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Total colectomy Part 15

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shellypoo
Veteran Member
Joined : Dec 2005
Posts : 896
Posted 5/31/2007 2:50 PM (GMT -7)
Hi Dana,

There is a surgeon in the u.S. who is highly recommended, I actually called and spoke with his secrectary when I didn't know who I could go to in my area.  He has a web site of his book, it's very interesting and gives you his contact numbers...http://www.constipation.net/Chapters/9_const_pcol.html

 

Just look on the left side of the page and click on the topics you want.  I hope it pulls up for you.  Take care. :-)


Michelle ><>

Co-Moderator MS forum

 

Ever stop to think, and forget to start again???


profile picture
Stuck42Long
Regular Member
Joined : Sep 2006
Posts : 250
Posted 5/31/2007 6:33 PM (GMT -7)
ADVISESEEKER - I'm so sorry for the delay in responding.  Yes, I did have very LARGE and hard stools.  In fact, I was at the point that I had to MANUALLY remove my stool.  On occasions, after taking LOADS of laxatives, I had the same thing as you are describing.  I was to the point of taking a box of 48 extra strength EX-LAX in a three day span.

As Danaalbertine stated..My BMs are what you describe: WIthout laxatives - nothing, and with laxatives at first harder but the loose and sometimes watery. I think when you have to take such high amounts of laxatives, a lot of water gets pulled into your intestines and that will make it very loose.  I experienced this too and I do think it has something to do with the colon pulling in the water.  However, this is a temporary fix and doesn't mean that your colon is OK and functioning. 

The most important thing I can relate to you is....EVENTUALLY the laxatives WILL NOT work like they're working now - it only gets slower and slower until you're extremely sick from the overdose of the laxatives on your body!! 

This is a big decision I know, but I cannot stress enough, the benefits outweigh EVERYTHING!!!  Time isn't on your side when you have this condition and at some point, if not now, you will have to decide what's best for you!!!

SHELLY/Michelle - Thank you for researching and helping Dana - You're a real blessing and I'm sure she appreciates it!!  We do have some great people here don't we?

HELENSC - Forgive me for asking, but was your surgery in 2007 rather than 2006?  I will try to answer your questions as best I can OK?  Yes, you can work out and try to trim the belly, however, I would ask your surgeon on how strenuous your workouts can be (better safe than sorry).  Regarding depression post-op - well, I've suffered with depression for many, many years and I did feel more depression symptoms after the surgery.  My psychiatrist said it's more than likely due to the "trauma" we've been thru.  As you well know, the surgery is big, as well as, recovery long.  I did start feeling "emotionally" better the better I began to heal and improve.

I have regained some of the weight I lost immediately post-op and I think it's only normal, we regain or appetites along with our strength.  Regarding your question on still having some pain...each one of us is different and we all heal in our own way and time.  I personally didn't feel like my old self until 16 weeks post-op or a little longer.  The good news, YES - you will feel normal again, only a little better than "normal"!!!!

Thanks for your encouraging words to those who haven't yet had this surgery.  I agree WHOLEHEARTEDLY with you and I too would do it all over again without hesitation!!!

 


Robin

 

God is SO good - His blessings are endless! 

Trust in Him with all your heart!

Know He's in control over every situation you face!!

 

 

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Stuck42Long
Regular Member
Joined : Sep 2006
Posts : 250
Posted 6/1/2007 5:57 PM (GMT -7)
ADVISESEEKER - I wanted to add one additional thing for you to think about.  If it weren't for the dulcolax would you have ANY BM's?  Probably not - that was my case.  In fact, it only got worse over time and even the "combinations" of different things (prescription medications) didn't work or made me seriously ill.

I cannot get over some of the things those people told you - they couldn't be farther from the truth.  I would ABSOLUTELY take what the surgeon said to heart and take his, and only his advise!!!

I know and understand your fears - you wouldn't be human if you didn't have them!!  Yes, this is a HUGE surgery and a painful recovery, however, 8 to 12 weeks of discomfort vs years of more toxins in the body, not to mention the pain and discomfort of the constipation and the overdose of medications and what they're doing to your body - the surgery IS in your best interest. 

You will gain a new lease on life, one that has been clouded, harmful and painful to this point.

I wish you all the best in your decision making and hope the surgeon can calm some or most of your fears.


Robin

 

God is SO good - His blessings are endless! 

Trust in Him with all your heart!

Know He's in control over every situation you face!!

