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

Omg...i Might Be On To Something


Rachel--24

Recommended Posts

Mtndog Collaborator

Just poppping into say hello and happy Memorial Day!

Patti- I hope you get better. You should definitely call your PC's office. They usually have a doc on call or a triage nurse you can talk to. If it gets worse- please go to the ER. :wub:

Carla- Can't believe you got to the race! So cool!

Rachel- I think I'm Racheling coffee enemas. :ph34r:

Gin- You are a funny girl.

OMG- Lucky Charms and tri-tip sandwiches. AHHHHHHHHHHHH!!!!!!!!!!!!! First of all, hubby loves Lucky Charms :ph34r: and we both fell in love with tri-tip while living in CA. It's very hard to find here. i am not a big steak fan, but that's a whole different thing! YUMMM!

Susie- What's up with Stinker? How old is she? Poor girl. And you must be worried. My BIL's border collie Cassie has seizures and it breaks my heart. If she has more than 3 in a 24 hour period they have to bring her in and i'm worried one day she's not going to come out. :( She's so sweet! Give the beautiful girls a pet for me. Angus is concerned. :(

I've had a pretty good weekend. I felt good on Friday, bad on Saturday, good yesterday and bad today. Bummed- it's beautiful here. was going to have my family over for a BBQ but just not up to it. Kurt's out riding his bike and I'm jealous.

I think I know what's making me sick. Lay's chips. There was awhile when I was convinced they bothered me but then I got this attitude like "well EVERYTHING bothers me" but I've realized, now that I have had a few good (or at least better days) that I am in Lay's denial :(

Must stop eating them.....shared lines and all that stuff. :angry: :angry: :angry:


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



Celiac.com Sponsor (A8-M):



  • Replies 33.4k
  • Created
  • Last Reply
DingoGirl Enthusiast
Dear Rachel,

Oops! Sorry, that is what I meant! Warm, not hot! :lol: Sorry Lisa! I did not want you to cook your colon or burn your butt! :o In my defense, I could have Lyme Brain. ;)

Sincerely,

Jin

:lol::lol::lol: she said - burned butt and cooked colon in the same sentence. ;) Jin is now part of the comedic relief team!

jin, yes juicing is a really good way of getting concentrated nutrition into your body, <_< maybe I should go back to it. My problem with it really is finances, I like to juice green things and it get's really pricey, perhaps when I have my country place with a garden. I think it can also really help to do it just for a few weeks at a time, perhaps borrow a juicer. I bet there are a lot of idle juicers out there. :lol:

:ph34r: In fact there is one fabulous juicer hiding itself, idle for months, in the cupboard here. Thanks for reminding me - got to pull her out!

But, the bright side is -- I caught a cold!!! How many of us couldn't do that when we were sicker?

This confuses me.......I have always had so many colds and sore throats - - in the last five or so yeasr before Celiac dx I was quite sick, quite frequently. The colds would turn into strep, or even bronchitis - something I'd never had in my life. I must have had a sore throat at least every two months....and then got this very mysterious kidney infection in Dec. of '05 (I was diagnosed Jan. '06) and ended up in the ER with the most excruciating pain I"ve ever known.....thought I was dying - 103 fever for five days.....pure misery.

And so what confuses me is that since removing gluten, I have had ONE sore throat (everyone at work was quite sick) that lasted for one day, and virtually nothing else! :o the only discomfort or sickness has been gluten contamination. I have not been sick - in the classic way I get sick - - for almost 16 months! I guess we all react differently - - but I"m confused as to why you would suddenly start catching colds and such, when in your extreme illness and weakness - - you never really got sick.....

Rinne - - my (former) boss is with Kaiser, and for six weeks, she had a fever, a constant fever (of course came to work every day). Her doctor seemed thorough, and did every single test, including infectious diseases. So I asked my boss if she'd researched her condition - - no, not a bit, she said, and they diagnosed her illness as "Fevers of Unknown Origin," and she was totally okay with that. Can you imagine?

