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

In Defense Of 20 Parts Per Million


psawyer

Recommended Posts

psawyer Proficient
Open Original Shared Link from Alessio Fasano, MD, of the University of Maryland Medical School's Center for Celiac Research regarding gluten-free labeling.

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



Celiac.com Sponsor (A8-M):



  • Replies 69
  • Created
  • Last Reply
Skylark Collaborator

Grrrr.... Time to write the FDA again. Stupid clinical trials studying a self-selected less sensitive population...

pricklypear1971 Community Regular

Grrrr.... Time to write the FDA again. Stupid clinical trials studying a self-selected less sensitive population...

I'm going to state flat-out I haven't read the above link....

But one study synopsis I read about wheat processed to remove the gluten really ticked me off. I don't remember the exact numbers but since a statistically insignificant number of celiacs were intolerant of the de-glutened wheat product it was deemed safe and non-reactive.

That kinda made me mad.

psawyer Proficient

I'm going to state flat-out I haven't read the above link....

Perhaps it would be a good idea to actually read Dr Fasano's writings before condemning them.

mushroom Proficient

Perhaps there is another way for the FDA to proceed. I know, it involves more label-reading for celiacs, but what celiac person doesn't read labels anyway :rolleyes: . If a company is going to test anyway, maybe they can label what their testing reveals and let the consumer decide whether they want to buy it or not :blink:

pricklypear1971 Community Regular

Perhaps it would be a good idea to actually read Dr Fasano's writings before condemning them.

I wasn't commenting on the letter. Besides, the letter correlated exactly with what I was discussing. So far

everything I've read "in defense of 20 ppm" says the same thing. Nothing new in his letter. The point is that the defense is almost always based on two things - that it works for most and it's prohibitively expensive to want to reach for lower ppm levels.

That's great for everyone else but not for people who are super sensitive. The hard part is there may not ever be a processed food or product that is safe for super gluten sensitives. Sometimes it's hard to find whole foods that are safe, especially since super sensitivity usually in involves more than one sensitivity, not just gluten (pesticides, waxes, preservatives).

These are just hard facts to face when you struggle to EAT. Kind of gives me a new perspective on things, considering celiacs apparentlyrun this risk, the longer we are gluten-free.

psawyer Proficient

I wasn't commenting on the letter.

Then why did you post here? This topic is about Dr Fasano's letter.


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



Celiac.com Sponsor (A8-M):



pricklypear1971 Community Regular

Then why did you post here? This topic is about Dr Fasano's letter.

Because it fits. Dr. Fasano's letter is based in part on scientific studies like the one I mentioned. A statistically insignificant number of people have a problem with 10 ppm. That's fine and dandy unless it's YOU they are talking about, then it becomes amazingly important.

It also adds insult to injury that Dr. Fasano is a leader in celiac research. While I can appreciate his stance, and am not surprised, I do understand the anger and potential problems this causes for those with opposing views.

Jestgar Rising Star

That's great for everyone else but not for people who are super sensitive. The hard part is there may not ever be a processed food or product that is safe for super gluten sensitives.

I guess I don't see why you (anyone) needs to eat processed food. Instead of stressing about what some packaged food tests at, why not just make all your own meals from whole foods? It's a different lifestyle, yes, but so much healthier for a lot of reasons.

pricklypear1971 Community Regular

I guess I don't see why you (anyone) needs to eat processed food. Instead of stressing about what some packaged food tests at, why not just make all your own meals from whole foods? It's a different lifestyle, yes, but so much healthier for a lot of reasons.

Because with today's lifestyle - work, travel, etc. that consistently takes people away from home it is almost impossible to not encounter processed food.

I'm sure we've all encountered something like this when trying to order a simple salad. Order lettuce, tomatoes and receive dressing all over it or croutons or cheese..,. Processed food just seems to magically appear.

As gluten free restaurants and options become more common people with sensitivities will have more options. And quite a few of them will have processed elements to

them.

Ironically, I find quite a bit of ready-made gluten-free food out there at gluten-free friendly restaurants. It seems to be "safer" for them to serve. And they have a point. It prevents cc, I'm sure.

