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Self-diagnosed Celiac


Link

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Link Rookie

Hello everyone:

I have hopefully diagnosed my 10 month battle with (first) bloating, gas; followed by numerous daily episodes of watery diarrhea, weight loss, plus fatigue; then, finally, hip joint pain and leg cramps...plus other symptoms that I'm sure I had just taken in stride. Unfortunately, I don't have medical insurance at present, but, frankly, I'm not sure if I would have put my health in the hands of my PCP because of the lack of knowledge MD's have concerning celiac disease. Anyway, I started myself on a gluten-free diet two weeks ago. I am an RN, and an avid good nutritional advocate, so I do have a good knowledge of the requirements needed to strictly adhere to this diet...including all the ways gluten is "hidden" in various added ingredients. I have been doing all my own cooking so I am sure I have not ingested any gluten for this two-week period. I have not, however, completely cut out dairy products...only limited them.

My guestion/concern is...I am still having watery diarrhea. I know that it will take some time to subside since I did endure 2-3 months of it before starting the diet. But, shouldn't I be noticing some improvement at this point? I'm getting discouraged!!!!!


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YoloGx Rookie

Hi Link,

Welcome to the board!

Maybe at some point as a nurse you could help start a local campaign to help improve the AMA's awareness of celiac? Despite the fact you don't have insurance, there are certain blood tests that are inexpensive that can indicate whether or not you potentially have celiac. I think by Enterolab?? Someone help me here...

At first there is a big learning curve--esp. getting rid of all trace gluten. It is in the most unlikely places. I would even check those disposable gloves they have at hospitals. What kind of powder do they use inside them?? Cetyl alcohol is OK but many other kinds of alcohol are gluten based. Even certain building materials have gluten in them like most pre mixed plasters, Fixall etc.

In addition, anything wooden like old cutting boards and wooden bowls and spoons, need to be replaced since they are so absorbent and will continue to give you "cross contamination" of gluten (CC). Similarly, iron pots either need to be replaced or put through a 600 degree cleaning cycle in your oven to destroy the glutenous residue.

I also had to replace shampoos and soaps as well as toothpaste and dental floss that had gluten in it. Lipstick and other beauty aids usually need to be replaced too. And boyfriends need to brush and floss their teeth (and rinse) before they get kisses from someone who has celiac!

There is a good list here on celiac.com that delineates various glutenous sources that one should avoid.

I have learned its important to always wash my hands before I eat in order to avoid trace gluten from some handshake or doorknob or whatever.

Also do not buy your food from bulk bins since they often are CC'd!

And yes--its very true--the milk products need to cease at least at first until your intestines heal except perhaps for yogurt. The lactose molecules are large and cause digestive disturbance at first in particular. In my case I do better when I make my own whole milk yogurt and let it ferment 24 hours or more in my oven (with just the pilot light on) since then all the lactose has been fermented out of it.

If you continue to have problems with D unabated, consider going off other grains as well and look into other sources of allergy. Many who have celiac develop a kind of "leaky gut" due to the flattened or scarred villi which then makes food sensitivities common. Sugar and various food additives too are often a no no.

Hope this is not overwhelming you! Eventually your dietary choices should improve as you heal.

Meanwhile, hot carob tea sweetened with stevia just might help stop the D for now--that or blackberry or raspberry leaf tea with some (pure unadulterated) cinnamon.... That plus enterically coated acidophilus...

Bea

ang1e0251 Contributor

I still had D for some time after going gluten-free. I had normally formed stools also. It was weird but I was getting trace gluten for some time as I felt my way through the maze. Wish I had found this forum right away! It would be worth a trial completely dairy free to see if that relieves some of the problem. You could have another food sensitivity or it could just be taking extra time for your healing. A food journal would be a good idea while you are figuring it all out.

ksymonds84 Enthusiast

If the D is very watery and hard to control you may want to consider ruling out Microscopic Colitis. Here is an Article from Science Direct (Dr. Peter H.R. Green is a very respected Celiac expert)

An Association Between Microscopic Colitis and Celiac Disease

Peter H.R. Green, Corresponding Author Contact Information, E-mail The Corresponding Author, Jun Yanglow Jianfeng Cheng

Ahorsesoul Enthusiast

Since you've just started going gluten free it might be a good idea to try cutting out the dairy and soy for a while until your intestines are healed. Also you might think you are gluten free but have overlooked something (spices, flavored coffee, gum, root beer). I thought I was doing good until I read this site. I've been nursing since 1974 so I too thought I was more aware. lol Now after being gluten free for years, I'm still learning. Let us know how you are doing.

