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  This may be a long story and im sorry but i have been threw hell and back ever since Dec 2019, when my j pouch was created, after 2 weeks i started having severe extreme painful painful pain in my stoma site, for 6 months i had this problem i had a partial blockage due to the looped stoma sorry if im not using tech health words, instead of my bag filling up within 20 mins it took all day to get output and air out of my system i was on my knees crying so bad and so hard, i warned my surgeon and she did nothing to fix this was during the first covid lock down and no surgeries were being accepted, my sugeon kept giving me tips of what to eat that was not the problem..

   Anyways 6 months later, i had my take down surgery and within 3 weeks had a full blown blockage and it almost killed, i had a drainage site with tube sticking out near my old stoma site to release fluid in my stomach, i ended on a TPN fluid only threw a pick line for 6 weeks no eating or drinking i was really pissed off about not being able to eat, anyways about 5 weeks in i had a CT scan and everything appeared to heal, so they told me i could start eating, my surgeon offered no pain control whatsoever and it was the worst pain ever im sure it was worse then cancer im not kidding they knew i was suffering at home, my parents and family called them several times about the issues, i couldn't go any where's i couldn't take care of my son.

  Maybe 2 weeks later i again suffered yet another blockage this blockage first and second was at the stoma site. however after a few days it went away by itself, im so sorry this is a long story but im still suffering from day one of my j pouch date.

  so im now 6 months passed my blockage and i ended with a completely narrow retum and caused my j pouch to fill up completely and i was back in the ER, i had severe painful contractions from gas moving around in the pouch it felt like a bowling ball moving around inside. they had to dilate me 4 times now they told they are going to have to remove scar tissue on April 1st 2021, ive had 10 operations since my j pouch ive been in the ER sooo many times im still heavily suffering because i have painful FIRE LIKE BURING not on the outside of my rectum but the piece that connects the pouch and retum is where i think its burning, on top of the im still having the contractions but i dont think its from my pouch filling up, i think it bursing inside the pouch and whenever gas enters the pouch it painful really painful and the contraction forces stool out from the pressure and movement of the pouch from the contraction.

  Ive seen others here say red meat is ok to eat, however i had a good 1 1/2 weeks of zero problems i went out to a steak house and had prime rib a salad and those breaded onion cuts, 15 hours later here comes the extremely fire feeling output and soon after the contractions, what really pisses me off about the NP at my surgeon center doesnt give a crap about me doesn't even read my messages i send, now my surgeon just now started to provide me with pain meds which does help its not that i want them its that my body needs them, i hate pain meds as much as they hate prescribing them but i feel its the only way during the times im not in remission.

Please help me, this has destroyed my life ive demanded several times for them to  remove the pouch i hate it because 3 weeks out of a month im in so much pain and i hate shitting myself when i have those contractions.

  I have thought several times about killing myself i want to do it because my surgeon refuses to remove the pouch, i do love my surgeon shes really good to me, shes always defended me in the hospital when they treated me like some prisoner, at strong hospital in Rochester NY these people in that hospital are tyrants i dont like a medical device in my nose scrapping my brain the PCR test are BS, 97% false positive's however the hospital will refuse to treat me for refusing the test, i dont trust the hospital  staff there i hate having  surgery there because im scared they will force that convid vax on me during surgery i know you'll say they cant do that, but if you went to this place you would question them as well some of them should NOT be working there. Just my opinion....

   Why am i having these contractions and why the fire burning inside my rectum, its so painful and like i said im over 1 year in and had maybe 7 weeks of good time that's it, i dont understand why they cant figure these issues out i feel its just a money maker in the long run, if they made it even near perfect i guess no money would be made and that's sad.. ive suffered way to long my death with be sitting in a car in a garage if things dont stop because i have trama and fear of pain i sometimes take a knife to my wrist i want to do it SOOO BAD like so bad soo freaking bad do i want to die



  Thank you much if you got this far im so sorry for the long message im just in darer need of direction

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I will not go into detail on my pouch experience.

It's in here on this site. Already

I was at the same place you are. Difference is it was going to kill me and I didn't care.

But I had it removed after two years of pure hell and from that day of removal everything turned around.

Now an end ileo is not for everyone. But it was for me.

It took all that pain  and suffering away. Period.

Long story short. I've had it a little ove five years now and had absolutely no regrets.

I hope you get help. Get help.  I know where you are at.  And there is a fix!

It  takes a huge toll on you body and mental state.  You cannot keep going through it.

Blockages are pure hell.

Richard.

Mysticobra
Last edited by Mysticobra

Hi

I understand you hating pain.  I have been dealing with my pouch for 35 years and I know the pain that we can go through but yours is horrific. Please check my message below and tell me if this helps.



I will try to make a suggestion, stay away from meat.  Try bone broth for a little while.  if your pain settles down then you know it's a matter of what you are eating.