Jestgar Rising Star

Because with today's lifestyle - work, travel, etc. that consistently takes people away from home it is almost impossible to not encounter processed food.

I'm sure we've all encountered something like this when trying to order a simple salad. Order lettuce, tomatoes and receive dressing all over it or croutons or cheese..,. Processed food just seems to magically appear.

I guess I don't get this. I manage to bring or store my own food for just about everything. Eating out is a choice, not a convenience. Even when traveling I buy whole foods and eat them raw, for the most part. I just skip the stuff that needs cooking.

pricklypear1971 Community Regular

I guess I don't get this. I manage to bring or store my own food for just about everything. Eating out is a choice, not a convenience. Even when traveling I buy whole foods and eat them raw, for the most part. I just skip the stuff that needs cooking.

It isn't that easy with business affairs. Especially when you have no control over the venue and you are away from home, in a different hotel room every night.

Jestgar Rising Star

It isn't that easy with business affairs. Especially when you have no control over the venue and you are away from home, in a different hotel room every night.

I don't travel for business, so I don't have that perspective, but I imagine that I could come up with a solution, if I really had too. Maybe not. I know when I backpack in other countries I hit the market for fresh veggies, and if I'm in a US city with no food, my first choice is the grocery store, not a restaurant. Meals with clients, I suppose, could be an issue.

pricklypear1971 Community Regular

I guess I don't get this. I manage to bring or store my own food for just about everything. Eating out is a choice, not a convenience. Even when traveling I buy whole foods and eat them raw, for the most part. I just skip the stuff that needs cooking.

I admit, fast food restaurants now are grocery stores. At least that's how I look at it.

It's difficult to be in a work situation - a 4 hour dinner meeting, at a nicecrestaurant in front if executives and whip out your own raw food. At least consistently... Then to

be running out the door into a car for a 2 hour drive to another hotel that may or may not have a kitchenette you requested. Up at 5 to make a breakfast meeting where you probably won't be able to eat the food - and you're running out of food because you couldn't get to a store last night or that morning because none were open en route.

It's exhausting, no?

So, this is the long route around but to make psawyer happy - Celiacs count on being able to find edible, safe food. If you aren't supersensitive you stand a decent chance. While Dr. Fasano's opinion may be conducive to supply, it Is supportive of a food supply that is unsafe for a number if sensitive individuals.

Personally, I'm more supportive of labeling that lists ingredients and derivatives, and tells what kind of facility it was manufactured in. For foods to be gluten free, they should be just that. Gluten free. Does that mean less gluten free labeled foods? Yes. That doesn't mean "no gluten ingredients" along with facility info won't work for most. Tested to 10 ppm is even better. Gluten free is the cherry on top.

weluvgators Explorer

I guess I don't see why you (anyone) needs to eat processed food. Instead of stressing about what some packaged food tests at, why not just make all your own meals from whole foods? It's a different lifestyle, yes, but so much healthier for a lot of reasons.

This can be incredibly problematic. As a celiac mother of three celiac kids, that is ALOT of food prep! SOMEBODY has to process the food that we eat, even if it is just washing it. Usually some additional form of processing is desireable for a fair chunk of it too, even if it is just cutting, dicing, grating it. And if you are a family with two working parents, trying to manage ALL of your own food processing - WOW - please share all of the tips and tricks that you have found to work. While I aspire for my kids to pull more of their own weight in food sourcing, processing and prep - they remain very young and are not yet skilled to do "their fair share" of this work.

And then there are the school issues. Schools want very much for you to be able to provide processed foods for your children. We need to maintain a shelf stable supply of food and drink at the school for unexpected events. There are several instances during the school year when processed foods really are a more reasonable answer to the school's requests. And I am simply overlooking the idea that celiac children deserve equal opportunity in our schools, including free and reduced breakfast and lunch. It simply isn't safe for my kids, and I leave it at that. But not every celiac child has that luxury of declining free/reduced food from school, and the schools rely very much on processed foods - how many pounds of processed food would a celiac child eating from our schools eat in a given day?

From Dr. Fasano's letter:

The three-month trial showed that a daily intake of 10 mg of gluten (that, translated in ppms, would be equivalent to the daily ingestion of more than a pound of gluten free products containing 20 ppm of gluten!) for three months by adults with celiac disease caused no intestinal damage.

