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

Any Celiacs Who Have Chronic Tailbone Pain?


fraggle

Recommended Posts

fraggle Newbie

Just wondering if any celiacs here have tailbone and sacroilliac problems?

I have had these for 7 years and since that time have had problems with gluten.


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



Celiac.com Sponsor (A8-M):



tarnalberry Community Regular

yep, but it looks to be structural, based on the MRI, so I don't think - in my case - it's necessarily connected.

GFdoc Apprentice

I had chronic problems with sacroileitis (~20 years on and off) that has virtually disappeared with the gluten-free diet (I use this as proof for me that the diet is worth it!- what a huge improvement in my life to not have back pain) :D

Sara

armymom3 Newbie

I have had "tail bone" issues for around 1 to 2 years now. My sacrum is off center and have problems lying on my back. In fact, sleeping is very painful anyway. I was diagnosed with mild diffuse osteoporosis which I believe was due to malabsorption of calcium due to Celiac. Chiropractic care has helped somewhat and I have not been gluten-free for too long so I can't see any improvement in that arena yet.

I'm hoping for something to change soon, though.

Leslie

tarnalberry Community Regular

armymom - have you been to PT? my problem is very similar, with my sacrum tending to stick on the right and causing a lot of pain on the left, but the PT I saw (and I know that not that many PT's can properly treat sacrum and tailbone issues) was able to help get in unstuck and give me appropriate exercises to allow the muscles to be strengthened and keep the sacrum in place better.

plantime Contributor

I have pain in my right sacroiliac, but it was caused by a car accident in '96. I'm afraid being gluten-free does not have any effect on injuries!

GinEva Newbie

Hi:

I, too, have had sacroilliac pain, on and off, for past year. Also getting shoulder pain (2 yrs) and knees are popping and grinding (1 yr). Could my heal pain also be due to not enough calcaum? Not only was I a Celiac baby but also born with an incomplete stomach lining. Couldn't have whole milk till I was 6 yrs old. Mom said she had to raise me on steak and banannas.

My painful knees drove me to search for a reason and I found the link to being a Celiac. Mom said it was only a childhood condition. But, with the help and information from this site, I've gone back to my "baby diet" and have left all forms of wheat behind.

It's been 2 months and much has improved, but I find I can't do too much work that will stress my bones and muscles. So don't try to push a grocery cart and then go home and mow the lawn. My sacroilliac is killing me today!


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



Celiac.com Sponsor (A8-M):



Guest gillian502

I have had debilitating SI Joint and now tailbone area pain and tightness for 2 years. I've never been given an adequate explanation as to why. I've tried chiropractic care and 3 months of PT plus ultrasound therapy applied directly to the SI Joint on both sides, as well as being injected with prednisone into the Si Joint, and nothing has improved. I've been gluten-free for 10 months now, also with no improvement to the back issues. My drs. have suggested it may be related to the celiac disease or my Colitis, but I have no clue. It's the most disabling part of my sickness by far. If anyone has any other ideas for treatment other than what I've mentioned, I'd love to hear it! I've seen an Orthopedist, and at this point I'm wondering if it'd help to go to a different type of specialist for this problem but wouldn't know where to start!

  • 4 years later...
dekefish Newbie

YES!!

and after about 2-3 weeks of zero gluten, my sacrum finally relaxes and the pain starts to subside. It feels like it's created a lot of major postural problems as well as weak back muscles. Stay away from sugar too!

Blessings Explorer

I have been fighting aches and pains for the last 15 years. At one time they thought it was fibromyalgia but not enough trigger points. In 1997, 2000, 2003, 2005, and then in 2007 I would go in for xrays test scopes nothing was ever found. Finally this March I was diagnosed with Celiac, April with Crohns and May with Spondylitis from the Crohns. Spondylitis is a form of artheritis that fuses the SI joint together. I think this may be part of my numbness. We'll see. It is very painful. You know how you feel after working in the yard all day. That's how I wake up in the am. I have started the Humira shot and am still waiting for it to kick in. A few nights ago I went to bed in so much pain, then at 5 am I had to wake up my hubby just to tell him "I have no pain!" It was a wonderful miracle and lasted for a little while. It comes and goes but usually is worse when I am still for a while. They found it through xray and then mri. I pray motrin can take your pain away.

God bless,

Vicky

purple Community Regular

My dd has had tailbone pain for over 7 years and only this year we found she was gluten intolerant. She fell when sledding so we always thought that's what caused it. She has had minor symptoms for years...could be gluten is causing it. Thanks for posting.

mftnchn Explorer
I have had debilitating SI Joint and now tailbone area pain and tightness for 2 years. I've never been given an adequate explanation as to why. I've tried chiropractic care and 3 months of PT plus ultrasound therapy applied directly to the SI Joint on both sides, as well as being injected with prednisone into the Si Joint, and nothing has improved. I've been gluten-free for 10 months now, also with no improvement to the back issues. My drs. have suggested it may be related to the celiac disease or my Colitis, but I have no clue. It's the most disabling part of my sickness by far. If anyone has any other ideas for treatment other than what I've mentioned, I'd love to hear it! I've seen an Orthopedist, and at this point I'm wondering if it'd help to go to a different type of specialist for this problem but wouldn't know where to start!