Some people are also sensitive to the xanthan gum in gluten free products.

https://www.celiac.com/articles/21710/1/Cou...very/Page1.html

Link Rookie
If the D is very watery and hard to control you may want to consider ruling out Microscopic Colitis. Here is an Article from Science Direct (Dr. Peter H.R. Green is a very respected Celiac expert)

An Association Between Microscopic Colitis and Celiac Disease

Peter H.R. Green, Corresponding Author Contact Information, E-mail The Corresponding Author, Jun Yanglow Jianfeng Cheng

Link Rookie
Hi Link,

Welcome to the board!

Maybe at some point as a nurse you could help start a local campaign to help improve the AMA's awareness of celiac? Despite the fact you don't have insurance, there are certain blood tests that are inexpensive that can indicate whether or not you potentially have celiac. I think by Enterolab?? Someone help me here...

At first there is a big learning curve--esp. getting rid of all trace gluten. It is in the most unlikely places. I would even check those disposable gloves they have at hospitals. What kind of powder do they use inside them?? Cetyl alcohol is OK but many other kinds of alcohol are gluten based. Even certain building materials have gluten in them like most pre mixed plasters, Fixall etc.

In addition, anything wooden like old cutting boards and wooden bowls and spoons, need to be replaced since they are so absorbent and will continue to give you "cross contamination" of gluten (CC). Similarly, iron pots either need to be replaced or put through a 600 degree cleaning cycle in your oven to destroy the glutenous residue.

I also had to replace shampoos and soaps as well as toothpaste and dental floss that had gluten in it. Lipstick and other beauty aids usually need to be replaced too. And boyfriends need to brush and floss their teeth (and rinse) before they get kisses from someone who has celiac!

There is a good list here on celiac.com that delineates various glutenous sources that one should avoid.

I have learned its important to always wash my hands before I eat in order to avoid trace gluten from some handshake or doorknob or whatever.

Also do not buy your food from bulk bins since they often are CC'd!

And yes--its very true--the milk products need to cease at least at first until your intestines heal except perhaps for yogurt. The lactose molecules are large and cause digestive disturbance at first in particular. In my case I do better when I make my own whole milk yogurt and let it ferment 24 hours or more in my oven (with just the pilot light on) since then all the lactose has been fermented out of it.

If you continue to have problems with D unabated, consider going off other grains as well and look into other sources of allergy. Many who have celiac develop a kind of "leaky gut" due to the flattened or scarred villi which then makes food sensitivities common. Sugar and various food additives too are often a no no.

Hope this is not overwhelming you! Eventually your dietary choices should improve as you heal.

Meanwhile, hot carob tea sweetened with stevia just might help stop the D for now--that or blackberry or raspberry leaf tea with some (pure unadulterated) cinnamon.... That plus enterically coated acidophilus...

Bea


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YoloGx Rookie

Whereas steroids may be what you need if you do actually have microscopic colitis, it wouldn't be my first choice since the side effects can be dangerous. Plus steroids just cover up symptoms rather than address them directly.

I agree however that the thing to look at here is the damage to the villi. There are non steroid ways to soothe and help heal the villi. Going off all irritating foods is a first of course--especially milk products and possibly for a while all grains and sugars--and only eat cooked vegetables (no raw lettuce etc.).

There are basic herbs however that can also help as well as taking enterically coated acidophilus that agrees with you.

The most useful herbs that I have found are marshmallow root and/or slippery elm (depends on the person). For me the marshmallow root works better--but others depend on the slippery elm. These two herbs are emollient. They soothe and take down inflammation in the intestines and the gut in general. Marshmallow root is also soothing and healing for the kidneys.

Carob, cinnamon, blackberry leaf and raspberry leaf all are good against diarrhea. The carob is nice sweetened with stevia and made into a tea.

Nattokinase, bromelain/papain and/or some other fibronilytic enzymes can help heal and get rid of scar tissue as well as get rid of excess fibrin built up in the heart and veins and the various organs. This is best taken on an empty stomach with a basic general digestive enzyme to balance it out.

I have found plant based enzymes are often good to take with meals to help with better digestion.

Once you feel a little better, it is a good idea to take 1/4 tsp. apple pectin and then when even better, take the pectin mixed in with raw flax seed (start with one tablespoon flax seed a day) ground up in your dedicated coffee grinder (dedicated for just the flax seed). If you put the pectin in the flax and then grind, the pectin will mix with the water better rather than separate into clumps. This is a very mild yet effective bulking agent. I personally cannot tolerate pre mixed varieties since most have gluten in them or some other often irritating agent that doesn't agree with me.

If you still are having problems, I would check to see if you might have some kind of parasites. I you have roundworms, pinworms or giardia for instance you would want to know about it!! Good simple general herbal anti parasitic agents are olive leaf and neem leaf. I like them mixed together. I use them not necessarily against parasites but against fungal overgrowth, bacteria and viruses etc. However both are known to be very good anti parasitics too. Initially however you might get worse for the first 2 to 3 days (the Herxheimer effect). However if you do, then you know its working, so just reduce the dose but stick with it. Ifyou follow this route, be certain to take extra acidlophilus--some hours apart from whatever anti parasitic agent you might be using.

