Surgery

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Wendy, puppies have amazing superkalifragilisticexpeialadocious healing abilities!!! Keona especially. I expect you will sleep tonight, dog farts and snores no doubt helping, and you will feel better in the morning.

Lets hear it for the dogs!!!

:hug:
Misty
 
too much excitement I guess. Got sick (excitement?? no sleep?? doing too much??) anyhow, my voice is back to being really hoarse and they asked me to consider tomorrow night. I have an appointment in am/advocate and then doctors/afternoon.. maybe evening ( i can of course have her back whenever I want her).. it also didnt occur to me how i would pick up after her until now..

charlie is good too ..
 
I guess you need a pooper picker upper!

Take it easy - I know you miss your cute pupper, but make sure you feel up to it first!

- Ames
 
I don't know how I missed this thread. I was wondering about you! Glad to hear the surgery went well, hope you're feeling up to speed real soon.

Get some rest and get well!
 
Hey Wendy, I hope things are continuing to improve for you. Is Keona home? Wishing you well!!
 
HAHA... thanks everybody!

KEONA is home as about 1/2 hour ago. I am really VERY HAPPY about that... :D The people who had her owns a farm (and was spoiled!!) and she was playing with all the animals and went on a lot of car rides (she lives for them). The person who took her was an advocate. She ran straight to the bath tub after we went grocery shopping -- to catch a nap... she is whopped :)
Amy I thought of te pooper picker upper but i live in an apartment building and didnt want to bring a dirty pooper scooper up .. I will get a lot of practice squatting :)

On another note - every thing looks good... incision wise. I went to the dietician and doctors yesterday and they think I have a partial bowel obstruction. I have been taking 2 senekott and 2 prescribed strength docusate sodium and 30 ml 2x's day of lactuloase....and still no pooping since surgery. I am feeling it in the area where the strictures are.. and I also feel a little nautaus after eating. I have been put on a soft food (soup, cottage cheese, smoothies, breakfast anytime) diet so I hope it helps. I think the fact that I had so many narcotics and anaesthetic likely contributes to the problem (not to mention lack of activity) so I will see how it goes... sort of a catch-22 b/c the more pain, the more meds I take.
Good thing I LOVE smoothies.
They keep reminding me to call 911 if I get extreme pain and start vomiting... i think it will start working soon...

click on my facebook link and you will see a new pic of Keona. :D I couldnt upload it here...says it is too large so just as soon as I figure out how to ... I will :)
 
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AWW! So glad you got Keona back. Love that she naps in the tub, haha! her new profile pic says, "Mommy, I'm so happy to be home!"

Glad your incision is healing well. I hope you don't have an obstruction! Yipes! I had terrible terrible pain from my partial. Can they not prescribe steroids while you are recovering from surgery or combine them with the other meds you are taking? I'm having a brain fart whether or not steroids and recovery mix. :)
 
i hope I dont either Marisa.. in fact, I think of you and your experience ..yikes! I am feeling the pain in the same spots as before but worse and different. I really feel they are listening to me now..they want me to call the on-call if anything changes or call 911..
i dont like that they ask about what my pain is like b/c there are a few different places and the pain is different in each. The new pain comes in short but intense waves like I am in labour and then it goes away..

oh..and just a tip to pass on.. my dietician told me to get Carnation Anytime (use to be Carnation Breakfast) as it is cheaper and doesn't have that vitamin aftertaste to it. There is also more to drink so you can feel a little more satisfied. You can add both to smoothies :D Im going to be a smoothie pro when Im finished... :D
 
So glad everything went well, but sorry to hear your are still in pain. : ( Hang in there, do call if you need to...those doctors work for YOU, remember...!

Oh, and your milky white medication is likely propofol, just in case you still needed the name. : )
 
YA! that's it... I didn't like it .. AT ALL .... :( Luckily it was for only a few seconds...
Michael Jackson used THAT to sleep ?!?! whoa.... :eek2:

thanks for the encouragement Doc.. I would get to hospital if I needed to...

Marisa, I dont know why he hasnt prescribed prednisone yet.. he mentions it almost every appointment... He wanted to see the biopsy results first I guess to make sure it isnt something else... . He keeps telling me that he wants to be 100 per cent sure I have it... he is pretty sure and every test points to that .. im confused why he's waiting.. but according to peoples experience on here with it.. IM a tad bit apprehensive myself :confused2: I haven't told him that though.
 
I must have been under a rock for the last year because I just realized right now that KEONA is the name of your dog. DUH!!!!!

Glad you are both home now!!! Hope you start passing stuff soon and that it is not an obstruction.

Take care of yourself and get plenty of rest!

- Amy
 
ROFLOL
laughdog.gif


yep..my dog's name is Keona :)

Thanks for the laugh Amy...
 
I am happy that your Keona is home. I know how empty a home can feel without your beloved doggie in it!

I really hope you do not have an obstruction. I am surprised that they have not done more for you with the pain and symptoms. I do not blame you for the percs. I get sooo nauseous with them.

I am glad that you are home and I hope that things start to get better.
 
Yipes...waves of pain and feeling like your in labor. That's exactly how I described it. It's good you are staying on a mostly liquid diet though. I tried that but I think it was oto late at that point. Are you feeling super nauseous too? I was and then the second I threw up I knew we had to go to the hospital. It was funny too because as we were sitting in the waiting room my pain eased up and was bearable. I was thinking "I hope these people don't think I'm faking it." I was taken back right away though. If you do go in, make sure you emphasize that you just had surgery and your docs think you have an obstruction. Usually they won't make you wait.

I hope the biopsy results come back. Maybe the docs, given your situation, put a rush on the results. That would be nice, so you don't have to prolong the suffering any more than you have to!

I love the laughing dog icon. ;)
 
The nausea comes in waves as well but not to the point where I'm going to throw up. I get a really full feeling even after drinking liquids. It's a burning feeling even up near my sternum. I am going to definitely call my GI if it doesn't improve by Monday. I am glad I am only drinking liquids. My dietician also thought it was a "mechanical" problem. I tend to always get really constipated and then have difficulty passing initially and then I have D until I am empty and then the pattern starts all over again with the constipation for awhile... then hurts to pass and then D..... I notice a big relief once the D starts... sounds weird but I would rather be going lots than none at all... I honestly don't know why they don't do anything more. I think it all comes down to my GI not wanting me to take steroids just in case it is something else. I think all of the arrows are pointing to Crohn's though... it obviously wasn't the endometriosis causing all of this.. but I have only just found that out (definitely)....
 
I just hope you get a definitive answer one way or the other so you can get on with your life!!!....which is so well lived even with the pain, I can't wait to see the output w/o it!!!
 
Thanks Dex.. Im calling tomorrow to get this ball rolling again.. I think I have been more than patient long enough...
 
More than long enough mate, you deserve a medal! Good luck with the call tomorrow, keeping my fingers and toes crossed that the ball gets bouncing along!!!

