blog title is pretty obvious, but eh.. sometimes you just need to be reminded...
it wasnt too shabby doing Thanksgiving with just gene, aidan, and myself.. due to some issues with our respective families (particular family members, rather, than the family as a whole), we have decided that we are going to do holiday activies with our little family instead of the whole rigamore of running from one house to another..
the idea of not buying gifts for a million people, and getting to focus on only buying for a few people is just LOVELY... i mean, Christmas shouldnt be about the gift giving, but rather the spirit of thanks and love and family... i fully intend of focusing on that rather than making sure that aidan gets the best of the best; i want him to really understand that it's more about spending time with family and helping people who arent able to have even basic necessities.
food wise, it was not difficult eating a ton of food and stuffing myself silly.. i was never a big eater on Thanksgiving for the past few years, so my 4oz. piece of turkey, with gravy, was pretty satisfying and yummy!!! aidan ate so much that he got sick that night.. poor guy looked sick, but eh.. its not uncommon, as his father was the same way..
on the not so holiday related, i have been feeling stupidly sick for the last 4 months... my crohns is not calming down (my GI doc has upped my Humera, so hopefully that will help with the flares and daily management), i had both my appendix and gallbladder removed on an emergency basis (see previous blogs), and then got a cold. a simple cold, you say?? not for this gal!!!
as crohns is an auto-immune disorder, a simple cold could end up with a hospital stay for me.. and i THOUGHT that with my Theraflu and various other OTC meds, i kicked it, but i continued to have a stupid runny nose, and headaches were getting pretty severe and common (by Thanksgiving, i was having daily headaches that lasted 2-3 hrs at a time, and occurred about 3-4 times a day.. i would go to bed with a headache and wake up with one too... it was frustrating, but i figured it was connected to my allergies, or perhaps just the change in weather... either way, i just stuck with Tylenol and loads of fluids..
but about a week ago, i started feeling SUPER lightheaded and dizzy when i stood up or sat up. whenever i got up from a laying/sitting position, i would be ok for about 5 seconds, then it would hit like a ton of bricks. i would feel like the room is spinning, everything would turn black, and i would feel like my heart was beating out of my chest... i would breathe through it and after about 10 seconds of that, i felt normal again. it is the most peculiar feeling!! by Thanksgiving, the fainting took over and gene and i decided an ER trip was in order..
you will never feel so low as when you leave your husband and step-son on the holiday to go to an ER, alone, on a holiday. i have never been so frustrated before.
they figured that my cold turned to a sinus infection, and the sinus infection turned into a brain infection... its an easy fix with antibiotics and Sudafed... they say the dizzy/lightheaded stuff is vertigo and another side effect of the infection.
im feeling really sad lately because of all of this. i wish that it were easier and my body wasnt so difficult. i thought the weight loss would end up HELPING with my various other body issues, not exacerbate and enhance further issues. i feel really low, but i know this too shall pass... i wish it would just end up passing quicker and not cause so much interruption to my life, work, and family. doesnt seem fair, but then again, their are many other people who have it far worse than i do, and i am pretty blessed... i will focus on that. i NEED to focus on that...
starting my journey to better health, less weight, more peace, and incredible love... excited to share the ups and downs with anyone who cares to listen and learn!
Showing posts with label ER. Show all posts
Showing posts with label ER. Show all posts
Sunday, November 25, 2012
Thanksgiving is Over!!!
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Saturday, August 11, 2012
appendix and heat
well, this last week has been crazy... once again, my body has showed me how much it hates me...
**BEWARE** THIS POST MAY HAVE SOME TMI MOMENTS, SO SHOULD YOU HAVE A WEAK STOMACH OR JUST NOT CARE TO HEAR ABOUT THE INNER WORKINGS ON MY BODY!!!!!
so on thursday, i went into the ER compaining on how i hadnt been able to have a bowel movement in nearly 7 days. yeah, that is NOT fun in itself... i figured maybe it had to do with the lack of fiber in my diet due to the high protien i have to have... gene stayed home, as i really figured they would give me a lovely suppository, and i would end up feeling better in a few hours.
side note, i never realized how freaking much it hurts not going number two... then again, it could've been my inflammed appendix, but im getting ahead of myself...
so, after consulting with my personal doctor, or rather my great, childhood friend, who happens to be a suergon and will tell me to go do something when i dont wanna hear it, i headed to the ER to get my lovely poop medicine.. well, after informing them of my amazing and heartwarming history with Crohns, they decided they wanted to do a CT scan...
now, i normally request unless its ABSOLUTELY necessary, they dont give me a CT...
http://www.webmd.com/a-to-z-guides/computed-tomography-ct-scan-of-the-body
you really dont want to get many CTs or X-Rays, if you can avoid it.. i mean, you dont want that much radiation in your body! so, pre crohn's "official" diagnosis, i was getting a CT scan at least once a month.. they were pretty free about filling my body with radiation because they didnt know what was going on! so im pretty hell bent now about not getting a CT unless they are worried about a blockage or something..