 

 

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Stuck42Long
Regular Member
Joined : Sep 2006
Posts : 250
Posted 6/3/2007 9:15 AM (GMT -7)
ADVISESEEKER - You're more than welcome!!!!  I do hope ALL goes well with your appointment with the surgeon and second opinion.  Please be sure and fill us in ASAP!!!

I can SO relate to having bm's once a month.  I pretty much lived that way for 43 years - YES - years! 

Thanks to Michelle and you for helping those still in the "decision making" process.  This is THE BEST forum/thread I've ever been a part of!!  I'm so blessed to have all you wonderful people an active part of my life.  I hope to continue helping and encouraging others who suffer with CI and how the TC has changed not only my life, but so many others!!!


Robin

 

God is SO good - His blessings are endless! 

Trust in Him with all your heart!

Know He's in control over every situation you face!!

 

 

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resa
Regular Member
Joined : Apr 2006
Posts : 141
Posted 6/3/2007 2:12 PM (GMT -7)
Hi Everyone,

SHELLYPOO - thank you for reiterating the http://www.constipation.net/Chapters/9_const_pcol.html website. I placed it here many post ago and asked people to check it out. I found it so informative. Anyway, thank you again for re-posting it. ADVISESEEKER - I do hope you found it helpful to your situation.

I am very happy I did this surgery. No regrets to this point. I am 2-1/2 months post op. I have started to walk to work which is 2 miles each way. I make better time in the morning I guess because the morning is cool and the afternoon is so hot. I must admit my leg muscle aren't too happy about this walking. I have held my initial weight loss of 30 pounds off and I continue to loose but at a much much slower rate - about 1 pound a month. The 30 pounds came off within 2 weeks post op. Eating FAT does make things move faster and more often. The surgeon did inform me not to eat Fat or Red Meat because they have that affect. The only thing I do not eat any more since surgery are sweets - cookies, cake, pie, soda. My body no longer craves sugar. At first I wanted an explanation but now it doesn't matter. The important thing is that I am free of an addiction that ruled my life. That is another plus of this surgery for me. I pray everyday that my craving stays gone. I would do this surgery over again in a heartbeat.
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Stuck42Long
Regular Member
Joined : Sep 2006
Posts : 250
Posted 6/4/2007 6:44 PM (GMT -7)
yeah  RESA - I hope your sweet tooth NEVER returns!!!  I have heard it said that once the cycle is broken on sweets, one usually doesn't desire them like they once did!!!  CONGRATULATIONS!!!! 

I will also agree with you about NOT HAVING ANY REGRETS having this surgery - it is the best thing I could have done - EVER!!!

:-)  ADVISESEEKER - I'm THRILLED that your decision was to go for the surgery.  The sooner the better for you!!!  I know that in this short period of time (10 to 20 days) that you will be anxious, have fears and concerns, but rest assured - this is the only way for you to reclaim and have your life back.  Please feel free if you want to talk - we are here for you 100% and we do understand EVERYTHING thing you're going thru right now!!

Please keep us posted on a confirmed date OK?


Robin

 

God is SO good - His blessings are endless! 

Trust in Him with all your heart!

Know He's in control over every situation you face!!

 

 

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danaalbertine
Regular Member
Joined : Apr 2007
Posts : 34
Posted 6/5/2007 11:34 AM (GMT -7)

ADVICESEEKER- I am happy and excited to hear that you made a decision. Good for you!

Unfortunately I am not doing well at all. It seems like my intestines are totally giving up. Even taking 7-10 Dulcolax AND MOM together doesn´t help! What is really strange is the fact that I never fell anything in my rectum. It seems like it´s stuck much further up. When the doctors( or myself) were examining my rectum manually, they could never feel any stool. And when I take laxatives, I can feel stool in my rectum but I cannot get it out. Has anybody experienced this before? EVen if I had diarrhea, I couldn´t pass any stools without removing them manually. This is soooo embarassing!

Oh, ADVICESEEKER, did you get my email? I sent it to the address you mentioned.

Take care everybody.

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Stuck42Long
Regular Member
Joined : Sep 2006
Posts : 250
Posted 6/6/2007 4:03 PM (GMT -7)
sad  DANAALBERTINE - I'm so sorry to hear you're not doing good!!  It really troubles me when someone cannot find the relief they need, or in your instance, help for their problems.  Are you still on the feeding tube?  Forgive me if I have you confused with someone else.  If in fact it is you on the feeding tube, how do you take the Dulcolax and MOM?  I'm sorry if that sounds stupid - I just don't understand the whole feeding tube thing and what is or isn't allowed.