Much love, :wub:
Dusty. xxxxxxxx
 
Good Morning ! (or at least it is morning where I live :) )

I hope you're awake and making that phone call and demanding the answers you so deserve !

Best of luck and hope you are feeling well !
 
Thanks :D for the friendly reminder Tracy!
I started with my OBGYN this morning to book the post-op appointment and to see if my biopsies are back and if so; do I contact my GI for the results or them. The receptionist is going to get the nurse to call me back with the answers. Im not too concerned with the OBGYN bit as I always knew in my head that I had endometriosis and it has now been confirmed. Just want to know the GI piece.
I'll let you now when they call back. I almost think it might be easier dealing with the OBGYN first.. than the GI.
 
Good Morning, my thoughts and prayers are with you today as I look over this thread and think what an incredibly strong person you are. This is my very first post and I can not tell you in words what I feel about the people who are part of this community. I feel like a lost soul in a sea of unknowns.

I wish you a lifetime of love, happiness and wellness.
thank you for ur inspiration, you may not know how much you inspire others.

as i was reading about ur surgery being cancelled at the last moments, i had 2 thoughts.
A) it was God's ( or an angels ) hand telling it was not your time to be in that O R. dont know why, but im not one to question something like that, and B) is that like being bumped from an Airline Flight ?? ( lol ) at least there you have the chance to get a free flight, any chance they offered you a discount on that following Monday ?? lol, just a giggle for the morning. I find if I dont make myself laugh at least once a day, I go crazy with thoughts of sorrow.
 
Good Morning PnaG
I know what you mean about having to laugh or else you would just cry all the time. If you think my story is inspiring (and thank-you for the compliment) wait until you read others stories... there are people on here who have had it way worse than I have and not to sound like it is at their expense, but it makes me grateful ... and truly inspired.... I am glad you found the forum!

I live in Canada so I dont have to pay for medical care (with cash anyway).. living in Canada, it takes forever to get an appointment or a test done. I did however get a free parking pass (that we never used) and a gingerale (that I refused as my way of protesting...lol...{and WAS very thirsty from fasting all night..so who won on that one?!?}) ..it is funny you use the flight analogy as I made a joke about accepting air miles (when I was on anesthetic) .. not so sure how funny that is in hindsight though
:rolleyes:
Anyhow... hope you found the "My story" section so that people can get to know you and offer support. It is truly a great forum - the members here can really keep you going when you have difficulty doing so..and it is a great place to share accomplishments!. WELCOME :D
 
Thnx hun. i went and posted My Story lol. as if peeps wanna hear my story LOL i still believe ur my inspiration.

i think i knew that canadians dont "pay" for medical treatments. seems the world is about $$ and because of that , compassion and empathy seems to have left the doctors offices LOL
 
people DO want to hear your story - going there now to read it...
i agree...a lot of the doctors are all about the mighty dollar
 
How ya doing, Wendy? Feeling better these days?

Thinking of you and hope you are doing alright.

xo - Ames
 
Hi Amy!
Thanks for thinking of me. Things are going well as far as the incisions..they're pretty well healed and every now and then I get a tearing sensation depending on how I move but otherwise, everything is going well.
I finally had a bowel movement and am at my whits end because Im not sure what to do. I had a very large bowel movement in which I seriously had to brace myself and thought I was going to black out passing it. It was very dark in colour for the first part and then was lighter the second part and consisted of a lot of pebbles so-to-speak. Im not surprised by the blood I saw - which wasn't a lot but right afterwards, there was another bowel movement that again was stringy and long...also blood streaked. Im not really concerned with blood as I have a feeling I might have internal haemorrhoids or a fissure or something.. I am concerned by the size and the pain passing it. I am still on a liquid diet and I cheated once with one of those fibre bars. I did this because I had some relief on the liquid diet, I wanted to see if it was all in my head..

I am not sure what to feel anymore other than sheer frustration... and confusion... if I have a blockage, how come such a large stool got through... also if I do have an obstruction...what are the doctors waiting for (medication wise)??? I am scared that passing such large stools is going to cause other issues.. or even being on a liquid diet will...or waiting ...

if anyone has any suggestions, advice or information about this PLEASE let me know. Is there something I can be doing differently at home that I'm not already doing? I did put a call through to all my doctors on Friday to get results of the biopsies.. I didn't get a call back except for the reception of my OBGYN with my next appointment in a few weeks.
Thanks in advance
Wendy

P.S: I am strongly considering quitting the dilaudid and going back to eating regular healthy diet ... if it sends me to the hospital and maybe then I will get some help. I really dont know what to do...
 
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Hey Wendy, I've read on here a few times that the pain meds can cause constipation. Are you drinking plenty of water?

Hope I'm not over simplifying by asking...
 
This is your first bowel movement since surgery???

When is your CT Scan?

Are you still taking psyllium husk?

Sorry about all the questions Wendy!

It is a concern that you are quite a lot of laxatives that don't appear to be working very well at all. Some of that may be due to the pain management medication and psyllium husks. If they are talking about partial bowel obstruction and you didn't have a bowel movement for ? 11 or 12 days I'm surprised you didn't actually pass out! It can be a vicious cycle with medication but that is something that can be managed. It is not working for you and therefore it can't be allowed to continue like this, I would be contacting the GI.

Thinking of you hun, :hug:
Dusty. xxxxxxxx
 
I would also guess that the dilaudid is causing constipation and the big poo you passed. All of the blood cannot be good! If you do have an internal hemmy or fissure you probably want to soften things up with a stool softener in addition to the psyllium husk and flax seed stuff.

Def call your GI on Monday and report what's going on.

Hang in there, Wendy. I hope things get better and start moving thru a little easier without so much strain.

xo - Ames
 
Ok, first....long amounts of poo are not necessarily a bad thing. I typically pass a long amount of stool when I do go (which is once a day typically). I've looked it up before, and long stool does not indicate anything negative, under normal circumstances. I had long stool all the way up until I ended up in the hospital due to my abscess. And when I was in the hospital they found out my intestines were severely narrow due to all the inflammation. That wasn't surprising since I obviously wasn't being treated for anything. And my stools were normal all the way up until I ended up in the hospital, which is why I didn't know anything digestive was wrong with me.

Now, when I had the partial obstruction, I knew there was something wrong because I wasn't passing anything. I had maybe one or two very small bits passed, but I could feel the full sensation and wasn't even able to pass any gas. It was a terrible feeling with extreme gurgly pain.

The pebble look to your stool definitely means you aren't getting enough water. Now...I don't know what your typical bowel habit are like, but since you described having very long stool, the part that was pebbly could have been from several days ago. Especially if you haven't had a proper bowel movement since surgery...could have been for a long while.

The long stool could just mean that the stool has just taken more time to get through your intestines. With no fiber to help it through, it could be why it took so long to pass and difficult to get out.

I have heard that some medications can constipate, so you may want to call the doc and double check with them about it. I agree with others about that. How much are you drinking a day? Just enough during meals? I know it sounds like a lot, but you should be drinking constantly.