My best friend - - same thing - - - won't EVER take an herb, because one doctor once told her that "echinacea is for the worms" - - she has never been even slightly proactive, never researched a single thing for herself, children, or friends......and she has the beginning signs of MS :o - - - she won't even let me TELL her if I've found something in my research (talk about DENIAL) - - - we have had very heated arguments over this - - - her son is wildly depressed adn can't eat - - WHAT TEENAGED BOY CAN"T EAT?????????????????? - - and she refuses to take any active rold in finding out what is wrong with him - - - (BTW he is 5' 11" and weighs 125 pounds....)

holy Loooooooooooooord - - - -I get furious when I think of these things, and how people blindly and passively accept what their doctors tell them - - - - :angry:

CarlaB Enthusiast

Susan, I think it's different for me and for you. My immune system was so burdened that it didn't even know I was exposed to an illness, so it didn't fight it at all. At my sickest, I never got "sick". Celiac Disease is an autoimmune illness though ... so your immune system would be hypersensitive.

I had many years before that where I caught everything that went around, just not the past few.

Rachel is probably better able to explain *why* than I can ... I've never really researched why, it's just that I've observed on the Lyme board that most people there talk about never getting sick. Sometimes when they do for the first time they actually get excited!

ROFL, My youngest just ran through the house singing, in a singing voice, "I've got to go number 2, Oh, Oh, Oh, Oh!" :lol::lol: Can you imgaine doing that as an adult?

I think it might be the high dose amoxy contributing to my feeling so bad still ... for those coffee enemas, do you use regular strength coffee? I wonder if that would help ... I know saunas sometimes do. Right now I'm too nauseous for a sauna though.

rinne Apprentice
Dear Rachel,

Oops! Sorry, that is what I meant! Warm, not hot! :lol: Sorry Lisa! I did not want you to cook your colon or burn your butt! :o In my defense, I could have Lyme Brain. ;)

Sincerely,

Jin

:lol:

I think I know what's making me sick. Lay's chips. There was awhile when I was convinced they bothered me but then I got this attitude like "well EVERYTHING bothers me" but I've realized, now that I have had a few good (or at least better days) that I am in Lay's denial :(

Must stop eating them.....shared lines and all that stuff. :angry: :angry: :angry:

:rolleyes: Been there, done.... :lol:

.....

Rinne - - my (former) boss is with Kaiser, and for six weeks, she had a fever, a constant fever (of course came to work every day). Her doctor seemed thorough, and did every single test, including infectious diseases. So I asked my boss if she'd researched her condition - - no, not a bit, she said, and they diagnosed her illness as "Fevers of Unknown Origin," and she was totally okay with that. Can you imagine?

......

Nope.

I can imagine something more dreadful than fever the next time though. :(

I had a friend, more of an acquaintance, turn yellow twice in two years and each time they ran their tests on him and found nothing and each year he went back to a life of a drink or two after work and a conventional diet. The third year he got sick they found pancreatic cancer and treated him for it but it wasn't pancreatic cancer after all. He died.

Last winter when I was at my most ill I made my sweetie promise me that we would go winter camping rather than the hospital. The idea being that I could go to sleep and not wake up, I've heard freezing to death is not a bad way to go. :P:lol:

That is how determined I am that they will NEVER get to mess with me again.

I suffered for three months after the CT scan even though I didn't drink the iodine and I am convinced they burned me. I felt so much worse after it and I kept telling myself that it couldn't be related and then after a month or so my sister told me she had heard of one young woman who died from a CT scan, she was already very ill with cancer and very thin and they over-radiated her. Apparently there is a problem with them under-radiating large men and over-radiating small women. :angry:

I am not saying that all doctors are bad or that I would never have any hospital procedures done but I would make sure that I was more informed than I was for that one.

Carla, sorry you are feeling so nauseous and I do remember you laying on the couch in between your :) adventures.

Murph Newbie
...there early, you leave with 500,000 other people, etc.

You have to see the 500 in person to believe it ... the stadium SEATS a half-million people!!!

The stadium seats 257,325, according to the Indy paper, w/ another 50-100,000 in the infield, tho probably not so many in the infield while it rains.

CarlaB Enthusiast
The stadium seats 257,325, according to the Indy paper, w/ another 50-100,000 in the infield, tho probably not so many in the infield while it rains.