And what concerns me about this is that it can be quite easy to eat a pound of "gluten free" food when looking at some celiac populations. What about celiac teenage boys? Don't they deserve adequate protection? What about a celiac family with three teenage boys?

And it goes well beyond "processed food"! Have you tried finding truly gluten free grains? So is our "gluten free" grain supply going to be "safe" at 20 PPM too? Now how easy is it to eat more than a pound of "gluten free" food on a daily basis?

So, really, what is wrong with at least aiming for 10 PPM (seems to be working well for GFCO certification, a gluten intolerant population recommendation! and only for now, as I truly think <5 ppm, and lower, is in the best interests of ALL celiacs) in our testing and giving more of these populations the ability to safely eat 2 pounds of "gluten free" food in a day??

For reference, I found that humans typically eat 3-5 pounds of food each day.

Skylark Collaborator

You all are missing the biggest problem. Only volunteers enter clinical trials. If you're super-sensitive, there is no incentive Faesano's clinic could offer that would make you participate in a trial where you eat 10 mg of gluten a day. They are probably paying on the order of $100-$150 to compensate people for the discomfort of being scoped. That means the study group is what we call "self selected". They are people who don't expect to get sick from the 10 mg of gluten. Even worse for the data, clinical trial participants are allowed to drop the trial at any time for any reason. Someone who feels ill after a couple days will simply drop and forego the cash.

This is an absolute necessity to run human trials fairly and safely, but it means the data from a trial like these gluten challenges is not necessarily a representative sample of celiacs.

pricklypear1971 Community Regular

You all are missing the biggest problem. Only volunteers enter clinical trials. If you're super-sensitive, there is no incentive Faesano's clinic could offer that would make you participate in a trial where you eat 10 mg of gluten a day. They are probably paying on the order of $100-$150 to compensate people for the discomfort of being scoped. That means the study group is what we call "self selected". They are people who don't expect to get sick from the 10 mg of gluten. Even worse for the data, clinical trial participants are allowed to drop the trial at any time for any reason. Someone who feels ill after a couple days will simply drop and forego the cash.

This is an absolute necessity to run human trials fairly and safely, but it means the data from a trial like these gluten challenges is not necessarily a representative sample of

celiacs.

I agree, this is a potential problem. However, I haven't read his methodology.

T.H. Community Regular

I thought some of the points about testing and 20 ppm that this couple made were pretty pertinent to the subject, actually.

Open Original Shared Link

They're knowledgeable about testing, and have some good points on the limitations. Their ideas made more sense to me than Fasano's, in part because while they acknowledge the financial and testing limitations, their proposal was that, at the very least, the FDA make a label that ensures ALL celiac's safety.

As a gluten free label's only purpose is the safety of people who react to gluten, that doesn't seem unreasonable to me.

Considering the statistics on unhealed celiacs, super-sensitives are not the only ones who seem to be getting sick on a 20 ppm diet. Maybe for different reasons (eating too many gluten-free products vs. eating them at all, at a guess), but it's still an issue.

So the above couple proposes to not call a food gluten free if it's not. Let us know the ppm, let us know it's safe for most celiacs, if need be, even. But at least that way, all celiacs have the opportunity to stay safe.

Yes, Fasano is a celiac expert. He's the one who got people to look at the biopsy as the gold standard for celiac diagnosis, which was great. He's also the one who, after more research, is trying to get the changed, because he's admitted he was incorrect.

I hope that a few years from now, he's going to have the same reaction to his pushing for a 20 ppm standard as safe and desirable. Because I've contacted his research center before and asked about any information they have on sensitive celiacs, or on unhealed celiacs trying a lower than 20 ppm diet, and I was told that the studies I was inquiring about didn't exist, to their knowledge.

With no studies on less ppm than this, how can any expert claim that they've investigated it fully, enough to make it a national standard?

Skylark Collaborator

I agree, this is a potential problem. However, I haven't read his methodology.

It is a problem with every clinical trial that has ever been run. Period. There is no way to both do ethical research AND get a truly representative sample of people.