BTW...the first listed side effect when I searched about Dilaudid was constipation. So, you may want to call up the doc and see if it's okay to stop it altogether.
 
HEy everyone
thanks for your replies. When I saw my dietician she asked how much water I was drinking and I told her and she was concerned I was drinking too much water (I am losing weight) and she thought the amount of water I was drinking was causing me to lose my appetite. Yes, dialudid does cause constipation but I was having these issues long before I started taking the dilaudid. Remember the 19 day stent I had?? that was before the dilaudid.
Yes, it was my first bowel movement since surgery.
@ Dusty I dont know when my CT is. I did call on Thursday and left a message. Monday is a holiday here as well so I have to wait until Tuesday.
Currently I am drinking smoothies..thats about it. It has lots of fruit in it...typically bananas, mango, blueberries flax seed, sometimes milk with carnation anytime..sometimes juice..and LOTS of ice with both; milk ones and juice ones. So, on top of all the water..all I am really doing is drinking. I was told to stop the psyllium husks until I see her next at my last appointment.
@ Marisa...lol...you say long amounts of poo aren't necessarily a bad thing yet your 2 examples describe you ending up in hospital both times after... hmm..

Before last night.. I wasn't passing anything either. And I was having the noises like you describe but lower down from my belly button area...In fact, some of the noises, I didn't know where it was coming from.
You know, I would say I give up but Im not even sure what that looks like anymore...and mentally I can say that but my body is still going to keep doing what it is doing... I was given the lactulose with the dilaudid...which I have been taking and the stool softener(S) I have been taking for a long time - long before the dilaudid.
So..if I stop taking dilaudid then Im not sure what I am supposed to do with pain... all pain meds cause constipation....
I'll call my GI..again... but Im not really sure how much that will help considering it hasn't helped that last x-amount of times I have called...
 
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Hi Wendy! I'd say congrats on getting all that out of you. Although painful, I do hope it brings you some relief in some way.

(I must say, this is an interesting forum...certainly nothing is sacred here, and wow am I grateful for that! :shifty-t:)

Because you aren't being treated for Crohns or UC yet, no doubt you ARE at the end of your rope! But soon, I hope REALLY SOON you will get that CT scan and hopefully some medication to help! I hope that after that this will not be your facebook page photo: :poo:

I will say my neighbour, bless his white cotton socks, didnt go for 14 days after surgery. He said he almost died when he did. (he has crohns too) He said it was horrendous. I can only hope you didnt scream as loudly as he did, but frankly I wouldnt blame you if you did! (he was also still on almost all liquids, he too had blood, quite a bit) I just hope you get some help and relief soon. Meanwhile, belly rub that baby dog of yours, and keep harassing for that CT scan. You need some help...NOW!

:rosette2:
Misty
 
Sorry, Wendy. I think I was unclear in my explanation about my typical stools. I've always had long stools. Before and after being diagnosed...and even now. So, long stools are not necessarily indicative of bowels not working properly, is what I was trying to convey. :)

Yes, I do remember you going that long period without having gone. This is why this all confuses me if you do have a partial obstruction. WHY AREN'T THE DOCS DOING ANYTHING ABOUT IT??? Making you wait to get a CT, prolonging the time you are on pain meds that could be constipating you, NOT putting you on steroids to help with inflammation in the mean time. I DON'T GET IT!!

Yeah...you shouldn't be on pain meds if they are constipating you or exacerbating your symptoms. The answer is for your docs to get on the ball and find out the cause of your pain so they can get you off the pain meds!! Sheesh. I just really don't understand a doc's line of thought with "I think you probably have a partial obstruction" and then not immediately schedule you for imaging to confirm and get you started on proper treatment.

I have heard that dairy products can cause constipation. I don't know if you've tried eliminating that from your diet (which again is easier said than done when you're on a liquid diet and aren't really eating anything!).

Also, have you read up on potential side effects of flax seed? If not, webmd had some good stuff to ponder over.

http://www.webmd.com/vitamins-suppl...ngredientId=991&activeIngredientName=FLAXSEED

I know you said you are drinking plenty of water, but given the possibility of a partial obstruction and you're still having difficulty passing stools, maybe it wouldn't hurt to stop taking and see if that improves anything. Though I'm not sure if your nutritionist suggested taking the flax seed or not.


Anyway...not trying to boss you around. So, I hope I don't sound like I'm telling you what to do. Just trying to maybe throw some things out there that maybe you might not have thought of yet. I know you've been through a lot and you are a very intelligent person, so I wouldn't be surprised if you've read about all of this stuff already. :)

Just trying to help from my side of the computer. ;) But maybe you weren't asking for help. Just support, which in that case I will shut my mouth from now on, haha.
 
The problem I see here Wendy is, you should be able to have a more than decent pain management regime and still not be constipated. The doc obviously felt that the amount of laxatives you are taking were sufficient to avoid the problem of constipation but it isn't and that is something they need to deal with.

Laxatives come with their own set of side effects and does constipation and these two things are, in my mind, further clouding the issues you already have.

My heart goes out to you Wendy and I don't know what to advise other than getting in contact with the GI. I wish I knew your health system better so I could perhaps suggest a way to circumvent all this crap you are dealing with. I guess the only thing I can say is if constipation is building again go to the hospital and lay it on thick with the abdo pain, recent surgery and inability to open your bowels.

Loads of love and hugs mate, :hug:
Dusty. xxxxxxxx
 
When I went to the Dietician she was the one who told me to take the flaxseed - ground flaxseed..not whole. She told me to go slowly. I have used it twice since I have seen her. I also stopped taking the flax-seed capsules the day of my pre-op appointment (March 29th). The anesthetist told me to...said I should only take the dilaudid and pantoprazole the day of surgery so I just stopped all but those two and haven't started up the others since. I took the ginger gravol only when I have been nauseous (maybe 4 or 5 since surgery) and have taken the tylenol when I get rebound from taking it every 4 hours with the dilaudid...so..only when I have to. I will change my signature. The dietician told me to stop taking the cod-liver oil as well because you can get too much vitamin K.

I think the problem is I have too many doctors and they aren't communicating. It was 2 interns and the dietician that said it was a partial obstruction.. "mechanical issue"... (in one appointment my GP was watching via video) and the other they left the room to consult with her. The 19 days was just before I got the results about having 2 strictures.

I dont know why they're not doing anything.. I dont have an answer for this.
I questioned the GP's prescriptions when I heard Im not supposed to be on omeprazole for 3 years ... which I was... AND without calcium supplements

The GI told me they (radiologists) would not do the CT until 2 weeks after the surgery. Im not sure if he knew the surgery was bumped or not.. but it has been just a little over 2 weeks. I haven't heard anything so that is (partly) why I called. (I was also wondering why they need to use an NG tube for the contrast when all the literature I have read, it explains how people can drink it now. If you know the difference, that would be helpful also.)

Dusty Im hesitant to go to ER as the last time I went all they did was a roll-up bedside ultrasound and chest x-rays (I still don't know why) and abdominal x-rays. They asked me if I wanted pain meds.., told me I needed a more nuanced ultrasound and to follow-up with my GP the next working day...and sent me home.