I stand corrected. In the old days, before all the changes to the track, the infield was more like a Woodstock event ... no law type thing! :lol: Back then the infield held a lot more. Someone told me yesterday it seated 500,000 ... next time I'll check my source.

It was much easier to get out this year than last time I went.

CarlaB Enthusiast

Murph, this is from USA Today and explains why a long time Indiana resident, though I no longer live there, wouldn't know how many it seated. Until yesterday, I thought the attendance was 500,000, then a "know-it-all" improperly corrected me and said it "seated" that many. Ha! Wish I had known this yesterday!

Indiana National Bank asked Tony Hulman to share Indianapolis 500 attendance figures when he borrowed an estimated $700,000 to purchase Indianapolis Motor Speedway in 1945.The bank never got the figures. Hulman paid off the loan.

Although Hulman died in 1977, his secret has lived on. No one connected with the Speedway has confirmed the size of any race-day crowd, and the limited number of people who know show no indication of breaking Hulman's unwritten rule.

Last fall, The Star decided to solve the mystery.

A six-month inspection of each grandstand resulted in a count of 257,325 permanent seats, which includes the five types of suites scattered around the Speedway. It is believed to be the only formal count of the seats in the facility's modern era.

Estimates had been left to journalists, many of whom have admitted to being influenced by the vastness of the Speedway and the enthusiasm surrounding the 500. Some have guessed as many as 500,000 fans on race day.


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



Celiac.com Sponsor (A8-M):



AndreaB Contributor
But, the bright side is -- I caught a cold!!! How many of us couldn't do that when we were sicker?

If I remember Rachel's posts on this I think it means your immune system is slowing down. I think she relates hers to being very active that nothing can get by.

I also take it to mean you're getting better. :)

Today I bought some bubble bath which I will add just a little to my epsom salt bath tomorrow after my massage! Then I will put on my jammies and maybe paint my toes green. Bought two shades of green polish...one sort of lime green and the other more of a seafoam. :lol:

Sounds nice and relaxing. Green polish.... :P:lol:

Must stop eating them.....shared lines and all that stuff. :angry: :angry: :angry:

Sounds like you realize the problem. Don't know if the desire for it has lessened though. :unsure:

And so what confuses me is that since removing gluten, I have had ONE sore throat (everyone at work was quite sick) that lasted for one day, and virtually nothing else! :o the only discomfort or sickness has been gluten contamination. I have not been sick - in the classic way I get sick - - for almost 16 months! I guess we all react differently - - but I"m confused as to why you would suddenly start catching colds and such, when in your extreme illness and weakness - - you never really got sick.....

I think I've briefly covered this above, but Rachel needs to post all her scientificness on it.

I still think it wouldn't hurt for you to get lyme testing done after you get another job and have the funds lined up for it. :)

dlp252 Apprentice
I still think it wouldn't hurt for you to get lyme testing done after you get another job and have the funds lined up for it. :)

Yes, and you can see the LLMD that Rachel and I go to...and don't feel bad if he shakes his head with you. With Rachel he had to put his head down on the desk I think...with me it was just hard head shaking and the head got halfway between where it was and the desk...bet you'd just get the head shake! :lol:

He likes my sense of humor...bet he'd LOVE you!!! :P

AndreaB Contributor
Yes, and you can see the LLMD that Rachel and I go to...and don't feel bad if he shakes his head with you. With Rachel he had to put his head down on the desk I think...with me it was just hard head shaking and the head got halfway between where it was and the desk...bet you'd just get the head shake! :lol:

He likes my sense of humor...bet he'd LOVE you!!! :P

I can totally see that. Ok Susan, we've got you a good doctor......... :D

dlp252 Apprentice

Oh, and Susan said something that stuck with me on Saturday at BioSET. We were talking about the lyme not showing up in BioSET again and she said something to the affect, your body isn't producing antibodies to it, that's why we can't find it...your immune system has to be healthy enough to produce antibodies!

I can't explain the cold thing, but I know that I haven't had a true cold in a long time. My good friend gets them all the time, but I don't seem to catch them. I thought at first that she wasn't getting colds, but maybe was going through what I had for those 3 years with the sinus infections, but she said they were colds.

