Poo question - sorry I don't have anyone else to ask

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So for the last 3 days when I have a bm it feels hard like it's going to be big and soild and I really have to push hard ( it hurts ) but as soon as I push it through it's straight D. Anyone else have a problem like this ? Also tonight I have a slight fever and am quite nauseous. Am I starting to flare ? Is it the beginning of an obstruction ? I feel pretty lousy but am in no more pain than than I'm normally in. Anyone have a clue what could be going on ? I don't know what to do ! Any advice would be greatly appreciated.
 
I've had that before. It could be a flare, especially with the diarrhea and nausea. I would try just eating clear liquids for a few days to see if it passes. Are you taking any medication? If your fever gets worse or you get worsening cramps, I'd give the doc a call.
 
I've had that before. It could be a flare, especially with the diarrhea and nausea. I would try just eating clear liquids for a few days to see if it passes. Are you taking any medication? If your fever gets worse or you get worsening cramps, I'd give the doc a call.

Thank you tzvia for replying. The only medications I'm on right now are aza 100mg daily and percocet as needed for pain. My fever got worse last night - sweating and freezing all night. I have no fever now today just a little back pain and some nausea.
 
It would be a good idea to talk to your doctor about this.
You may have some kind of blockage going on,and the sooner they know the better it is for you.
Hugs and best wishes
trysha
 
Yes, call your doc ASAP. You may need something temporary like prednisone to get the flare to calm down before things get worse.
 
Periodic constipation seems to be a problem that all of us have to deal with. I'm sorry it's bothering you at this time. Talk to you doctor - they may suggest a stool softener or some fibre supplements to soften your bowel movements. Prednisone may make you more constipated so you should definitely mention this to your doctor. Take care!
 
Thanks guys.I don't have a good GI doctor . He said go to the Er or call back on Monday if things get worse.
 
I hate to guess since I'm not a doctor, but if you start getting pain and a fever, go to the ER asap since an obstruction could be coming. You would know if it was an obstruction or partial obstruction, as you would be in the worst pain you have ever felt!

Hope you feel better soon and it passes.
 
I hate to guess since I'm not a doctor, but if you start getting pain and a fever, go to the ER asap since an obstruction could be coming. You would know if it was an obstruction or partial obstruction, as you would be in the worst pain you have ever felt!

Hope you feel better soon and it passes.

Thanks badbelly. I have had a few partial obstructions in the past thet are very painful ! At first I always went to the ER but the last one I had I passed it at home using percocet for pain and a clear liquid diet. Still very painful but I got through it.
 
Thanks guys.I don't have a good GI doctor . He said go to the Er or call back on Monday if things get worse.

I urge you to look into a different GI.You need a Dr. you feel confident with,someone who will work with you.Since you have a had a few partial obstructions already...perhaps you can find someone who will be proactive in your treatment and more competent.

My introduction to CD was by emergency surgery for blockage...I don't want that to happen to anyone.It can progress quickly,stay on top of it.

Sorry...trying not to preach...just concerned :smile:
 
I urge you to look into a different GI.You need a Dr. you feel confident with,someone who will work with you.Since you have a had a few partial obstructions already...perhaps you can find someone who will be proactive in your treatment and more competent.

My introduction to CD was by emergency surgery for blockage...I don't want that to happen to anyone.It can progress quickly,stay on top of it.

Sorry...trying not to preach...just concerned :smile:

Thanks Dave my primary care doc has tried to refer me to 3 different GI doctors but none of them will take me as a patient due to hospital affiliations and insurance issues. So I'm kinda just stuck with this guy for now. :angry-banghead:
 
Zep- lately this is an everyday occurrence with me.You're not alone! My issue is a very narrow stricture and increased inflammation- I told my GI it was like a cork: and after the cork, came the D or soft, loose stool. I'm so sorry you're stuck with a GI that's hard to get into to. I'd say no raw foods,and definitely low residue for a bit to see if it calms down "in there". Hope you feel better soon!
 
Zep- lately this is an everyday occurrence with me.You're not alone! My issue is a very narrow stricture and increased inflammation- I told my GI it was like a cork: and after the cork, came the D or soft, loose stool. I'm so sorry you're stuck with a GI that's hard to get into to. I'd say no raw foods,and definitely low residue for a bit to see if it calms down "in there". Hope you feel better soon!

