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

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.

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Mari replied to Jmartes71's topic in Related Issues & Disorders
      15

      My only proof

    2. - Rejoicephd commented on Jefferson Adams's article in Gluten-Free Cooking
      1

      Your Complete Gluten-Free Thanksgiving Plan: Recipes, Tips & Holiday Favorites

    3. - marion wheaton replied to marion wheaton's topic in Gluten-Free Foods, Products, Shopping & Medications
      3

      Are Lindt chocolate balls gluten free?

    4. - trents replied to marion wheaton's topic in Gluten-Free Foods, Products, Shopping & Medications
      3

      Are Lindt chocolate balls gluten free?


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,422
    • Most Online (within 30 mins)
      7,748

    HAUS
    Newest Member
    HAUS
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • Mari
      Years  ago a friend and I drove north into Canada hoping to find a ski resort open in late spring,We were in my VW and found a small ski area near a small town and started up this gravelled road up a mountain. We  got about halfway up and got stuck in the mud. We tried everything we could think of but an hour later we were still stuck. Finally a pickup came down the road, laughed at our situation, then pulled the VW free of the mud. We followed him back to the ski area where where he started up the rope ski lift and we had an enjoyable hour of skiing and gave us a shot of aquavit  before we left.It was a great rescue.  In some ways this reminds me of your situation. You are waiting for a rescue and you have chosen medical practitioners to do it now or as soon as possible. As you have found out the med. experts have not learned how to help you. You face years of continuing to feel horrible, frustrated searching for your rescuer to save you. You can break away from from this pattern of thinking and you have begun breaking  away by using some herbs and supplements from doTerra. Now you can start trying some of the suggestions thatother Celiacs have written to your original posts.  You live with other people who eat gluten foods. Cross contamination is very possible. Are you sure that their food is completely separate from their food. It  is not only the gluten grains you need to avoid (wheat, barley, rye) but possibly oats, cows milk also. Whenever you fall back into that angry and frustrated way of thinking get up and walk around for a whild. You will learn ways to break that way of thinking about your problems.  Best wishes for your future. May you enjpy a better life.  
    • marion wheaton
      Thanks for responding. I researched further and Lindt Lindor chocolate balls do contain barely malt powder which contains gluten. I was surprised at all of the conflicting information I found when I checked online.
    • trents
      @BlessedinBoston, it is possible that in Canada the product in question is formulated differently than in the USA or at least processed in in a facility that precludes cross contamination. I assume from your user name that you are in the USA. And it is also possible that the product meets the FDA requirement of not more than 20ppm of gluten but you are a super sensitive celiac for whom that standard is insufficient. 
    • BlessedinBoston
      No,Lindt is not gluten free no matter what they say on their website. I found out the hard way when I was newly diagnosed in 2000. At that time the Lindt truffles were just becoming popular and were only sold in small specialty shops at the mall. You couldn't buy them in any stores like today and I was obsessed with them 😁. Took me a while to get around to checking them and was heartbroken when I saw they were absolutely not gluten free 😔. Felt the same when I realized Twizzlers weren't either. Took me a while to get my diet on order after being diagnosed. I was diagnosed with small bowel non Hodgkins lymphoma at the same time. So it was a very stressful time to say the least. Hope this helps 😁.
    • knitty kitty
      @Jmartes71, I understand your frustration and anger.  I've been in a similar situation where no doctor took me seriously, accused me of making things up, and eventually sent me home to suffer alone.   My doctors did not recognize nutritional deficiencies.  Doctors are trained in medical learning institutions that are funded by pharmaceutical companies.  They are taught which medications cover up which symptoms.  Doctors are required to take twenty  hours of nutritional education in seven years of medical training.  (They can earn nine hours in Nutrition by taking a three day weekend seminar.)  They are taught nutritional deficiencies are passe' and don't happen in our well fed Western society any more.  In Celiac Disease, the autoimmune response and inflammation affects the absorption of ALL the essential vitamins and minerals.  Correcting nutritional deficiencies caused by malabsorption is essential!  I begged my doctor to check my Vitamin D level, which he did only after making sure my insurance would cover it.  When my Vitamin D came back extremely low, my doctor was very surprised, but refused to test for further nutritional deficiencies because he "couldn't make money prescribing vitamins.". I believe it was beyond his knowledge, so he blamed me for making stuff up, and stormed out of the exam room.  I had studied Nutrition before earning a degree in Microbiology.  I switched because I was curious what vitamins from our food were doing in our bodies.  Vitamins are substances that our bodies cannot manufacture, so we must ingest them every day.  Without them, our bodies cannot manufacture life sustaining enzymes and we sicken and die.   At home alone, I could feel myself dying.  It's an unnerving feeling, to say the least, and, so, with nothing left to lose, I relied in my education in nutrition.  My symptoms of Thiamine deficiency were the worst, so I began taking high dose Thiamine.  I had health improvement within an hour.  It was magical.  I continued taking high dose thiamine with a B Complex, magnesium. and other essential nutrients.  The health improvements continued for months.  High doses of thiamine are required to correct a thiamine deficiency because thiamine affects every cell and mitochondria in our bodies.    A twenty percent increase in dietary thiamine causes an eighty percent increase in brain function.  The cerebellum of the brain is most affected.  The cerebellum controls things we don't have to consciously have to think about, like digestion, balance, breathing, blood pressure, heart rate, hormone regulation, and many more.  Thiamine is absorbed from the digestive tract and sent to the most important organs like the brain and the heart.  This leaves the digestive tract depleted of Thiamine and symptoms of Gastrointestinal Beriberi, a thiamine deficiency localized in the digestive system, begin to appear.  Symptoms of Gastrointestinal Beriberi include anxiety, depression, chronic fatigue, headaches, Gerd, acid reflux, gas, slow stomach emptying, gastroparesis, bloating, diarrhea and/or constipation, incontinence, abdominal pain, IBS,  SIBO, POTS, high blood pressure, heart rate changes like tachycardia, difficulty swallowing, Barrett's Esophagus, peripheral neuropathy, and more. Doctors are only taught about thiamine deficiency in alcoholism and look for the classic triad of symptoms (changes in gait, mental function, and nystagmus) but fail to realize that gastrointestinal symptoms can precede these symptoms by months.  All three classic triad of symptoms only appear in fifteen percent of patients, with most patients being diagnosed with thiamine deficiency post mortem.  I had all three but swore I didn't drink, so I was dismissed as "crazy" and sent home to die basically.   Yes, I understand how frustrating no answers from doctors can be.  I took OTC Thiamine Hydrochloride, and later thiamine in the forms TTFD (tetrahydrofurfuryl disulfide) and Benfotiamine to correct my thiamine deficiency.  I also took magnesium, needed by thiamine to make those life sustaining enzymes.  Thiamine interacts with each of the other B vitamins, so the other B vitamins must be supplemented as well.  Thiamine is safe and nontoxic even in high doses.   A doctor can administer high dose thiamine by IV along with the other B vitamins.  Again, Thiamine is safe and nontoxic even in high doses.  Thiamine should be given if only to rule Gastrointestinal Beriberi out as a cause of your symptoms.  If no improvement, no harm is done. Share the following link with your doctors.  Section Three is especially informative.  They need to be expand their knowledge about Thiamine and nutrition in Celiac Disease.  Ask for an Erythrocyte Transketolace Activity test for thiamine deficiency.  This test is more reliable than a blood test. Thiamine, gastrointestinal beriberi and acetylcholine signaling.  https://pmc.ncbi.nlm.nih.gov/articles/PMC12014454/ Best wishes!
×
×
  • 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.