I have experienced the stool being in the rectum and even up higher.  I was to the point that I was having to "manually" remove ALL of my stools, which is quite painful to say the least (and embarassing)!!!

I really hope your doctors can find some kind of help for you in the very near future.  This is not healthy and is surely playing a role on your overall health.   


Robin

 

God is SO good - His blessings are endless! 

Trust in Him with all your heart!

Know He's in control over every situation you face!!

 

 

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danaalbertine
Regular Member
Joined : Apr 2007
Posts : 34
Posted 6/7/2007 5:01 AM (GMT -7)
STUCK42LONG- You didn´tget it mixed up, I AM the one with a feedn tube.
I put MOM through the tue, and Dulcolax I have to take by mouth( which is very hard for me, but what choice do I have?). I need this tube because my stomach and intestines don´t show much motility at all, and if I eat or drink something orally, I feel extremely nauseous or have to vomit because it just rots in my stomach. This maks it all very complicated since it´s just not only the colon that´s bugging me...but nobody here seems to think that surgery is a solution to "constipation"( I would rather call it something else, it sounds so harmless!). Like I said before, I don´t even know if it´s right for me because I don´t know what my stomach and small intestine would do if there was no colon any longer. Maybe they´d start working better because there is no longer any blockage further down, but who knows? I did notice though that my stomach did feel much better everytime I was able to fore a BM and I didn´t feel as full and nauseous.
Right now I am trying to find a good doctor here who undrstand me, maybe he would be willing to work together with someone from the States...this would be great!

Take care.
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Irish_Mom
Regular Member
Joined : Apr 2007
Posts : 385
Posted 6/9/2007 1:57 AM (GMT -7)
Sorry if I have missed anybodys news. I've been kind of out of it since my reconstruction surgery, but I'm back to normal more or less. In fact, I'm going back to work on Monday.

Today I met with the surgeon that did my colon resection three years ago. We went over how things are going (or not going LOL) and he has come up with a plan. He's going to remove everything but six inches of colon which will give me somewhat normal stools. He said that he normally hooks things back up at the sigmoid colon, but I don't have that since it was removed during the first surgery so he'll use a different approach. He's also going to have a GU doc put stents into my ureters right before he starts the surgery to help ID them. I've had a lot of open abdominal surgeries due to ovarian remnant syndrome and have a lot of scar tissue and adhesions that makes things more difficult to dig out and ID. He said that he will try and do it laparoscopically but can't guarantee it. He's going to be on a couple of vacations with the last one being the middle of July. He doesn't want to do the surgery until he's available for a long period of time to be able to follow me. So we're shooting for the end of July.


Breast Cancer at 36. Diagnosed in 2000. Bilateral mastectomy with reconstruction.

Status post partial colectomy, but now heading towards a left hemicolectomy.

Son diagnosed with Crohn's at 17 (now 20). Taking Asacol and 6MP with Prednisone and Rowasa added during flareups.

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Stuck42Long
Regular Member
Joined : Sep 2006
Posts : 250
Posted 6/10/2007 3:28 PM (GMT -7)
sad  DANAALBERTINE - My heart goes out to you and I wish there were more we could do to help with your situation.  It is so sad that the doctors where you're at don't feel that "constipation" is a serious condition and that it's more than likely the root to your problems.  There is a name for this condition and it's Colonic Inertia.

I recently found out (yesterday) that I have a lazy small intestine and my transit time has decreased, so I will more than likely start using MiraLAX on a daily basis again (NOT at the extent and dosage I took it pre-op though).  Thankfully my stomach does NOT have any problems moving things along.

I do hope and pray that there is a doctor/surgeon who is willing to take on your case and team up with a surgeon experienced in this field here in the states.  Don't give in or give up. 

:-)  IRISH_MOM - So nice you're feeling "back to normal" - So nice to see you post and giving up an update on your situation!!!

Nice to hear that mid-July will be the beginning of a new life for you!!  I think it's wonderful that the surgeon wants to wait until he will be available to watch over your progress and healing process!!

***** I hope everyone else is doing good.  It's so nice to hear how others are doing ******


Robin

 

God is SO good - His blessings are endless! 

Trust in Him with all your heart!

Know He's in control over every situation you face!!