Misty - nope I didn't scream but I could see why your neighbour did. I think I did a lot of swearing though...

I dont cry in front of people but sometimes I wonder is that what they are waiting for?? For me to go in and start crying in front of them??
 
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Maybe you should go to your GI's office and stand yourself at the front desk until you have a CT scan appt? I dont cry in front of others either Wendy. I wait til everyone is asleep.

They seem just disorganized as hell. Perhaps they need a shove in the right direction? YOU GO GIRL!!! Dont let them ignore you. Whether by glaring or bambi eyes....get your CT scan!

Misty
 
Im not sure if Doctors offices are open tomorrow or not. Easter Monday?? I know some places are open some not. He works out of the hospital so maybe... Regardless, I will call.

I know constipation is not a life threatening condition however I am getting really really tired of this dragging on. I have missed every holiday for 2 years now. At least one of the interns who gave me the dilaudid and recognized my pain also recognized that there is poor communication between my GI and GP's office (and me). I LOVE to exercise..run...hike, etc... I haven't done any of that for 3 years now... 3 YEARS!!!
I am single... I havent gone on a date in ... umm... I dont know how long and guys have asked me out (one in particular) however, I am waiting to feel better... and i never do.
 
Tell them that! You deserve a life. Period.

If you dont do it for you, do it for your dog! Methinks running and walking are things she misses too!

Misty
 
I know constipation is not a life threatening condition

Under normal circumstances it isn't Wendy but we aren't talking normal circumstances. If you do indeed have a partial blockage then constipation can become life threatening...perforation. This is the aspect of your problem that really concerns me and something that the docs really need to get on top of. I know you are trying and doing your very best to get this sorted and I hope more than anything they sit up and take notice now!

Thinking of you mate, :hug:
Dusty. xxxxxxxx
 
Hi Wendy- just catching up here!
Hope you can get this problem sorted pronto. Hang on in there, easier said than done sometimes I know!!
Hugs, And xx
 
I called to get a GP appointment today - there is nothing until Friday. They want me to call back before 8:30 am tomorrow to make an "open appointment" - there were no doctors there but yet the office was open?? WTF??? I hadnt even given them my name....
I called the OBGYN for the results of the biopsies and it was an answering machine.... 3rd message I have left.

I called the GI to ask for the results of the OBGYN - they told me I had to call my OBGYN. I asked about the CT - they told me my last MRI came back normal and there is to be no further follow-up (radiologist). I got angry at this point and said that he wanted the CT BEFORE the last MRI because it wasn't getting good images and he told me to go ahead and have it done anyway since I was scheduled. I also sad "know what I did this entire week-end?...nothing. Know what I ate this week-end?...liquids and I am STILL in pain. She said "oh well that was probably due to your surgery"...I told her I had surgery over 2 weeks ago... (she kept calling it a "laparotomy" and I kept correcting her it was only a LAPOROSCSOPY!!!) and it is healed and the same pain is in the same spots as before. I told her I asked the OBGYN if endometriosis causes strictures and thickening of the bowel walls and she said no - that is Crohn's disease. I could then hear her shuffle some papers and read verbatim something about "if that doesn't prove to be helpful then schedule the CT enterography". Im not sure what "THAT" refers to... but nothing is helpful and THEY ARE NOT HEARING ME.... she said "well, we will have to see what Dr. M has to say about this then. That was it... Im not sure if Im doing something wrong here or if it is because I am basically doing this on my own or what... I dont understand how we get from talking about a resection in the last appointment to "no further follow-up" over the phone with the receptionist.
This is all fuc*ed if you ask me....

to top it all off.... I had to send regrets in an email for not attending a meeting today (I haven't attended one since January). I felt bad and told the person why ... she is a lawyer..(not that that makes any difference) but her response was, "Thanks Wendy. Hope you feel better soon! And it does get better (Chrons runs in my family- I control mine with diet and vitamins. The meds didn’t work for me). " I'm not sure why this pissed me off further but I am now even more pissed off....

Makes me wonder how long now I have to wait for the GI to call and how long it is going to take to get the CT. Have you ever been so angry it makes you want to cry??? I seriously don't know what to do anymore...nobody is communicating with anyone and I seem to be doing all the leg work here... THATS THEIR JOB!!!
 
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update: Since this... I have gone from crying out of sheer frustration to looking up at my laptop and reading this posted on FB by a member here:
"PLEASE put this on your status if you know someone who has been eaten by dragons. Dragons are nearly unstoppable, and in case you didn't know, they can breathe fire. 93% of people won't copy and paste this, because they have already been eaten by dragons. 6% of people are sitting in the shower, armed with fire extinguishers. The remaining 1% are awesome, and will re-post this."

to laughing.....

I dont even know anymore.....
 
I know you are tired and weak, but can you go directly to the GI's office and sort them out?

:devil:
Misty
 
I called the advocate and they are sending an email to see their doctor. She is a family doctor but she works right out of their office or will go to you - which Dr's don't do here anymore... I cant even get in to see my GP...I see her interns who tell me conflicting info like drink milk/instant carnation anytime and take percocets and dilaudid... (Im sorry Marisa if I seemed bitchy in my response) I am just so tired of being pulled in so many different directions and the person with the power (the GI) isn't doing anything. He has the power to order the CT and if it's Crohn's then do something... if not..send me in the right direction... I have been on liquids for 2 weeks .. milk based smoothies and taking dialudid and on top of it all taking loads of laxitives..I am going to get the new GP to see if she can order the CT scan.,.. the GI works out of the hospital
 
Hi Wendy, I am so sorry that you are still having to put up with this c**p! It's so wrong and damn unfair. I agree that your GI either needs to help or point you in the right direction to allow someone else to help..
Hang in there, easier said than done I know.
Thinking of you and sending a big virtual hug xx
 
Wendy....I'm with Joan on that one! (isnt she great!)

Go get em....or have the advocate go get em!!

Work on that rrrrrrrrrrrraaaaaaaaaaaaaaaaaaarrrrrrrrrrrrrrrrr!!!!!!!

Misty
 
It's okay, Wendy. :) I understand you are dealing with A LOT. And I know how frustrating it can be when you are doing everything you possibly can and then someone thinks they have the magic answers to your problems. So, I'm the one who is sorry :). You're just trying to follow doctor's orders (when they actually give you some!). I didn't mean to over step my bounds!

Wish I could be there to yell at all your doctors for you. I'm doing it already from this side, haha, but it's not doing any good. ;)

What does the advocate say about the back and forth with scheduling the CT scan?
 
I just received a call from my OBGYN's office. She did not take any biopsies for my GI because she dod not receive anything from him asking her to.
 
