Ever thought it was your UC but was internal hemroid?

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TheLori
Regular Member


Date Joined Aug 2007
Total Posts : 277
   Posted 1/9/2008 1:09 PM (GMT -7)   
Have you ever thought you were flaring (because of blood) and found out it was an internal hemroid?  I go at 4:00 for a scope, been bleeding for 7 weeks but no other symptoms, just wondering if it may not be my UC.  We shall see!
Lori
38/F
UC diagnosed 1991
Asacal, zoloft, levoxyl, colocort enemas, prednisone 40m


blessteve
Regular Member


Date Joined Jan 2008
Total Posts : 121
   Posted 1/9/2008 1:17 PM (GMT -7)   
Blood in stool UC. Blood on TP hemroid.
That is my general rule.
Diagnosed Colitis 1990.
Current Meds Asacol x4
twice a day.
Pred for flares.
I still have my colon THANK YOU GOD!!!
Started 1/08
raw milk-kefir made with raw milk
natto
caprylic acid-oregano oil
probiotic
 


Beth75
Veteran Member


Date Joined Jul 2007
Total Posts : 2148
   Posted 1/9/2008 1:20 PM (GMT -7)   
Steve I think you are right!!

My hemi blood was more watery and on the tp mostly. I had one a few weeks ago, it was horribly painful and it is pretty much gone now. Mine was right near the end so I could get at it.......can they be farther up?

Lori - good luck w/your scope, keep us posted!
Beth, 32
Major Flare Sept/Oct 07 ~ working on remission almost there
UC Diagnosed March 2000 (30 cenitmeters)
Azathioprine 200mg 1xday nightly; Calcium and Vit D 500mg 3xday, Multi Vit, Folic Acid 400mg 2xday, Probiotics.
Minimal Change Disease (Kidney Disorder) Diagnosed Sept 2007
Prednisone 60/40mg alt days 1xday, Simvastatin 20mg 1xday, Diovan 160mg 2xday. Potassium 600mg 2xday, Fosomax 70mg 1xweek. MCD may be from hypersensitivty to 5ASA drugs.


Lou95
Regular Member


Date Joined Dec 2007
Total Posts : 47
   Posted 1/9/2008 1:33 PM (GMT -7)   
Well, my internal hemis give me more pain and blood than my UC ever has.  I haven't been in a flare in well over a year, but for the past few months I have tried everything I know of to help my hemis.  I don't have anything visable to the eye- just internal.  They have left blood in the stool as well as the paper.  My colonoscopy in December confirmed this wasn't my UC, just internal hemis, so I guess it is different for everyone.  But, hemis usually make me feel extreme pressure and a burning pain.

Age/Sex:  50 & female
Diagnosed:  2005 pancolitis
Medications:  800 mg. Asacol twice a day - in remission; 1200 mg. fish oil supplement nightly,
1 Dulcolax stool softener nightly, Effexor-XR 75 mg. daily
 


blessteve
Regular Member


Date Joined Jan 2008
Total Posts : 121
   Posted 1/10/2008 6:06 PM (GMT -7)   
Internal hemeriods just great. Did not know there was such a thing but
I probably will get if I do not have already. I hate my @ss sometimes.
Pun intended.
Diagnosed panColitis 1990.
Current Meds Asacol x4 twice a day.
Pred for flares. I still have my colon THANK YOU GOD!!!
veggie juice-wheat grass juice--fish oil
Started 1/01/08
raw milk-kefir made with raw milk--natto--caprylic acid-oregano oil
probiotic
1/10/08 Started healthy diet again.
 


TheLori
Regular Member


Date Joined Aug 2007
Total Posts : 277
   Posted 1/10/2008 6:27 PM (GMT -7)   
HAHAHAHAHA Blessteve That was FUNNY! Turns out mine is my UC acting up not a hemi.
Lori
38/F
UC diagnosed 1991
Asacal, zoloft, levoxyl, prednisone 40m, Azathioprine (started 1/9/08)

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