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Gabes-Apg
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Post by Gabes-Apg »

Erica
I think there is a couple of factors that have contributed to external symptoms;

- alcohol depletes magnesium and interrupts methylation cycle (ie disrupts use of B6 by the body)
- found the info below, and in line with your candida, the imbalance in your gut could be contributing to the increased histamine/DAO etc

https://paleoleap.com/histamines/
The biggest nonfood source of histamines in most people’s bodies, though, is their gut flora. Some kinds of bacteria produce histamines, while others degrade them. Too many histamine-producing bacteria can fill up your “sink” faster than DAO can empty it. If you think about it, this makes perfect sense: it’s the same reason why fermented foods are off the table, only the reaction is happening internally instead of externally.
The importance of gut flora in creating and destroying histamine can give rise to a sudden onset of histamine intolerance later in life, if you take antibiotics or make a drastic change to your diet. When the gut flora start growing back after this kind of trauma, the environment is ripe for bacterial overgrowth problems, and a predominance of histamine-producing bacteria might be just one of those issues. And in a cruel coincidence, the probiotic fermented foods that you eat to heal your gut are all high in histamine, so they only make the problem worse.
And the gut problems don’t stop there. DAO, the “emergency drain” in the histamine sink, is mainly produced by the mucous lining the intestinal wall. If the lining of the gut is irritated (by inflammatory foods like grains and legumes), DAO production decreases, and the symptoms of histamine overload only get worse.
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tex
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Post by tex »

Erica wrote:Tex, my DAO must really be shot right now....is there anything else besides foods that raise histamine? Like heat, stress, insufficient sleep etc....
Yes. For me at least, getting hot, or taking a hot shower, can make my itching worse. Interestingly, that effect seems to be amplified if I am taking Allegra. Stress makes it worse, I believe. In line with what Gabes posted about above, have you ever read the article at the link below? It discusses the gut bacteria connection and how certain types of gut bacteria are capable of producing histidine. As you may know, in the body, histamine is produced (naturally) from histidine. Too much histidine presumably means that we will produce too much histamine. The article that Gabes took the quote from may present a dumbed-down interpretation of what actually happens. Certain gut bacteria have been shown to be capable of producing histidine. I don't believe they have been shown to capable of producing histamine, the body has to make that conversion. At any rate, this will be discussed in my next book.

How a chronic magnesium deficiency can cause inflammation, and how antibiotics can amplify the problem

Tex
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It is suspected that some of the hardest material known to science can be found in the skulls of GI specialists who insist that diet has nothing to do with the treatment of microscopic colitis.
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Erica P-G
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Post by Erica P-G »

Thank you Gabes & Tex,
I've read both scenarios and I have to say...WOW where do I begin to fix this....besides upping my Magnesium once again....and I'll probably have to use it topically now since I can't be sure internally it is absorbing properly.

I'm really interested in your research Tex....

I'll really watch my food and drink and increase my Mag and B6....it's crazy how my gut is dealing with things and I'm sure it's been slowly coming on over time since May.... otherwise my lip/nose wouldn't have erupted with a rash to begin with.

Sure hope I can figure this out soon.
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Erica
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Erica P-G
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Post by Erica P-G »

Ok...I have pressure urticaria going on so for that I will take antihistamine, then I have Metronidazole to apply to the skin yeast for a while and then as needed.....aka Candida albicans.

So antihistamine 2-4 times a day...which one would be best Claritin, Zyrtec or Allegra??? And 50mg Benedryl right at bed time. For how long I was not advised....so I guess I punt with that based on how I feel.

Im kinda miserable, everything itches... :sad:
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Post by tex »

Whichever one works for you is the one to use. Some brands might not help as much as others. I got no relief from Claritin, so I used Allegra. Please be aware that Benedryl has some anticholinergic action so it increases the risk of Alzheimer's and age-related dementia after taking something like 180 doses during your lifetime. I've forgotten the exact details of the research so that total number may not be correct, but I believe it's somewhere in that neighborhood.