 

 

Post Edited (Stuck42Long) : 6/10/2007 4:31:56 PM (GMT-6)

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Nonna
Regular Member
Joined : Jan 2006
Posts : 23
Posted 6/10/2007 9:35 PM (GMT -7)
PHYLLIS:  I had my surgery on 31 Jan 06.  Things have been wonderful; however the last week or so, I have gone from having three BMs daily to only one and the stool is somewhat hard in the beginning.  Slight constipation (I HATE THAT WORD) and am leary about even using it.  I have noticed some bloating and I think that is because I am not going like after every meal?  Is is possible for the small intesting to become sluggish and do you know of anything I can take to resume the three times a day BMs?  I do not hurt or cramp - just a slight full feeling and it is a slight reminder of the way I was before and then I become concerned.  I am at 15 months out and just concerned about the sudden change.  I am also anemic and am taking B-12 shots.  (I refused to take iron for fear of constipation).  I seem to have some trouble with vegetables and have added more into my diet and am thinking maybe that is the problem.  I do best on chicken, potatoes, pasta, etc.  I have been eating hot peppers though and they don't seem to bother me.....  Hamburger or red meats don't settle well - they don't hurt, just feel full - however once in awhile, I will eat 1/2 cheeseburger.  I read in an earlier post that 100% pure grape juice was good if you felt constipated.  Do you ever just go only one a day? 
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Phyllis B
Regular Member
Joined : Feb 2006
Posts : 196
Posted 6/10/2007 10:14 PM (GMT -7)

Hi Nonna

I am  a few days shy of being a year out from surgery.  I go 8-12 times a day (and bless each time I go) so I am not the person to ask about the slowing to once a day.  From other posts I have read, people use stool softeners to help with the hardness.  Are you drinking enough water?  Also, has the doctor done any testing to find cause of the anemia?  This sounds crazy but Lays makes a potato chip that is made with Olean and that really softens things up plus I can say I am eating chips for medicinal reasons...  Even though I go often, I am so glad I had the surgery...

Hopefully others will post and give you other ideas..

Take care...Phyllis

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Stuck42Long
Regular Member
Joined : Sep 2006
Posts : 250
Posted 6/11/2007 10:54 AM (GMT -7)
:-)  NONNA - I can very much relate to your situation.  I was seven months post-op on June 9th and for about a little over a month I've also noticed that "old bloating - full feeling" you're speaking about, as well as, the decrease in daily bowel movements with added "hardness" of the stool.  I also HATE to use the word "constipation" so I called my surgeon and told him what was going on and my fears.  He ordered a CAT scan and a colonoscopy in order to rule anything out.

My CAT scan was last Wednesday and came back OK and my colonoscopy was this past Saturday and the results also OK.  I did have a few polyps that needed to be removed and was.  The purpose of the colonoscopy was to rule out any narrowing where they connected the small intestine to the rectum.  Other than the polyps he said eveything else looked good, that I more than likely have a "lazy" small intestine (not paralyzed as the colon was).  He told me that I could start taking MiraLAX again - it's an OTC medication now.  I took it once everyday until my appointment with the surgeon and it did help, but only if I was taking it consistantly everyday.  The best part of the MiraLAX is it has NO taste.

There are other things you could try that I find helpful if taken regularly too....Mott's 100% apple juice with no sugar added OR Welsch's grape juice.  Another thing that really moves things...sugar free chocolate (I'm sure any sugar free candy will do).  I do take stool softeners everyday and that will not hurt you to do so.  I also supplement my diet with magnesium capsules.

I hope this information is helpful to you.  I was just like you when things changed sort of all the sudden.  Of course the first thing we're going to do is worry because we don't want to live like we did pre-op. 

Also, I remember the surgeon telling me that over time, once the small intestine gets used to the roll of the colon - reduced bowel movements were a possibility. 

He did say that I have very little colon that could still be removed, however, that would be a last ditch decison and that trying all other options first is the way to go.  So, I'm going to start incorporating the MiraLAX everyday to see how that goes (plus all the other little tips that have been helpful so far).


Robin

 

God is SO good - His blessings are endless! 

Trust in Him with all your heart!

Know He's in control over every situation you face!!

 

 

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Irish_Mom
Regular Member
Joined : Apr 2007
Posts : 385
Posted 6/12/2007 7:31 AM (GMT -7)
Phyllis

I'm happy to hear that you're doing so well being one year out, and I must say, I would have never thought about those chips! That's a great idea. I'm going to stop at the store on the way home from work to pick some up.

