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Guest celiacbuzzroom

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Discovery Rookie
I FOUND THIS............I WILL TRY THIS (VITAMIN E)

IN MY CASE, I HARDLY WALK.

Case of the Month

Reversible inflammatory and vacuolar myopathy with vitamin E deficiency in celiac disease

Kleopas A. Kleopa, MD, Kyriacos Kyriacou, PhD, Eleni Zamba-Papanicolaou, MD, Theodoros Kyriakides, FRCP

Department of Clinical Neurosciences,

Cyprus Institute of Neurology and Genetics,

P.O. Box 23462, Nicosia, Cyprus

Department of Electron Microscopy and Molecular Pathology, Cyprus Institute of Neurology and Genetics, Nicosia, Cyprus

email: Theodoros Kyriakides (Open Original Shared Link)

*Correspondence to Theodoros Kyriakides, Department of Clinical Neurosciences, Cyprus Institute of Neurology and Genetics, P.O. Box 23462, Nicosia, Cyprus

setDOI("ADOI=10.1002/mus.20144")

Keywords

anti-gliadin antibodies • ataxia • gluten enteropathy • inclusion-body myopathy • malabsorption • neuropathy

Abstract

We report a patient with late-onset celiac disease and neurological manifestations including myopathy, polyneuropathy, and ataxia.

Laboratory investigations showed anti-gliadin antibodies and severe vitamin E deficiency.

Muscle biopsy revealed inflammatory infiltrates and rimmed vacuoles, similar to those found in inclusion-body myositis.

A gluten-free diet and vitamin E supplementation reversed both the clinical neurological manifestations and the abnormalities in the muscle biopsy.

Anti-gliadin antibodies were no longer present.

This case illustrates the spectrum of neurological complications of celiac disease and documents the occurrence of reversible pathology resembling inclusion-body myopathy in the muscle. Muscle Nerve 2004

===================================================

Let's cut the chase for those who are suffering and let them see who has helped you in your State.

I am In Salem, Or. and this Neurologist below helped me before any MD would.

Dr. Benton Davidson

Salem, Oregon

He tested for Vitamin K.

I had 2 years with my MD who would not do any testing.

I slipped hehind his back and got to this Neurologist.

Bye

THANK YOU THANK YOU THANK YOU! This is WONDERFUL information. :):):)


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  • Replies 113
  • Created
  • Last Reply
Discovery Rookie

Does anyone know of a GOOD doctor in Glendale, CA?? I have been to more quacks than ever imagined, from HMOs to out-of-pocket docs...I finally ordered all lab tests on my own and am waiting for package to come in the mail. I have cut out the middle-man (doctor) in that regard, but would still like a GOOD one to help me on my lone journey....I am doctor, patient, nutritionist and insurance company (payer) and this disease is in the ring with me, how the heck am I gonna get through this? My dad had ALL the symptoms I have and he was never diagnosed and died in his 70's from colon cancer...poor man, so much suffering.

thank you for listening, really gotta get this out somehow, because don't have a friend in sight that is going thru any of this strife.

:P

JulesH Rookie

I just want to recommend my doctor, Dr. Bill Kirsh, in Miami, FL. He's not a celiac expert or anything, but he's excellent at diagnostics. My whole family goes to him, and he always goes above and beyond what other doctors do. Never takes the easy way out when coming up with a diagnosis.

He actually works with Dr. Agatson, the South Beach Diet guy, but I would definitely consider Dr. Kirsh the better doctor in the practice, at least in bedside manner. Agatson never has any idea who you are or what your history is without looking at his chart a million times. Kirsh actually remembers you and your family and everything.

He was also happy to run vitamin deficiency tests when I had an eye issue and the opthamologist decided I was vitamin B deficient. (I wasn't, but I was vitamin D deficient.)

  • 1 month later...
mumseyh Rookie

My sister needs a doctor in the Detroit area who accepts HAP insurance. She has not been diagnosed yet, but has many symptoms like mine. She would prefer someone out of St. Mary's or Henry Ford Hospital. Any suggestions? I have not lived there in many years so I am not familiar with anyone. Thanks

itchygirl Newbie
No help here in North Carolina...still trying to seek a DR. who cares enough to do some research. <_<

I can't help you with North Carolina but if you'd care to hop over to South Carolina everybody at MUSC Digestive Disease Center has been great

Open Original Shared Link

My primary doc recently retired but if you call you should find someone sensible :)

Their diet sheet is kind of amusing. Oh look, you can eat a dead fish! :lol:

Open Original Shared Link

Nobody actually gave me this, however, I just found it online just now.

