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

Ugh Displaced Mind


Lister

Recommended Posts

Lister Rising Star

what diffrent things mess with your vision?? i got really blurred/stoned like vision today and yesterday all day long.. would say its from gluten but i know its not. but one thing that may help figure it out is the vision seems to alwasy come with one other thing, a pressure like it feels like someone has two fingers on top of my nose and is pushing down, i can relive the vision and the pressure by applying force to my nose but it only gives relife for about 10 seconds any clues??? ugh i feel like crap, i already gotta deal with my stomic why my vison also

_________________

if anyone thats had to do a stigomoidoscopy would be willing to talk to me about it in a privete message it would be much apretated, im really nervis/scared/dreading the whole thing im not sure if im more frightend of the prep or the procedure and im making myself a wreck dwelling on it


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



Celiac.com Sponsor (A8-M):



  • Replies 411
  • Created
  • Last Reply
Lister Rising Star

The gastrointologist is 98% sure its chrons disease, so i meen if he is that positive im thinking about cancaling the scope ( i really dont wanna go thru with it anyways) because i meen if it is chrons then there is nothing they can do for me just send me home and tell me to deal with it..so i meen atleast then i would not be butt hurt and poor because of the diagnosis... i dont know :(

ravenwoodglass Mentor
The gastrointologist is 98% sure its chrons disease, so i meen if he is that positive im thinking about cancaling the scope ( i really dont wanna go thru with it anyways) because i meen if it is chrons then there is nothing they can do for me just send me home and tell me to deal with it..so i meen atleast then i would not be butt hurt and poor because of the diagnosis... i dont know :(

Your GI can not be sure it is Chrons without doing tests and biopsies. Chrons patients also often see a great deal of improvement on a gluten-free diet, read misdiagnosed celiacs here. My 'Chrons' symptoms are in complete remmission on the gluten-free diet, no pills, no pain. Also the symptoms of chrons, colitis and Celiac are all similar. And none are a death sentence. You need to get the test done to set your mind at ease. Also many of the previous bills were absorbed by the hospital and you will be able to get some help with at least a payment plan if you ask for it. Having things on paper may also assist you in getting some help with finding another job or job training, if you check at the SSI office and explain your situation they can help.

Green Fingered Gaelic Newbie

Wise words Raven

Turtle Enthusiast

You might also want to look into the Vocational Rehabilition program in your area....SSI could probably direct you to them if you cannot locate them on your own!

ravenwoodglass Mentor
You might also want to look into the Vocational Rehabilition program in your area....SSI could probably direct you to them if you cannot locate them on your own!

Lister this is what I was talking about when I mentioned what they call Vesid in my state. I really hope you check this out, with your educational history and your newly diagnosed celiac they really will help you with getting into another occupation or job. You have shown good determination and a good work ethic by the number of times you have gone to work or stayed at work when you were feeling ill. Try and channel some of that strength in to walking to that office and starting the process. It could open a whole new world for you.

Turtle Enthusiast

Also, they could link you up with other services that could be helpful and beneficial to you that we may not even know about or have thought about yet! PLEASE consider this!!! If you need help, let us know...i'm a social worker and could possibly assist you with finding your local office if you are unable to find this information on your own.


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



Celiac.com Sponsor (A8-M):



jerseyangel Proficient
Lister this is what I was talking about when I mentioned what they call Vesid in my state. I really hope you check this out, with your educational history and your newly diagnosed celiac they really will help you with getting into another occupation or job. You have shown good determination and a good work ethic by the number of times you have gone to work or stayed at work when you were feeling ill. Try and channel some of that strength in to walking to that office and starting the process. It could open a whole new world for you.

Yes, this is excellent advice, Lister. Take what these ladies said to heart--we know you can do this!

