine, which is where you absorb your minerals.

I tend to tense up in my buttock muscles and hips, and once I got full blown tetany, which is when you get really rigid all over, including that lockjaw thing. That's caused by low blood calcium, but again, low blood calcium can be complicated. And really low vitamin D can cause that, I think.  And you need vitamin D to absorb calcium. Don't know if it affects absorption of magnesium and potassium.

Good luck.

 

 

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,964
    • Most Online (within 30 mins)
      7,748

    Cbear
    Newest Member
    Cbear
    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

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • 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.