Unmentionable Bits


I imagine that many of you with MS read the NMSS Blog. A few days ago Trevis Gleason dealt with the dreaded B&B issue; not the second B [Bladder] which gets lots of attention. We either pee too often, or not enough, or get UTIs all the time, or wet our bed, or our pads, or ourselves. But the first B [Bowel] is the one that rarely gets talked about, and when it does get talked (or written about in neat little pamphlets explaining the various symptoms of MS that may affect us) it leans toward one end of the spectrum -- constipation. Oh, the dreaded bloating and feeling that you have to take a dump, but you just can't.

It doesn't tell you that constipation can be so bad that you need to see a gastroenterologist to find ways to manage it. Like taking doses of various meds, laxatives, eat more fiber, or even using your fingers to pry the stool from you. Oh happy, oh joy. Of course, you know you might be able to go if you just drank enough water to wash things out, but when you do that you can't control the other B [Bladder] (see paragraph one.)

It also doesn't tell you about the other problem: incontinence. Yes, that kind of incontinence. Going without warning wherever you might be. I have known someone to whom that happened - in a high end department store, no less. The sales clerks were very kind to her and led her to a private bathroom so she could clean up, and brought her a change of clothes. Yes, they were very kind indeed. She never set foot in that store again. They don't mention that in those pamphlets. N'uh uh. And another woman told me that she was in a mall when it happened to her; suddenly it started running down her leg. She said she never wanted to be a runner, but she did that day. She was mortified, and lucky too, in a way, because though  she left a trail of sorts, it just led to an empty parking spot. She retained her anonymity, at least.

What if the problem you have is that you can't feel when you have to go until, well, until it's actually TIME TO GO? And what if that happens when you're in the middle of a dream that starts telling you to get to a bathroom ... any bathroom ... like right now? And you wake up in a stupor, and you can barely move your legs because the blankets were a little too warm and you try to stand up, and you can't? You try and you try and you keep falling back onto the bed, and you start going and you know you can't control it? What do you do? This is no nightmare; well, yes it is, it is a nightmare, and this nightmare is part of MS. This is what happened to me the night before last.

So I look around to see what I have nearby that might save the situation. I find one of those thin blue plastic absorbent lined pads that they use at every urologist appt. [Don't mock me- I think it's foolish to  let all that Dr. office stuff go to waste - so I bring it home; you never know when it might come in handy] This seemed like the perfect thing to use it for - to catch my poop unmentionable bits so they didn't get all over my sheets. I turned to lay on my side and managed to get it beneath and behind me. My sheets were saved; I just lost my dignity as I had to call my husband to help at that point. I had no TP. I couldn't clean myself. I still couldn't stand. I was exhausted. I just wanted to cry but couldn't thanks to my antidepressant.

I needed more sleep, so after DH cleaned things up (he's so good, he takes these things in stride), I took a long nap, after which I was able to (barely) stand, at least enough to use a walker to go to the bathroom, take a shower and get dressed.

MS just keeps getting better and better. I know; you don't have to say it, I was happy to share.

Good Night, TTYL and Be Well,

Comments

  1. My dear Webster...happy to share too. (not)

    The whole time I was reading your post I was nodding my head (except I don't take anti-depressants) and I haven't gotten that far yet with "crusty bits" but I have wet the bed repeatedly. It makes a bigger mess than the other, I would think...

    Great post!

    ReplyDelete
    Replies
    1. Been there, done that, and it still happens occasionally. I'm told that in absence of an infection, bladder spasms are the culprit. So my solution is to sleep on a crib liner. Sometimes the wet feeling will wake you and then all you have to change is the liner, well and your PJ's [if you were wearing any]. ;p.

      Delete
  2. This had to be a difficult post for you, and I admire your honesty. I, too, wrote about this in my blog back in October of '10. It's the often unspoken topic of this disease. If you read Trevis Gleason's blog on http://www.everydayhealth.com, he just wrote a post about this issue. Hang in there, Webster, we understand.
    Peace,
    Muff

    ReplyDelete
    Replies
    1. Actually I did read Trevis' article and that's what prompted me to tell my experience. Now I'll have to go back and read what you had to say about it!