Puddy Explorer

Does anyone know of a doctor in Nassau County on Long Island, NY? Thanks. (I'll even take somone in western Suffolk County.)

Dennis wayne Newbie
Dr. Kristie Gering

Chippewa Falls, WI

She's fantastic.

i believe that the name under that quote is Raoul Duke. :rolleyes::)


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Guest mjhere
I FOUND THIS............I WILL TRY THIS (VITAMIN E)

IN MY CASE, I HARDLY WALK.

Case of the Month

Reversible inflammatory and vacuolar myopathy with vitamin E deficiency in celiac disease

Kleopas A. Kleopa, MD, Kyriacos Kyriacou, PhD, Eleni Zamba-Papanicolaou, MD, Theodoros Kyriakides, FRCP

Department of Clinical Neurosciences,

Cyprus Institute of Neurology and Genetics,

P.O. Box 23462, Nicosia, Cyprus

Department of Electron Microscopy and Molecular Pathology, Cyprus Institute of Neurology and Genetics, Nicosia, Cyprus

email: Theodoros Kyriakides (Open Original Shared Link)

*Correspondence to Theodoros Kyriakides, Department of Clinical Neurosciences, Cyprus Institute of Neurology and Genetics, P.O. Box 23462, Nicosia, Cyprus

setDOI("ADOI=10.1002/mus.20144")

Keywords

anti-gliadin antibodies • ataxia • gluten enteropathy • inclusion-body myopathy • malabsorption • neuropathy

Abstract

We report a patient with late-onset celiac disease and neurological manifestations including myopathy, polyneuropathy, and ataxia.

Laboratory investigations showed anti-gliadin antibodies and severe vitamin E deficiency.

Muscle biopsy revealed inflammatory infiltrates and rimmed vacuoles, similar to those found in inclusion-body myositis.

A gluten-free diet and vitamin E supplementation reversed both the clinical neurological manifestations and the abnormalities in the muscle biopsy.

Anti-gliadin antibodies were no longer present.

This case illustrates the spectrum of neurological complications of celiac disease and documents the occurrence of reversible pathology resembling inclusion-body myopathy in the muscle. Muscle Nerve 2004

===================================================

Let's cut the chase for those who are suffering and let them see who has helped you in your State.

I am In Salem, Or. and this Neurologist below helped me before any MD would.

Dr. Benton Davidson

Salem, Oregon

He tested for Vitamin K.

I had 2 years with my MD who would not do any testing.

I slipped hehind his back and got to this Neurologist.

Bye

Guest mjhere

I had an appointment with Dr Benten Davidson, and had to cancel because I was so sick. Reading your report on his knowledge of celiac, I am going to make another appointment, as my md isnt doing anything. could you please email me and let me know how it helped,..Mary mjhere

hapy4dolphins Contributor

Dr.Safwan Malas, MD

1200 E. Michigan Ave

Suite 460

Lansing MI 48906

ph 517-364-5490

A peds. gastro doc. Very familiar with celiac and food allergies. He came to speak at our group last year and my son just saw him last week.

  • 4 weeks later...
rick-spiff Rookie

Jon Mundall

preventitave medicine

conell,wa and visits vancouver, wa

Open Original Shared Link

Virginia Frazer

ND/Midwife

Kennewick, wa/grandview, or

dr. mundall has been my mom's dr since early 90's. virginia delivered my babies and is our only dr. we went in for allergy tests and the gluten was very high so we were diagnosed very easily. both listen to all questions and are very good!! Highly recommended!!

  • 10 months later...
pljahr Newbie

Do you have Inclusion Body Myositis?

babinsky Apprentice

Dr. Yen Lai

Pomona, California

I was her first Celiac case, but she refused to give up until she found out what was wrong with me....she knew I was very sick, just didn't know what it was. Since my diagnosis she has been trying to research the disease and she told me last time I was in that she now tests all patients with "suspect symptoms" I wish all doctors were as caring and concerned!

Donna

mimommy Contributor

Dr. Truding, Pediatric GI

Royal Oak Beaumont Hospital

Royal Oak, Michigan

Thank you, thank you, thank you Dr. Truding!