Good luck Steven!!

M

When it comes to trying different things to eat and such I reached a point if I didn't do the removal I'd have passed from it.

I tried alot of different things in a two year period that didn't work. I just kept going downhill.

I was also working full time during this.

I was down to 128 pounds and a walking skeleton.

My mind was mush. We (I) fight the obvious until you can't. The bag is the "obvious".  I didn't want it even being rolled in for removal surgery.

But it was the smartest and best thing I could have done. No one wants it.  But I will say that in my experience it works perfectly.  And I should have done it sooner.

Time is limited. As for trying this or that diet. Because if it doesn't work your just further down the road of no return.

I didn't have the luxery of time anymore.  I wouldn't be here had I not had my removal. It was that serious.

It sucks going through it. But it can be fixed.  You may not like my answer but an end ileo is a fix.

Richard.

Mysticobra

I've heard of these contractions and people went in anti anxiety pills that cured them.look up Emily Parris on youtube a one year post takedown and she talks of them and being put on anti anxiety pills fixed it.go to the six minute mark on her one year jpouch video she talks of the same as you.goodluck.

FM
Last edited by Former Member
@Former Member posted:

I've heard of these contractions and people went in anti anxiety pills that cured them.look up Emily Parris on youtube a one year post takedown and she talks of them and being put on anti anxiety pills fixed it.go to the six minute mark on her one year jpouch video she talks of the same as you.goodluck.

So true! I have told other people about that as well! Soo cool that you posted that here

FM

As far as the depression, which is 100% understandable, I would seek help from a psychiatrist.  I did, and I went on Paxil, an antidepressant, and it helped my mental state immensely.  I became more hopeful.  I was still very physically sick when I started the Paxil, but my mental outlook just got better.  It was really remarkable.  See if your primary care doctor can recommend at psychiatrist.  I am obviously no doctor, but see if your primary care doctor thinks it makes sense.  What you are going through is absolute hell, and anyone would feel hopeless, but help is around the corner, and a few months from now you could feel great!  Let us know how things go.

DK

thank you everyone for your kind words and support i don't even know what to say, im so tried right now haven't had any real sleep this past week , ive had a lot of sleepiness nights i feel my body has had enough, my surgeon does not want to do a take down of the j pouch, because before when i had an ilo i had so much depression, i feel stuck in a corner because either a ilo or a j pouch hasn't worked out for me,

i knew the j pouch wasn't going to be  perfect but i had no idea it was this extreme I wish the Lord would have mercy on me for I am sinner i used to have a drug problem im now 2 years clean and for that i am very proud of my last relapsed was when  my wife passed away in 2018 she was there for me with everything, if she was here she would takeb care of me ive been locked up in my room for over 2 years i cant even leave my room  because of the pain, my poor son James has lost years of time with his father, he is always worried for me, he has seen me being taken off to the hospital so many times, i know life isn't fair i get it and I understand but these problems are getting old, if its not fire in my rectum it is painful contractions i fee like the burning pain is fighting over the pain from contractions as if its a sport , who is going win causing the most pain.  and a lot of times ill have both at the same time that when i really start thinking ive got to stop this pain ive got to do something, the feeling of emergency to get back on the toilet is horrible ive been on the toilet about 20 times within 8 hours. i wouldn't wish this on my worst enemy. I just don't know  anymore my hopium has run dry

Thanks again everyone for the support it is a relief knowing there are voices who want to help and may god bless your hearts and souls.

S
Last edited by StevenChar78

i had a psychiatrist before and it did not help put me on a bunch of meds that just made me sleepy and unstable, thankful today i woke up and i havent had one contraction I feel really good today, i did watch the Emily Parris video and what it sounds like is exactly my problem so I took down the medication she took to cure the issue I see my surgeon tomorrow, these contractions come and go, when they did a scope they found no problems with my pouch, these contraction started after my j pouch filled up and i couldn't empty i had to go to the ER and they dilated me and emptied my pouch ever since then I've got these contractions every 2 or 3 times a month and last over a week its so weird because i didn't have contraction in the beginning just the blockages at my stoma site

  When I have no problems my pouch works good and i feel no pain when i use the bathroom I can stop and go, i normally spend 10/15 mins on the toilet.



Thanks again for all your help so far so god today this is such a loving community and i am so thankful and feel blessed.

 

S

Promise that you will NOT kill yourself - that is a permanent solution to a temporary problem. A lot of us have been where you are (maybe not in every exact way), but a lot of us have been through hell and back (or stayed in hell for a while) with this disease and subsequent surgery, so as much as you want to, you can't give up. Is there another surgeon you could go to? Yours sounds awful. If there isn't one in your network, could you afford at least one visit, out-of-pocket, to one of the well-known colorectal surgeons? It seems that you may need a permanent ileostomy, but there might be other options if you're able to hook up with a good med GI, as well as surgeon. Another suggestion is (again, if you have the funds, or your family can help you out,) to travel to the Mayo Clinic in Rochester, MN. They're known for they're excellent diagnosticians - they almost always get to the bottom of something, esp if you haven't had luck with other doctors or medical centers.