      Delete
  3. Webster - such a well written post about a really horrible, taboo subject. I know folks will write about bladder issues, but rarely are bowel issues broached anywhere, much less a blog. For us, I've decided not to discuss Skip's bowel program on my blog, but it definitely causes me crankiness at times.

    It's amazing you were able to get that chux under you before making a complete mess of the sheets. You may want to buy a small package of them ... Amazon and eBay carry many different brands for relatively small dough. (I admire your frugality. It always used to bother me that the kit of scissors and tweezers at the wound center would be thrown out after 1 use. After I accumulated a half dozen of them, I finally let them be tossed.)

    ReplyDelete
    Replies
    1. Actually, I haven't always been so frugal, but you'd better believe I will be in the future. These things add up! I took home one of kits too, and they are great. Still have and use the items - Stainless steel tweezers, two very sharp and pointy scissors, one of those clamp thingys... I can't believe they just throw those kits away.

      I know you don't want to, but I would be interested in the nuts and bolts of an actual bowel program. Just sayin'. And I'm sure I'm not the only one. No pressure, though. lol

      Delete
  4. I won't say it really I won't but . ... OK you explained it much better than I ever could.

    ReplyDelete
    Replies
    1. Thanks Jan. But you explain all those geeky things much better than I ever could. Truck spring things, too.

      And aren't you glad I don't take pictures???

      Delete
    2. I am not sure if explaining geeky things is a a good thing LOL. I would dare you to take a pic but well ... I suspect that would be TMI.

      Delete
  5. I'd like to say that this has never happened to me but it has. I've been doing well for years now but I do so remember.

    I am so sorry. Life just sucks sometimes.

    ReplyDelete
  6. I have swallowed my pride, and wear incontinence undies (aka diapers),when the need arises.

    ReplyDelete
    Replies
    1. Oh I remember the first time I "used" my Depends when out in public. It is a very odd sensation.

      I don't know, it seems they would just cause a worse mess.

      Delete
  7. Oh gosh. Big huge hugs.. so much to deal with. :(

    ReplyDelete
    Replies
    1. Yeah Ami, MS is not for sissies. It's a tough disease to have.

      Thanks for the hugs.

      Delete
  8. It is a really, really sucky part of the disorder isn't it? Hugs. You said it so well, for so many of us.

    ReplyDelete
    Replies
    1. Thanks. I think more of us need to take this out of the closet. What do you think? Would it scare too many newbies?

      Delete
  9. Oh man, this explains alot. I learn more from the MS blogs than I do my neurologist and Drs. Thank you for your courage...I have some topics that I need to get out there, but I have not been ready yet, heck, I am still learning what is happening to me. Your courage gives me strength! Funny, I can feel myself cry inside, but the tears don't come, I have never related it to the antidepressants.
    Big giant squishy hugs your way.
    xo
    Olivia

    ReplyDelete
    Replies
    1. Usually, I am not a crier, Olivia, but this time I just wanted the release- and I couldn't. I figured that it HAD to be the antidepressants, because that's why I went on them in the first place! I used to cry at sappy commercials!!

      As for learning what is happening to you, just know that MS is different for everyone, and for each person at different times. I learn a lot from blogs, but there is also a lot of misinformation out there, so be careful.

      Delete
  10. These are common problems with MS...so glad you were brave enough to write about it. I have had all these before

    ReplyDelete
  11. just ugh... nothing more really to say about that

    i have been mostly lucky in the waste management department so far... i do have the problem of not knowing i have to go until I HAVE TO GO... but so far i've been in a situation that the potty has been close by - and i had the ability to get there....

    i do, however, have the piddles... i hate that... coughing, bending, picking something up, setting something down, blinking too fast... well you know...

    sorry that happened to you... and so glad you have a man that takes it in stride...

    ReplyDelete

Post a Comment

Popular posts from this blog

jinxed !!

My MS Update 2017

my back yard pt. 2