I havent been sleeping and she woke me out of sleep. When she told me who she was she said there were no results to give that I need to speak directly to my OBGYN on my post op appointment. I asked her "wait.. didnt she take biopsies? My GI thinks I have Crohn's" and she said no that there was nothing from him. All I kept saying was What?? She seemed a little short trying to get me off the phone or maybe I was just really out of it..I dont know.. I heard him say that he was going to ask her to take biopsies for him. I had an advocate there with me when he said that.
She just kept saying I need to speak directly with my OBGYN..when is my post op appointment..
it is on the 11th of May.

I need new doctors...
 
Wendy- I'll send Joan over pronto to get this sorted for you!!
This is so bloody wrong...and I agree that you need some new doctors!! xx
 
Holy moly...what the heck is going on with your GI?? What is he getting paid for, seriously? Doesn't sound like he's done anything helpful lately AT ALL. I'm glad your advocate was there, at least, to hear what your GI said. In case you have a hard time convincing a GP to refer you to another GI, hopefully having your advocate as proof that your GI is dropping the ball will help!

I'm really sorry. I seriously never have heard a group of doctors have more communication problems than you have had to deal with. It's unbelievable! I can barely keep up with all these blunders!
 
I want to scream in frustration so I can't imagine how you must be feeling about this. We have a hard enough time just being as sick as we are, let alone having to constantly wrangle these crazy, incompetent docs who don't know how to communicate. I think it is so insane that this happened to you, there are really no words!

That is really just unbelievable.
 
I just fired my GP and the advocates put in a referral for their GP. It is a temporary thing until I can get a new one.

I also called the GI's and the reception was not happy with me and told me very sternly that the GI does not request anything from the surgeon. The surgeon does what the surgeon wants and sends the info to them. Well, this is not what I heard nor what the advocate heard and besides, the GI still did not ask for anything to be sent to him so either way..where is the communication?? The nurse who sat in on the appointment is calling me tomorrow.
 
I really do not like confrontation..especially when it is with people of power...and with people who have my health in their hands. I am doing better now. Thank-you everyone. A little anxious about the call tomorrow from the nurse. What if they tell me to find a new GI?? That could mean another year wait. I am still waiting for word from my recently fired GP about the last "new referral". Never heard anything since. Maybe I would be better off getting a new one...

I am hopeful with the new GP. I don't know when I can get in to see him/her but they are being referred by people I know and the advocates will catch him/her up to speed for me in terms of care (lack of) so far. I am looking forward to starting anew...this is a mess. Who goes from one appointment with a GI & being told about having a resection and SBS to a phone call from a receptionist saying no follow-up care required??? Then back to needing a CT all in one day??

Thank-you for being there everyone.
W.
 
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And Marisa...you dont need to apologize. You didn't over step boundaries at all... I asked for advice, feedback, suggestions.. I think I was frustrated that what you had pointed out is correct..they told me to drink milk based drinks and take painkillers and flax seed all the while telling me I have a "mechanical problem.."

I am mostly pissed off that they were inside me and had the chance to take biopsies which could prove to be helpful in diagnosing why I am like this and what...forgot??

The advocate said (there are many, not just one) but they can go to bat for me regarding the lack of care I have been receiving. The 2 I spoke with, one was very supportive of my feelings and the other was very calm and level headed..factual and walked me through the referral forms on the phone. I have to sign a release of information tomorrow for them to speak to the new GP.
 
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I wish there was way to review doctors because people need to know about how terrible these docs have been treating you. Thank goodness for advocates. If I were in your sheos I surely would have lost my mind long ago.

Really hoping and praying your advocate's GP is the right one for you!
 
there is: rate your doctor . com. Only the problem with that is it is very biased b/c people who had good experiences with their doctor wouldn't really take time to write a good report - they are busy living their lives. I suppose it would be a helpful guide. I am waiting for the call from the GI nurse tomorrow and see how that goes. If they say he never said he was going to request biopsies I'm gonna flip. I had someone with me...she heard him.

Ya Marisa...thank goodness for advocates....
 
I just got off the phone with the GI nurse and apparently I have irritable bowel Syndrome. She said he wants me to take Donnatal. I have had t before - it didn't work.
 
ha..thanks Misty :)

Yesterday was a rough day with pain, no sleep, a lot of crying, (lost 6 pounds this week-end) and BS from receptionists and nurses. I haven't spoken to any of the doctors. And I couldn't get any appointments with any of them..

If it weren't for the worsening pain and the MRI's showing strictures and thickening of the bowel wall .. I would probably be second guessing things as well. I have been told for over 15 years that I have IBS. Maybe I do...maybe I don't but I have tried the drug already, which did nothing.

so now... Im angry. And there is something empowering about that. On the phone today I had all of you in my thoughts as I questioned the clinical nurse after every attempt she gave to dismiss it as IBS. IBS does not account for structural changes in the bowel - and I told her that (much to my surprise). She was not impressed but neither am I and at the end of the day - it is my health - not hers and she gets to go home and celebrate special occasions and eat turkey and walk her dog if she has one. I cant at the moment.
The last thing she said was she would go back and talk to the doctor.

My new GP appointment cant come soon enough and although I dont have any proof of this... I know that it will work out between the new doc and I. They are aware of these sorts of cases...that is why they are reserved for people without doctors. And I have great advocates on my side as well... :D
 
Not glad to hear your GI has proven to be worthless yet again, but hey we weren't really surprised by that were we?

I think it's good that you are angry :) Sometimes it's required to get people to take you seriously. And I think it's given you a voice that you've been wanting to let loose for a long time!

Your positive attitude, despite what's going on, is encouraging and inspiring. :)

Keep going, Wendy!
 
Thank-you Marisa.
I have learned that it is much easier to fight for other people than it is ourselves. I suppose because I am really close to this issue..

and you are right.. I did find my voice!

One thing I didn't mention is that the GI nurse told me that when the OBGYN did the surgery she noted she looked at my bowels and said she didn't see any strictures or swelling. I find this interesting as my very first (and only) appointment with the OBGYN, I had asked her after we decided on the surgery if she would be able to tell if I had Crohn's disease. I believe I posted that conversation here already in this thread, and she told me, "no...that was not her area." The last laporoscopy I had, they said they didn't think I had endometriosis either. Ten years later of insisting I do, I am unable to have children because of this (but as everyone has proved, doctors can be wrong).

Anyhow, I came on to ask Marisa if you (or anyone) know if liquid capsules of flax seed cause constipation or just the ground ones? Is there a difference? I figure if I have to rely on my own devices for awhile, I ought to try alternative measures of relief. I stopped the lactulose because I am scared that it will screw up my bowels even more. I also stopped the dialudid (they wanted me to take it every 4 hours regardless of pain to make a "base-line"....). I have them and the percocet if needed... but thought I would just ride the pain out more with alternative measures. Im sure the dilaudid isnt helping the serious lack of energy either.
 
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I'm with Mark.... miss one day and holy shiite! I'm so sorry for all this crap you are dealing with, on top of recovering from the surgery.

