Jump to content
  • 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):

Zoinks celiac , fibromyalgia, "big pill to swallow"


Awol cast iron stomach

Recommended Posts

Awol cast iron stomach Experienced

After my crash and burn gluten challenge of 2016, I wander off yet again Into the land of eastern and alternative medicine to heal. While I am grateful to many (not all) western medicine  Dr s of the past , for the past 2 decades the ones who give me relief for my lifetime ails are the alternative/eastern practitioners. I'm not starting a debate as both branches have their strengths, often the shame is they are seperated in healthcare, for likely humanity and public health imo would be best served by their encouraged collaboration/mutual recognition,but alas not my problem to solve. Much bigger then me and quite frankly, I'm too busy healing to tackle that mountain.

Regardless, I now have "shoes that fit my carpet bag " of decades of multiple misdiagnosis /undiagnosis collection. They can be combined and labeled celiac and fibromyalgia.

I was shocked at first at the news, I consider those really serious. Is AWOL really that ill? I've read up more  on both disciplines descriptons etc for these conditions, I'm in shock for the "shoes" fit perfectly . I know based on western test results I'm far from textbook/ gold standard celiac (but I failed to get past day 6 of my gluten challenge -likely speaks for itself) and fibromyalgia is quite demeaned/dismissed from my past knowledge amongst the western medicine world and greater society. (Friends /family in western medical fields) Is this still the case?

My lifetime gi issues, the 30 plus years multiple chemical sensitivities ( go back to childhood-I keep very close to the vest), 20 plus years symptoms of muscle issues / myalgia, now have the names of celiac & fibromyalgia. Mixture of feelings of relief to be recognized, but also knowing my named illnesses are likely not recognized or are minimised by my western medicine trained family and friends and greater society.

Can anyone offer some encouragement to help me cope at this time of healing? My accupuncture visits have been truly helpful, but my last visit is giving me a lot to process chemically, biologically, and spiritually. It's like someone unleashed the flood gates of all the symptoms of both illnesses at once in a combined package for me to experience in a one transparent package.  Very enlightening and to be blunt I feel like crap. So it's time to accept the package names and all, the curtain was lifted and the waxing and waning symptoms of fibromyalgia we're released.

Please share any positive support or stories you have on coping with celiac recovery, celiac/fibromyalgia, and  healing by accupuncture. It will be much appreciated. As it is abundantly clear AWOL is here to stay on the celiac.com forums.

Thanks

 


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



Celiac.com Sponsor (A8-M):



RMJ Mentor

I'm glad you have a diagnosis.  Fibromyalgia is recognized by western medicine, FDA has even approved several drugs for its treatment.  This article from the NIH is interesting, saying that not all doctors are familiar with it ( those are probably the ones who minimize it).   I hope your health improves now that you know what you have and can begin to do something for it.

Open Original Shared Link

ravenwoodglass Mentor

Now you know and can continue on the path to healing. I did acupuncture before I was finally diagnosed. It helped  a bit even still eating gluten. I have liverdo reticularis that was very pronounced prediagnosis. I was basically purple. It amazed me that when I would get done with an acupuncture session my skin would be a normal color. Natually when I went home and ate I would again turn purple.  I would also get a small amount of relief from pain. Keep at your sessions and you may want to look for a book on acupressure.  I found that to be helpful and easy to do.

I was also considered to have fibro but mine was relieved after I had been gluten and soy free for a few months. I hope that is the case for you also.

Stay strong things will get better.

Awol cast iron stomach Experienced

Thank you RMJ. It is helpful to hear kind/ encouraging words.

From my symptoms I likely have had (undiagnosed) fibromyalgia for over 20 years, my celiac (misdiagnosed as IBS I likely had longer) 

Additionally, in 2016 I was diagnosed with Barrett s esophagus and multiple food intolerance s as well as gluten being an issue.

Thanks for the link for the info, although for this stage of my life I'm hoping to manage it non pharmaceutical, but it is good to get the details. 

Thanks again

Awol

Awol cast iron stomach Experienced
6 hours ago, ravenwoodglass said:

Now you know and can continue on the path to healing. I did acupuncture before I was finally diagnosed. It helped  a bit even still eating gluten. I have liverdo reticularis that was very pronounced prediagnosis. I was basically purple. It amazed me that when I would get done with an acupuncture session my skin would be a normal color. Natually when I went home and ate I would again turn purple.  I would also get a small amount of relief from pain. Keep at your sessions and you may want to look for a book on acupressure.  I found that to be helpful and easy to do.

