Alright so..depending on who is reading this (friends/family of mine interested in my story or other UC/IBD sufferers) you may or may not have had to prepare for a colonoscopy in your lifetime.
If you haven't, damn you're lucky.
I talked before about how terrible prep for this is, and how I really struggled with it when I was first sick and they were trying to diagnose me. This time I used a method I had never used before. My surgery was Monday, and I had to stop eating at midnight on Saturday, so no foods on Sunday at all. I could have liquids (popcicles and jello, but that doesn't count...SO not real.) At any rate...
I took some antibiotics the day before surgery, and then this little pill that came along with my bowel prep kit. It acted as a minor laxative to sort of ease me into the process. You're supposed to take the pill at like...4 or something (I don't have the paper near me...) and then the next step is waiting for a bowel movement which could happen as soon as 30 minutes or as long as 4 hours after taking the pill. After you have your first bowel movement you have to start drinking the liquid that will make the rest of your evening, and well into the next day, a living hell.
I prepped for my surgery at my sister and brother in law's apartment in Indy. That way we would already be in town, not 10 minutes from the hospital where my procedure was going to take place, rather than an hour or so away. We watched Harry Potter and the Prisoner of Azkaban while we waited for my little pill to take effect. I don't know why I remember that...
I believe it's something like...64 ounces of liquid that you have to drink, total. You drink one 8 ounce glass every 10 minutes. The liquid is flavored, in an attempt to make it less horrible, but it doesn't work. (I seriously just gagged thinking back to it what it was like..) I think I picked orange flavor...or something. But you really don't taste the flavor much. The mixture is very salty...:shudders: I drank the first glass down just fine. Yeah, it was disgusting and extremely unpleasant, but I chugged that drink like a trooper and started timing 10 minutes until I had to chug the next one. I got the next one down a little less easy than the first (it's harder to do it once you KNOW how unpleasant it is...not like I expected it to be tasty, but before you know how awful it really is, you can delude yourself into thinking that it might not be that bad...) and then I started feeling like SHIT.
Only 6 more glasses to go....
You don't leave the bathroom during processes like this. You just don't. It's not worth it, because even if you do go somewhere else, you aren't going to be staying there for very long...if you catch my drift...
It just got harder and harder. Probably by the 4th glass, I couldn't bring myself to just chug it down all at once anymore. It was just so terrible. I could probably get it down in two chugs, and then soon after that, I couldn't even do it that well. It was so awful.
I wish I could accurately describe the feeling that this medicine started giving me...I would swallow just one little gulp of it and my stomach would automatically start twisting and turning...it felt like it was literally flipping over in my abdomen and twisting its self into knots. It was so difficult to get that medicine down. I was maybe only half way done when my stomach started undulating with every tiny sip of the medicine that I swallowed. My body wanted that shit out. It wanted me to puke. But all I kept thinking was that if I threw up, then I wasn't going to be able to have my surgery done, and I was going to have to go through all of this again another day, and I knew I couldn't do that. So I would swallow my medicine and immediately clasp my hand over my mouth to keep everything in. You know that thing your mouth does when you're about to puke? Where you just salivate like crazy, and you just KNOW that your body wants you to vomit? That was happening constantly. I just kept swallowing and trying to think of ANYTHING else to get my mind off of how much I just wanted to throw up.
I still had so much left to drink. It was becoming so hard to keep going....I had already given up trying to drink the solution exactly 10 minutes apart like I was supposed to. I knew if I had kept that up, I would have been throwing up uncontrollably...so I sacrificed doing the prep in a timely fashion, to try and be able to do it without throwing the medicine right back up again.
The only problem with this is that I was supposed to stop consuming anything after 11pm...even water, and my medicine. 11 just kept getting closer and closer...
I was down to my last 2 glasses. I got one of them down and threw it right back up. I couldn't prevent it. I started bawling my eyes out. I was just convinced that they weren't going to be able to do my surgery because I didn't complete my prep...One glass left...I drank about half of it and just couldn't bring myself to finish those last 4 ounces. I know it seems stupid that after drinking 60 ounces I couldn't bring myself to chug a few more, but like I said, if you've never done a prep like this before, you don't understand just how awful it is. My body ached from not moving from the bathroom for hours upon hours...I was crying, worrying about my procedure the next day and whether or not it would even be able to happen...I wanted to throw up and get all the terrible medicine out of my system more than anything in the world...
Then my time ran out. My sister came in and measured how much medicine I hadn't finished, it was just under 4 ounces. She said "you're done..now rest" I cried to her and my mom because I was so worried that if I got to the hospital and told them I couldn't finish my prep that they were going to tell me they couldn't do the surgery...I cried because I hurt...I cried because I was terrified even if it turned out that they could do the surgery...I was just so sick and so scared...
They made me feel a little bit better by reminding me that they don't adjust the dosage of preps like this for your size. So what I mean is that a fully grown man that could weigh 300 lbs would have to drink the same amount of this liquid as me...a 21-year-old girl that probably weighed about 97 lbs at the time this was taking place.
I slept in the bathroom that night. That's just what you have to do when you prep like this. You don't have any other choice. It was a long time before I even felt comfortable getting up off the toilet, it's that bad of a situation. But when I finally did, Sandy had gotten me some blankets and a pillow and I curled up in the corner of the bathroom. I still had to get up every little while, and I got no real rest. I just laid on the hard floor listening to my ipod and trying to calm myself down. I was terrified of so many things that could go wrong...
Morning came too soon...there was a definite air about the house. Everyone was on edge..everyone was worried. I was still going to the bathroom, which was terrifying to me. I was just all the more convinced that they were going to tell me that they couldn't do the surgery because of something that I did wrong...
They told me to be at the hospital at 5:30...so we hopped into the car and made our way there...
Thursday, July 1, 2010
Tuesday, June 15, 2010
My Surgery.
So I've been getting a lot of questions (understandably) about what kind of procedure I'm having done so I thought this was a necessary post. I must say though, it's pretty funny because every time I tell someone I'm having my colon removed their first response is something akin to...
"...but..uhm..really? Don't you need that?"
The short answer is no. Not anymore! It's terrible. It wants to give me cancer and make me sick everyday. Get it outta here!
I received a packet of information from the Midwest Colon and Rectal Surgery center giving me instructions for preparing for my surgery. It states...
Type of surgery: Laparoscopic Assisted Total Proctocolectomy Ileo J-Pouch Anal Anastamosis with possible Temporary Loop Ileostomy.
What a mouthful, huh?
Okay, let's go through this word by word..
Laparoscopic Assisted-When a surgery is done laparoscopically, it basically means they don't have to completely cut me open to get this organ out. Here, when I googled it, this is the explanation I got for laparoscopic proctocolectomy...
"A laparoscopic proctocolectomy is a minimally invasive surgery to remove the rectum and colon;
So yes. Rather than having one huge incision along my entire midsection, I'll have a few smaller incisions. This is good.
Alright, what's next...
Ileo J-Pouch Anal Anastamosis..
The mayo clinic describes this by saying...
"The ileal pouch-anal anastomosis (IPAA) is a complex surgical procedure developed to avoid a permanent stoma (opening for collecting waste) in cases where the entire colon and rectum needs to be removed. This procedure is most often used to treat patients with chronic ulcerative colitis. The IPAA procedure involves removal of the entire colon and rectum with preservation of the anus and sphincter muscles. After removal of the colon and rectum, the surgeon constructs a pouch from the end of the small intestine and attaches it directly to the anus. In order to allow time for the pouch to heal, a temporary ileostomy (opening in the front of the abdomen) is created. The ileostomy is reversed a few months later in a second operation and the patient begins to pass bowel movements through the anus, with only slight alterations in the frequency of bowel movements. In most cases the IPAA procedure can be performed laparoscopically, which minimizes the incision length and decreases postoperative discomfort and the hospital stay."