Robin

I'm glad to hear that your colonoscopy came out okay. You're right about MiraLax not having any taste. It's great that you can put it in just about anything without worrying about it messing up the taste. I used to put it in my morning coffee. Unfortunately it didn't work for me. I'm going to try the Mott's that you mentioned.

Adviceseeker

The main risk for infection would be if you're not cleaned out before the surgery. My doctor is going to have me do a three-day prep just to be sure. Other than that, you can get an infection after any type of surgery. I had ACL reconstruction (knee) and ended up with osteomyelitis and was in the hospital for three months and was on home IV antibiotics through a PICC line for 16 weeks after that.


Breast Cancer at 36. Diagnosed in 2000. Bilateral mastectomy with reconstruction.

Status post partial colectomy, but now heading towards a left hemicolectomy.

Son diagnosed with Crohn's at 17 (now 20). Taking Asacol and 6MP with Prednisone and Rowasa added during flareups.

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shellypoo
Veteran Member
Joined : Dec 2005
Posts : 896
Posted 6/12/2007 6:41 PM (GMT -7)
Hi All,

It will be 6 weeks since my surgery this Friday.  I just got out of the hospital after being in there since Sunday.  The surgeon (that's who I called) admitted me for a partial bowel obstruction.  I had severe cramping pain in the center of my abd. around my belly button and no bm's. 

 

They did abd. xrays and labs 3 days in a row.  The radiologist read my first 2 as my left "large" intestine being dialated and distended!  The doc got a laugh about that but said my left side of my small intestine was severly dialated and distended and probably partially blocked.

 

I had iv fluids until today and then full liquids/soft stuff today.  She let me come home because I told her I would go back if things worstened. 

 

 I still have some pain in my intestines but at least I'm passing liquidy stools. She didn't know what caused it but said I could have had a stomach bug that shut my intestines down.  I'm dissapointed she didn't call my GI doc and at least send a stool culture off.  I hope I'll be well soon, this is rediculous.  I'm very weak and woozy.


Michelle ><>

Co-Moderator MS forum

 

Ever stop to think, and forget to start again???


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Nonna
Regular Member
Joined : Jan 2006
Posts : 23
Posted 6/12/2007 7:44 PM (GMT -7)
STUCK42LONG:  Thanks for all the information.  I was on MiraLAX for 10 years before my surgery.....Does the MiraLAX make your stomach swell now?  It did make mine swell before - but don't know if it was so much the MiraLAX or the paralized colon. 

My greatest fear is that my small intentine will become lazy and things go back to the way they were.  I had a really hard time during my surgery, I was in the hospital for 14 days, home a week and back for another four days.  I stayed the first 24 hours in ICU and was on a ventilator for a while (due to a major anxiety attack coming out of the anst), had an NG tube for six days and threw my insides up after it was removed several times; however, I would do it again tomorrow. 

I was under the impression that we would never have to have a colonoscopy again?  What was the prep for that, please don't tell me you had to drink the fleet phosa soda?  Where did they remove the polups from, your rectum?  Did you have your entire colon (except for your rectur) removed?  I am concerned about scar tissue and that has crossed my mind.  I do not cramp or hurt, I just have a little full/bloated feeling and that makes me really nervous, as up until about a month ago, there was a definite feeling when I needed to have a BM and now it is some what supressed.  I am obsessing.  LIFE was WONDERFUL and I am so blessed because like you, with each and every BM I thank  GOD for the miracle  - once a day is far better than before, but three times a day was perfect. 

Is it possible for the small intestine to become paralized like the colon?  Can part of the small intestine be removed?

prior to my surgery, I was having severe heartburn and that stopped afterwards also.  Then slowly about a month ago, that stated as well.  I went to see the Gastro doctor and had an endoscopy performed and he found a hernia and some irritation, he also said it did not have anything to do with my intestine/colon problems and was glad that I was enjoying life and feeling like living.

He mentioned that within the next five years they would scope my rectum for polups as I had some removed from my colon before I decided to have the Total Colectomy.  the prep work for that is only one fleet enema.

Due to the anemia - I am tired and I refused to take iron because you know that will cause constipation and so I am on B-12 shorts once a month because they think the anemia was due to a B-12 deficiency.  It is helping somewhat.  I have a very stressful job and I was thinking that maybe the stress is affecting my stomach.

I cannot imagine life like before - maybe I should call my surgeon and have them run some test as well. 

Thanks for all the information and please keep me posted....