AndreaB Contributor

Nikki was so kind to give me a link with DH pictures. One of them definately looks like what my brother has. I've already called him and told him it's gluten free for life, as long as he can live without a piece of paper telling him he can't eat gluten then to go gluten free and never look back.

I've also got to get my mom to understand the seriousness of cc. My brother is more sensitive than we are. She's pretty good though. We haven't gotten sick since the time she used white flour to coat the pot roast. She keeps an immaculate house (so did her mother......I lost it somewhere :P).

Rachel--24 Collaborator
But, the bright side is -- I caught a cold!!! How many of us couldn't do that when we were sicker?

I never caught colds when I was healthy either. :P

I was always the least likely to get sick....I guess thats still true as far as colds and such....not so much for poisonings though. <_<

I guess I was the most likely to become toxic...I just didnt know it. :rolleyes:

Rachel--24 Collaborator
Now that I FINELY have a grandbaby I also go by Grandpa Grump, lol........

:lol::lol:

So cute.

Well, I went out for a little shopping today...I am now all prepared for my day of luxury tomorrow!

WOO-HOO

Donna, you've inspired me...tonight I will bathe in epsom salts. :)

I'm not consistent but I wanted to do about 2 a week.

Oh Susie...I looked at candles today too. Decided against it though because the last time I burned one I had some sort of reaction. I wanted to light candles in the bathroom whilst I had my bubble/epsom salt bath. I have a couple left around here somewhere that I may try, but didn't want to buy new ones if I react to it. :(

I miss candles. :(

Maybe some candles are ok...like unscented and chemical free?? :unsure:

Just poppping into say hello and happy Memorial Day!

Hi Bev....happy Memorial Day to you too!!

I actually entered this crazy world on Memorial Day....lots of years ago. :P

Rachel- I think I'm Racheling coffee enemas. :ph34r:

:o

No Racheling the coffee enemas! Be careful and dont overdue it. ;)

Are you finding it to be helpful?? Well...I know it cleans you out and all :ph34r: ....but do you feel any better??

and we both fell in love with tri-tip while living in CA. It's very hard to find here. i am not a big steak fan, but that's a whole different thing! YUMMM!

I thought tri-tip was everywhere?? :huh:

I thought it was kinda strange that Rinne didnt know what tri-tip was :unsure: ....chalked it up to her being way more sophisticated than me. :P

When I think of tri-tip I think of the CA State Fair...they have AWESOME tri-tip sandwiches there.

Also the grocery store by my house sells some really good tri-tip...its already cooked...just ready to be eaten. They have it in the deli with all the ready to eat roasted chickens. YUMMY!

How do some places NOT have tri-tip??!! :blink:

Rachel--24 Collaborator
I think I know what's making me sick. Lay's chips. There was awhile when I was convinced they bothered me but then I got this attitude like "well EVERYTHING bothers me" but I've realized, now that I have had a few good (or at least better days) that I am in Lay's denial :(

Yeah...the potato chips are not a good choice for alot of reasons.

I saw a list of the top 5 WORST foods to eat....potato chips was on that list. Donuts were #1 but when I get better...I wont let that deter me. ;)

I'm for sure gonna be having me some donuts...all different kinds...definately a jelly filled and one with sprinkles and a glazed cinnamon twist and a maple bar and a chocolate bar...OMG....somebody stop me!! :ph34r:

In fact there is one fabulous juicer hiding itself, idle for months, in the cupboard here. Thanks for reminding me - got to pull her out!

I have a juicer too...I just dont have enough foods (which I can eat) that I can actually juice right now. :(

So I asked my boss if she'd researched her condition - - no, not a bit, she said, and they diagnosed her illness as "Fevers of Unknown Origin," and she was totally okay with that. Can you imagine?

Honestly....I CANT imagine. :blink:

I know there are a gazzilion people who just "accept" their illness and do nothing to try to understand it or to change it. It totally boggles my mind...its beyond my comprehension I think. :huh:

I just dont think I'm "wired" that way....my brain is always wanting to seek answers....my entire being wants to be well again...there is absolutely no way I could be OK with any kind of "unknown origin" diagnosis. :blink:

ROFL, My youngest just ran through the house singing, in a singing voice, "I've got to go number 2, Oh, Oh, Oh, Oh!" :lol::lol: Can you imgaine doing that as an adult?

