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

Pain Management


melmak5

Recommended Posts

melmak5 Contributor

I was prescribed Levsin (digestive muscle relaxant) prior to being diagnosed (2+ weeks ago) for the abdomen pain I was experiencing.

It causes constipation, which I have recently been battling, so I have stopped taking it.

Any recommendations on pain management?

(Sometimes walking helps, but often it makes it worse.)


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



Celiac.com Sponsor (A8-M):



jennyj Collaborator

I take tylenol for pain. My doc said it was ok. Hope you feel better soon.

grantschoep Contributor

Advil is gluten free, I've checked with some generics and they are too. Advil was the only thing that ever help me with headaches and so on. I can't take it anymore as I take blood thinners and it basically magnifies that. Aspirin/Aleve etc is out too, same thing. I'm basically stuck with Tylenol. I do actually have Vicoden for the really bad knee pains I have at times. But thats prescrip. of course. And a narcotic, so you don't really want to take it too much.

lfij Newbie

i'd say take some tylenol and lie down. I don't think walking around is really the best thing if your stomach hurts enough to have to take medicine. But, really, you should be asking your doctor and not a bunch of stay at home moms and other non doctors (like me).

Dandelion Contributor

Please, please, please watch how much advil, alleve and excedrin you take. I used to be in constant pain prior to going gluten free - abdominal pain, joint pain, terrible headaches and took tons of over the counter pain relievers to get through it. Well now I have three almost bleeding ulcers because of it. I am lucky that I do not need surgery (yet). I am on a very restrictive diet to help them heal. Like we need any more restrictions on what we can eat. So please be careful of what you take. Tylenol is ok, but the other NSAIDS are what you should watch out for. If I can keep one person from going through the excruiating pain of an ulcer I would be very happy.

I hope you feel better.

Beth

  • 2 weeks later...
melmak5 Contributor

Thank you all for your input/advice.

I am going to doctor #4 tomorrow, hopefully he can figure out why I am still in so much pain and/or offer some useful suggestions.

grey Explorer

Like Beth, I also ended up with an ulcer from NSAIDs. I also don't tolerate Celebrex and advil anymore, I get a severe fatigue rxn (like I needed more fatigue) and I'm allergic to percadan/percacet. The pain before dx was pretty bad, and I ended up with Alleve (because I could tolerate it, I thought) and other drugs for migraines. Both turned out to be doing a number on my liver and kidneys, as well as my electrolyte levels. Now I have Tramadol, which is from a different family of pain killers, for pain and take it with a tylenol (as prescription) - one bonus is it doesn't make me extra-woozey.

I've learned to be very very careful with OTC pain relievers! I'm also a huge fan of hot baths, heating pads, and microwaved hull pillows. And massage; it sounds a bit silly but foot and hand reflexology have been helpful to me.

My digestive pain decreased dramatically, although it didn't go away, about 6 weeks into gluten-free. I'm also pretty careful about eating to digest foods, more so than I was before dx, which has helped.

Good luck!


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



Celiac.com Sponsor (A8-M):



Karen B. Explorer

I use enteric coated aspirin (very sparingly) or Naproxen (even more sparingly) for pain. I'd be very cautious about taking oral pain medication for abdominal pain because of the risk that the area hurting is also the area having to metabolize the pain killer. Taking aspirin for a bleeding ulcer is about the worst thing you can do and can become life threatening very quickly.

When they thought I had colon cancer, they wouldn't let me take anything for the severe back pain I was experiencing (due to sciatica, due to undiagnosed Celiac) until they had gone in with an EGD and colonoscopy and ruled out colon cancer.

If the drug your doc suggests works but causes constipation, can you approach it from the angle of treating the side effects? i.e. taking a stool softener (not a laxative)? The problem with a lot of pain drugs is that they slow down the lower bowel track and the longer fecal material sits there, the more moisture gets pulled out and the more hardened and compacted it becomes. A stool softener is an old fashioned approach and docs don't usually think of it because they are OTC, cheap and don't have pharm. reps pushing them at every visit. I look for docusate calcium, but I've been told docusate sodium works well too.

You may want to ask your doc about using something like this with the drug already prescribed.

melmak5 Contributor

Thank you to you all. I have been "grinning" through it all and not taking any otc meds, until yesterday when I broke down and took Tylenol. (I spend 2 hours in so much pain that only laying flat on the floor was tolerable.)

New dr. today prescribed a different antispasmatic, and since I am battling a crazy amount of D, I think the "side effects" will be a welcome relief at this point.

They are also going to do a colonoscopy to make sure there isn't something else going on.

Thanks again.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,951
    • Most Online (within 30 mins)
      7,748

    SY8
    Newest Member
    SY8
    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

    • 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
    • DebJ14
×
×
  • 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.