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Post by Erica P-G »

I asked the Dr what she would choose over the three and she said Zyrtex....so I have Allegra 180 at home (I know it isn't the greatest to take long term either - might have to give Zyrtec a chance) I suppose it isn't overkill to take one in the morning and one after I get home from work/dinner time and then take the Benedryl at night for a few days (don't want to take this very long either) just to get these wheals to go the heck away....I have gotten them 4 times now and exactly at pressure points....they get huge like 4-5 inches in diameter across the top of the skin...super uncomfortable.

LOL..so no underwear, no bras :lol: GEESH!!! my jeans are killing me at work today because my last wheal erupted right at the bend in my hip/leg near the pelvic.....ARGH that hurts to sit today.

Thank you Tex....it just helps to talk thru these things sometimes....
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Post by tex »

I hear you. That's where I seem to be most likely to get them (at the waist or near the bend line at the top of my legs). I suppose that's because those areas are under more stress due to bending, perspiration, chafing, etc. I wear an elastic belt to help hold my ileostomy bags in place, and right at the edge of that belt is a favorite place for them to spring up, especially during the summer.

Tex
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Post by sunny »

Gabes & Tex... thanx for explanation of PSP....simple when you know what you didn't know before!

Erica, I'm so sorry that this is such a problem just now for you! Just what you need in the midst of wedding plans! Urgh! You must be feeling so miserable .. hope the Allegra helps...
Sunny
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Erica P-G
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Post by Erica P-G »

Update....

Histamine can be the hidden symptom that you least expect to derail you.

I think I've gotten plenty of magnesium, VitD, B vitamins etc...but what I haven't given much thought to is the fact my body isn't and hasn't been eliminating histamine very well and since I haven't used an antihistamine since early Spring I need to make yet another note that Summer may be my worse time for it to build up.

Since going on the high dose antihistamine I have gotten to Norman in a matter of 4 days. Previously I have had WD for quite a few days this month, but I began to attribute it to wedding plan stress since my daughter is getting married outdoors at our home with reception here to.

I don't itch nearly what I had been and I'm sleeping really well again. I was hoping I could forgo the antihistamine but it appears my body isn't ready or capable of not having it at this time. I may still have a while to heal before I'm able to remove excess histamine. I'm also taking a 70 billion probiotic by Mercola since I am having an issue with Candida Albicans and the gut flora is out of balance.

Without being able to eat fermented type foods ( due to their high histamine!!) it is a catch 22 to balance this situation.

Just thankful I'm understanding what's going on and able to take steps in correcting it. Thanks again to all the helpful advice here!
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Erica
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Post by tex »

:thumbsup:

Tex
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It is suspected that some of the hardest material known to science can be found in the skulls of GI specialists who insist that diet has nothing to do with the treatment of microscopic colitis.
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Post by Barbara1 »

:mad: Hello! This is my very first post (I think), and I need help! I am a Type1 Diabetic and for the past several days have been in a MAJOR flare of MC. Everything that is good for DM (diabetes) is terrible for MC, and vice versa. Yesterday my blood sugar dropped to 48 (WAY TOO LOW, RANGE IS 80-120), and things I would normally eat to bring it back up to a normal range sent me running to the bathroom.
What can I eat (that will stay in me) and is high in protein and carbs to quickly bring my glucose back up and at the same time not irritate my MC? I ate tons of applesauce, a banana, saltine crackers at mealtime, all of which are OK in moderation for DM, but what else can I eat that won't send me running for the bathroom? Any ideas would be greatly appreciated - thank you! On, of course I'm lactose intolerant, too..
Barbara[/b][/quote]
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Erica P-G
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Post by Erica P-G »

It's been a while since I made an update here....

A new feeling/situation has arised and I have to say I really hate not being normal, people don't know how to accommodate me, perhaps they are uncertain what to ask me, what I might say, maybe they don't have the resources to try if I give an answer.