:lol:

I'm sure I've run through the house singing crazy stuff even as an adult....I have no shame. :P

I think it might be the high dose amoxy contributing to my feeling so bad still ... for those coffee enemas, do you use regular strength coffee?

For the coffee enemas you would need to use oragnic caffienated coffee...I had read that light roast is preferable...but not sure if it really matters. :unsure:

3. The coffee must be regular, non-instant, non-decaffeinated coffee. It must be prepared in enamelware, Corning Ware
CarlaB Enthusiast
I thought tri-tip was everywhere?? :huh:

I thought it was kinda strange that Rinne didnt know what tri-tip was :unsure: ....chalked it up to her being way more sophisticated than me. :P

Nope. We don't have it, but you guys had already told Rinne what it was so I didn't have to ask. It CAN'T be as good as Cincinnati chili no matter how good it is! :P:lol:

Rachel, do you think the coffee can be made in a french press? I don't have a drip coffee maker. So, the coffee would be weaker than you make it to drink?

Rachel--24 Collaborator
Oh, and Susan said something that stuck with me on Saturday at BioSET. We were talking about the lyme not showing up in BioSET again and she said something to the affect, your body isn't producing antibodies to it, that's why we can't find it...your immune system has to be healthy enough to produce antibodies!

Donna...your body IS producing antibodies...thats why you tested positive on your Western Blot. So next time you can tell Susan that you ARE producing antibodies. :P

What Denise said makes alot more sense. BioSET isnt looking for immune system attacks (antibodies)....its looking for sensitivities.

Its totally different from ART. Its totally different from antibody testing.

Your immune system can be fighting something and yet its not actually sensitive to what its fighting...in an allergic type way.

My body is reactive to EVERYTHING...every toxin that gets stirred up, the metals, the Lyme, candida, food, chemicals, mold...the whole she-bang. Your immune system might not have become sensitized to the lyme...but this has nothing to do with antibody production.

Your immune system could be producing plenty of antibodies and putting up a good fight...its just not "reacting" to Lyme in an "allergic" way...which is what BioSET identifies and treats. They de-sensitize you to the stuff that your reactive to. You're obviously not at the point that you react to the Lyme in that way...which is good.

If you were sensitive to it...it would just cause more stress on your immune system.

This is what I think Denise was explaining and as far as I know BioSET cant identify antibodies...whether your immune system is producing them or not. Its a totally different type of testing...its more of an allergy test. '

If you had showed up as "sensitive" to all the Lyme panel...then it would have been a good clue that the Lyme was there....cuz why else would you be sensitive to it...unless it was there.

Thats what Anna had explained to me...she did feel I had Lyme because I definately was reactive to all these Lyme antigens....but she did say it didnt mean that Lyme was my main issue...or that the Lyme was an active infection.

She said it could be inactive but its presence still caused my "freaked out" immune sytem to become sensitized to it.

Hope this makes sense. :)

Rachel--24 Collaborator
Rachel, do you think the coffee can be made in a french press? I don't have a drip coffee maker. So, the coffee would be weaker than you make it to drink?

OMG...you are sooooo asking the wrong person. :lol:

I never made coffee (to drink) in my life. French Press?? :unsure:

I never drank coffee...except right before I got sick I broke down and tried Starbucks Caramel Frappacino (couldnt resist the whip cream, caramel and sprinkles :P ). I fell in LOVE. :wub:

But really...I'm very clueless about coffee :ph34r: ....hate it when customers ask me about coffee....how to make it etc. I tell them I dont know a thing about coffee....I never drank it.

I think the customers feel I should know about every product on the shelf...how to make it, what it tastes like, which brand is best, which flavor is best..etc.

WTH?? Even if I could eat whatever I wanted...would it really be possible to eat everything in the entire grocery store?? :blink:

rinne Apprentice
I thought tri-tip was everywhere??

I thought it was kinda strange that Rinne didnt know what tri-tip was ....chalked it up to her being way more sophisticated than me.

:lol:

Nope, just Canadian. :P

Rachel--24 Collaborator
If I remember Rachel's posts on this I think it means your immune system is slowing down. I think she relates hers to being very active that nothing can get by.