Yes just like a cork ! That is good way to decribe it. Thank you . I hope you feel better also. :hug:
 
So I had to go to the ER today they said I'm definitely flaring . They gave me prednisone and percocet which is not helping with the pain at all. I am curled up in bed crying. I hate this disease ! I've been on aza for over 6 months now.I feel like I am never going to find a medication that is going to work for me. I am sick and sad don't want to worry my children and overwhelm my husband . I feel like my doctor doesn't care about me. All I can do is cry this stupid Crohn's has really got me down.
 
I think we can all relate to meds not working and feeling guilty with regard to our families. This disease can be so overwhelming and frustrating! I'm so sorry you ended up in the ER and without much relief. Have you discussed Biologics with your GI? I've had some relief with Cimzia and others are on Humira and Remicade. It may be time for one of those? Hang in there...and we are all here for you! This forum is such an important lifeline when we need to talk to someone who REALLY understands.:hug:
 
I think we can all relate to meds not working and feeling guilty with regard to our families. This disease can be so overwhelming and frustrating! I'm so sorry you ended up in the ER and without much relief. Have you discussed Biologics with your GI? I've had some relief with Cimzia and others are on Humira and Remicade. It may be time for one of those? Hang in there...and we are all here for you! This forum is such an important lifeline when we need to talk to someone who REALLY understands.:hug:

Hi 4peace, before the aza I was on pentasa first for about a year- it did nothing for me so then I was but on Remicade for about a year and a half- but felt terrible on it. So now I'm on aza for the last 6 months and have had 2 or 3 partial obstructions and a couple really bad flares. How long should I give the aza? I think all I have left I can try is Humira. If that doesn't work I don't know what I'm going to do ! :cry:
 
Predinose works well and works fast. You should be feeling better very soon on it. Next step is to talk with your doc about stronger medications than what you have been taking. Also, be very cautious about what you eat--only eating very digestable smooth food like smoothies, soup, yogurt, avocado, very cooked veggies if you can. And excersize and help too. I hope you feel better!
 
I agree with tzvia: Pred usually helps fast but it isn't a permanent solution. My Gi told me Aza usually takes 6-8 week to start working, so 6 months seems like a long time to be on it without any relief. I'd ask about Cimzia or Humira (I'm on Cimzia and just started Aza 4 weeks ago for combo therapy). You could also read up on Low Dose Naltraxone (sp?). I know there's a sub forum about LDN and some people have had relief with it, but from what I understand it may be most beneficial to mild/moderate patients not necessarily moderate/severe.
Keep your chin up, or at least put it up after giving yourself permission to have a little pity party (I know I do sometimes!):lol:
Hope you have a better week!
 
Predinose works well and works fast. You should be feeling better very soon on it. Next step is to talk with your doc about stronger medications than what you have been taking. Also, be very cautious about what you eat--only eating very digestable smooth food like smoothies, soup, yogurt, avocado, very cooked veggies if you can. And excersize and help too. I hope you feel better!

Thanks tzvia, Your right the predinose is already starting to work a little. The pain is not as bad today as it was yesterday. My cheeks are really flushed though and I went from constipation to D. I am being careful with what I eat - Thanks again.
 
I agree with tzvia: Pred usually helps fast but it isn't a permanent solution. My Gi told me Aza usually takes 6-8 week to start working, so 6 months seems like a long time to be on it without any relief. I'd ask about Cimzia or Humira (I'm on Cimzia and just started Aza 4 weeks ago for combo therapy). You could also read up on Low Dose Naltraxone (sp?). I know there's a sub forum about LDN and some people have had relief with it, but from what I understand it may be most beneficial to mild/moderate patients not necessarily moderate/severe.
Keep your chin up, or at least put it up after giving yourself permission to have a little pity party (I know I do sometimes!):lol:
Hope you have a better week!

Hi 4peace. I will ask my GI about adding Humira he already said no to LDN. This prednisone is making me really sensitive - I feel like a crybaby. I will try and keep my chin up though ( or chins up as I will soon be getting the lovely moon face :tongue: ) Thanks You !
 
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