I was also considered to have fibro but mine was relieved after I had been gluten and soy free for a few months. I hope that is the case for you also.

Stay strong things will get better.

Thanks Ravenswood. I need the strength and encouragement to keep going. The last sessions fall out was 4 days of my body revolting on a nervous system level. 

I'll look into your acupressure book suggestion. I have done sinus acupressure for myself and my daughter for years but did not explore more. 

In the past when gluten-free my fibromyalgia symptoms improved but since they come back the concern is it might be actual fibromyalgia. 

After 2016 I found out I have Barrett s esophagus, fibromyalgia, additional food intolerance plus the gluten. I had in my head I was ncgs and it was all related to  that and leaky gut that occurred after my challenge., So I wasn't prepared to digest all the above. Pun intended.

Thanks for the encouragement

Awol

knitty kitty Grand Master

Awol, 

Be encouraged!  There are things that will help! 

I found this article about nutrition and Berrett's esophagus.  

Open Original Shared Link

"The existing epidemiological evidence is strongest for an inverse relationship between intake of vitamin C, β-carotene, fruits and vegetables, particularly raw fruits and vegetables and dark-green, leafy and cruciferous vegetables, carbohydrates, fiber and iron and the risk of esophageal adenocarcinoma, and to a lesser degree, Barrett’s esophagus."

An inverse relationship is like a seesaw.  The more of one thing (the heavy end of the seesaw on the ground) means less of the other (the end of the seesaw in the air).  So, more fresh veggies means less symptoms.   

After a lifetime of a hodgepodge of problems, I found I benefited greatly by eating unprocessed foods and correcting vitamin deficiencies.  Celiac Disease causes malabsorption which results in malnutrition.  Celiacs often have low vitamins A, D, E and B Complex vitamins.  Sometimes the deficiencies are overlooked by physicians.  They don't recognize deficiency symptoms.  They don't value the importance of vitamins to one's health.

Here's another article about a B vitamin, a form called P5P, that helped me.  

Open Original Shared Link

Hope this helps on our journey to health.

 

 

 

Awol cast iron stomach Experienced
On 5/30/2017 at 11:57 AM, knitty kitty said:

Awol, 

Be encouraged!  There are things that will help! 

I found this article about nutrition and Berrett's esophagus.  

Open Original Shared Link

"The existing epidemiological evidence is strongest for an inverse relationship between intake of vitamin C, β-carotene, fruits and vegetables, particularly raw fruits and vegetables and dark-green, leafy and cruciferous vegetables, carbohydrates, fiber and iron and the risk of esophageal adenocarcinoma, and to a lesser degree, Barrett’s esophagus."

An inverse relationship is like a seesaw.  The more of one thing (the heavy end of the seesaw on the ground) means less of the other (the end of the seesaw in the air).  So, more fresh veggies means less symptoms.   

After a lifetime of a hodgepodge of problems, I found I benefited greatly by eating unprocessed foods and correcting vitamin deficiencies.  Celiac Disease causes malabsorption which results in malnutrition.  Celiacs often have low vitamins A, D, E and B Complex vitamins.  Sometimes the deficiencies are overlooked by physicians.  They don't recognize deficiency symptoms.  They don't value the importance of vitamins to one's health.

Here's another article about a B vitamin, a form called P5P, that helped me.  

Open Original Shared Link

Hope this helps on our journey to health.

Hi knitty kitty,

Thanks for the info. I completely shocked the Dr s from the Barrett s finding for I do not fit the profile nor had symptoms . It was only found during my endoscopy following gluten challenge. I will focus more on the nutritional areas you mentioned based on your link,  which is great come summer gardening wise  me luck . I bought many to grow from the group's you mentioned additionally I actually believe I crave them.

Thanks for the details on the common vitamin deficiencies my challenge unfortunately is finding products that are corn free. It's everywhere. Those darn fillers, binding agents etc. I am awaiting another response from my inquiry from a manufacturer  regarding sourcing they are quite as slow which does not appear promising. I was diagnosed with a vitamin d deficency 4 1/2 years ago but they have never tested the others you mentioned as you predicted. I do know that I know b' s seem important to  me particularly during my   m. cycle .