Basically that explains all of it. It's being done with little cameras so I don't have to be cut completely open, and therefore don't have to be in the hospital as long (though if you ask me, 4-7 days is long enough for me). I'm having my colon and rectum removed. Then a pouch will be constructed from my small intestine and attached to my anus. I will then (most likely) have a temporary loop ileostomy. This is where the end of the small intestine is brought to the surface of my skin on my abdomen and I will have a pouch outside of my body to collect my waste. This is only temporary, to allow for my j-pouch to heal before waste will be passed through it. A few months after this first surgery, I will have yet another surgery where they get rid of my ileostomy and hook up my new pipeworks!
Basically they're constructing a new makeshift colon inside of me using my small intestine. It won't be exactly the same, but then again, I don't want to be the same as I am now. My digestive system is being considerably shortened, so I will go to the bathroom more often than "normal" people, but I do that already anyway thanks to the UC. At least I won't be in pain anymore! So yes, waste will go from my small intestine, into this new pouch (which is also part of my small intestine, just reconfigured) and then out of my body. The pouch acts for me as a colon does for everyone else. Your colon basically holds your poo until you're ready to go to the bathroom. That's exactly the purpose of my j-pouch. Make sense??
There is a chance I will not have to have an ostomy bag. I won't know until I wake up whether or not I'm going to have one. This is a little worrysome to me, but I trust my doctor. Sometimes they do this procedure all in one step where they just hook you right up and let you go. The nurse told me he will not be able to tell what I'm going to need to happen until he gets in there...so yeah..I may wake up with a stoma and I may not. I'm prepared either way.
Prepared to feel better and to be healthy goddamnit!
"...but..uhm..really? Don't you need that?"
The short answer is no. Not anymore! It's terrible. It wants to give me cancer and make me sick everyday. Get it outta here!
I received a packet of information from the Midwest Colon and Rectal Surgery center giving me instructions for preparing for my surgery. It states...
Type of surgery: Laparoscopic Assisted Total Proctocolectomy Ileo J-Pouch Anal Anastamosis with possible Temporary Loop Ileostomy.
What a mouthful, huh?
Okay, let's go through this word by word..
Laparoscopic Assisted-When a surgery is done laparoscopically, it basically means they don't have to completely cut me open to get this organ out. Here, when I googled it, this is the explanation I got for laparoscopic proctocolectomy...
"A laparoscopic proctocolectomy is a minimally invasive surgery to remove the rectum and colon;
So yes. Rather than having one huge incision along my entire midsection, I'll have a few smaller incisions. This is good.
Alright, what's next...
Ileo J-Pouch Anal Anastamosis..
The mayo clinic describes this by saying...
"The ileal pouch-anal anastomosis (IPAA) is a complex surgical procedure developed to avoid a permanent stoma (opening for collecting waste) in cases where the entire colon and rectum needs to be removed. This procedure is most often used to treat patients with chronic ulcerative colitis. The IPAA procedure involves removal of the entire colon and rectum with preservation of the anus and sphincter muscles. After removal of the colon and rectum, the surgeon constructs a pouch from the end of the small intestine and attaches it directly to the anus. In order to allow time for the pouch to heal, a temporary ileostomy (opening in the front of the abdomen) is created. The ileostomy is reversed a few months later in a second operation and the patient begins to pass bowel movements through the anus, with only slight alterations in the frequency of bowel movements. In most cases the IPAA procedure can be performed laparoscopically, which minimizes the incision length and decreases postoperative discomfort and the hospital stay."
Basically that explains all of it. It's being done with little cameras so I don't have to be cut completely open, and therefore don't have to be in the hospital as long (though if you ask me, 4-7 days is long enough for me). I'm having my colon and rectum removed. Then a pouch will be constructed from my small intestine and attached to my anus. I will then (most likely) have a temporary loop ileostomy. This is where the end of the small intestine is brought to the surface of my skin on my abdomen and I will have a pouch outside of my body to collect my waste. This is only temporary, to allow for my j-pouch to heal before waste will be passed through it. A few months after this first surgery, I will have yet another surgery where they get rid of my ileostomy and hook up my new pipeworks!
Basically they're constructing a new makeshift colon inside of me using my small intestine. It won't be exactly the same, but then again, I don't want to be the same as I am now. My digestive system is being considerably shortened, so I will go to the bathroom more often than "normal" people, but I do that already anyway thanks to the UC. At least I won't be in pain anymore! So yes, waste will go from my small intestine, into this new pouch (which is also part of my small intestine, just reconfigured) and then out of my body. The pouch acts for me as a colon does for everyone else. Your colon basically holds your poo until you're ready to go to the bathroom. That's exactly the purpose of my j-pouch. Make sense??
There is a chance I will not have to have an ostomy bag. I won't know until I wake up whether or not I'm going to have one. This is a little worrysome to me, but I trust my doctor. Sometimes they do this procedure all in one step where they just hook you right up and let you go. The nurse told me he will not be able to tell what I'm going to need to happen until he gets in there...so yeah..I may wake up with a stoma and I may not. I'm prepared either way.
Prepared to feel better and to be healthy goddamnit!
Sunday, June 13, 2010
My Story Continued
So when I left off, I was at the hospital and had just been told that I had UC. The biopsy was to make sure there was no cancer, if I'm not mistaken in my remembering (and there wasn't).
I'm pretty sure at this point in time I still didn't have a GI (gastrointerologist) yet. I was just seeing my family doctor. After my diagnosis, however, it was time to get referred to a specialist. I think my first specialist was a man named Doctor Yoo. The first drug I was put on was called Imuran/Azathioprine. This medicine was pretty risky. I was given a paper explaining all the possible risks, to make sure I knew what I was getting into. This medicine is most often used to treat rheumatoid arthritis and is also used in patients who have had organ transplants to make sure that the organs take. It was also found, however, it could be used for UC treatment. I've found that a good percentage of drugs used to treat UC weren't developed to help UC patients originally, it was just found that they can help them as well. As a side note, this is extremely frustrating to me. It's the most annoying thing to realize that you have a disease that all these amazingly brilliant people in the world can't figure out how to fix. Why would something like this ever be real?
At any rate...Imuran is an immunosuppressant drug. You see, my disease is basically my immune system attacking the lining of my colon, because it thinks it shouldn't be there. So it makes sense that they would use the same type of drug for UC as they do when someone has an organ transplant. They're basically trying to prevent the same thing from happening in both cases. At any rate, it comes along with a lot of scary side effects (as I would eventually learn that many UC medications do). Neoplasia, lymphoma, severe infections, bone marrow issues...It was scary to hear all the things that could go wrong with me because I was taking a medicine to make myself better. It's quite overwhelming to think that I could just be trading off some symptoms for others.
I was on prednisone during this time as well. Prednisone is a type of steroid. It also disables your immune system. Now prednisone is a terrible drug. If you haven't seen my posts on here from when I was taking it, let me give you a rundown. It gives you trouble sleeping, makes you an overemotional wreck, makes you fat, gives you cushings syndrome where parts of your body just start puffing up and looking ridiculous, and it completely fucks up your body. There have been people with UC that end up having to have hip replacements in their 40s because they were on steroids so long or so often that it completely killed their bones. It's obviously terrible for your organs as well. It's the worst drug that I've ever had to take in my entire life.