GOD BLESS YOU

 

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Julia506
New Member
Joined : May 2007
Posts : 9
Posted 6/13/2007 5:52 AM (GMT -7)
I have read all the postings for colectomies. I have a few decisions to make. I have had Crohn's disease for 25+ years. I now have an obstruction in my left colon and not quite sure if there are more. This is where the disagreement comes in. I had two tests...a ct enterography and a gastrogaffin enema. The ct showed multiple obstructions all over my colon but the enema only showed one large one on the left. Surgery is scheduled for 7/25 but the surgeon is only going to remove the left colon. My GI told me a while ago that I should have a subtotal colectomy, not a partial one, for many reasons. I have a second opinion with a surgeon from Mt Sinai in a few weeks.

The surgeon wants to keep part of my colon for better quality of life but my GI feels that it is risky to leave some of it as it would be difficult to screen for cancer and she feels eventually the rest of it would have to be removed. So, she feels that although I would have better quaility of life in the immediate future, long term I would be a good candidate for developing colon cancer and it would be diffcult to monitor. My GI recommended me to both doctors.

Another thing, my present surgeon (who is a colo-rectal guy and experienced in lap surg) wants to do my surgery open while the surgeon in Mt Sinai would probably do it via a lap (although I don't know that for a fact yet).

My question....is there anyone out there that had partial colon resections and then had to have the rest of the colon removed? If so, would you have gone with the entire colon removal originally?

Thanks.
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Irish_Mom
Regular Member
Joined : Apr 2007
Posts : 385
Posted 6/13/2007 7:57 AM (GMT -7)
Hi Julia,

I don't have Crohn's (my 20-year-old son does though), but I did have a colon resection three years ago due to recurrent diverticulitis and fissures. My problems actually started after the resecton, i.e., severe constipation only relieved with heavy does of MOM or one of the preop cleansers. I've now been diagnosed with colonic inertia/dysmotility disorder. My GI doc said that a total colectomy would be best, but when I saw the surgeon he's recommending removing everything but about six to seven inches to prevent the frequent BM"s after a total or subtotal colectomy. I had the colon resection almost three years ago and I'll be having the other surgery at the beginning of September. It was going to be at the end of July, but I pushed it back a bit more because of things I need to take care of. I figured that a couple extra months of this isn't going to make much of a difference.


Breast Cancer at 36. Diagnosed in 2000. Bilateral mastectomy with reconstruction.

Status post partial colectomy, but now heading towards a left hemicolectomy.

Son diagnosed with Crohn's at 17 (now 20). Taking Asacol and 6MP with Prednisone and Rowasa added during flareups.

profile picture
Stuck42Long
Regular Member
Joined : Sep 2006
Posts : 250
Posted 6/13/2007 8:19 AM (GMT -7)
I'M GOING TO TRY AND ADDRESS AS MANY QUESTIONS AS I POSSIBLE CAN - I MAY OR MAY NOT KNOW ALL THE ANSWERES BUT WILL TRY MY BEST OK?

 

ADVISESEEKER - I was told that once the small intestine finally realizes its roll (it takes anywhere from a year to a year and a half for our bodies to heal and get used to it's new way of transit) the amount of bowel movements CAN decrease compared to right after surgery.  This may be a question to ask the surgeon for your own personal peace of mind. 

 

I think (as I'm sure others have too) that we get extremely paranoid over the smallest of things....we just don't want to go back to our old non-existent lifestyle. 

about the risk of infection...during any procedure there's a risk for ANYTHING.  From my own personal experience, antibiotics were given from the very beginning until I was released from the hospital (it's possible I was given some after I left the hospital but it been so long that I can't remember).

 

IRISH_MOM - The MiraLAX really didn't work for me pre-op either and I was taking it three times a day on top of the Zelnorm, Amitiza, and something else that I can't remember the name of.

 

I think you will find the Mott's apple juice a good choice.  Sugar free candy is another real boost!!

 

SHELLYPOO - Oh my goodness - my heart goes out to you.  If it makes you feel any better, I too caught a stomach bug in the early post-op stage and my entire abdomen region had a lot of cramping, pain, tenderness, and discomfort.  My stomach was also distended.  I did have bowel movements but very few at that time.  Once the "bug" was over I went back to my normal routine.  I think it was somewhere in the range of two or three weeks post-op, I was readmitted in the hospital for three days, had two CAT scans (which didn't show anything) and they took a look at where they connected the small intestine to the rectum for a possible blood supply problem - all came back OK.