Thanks again.

 

 

 


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



Celiac.com Sponsor (A8-M):



Archived

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

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

    • Total Members
      134,108
    • Most Online (within 30 mins)
      10,442

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

    • Total Topics
      121.7k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • Wheatwacked
      Chronic fatigue in the producer was the inspiration for the episode but I feel it touches on anyone that suffers and is dismissed as psycosomatic. The patient expressed my feelings elequently.  In episode 2 the doctor explains the problem well. I stopped all commercial milk protein like skim milk added to processed foods and in a few days there was a definate improvement in my  gut, bowel movements, discomfort etc. Still drinking several glasses of Pasture Fed grass fed milk with no negative effects.   Specifically, for myself Clonidine is the only medication that lowers my BP and the doctor did not renew it, insisting that I continue Losartan.  I think that she thinks I am abusing Clonidine and the reason the Losartan doesn't work is because I am non-compliant.  Absolutely not. Surprisingly after a few days withdrawal from the Clonidine my fasting blood sugar has gotten under control.  Fasting blood sugar near normal instead of over 160.  Last few days its been below 100.  I still need Glimiperide.  Without the clonidine my pulse rate is around 100 bpm, with it around 60.   Prescription of angiotensin receptor blockers in celiac disease is associated with persistent symptoms and surrogate markers of malabsorption.  https://pmc.ncbi.nlm.nih.gov/articles/PMC12323722/ Angiotensin receptor blocker-associated enteropathy (ARB-e) is an increasingly recognised clinical entity with symptoms and histological findings identical to coeliac disease (celiac disease). There is evidence to suggest immune-mediated mucosal injury in ARB-e with a high prevalence of DQ2/DQ8; however, as IgA anti-tissue transglutaminase (anti-TTG) is usually negative   https://onlinelibrary.wiley.com/doi/full/10.1002/ueg2.12117 NEW research [Nov 2024] presented at the American College of Gastroenterology (ACG) Annual Scientific Meeting suggests that angiotensin receptor blockers (ARBs), a class of drugs commonly used to manage hypertension, may be associated with poorer outcomes in patients with coeliac disease. Findings indicated that patients taking ARBs had a higher likelihood of experiencing persistent symptoms and markers of poor small bowel healing, such as anaemia and iron deficiency.  https://www.emjreviews.com/en-us/amj/gastroenterology/news/angiotensin-receptor-blockers-may-worsen-coeliac-disease-outcomes/
    • mermaidluver22
      @BarcinoHi! I am so sorry abt your son but also relieved to know I am not alone! My ttg iga is still mildly elevated but going down. Last time we checked I had some small erosions in my ileum but recently got an MRE that showed no inflammation. Calpro 70. We are still in limbo but we are taking a conservative approach as well. Please keep me updated about his situation and outcomes! I always love to hear others opinions/experiences especially ibd specialists. 
    • Scott Adams
      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:    
    • BelleDeJour
      Oh, thank you all so so much! I have found my people.   ❤️ I am so sorry that we have all suffered with this torturous itching and resulting sore skin. Sue, I can relate to what you wrote about the dark thoughts, I have had them, too. It's very tough and painful.  I have now had a 2 day straight run of only minor itching. I woke up this morning and did not want to get out of bed because it is the first time in months that I have felt comfortable and actually been able to appreciate the lovely feeling of the duvet on my skin, rather than just waking in pain and thinking about where I need to put cream on before I dress for work. If I can continue like this, then I think I could manage without medication but every time I say this, I then have a flare up. I plan to be very careful about what I eat over the weekend and it won't be easy as we are out with friends for dinner on Saturday (the pub do have very good gluten-free options, I checked of course!).  I really, REALLY appreciate your words so much and am so glad to have found this forum. I am going to read the articles kindly posted now, thank you Scott.
    • Scott Adams
      I don’t know how common this is with celiac disease specifically, but significant inflammation, weight changes, aging, genetics, and skin elasticity can all play a role. It may be worth talking with both your doctor and a board-certified dermatologist or plastic surgeon to see what options are realistic, from skin-tightening treatments to surgical approaches, while also making sure there isn’t ongoing inflammation, thyroid imbalance, or nutritional deficiency contributing. You deserve support for both the physical and emotional side of this.
×
×
  • Create New...