Jestgar Rising Star

I guess I don't see why you need a label to choose your food. For the majority of people, the 20ppm will work. Most won't react, some won't care. For those that do react at that level, would you believe a lower level stamp anyway? Wouldn't you make your choices based on previous experience with that food?

Has your experience with government labeling been so good that you believe companies wouldn't find a way to skirt the truth even with proper testing? You could add water to something to get it below the acceptable threshold, or dust it with sugar or something.

And even if it's completely legit and accurate, your dose totally depends on how much you eat. You can take the "gluten-free" label as 20ppm and only eat 1/4 of the serving size. Now you've ingested the same amount of gluten as you would have had you eaten something tested at 5ppm. For how many of you would this work?

Ultimately, your health is up to you. It doesn't really matter what a company puts on a box.

sariesue Explorer

I think that there is a need for a testing standard because than it can be enforced and universally applied to products. And if there is a standard you can still make the decision to not eat/buy a product. Just like it is now only it would be safer for a majority of people. If the super sensitive population want's their needs to be met than they need to sign up for clinical studies. You can't expect that your exact needs to be met if you won't volunteer to be part of a study. Plus, many people who are considered super sensitive have allergies or intolerances with other food which makes a national standard useless because even if the product was completely gluten-free they'd still have to look for other ingredients. Personally, I'd like to be able to look at a package and know that the gluten free label means that it was tested to a specific standard, not the companies best guess that they don't use gluten so their product should be gluten free.

For those who complain that it's too difficult for them to have food based meetings or to travel for business, use the American with Disabilities Act to get the accommodations that you need like that your meetings not be food based, that you can only travel for 2 night in a row, or that you need access to a grocery store during your stay and a room with a kitchenette. Plus keep a jar of peanut butter and some gluten-free pretzels and keep them in your bag. That way you always have a high protein snack regardless of what's around you.

Gemini Experienced

I guess I don't see why you need a label to choose your food. For the majority of people, the 20ppm will work. Most won't react, some won't care. For those that do react at that level, would you believe a lower level stamp anyway? Wouldn't you make your choices based on previous experience with that food?

Has your experience with government labeling been so good that you believe companies wouldn't find a way to skirt the truth even with proper testing? You could add water to something to get it below the acceptable threshold, or dust it with sugar or something.

And even if it's completely legit and accurate, your dose totally depends on how much you eat. You can take the "gluten-free" label as 20ppm and only eat 1/4 of the serving size. Now you've ingested the same amount of gluten as you would have had you eaten something tested at 5ppm. For how many of you would this work?

Ultimately, your health is up to you. It doesn't really matter what a company puts on a box.

This is a very good point and one I pretty much follow. If you eat a diet based heavily on whole foods and use gluten-free treats and baked goods as such...a treat and not part of your daily diet, then you should not have a problem. All this obsession with ppm doesn't mean you will be eating a completely gluten-free diet...but there is no way to prove that anyway. Super sensitivity usually means other food intolerances also so many times it's a guess to try and figure it out.

I find I cannot eat the vast majority of items made in shared facilities. So I pretty much stick with stuff from dedicated facilities and have never been glutened from one and I am a fairly sensitive, full blown Celiac who has healed well. I eat a mostly whole foods diet with treats thrown in and this has worked very well for the majority of Celiacs I know. Some will take longer to heal, that's pretty normal. If you are that sensitive, why would

this suggested standard bother you? You probably don't eat the stuff anyway. Most companies worth their salt test to a certain standard, and yes, it can vary, but most Celiacs do just fine with that. If you are unsure of a product or have become ill from it, don't eat it again.

All I know is I have found certain staples like bread that are quite good and don't want them to cost $20.00 per loaf. I have never become ill from the bread and have no doubt if there is any gluten in it, it's well below what this standard would be or I'd get sick. I trust what my body tells me and don't heavily rely on what the package says other than "dedicated facility". The same would apply when I make my own bread...if the flours come from dedicated facilities and I have zero reaction from it, it's not something I worry about.

Scott Adams Grand Master

There is a lot more scientific research posted on this site about this topic at:

https://www.celiac.com/categories/Gluten%252dFree-Diet%2C-Celiac-Disease-%26-Codex-Alimentarius-Wheat-Starch/

The problem with a lower level, say 5ppm, is that many companies will no longer put "gluten-free" on their labels due to the vastly increased liability factor, and the huge expense of trying to maintain such levels in all batches. While the idea of being more strict sounds like it would make you more safe--this might not actually be the case. More strict could mean less choice and more cost.