You might check out the lyme disease thread on this forum. I have pain too but it really seems related to lyme disease, even though the fatigue and brain fog seems to be both celiac and lyme related.

mftnchn Explorer
I have been fighting aches and pains for the last 15 years. At one time they thought it was fibromyalgia but not enough trigger points. In 1997, 2000, 2003, 2005, and then in 2007 I would go in for xrays test scopes nothing was ever found. Finally this March I was diagnosed with Celiac, April with Crohns and May with Spondylitis from the Crohns. Spondylitis is a form of artheritis that fuses the SI joint together. I think this may be part of my numbness. We'll see. It is very painful. You know how you feel after working in the yard all day. That's how I wake up in the am. I have started the Humira shot and am still waiting for it to kick in. A few nights ago I went to bed in so much pain, then at 5 am I had to wake up my hubby just to tell him "I have no pain!" It was a wonderful miracle and lasted for a little while. It comes and goes but usually is worse when I am still for a while. They found it through xray and then mri. I pray motrin can take your pain away.

God bless,

Vicky

Sure sounds like you need to rule out lyme disease....

frec Contributor

I've had SI joint pain for 6 years. It started with a herniated disk that wouldn't heal. The disk and the celiac were diagnosed the same week. In my case I think all those years of malabsorption--I have other allergies, and it took a while to figure them out--slowed down my healing. This year my back is hugely better because of a series of prolotherapy and PRP (platelet rich plasma) shots to strengthen the tendons, ligaments and cartilage in the SI joints. There are lots of sites on the Internet about both. I can sit for the first time in six years!

Candy Contributor

Yeah,my backside hurts regularly,but I'm not sure what to do about it.I thought it has something to do with malabsorption of Calcium,or vitamin B. If I take more Co-enzyme Vitamin B Complex,it seems to subside a little,but I heard/felt my hip grinding too,and I thought ,"Oh no, I hope my hip doesn't break Off-I have enough problems".

1grnthmb Newbie

I also have sacroilitis and Spondylitis the latter I was told was connected to the celiac disease ( the doctor said that is why I developed it when it is not something in my family history) which both cause tail bone pain that seems to come and go as the inflammation comes and goes. Mine has not been reduced by being on the gluten free diet. I think because the damage was done before I was diagnosed with Celiac Disease. I was diagnosed with the sacroilitis in 1994 before I was diagnosed with the Celiac Disease. I was not diagnosed with the Spondylitis untill 1999 but was told I had suffered from it for at least twenty years before being diagnosed.

GermanMia Newbie

I was very surprised to read this... Yes, I also have chronic pain in the tailbone. Sometimes not very much, but sometimes so violent a pain that I can barely sit. It didn't get better after eating gluten-free, but on the other hand my gastro-intestinal problems didn't get better either. Now that I think about it, I think that there is a relation between the violence of the intestinal problems and that pain. A friend of mine is a doctor of osteopathic medicine and he treated the tailbone pain several times; it brought some release, but no healing.

Amber M Explorer
My dd has had tailbone pain for over 7 years and only this year we found she was gluten intolerant. She fell when sledding so we always thought that's what caused it. She has had minor symptoms for years...could be gluten is causing it. Thanks for posting.

I can't believe it. I have had tail bone problems all lower back problems (fused last 2 vert. naturally). They never knew why. Said it might have been conj. I get up every day with a horrible back ache. Had a Bone Density yesterday and the Tech. said there is a problem in the lower area and suggested Thyroid panel and Back Exray. Haven't gotten the full results yet.(on the bone density) Every area I read on this site seems to sound like my life story! Wow. Thanks All.

  • 5 months later...
dekefish Newbie

wow i can't believe i found other people with these issues. i am a year into being gluten free and it feels like my stomach has finally relaxed and gotten small enough that my tailbone and sacrum have finally opened up. i was having to take massive medications and be super inactive and I am just praying that I can re-strengthen and hold my joints together as go through my day! this has been a profound change, and finding my own cranial-sacral adjustments has helped infinitely more than a 'professional' could have. the sacral bone controls so much of your nervous system's input, my vision and mental energy have changed a ton, i'm getting feeling back in my back, and i'm finally able to breathe into my muscles to relax them. truly amazing.

  • 5 months later...
knowurgluten Rookie

I have tailbone pain too. I know this is an older thread, but I just wanted to see if anyone else had it that could help.