I was on these two medicines for a bit, but wasn't getting better fast enough. They switched me from the Imuran to a drug called Asacol, and upped my dosage on the Prednisone. I was taking somewhere near 60 mg of Prednisone a day, which is an insane amount. Asacol is part of a group of drugs with the main ingredient mesalamine. Mesaslamine is supposed to discourage the substance in the body that causes inflammation, therefore stopping tissue damage, etc. It is not, however, an immunosuppressant.
Steroids are not a long-term medicine to help the symptoms of UC. It works, don't get me wrong, but as I said, they're extremely bad for you. The reason I was on steroids coupled with other medications is so the steroids could get my disease under control quickly, and then the other medicines (which take a bit to start working) could start doing their job easier. Then what they do is taper you off of the steroids (it's extremely unsafe to just stop taking steroids, especially at high dosages) and then the other medicine is supposed to pick up where the steroids left off. ...I hope that makes sense to someone other than me...
It took a little while, but I started getting better! It was amazing. I was at home from school a little while longer, but then I got to go back. It was...more than weird. I had missed over a month. I still only weighed 80 lbs, and no one really knew why I had been gone so long. No one had ever heard of ulcerative colitis. It was embarrassing to have to actually explain my disease, so I told everyone that I simply had ulcers in my digestive system. Even though I was sickly skinny, and pale as a ghost, no one at my school got to see me while I was deathly ill. So to them, it seemed like I magically disappeared from school with no previous signs of anything wrong with me, and then I came back a little bit thinner, but that was it.
The rumor was that I had gone to rehab for an eating disorder.
And that was started by one of my friends.
High schoolers are bitches, especially when you're from a small town when there isn't anything better to talk about.
I busted my ass to catch up. I had to do what we were currently learning, and the current homework, while catching up on the month of learning and homework I had missed. I stayed up until all hours of the night studying, reading, and working harder than any of those people in that damn school had all year. I was happy to do it though, because I felt fantastic. I'm pretty sure at this point I was taking somewhere near 13 pills a day. I had to take an iron supplement because of all the blood I has lost due to my disease. I didn't even care though, I was healthier, and I was back to my life. It was wrestling season. I got to cheer my boys on and hang out with my friends, it was fantastic.
I definitely developed a terrible case of cushings syndrome though. I had not really been warned about the side-effects of my steroids. I had a lot of trouble sleeping because of them, and my face ballooned up like a chipmunk trying to hoard nuts for winter...it was gradual, but damn when I realized how bad it was, that was all I could see when I looked in the mirror. Maybe I'll dig up an old picture of it, because looking back, it really is hilarious. One good thing, though, I never had to deal with the mood swings during my first time on steroids. I was just so happy to be feeling good.
It wasn't all sunshine and lollipops though. The teachers didn't really believe I had a reason to miss school for a month. They wouldn't admit it, but I could tell. People made fun of me because my face looked funny. It was still rumored that I had left because of an eating disorder.
I was okay though. So what if I didn't get to have any senior photos taken of me. So what if a few people thought I looked silly, and was way too skinny. Honestly, both of those things were true! I didn't have to run to the bathroom anymore. I wasn't in pain. I was weaned off my steroids, and my face slowly returned to normal. I got back up to my normal weight, and my jeans no longer sagged off my body. I didn't have to hide under sweatshirts because I was too embarrassed for people to see how skinny I was. The asacol was doing the trick. I went off to college at IUB in the fall, and was ready to start a new and fantastic life. I wasn't perfect, but I was better.
At least for a little while...
I'm pretty sure at this point in time I still didn't have a GI (gastrointerologist) yet. I was just seeing my family doctor. After my diagnosis, however, it was time to get referred to a specialist. I think my first specialist was a man named Doctor Yoo. The first drug I was put on was called Imuran/Azathioprine. This medicine was pretty risky. I was given a paper explaining all the possible risks, to make sure I knew what I was getting into. This medicine is most often used to treat rheumatoid arthritis and is also used in patients who have had organ transplants to make sure that the organs take. It was also found, however, it could be used for UC treatment. I've found that a good percentage of drugs used to treat UC weren't developed to help UC patients originally, it was just found that they can help them as well. As a side note, this is extremely frustrating to me. It's the most annoying thing to realize that you have a disease that all these amazingly brilliant people in the world can't figure out how to fix. Why would something like this ever be real?
At any rate...Imuran is an immunosuppressant drug. You see, my disease is basically my immune system attacking the lining of my colon, because it thinks it shouldn't be there. So it makes sense that they would use the same type of drug for UC as they do when someone has an organ transplant. They're basically trying to prevent the same thing from happening in both cases. At any rate, it comes along with a lot of scary side effects (as I would eventually learn that many UC medications do). Neoplasia, lymphoma, severe infections, bone marrow issues...It was scary to hear all the things that could go wrong with me because I was taking a medicine to make myself better. It's quite overwhelming to think that I could just be trading off some symptoms for others.
I was on prednisone during this time as well. Prednisone is a type of steroid. It also disables your immune system. Now prednisone is a terrible drug. If you haven't seen my posts on here from when I was taking it, let me give you a rundown. It gives you trouble sleeping, makes you an overemotional wreck, makes you fat, gives you cushings syndrome where parts of your body just start puffing up and looking ridiculous, and it completely fucks up your body. There have been people with UC that end up having to have hip replacements in their 40s because they were on steroids so long or so often that it completely killed their bones. It's obviously terrible for your organs as well. It's the worst drug that I've ever had to take in my entire life.
I was on these two medicines for a bit, but wasn't getting better fast enough. They switched me from the Imuran to a drug called Asacol, and upped my dosage on the Prednisone. I was taking somewhere near 60 mg of Prednisone a day, which is an insane amount. Asacol is part of a group of drugs with the main ingredient mesalamine. Mesaslamine is supposed to discourage the substance in the body that causes inflammation, therefore stopping tissue damage, etc. It is not, however, an immunosuppressant.
Steroids are not a long-term medicine to help the symptoms of UC. It works, don't get me wrong, but as I said, they're extremely bad for you. The reason I was on steroids coupled with other medications is so the steroids could get my disease under control quickly, and then the other medicines (which take a bit to start working) could start doing their job easier. Then what they do is taper you off of the steroids (it's extremely unsafe to just stop taking steroids, especially at high dosages) and then the other medicine is supposed to pick up where the steroids left off. ...I hope that makes sense to someone other than me...
It took a little while, but I started getting better! It was amazing. I was at home from school a little while longer, but then I got to go back. It was...more than weird. I had missed over a month. I still only weighed 80 lbs, and no one really knew why I had been gone so long. No one had ever heard of ulcerative colitis. It was embarrassing to have to actually explain my disease, so I told everyone that I simply had ulcers in my digestive system. Even though I was sickly skinny, and pale as a ghost, no one at my school got to see me while I was deathly ill. So to them, it seemed like I magically disappeared from school with no previous signs of anything wrong with me, and then I came back a little bit thinner, but that was it.
The rumor was that I had gone to rehab for an eating disorder.
And that was started by one of my friends.
High schoolers are bitches, especially when you're from a small town when there isn't anything better to talk about.