I am aware of at least one manufacturer who have already removed "gluten-free" from their labels due to the new 5ppm Canadian laws. Their products haven't changed a bit, and are still gluten-free according to the 20ppm standard and they regularly test below 5ppm, however, they occasionally get a batch that is slightly above 5ppm. Such a test would, under current Canadian standards, set of a nationwide recall of their products, the cost of which could put them out of business.

Additionally, it is my understanding (correct me if I am wrong here), that Schar products are not available in Canada. I have heard that if you contact them they will tell you it is because they don't have French/English labels, however, I suspect that the 5ppm regulation might be the real culprit.

In any case, the "zero tolerance" position expressed by some on this board and in the celiac community would actually backfire and create less choices, and more expensive products. Additionally I doubt the super-sensitive folks would eat them anyway, as they could contain up to 5ppm...right?

Take care,

Scott

jerseyangel Proficient

This is a very good point and one I pretty much follow. If you eat a diet based heavily on whole foods and use gluten-free treats and baked goods as such...a treat and not part of your daily diet, then you should not have a problem. All this obsession with ppm doesn't mean you will be eating a completely gluten-free diet...but there is no way to prove that anyway. Super sensitivity usually means other food intolerances also so many times it's a guess to try and figure it out.

I find I cannot eat the vast majority of items made in shared facilities. So I pretty much stick with stuff from dedicated facilities and have never been glutened from one and I am a fairly sensitive, full blown Celiac who has healed well. I eat a mostly whole foods diet with treats thrown in and this has worked very well for the majority of Celiacs I know. Some will take longer to heal, that's pretty normal. If you are that sensitive, why would

this suggested standard bother you? You probably don't eat the stuff anyway. Most companies worth their salt test to a certain standard, and yes, it can vary, but most Celiacs do just fine with that. If you are unsure of a product or have become ill from it, don't eat it again.

All I know is I have found certain staples like bread that are quite good and don't want them to cost $20.00 per loaf. I have never become ill from the bread and have no doubt if there is any gluten in it, it's well below what this standard would be or I'd get sick. I trust what my body tells me and don't heavily rely on what the package says other than "dedicated facility". The same would apply when I make my own bread...if the flours come from dedicated facilities and I have zero reaction from it, it's not something I worry about.

I agree. I'm very sensitive and find that I do best to start with whole foods and make meals from scratch. I do use some mixes and flours from dedicated facilities (for treats as well) and find it works very well for me.

Skylark Collaborator

What I'd like to see is the 10 ppm standard as applied by GFCO. I get sick from Amy's, who is putatively manufacturing to 20 ppm. I have never gotten sick from a GFCO certified food, and plenty of companies seem perfectly capable of manufacturing to those standards. I told the FDA this, and am praying they'll listen.

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. - Jmartes71 replied to Jmartes71's topic in Related Issues & Disorders
      16

      My only proof

    2. - Dakota01 commented on Scott Adams's article in Winter 2026 Issue
      1

      Are Gluten-Free Processed Foods Making You Sick? (+Video)

    3. - JoJo0611 posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      0

      Awaiting Biopsy results

    4. - cristiana replied to emzie's topic in Related Issues & Disorders
      1

      Stomach hurts with movement


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,455
    • Most Online (within 30 mins)
      7,748

    Suelle
    Newest Member
    Suelle
    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

