constipation

Hysterectomy, Ovary Removal, SIJD, Piriformis Syndrome etc
pn_person
Posts: 94
Joined: Fri May 13, 2011 10:11 pm

constipation

Post by pn_person »

No doubt the most significant quality of life issue from the PN damage for me has been constipation.
Never even thought about going to the bathroom prior to the PN issues, everything, in that regard, 100% normal.

I know from previous posts that others are dealing with this same issue.

My doctors insist that the only safe laxative for long term use is Miralax (adding water to the stool).

For me, the Miralax is somewhat helpful in that when I do finally go, I will typically do not get a fissure from a hard stool (had that several times now), but going is still a BIG problem.

The believe that the nerves responsible for push things through are just not working properly, and the spasms at the opening, are not helping. Of course, any straining causes the PN to stretch and thus get worse, so getting the constipation issue resolved would be a huge help for me.

I recently tried ex-lax (stimulant laxative) which the doctors are all very against as they cause things just to get worse long term (paralyzing the nerves even more), but I find it is incredibly helpful.

So my question is, is there any natural food, drink, etc, that would have a stimulant effect analogous to ex-lax, but that would not be harmful long term. Caffeine is a little helpful, but not great, for me at least. I am drinking several cups of coffee a day, which I think might help a little, if any.

Thanks all...have not posted for a bit..hope all is well with everyone.

Rob
Lernica
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Joined: Fri Jan 14, 2011 10:31 pm

Re: constipation

Post by Lernica »

I completely agree with you. Constipation sucks. I spend WAY more time than I want to on the toilet. And a distended tummy puts pressure on my pelvis and adds to my pain levels. I have to completely stay away from opiates because of it. (I will take one if I'm desperate, or travelling. But then I pay for it for days.)

Unfortunately I don't think you'll find any "natural" product that has the same effects as a laxative. Try doubling up the Miralax that you're taking. I think that at one point Calluna was taking up to six sachets a day! I sometimes have to take two to get things moving. I also take 1 - 3 docusate sodium tablets at night. They are also safe for long term use, I think.

Enemas are also helpful to get things moving. And the odd time I have taken a tablespoon of mineral oil at night. I have never taken ex-lax.

Try searching "constipation" on the right hand corner above to get more ideas.

PN Person, have you ever had a painful colonoscopy? I am trying to figure out if some of my symptoms are diagnostic of another condition, e.g. hernia.

Good luck with your toilet troubles. ;)
Athlete until pain started in 2001. Diagnosed with PN in Nov. 2010. Probable cause: 3 difficult labors, 5 pelvic surgeries for endometriosis, and undiagnosed hip injuries. 60% better after 3 rounds of shockwave therapy in Cornwall, Ontario (Dec - Feb/12). 99% better after bilateral hip scopes for FAI and labral tears (April and July/12). Pelvic pain life coach Lorraine Faendrich helped me overcome the mind/body connection to chronic pain: http://www.radiantlifedesign.com
calluna
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Re: constipation

Post by calluna »

I was indeed taking a lot of Movicol/Miralax before I had the mesh surgery to repair prolapse - 3-12 sachets a day - my problems then were due to prolapse, not PN. I don't recommend it. PN started when I woke up after the mesh surgery.

After the mesh surgery I was on a regime of Movicol + senna for a while, gradually decreased it down to nothing and all was basically ok in that department - apart from the PN pain. I was told that senna is ok for a few weeks (3 - 4) but no longer than that or else the bowel becomes dependent on it, and you start to need more and more to get the same effect.....

Nowadays I am having problems again - the previous mesh was taken out and rectopexy with new mesh to prevent further prolapse, the bowel seems to have forgotten how to work. :oops: :? Back on the Movicol again at first, but difficult to get the balance right, because unfortunately I'm also having continence issues now. Seems to be a control issue, related to nerve damage - no surprises there. I have been referred for biofeedback, haven't got an appointment yet. In the meantime my best help has turned out to be Magnesium capsules, if I take 400mg a day then mostly I'm fine.

Other things that help - a couple of prunes or dried figs, can't have this every day as I have PCOS and need to stay away from carbs. Also, we eat lots of green leafy veg. And we do keep the fluid intake up - 1.5 to 2 litres a day, and I don't include coffee there.

I hope you find a solution that works for you.
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Violet M
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Re: constipation

Post by Violet M »

Rob, there's a bunch of ideas at this link: http://pudendalhope.org/node/32

A doctor of oriental medicine recommended magnesium citrate tablets and my regular physician thought it would be fine to take them indefinitely so I've been taking them for about 5 years now with no problems. If I eat a high fiber diet I can get by with 800 mg. a day but if you are on narcotics you might need more. The goal is to keep your stools the consistency of applesauce and adjust the amount you take accordingly.
PNE since 2002. Started from weightlifting. PNE surgery from Dr. Bautrant, Oct 2004. Pain now is usually a 0 and I can sit for hours on certain chairs. No longer take medication for PNE. Can work full time and do "The Firm" exercise program. 99% cured from PGAD. PNE surgery was right for me but it might not be for you. Do your research.
pn_person
Posts: 94
Joined: Fri May 13, 2011 10:11 pm