I busted my ass to catch up. I had to do what we were currently learning, and the current homework, while catching up on the month of learning and homework I had missed. I stayed up until all hours of the night studying, reading, and working harder than any of those people in that damn school had all year. I was happy to do it though, because I felt fantastic. I'm pretty sure at this point I was taking somewhere near 13 pills a day. I had to take an iron supplement because of all the blood I has lost due to my disease. I didn't even care though, I was healthier, and I was back to my life. It was wrestling season. I got to cheer my boys on and hang out with my friends, it was fantastic.
I definitely developed a terrible case of cushings syndrome though. I had not really been warned about the side-effects of my steroids. I had a lot of trouble sleeping because of them, and my face ballooned up like a chipmunk trying to hoard nuts for winter...it was gradual, but damn when I realized how bad it was, that was all I could see when I looked in the mirror. Maybe I'll dig up an old picture of it, because looking back, it really is hilarious. One good thing, though, I never had to deal with the mood swings during my first time on steroids. I was just so happy to be feeling good.
It wasn't all sunshine and lollipops though. The teachers didn't really believe I had a reason to miss school for a month. They wouldn't admit it, but I could tell. People made fun of me because my face looked funny. It was still rumored that I had left because of an eating disorder.
I was okay though. So what if I didn't get to have any senior photos taken of me. So what if a few people thought I looked silly, and was way too skinny. Honestly, both of those things were true! I didn't have to run to the bathroom anymore. I wasn't in pain. I was weaned off my steroids, and my face slowly returned to normal. I got back up to my normal weight, and my jeans no longer sagged off my body. I didn't have to hide under sweatshirts because I was too embarrassed for people to see how skinny I was. The asacol was doing the trick. I went off to college at IUB in the fall, and was ready to start a new and fantastic life. I wasn't perfect, but I was better.
At least for a little while...
Tuesday, June 8, 2010
My story.
So I just realized that I haven't actually shared my UC story from the beginning. I think it's time to do that, considering I'm getting this surgery done, and therefore my disease is a bit more public with people I know, and they're (understandably) curious.
As I go to write this...it's strange to me how fuzzy my memories of it all are...It's been so long, and so much has happened, that I'm having a tough time remembering just how it all got started...
It was '06..I remember that much. I was a senior in high school with big plans and lots of activities, as most of the seniors did. I was a runner (both track and cross country) and I was also in the school play. When my symptoms first started, I ignored them. They were typical UC symptoms (obviously) bleeding, urgency, intense pain, etc. Pretty serious symptoms, right? Well, my pride won out over the terrifying symptoms. I was absolutely mortified just at the thought of having to tell someone what was going on with me, so I didn't. I dealt with the pain for 6 months without telling a single soul what was going on with me. It was during cross country and simultaneously play (thespians) season. I remember being outside during XC practice and having to sprint to the bathroom in crazy pain. I could barely make it through practices, and spent a lot of my time hiding out in the bathroom hoping no one noticed I had disappeared during what was supposed to be an hour long run. I had no idea what I was going to do when the season really started and I actually had to race. You can't just run off the course to use the bathroom and start up again! All the while, the play was happening. I was in the running for the lead role, which I wanted more than anything else in the world at that time. Quitting XC was already on my mind because of the complications with my health, but when I spoke to the play director and she told me that I got the lead, quitting XC became that much easier. I tried balancing the two for a while, but being the lead in the play meant that I had to be at every play practice. So I quit cross country and focused all my energy on the play. Play practices were intense to say the least. Especially when it gets close to time for the production, you're there from right after school ends at 3 until 10 pm. Not to mention this happens right around midterms/finals or something..I just always remember having to cram for exams on my breaks offstage. I loved the play, but it was also an event where if I had to, I couldn't just run offstage to take care of my current health problems. I spent a lot of time with my fellow castmates. We ate dinner together almost every night and were around each other constantly. It was hard for them not to notice that something was weird with me. However, no one mentioned anything to me, at least not then, and not to my face.
The play went fantastically. Despite extreme nerves, and having to be on the stage damn near constantly, I made it through all the productions without having to run offstage to the bathroom, or miss a cue due to my illness. The last performance was on Saturday. I didn't make it to school that next Monday.
You wanna hear the funny part? I still didn't want to tell anyone about my disease. I would have kept it a secret. You know why I finally decided to tell someone that Monday? I just didn't want to go to school...plain and simple. I was tired, and I didn't want to do it. Forget the fact that I was in intense pain, with something clearly wrong with me...I was feeling lazy, and I wanted an excuse not to go to school. Bleeding colon? As long as it gets the job done! I texted my mom that I wasn't going to school because I was bleeding when I went to the bathroom. That was exactly how I worded it. She just assumed I meant when I peed. Nope. Of course not, that's not NEAR mortifying enough for me...When she found out what was really going on, she freaked. Understandably.
I had been dealing with it so long without anyone else knowing (about 6 months, like I said) that it had become no big deal to me. It took her freaking out for me to realize how serious whatever was going on with me had to be.
My health took a real quick downward spiral around this time. I'm really not sure how I dealt with it so long without medicine, without doctors knowing...without anyone knowing...I'm lucky I didn't wind up in the ER, or worse. Not telling anyone about what was going on with me was the dumbest thing I've ever done in my life. So many things could have happened...but I let my pride get to me, and keep me from doing what I knew I should have done. Never again. And please take my advice here..no matter how embarrassing a medical condition is...go to a fucking doctor. They don't give two shits, (no pun intended), I promise you. It's they're job to deal with these things.
At any rate, they couldn't figure out what was wrong with me at first. They thought maybe hemorrhoids, a fissure, I don't even remember all the possibilities they ran through. All the while, I was getting sicker and sicker.
I couldn't eat. I wouldn't eat. I laid curled up in a ball in a chair in the living room. I had no energy because I had no nutrients. I was out of school indefinitely. I lost 20 pounds in 2 weeks. I weighed 80 pounds. I was a (barely) walking bag of bones. I only got up out of my chair to go to the bathroom. I didn't even have enough energy to stay awake through a half hour long TV show, yet when nighttime came, I couldn't sleep for the pain. My skin was almost green.
My mom thought I was going to die.
I remember being alone a lot. I don't think my mom could bear the sight of me. I remember a few times of my family coming over to check on me, but I couldn't stay awake long enough to really interact with them. They were all so worried...
The doctor decided we had to do a colonoscopy to find out what was going on. At this point they still had no idea what was wrong with me. I don't know how many of you have ever known someone that had a colonoscopy done, but the prep for it is absolutely terrible. They have to clean your bowels out, obviously so they can see what's going on, and let me tell you..it's absolutely awful. There are many different ways that you can go about the prep, but the one they were going to have me to do was a medicine that was mixed in with a sports drink. You had to drink somewhere near 64 ounces of gatorade with this medicine in it that made you shit water. Literally. Somewhere about halfway through you're literally shitting clear as water, and it's absolutely awful for so many reasons.
At any rate, I couldn't do it. As I said, I hadn't been eating, and I'd barely been drinking anything. My stomach couldn't handle all those fluids. I couldn't force myself to drink it. I remember crying..my mom was crying...If I couldn't get the medicine down, I couldn't have my colonoscopy. If I couldn't have my colonoscopy, we couldn't figure out what was wrong with me...
I couldn't force it down. My mom was so upset, almost angry with me. I just curled up in a ball and stayed that way all night. We went to the hospital the next day and were told as we suspected that they could not perform the procedure since I couldn't finish my prep. We were devastated. That meant I had to wait another week and then try a different approach to the situation. Another painful and scary week...