 

It's hard to accept these setbacks, but they are possible, as we all can see.  I have no doubt that you will regain your strength and begin feeling better very soon.  I do wish you the best of luck - keep us posted OK and try not to get too discouraged (easier said than done I know). 

 

NONNA - You're more than welcome!!  The MiraLAX pre-op did cause my stomach to swell, however, I was taking the stuff three times a day then.  I have noticed that taking it once a day isn't too bad - I can't say I'm happy with the bloating but at least I can pass some gas now which helps a lot.

 

It sounds like you and I have a very similar situation and I also fear the small intestine being "lazy" as I was told Saturday - I too was readmitted after surgery for three days, had a host of tests ran, and was released with no definitive cause for my pain and discomfort and given stronger pain medications.  Thankfully my hospital stay wasn't anywhere close to your experience.

 

I was also under the impression that I'd never have to have another colonoscopy and the prep WASN'T the Fleet phosa soda thank God!!  It was that "gallon" of salty stuff that had to be chugged down by the glass full every ten minutes until gone (the surgeon thought it would only take half the bottle for me - but seeing I'm unusual - it took the whole darn thing).

I did have my entire colon removed and guess it was all except for the rectur.  I do not cramp, just a little full and bloated look/feeling which can cause me to hurt (tender) a little.  The very same goes for me, that up until about a month and a half ago there was a definite feeling when I needed to have a BM but now it is somewhat supressed.  I too began obsessing over it because things moved plenty and wonderfully.  Now I really feel blessed with each and every BM I thank GOD for each one!  Once or twice a day is far better than before, but three times a day was perfect.

I'm not sure if the small intestine can become paralyzed or even removed, but my surgeon did tell me that if my syptoms do not improve or they worsen, then and only then would he take out the remainder of the colon (he didn't mention anything about having to remove any part of the small intestine).

I've been on Protonx since before my surgery due to an ulcer, but now it's basically for preventitive measures. 

I know how easy it is for ALL of us to fret and worry over the smallest of things.  We're human and that's only normal.  Also, for those who've been thru so much - just the thought of something going wrong increases our anxiety.  I hope I was able to address your questions and the best piece of advise I can give you is to call and ask/express your fears with your surgeon.

 

JULIA506 - I'm happy to hear you're doing as much homework as possible.  I'm not real sure, and forgive me if I'm wrong, but I think there is a difference in the purpose/reasons for having a colectomy for Colonic Inertia (paralyzed colon) vs Crohn's Disease.

 

Maybe there is someone here who is more familiar with this and I wish you the best of luck in whatever decision is made in your best interest.

 

OK - forgive me if I've made any typo's - my hands have trouble typing for any extended period of time!!!!   

 

 


Robin

 

God is SO good - His blessings are endless! 

Trust in Him with all your heart!

Know He's in control over every situation you face!!

 

 

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danaalbertine
Regular Member
Joined : Apr 2007
Posts : 34
Posted 6/13/2007 11:13 AM (GMT -7)

NONNA- If you have read my earlier posts, you will have noticed that the small intestine can have dysmotility as well, as in my case. In fact, every part of your digestive system can be slow. I have general dysmotility in all of my gut. SHortening the small intestine is NOT the way to go though. It´s not done unless absolutely necessary, for example when you have a tumor. It´s very dangerous because you absolutely need every part of your small intestine because that´s where all the nutrients are absorbed. Most people who have had a partial resection of the small intestine develop short bowel syndrome and have to have intravenous nutrition and/or fluids for the rest of their life. I know we can get a bit "obsessed" about our intestines, BM, etc. but please remember that going once a day is okay! I wish I would be able to even go once a week...(I haven´t had surgery yet).

Stuck42long gave you some good advice on what foods to try.

Take care.

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Stuck42Long
Regular Member
Joined : Sep 2006
Posts : 250
Posted 6/13/2007 3:28 PM (GMT -7)
:-)  DANAALBERTINE - Thank you for the information regarding the small intestine!!!  If my small intestine is indeed "lazy" but working, I am blessed.  I really don't mind taking the MiraLAX daily.  At least with MiraLAX I can move at least once a day, maybe two if I'm lucky.  Before the TC I couldn't go for nearly three weeks (sometimes longer) and I was taking MiraLAX three times a day - Zelnorm - Amitiza - MOM - all at the same time with NO success. 

At least when I eat or drink certain things (prunes, apple and grape juice, sugar free candy) they do aid in the moving process. 

