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-   -   This is new (to me) (https://www.neurotalk.org/multiple-sclerosis/36995-this-is-new-to-me.html)

Taffy 01-24-2008 08:18 PM

Quote:

Originally Posted by AfterMyNap (Post 195266)
Twippy! IT WORKED, IT WORKED!!!!!

THANK YOU EVERYBODY! :grouphug: It went away for now!!!! I am so relieved that I relieved myself this morning! I called it in and my nurse said that we might be looking at spasms, but we'll wait for the doc to weigh in on it.

It's funny, I've never really paid a lot of attention to this function and I realized this morning that everything felt relaxed and nothing felt like it was "fighting" the process. Man, I am so so happy about that!

Congrats! I will never feel bad about wetting my pants again! I guess that is a good things after all!:D

NurseNancy 01-24-2008 08:54 PM

very glad to hear about this cindy.

Riverwild 01-24-2008 11:11 PM

Cin,

Glad to hear the water's running again!:)

Let us know what the doc has to say when you see her/him!

Twinkletoes 01-25-2008 12:20 AM

There once was a gal from Grand Rapids

Whose bladder became rather vapid.

Her urine backed up
Till she tried Taffy’s cup:

Now she’s happy she won’t have to cath it!

tkrik 01-25-2008 09:16 AM

LOL, Twink. You are always so creative with words. Sorry AMN it was at your expense. LOL

mbsews 02-01-2008 11:09 PM

Quote:

Originally Posted by AfterMyNap (Post 195266)
Twippy! IT WORKED, IT WORKED!!!!!

THANK YOU EVERYBODY! :grouphug: It went away for now!!!! I am so relieved that I relieved myself this morning! I called it in and my nurse said that we might be looking at spasms, but we'll wait for the doc to weigh in on it.

It's funny, I've never really paid a lot of attention to this function and I realized this morning that everything felt relaxed and nothing felt like it was "fighting" the process. Man, I am so so happy about that!

Johnny on the spot I am, as usual. :rolleyes:;)

I'm so glad you're better, Cin. It's such a pain. In the months before I started Tysabri it was so hard to pee that I could have pushed a baby with less effort. It was exhausting. :o But every time I checked by self-cathing I was emptying adequately so my neuro didn't insist on urodynamic studies.

I'm amazed and chagrinned by how much time I spend thinking about pee and poop since MS invaded my life. :rolleyes:


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