Re: constipation

Post by pn_person »

using senna (ex-lax), and HUGE help...understand stimulant laxatives long-term is NOT recommended as it might become a dependency, but hey, I figure gotta do what you gotta do, and nothing has help like this...miralax keeps it from getting hard (sorry about the details), definitely important, but when the nerves that move things along are not working properly, the senna has been great..been a few weeks, taking 15mg of ex-lax 2x/day..along with a single dose of miralax

will try to reduce at some point, but right now, I am going to stick with it
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Karyn
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Location: Lowell, MA

Re: constipation

Post by Karyn »

All of the above responses are really good. I'd like to add GRAPES to list. I personally prefer the white, seedless ones. :D
Ultra Sound in 03/08 showed severely retroverted, detaching uterus with mulitple fibroids and ovarian cysts.
Pressure and pain in lower abdomen and groin area was unspeakable and devastating.
Total lap hysterectomy in 06/08, but damage was already done.
EMG testing in NH in 04/10 - bilateral PN and Ilioinguals
3T MRI at HSS, NY in 09/10
Bilateral TG surgery with Dr. Conway on 03/29/11. Bilat ilioinguinal & iliohypogastric neurectomy 03/12. TCD surgery 04/14.
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birdlife
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Location: London, UK.

Re: constipation

Post by birdlife »

Concentrated prune juice with additional Sorbitol was more useful for me than the macrogol sachets (same as your miralax I believe). I had boxes and boxes of those, plus Senecot, but was getting nowhere for 3 months till I had the prune juice. Did sound like I had deep plumbing problems for a while, but hey - just stay indoors for a day! :). Also dark chocolate and bananas helped ...
PN, possible entrapment at ischial spine -Dr.Natasha Curran, National Hospital for Neurology, London.
2 -Xray guided double nerve blocks -Dr.Baranowski - no relief.
TP self-massage reduced piriformis pressure on p nerve.
Dr.Greenslade/Bristol:
CT guided block (left) 16.7.12- success! Could sit without a cushion! On a brick wall!
06/2/13 - Sit pain gradually returned, L3. Offered further CT-guided block, or an op. Had to decline at time.
Feb '15. Applying to be referred again to Dr G.
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kia kaha
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Re: constipation

Post by kia kaha »

here in New Zealand I buy and drink ''alpine tea''
its a miracle!!
Chronic Pain pudendal area for 3 years, after a hard jolt to right side.
18 months later discovered sprained/fused sacro-illiac injury. Told to 'live with it' then saw this forum October 2011 = symptoms matched. Attempting to get this investigated in the face of lack of skilled docs in New Zealand.
Been told I have IC Dec 2011
FINALLY - 3T MRI in Christchurch 5th May 2012 - Pudendal nerve block, unguided 8th June 2012 - still waiting on results and progress from these.
pn_person
Posts: 94
Joined: Fri May 13, 2011 10:11 pm

Re: constipation

Post by pn_person »

thanks all for the suggestions!!!

guess it is a matter of finding what is best, and can be used consistently without doing harm

still using the miralax + the senna (ex-lax)...miralax adds water, and the senna moves things along

seems, at least for me, no matter how much water is added with miralax or something similar, without the stimulant, it is not much use...would still have to strain exacerbating the perineal decent, stretching the PN, and making the condition worse (mostly numbness for me)

going to try and substitute prunes/prune juice for some of the senna, since the prunes act as a stimulant also..not sure if the prunes are less harmful, but natural is always better I would think

already started with one glass of prune juice today..gonna see how it goes..if I can get off the ex-lax, I will feel that is progress

bloated to some extent all the time...feels hoorrible, and makes all symptoms worse

hard to believe that just over a year ago, I did not even know what the PN was, lol, and going to the bathroom never entered my mind..had to go, went..wow, the new reality sucks!!!!

have to experience it to understand as all of you do..try and explain it to a "normal" person, they cannot relate

I hear things like just increase fiber, etc, lol, they have no idea...I include the VAST majority of doctors in this category
shljk
Posts: 27
Joined: Wed Feb 02, 2011 4:18 am

Re: constipation

Post by shljk »

I suffered for YEARS from very severe constipation, had to have surgery for anal fissures, and still have to work hard at going regularly. Five things have made a huge difference for me: 1. keeping a fiber/water/bladder & bowel diary so I can see how much fiber I'm really getting with daily goal of 35-40g; 2. taking a daily non-stimulant supplement whether it's Miralax, magnesium or a Colace-type product; 3. eating a mixture of applesauce and uncooked oat bran every night (some use wheat bran instead and add prune juice); 4.) making sure I go when I feel the urge with absolutely no pushing or straining and giving my body enough time to sit, relax the muscles and go (apparently lots of people rush the process) and 5.) doing the I L U colon massage every night before bed (absolute number one thing that has helped me). My PT gave me all these tips, and done together, boy was she right!
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