Bea

Link Rookie

Thank you, everyone, for all your ideas and suggestions for my ongoing diarrhea after starting, what I perceived to be, a gluten-free diet two weeks ago.

Several of you felt that I should eliminate dairy and another recommended I try cutting out other grains as well. One of you thought that keeping a food journal would help me to identify any offending food or ingredient. Still another suggested I investigate for possible gluten in flavored coffee or spices or trace gluten in other areas of the kitchen.

Some of you discussed the possibility of cross contamination, while others offered other possible causes such as microscopic colitis, which I have to admit, I have considered. I can't say that I am thrilled at the thought of taking steriods for that.

I appreciate all these suggestions and ideas. I did find the list of foods that may be gluten ladened on celiac.com and I will try the hot carob tea with stevia...if I can find carob tea somewhere!

I appreciate all these suggestions as I face the daunting task of living with celiac disease. I look forward to healing myself and feeling better, and I just MAY undertake the AMA to raise awareness of Celiac Disease when I do!!! :)

Link Rookie
Whereas steroids may be what you need if you do actually have microscopic colitis, it wouldn't be my first choice since the side effects can be dangerous. Plus steroids just cover up symptoms rather than address them directly.

I agree however that the thing to look at here is the damage to the villi. There are non steroid ways to soothe and help heal the villi. Going off all irritating foods is a first of course--especially milk products and possibly for a while all grains and sugars--and only eat cooked vegetables (no raw lettuce etc.).

There are basic herbs however that can also help as well as taking enterically coated acidophilus that agrees with you.

The most useful herbs that I have found are marshmallow root and/or slippery elm (depends on the person). For me the marshmallow root works better--but others depend on the slippery elm. These two herbs are emollient. They soothe and take down inflammation in the intestines and the gut in general. Marshmallow root is also soothing and healing for the kidneys.

Carob, cinnamon, blackberry leaf and raspberry leaf all are good against diarrhea. The carob is nice sweetened with stevia and made into a tea.

Nattokinase, bromelain/papain and/or some other fibronilytic enzymes can help heal and get rid of scar tissue as well as get rid of excess fibrin built up in the heart and veins and the various organs. This is best taken on an empty stomach with a basic general digestive enzyme to balance it out.

I have found plant based enzymes are often good to take with meals to help with better digestion.

Once you feel a little better, it is a good idea to take 1/4 tsp. apple pectin and then when even better, take the pectin mixed in with raw flax seed (start with one tablespoon flax seed a day) ground up in your dedicated coffee grinder (dedicated for just the flax seed). If you put the pectin in the flax and then grind, the pectin will mix with the water better rather than separate into clumps. This is a very mild yet effective bulking agent. I personally cannot tolerate pre mixed varieties since most have gluten in them or some other often irritating agent that doesn't agree with me.

If you still are having problems, I would check to see if you might have some kind of parasites. I you have roundworms, pinworms or giardia for instance you would want to know about it!! Good simple general herbal anti parasitic agents are olive leaf and neem leaf. I like them mixed together. I use them not necessarily against parasites but against fungal overgrowth, bacteria and viruses etc. However both are known to be very good anti parasitics too. Initially however you might get worse for the first 2 to 3 days (the Herxheimer effect). However if you do, then you know its working, so just reduce the dose but stick with it. Ifyou follow this route, be certain to take extra acidlophilus--some hours apart from whatever anti parasitic agent you might be using.

Bea

YoloGx Rookie
Thank you, everyone, for all your ideas and suggestions for my ongoing diarrhea after starting, what I perceived to be, a gluten-free diet two weeks ago.

Several of you felt that I should eliminate dairy and another recommended I try cutting out other grains as well. One of you thought that keeping a food journal would help me to identify any offending food or ingredient. Still another suggested I investigate for possible gluten in flavored coffee or spices or trace gluten in other areas of the kitchen.

Some of you discussed the possibility of cross contamination, while others offered other possible causes such as microscopic colitis, which I have to admit, I have considered. I can't say that I am thrilled at the thought of taking steriods for that.

I appreciate all these suggestions and ideas. I did find the list of foods that may be gluten ladened on celiac.com and I will try the hot carob tea with stevia...if I can find carob tea somewhere!

I appreciate all these suggestions as I face the daunting task of living with celiac disease. I look forward to healing myself and feeling better, and I just MAY undertake the AMA to raise awareness of Celiac Disease when I do!!! :)

Yay! Go girl!!