Andrea...yup...thats the "theory". ;)

I dont think there is any "scientificness" behind it...and not every person with Lyme experiences this. Some people catch everything that comes their way...some people dont.

It just depends on the persons immune system. Even without Lyme some people never get sick and others catch everything.

A person that catches things has a weaker immune system...or its busy with other stuff. Or its just not in a really heightened state.

A person that doesnt catch things could have an overactive immune system which is ready to attack every little thing. I would say my immune system is definately in overdrive. :rolleyes:

So some people have speculated that when a person with Lyme isnt getting "sick"...even though they are SICK...its because the immune system is on "heightened alert". Because Lyme hides...comes out...changes form...etc...the immune system is really challenged and is just constantly in a heightened state....so nothing gets by.

On the other hand some peoples immune systems are really burdened and not even putting up a strong fight against the Lyme...let alone other "unwanted" guests.

I think people who never got sick while they had Lyme feel like once they are rid of Lyme and start catching colds...its because their immune system is no longer in that "heightened state" that it was in when it was stressed by the Lyme.

Mtndog Collaborator

Words of encouragement: Just got off the phone with my SIL's older sister. She had Lyme from 2001-2004. Saw an LLMD in NYC and was tested through Igenix. You know the routine.

She told me what she felt like before she was diagnosed (VERY bad case of neuro Lyme- thought she was having a nervous breakdown, brian tumor etc Tons of food intolerances.)

She is now clear and pregnant with her first baby and SHE HAD HER FIRST PIZZA last week!!!!!!!!!!! See THERE is a light at the end of the tunnel!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!

AndreaB Contributor
She is now clear and pregnant with her first baby and SHE HAD HER FIRST PIZZA last week!!!!!!!!!!! See THERE is a light at the end of the tunnel!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!

Sounds very promising Bev. :D

Judyin Philly Enthusiast

Dear Judy,

Hugs to you too! Severe weather sure is something we have in common! We get it all of the time! Evansville is right in Tornado Alley! I am used to it, though. The new people in town are so obvious. They freak when the weather gets bad.

Sincerely,

Jin

jin...thanks kido.

i was looking on line for you for the toaster bags on QVC and another site...but they were'nt there. I know your finances are limited so when i got the toast bags i also got the sheet you put on a cookie sheet or pizza pan and you'll always be protected from gluten.

you can wash up to 100 times.

If Patti sees this maybe she can find the link again.

mine was old but didn't come up in a new search either.

they saved me while traveling b/c you just put on any counter etc and your safe.

the toaster bags you put bread etc in or do a grilled cheese..( I can't b/casue of lactose and casein. NOt sure of your issues ..........

anyway.........have you been through a tornada?

We had one that was 15 miles away and the debris from it came clear over to us..like pictures etc...the Easter Tornado in Zenia Ohio.

I'm not scared fro myself in stores.......just don't wnat my computer to get zapped.

i've never done the fast reply so have no idea where this will show up

i am 3 pages behind.

wish i could answer all of you.

will in time.

let's see where this goes...hopefully at the end of the thread???

judy

oh good it's on the end of thread

bev see you

read you have not had a good weekend health wise and hubby went out on the bike.

we'll get better i know

so far the SIBO meds are agreeing with me BUT...........BOTH ANKLES ARE SO SWOLLEN.

EVEN THE SMALL 'R' ONE...

TIME WILL TELL

THE PT FOR MLD IS TO CALL ME TOMORROW AS HAVE A NEW REFURAL JUST IN TIME I GUESS.

HOPE YOUR OK.

HAVE SO MUCH TO CATCH UP ON.

WAS HOPING PATTI HAD POSTED ABOUT TODAY...

I SURE HOPE SHE'S BETTER.

HUGS

TO ALL i GET TO EVERYONE SOMEDAY.

NOW HAVE TO GO AND READ.

JUDY

Judyin Philly Enthusiast
She is now clear and pregnant with her first baby and SHE HAD HER FIRST PIZZA last week!!!!!!!!!!! See THERE is a light at the end of the tunnel!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!

THIS IS SO INCOURAGING...THANKS FOR THE POST BEV.