Guest ~jules~

Lister, I was curious if you have applied for the oregon health plan. I was on it years ago in my early 20's before kids and marriage came along. I'm not sure what the qualifacations are these days but its something you might want to look into. So the doc says he's pos. its chrons? Follow through with all your testing even if he said that, this whole experience has shown me that doctors love to slap a label on you and send you home. I do know if you have chrons they treat it with medication, diet, no smoking the usual....I know how you are feeling, it sucks. Before I was diagnosed I went through almost 2 years of WTF? I was told I had parasites, even though they found none. I was sent home with pill upon pill, poked and prodded at, colonosopy came out normal, sent me home with IBS. I had no idea what was going on, I would sit on the internet trying to figure it all out, finally after more tests my gi, dx me with celiac. You will figure it all out unfortunetly we are at the mercy of our doctors and have to jump through their hoops and wait....Take care, things will get better Julie

Lister Rising Star

unfortuntly i still dont have a dx to back up anything for social security doctor has not put down any offical diagnosis in his records besides IBS :(

Guest ~jules~

Hey lister, I just wanted to add a few about the stig. or colonoscopy, whichever you may...I wanted you to know that I was totally freeked out about it. BUT...it turned out to be nothing really. The worse thing about it was the liquid diet you have to go on before you get it done, I was starving! The procedure is a piece of cake, trust me. You go in, get a IV ( no big deal just a prick, and don't watch! ) Then you go into a room with the doc, and a r.n. and they set up their equipment (you can't see it) then, they give you strong drugs, the next thing you know your waking up. You wont remember a thing, or feel a thing afterward, I had no idea anything had happened to me at all. So, you will be okay. I am spreading the word on how easy the colonoscopy is so people wont be so afraid to get one, it is a very important procedure. Take care Julie

Lister Rising Star

whats the reason for the iv? do you feel the drugs kick in or does it just happen? i think im more nervise about the prep then the procedure really, i have to give myself 2 ummm well enemas beforehand plus a laxative before i go to sleep the night before..... sounds so miserable plus since i cant eat i cant take my meds or probably even smoke a cig :( man wensday is going to suck, i just hope they find something so i dont have to go in for the colonoscopy and just the stigomiodioscopy. I hope its like a 30 foot worm thats eating all my food and causing stomic pains and not something really bad like cancer or something i guess no reason worrying about it now will know on wensday just hard to not think about. but thank you for your words that really helps me get into the mind set to go thru with it

__________

what laxatives are gluten-free?

Turtle Enthusiast

Lister:

I understand what you are saying about not having a diagnosis for SSI.

Below is the link for Vocational Rehabilitiation. You don't have to have SSI to go there and talk w/ them.

Open Original Shared Link

This link is for the entire state of Oregon. So you'll need to click on "Locations and Contacts" (it's the 3rd link down on the left hand side of the website, under MENU). Look to find the location closest to where you live and call them to arrange an appointment. Usually they will ask you a bunch of questions and evaluate you to see how they can best assist you.

Hope this helps! GOOD LUCK!

Guest ~jules~

The IV is to administer the drugs they give you, if you've never had an IV it just feels like a beesting for a second then it goes away. As far as the drugs they give you its within a minute if not shorter your just gone, they told me its a semi-consious state but I can't remember anything. I don't remember a single thing about the procedure accept prep, then waking up. As far as the worm theory I'm not too sure I'd want that either :P Although worm vs. cancer, Okay I'll take the damn worm. You'll be fine, try not to stress it too much. Julie

Lister Rising Star

2 more days until the test, man im so scared about what the results will be, i cant keep my mind off cancer since my dad keeps bringing up the fac t that that colon cancer runs in the family and that i match all the signs hes a jerk scaring me like this

CarlaB Enthusiast

Lister, you are very young, your chances of it being cancer are low.

I thought you didn't communicate with your dad?

I think a lot of your problems are aggravated by stress ... try to not worry so much! Not all stress is worrying either .... and it does affect you physically.

It will go fine, and you won't remember a things. The IV is pretty much the same as having blood taken for a blood test. The worst part of all of it is the prep the night before!!