I just know that because I am not able to eat what Every Body else can eat I get left out and that really hurts.

I HATE being who I am right now. :cry:

I used to be included in Everything at my job, even felt like I was part of the Circle (managers) but lately with Spring Break and no cooking going on (because I work in a education foodservice environment) there has been a cleaning crew and food has been ordered and I have not been included at all, plus I have not been included while the Circle enjoys the ordered food. They know I bring my own.....but I have not been encouraged to eat my meager foods along with the Circle.

So I sit at my desk unsure how I want to choose to feel about this because I know it is a choice whether to just accept because it truly isn't something I can make any different due to my food intolerances, or whether I would just be selfish and needy if I said anything to anyone about how I feel. It isn't their fault I have to be this way.

It's times like this that I feel I will retire sooner than later and I'm only 50 :sad:

I just needed to vent....I really don't like my lifestyle anymore, I feel less of a person the more I have to be this way.
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Post by jlbattin »

Oh Erica, my friend, my heart hurts for you, and rest assured, if I were closer, I'd come and eat lunch with you!

I've been where you are. Teachers are notorious for always having food around, but quite honestly, the first two years I was there, I could count on one hand the number of times we ever ate together or had food catered or anything like that. Then comes my diagnosis, and just like magic, it seemed like every single time I turned around there was food being catered in. Lucky for me, I was only working mornings and I usually always left and came home to eat lunch. But one day, we had a morning training with lunch catered in and as I got up to leave, my principal called me out. I walked over to see what she wanted, and she said, "You never stay anymore. You don't sit with us or socialize or anything." I looked at her and said, "Oh, you want me to sit in a room and smell the food and sit across from you and visit while you eat the food I can't have! I get it!" And I promptly walked out! That was the last time that happened. She apologized profusely and after that, if something was catered in, the secretary would go get me a Chipotle rice bowl.

People who don't understand can be so very cruel. They don't understand, and sometimes they choose to not understand. I still deal with it on a regular basis. Some folks try hard to include me and will work really hard to find something I can have, and others are just downright rude. Another example, one of our teachers who knows I can't have gluten, dairy, or soy, brought Valentine's cupcakes to our meeting that morning. As he passed them out, he just looked at me and said, "Sorry, Jari, I know you can't have this." And went right on. It does make you feel like a nobody, like you are invisible.

Hang in there. Sometimes I think you have to release that frustration and let them know how you are feeling. Depends on the situation. I sometimes will now join them at a catered event with my own food, but more often that not, I don't. I just don't stay around. Sadly our society has gotten into a pattern of food being the center for get togethers, and it's frustrating for the minority of us in the world that don't center around food anymore.

But my dear Erica, you are not less of a person, and don't ever let anyone make you feel like that! Those kind of folks are folks you can do without!
Jari


Diagnosed with Collagenous Colitis, June 29th, 2015
Gluten free, Dairy free, and Soy free since July 3rd, 2015
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Erica P-G
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Post by Erica P-G »

I certainly could use Jari (Hugs), or insert your name here______

to be able to sit with me, have something in common with, to not feel bad that we Both had to bring different foods to the table.

I'm tired of being different.....as I know a lot of who reads this have felt that way at one time or another, and there is nothing that can really be done about it except to accept it (or find a job that isn't in the food business - cripe it is a double edge sword I tell ya).

I really appreciate the outreached hand Jari, you did make me smile :smile:

Just another Progress not Perfection moment to mark on the calendar.
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Post by LauraAnn »

I know and feel you pain! I guess I’m lucky that I am retired and don’t have to socialize every day. When I do get to go out with friends and family it is not always fun. My sister, who has been with me through this, is the only one who “gets” it. Others can be down right rude and cruel. I try not to wear my feelings on my sleeve, but some days it’s not easy to smile through the comments.

Please know that you are not alone and remember how strong you are. Just look at what you have accomplished and you did all on your own....well, maybe some of your “potty peeps” helped along the way. :smile:
Laura Turner
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