which was a possiblity with the amount of pain i was in, along with other symptoms.. so they did the CT, and within 30 mins of coming back to my room, my ER doctor came in a looked pretty serious... she told me "your CT scan was abnormal, and im having the suregon come down and review your films."
being the dosages of Ativan. I started panicking!! i mean, i knew i was in a lot of pain, but at this point, i was freaking the eff out... she came back in and said "well, it looks like your appendix is inflammed, along with the intestines (or colon, im not sure). the suregon will be in here in a moment to discuss surgery." i immediately got on the phone and called gene to come down. i mean, at this point, they were discussing surgery! i mean, i was thinking i was going to get some sort of enema or suppository, and here they are discussing cutting me open!!! seriously?? cant i catch a freaking break!?!
well, the surgeon came into the room, and from start to finish, i was in the OR within 40 mins. honeslty, i dont remember much after that, except i refused to take out my lip ring because i didnt want the hole to close (the anestesiolgist was NOT happy about that.. but im stubborn. they let me keep it in!), crying for gene post-op and confused about where i was..
i guess the surgery was only suppose to take 30-50 mins, but due to my inflammed innards and whatnot, the whole thing lasted 3 hrs. gene's grandma came and sat with him, which im really thankful for... i guess they didnt even update him till 1.5 hrs in, which is totally unacceptable! i mean, if gene was in there for 5 minutes more that i expected, i would freaking be banging on the OR doors.. but gene said he raised a little hell to find out wtf was going on with his wife, which is oddly sweet.. oh, the things i find romantic!
well, i was in the hospital from thursday night till sunday afternoon.. oddly enough, i wasnt feeling too crappy till sunday afternoon when they let me go home.. my mom came by sunday and helped put away some laundry while i laid in bed and hurt, complained, and sweat. idk if you remember, but it was stupid hot out that weekend...
which is awesome. and by awesome, i mean the stupidest and most hateful thing in the world. i hate the heat. anything over 70, and i vote to turn on the AC... gene and i have had the AC running
since may with shouldnt be a suprise if you know us evena little.. i was happy to have the AC running crazy in our room, which made the nurses and staff come check up on me more than usual.. hey, i would've done the same thing!!
so here we are a week later, and im still in a decent amount a pain.. im finding that its a completely different type of pain than the sleeve, so i wasnt ready for it at all... in fact, the pain has been getting a little worse over the last few days, but i figure its all normal so im just sticking to my belly ice packs and pain meds... i showed aidan my scar and he was excited about that... little boys love that kinda thing!!
**BEWARE** THIS POST MAY HAVE SOME TMI MOMENTS, SO SHOULD YOU HAVE A WEAK STOMACH OR JUST NOT CARE TO HEAR ABOUT THE INNER WORKINGS ON MY BODY!!!!!
so on thursday, i went into the ER compaining on how i hadnt been able to have a bowel movement in nearly 7 days. yeah, that is NOT fun in itself... i figured maybe it had to do with the lack of fiber in my diet due to the high protien i have to have... gene stayed home, as i really figured they would give me a lovely suppository, and i would end up feeling better in a few hours.
side note, i never realized how freaking much it hurts not going number two... then again, it could've been my inflammed appendix, but im getting ahead of myself...
so, after consulting with my personal doctor, or rather my great, childhood friend, who happens to be a suergon and will tell me to go do something when i dont wanna hear it, i headed to the ER to get my lovely poop medicine.. well, after informing them of my amazing and heartwarming history with Crohns, they decided they wanted to do a CT scan...
now, i normally request unless its ABSOLUTELY necessary, they dont give me a CT...
http://www.webmd.com/a-to-z-guides/computed-tomography-ct-scan-of-the-body
you really dont want to get many CTs or X-Rays, if you can avoid it.. i mean, you dont want that much radiation in your body! so, pre crohn's "official" diagnosis, i was getting a CT scan at least once a month.. they were pretty free about filling my body with radiation because they didnt know what was going on! so im pretty hell bent now about not getting a CT unless they are worried about a blockage or something..
which was a possiblity with the amount of pain i was in, along with other symptoms.. so they did the CT, and within 30 mins of coming back to my room, my ER doctor came in a looked pretty serious... she told me "your CT scan was abnormal, and im having the suregon come down and review your films."
being the dosages of Ativan. I started panicking!! i mean, i knew i was in a lot of pain, but at this point, i was freaking the eff out... she came back in and said "well, it looks like your appendix is inflammed, along with the intestines (or colon, im not sure). the suregon will be in here in a moment to discuss surgery." i immediately got on the phone and called gene to come down. i mean, at this point, they were discussing surgery! i mean, i was thinking i was going to get some sort of enema or suppository, and here they are discussing cutting me open!!! seriously?? cant i catch a freaking break!?!