The next approach was pills. 32 pills, to be exact. You take two every 15 minutes, and are supposed to drink 8 oz of water with them, because they dehydrate you so much. It was hard enough for me just to get the pills down, so we settled for that. My oldest sister was there, I remember...I was crouched on the floor crying and saying that I couldn't do it...They were crying too because they knew how hard it was for me, but we all knew that I had to get those damn pills down...
My mom promised me a new winter coat if I finished my prep...
Hardest thing I've ever had to do for a damn coat in my life!!
I got the pills down though..spent the entire night completely miserable and running to the bathroom more often and more urgently than usual, which is saying something.
I remember getting to the hospital and being put on the bed. It was the first time in a while that I didn't have to go the the bathroom..I was fucking empty. Stupid nurse kept missing my vein for my IV...I bled everywhere...They wheeled me back and the nurse said
"At least you have long eyelashes..."
Looking up at the lights in the room, just like in the movies..Doctors in masks over me...told me to count backwards from 10...I was out before I even got to 8. I woke up and remembered really needing to go to the bathroom, immediately. The nurse told me I couldn't go until I had been awake for a while but that she would get me a bedpan. I absolutely refused. I wouldn't sink that damn low, come on now...I waited for another nurse to walk by less than a minute later and acted as normal as I could...She let me get up and go to the restroom.
They showed me, my mom, and my sister Sandy the pictures of the inside of my colon. I'm pretty sure they took a biopsy too. I was in a wheelchair..I didn't want to look at the pictures. I wouldn't do it. Everything is so fuzzy...They diagnosed me with ulcerative colitis.
Now what??
(I appreciate all of you who read through all this...it's really intense for me to basically relive it all...so I'm going to take a little break...let this bit sink in, and I'll update this again soon with the rest of the story...)
As I go to write this...it's strange to me how fuzzy my memories of it all are...It's been so long, and so much has happened, that I'm having a tough time remembering just how it all got started...
It was '06..I remember that much. I was a senior in high school with big plans and lots of activities, as most of the seniors did. I was a runner (both track and cross country) and I was also in the school play. When my symptoms first started, I ignored them. They were typical UC symptoms (obviously) bleeding, urgency, intense pain, etc. Pretty serious symptoms, right? Well, my pride won out over the terrifying symptoms. I was absolutely mortified just at the thought of having to tell someone what was going on with me, so I didn't. I dealt with the pain for 6 months without telling a single soul what was going on with me. It was during cross country and simultaneously play (thespians) season. I remember being outside during XC practice and having to sprint to the bathroom in crazy pain. I could barely make it through practices, and spent a lot of my time hiding out in the bathroom hoping no one noticed I had disappeared during what was supposed to be an hour long run. I had no idea what I was going to do when the season really started and I actually had to race. You can't just run off the course to use the bathroom and start up again! All the while, the play was happening. I was in the running for the lead role, which I wanted more than anything else in the world at that time. Quitting XC was already on my mind because of the complications with my health, but when I spoke to the play director and she told me that I got the lead, quitting XC became that much easier. I tried balancing the two for a while, but being the lead in the play meant that I had to be at every play practice. So I quit cross country and focused all my energy on the play. Play practices were intense to say the least. Especially when it gets close to time for the production, you're there from right after school ends at 3 until 10 pm. Not to mention this happens right around midterms/finals or something..I just always remember having to cram for exams on my breaks offstage. I loved the play, but it was also an event where if I had to, I couldn't just run offstage to take care of my current health problems. I spent a lot of time with my fellow castmates. We ate dinner together almost every night and were around each other constantly. It was hard for them not to notice that something was weird with me. However, no one mentioned anything to me, at least not then, and not to my face.
The play went fantastically. Despite extreme nerves, and having to be on the stage damn near constantly, I made it through all the productions without having to run offstage to the bathroom, or miss a cue due to my illness. The last performance was on Saturday. I didn't make it to school that next Monday.
You wanna hear the funny part? I still didn't want to tell anyone about my disease. I would have kept it a secret. You know why I finally decided to tell someone that Monday? I just didn't want to go to school...plain and simple. I was tired, and I didn't want to do it. Forget the fact that I was in intense pain, with something clearly wrong with me...I was feeling lazy, and I wanted an excuse not to go to school. Bleeding colon? As long as it gets the job done! I texted my mom that I wasn't going to school because I was bleeding when I went to the bathroom. That was exactly how I worded it. She just assumed I meant when I peed. Nope. Of course not, that's not NEAR mortifying enough for me...When she found out what was really going on, she freaked. Understandably.
I had been dealing with it so long without anyone else knowing (about 6 months, like I said) that it had become no big deal to me. It took her freaking out for me to realize how serious whatever was going on with me had to be.
My health took a real quick downward spiral around this time. I'm really not sure how I dealt with it so long without medicine, without doctors knowing...without anyone knowing...I'm lucky I didn't wind up in the ER, or worse. Not telling anyone about what was going on with me was the dumbest thing I've ever done in my life. So many things could have happened...but I let my pride get to me, and keep me from doing what I knew I should have done. Never again. And please take my advice here..no matter how embarrassing a medical condition is...go to a fucking doctor. They don't give two shits, (no pun intended), I promise you. It's they're job to deal with these things.
At any rate, they couldn't figure out what was wrong with me at first. They thought maybe hemorrhoids, a fissure, I don't even remember all the possibilities they ran through. All the while, I was getting sicker and sicker.
I couldn't eat. I wouldn't eat. I laid curled up in a ball in a chair in the living room. I had no energy because I had no nutrients. I was out of school indefinitely. I lost 20 pounds in 2 weeks. I weighed 80 pounds. I was a (barely) walking bag of bones. I only got up out of my chair to go to the bathroom. I didn't even have enough energy to stay awake through a half hour long TV show, yet when nighttime came, I couldn't sleep for the pain. My skin was almost green.
My mom thought I was going to die.
I remember being alone a lot. I don't think my mom could bear the sight of me. I remember a few times of my family coming over to check on me, but I couldn't stay awake long enough to really interact with them. They were all so worried...
The doctor decided we had to do a colonoscopy to find out what was going on. At this point they still had no idea what was wrong with me. I don't know how many of you have ever known someone that had a colonoscopy done, but the prep for it is absolutely terrible. They have to clean your bowels out, obviously so they can see what's going on, and let me tell you..it's absolutely awful. There are many different ways that you can go about the prep, but the one they were going to have me to do was a medicine that was mixed in with a sports drink. You had to drink somewhere near 64 ounces of gatorade with this medicine in it that made you shit water. Literally. Somewhere about halfway through you're literally shitting clear as water, and it's absolutely awful for so many reasons.
At any rate, I couldn't do it. As I said, I hadn't been eating, and I'd barely been drinking anything. My stomach couldn't handle all those fluids. I couldn't force myself to drink it. I remember crying..my mom was crying...If I couldn't get the medicine down, I couldn't have my colonoscopy. If I couldn't have my colonoscopy, we couldn't figure out what was wrong with me...
I couldn't force it down. My mom was so upset, almost angry with me. I just curled up in a ball and stayed that way all night. We went to the hospital the next day and were told as we suspected that they could not perform the procedure since I couldn't finish my prep. We were devastated. That meant I had to wait another week and then try a different approach to the situation. Another painful and scary week...
The next approach was pills. 32 pills, to be exact. You take two every 15 minutes, and are supposed to drink 8 oz of water with them, because they dehydrate you so much. It was hard enough for me just to get the pills down, so we settled for that. My oldest sister was there, I remember...I was crouched on the floor crying and saying that I couldn't do it...They were crying too because they knew how hard it was for me, but we all knew that I had to get those damn pills down...