I don't have much to add that hasn't already been covered, but just wanted to send a hug and let you know I am wishing you good luck.

xo - Ames
 
Here's a good link about flaxseed oil (liquid capsules qualify for this too, I think).

http://www.webmd.com/vitamins-suppl...dientId=990&activeIngredientName=FLAXSEED OIL

Looks like there could be a chance of loose stools and/or diarrhea if dosage is higher than 30 mg. Also, unlike the whole or powdered form of flaxseed, the liquid/oil form is highly susceptible to oxidation, so make sure you store it in the fridge. You wouldn't want to ingest rancid flaxseed oil. Yuck!

I imagine the whole/ground flaxseed form causes constipation is due to the fiber found in the seed coat. You don't get that if you use the liquid form. You just get the alpha-linolenic acid that helps to thin blood, similar to krill oil supplements.
 
Thanks everyone..:D

Just an update: I signed the release of information for the advocates to talk to the doctors so I dont have to repeat everything. This is usually a temporary solution getting this GP but they told me today that they are going to request that they take me on long-term so I dont have to keep repeating everything over and over.
As far as the liquid diet, I am concerned with the weight I am losing...as are they, so they are going to get me into their nurse ASAP to see if she can do anything. Unfortunately, today was the day that she works there but they are going to look in to it. I am okay with the waiting as I know that at least there are people helping me on my behalf and doing their best. Not what I experienced with the GI's et al. I have the option of ER as well but the last time, I was given a roll-up bedside ultrasound, chest and abdominal x-rays and sent home with instructions to follow-up with my GP. I couldnt get in to see my GP so the frustrating cycle continued.

So, I am inching along here and do feel confident that someone somewhere will eventually help me..just a matter of when. "Hopefully" this doctor will be the one.
W.
 
Hi Wendy! I'm glad to see you up and about on the forum. You are in my thoughts and prayers, sweetie.
 
Thank-you Andi :) I have been reading your posts, just haven't had much energy to respond to them....yet.... I am also thinking about you and hope things are improving for you. Still try to picture what it would look like seeing a massive iceberg :D

iceberg-subconscious-300x266.jpg


:D
 
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No worries. My CD is going anywhere I'm afraid, so I'll be here a while. LOL! You need to rest up and heal.
 
Oh man Wendy, after all the crap, setbacks and let downs this is finally starting to sound positive. I hope more than anything that this is the case hun and this is a turning point for you, god knows you deserve it mate.

Loads of love, :wub:
Dusty. xxxxxxxx
 
Sounds like a very promising update! :) The ball is rolling and there are people who seem to be genuinely concerned for your health, which is good!

Yay!
 
Hey Wendy

Far out - what an emotional circus you have been through. Time to bring on the op and get you some answers.:goodluck:

Wouldn't it be good if we could get all the 'ologists that we have in the same room at the same time so they can hear what each other has to say and to realise the impact of the differing treatments they suggest.

I would so love to have my gyno, gastro, uro, neuro, ent, and gp all in the same room. I wonder how they would go at changing a light bulb?

I am thinking of you Wendy. A few of us have endo and crohns - it's possible and its manageable at times - take care hun. Be comfortable - I love watching movies, reading books and being snuggled up in a comfy duvet. Do what works for you, and makes you feel good.

:hug:
 
Yes... I think this is a good move. I am also going to get help with writing a letter and others are willing to write letters on my behalf as well. I don't know where to send them yet or if the letters will even do anything but it is another option.

I have taken the suggestions..I cut back significantly on the dilaudid, but had to take perc today. I have also stopped all the milk and the laxatives and flax seed. Now I have D. Im still only drinking smoothies but tried some turkey soup I made myself (had defrosted it). It tasted good and it was good to eat with a spoon but caused a lot of pain. I am going to try the soup again in a couple of days as I have another bowl frozen (don't like store bought soups). Maybe the D is all the meds coming out of my system, who knows??
I want to get back to school and to start working again. First thing I am going to do is ask the doc to check my magnesium levels.
 
These are our rights as patients in NZ

You will have the right to:

•always be treated with respect
•not be discriminated against, pressured or taken advantage of
•services that promote dignified and independent lives
•be treated with care and skill and receive correctly administered treatment
•medical staff who listen to you and communicate clearly
•an interpreter if required
•a clear explanation of your medical condition and the types of treatment available
•an honest description of the risks and costs as well as the benefits of proposed treatment
•ask questions and receive competent answers
•make your own decisions
•change your mind if you have already said yes or no to a course of treatment
•refuse to participate in teaching or research
•have a support person present at most times
•register a complaint.


Do you have something similar? I think the letter is a good start, and they deserve a lot more than a letter
 
I wish we had health care like that.
I am going to respond to that when I return.

Had a doctors appointment with my clinic today as I went to the other clinic doc and they had to turn me away. She sent me to the nurse who basically gave me a number I already have to get a new doctor. So, that didnt work (they were hoping they would see me in the meantime before the new doc). I ended up going back to my last clinic and once again was sent to someone brand new and an intern on a different team. I have oral thrush again and it is hurting my throat and I had to ask her to take a swab. She also asked me to do an HIV test. Which I did just so they would stop asking me screening questions. I also asked for my records and they said I would have to pay for them. 5 cents a page and a fee but she wants me to see the intern I had seen with the dietician for the test results. She said she didnt think I had it but wanted to make sure. I think I keep getting oral thrush b/c I am only drinking smoothies and fruit is high sugar.. but who am I, right??
Okay - gotta go.. but am going to respond to Auras post when I get home. I have to go to an awards ceremony that I dont feel like going to. (I nominated someone for an award. I hope this person wins!!!!)
W.
 
I don't understand what is going on with your treatment at all. I'm sure you feel the same way. Guh!?

I hope your thrush goes away. I have a phobia of fungus so just the thought of thrush terrifies me!

Keep us posted on what's going on.
 
Well, yuck. Was the doctor that had to send you away the one your advocate's set up for you?

Usually yogurt ha lactobacillus in it, which should help deter thrush. But, yeah, if you are susceptible to getting it, it could be all the fruit you are eating, plus whatever sugar may be in any of the juice you are adding to the smoothies. What a nightmare!

How did the thrush go away the last time? I remember you tried basically every medication known to man to try and get rid of it. Or did it just basically run its course and go away after a while?

I never understood why patients must pay for their own records. I've seen that a lot here too. For some reason, it seems like you don't have to pay anything if you ask for results as you get labs and procedures done. But, if you request your whole health record at once you have to pay. Too bad there's not a charge if you offer to bring in your own paper for printing! ;)
 
Keona,

OMG I can't imagine what you are going through finally ready for your surgery and then having that happen! I hope by now you've had your surgery and are doing better? I just got my resection surgery scheduled today for 6/6 via laproscopic incision. My GYN surgeon will also be there as they too think I have endo and probable on my bowels and maybe my bladder. I am curious to see how you turned out and how you feel.... hoping for the best!

Hugs
 
Sorry Wendy! It's always up one hill and down another with your hc situation it seems! I know you're having a hard time staying positive but you've got a lot of good living to do so hang in there. Some day you're going to fall into the right situation for you so don't stop trying!!
 