    • Jmartes71
      Doterra is a life saver and yes I feel like im waiting because Im getting yes you are celiac, no your not celiac. Im so FRUSTRATED, exhausted and tired of explaining to medical why I feel this way.Im stressed because my body isn't feeling well.Yes I am and no it's not just a food allergy as downplayed with doctors Ive seen.I even went to the " celiac  specialist " Dr Fernandez-Becker who down played my ailments and stated im not and then yes I am I even had one her " care team" ask my why do you want that diagnosis. UNMMMMM. I don't want it, its been my life confirmed in 1994.Menopause intensified extra sensitivity and medical has down played my sibo, ibs, CELIAC, now im having skin and eye issues. I thought help was available but its been a complete medical disaster. 
    • JoJo0611
      I have had my endoscopy this morning with biopsies. My consultant said that it looked like I did have coeliac disease from what he could see. I now have to wait 3 weeks for the biopsy results. Do I continue eating gluten till my follow appointment in three weeks.  
    • cristiana
      Hi @emzie and welcome to the forum. Perhaps could be residual inflammation and bloating that is causing sensitivity in that area.  I was diagnosed with coeliac disease in 2013 and I remember some years ago my sister telling me around that time that she had a lady in her church, also a coeliac, who  had real pain when she turned her torso in a certain direction whilst doing exercises, but otherwise was responding well to the gluten-free diet. As far as I know is still the picture of health. I often end up with pain in various parts of my gut if I eat too much rich food or certain types of fibre (for some reasons walnuts make my gut hurt, and rice cakes!) and and as a rule, the pain usually hangs around for a number of days, maybe up to a week.   When I bend over or turn, I can feel it.  I think this is actually due to my other diagnosis of IBS, for years I thought I had a rumbling appendix but I think it must have just been IBS.  Reading the experiences of other sufferers, it seems quite typical.  Sensitized gut, build up of gas - it stands to reason that the extra pressure of turning can increase the pain. When I am glutened I get a burning, gnawing pain in my stomach on and off for some days - it isn't constant, but it can take up a few hours of the day.  I believe this to be gastritis, but it seems to hurt irrespective of movement.   Anyway, you are doing the right thing to seek a professional opinion, though, so do let us know how you get on.   Meanwhile, might I suggest you drink peppermint tea, or try slices of fresh ginger in hot water? A lot of IBS sufferers say the former is very helpful in relieving cramps, etc, and the latter is very soothing on the stomach. Cristiana
    • emzie
      Hi! One of the usual symptoms I have with a gluten flare up has deviated a bit and I thought I'd search for advice/opinions here. Also to see if anyone goes through similar stuff. Monday all of a sudden I got really bad pain in my stomach (centre, right under the chest, where the duodenum would be located). I ended up having to throw up for 2 hours, my body was trying to get rid of something from all sides and it was just horrible. Since then I havent been nauseous anymore at all, but the pain has stayed and it always worsens the moment i start moving. The more I move the more it hurts, and when i rest longer it seems to dissapear (no movement). I've had this before, but years ago I think around when I first got diagnosed with coeliac, where each time I moved, my stomach would hurt, to the point where I went to the ER because doctors got freaked out. That only lasted 1 night though, and Now it's already wednesday, so 3 days since then, but the pain persists and remains leveled. it doesn't get crazy intense, but it's still uncomfortable to the point I cant really go out because Im afraid itll turn into a giant flare up again. I couldn't think of where I could possibly have been glutened at this bad of a level and why it hasn't passed yet. I went to the GP, and as long as I have no fever and the pain isnt insane then its fine which I havent had yet. Tomorrow im also seeing a gastroenterologist specialized in IBS and coeliac for the first time finally in years, but I thought I'd ask on here anyway because it still hasnt dissapeared. It also hurts when someone presses on it. Maybe it's just really inflamed/irritated. I'm just frustrated because I'm missing out on my uni lectures and I do a sports bachelor, so I can't get behind on stuff & next to that i'm also going to go to the beach with my boyfriend's family this weekend: ( 
    • Flash1970
      Hi. So sorry to hear about your shingles. There is a lidocaine cream that you can get at Walmart that will help numb the pain.  That's what I used for mine. It can't be put near your eyes or in your ears. I hope your doctor gave you valacyclovir which is an antiviral.  It does lessen the symptoms. If it is in your eyes,  see an ophthalmologist.  They have an antiviral eye drop that can be prescribed.  Shingles in the eye could cause blindness.  I was unsure whether you have celiac or not.  If you do,  follow the diet.  I believe that extra stress on your body does affect everything. Shingles can recur. If you start getting the warning signs of nerves tingling,  see the dr and start taking the valacyclovir to prevent a breakout. If I sound technical,  I am a retired pharmacist. 
×
×
  • 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.