My mom promised me a new winter coat if I finished my prep...
Hardest thing I've ever had to do for a damn coat in my life!!
I got the pills down though..spent the entire night completely miserable and running to the bathroom more often and more urgently than usual, which is saying something.
I remember getting to the hospital and being put on the bed. It was the first time in a while that I didn't have to go the the bathroom..I was fucking empty. Stupid nurse kept missing my vein for my IV...I bled everywhere...They wheeled me back and the nurse said
"At least you have long eyelashes..."
Looking up at the lights in the room, just like in the movies..Doctors in masks over me...told me to count backwards from 10...I was out before I even got to 8. I woke up and remembered really needing to go to the bathroom, immediately. The nurse told me I couldn't go until I had been awake for a while but that she would get me a bedpan. I absolutely refused. I wouldn't sink that damn low, come on now...I waited for another nurse to walk by less than a minute later and acted as normal as I could...She let me get up and go to the restroom.
They showed me, my mom, and my sister Sandy the pictures of the inside of my colon. I'm pretty sure they took a biopsy too. I was in a wheelchair..I didn't want to look at the pictures. I wouldn't do it. Everything is so fuzzy...They diagnosed me with ulcerative colitis.
Now what??
(I appreciate all of you who read through all this...it's really intense for me to basically relive it all...so I'm going to take a little break...let this bit sink in, and I'll update this again soon with the rest of the story...)
Don't feel bad for me because I'm getting surgery.
There's something I really want to make clear with all of this. It seems to be a trend, when talking about my surgery, for people to tell me that they feel really sorry for me that I'm getting this surgery done, and they're sure that I'm worried, and upset about it...
I am worried, it's natural. I'm having a large, quite important organ removed from my body, and it's terrifying. That aside,
don't feel sorry for me because I'm getting surgery.
If you want to feel sorry for me (which, let me make clear, is not at all what I'm wanting or asking for) then feel sorry that I've had to live sick, with this terrible disease, for the last four years of my life.
This surgery is a GOOD thing.
no
a GREAT thing.
I'm getting this diseased organ out of my body. It doesn't belong, and frankly, I don't want it anymore.
It's five days until my surgery and though I am terrified, all I can think about is all the things I'm going to be able to do once it's over with. I'm going to have my life back. I'm going to be healthy. I'm not going to hurt every day of my life anymore.
So be happy for me. Be excited.
I know I am.
Of course, all thoughts/prayers are more than welcome. As I said, it is terrifying. I'm beyond scared. But the outcome will be worth it, I know.
Thanks to everyone who has been there for me the last 4 years, and helped me with this. And thanks to those who had no idea I was even sick, but are there for me now. <3
I am worried, it's natural. I'm having a large, quite important organ removed from my body, and it's terrifying. That aside,
don't feel sorry for me because I'm getting surgery.
If you want to feel sorry for me (which, let me make clear, is not at all what I'm wanting or asking for) then feel sorry that I've had to live sick, with this terrible disease, for the last four years of my life.
This surgery is a GOOD thing.
no
a GREAT thing.
I'm getting this diseased organ out of my body. It doesn't belong, and frankly, I don't want it anymore.
It's five days until my surgery and though I am terrified, all I can think about is all the things I'm going to be able to do once it's over with. I'm going to have my life back. I'm going to be healthy. I'm not going to hurt every day of my life anymore.
So be happy for me. Be excited.
I know I am.
Of course, all thoughts/prayers are more than welcome. As I said, it is terrifying. I'm beyond scared. But the outcome will be worth it, I know.
Thanks to everyone who has been there for me the last 4 years, and helped me with this. And thanks to those who had no idea I was even sick, but are there for me now. <3
Tuesday, May 25, 2010
i am a depressed hermit.
It's so hard to be able to be positive about anything when you have a chronic illness that affects you every single day.
Even things that are supposed to be happy in my life are tarnished by this damn disease.
I can't handle it anymore.
I'm breaking down. It's so god damn hard.
I pretty much go into everything in my life with a slightly negative attitude because that's just what I have to deal with. I could at any minute feel like instant shit; and I spend my life worrying whether or not that is going to happen.
I so depressed I don't even want to leave my house anymore.
I hate people that are all doom and gloom and **feel sorry for me** but I'm posting this so hopefully...you will be able to see the improvement after I have my surgery...I can't wait...I really...really..can't.
Even things that are supposed to be happy in my life are tarnished by this damn disease.
I can't handle it anymore.
I'm breaking down. It's so god damn hard.
I pretty much go into everything in my life with a slightly negative attitude because that's just what I have to deal with. I could at any minute feel like instant shit; and I spend my life worrying whether or not that is going to happen.
I so depressed I don't even want to leave my house anymore.
I hate people that are all doom and gloom and **feel sorry for me** but I'm posting this so hopefully...you will be able to see the improvement after I have my surgery...I can't wait...I really...really..can't.
Tuesday, May 18, 2010
Every day is a bad day.
I remember when I used to go to an appointment with my GI, and though I wasn't feeling 100% great all the time, when he asked how I was doing I would respond
"There are good days, and there are bad days."
Now, there are ONLY bad days.
I feel worse than terrible for at least 3 hours of EVERY DAY.
Just take a second and imagine that.
I don't know how I'm going to be able to last for another month. I really, really don't.
If you had told me before all this happened, that this would be my life for 4 years, I wouldn't have believed you for a second. I honestly don't know how I've done it this long...probably because I had no other choice.
It's hard guys...it really is. For those of you who have no insight into this disease, it's unexplainable. I have had to adjust literally EVER SINGLE ASPECT of my life for this disease. I have to plan everything. I have to think about it constantly. There are so many things I can't do because of it.
Walk the canal?---NOPE.
Mushroom hunting?--NOPE.
Camping?--NOPE.
Car ride that lasts more than 1 hour (and sometimes even that's too long)--NOPE.
Traveling of any sort, really...---NOPE.
Spending the night away from home?--Not unless it's someone who already understands everything I'm going through...3 hours in the bathroom every morning is kind of hard to explain...
Eating?--Better not try more than 1.5 meals a day unless you want to die tomorrow!!!
Playing with my nephew?--not unless it's video games, girl.
The list goes on and on.
And the worst part is, people don't understand. I look like a loser that just wants to sit at home and not do anything. I have to cancel plans frequently when I'm having an exceptionally bad day, and I look like a jerk that just doesn't want to hang out with my friends. Or god forbid I have to cancel something more important than that, like a photoshoot, or call into work....
Everywhere I go the first thing I must know is where the bathroom is at. If there isn't one, I better get the fuck out of there quick, because you can be damn sure that I'm going to need to use it, ESPECIALLY if it isn't there.
I'm just so tired.
I'm tired of feeling awful constantly. My pain is excruciating for at least three hours every morning (so yeah..guess when I need to wake up if I need to be somewhere at oooh...8am? yeah...it blows) but it never really goes away either. Even when I'm not locked in the bathroom, I'm not well. I'm so very, very, ill, all the time. One of my instructors said it best when he told me
"...you have seemed a little wilted lately..."
That's exactly what I am. I'm wilted...I have bags under my eyes that I can't cover up. If you were to touch me, all you would feel is bones. I'm sleepy. I'm sad.
But you know what?
I'm a fucking fighter.