Lister Rising Star

night before is just pure liquids and a laxative i can deal with that, the next morning is the bad prep the fricking enemas ughhhhhhhhh does not sound fun... but i am paining a frowny face on my butt cheak tonight so when they go to put in the tube they will find a little frowny face :) figure if i can keep a sense of humor to it it will go better

CarlaB Enthusiast
night before is just pure liquids and a laxative i can deal with that, the next morning is the bad prep the fricking enemas ughhhhhhhhh does not sound fun... but i am paining a frowny face on my butt cheak tonight so when they go to put in the tube they will find a little frowny face :) figure if i can keep a sense of humor to it it will go better

I didn't have to do enemas, only laxatives ...

frowny face :lol::lol::lol:

Lister Rising Star

i dont really talk to my dad i just email him every once and a while and he responds sometimes, but as you can see not very positive responses from him

ravenwoodglass Mentor
2 more days until the test, man im so scared about what the results will be, i cant keep my mind off cancer since my dad keeps bringing up the fac t that that colon cancer runs in the family and that i match all the signs hes a jerk scaring me like this

Lister you'll do fine and as Carla said the chances of your having cancer are low. Try to relax and do as much as you can to keep your mind off it. You'll get through the prep okay, it's no fun but if it helps give you some answers it is worth going through. Has your Dad been getting the regular colonoscopies that he should? If not his fear may be more for himself. If he says that again I would ask what the outcome of his last one was. As for you, you can do this.

jerseyangel Proficient

Lister,

Because of your family history, and the problems you've been having, I think you are absolutely doing the right thing by having the test. Like everyone said, the prep is the worst part--and it's not really all that bad. I remember nothing from my procedure--no pain at all--even after.

Colon cancer "runs" in my family, too. I think I told you that my dad had it, but it was caught very early. He's 80 now, and has been followed closely for the last 30 years. (He was 50 when it was found).

The important thing is to get screened--this is curable if caught early! That's the good news. Even if they find a polyp--they'll remove it and it will never have a chance to grow into something more serious. You should look at this as a positive in that respect. Because you are so young, chances are they will find nothing--but always better to be safe!

I don't know why your dad is trying to scare you. Some people have a hard time showing concern--they make jokes or say unnecessary things. Could be he's scared of this himself....Maybe he dosen't know the facts.

Really, there's nothing to be afraid of here--you'll come through it fine. Try and relax, get your mind on something else if you can.

gfp Enthusiast
Lister, you are very young, your chances of it being cancer are low.

I thought you didn't communicate with your dad?

Yep and his dad winding him up like this i can see why...

CarlaB Enthusiast
i dont really talk to my dad i just email him every once and a while and he responds sometimes, but as you can see not very positive responses from him

Lister, if you're like me, you keep trying to establish the relationship, but keep getting treated badly each time. I don't want to post much for public view, but let's just say that I know exactly how you feel. I finally cut off ties, but it took me till I was 40 to do it. I found friends and mentors who I rely on and go to in times like these. If the relationship causes you stress each time you try, you might want to just stop emailing your dad until you're healthy again.

Guest ~jules~

lmao! Man I wish I was a fly on the wall when the doctor sees that! ha hahahahahahah!!! I agree with the stressing out though, you've got to chill a little its probably making you feel worse. Well at least you'll find out that the procedure is no biggie, so when you need to start getting checked routinely when your older you wont be so afraid of it. Just a thought.

Lister Rising Star

i think i have calmed myself for the procedure yeah im still woried about it but im not letting it get to me anymore. but im starting to think about the night before now so i meen i guess tomorrow.. the not eating part i meen yeah they said i could eat all the way up until 4pm but then no more food.. usualy if it was like 5 months ago that would not be a problem but eating is the only thing that keeps my stomic from always hurting so i am going to be in constant stomic pain all night long and then they want me to take a laxative before sleep... so how am i supposed to sleep laxative+empty upset stomic= really really upset stomic.... man tomorrow is going to suck

on a side note

are spicy things naturaly hard on the stomic? me and my girlfriend made some home made salsa tonight but i dont wanna eat it now that i was thinking that it could irratate my stomic it has cilantro,white onion,jalapeno, and tomatoes.. would this be cool or am i going to give myself a stomic ake?

also anyone know gluten-free laxatives??