Just done reading your story. Just hope it all gets better soon, keep fighting.
 
Thank-you all for your responses. I am doing okay., actually had a great night because the person I nominated for an award won. It was a lot of work (I needed to gather 5 letters of support, write a letter of nomination myself and also write a profile of the person.) This person has done a great deal for the community and has touched many so I was very proud to see her win. Her husband even teared up :)

So...ya, I am pretty sure the thrush is back b/c I havent been eating and when I do, it is smoothies with sugar and juice and I also went to a friends place for the week-end and we drank several beers so the alcohol likely has to do with the mouth sores and thrush I think. The sore throat/sinus's is likely from me chasing her 1 year old around with a kleenex - he had a bad cold. I dont typically get colds or flus but I do get congested sinuses and sore throats...thats about it.. I rarely get them. I took some very expensive pills that werent covered Marisa and also took nystatin on top of that and also dex suggested a mouth wash without alcohol.
I did look up the symptoms of HIV and officially scared the **** out of myself. The symptoms really do overlap and I can see why they may think that. Especially with my sore throat/swollen glands, etc. It is going to be a long 2 weeks.. and I have been scared ever since they took it. I had the lecture about having to have the health department involved, etc and how if it comes back + I need to tell them who my last partner was. He did cheat on me so the fear is there but I dont think it is the problem.


Rapid weight loss
Dry cough
Recurring fever or profuse night sweats
Profound and unexplained fatigue
swollen lymph glands in the armpits, groin, or neck
Diarrhea that lasts for more than a week
White spots or unusual blemishes on the tongue, in the mouth, or in the throat
Pneumonia
Red, brown, pink, or purplish blotches on or under the skin or inside the mouth, nose, or eyelids
Memory loss, depression, and other neurological disorders
fever
headache
joint pain
rash
yeast infections that last a long time or occur frequently

I dont have a cough, pneumonia (the chest x-ray would have picked it up), I do have a brown mark by my right eye but that is from the sun (came right after I was in Hawaii for a month and hasnt changed at all)
other symptoms are rashes, gynae problems, pains in stomach... etc..etc... so the list goes on and on..
they still haven't explained the thickening of the bowel wall or strictures. I dont think HIV causes that..lol. (Im not laughing at HIV, I am laughing at the fact that I am not getting anywhere with these people and they are running me around the block, scaring the crap out of me and then telling me to "reduce your stress levels".
In my next appointment on the 18, I will get the results...couldn't get an appointment with my doc but she is supervising interns that day and she did put in her schedule to pop in. She also put in her schedule that I will be seeking a new doctor.
I consented to the HIV test just so they can stop asking me the questions about my sex life. They ask you certain questions as if they think they are being non-challant...as if you dont know what they're getting at.

@logansmom, yes, I had my surgery and it really wasnt that big of an ordeal for me. It took a few days to move around ok but they prepared me for MUCH worse and it wasnt as bad as they thought. One hand I am grateful the endo isnt that bad but on the other I was sort of hoping that I could blame everything on endo... not the case. I only had 2 implants. The worst part for me was the medication they gave me. I was on a lot of drugs for pain and once I was able to get of them, I found it a lot easier to move around without nausea etc. Im not too big on pain pills.
I am glad your doctors will both be there - I asked for that and they said no. If it were an emergency situation he would have been able to been called though as they were in the same hospital. Doctors make me shake my head - they seem so counter productive.

Im not giving up Dex. I am a little low key just because of my throat and sinuses. I have been taking Buckelys non drowsy capsules for sinuses and congestion but I am far from giving up.
You guys were right about the Dilaudid and milk. I stopped and now I am back to D. It is explosive. At the awards ceremony tonight I was able to hold it in until I got home. I think about an hour. I ate a good dinner though :) first time eating food in awhile.

I was proud of the way I told the intern how I felt. I dont think she was very impressed but did agree that I have been seeing far too many doctors and she made the appointment with my team. I also told her that I have thought many times about saying f-it and giving up but I cant... its my health and its not like Im going to magically get better if I do that. I have a lot of things I want to do. I still think I have IBD and I told her that but she gave me the impression there wasnt anything she could do. That I would have to wait for the GI doc on June 20th. Thats when I asked for my records. All these months waiting; add up to waiting years, and I am not able to do much in between. Ive had it in a good way meaning I am starting to push back. I dont care if I hurt anyones feelings and Im not so concerned with saying something wrong anymore.

My brother has severe crohns, I smoked for 10 years, I have strictures in the jejunum and thickening of the bowel wall (ilium), endometriosis, gastritis, GERD, hiatus hernia, oral thrush, and the list goes on. Sounds like IBD to me.... Im not sure why they are having a hard time coming to terms with that.. lol...usually it is the doctors trying to snap the patient out of denial. I dont get it either diesandhur...are steroids really that dangerous that they wont stop with the testing and theorizing and just let me try them to see what happens? I need my life back.

Im going to be okay though... I have a lot of good people on my side. I just need to find the good doctors.
 
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Hey Wendy,

Just catching up hun, been incommunicado 'cause the modem S*** itself! ugh! That, and Matt has been hogging the dongle. :eek2:

It's so good to know that you people looking out for you...:), now if you can just find those bloody doctors to do their bit!

Keeping for fingers, toes and everything crossed hun!

Sending loads of love and hugs your way...:wub::hug::wub:
Dusty. xxxxxxxx
 
Thank-you Dusty.yes, I do have good support people on my side, no doubt about that. They are still helping me to find a doctor and they are taking some of the frustration off my back by doing some of the leg work for me. I think they are getting just as frustrated. I am going to see if I can get another referral to a different GI at McMaster Hospital. I know some people on here have gone there so maybe that is an option. It is the wait that I am wondering about.
What the heck is dongie??? You're starting to sound like Joan :p
How is Matt??
 
Well, thanks for that Dex! :yrolleyes:

Good luck with the referral Wendy and who knows, with all the waiting around you've already endured maybe it won't be too long! Fingers crossed!

Dongle Wendy, Dongle! :ylol:

If I describe it well enough you will know what it is...a piece of USB hardware, like a memory stick, that is used for mobile broadband.

All is fine with Matt, thanks for asking hun.

Much love, :karl:
Dusty. xxxxxxxx
 
I wouldn't get too worked up about that list of symptoms for HIV Wendy. A LOT of those things also correspond with IBD and basically having an out-of-whack- immune system.

Have you ever been tested for allergies? A few years before my diagnosis, I started having what you described as constant sinus congestion and sore throats. I wouldn't get sick, but I;d go through a period of about a week where I was constantly blowing my nose from all the congestion and getting terrible sore throats with post-nasal drip.

They would get more prolonged when they came on when I finally got walking pneumonia. I was tested for allergies and found out I was allergic to mold dust, cats (that was no surprise), and mosquitoes (again, no surprise). I started on allergy shots right away and the sinus and throat problems stopped. I haven't had any of those problems since. That was back in 2005 when all that started.