It may sound bad, but this disease has made me lose a lot of sympathy for other people, it really has. It really is true; Whatever you happen to be going through in life IT COULD BE WORSE. I know this is true for myself, even with all the pain and suffering I'm going through. It could be fucking worse...Don't get me wrong, there are still days where I feel extremely sorry for myself. Today is one of them.
I think I'm entitled to one every now and again...
"There are good days, and there are bad days."
Now, there are ONLY bad days.
I feel worse than terrible for at least 3 hours of EVERY DAY.
Just take a second and imagine that.
I don't know how I'm going to be able to last for another month. I really, really don't.
If you had told me before all this happened, that this would be my life for 4 years, I wouldn't have believed you for a second. I honestly don't know how I've done it this long...probably because I had no other choice.
It's hard guys...it really is. For those of you who have no insight into this disease, it's unexplainable. I have had to adjust literally EVER SINGLE ASPECT of my life for this disease. I have to plan everything. I have to think about it constantly. There are so many things I can't do because of it.
Walk the canal?---NOPE.
Mushroom hunting?--NOPE.
Camping?--NOPE.
Car ride that lasts more than 1 hour (and sometimes even that's too long)--NOPE.
Traveling of any sort, really...---NOPE.
Spending the night away from home?--Not unless it's someone who already understands everything I'm going through...3 hours in the bathroom every morning is kind of hard to explain...
Eating?--Better not try more than 1.5 meals a day unless you want to die tomorrow!!!
Playing with my nephew?--not unless it's video games, girl.
The list goes on and on.
And the worst part is, people don't understand. I look like a loser that just wants to sit at home and not do anything. I have to cancel plans frequently when I'm having an exceptionally bad day, and I look like a jerk that just doesn't want to hang out with my friends. Or god forbid I have to cancel something more important than that, like a photoshoot, or call into work....
Everywhere I go the first thing I must know is where the bathroom is at. If there isn't one, I better get the fuck out of there quick, because you can be damn sure that I'm going to need to use it, ESPECIALLY if it isn't there.
I'm just so tired.
I'm tired of feeling awful constantly. My pain is excruciating for at least three hours every morning (so yeah..guess when I need to wake up if I need to be somewhere at oooh...8am? yeah...it blows) but it never really goes away either. Even when I'm not locked in the bathroom, I'm not well. I'm so very, very, ill, all the time. One of my instructors said it best when he told me
"...you have seemed a little wilted lately..."
That's exactly what I am. I'm wilted...I have bags under my eyes that I can't cover up. If you were to touch me, all you would feel is bones. I'm sleepy. I'm sad.
But you know what?
I'm a fucking fighter.
It may sound bad, but this disease has made me lose a lot of sympathy for other people, it really has. It really is true; Whatever you happen to be going through in life IT COULD BE WORSE. I know this is true for myself, even with all the pain and suffering I'm going through. It could be fucking worse...Don't get me wrong, there are still days where I feel extremely sorry for myself. Today is one of them.
I think I'm entitled to one every now and again...
Sunday, May 9, 2010
6-21-2010
That's the day that my life is going to change forever.
I met with a surgeon this past Tuesday, and he's going to perform my surgery for me! I went into the appointment completely skeptical, and assuming he was going to be like the last surgeon that I met with, and my GI, and tell me that I shouldn't want to have this surgery done, and that he wasn't going to do it for me, but that wasn't what happened at all!
We went through an abbreviated history of my disease, and all the medications I've tried and such, and how I've been feeling lately and everything that I've been going through. He listened very carefully, making notes as I told my story, and when I finished, he basically said that what I'm going through is terrible. It was such a relief to hear that, as strange as that sounds. I think too many doctors become desensitized to their patients problems. I honestly expected a response like those I get from my GI so often; "Well my patient so-and-so has it worse because they had to deal with such problem and such and such problem...You should be glad you don't have to deal with that..." etc. But that's now how this surgeon was at all. He was so incredibly sympathetic. He said that he can tell my quality of life isn't high, and that he knows that I'm living okay now, because I don't have any other choice, but that he could tell from what I told him that my life is rough, and no one should have to live the way that I do every day.
Him saying that, and agreeing that I can't keep living the way I am right now, was the biggest relief of my life. I honestly almost cried.
I assume most people that read this blog as of right now are fellow UC sufferers, which is great. But to any of you out there that do not have UC or crohn's or anything like it, it really is indescribably terrible, and almost impossible to describe to someone who doesn't have to go through it. I'm thinking about posting this blog onto my facebook once the time of my surgery approaches. That way, those close to me, or those wondering why I'm not around school, and permanently attached to Liesl's side anymore can read up and see how I'm doing. I guess I'm just apprehensive since my disease and this surgery process are going to be very...personal? I don't know if that is the word that I'm looking for. My disease is just gross, okay? I realize this. It's been around for four years, how could I not realize it?? But it's important for me to share my story with others. I know for me, the blogs of others with my condition have been so helpful in trying to deal with my condition. Beyond that, I know some people that know me are curious about my condition..if I share my blog, maybe they can understand it more? :sigh: I don't know. I'm going to do it either way.
So...if you're reading this, and you don't want to feel awkward, or have the possibility of being grossed out, read no further. This disease is gross, it's terrible, and it's been doing it's best to ruin my life for the past four years. I'm putting a stop to that right now. This is my story about it. If you're interested, that's fantastic, if not, go away.
I met with a surgeon this past Tuesday, and he's going to perform my surgery for me! I went into the appointment completely skeptical, and assuming he was going to be like the last surgeon that I met with, and my GI, and tell me that I shouldn't want to have this surgery done, and that he wasn't going to do it for me, but that wasn't what happened at all!
We went through an abbreviated history of my disease, and all the medications I've tried and such, and how I've been feeling lately and everything that I've been going through. He listened very carefully, making notes as I told my story, and when I finished, he basically said that what I'm going through is terrible. It was such a relief to hear that, as strange as that sounds. I think too many doctors become desensitized to their patients problems. I honestly expected a response like those I get from my GI so often; "Well my patient so-and-so has it worse because they had to deal with such problem and such and such problem...You should be glad you don't have to deal with that..." etc. But that's now how this surgeon was at all. He was so incredibly sympathetic. He said that he can tell my quality of life isn't high, and that he knows that I'm living okay now, because I don't have any other choice, but that he could tell from what I told him that my life is rough, and no one should have to live the way that I do every day.
Him saying that, and agreeing that I can't keep living the way I am right now, was the biggest relief of my life. I honestly almost cried.
I assume most people that read this blog as of right now are fellow UC sufferers, which is great. But to any of you out there that do not have UC or crohn's or anything like it, it really is indescribably terrible, and almost impossible to describe to someone who doesn't have to go through it. I'm thinking about posting this blog onto my facebook once the time of my surgery approaches. That way, those close to me, or those wondering why I'm not around school, and permanently attached to Liesl's side anymore can read up and see how I'm doing. I guess I'm just apprehensive since my disease and this surgery process are going to be very...personal? I don't know if that is the word that I'm looking for. My disease is just gross, okay? I realize this. It's been around for four years, how could I not realize it?? But it's important for me to share my story with others. I know for me, the blogs of others with my condition have been so helpful in trying to deal with my condition. Beyond that, I know some people that know me are curious about my condition..if I share my blog, maybe they can understand it more? :sigh: I don't know. I'm going to do it either way.
