Constipation after laproscopic surgery

Red_34

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Posted 9/16/2007 6:33 AM (GMT -7)

My last bm was Wednesday and I had my lap surgery on Thursday. I haven't had a bm since then and I am getting very uncomfortable! How concerned should I be with having constipation after a lap procedure? I have tried fiber supplements, lots of water, drinking coffee, stool softener and nothing seems to be working. I'm getting nauseas and I have a burning pain on my left side. Any suggestions? Why can't I ever just have a happy medium??? Why one extreme or the other??

^{@--->--SHERRY--<---@}

^{Left sided Uc -'92 - Colazal, Canasa, 6mp, Prilosec, Biotin, Forvia}

^{Secondary Reynauds Syndrome - '04 - Norvasc}

^{Fibromyalgia - '06}

^{PLEASE HELP HEALINGWELL CONTINUE TO HELP OTHERS BY CLICKING HERE: DONATE}

^{@--->--Moderator for Allergies/Asthma and Co-moderator for UC--<---@}

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ks1905

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Joined : Sep 2005

Posts : 5248

Posted 9/16/2007 7:41 AM (GMT -7)

I would suggest calling your GI, he or she probably has an after hours phone number for medical issues/emergencies and someone will call you back.

Sometimes enemas make me go; if you have an extra one around you might want to try that.

I hope that you feel better soon.

--Keith

DX'd with Pan-Colitis June 2005

Current Status: Flaring since May

Current Meds: 6-mp & Colocort

Supplements: None

Another UC wife

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Joined : Jun 2007

Posts : 2111

Posted 9/16/2007 10:06 AM (GMT -7)

Oh Sherry - I was hoping things were improving...it must be kind of all packed in there now...maybe a gentle enema to help dislodge things??? It might just need that little penetration and liquid from the other end. Maybe everything will meet up and finally let loose.....

60 yr old male~Colitis 1st diagnosed Jan '05-cleared up within a few wks. Flared again in May '06 ... left sided UC now, fully involved and trying to get in remission. Acute inflammation-pancolitis-tenesmus rectal pain-granulation is showing some healing started. Osteopena of spine from prednisone DX 8/07 July 07 good days & bad days 75mg Imuran 40 mg prednisone (tapering 8/07) 12 Asacol, Lidocaine Hydrochloride Jelly 2%,multi vitamin, iron 3X day, DanActive, chewable calcium, Prilosec 20mg, enalapril 10mg, glipizide 5 mg, zocor 20 mg, baby aspirin, (Fentanyl pain patch 50mg 72 hrs Morphine Sulf 15 mg twice daily)Colocourt enemas at night. Fosamax and mthly B12 shots folic acid 1mg

Red_34

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Joined : Apr 2004

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Posted 9/16/2007 10:26 AM (GMT -7)

Thanks for the replies. I have a call into the on call GI and I'm just waiting for him to call me back. So we will see what he has to say. When I go to the bathroom (or try to), I feel no need to expel and when I strain, I see small bits of blood and mucous when I wipe. The only enemas I have here are the Colocort and I've been using my Canasa every night. On a brigther note, at least I'm feeling better now from the procedures I had! :) lol Now! If only my colon would behave itself!

^{@--->--SHERRY--<---@}

^{Left sided Uc -'92 - Colazal, Canasa, 6mp, Prilosec, Biotin, Forvia}

^{Secondary Reynauds Syndrome - '04 - Norvasc}

^{Fibromyalgia - '06}

^{PLEASE HELP HEALINGWELL CONTINUE TO HELP OTHERS BY CLICKING HERE: DONATE}

^{@--->--Moderator for Allergies/Asthma and Co-moderator for UC--<---@}

http://www.myspace.com/82595818

pb4

Elite Member

Joined : Feb 2004

Posts : 20577

Posted 9/16/2007 12:08 PM (GMT -7)

If you were under anestetics that slows things down.

:)

My bum is broken....there's a big crack down the middle of it! LOL :)

Red_34

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Joined : Apr 2004

Posts : 23569

Posted 9/16/2007 1:14 PM (GMT -7)

Oh yeah, I would say I'm slowed down! lol The doc called me back and told me to take Miralax and to call my regular doc tomorrow morning. So far all I'm getting is intense abdominal cramping but no results yet *sigh* I don't know whats worse, D or C!