Country Girl Newbie

Dr. Elizabeth Schaeffer with St. Vincent Hospital in Indianapolis is fabulous pediatric GI doctor. She even spent an half-hour on the phone with me on a Sunday b/c I had questions

  • 3 weeks later...
diannalynn0711 Rookie

Hi,

I'm new to the forum. I am hoping that someone can help me. I have recently decided to move to the northwest part of ohio. I moved from Pittsburgh, Pa. I can not drive the 6 hours to get to my doc back home that was excellent with celiac. Is there any chance that anyone knows of a doc that has some knowledge of celiac in the toledo, fort wayne, lima area? I would appreciate any information anyone has. I have tried so many doctors in this area and it seems that I know more than they do and I'm tired of having to tell them what is what and what to do rather than them knowing. :(

Thanks

mindiloo Rookie

Dr. Murdocco

360 Kingstown Rd

Narragansett, RI 02882

401 789 0226

He has Celiac himself and was the first person, after six years of tests and "I don't know"s from other doctors, to even consider the possibility of Celiac. He's awesome, understanding, and really nice.

diannalynn0711 Rookie
Dr. Murdocco

360 Kingstown Rd

Narragansett, RI 02882

401 789 0226

He has Celiac himself and was the first person, after six years of tests and "I don't know"s from other doctors, to even consider the possibility of Celiac. He's awesome, understanding, and really nice.

I am in Ohio.... RI isnt close to me :( Toledo, oh Lima, oh and fort wayne, in are an hour away from me..... I'm hoping to find a doctor within an hour or so of me.

jaime1103 Rookie

Central New Jersey

Dr. Armen Simonian

416 Bellevue Ave

Mercer Gastroenterology

Trenton, NJ 08618

Highly recommended!

  • 3 weeks later...
SLB5757 Enthusiast
Hi,

I'm new to the forum. I am hoping that someone can help me. I have recently decided to move to the northwest part of ohio. I moved from Pittsburgh, Pa. I can not drive the 6 hours to get to my doc back home that was excellent with celiac. Is there any chance that anyone knows of a doc that has some knowledge of celiac in the toledo, fort wayne, lima area? I would appreciate any information anyone has. I have tried so many doctors in this area and it seems that I know more than they do and I'm tired of having to tell them what is what and what to do rather than them knowing. :(

Thanks

If you find anyone in this area, or get any responses PLEASE let me know. I am almost 100% sure that Celiac is what I have and cannot get anyone to do testing:( Even though having a wheat allergy come up positive, the primary care doc here states that I cannot have Celiac because it is a malabsorption disease and I am gaining weight. He said back when I was 92 lbs. two years ago they would have considered it, but now that I am 105 it couldn't be malabsorption?? I have always been small and I do not feel my weight has any bearing on whether I have Celiac or not. The docs just want to write me off as IBS...and I am not accepting it. Ughhh....Ohio docs :(

diannalynn0711 Rookie
If you find anyone in this area, or get any responses PLEASE let me know. I am almost 100% sure that Celiac is what I have and cannot get anyone to do testing:( Even though having a wheat allergy come up positive, the primary care doc here states that I cannot have Celiac because it is a malabsorption disease and I am gaining weight. He said back when I was 92 lbs. two years ago they would have considered it, but now that I am 105 it couldn't be malabsorption?? I have always been small and I do not feel my weight has any bearing on whether I have Celiac or not. The docs just want to write me off as IBS...and I am not accepting it. Ughhh....Ohio docs :(

Well I haven't been able to find a specialist. The closest I found was in Chicago... but i found a Nurse Practitioner in Defiance Hospital off Sessions St that is willing to do tests and learn and she is looking for a specialist for me. She is really awesome! Id recommend her as a primary doctor, but for anything that involves scopes she would have to refer you to a specialist. One thing though, are you still eating gluten? The test will not help if you have cut gluten out of your system you must continue on gluten. But she would definitely run the tests if you went to her (if your eating gluten). Also I was small until this year I wasn't able to gain any weight at all and I'm going on 6 years of gluten-free. IBS kinda comes with the disease for most, I have it and some other issues like a lot of others on the board. Does anyone else in your family have the disease? That's another thing I'd look at. The disease killed my grandmother because it went undiagnosed. My mother does not have the disease, but I do. If your still on gluten you will need a GI to do scopes and a biopsy. But if you have cut wheat out of your diet and are doing fine, I'd say its a wheat allergy then... You can have a wheat allergy and not be Celiac. I'm not sure about the weight thing, mine was so bad that it almost killed me so I was a severe case. You might wanna post a separate topic about the weight loss/gain issue and see what their experiences are.

The Nurse Practitioner that I am seeing is Carolyn Badenhop, CNP.