The most important thing that I have to keep reminding myself.....I'm blessed and thankful for the TC and would do it all over again!!!  I know that because I have an obsessive personality - I stress over the smallest of things, especially with the TC.  I think what I'm experiencing now is totally normal - that my small intestine is finally taking on its responsibility, doing what the colon used to do. 

Thanks again for the small intestine info!!!


Robin

 

God is SO good - His blessings are endless! 

Trust in Him with all your heart!

Know He's in control over every situation you face!!

 

 

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resa
Regular Member
Joined : Apr 2006
Posts : 141
Posted 6/13/2007 6:56 PM (GMT -7)
Hi Everyone,

I was watching a documentary type film about the different types of weight loss surgeries. In one the surgeon did reduce the size of the woman's small intestine so that she would not absorb all the calories/nutrients she ate in the day. This is way to drastic I think. But when I was getting my surgery I asked the doctor about that because I was curious and he said obsolutely not. You can live without a colon but you really need your small intestine.

Infection - some people I believe took oral antibiotics for a few days before surgery. My surgeon did not give oral to me. During surgery he gave me IV antibiotics and after surgery he gave me more IV antibiotics. I was fine with that.

Yesterday was my three months post-op and doing fine. Some days I go a lot and my anus hurts so much. It hurts to walk. My stools are still watery at times. But I love that I did this surgery. This year's birthday present to myself was this surgery.

When I was diagnosed with colonic inertia the sitzmarker test showed all rings throughout my bowel. Most of them accumulated in the descending colon. I asked the doctors if they could remove just the worst section and both surgeons I saw said no. They found that if they just removed a section of colon the patient would be back within the year to have the rest removed so they just do it the first time.

The only medication I am on at this time is my allergy pills and an occasional Ibuprofen for leg pain. After surgery my leg pain disappeared about 95 percent. But it does flare sometimes. Before surgery it was unbarable leg pain. My cholesterol even went down.

I had fluid leak from my belly button for about 2 weeks. By the time I went to the doctor it had stopped and the PA said nothing to worry about.

Take care everyone.
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Nonna
Regular Member
Joined : Jan 2006
Posts : 23
Posted 6/13/2007 7:34 PM (GMT -7)
Thank ya'll so much for the information. I know I have an obsessive personality and this is like MAJOR to me as I know you understand. It was the most incredible thing I have ever been through, even the bad parts of it and I would do it again as I have already stated. Going once a day is wonderful especially compared to before the surgery and I am so thankful and blessed. My surgeon told me that usually how you were doing at your six month would be the norm and I guess I just expected it to be three times a day and some days I do go two or three times, but like I said, just lately, it has changed to only once. I am so sensitive to every little pain or change.

Thank you for all the information - I did go to Walmart and get grape juice, apple juice, prunes, etc., today and will start adding those to my diet.

I too was on MuriLAX three - four times a day prior to surgery for 10 years. It got to where it would bloat me and make my intestines grumble. The night before my surgery, I discarded all the bottles of it as well as all the laxitives I had in my medicine cabinet.

I am so thanful for this site as you all understand perfectly - and when you try to explan this to some who has not had constipation or been through this surgery, they cannot even comprehend what you are saying.

Thanks guys and may God continue to bless each and every one of you.
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shellypoo
Veteran Member
Joined : Dec 2005
Posts : 896
Posted 6/18/2007 5:12 AM (GMT -7)
Hi all.

I am back in the hospital since Friday.  Same probelms only worst than ealier last week when I was hospitalized. Severe abdominal pain, nausea and dry heaves, and severe weakness.....I thought I would have to go by ambulance but my hubby got me there.  A security guard was nice enough to bring a wheelchair out and when she saw how ill I was she informed the admissions d  ept. that she would take me to my room and my hubby could register me.  The doc still sat partial obstruction and I have a PIC line and NG tube and no food since last Thurs.  I do have diarrea everytime I go to the bathroom.  Today I am supposed to have a ct w/gastrographen enema t see if the probelm is a stricture around the anastimosis sight.  If that is the case I will need surgery.  I am so scared!  Yest. my potassium levels were critical, I got extra potassium and feel less weak and weird.

 

I'll try to keep you all posted.  Anyone else had these problems?  The doc said if it is the anastimosis sight it usually happens about 5-6 weeks out.  I am 6 weeks out.


Michelle ><>

Co-Moderator MS forum

 

Ever stop to think, and forget to start again???


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