^{@--->--SHERRY--<---@}

^{Left sided Uc -'92 - Colazal, Canasa, 6mp, Prilosec, Biotin, Forvia}

^{Secondary Reynauds Syndrome - '04 - Norvasc}

^{Fibromyalgia - '06}

^{PLEASE HELP HEALINGWELL CONTINUE TO HELP OTHERS BY CLICKING HERE: DONATE}

^{@--->--Moderator for Allergies/Asthma and Co-moderator for UC--<---@}

http://www.myspace.com/82595818

marty1976

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Joined : Nov 2005

Posts : 2045

Posted 9/16/2007 1:15 PM (GMT -7)

Sherry how aree you now. I missed out on a lot of post due to Beth being ill.

keep the faith

Pred40mgs/asacol/proctifoam/omoparazole 40mgs/Domperidone10mgs x 3 daily

http://www.myspace.com/martybuzz1<FONT]

Seahorselover

Regular Member

Joined : Sep 2007

Posts : 30

Posted 9/16/2007 1:58 PM (GMT -7)

When I had my colonoscopy this past thursday, I did'nt have a bowle movement until Saturday morning, I did have anethisia and friday night I took one dolcolax... maybe you should take a dolcolax.

Seahorse Lover

Old Hat

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Joined : Feb 2007

Posts : 5195

Posted 9/16/2007 3:47 PM (GMT -7)

What have you been able to eat post-procedure? Did you try any steamed veggies? I have found steamed yams very helpful in "restarting" a sluggish colon-- leave it in the steamer extra long so that you can mash it easily w/o adding anything to it. Best wishes for you to get back on track ASAP & w/o additional meds. / Old Hat (P.S. Did your doctor ever mention possible effect of caffeine consumption on development of gyno cysts? The reason I ask is that Dr. Susan Love [breast surgeon] mentions the connection btw caffeine & breast cysts in her books. My internist thinks it is a valid cause for caution re coffee-drinking.)

Red_34

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Joined : Apr 2004

Posts : 23569

Posted 9/16/2007 5:15 PM (GMT -7)

Old Hat, no my doc never said if there were any correlation to my ovarian cysts and caffeine. She did however mention it when I had a large cyst drained out of my breast and I have cut down on my caffeine consumption alot. Thanks for the tip on the steamed yams. I may have to try that next time.

The Miralax worked but man did it hurt! I felt like I was giving birth! And, not to sound gross, but when you spend that much time working on a bm you expect it to be the size of a football not a pencil! Ah well, I knew I had inflammation in there because of the pain but now I know for sure. I'm gonna give my Canasa a few days to do it's magic and if it doesn't work then I will call my GI.

Thank you everyone for the suggestions....I'll file it away for future reference.

^{@--->--SHERRY--<---@}

^{Left sided Uc -'92 - Colazal, Canasa, 6mp, Prilosec, Biotin, Forvia}

^{Secondary Reynauds Syndrome - '04 - Norvasc}

^{Fibromyalgia - '06}

^{PLEASE HELP HEALINGWELL CONTINUE TO HELP OTHERS BY CLICKING HERE: DONATE}

^{@--->--Moderator for Allergies/Asthma and Co-moderator for UC--<---@}

http://www.myspace.com/82595818

ks1905

Veteran Member

Joined : Sep 2005

Posts : 5248

Posted 9/16/2007 5:23 PM (GMT -7)

Sherry,

Have the cysts gotten more frequent and worse since you started taking 6-mp?

--Keith

DX'd with Pan-Colitis June 2005

Current Status: Flaring since May

Current Meds: 6-mp & Colocort

Supplements: None

Red_34

Forum Moderator

Joined : Apr 2004

Posts : 23569

Posted 9/16/2007 7:01 PM (GMT -7)

10xs worse! Neither my GI nor my primary can see any correlation to my increase of cysts and 6mp. It may be just an odd coincidence. Every year something new crops up and this time around it was cysts. They have slowed down considerably though. It has been proven that women with Uc have a higher incidence of ovarian cysts then the normal population but I don't know why.

^{@--->--SHERRY--<---@}

^{Left sided Uc -'92 - Colazal, Canasa, 6mp, Prilosec, Biotin, Forvia}

^{Secondary Reynauds Syndrome - '04 - Norvasc}

^{Fibromyalgia - '06}

^{PLEASE HELP HEALINGWELL CONTINUE TO HELP OTHERS BY CLICKING HERE: DONATE}

^{@--->--Moderator for Allergies/Asthma and Co-moderator for UC--<---@}

http://www.myspace.com/82595818

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