So, could be something to possibly look into if you haven't. I know a lot of people with Crohn's have talked about having allergies. Another thing corresponding to an overly active immune system!
 
I did have an allergy test once where they scratched part of my back and then put some stuff on it but I had taken a gravol that day and learned later that it probably screwed up my test. I havent had one since. I have thought about doing it again. I hope I didnt give the wrong impression but I rarely get sick but if I do, it is usually only a sore throat or sinuses. I use to run a lot so I attributed it to that. These moods are crazy. One moment I am bummed out and then the next I am very hopeful. I am back to being very hopeful and I know that I ought to put the HIV scare out of my mind. I dont think I have it but it is one more piece of paper I can put in front of the new doctor to say that I have been nothing but co-operative and patient... now it is time for them to do something. I dont know why but I do believe I will get the answer soon (and I realize I have been saying that for months)... I dont have anything to back that up so maybe I am a little delusional.. It just works for me to think that way. If I think otherwise, I get really crabby.
 
Yup, that sounds like an allergy scratch test to me. When I had mine done, they told me not to take any antihistamines for a couple days prior to the test. I'm not sure how/if Gravol would affect the test, but it could be possible.

I would have described myself as someone who rarely got sick. I didn't even consider my sinus/congestion problems as sicknesses. I never took it seriously until I ended up with walking pneumonia and felt like I was going to die. That's when I finally decided to get treated for my allergies because I didn't want to have to go through that again. I was on 3 different antibiotics at that point to clear it up because it came back again after a couple weeks.

So, I don't know. It couldn't hurt to possibly get it checked out again. How long ago were you tested? I know in Florida the pollen levels are outrageous right now and my mom (who is a nurse at an allergy clinic) says even the people who are treated already are coming in asking for more frequent injections and more medicine because everything is out of whack. If it's anything like that where you are, you could experience a worsening of sinus issues and congestion.

I think the mood fluctuations are normal, considering what you are going through :) don't feel bad for constantly being hopeful about things, even when they don't pan out. Sometimes that's the only thing that can get us through it! Better to be positive than crabby ;)

You are awesome, Wendy! :)

:::HUGS:::
 
Marisa may be right about the pollen and your sinus/laryngitis issues! I almost never have any allergy issues but this year is off the charts!!
 
I thought it may be a cold because the kid I was chasing around (wiping his nose) was also sick. I have had it for almost a week. A lot of people here seem to be getting sick starting with sore throat first. I have some reactine I got free as a sample so I may try that and see what happens. It says it is for allergies. I have been using Buckely's cold and sinus gel caps (non-drowsey) but they don't appear to be helping at all. I still have very little voice and I am supposed to be going to a conference tomorrow (Sun) until the 12th. I feel sorry for the person sharing the hotel room with me because as soon as I lay down I am hacking and blowing my nose...it gets worse at night.
I just hope if it is a cold, I dont give it to anyone - it is brutal. Have had a sore throat for a week now!!
 
Marisa may be right about the pollen and your sinus/laryngitis issues! I almost never have any allergy issues but this year is off the charts!!

Here in Pennsylvania, too. I have been popping Benedryl like tic tacs. Harrison has post-nasal drip so bad it's giving him stomach aches!

Wendy - can't beleive all the BS you are going thru. It seems you take a step forward and three steps back. I hope you start to make significant progress soon. Good luck with your appt on the 18th.

- Ames
 
lol.. I told him its not worth risking all of my school/career, etc. He wasn't happy but oh well.. Im not the best person to be asking to do illegal stuff with. I think I really took him off guard when I started to laugh hysterically when he told me...

As far as the sinuses... it is definitely them that is bothering me... I took the Reactine and it seemed to dry them out for a bit but my throat (top of roof of mouth) still hurts. When I get the new doctor I will look in to it.
 
In the meantime, Wendy, you could use a netipot (nasal irrigation pot). The salt water is supposed to lubricate the sinuses and flush out any nasty allergens that are hanging out in your nasal passages. It could give you some relief from the dry sinuses as well as maybe lessen some of the congestion you are experiencing. It may take a while to figure out how to do properly, but it's worth it. You can do it twice a day (once in morning, once before bed) or just before bed (to make sure all the allergens are out before you go to sleep).

That's one of the downfalls with some of these allergy medications out there. They can really dry your sinuses out. Also, if you have a humidifier, it can help keep your nasal passages moist and could help lessen the coughing at night. The reason it worsens at night is because all the congestion in your sinuses is trickling down into your throat and irritating it.

To help with losing your voice....you should really go on vocal rest and do an apple cider rinse gargle. My high school singing teacher recommended this for me when I lost my voice to laryngitis 2 days before a music audition. I didn't talk for the 2 days prior and did an apple cider gargle about every hour for the first day, then every 3-4 hours the next day. I had enough voice back the 3rd say to sing! You may not have enough voice back for the conference, but it could help your symptoms improve more quickly in the meantime.

You've really had a hard time with all this stuff. I always say when something dumb happens to me, it always happens in 3s. It can't be just one thing to go wrong, but several. Waves of bad luck, haha. I hope your luck turns around soon! :)
 
Oh, Wendy! Dang, perhaps HIS kind of treatment could help you? Just kidding! That just sucks but better to find out earier rather than later I guess.

I am with Marisa on the neti pot suggestion - love the neti pot! once you get used to using it, it's great!

- Ames
 
Ha..funny how you mention happening in threes. My sinuses are still congested and while I was away I slept very little as I was hacking or my sinuses got so congested I couldnt breathe. There seems to be a lot of people around me with the same thing going on so I am wondering it it is a cold. I am going to get a net pot as I tried 3 reactine now and none of them worked. Someone also suggested trying Oregeno oil. Apparently burns but they got better quick. I know someone who was using it and stopped and then got it again.

The good news is when I returned, there was a message from the GI nurse saying she spoke to my GI and he has sent radiology a request to book a CT entercolisis.
http://en.wikipedia.org/wiki/Enteroclysis

so..looks like they want to put the tube down anyway. Luckily the answering machine picked it up as I would have not remembered the name. The link explains my previous question about the difference between enterography and the NG tube. I dont really care so long as they figure out what is going on. I dont have a date yet but they will call when they do. My guess is I will be waiting a couple of months.

While I was away, I have had some pain but not much and typically after eating. I am back to eating solids - thanks to you guys. I am also back to taking a few dilaudids here and there when I have pain or d.
I have my post op tomorrow and I saw a string coming out of my bellybutton today. I thought it was a scab (one of the incisions was in my BB)... It has a knot on the end of it and when I tug on it it doesnt cause any pain at all....lol.. freaky though... I was told I didnt have to have any stitches removed - they would disolve. It looks like thin white string though..lol.. weird, huh? I guess she will look at it tomorrow.
Anyhow.. gotta go to bed. Sooo tired from little sleep. GREAT conference though.
Hope everyone is well.
Wendy
 
Glad you had a good time Wendy...and no roomie to keep awake:)!

How did the post-op go? What about the string?
 

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