I was doing situps on a hard floor a couple of months ago. I had lost weight and my butt sagged so much I can feel my tailbone sticking out. It hurts to sit and throbs at times even at rest or standing.

Anyone else get relief from gluten-free diet?

jkr Apprentice

I started having tail bone problems about 3 years ago - I only have known about my celiac for about 1 year, but looking back I think I've had celiac since I was five. I had a back x-ray and it showed arthritis in my tail bone. Is that the same as spondylitis? Anyway the tail bone pain started after I had horrible constipation. I have read the pressure from straining can cause tail bone pain.

The pain lasted about a year. Anti-inflammatory meds helped so I don't know if the celiac had anything to do with it.

It was so painful to get up from a sitting position.

knowurgluten Rookie
I started having tail bone problems about 3 years ago - I only have known about my celiac for about 1 year, but looking back I think I've had celiac since I was five. I had a back x-ray and it showed arthritis in my tail bone. Is that the same as spondylitis? Anyway the tail bone pain started after I had horrible constipation. I have read the pressure from straining can cause tail bone pain.

The pain lasted about a year. Anti-inflammatory meds helped so I don't know if the celiac had anything to do with it.

It was so painful to get up from a sitting position.

Have you tried more magnesium and less calcium to see if that helps? Just curious.

jkr Apprentice
Have you tried more magnesium and less calcium to see if that helps? Just curious.

No I haven't but I have been thinking about taking magnesium after reading lots of posts. I only take a multi-vitamin that has magnesium (200 mg) but I think I need to take more magnesium. What brand do you recommend?

Thanks

noglut4me Newbie
No I haven't but I have been thinking about taking magnesium after reading lots of posts. I only take a multi-vitamin that has magnesium (200 mg) but I think I need to take more magnesium. What brand do you recommend?

Thanks

I am taking the "Now" brand Magnesium citrate powder

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,869
    • Most Online (within 30 mins)
      7,748

    Stacy W
    Newest Member
    Stacy W
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      I totally get this. It's absolutely a grieving process, and it's okay to feel gutted about the loss of those simple joys, especially at 18. Your feelings are completely valid—it's not about being ungrateful for your amazing boyfriend, it's about mourning the life you thought you'd have. That "tortured by the smell" feeling is so real. It does get easier, I promise, but it's okay to sit in the sadness and just vent about how much it stings right now. Thanks for sharing that. Celiac.com has published a book on our site by Jean Duane PhD called Gluten-Centric Culture, which covers many of the social aspects of having celiac disease: This chapter in particular covers issues around eating with family and others - Gluten-Centric Culture: Chapter 5 - Grabbing A Bite Together:    
    • Scott Adams
      Many of us with celiac find that the fillers in medications can cause a reaction, and sometimes our bodies just process things weirdly. That "rebound muscle pain" and "burning feet" you described sounds awful and is a huge red flag. It's frustrating enough managing the diet without medication causing setbacks. So sorry you're dealing with this, but you're definitely on the right track by connecting the dots. You can search this site for prescriptions medications, but will need to know the manufacturer/maker if there is more than one, especially if you use a generic version of the medication: To see the ingredients you will need to click on the correct version of the medication and maker in the results, then scroll down to "Ingredients and Appearance" and click it, and then look at "Inactive Ingredients," as any gluten ingredients would likely appear there, rather than in the Active Ingredients area. https://dailymed.nlm.nih.gov/dailymed/   
    • Scott Adams
      It's so tough when you're doing everything right and still get hit with it. I'm glad you're figuring out a system that works for you—the peppermint tea and rehydration powders are smart moves. It sounds like you've really learned to listen to your body, and that's half the battle. Sticking to simple, safe food at home is the best way to build yourself back up. It's great you can take the time to rest properly. Thanks for sharing what works; it's a big help to others figuring this out too. This article, and the comments below it, may be helpful:    
    • Scott Adams
      I am so sorry you're going through this. It's bad enough to fight for a diagnosis and manage this disease, but to have your partner use it as a weapon against you is truly devastating. What you're describing isn't just a lack of support; it's abuse, full stop. Controlling your food and money is cruel, and his pleasure in your misery is chilling. Please hear this: the kindness from that woman at the food pantry is what you deserve. It's a glimpse of the real world, where people care. You deserve to eat, to heal, and to have peace. His actions are the biggest barrier to your health right now, and you are not broken—you are surviving in an impossible situation. Don't give up on that lifeline you've found.
    • Colleen H
      Thank you.. Christina My anxiety is through the roof.  I think it was from eggs.  I really don't know because my eyes feel sore. Like I'm allergic to them.  I was defient in B12.   My heart is pounding and it won't stop.  Not sure what to do.   I don't have much support other than this forum.    Colleen 
×
×
  • 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.