Hang in there and good luck!!

Katt

yeah I kind of spoke to soon today, a few hours after I wrote my reply, the burning discharge came back on top of the evil mean contractions so instead of just the one problem I ended up with both of them, i see my surgeon tomorrow, and my Surgeon is awesome i love her so much, its the NP who let me suffer for almost a year, while i was in phoenix(i live in NY now) every ER visit due to UC they provided me something for pain at least 2 weeks and im telling ya, that pain was nothing compared to this pain but every pain is different, i have message after message explaining to the NP that I am SUFERING and have severe TRAMA from being in so much pain all she did was say keep me updated or played message tag, the NP  works for my surgeon so when I called I asked them to have my surgeon call me NOT the NP, I explained what's going and she right away sent over a pain med script and as much as I HATE taking them, right now for me its the only way to get passed just one more day, I really think Doctors and Nurse under-rate the pain we feel its so bad it is torture, I've seen people with way less pain they have no issues getting help, I really hope the medication from Emily Parris works because to be honest i just don't wanna be on any pills at all

As for killing myself the only time i wanna kill myself is when i feel backed in to a corner and the pain feels like its killing anyways, before I got the J pouch i did watch Emily Parris channel and a few others i was aware of the challenge's but not on this level im dealing with now, i enjoy feeling normal when my pouch isnt acting up but when it is i want it out as I said I get 1 week per month and the remaining 3 weeks of hell, and also to answer your question about finding a new surgeon it wont happen because im so far in to this with my surgeon no one would want to take me, my surgeon made the j pouch she knows how it was installed, i do trust her, these problems do happen she is just the sweetest lady i gave her a hug my last operation and i can just feel how much she cares about me. shes just as disappointed as I am she wants to see the pouch work once and for all.

Anyways thank you Kath for your enlightening words makes me feel better that I'm not in this fight alone. I just ask the question all the time who came up with the j pouch and why have it if there is so many problems with it

S

This can be a very difficult journey, for sure.  You have definitely been through a lot and I hope things begin to improve for you soon.  I can relate to being on TPN.  I was on it for a little over 2 1/2 months, most of it during the summer.  I had my infusions at night eventually so that I didn’t have to carry the bag around in a suitcase when we spent a week at a cottage.  I just had a sleeve to cover the tubes hanging out of my arm, but on a hot day that can be annoying.  It’s good that you have a surgeon that you are happy with.  If things don’t get better, you can choose what is best for you.  Good luck!

C

So here's the good news.. my Surgeon prescribed a month worth of nortripyline within 20 mins the contractions started fading away thank you guys so much,  all the pressure is gone, i don't feel like i have to go to the bathroom all the time, no more accidents , its been 8 hours and no contractions no bowling ball feeling, it worked quickly. I was able to lay down and sleep without discomfort, thank you for all the support with you guys id still be in pain, my surgeon didnt think it was going to work she believes my pouch is just filled up but I told her i can empty my pouch just fine.

   I'm going to wait a few days to let my surgeon know just in case,  but I know its working. I'm so much better. Now I can spend time with my son!!

  Thanks again!

   

S

So here's the good news.. my Surgeon prescribed a month worth of nortripyline within 20 mins the contractions started fading away thank you guys so much,  all the pressure is gone, i don't feel like i have to go to the bathroom all the time, no more accidents , its been 8 hours and no contractions no bowling ball feeling, it worked quickly. I was able to lay down and sleep without discomfort, thank you for all the support with you guys id still be in pain, my surgeon didnt think it was going to work she believes my pouch is just filled up but I told her i can empty my pouch just fine.

   I'm going to wait a few days to let my surgeon know just in case,  but I know its working. I'm so much better. Now I can spend time with my son!!

  Thanks again!

   

Your welcome, keep us updated

FM
@Anais posted:

My son started Cymbalta but it did not help with the painful contractions.  He is been suffering for almost a year, right after connection surgery. Contractions are constant.  Do you think the other one you are taking might be better.  Please let us know.

Thanks!

I am sorry that did not work honey, I would reach out to the gastro/surgeon at this point.

FM

sorry Anais to hear that, my contractions started a year after the first j pouch surgery the nortriptyline does work but I found out after over taking it it will completely stop working,  my contractions started back up on Saturday and have been suffering since i stopped taking the  nortriptyline  for about 30 hours and i started taking it again and my contractions are gone i would try this medication it helped me a lot just make sure he takes as directed, because i had a small contraction i freaked out and i took another one on top of the already 2 doses and it just completely stopped working.

S

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