_______

omg mmmmmm, i wish i would have known how good cilantro was before, i just boiled some with my chicken and omg so fricking good im drooling

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,896
    • Most Online (within 30 mins)
      7,748

    debbiebryant12
    Newest Member
    debbiebryant12
    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

    • Gigi2025
      No, I've not been diagnosed as celiac.  Despite Entero Labs being relocated to Switzerland/Greece, I'll be doing another test. After eating wheat products in Greece for 4 weeks, there wasn't any reaction.  However, avoiding it here in the states.   Thanks everyone for your responses.  
    • Rejoicephd
      Thank you @JulieRe so much for sharing this extra information. I'm so glad to hear you're feeling better and I hope it keeps moving in that direction. I feel I'm having so many lightbulb moments on this forum just interacting with others who have this condition. I also was diagnosed with gastric reflux maybe about 10 years ago. I was prescribed ranitidine for it several years back, which was working to reduce my gastric reflux symptoms but then the FDA took ranitidine off the shelves so I stopped taking it. I had a lot of ups and downs healthwise in and around that time (I suddenly gained 20 pounds, blood pressure went up, depression got worse, and I was diagnosed with OSA). At the time I attributed my change in symptoms to me taking on a new stressful job and didn't think much else about it. They did give me a replacement gastric reflux drug since ranitidine was off the shelves, but when I went on the CPAP for my OSA, the CPAP seemed to correct the gastric reflux problem so I haven't been on any gastric reflux drug treatment for years although I still do have to use a CPAP for my OSA. Anyway that's a long story but just to say… I always feel like I've had a sensitive stomach and had migraines my whole life (which I'm now attributing to having celiac and not knowing it) but I feel my health took a turn for much worse around 2019-2020 (and this decline started before I caught covid for the first time). So I am now wondering based on what you said, if that ranitidine i took could have contributed to the yeast overgrowth, and that the problem has just been worsening ever since. I have distinctly felt that I am dealing with something more than just stress and battling a more fundamental disease process here. I've basically been in and out of different doctor specialties for the past 5 years trying to figure out what's wrong with me. Finally being diagnosed with celiac one year ago, I thought I finally had THE answer but now as I'm still sick, I think it's one of a few answers and that maybe yeast overgrowth is another answer. For me as well, my vitamin deficiencies have persisted even after I went gluten-free (and my TTG antibody levels came down to measurably below the detectable limit on my last blood test). So this issue of not absorbing vitamins well is also something our cases have in common. I'm now working with a nutritionist and taking lots of vitamins and supplements to try and remedy that issue. I hope that you continue to see improvements in working with your naturopath on this. Keep us posted!
    • ElenaM
      Hello everyone. I am Elena and am 38 years old. I suspect I have a gluten intolerance even if my celiac panel is ok. I have the following symptoms : facial flushing, Red dots not bumps în face, bloating abdominal distension, hair loss, depression anxiety even with meds and even bipolar. Fatigue extreme to the point of not being able to work. All of these after I eat gluten. Could I have non celiac gluten sensitivity? Thanks anyone else with these symptoms?
    • JulieRe
      Hi Everyone,  I do appreciate your replies to my original post.   Here is where I am now in this journey.  I am currently seeing a Naturopath.  One thing I did not post before is that I take Esomeprazole for GERD.  My Naturopath believes that the decrease in the gastric acid has allowed the yeast to grow.    She has put me on some digestive enzymes.  She also put me on Zinc, Selenium, B 12, as she felt that I was not absorbing my vitamins. I am about 5 weeks into this treatment, and I am feeling better. I did not have any trouble taking the Fluconazole.  
    • Ceekay
      I'm sure it's chemically perfect. Most of them taste lousy!        
×
×
  • 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.