So...if you're reading this, and you don't want to feel awkward, or have the possibility of being grossed out, read no further. This disease is gross, it's terrible, and it's been doing it's best to ruin my life for the past four years. I'm putting a stop to that right now. This is my story about it. If you're interested, that's fantastic, if not, go away.
Sunday, May 2, 2010
this is the worst medication ever invented.
I don't understand why anyone would look at the side-effects of steroids and think that it's an okay thing for people to put into their bodies.
So far I'm experiencing every terrible side effect that I always get when on this damn medication, and not ONE glimpse of the help it's supposed to give me in making my disease less terrible. I'm biting everyone's heads off, I don't want to talk to anyone, go anywhere, say anything, eat anything (which I realize is unusual since steroids normally make your appetite ridiculous)...I can't sleep for shit...and the little amount of sleep I do get is constantly interrupted by my ceaseless thirst and then inevitable need to piss; ALOT. I'm depressed, to say the least. I'm just waiting for my face to balloon up so I can crawl even further into my whole of isolation and hatred for fucking everything.
So far I'm experiencing every terrible side effect that I always get when on this damn medication, and not ONE glimpse of the help it's supposed to give me in making my disease less terrible. I'm biting everyone's heads off, I don't want to talk to anyone, go anywhere, say anything, eat anything (which I realize is unusual since steroids normally make your appetite ridiculous)...I can't sleep for shit...and the little amount of sleep I do get is constantly interrupted by my ceaseless thirst and then inevitable need to piss; ALOT. I'm depressed, to say the least. I'm just waiting for my face to balloon up so I can crawl even further into my whole of isolation and hatred for fucking everything.
Friday, April 30, 2010
back on the 'roids.
Fan-fucking-tastic.
I'm back on prednisone. In February the pharmacy messed up and didn't order my Asacol HD. I had to take the lower dosage of Asacol for a weekend, and it completely messed up my entire system. I had been fairly okay before the mix up, but it all went downhill from there. I completely relapsed into my flare-up. I got back on the HD Asacol after a few days, but it just wasn't the same. And now I'm back on my steroids. This coming Tuesday I'm meeting with another (different) surgeon. My GI still disagrees with my feeling of needing surgery, but I just don't know what else to do anymore. He thinks this surgeon will disagree with me just as the last one did.
I'm just lost. I've been on my steroids for about a week and am already experiencing some of the terrible side effects. My emotions are out of control and I can't sleep. I started a new job recently and have already had to leave work once because of my UC. No one understands, and I can't explain it to them. It's so weird. Total TMI moment if I really explained to them what my disease is.
"You're too young to have ulcers."
"You're telling me...I've had them since I was 17..."
I don't know what to do.
I'm back on prednisone. In February the pharmacy messed up and didn't order my Asacol HD. I had to take the lower dosage of Asacol for a weekend, and it completely messed up my entire system. I had been fairly okay before the mix up, but it all went downhill from there. I completely relapsed into my flare-up. I got back on the HD Asacol after a few days, but it just wasn't the same. And now I'm back on my steroids. This coming Tuesday I'm meeting with another (different) surgeon. My GI still disagrees with my feeling of needing surgery, but I just don't know what else to do anymore. He thinks this surgeon will disagree with me just as the last one did.
I'm just lost. I've been on my steroids for about a week and am already experiencing some of the terrible side effects. My emotions are out of control and I can't sleep. I started a new job recently and have already had to leave work once because of my UC. No one understands, and I can't explain it to them. It's so weird. Total TMI moment if I really explained to them what my disease is.
"You're too young to have ulcers."
"You're telling me...I've had them since I was 17..."
I don't know what to do.
Thursday, April 1, 2010
i hate doctors.
why can't i force myself to make an appointment with my GI even though I'm experiencing ridiculous, terrible pain?
i hate doctors.
hate them
hate them
hate them.
i hate that they still get paid even if they can't find out what's wrong with you.
i hate that they will get paid even if they can't make you better if they do find out what's wrong with you.
i hate that they're so pompous about 99.9% of the time.
ugh.
i don't want to go back and be told that no one is going to perform this surgery on me.
i don't want the #1 think on my mind at all times to be where the bathroom is located in a new location, and how fast I can get there without looking weird.
*sigh*
i hate doctors.
hate them
hate them
hate them.
i hate that they still get paid even if they can't find out what's wrong with you.
i hate that they will get paid even if they can't make you better if they do find out what's wrong with you.
i hate that they're so pompous about 99.9% of the time.
ugh.
i don't want to go back and be told that no one is going to perform this surgery on me.
i don't want the #1 think on my mind at all times to be where the bathroom is located in a new location, and how fast I can get there without looking weird.
*sigh*
Sunday, March 28, 2010
apologies...
It has been quite some time since I've posted...I apologize. ( I do, after all, have ONE whole follower..I'm sure I've been disappointing them.)
At any rate, I guess I just became extremely discouraged after meeting with my surgeon and basically lost all motivation to keep up with this blog.
It didn't go well, to say the least. I had an entire list of questions to ask him about the surgery, so I could be informed and ready for all ahead of me. Well, it didn't even get far enough for me to ask a single question on the list.
It was the same situation that happened when I mentioned surgery to my GI specialist. He acted like I was a crazy person for even considering this surgery as young as I was. He was telling me all the negatives ( that I already knew, thanks to my extensive research ) as though he was trying to scare me out of the surgery. My mom started crying. She was so upset that he wasn't going to even consider the surgery. She hates seeing me in pain, and is afraid that I'm going to get extremely ill again like before. I was just stunned. I didn't say half the things I would have loved to say; I knew it would have been pointless anyway. I believe fairly close to his exact words were "You're not going to scare me into performing a surgery that I don't want to perform." Meaning I could threaten to go to another surgeon, etc. but I wasn't going to change his mind, which I think was made up almost immediately.
It infuriates me that I, weighing just over 110lbs could walk into a plastic surgeons office and say that I wanted to have liposuction, and they would do it, no problems; but I can't walk into this surgeons office wanting to have a diseased organ removed to stop my chronic illness, without being shot down almost immediately.
Absolutely ridiculous.
I will be updating more often, as I think it's nice to have a journal of how I'm doing with this disease.
Expect another post tomorrow...
At any rate, I guess I just became extremely discouraged after meeting with my surgeon and basically lost all motivation to keep up with this blog.
It didn't go well, to say the least. I had an entire list of questions to ask him about the surgery, so I could be informed and ready for all ahead of me. Well, it didn't even get far enough for me to ask a single question on the list.
It was the same situation that happened when I mentioned surgery to my GI specialist. He acted like I was a crazy person for even considering this surgery as young as I was. He was telling me all the negatives ( that I already knew, thanks to my extensive research ) as though he was trying to scare me out of the surgery. My mom started crying. She was so upset that he wasn't going to even consider the surgery. She hates seeing me in pain, and is afraid that I'm going to get extremely ill again like before. I was just stunned. I didn't say half the things I would have loved to say; I knew it would have been pointless anyway. I believe fairly close to his exact words were "You're not going to scare me into performing a surgery that I don't want to perform." Meaning I could threaten to go to another surgeon, etc. but I wasn't going to change his mind, which I think was made up almost immediately.
It infuriates me that I, weighing just over 110lbs could walk into a plastic surgeons office and say that I wanted to have liposuction, and they would do it, no problems; but I can't walk into this surgeons office wanting to have a diseased organ removed to stop my chronic illness, without being shot down almost immediately.
Absolutely ridiculous.
I will be updating more often, as I think it's nice to have a journal of how I'm doing with this disease.
Expect another post tomorrow...
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