SO PATTI HASN'T BEEN ON TODAY.

GOD HOPE SHE'S OK

CALRA...YOU SURE PAID BIG TIME FOR YOU NYC AND RACE DAYS...POOR LADY

SUSAN...POOR STINKER...IS SHE BETTER TODAY

ANDREA..GLAD THE SITE HELPED WITH YOUR BROTHERS ISSUE.

RACHEL..LORD..READ ABOUT THE LOST CELL PHONE..THE OATS...WILL IT EVER END ...SURE ONE DAY...ONE DAY...IF WE LIFE LONG ENOUGH RIGHT.

HAS ANYONE HEARD FROM PATTI

PRAYERS FOR HER APT TOMORROW.

HUGS

J

Judyin Philly Enthusiast

RINNE. HOW ARE THOSE BARS COMING ALONG.

I SURE COULD USE ON RIGHT ABOUT NOW.

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,857
    • Most Online (within 30 mins)
      7,748

    LowellFrancis
    Newest Member
    LowellFrancis
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Rogol72
      Some interesting articles regarding the use of Zinc Carnosine to help heal gastric ulcers, gastritis and intestinal permeability. I would consult a medical professional about it's use. https://www.nature.com/articles/ncpgasthep0778 https://www.rupahealth.com/post/clinical-applications-of-zinc-carnosine---evidence-review https://pmc.ncbi.nlm.nih.gov/articles/PMC7146259/ https://www.fallbrookmedicalcenter.com/zinc-l-carnosine-benefits-dosage-and-safety/
    • Jillian83
      He is. Which makes everything even more difficult. I’m not a believer in “staying for the kids” but I have nowhere to go and it’s not just me, it’s me plus my babies. We live in a beautiful place, lots of land in the country and me and the kids love the place we’ve called home for their entire lives. But Im seeing that he’ll never change, that my kids deserve a happy healthy Momma, and that staying in this as is will be the early death of me. Then I look at the scars covering my entire body…this disease and the chronic stress I’ve been enduring for years that tell me I’m no longer beautiful and no one will ever look at me with interest again. I try self care, try to give myself grace so I can just start loving myself enough to gain strength but the slightest sparkle in my eye and skip in my step attracts his wrath and it all comes crashing ten fold. Life is just absolutely railing me from every single direction leaving me wanting to wave that white flag bc I don’t feel like there’s much hope no matter what happens. 
    • trents
    • Jillian83
      Hi, I was recently diagnosed with Celiac and dermatitis herpetiformis after years of suffering without answers. I lost my mind. I lost my job. I lost so much time. I lost Me. Conventional doctors are opulent come near me and the one who did sat across the room, misdiagnosed me, pumped me full of steroids which collapsed my entire hip for 6 months. So without answers I began my holistic journey. Fast forward a couple of years and still struggling with a mysterious whole body itchy, crawling “skin hell”, perfect teeth now deteriorating, thick hair now thinning rapidly and no more than a day or 2 at most relief….An acquaintance opened up a functional medicine practice. Cash only, I found a way. Within a month tests clearly showing my off the charts gluten allergy/sensitivity as well as the depletion of vital nutrients due to leaky gut and intestinal damage. dermatitis herpetiformis was more than likely what I was experiencing with my skin. I was happy. I thought this is easy, eat healthy Whole Foods, follow the diet restrictions and I finally get to heal and feel confident and like myself again very soon! 😔 Supplements are very pricey but I got them and began my healing. Which leads to the other major issue: not working, stay at home Mom of young kids, entirely financially dependent on my man of 7 plus years. He’s never been supportive of anything I’ve ever done or been thru. He controls everything. I’m not given much money ever at a time and when he does leave money it’s only enough to possibly get gas. His excuse is that I’ll spend it on other things. So my “allowance” is inconsistent and has conditions. He withholds money from me as punishment for anything he wants. Since being diagnosed, he’s gained a new control tactic to use as punishment. He now is in control of when I get to eat. He asked for proof of my diagnosis and diet bc he said I made it up just to be able to eat expensive organic foods. Then after I sent him my file from my doctor he then said she wasn’t a real doctor. 