well, the surgeon came into the room, and from start to finish, i was in the OR within 40 mins. honeslty, i dont remember much after that, except i refused to take out my lip ring because i didnt want the hole to close (the anestesiolgist was NOT happy about that.. but im stubborn. they let me keep it in!), crying for gene post-op and confused about where i was..
i guess the surgery was only suppose to take 30-50 mins, but due to my inflammed innards and whatnot, the whole thing lasted 3 hrs. gene's grandma came and sat with him, which im really thankful for... i guess they didnt even update him till 1.5 hrs in, which is totally unacceptable! i mean, if gene was in there for 5 minutes more that i expected, i would freaking be banging on the OR doors.. but gene said he raised a little hell to find out wtf was going on with his wife, which is oddly sweet.. oh, the things i find romantic!
well, i was in the hospital from thursday night till sunday afternoon.. oddly enough, i wasnt feeling too crappy till sunday afternoon when they let me go home.. my mom came by sunday and helped put away some laundry while i laid in bed and hurt, complained, and sweat. idk if you remember, but it was stupid hot out that weekend...
which is awesome. and by awesome, i mean the stupidest and most hateful thing in the world. i hate the heat. anything over 70, and i vote to turn on the AC... gene and i have had the AC running
since may with shouldnt be a suprise if you know us evena little.. i was happy to have the AC running crazy in our room, which made the nurses and staff come check up on me more than usual.. hey, i would've done the same thing!!
so here we are a week later, and im still in a decent amount a pain.. im finding that its a completely different type of pain than the sleeve, so i wasnt ready for it at all... in fact, the pain has been getting a little worse over the last few days, but i figure its all normal so im just sticking to my belly ice packs and pain meds... i showed aidan my scar and he was excited about that... little boys love that kinda thing!!
Thursday, May 31, 2012
a bit of a setback...
well, looks like the healing isn't going as it should be... which shouldn't be surprising, but lo and behold, still as frustrating...
about 3 weeks ago, i started vomiting anytime i ate or drank. i was aware that this could be a problem going INTO the surgery, but this just seemed excessive. i slowed down my eating and drinking, went back to mushy foods, etc... Dr. Halpin said that this could be all normal, but i really don't feel like it is..
so on Wednesday, i went to the ER after getting some blood tests results, and being dehydrated. i was TOLD that i could get the upper GI that night if we went all the way to Good Sam from Oregon City, but yet again, there was some crap miscommunication.
this morning, i went and got the upper GI, and in the process of drinking the contrast, i threw it up.. SHOCKING. ugh. the radiologist who took the series was somewhat concerned with why the contrast wasn't going down and through my tummy like it should've, so at least now i know its not all in my head. so for now, i am waiting on a call from Dr. Halpin after she's reviewed the study, and we'll go from there..
I'm still not regretting my choice to get the sleeve. overall, its helped my health more than i every though.. I'm just frustrated with the fact my body isn't healing how it should've been... i get annoyed that gene is stuck coming to the hospital to visit me or make sure I'm not dying. i am frustrated that I'm told one minute things are fine, and the next they may not be. i frustrated that the ONLY person in my family that seems to care about how my health is is my dad. I'm frustrated. period. end of story.
i just hope i can get some answers here shortly. i cant keep stringing along my husband. i cant keep hoping for better health.
I'm exhausted. I'm weak. I'm tired. its getting old.
about 3 weeks ago, i started vomiting anytime i ate or drank. i was aware that this could be a problem going INTO the surgery, but this just seemed excessive. i slowed down my eating and drinking, went back to mushy foods, etc... Dr. Halpin said that this could be all normal, but i really don't feel like it is..
so on Wednesday, i went to the ER after getting some blood tests results, and being dehydrated. i was TOLD that i could get the upper GI that night if we went all the way to Good Sam from Oregon City, but yet again, there was some crap miscommunication.
this morning, i went and got the upper GI, and in the process of drinking the contrast, i threw it up.. SHOCKING. ugh. the radiologist who took the series was somewhat concerned with why the contrast wasn't going down and through my tummy like it should've, so at least now i know its not all in my head. so for now, i am waiting on a call from Dr. Halpin after she's reviewed the study, and we'll go from there..
I'm still not regretting my choice to get the sleeve. overall, its helped my health more than i every though.. I'm just frustrated with the fact my body isn't healing how it should've been... i get annoyed that gene is stuck coming to the hospital to visit me or make sure I'm not dying. i am frustrated that I'm told one minute things are fine, and the next they may not be. i frustrated that the ONLY person in my family that seems to care about how my health is is my dad. I'm frustrated. period. end of story.
i just hope i can get some answers here shortly. i cant keep stringing along my husband. i cant keep hoping for better health.
I'm exhausted. I'm weak. I'm tired. its getting old.
Labels:
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gastric sleeve,
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Location:
Oregon City, OR, USA
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