Bea

PS--they sell carob in containers at Whole Foods as well as in bulk at bulk herb stores (which should be OK__just not in the same store where they sell bulk glutenous items). Usually the carob has trace nut contamination so keep that in mind...I find it best to take it every other day or more apart than that for this reason...since I am allergic to most nuts. Meanwhile I often top it off with a little coconut milk--something I can have every few days but not every day for the same reason.

Link Rookie
Whereas steroids may be what you need if you do actually have microscopic colitis, it wouldn't be my first choice since the side effects can be dangerous. Plus steroids just cover up symptoms rather than address them directly.

I agree however that the thing to look at here is the damage to the villi. There are non steroid ways to soothe and help heal the villi. Going off all irritating foods is a first of course--especially milk products and possibly for a while all grains and sugars--and only eat cooked vegetables (no raw lettuce etc.).

There are basic herbs however that can also help as well as taking enterically coated acidophilus that agrees with you.

The most useful herbs that I have found are marshmallow root and/or slippery elm (depends on the person). For me the marshmallow root works better--but others depend on the slippery elm. These two herbs are emollient. They soothe and take down inflammation in the intestines and the gut in general. Marshmallow root is also soothing and healing for the kidneys.

Carob, cinnamon, blackberry leaf and raspberry leaf all are good against diarrhea. The carob is nice sweetened with stevia and made into a tea.

Nattokinase, bromelain/papain and/or some other fibronilytic enzymes can help heal and get rid of scar tissue as well as get rid of excess fibrin built up in the heart and veins and the various organs. This is best taken on an empty stomach with a basic general digestive enzyme to balance it out.

I have found plant based enzymes are often good to take with meals to help with better digestion.

Once you feel a little better, it is a good idea to take 1/4 tsp. apple pectin and then when even better, take the pectin mixed in with raw flax seed (start with one tablespoon flax seed a day) ground up in your dedicated coffee grinder (dedicated for just the flax seed). If you put the pectin in the flax and then grind, the pectin will mix with the water better rather than separate into clumps. This is a very mild yet effective bulking agent. I personally cannot tolerate pre mixed varieties since most have gluten in them or some other often irritating agent that doesn't agree with me.

If you still are having problems, I would check to see if you might have some kind of parasites. I you have roundworms, pinworms or giardia for instance you would want to know about it!! Good simple general herbal anti parasitic agents are olive leaf and neem leaf. I like them mixed together. I use them not necessarily against parasites but against fungal overgrowth, bacteria and viruses etc. However both are known to be very good anti parasitics too. Initially however you might get worse for the first 2 to 3 days (the Herxheimer effect). However if you do, then you know its working, so just reduce the dose but stick with it. Ifyou follow this route, be certain to take extra acidlophilus--some hours apart from whatever anti parasitic agent you might be using.

Bea

Link Rookie

Bea,

You are a wealth of information on celiac disease and everything else closely related for that matter. I wanted to pick your brain about microscopic colitis.

From everything I have read, IBS is the new name for microscopic colitis. Since IBS and IBD are associated with Celiac Disease, than I am assuming that if I can get the celiac disease under control, then the microscopic colitis/IBS will improve as well. Do you concur?

I really don't want to get into the whole steroid thing...much perfering your line of thought as to the marshmallow root or slippery elm to soothe the inflammation. And I will look for the carob at our local herb shop...closest Whole Foods is 2 hrs. away. I live in the mountains of Western MD.

I would be grateful for your shared thoughts.

Linda

ksymonds84 Enthusiast

Microscopic Colitis is an actual disorder whereas IBS is a syndrome diagnosed only after all other possible disorders have been found negative. Microscopic Colitis can be seen during a colonoscopy when the GI uses a certain instrument siga something....others can jump in here, don't remember the exact name, because it is hard to see otherwise. I belong to another board called perskyfarms.com where they suffer from microscopic colitis and there are celiacs there as well plus actual doctors. Many of them are healed by just going gluten free, so a gluten free diet is highly emphasized. A warm group of people if you want to ask them any questions as well. I don't have MC but thought I might in the past so I joined their forum and just haven't left because we face alot of the same issues and they are so friendly. Don't get me wrong.... I love this forum too! :)

Isn't Bea wonderful!

Swimmr Contributor
I still had D for some time after going gluten-free. I had normally formed stools also. It was weird but I was getting trace gluten for some time as I felt my way through the maze. Wish I had found this forum right away! It would be worth a trial completely dairy free to see if that relieves some of the problem. You could have another food sensitivity or it could just be taking extra time for your healing. A food journal would be a good idea while you are figuring it all out.

I was told that a tell-tell sign of being "glutened" is if your stools are loose and float instead of sink. Is this true? Because my stools rarely EVER sink.

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    • 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!
    • 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 
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