1250 Ralston Ave., Suite 204

Defiance, OH 43512

419-782-8332

Good luck and let me know if you need anything else. Ive found a lot of info for the area that may help.

diannalynn

Crystalkd Contributor

I love my internist Dr. Steven Patten in Tucker GA (Right out side of Atlanta.) I started going to him after I had all my testing and it came back inconclusive. After going through the whole thing he told me no matter what the test results said that it didn't mean I didn't have celiac or an allergy so NOT to ever eat gluten agian. I have Cerebral Palsy and when I come in with a complaint he always investigates. He never makes me feel like I'm crazy. He's the one that found the fibro and in looking at sleep tests my old neourologist had done relized I had a sleep problem that needed treatment so after a total of 14 years of complaints to various docs he's the one putting it all together! I'm so thankful to him!! My family and I believe he saved my life. I was in pretty bad shape by the time I got to him!!

Also Dr. Mark Stern might be worth a try. He's the GI that suggested celiac in the first place. Even though the tests came back inconclusive he was suppotive of the gluten-free diet if I was feeling better and not losing weight any more.

I need a little help though! Anyone know of a good celiac specialist in the Atlanta area that will be willing to talk to me even if I refuse to go back on a gluten diet to re run the tests. I've been to a couple who wanted me to go back on the diet so they could retest or told me "we don't think you'll have to stay gluten-free for ever."

caek-is-a-lie Explorer

I've had a lot of luck with the NCNM Community Clinics in Portland, OR. It's relatively inexpensive and they listen and really work with me:

National College of Natural Medicine

Open Original Shared Link

For appointments: (503) 552-1515

frecOregon Newbie

gastroenterologist Dr. Alan Kaynard 503 297 8081 near St. Vincent's in Beaverton, Oregon

I sure wish I'd known him when I was diagnosed 7 years ago! He is patient, listens well, and answers odd questions very respectfully. He did all the followup blood/nutritional type tests that my former gastroenterologist (who sent a letter telling me I had celiac) SHOULD have done.

Skysammy Newbie

I am new to this group and conversations. Not sure I am even typing in the right place ;) .

I live in Gilbert,AZ and was diagnosed with Celiac Disease at age 50 - 8 years ago. And still struggling to maintain a gluten free diet and stay healthy. more on that topic at a later date. But I am looking for doctors in the area that are more aware of Celiac and base their treatments with that knowledge.

Is Dr. Shimamoto, San Tan Allergy and Asthma "Celiac aware"? I have developed more intense allergies in the last few years and struggle to get through our high pollen seasons - which I believe are now 365 days a year. Are you recommending this doctor because he/she is a great Allergist and of the knowledge level of Celiac?

Thank you for your response.

Sam

***ARIZONA***

Dr. Shimamoto, SanTan Allergy and Asthma, Mesa (or Gilbert?), Arizona -- This is the single best doctor I have ever known! All 3 of our kids are being treated by him. He is the most down-to-earth, easy-going, yet extremely knowledgeable person you'd ever meet. My kids love going to him and the 35 minute drive to his office is so worth it. I would probably drive 2 hours to go to this guy if I had to...just can't say enough. It took 7 months and 4 doctors to make even a slight dent in my youngest son's issues. I had more answers in my first visit with this doctor than I did with all the rest put together.

Dr. Nancy Yokois, Pediatric GI, Scottsdale, AZ -- We've only been to her once. She was patient, extremely thorough, answered all our questions, very knowledgeable of celiac and eosinophilic disorders. No one can compare to Dr. Shimamoto, but she does come in a close second and I would highly recommend. She came highly recommended to us by several different people and it's easy to see why once you meet her.

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    • 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!
    • Jmartes71
      I have been diagnosed with celiac in 1994, in remission not eating wheat and other foods not to consume  my household eats wheat.I have diagnosed sibo, hernia ibs, high blood pressure, menopause, chronic fatigue just to name a few oh yes and Barrett's esophagus which i forgot, I currently have bumps in back of my throat, one Dr stated we all have bumps in the back of our throat.Im in pain.Standford specialist really dismissed me and now im really in limbo and trying to get properly cared for.I found a new gi and new pcp but its still a mess and medical is making it look like im a disability chaser when Im actively not well I look and feel horrible and its adding anxiety and depression more so.Im angery my condition is affecting me and its being down played 
    • marion wheaton
      Wondering if anyone knows whether Lindt chocolate balls are gluten free. The Lindt Canadian website says yes but the Lindt USA website says no. The information is a bit confusing.
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