😡. I go days upon days starving, sometimes breaking down and eating things I shouldn’t bc I’m so sick then I pay horribly while he gets annoyed and angry bc I’m not keeping up with all the duties I’m supposed to be doing. His abuse turns full on when I’m down and it’s in these desperate times when I need his support and care the most that I’m punished with silence, being starved, ignored, belittled. He will create more of a mess just bc I’m unable to get up and clean so that when I am better, I’m so overwhelmed with chores to catch up that the stress causes me to go right back into a flare from hell and the cycle repeats. I’m punished for being sick. I’m belittled for starving and asking for healthy clean water. I’m purposely left out of his life. He won’t even tell me he’s going to the grocery or to get dinner bc he doesn’t want me to ask him for anything. I have no one. I have nothing. Im not better. My supplements ran out and I desperately need Vitamin D3 and a methylated B complex at the very minimal just to function….he stares at me blankly…no, a slight smirk, no words. He’s happiest when im miserable and I am miserable.  this is so long and im condensing as much as I can but this situation is so complicated and disgusting. And it’s currently my life. The “IT” girl, the healthy, beautiful, perfect skin, perfect teeth, thick and curly locks for days, creative and talented IT girl….now I won’t even leave this house bc Im ashamed of what this has dont to my body, my skin. Im disgusted. The stress is keeping me from healing and I think he knows that and that’s why he continues to keep me in that state. He doesn’t want me confident or successful. He doesn’t want me healed and healthy bc then how would he put the blame of all his problems on me? This journey has been hell and I’ve been in Hell before. I’ve been killed by an ex, I’ve been raped, robbed, held hostage, abused beyond nightmares but the cruelty I’ve experienced from him bc of this disease is the coldest I’ve ever experienced. I’ve wanted to give up. Starving and in tears, desperate…I found a local food pantry in our small town so I reached out just saying I had Celiac and was on hard times. This woman is blessing me daily with prepared gluten free meals, donations, educational info, people who know this disease and how they manage life and the blessings just keep coming. But it’s overwhelming and I feel like I don’t deserve it at all. He just glared and I know he’s going to sabotage it somehow. I don’t even know what to do anymore. I’m so broken and just want peace and healing. 
    • cristiana
      @Colleen H   I am just curious,  when you were tested for coeliac disease, did the doctors find out if you had any deficiencies? Sometimes muscle pain can be caused by certain deficiencies, for example, magnesium, vitamin D, calcium, and potassium.   Might be worth looking into having some more tests.  Pins and needles can be neuropathy, again caused by deficiencies, such as iron and B12,  which can be reversed if these deficiencies are addressed. In the UK where I live we are usually only tested for iron, B12 and vitamin D deficiencies at diagnosis.   I was very iron anemic and supplementation made a big difference.  B12 was low normal, but in other countries the UK's low normal would be considered a deficiency.  My vitamin D was low normal, and I've been supplementing ever since (when I remember to take it!) My pins and needles definitely started to improve when my known deficiencies were addressed.  My nutritionist also gave me a broad spectrum supplement which really helped, because I suspect I wasn't just deficient in what I mention above but in many other vitamins and minerals.  But a word of warning, don't take iron unless blood tests reveal you actually need it, and if you are taking it your levels must be regularly monitored because too much can make you ill.  (And if you are currently taking iron, that might actually be making your stomach sore - it did mine, so my GP changed my iron supplementation to a gentler form, ferrous gluconate). Lastly, have you been trying to take anything to lessen the pain in your gut?  I get a sore stomach periodically, usually when I've had too much rich food, or when I have had to take an aspirin or certain antibiotics, or after glutening.  When this happens, I take for just a few days a small daily dose of OTC omeprazole.  I also follow a reflux or gastritis diet. There are lots online but the common denominators to these diets is you need to cut out caffeine, alcohol, rich, spicy, acidic food etc and eat small regularly spaced meals.   When I get a sore stomach, I also find it helpful to drink lots of water.  I also find hot water with a few slices of ginger very soothing to sip, or camomile tea.  A wedge pillow at night is good for reflux. Also,  best not to eat a meal 2-3 hours before going to bed. If the stomach pain is getting worse, though, it would be wise to see the doctor again. I hope some of this helps. Cristiana    
×
×
  • 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.