Reply
 
Thread Tools Display Modes
Old 10-13-2008, 06:58 PM #1
Judy2's Avatar
Judy2 Judy2 is offline
Senior Member
 
Join Date: Sep 2006
Location: PA
Posts: 1,236
15 yr Member
Judy2 Judy2 is offline
Senior Member
Judy2's Avatar
 
Join Date: Sep 2006
Location: PA
Posts: 1,236
15 yr Member
Default

Hi Annie,

So sorry you're dealing with this "lovely" problem, but kind of glad you've brought up this subject. Even though it's such a common problem in MS, it's still embarrassing to talk about -- whether you "can" or "can't".

Of course there can be other reasons for incontinence, MS can be the culprit. Over the past couple years, my urgency has become a real problem. I'm past the pad stage and into "Depend's" which at night still aren't enough. It takes me about 1/2 hour to get out of bed, so there's no sense trying to get to the bathroom. Those mattress pad thingys that tuck in on each side save the rest of the bedding! But it sure isn't enjoyable getting up just about every day all wet. YUCK! Guess the Lord had a good reason for me not marrying again after my divorce 18 years ago! The thing you mentioned with not knowing you have to go is true with me also. By that time, it's too late. Being in this "chair", by the time I stand up, shuffle my feet enough to turn around hanging on for dear life -- too late. Thank heaven for washing machines!! Personally, I can no longer do the kegel (sp?) exercises since I can't move those muscles. One of these neuro visits I have to speak with him about the nightly stuff. Where does it all come from? Heard something about nocturnal urination?? When I have to go, if it starts, I'm sunk when I stand up. The flood-gates open!!

Yes, I've tried different meds, Enablex worked at first but then stopped, take oxybutynin but it doesn't do much either. The LDN does help somewhat. On the days when I have coffee or tea, forget it. Wonder if that herbal tea your doctor recommended would have the same effect? And yes, a diuretic does make the situation worse. My ankles/feet swell but the neuro says it's lymph due to immobility. The Detrol isn't covered by my insurance and it's very expensive. I'd like to try one of the others, but my dr. says they're all about the same. So far at least, I've never had to cath or had the usual bowel problem. If anything, it tends to go the other way -- HURRY -- HURRY!!!

Don't you find the "simple" task of pulling your pants back up is the hardest thing to do since we have to hold on all the time? I tend to fall backward. Wherever this disease came from, I wish they'd take it back!!!

Sorry I'm no help in finding a solution, but hopefully it will help knowing you're not alone. You sure helped me!!

Good luck..........
__________________
_____________________________________________

.....Judy
SPMS -- FIBROMYALGIA -- Ouch! and Ouch!
.
Judy2 is offline   Reply With QuoteReply With Quote
Old 10-13-2008, 09:22 PM #2
Koala77's Avatar
Koala77 Koala77 is offline
Legendary
 
Join Date: Jan 2008
Location: Australia
Posts: 12,030
15 yr Member
Koala77 Koala77 is offline
Legendary
Koala77's Avatar
 
Join Date: Jan 2008
Location: Australia
Posts: 12,030
15 yr Member
Default

Thank you Judy! I'm sorry to read that you're going through a similar thing to me but it's nice to know that you, and others, understand what I've been going through.

I found out the name of the herbal tea that started with "H" that my doctor recommended. It's actually called Epilobium Tea, so I don't know where she got the "H" from.

I'm with you on the pad thing. I've been buying packets of full continence briefs for night use, and using stick on ones for day time use..... unless I have to be away from home for a while.... the I use the briefs.

Lately I've discovered that it's cheaper to buy them by the carton, and since I order on line and have them delivered, I'm so glad the boxes are "discretely" packaged.

I think the tea is rather expensive at $25 for 12 tea bags, so unless I find a cheap stockist to order them from, I probably will have to give them a miss.
__________________
Eastern Australian Daylight Savings Time
and
my temperature


.

Koala77 is offline   Reply With QuoteReply With Quote
Reply


Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off


Similar Threads
Thread Thread Starter Forum Replies Last Post
Urinary and bowel issues, help! weeble37 Multiple Sclerosis 11 07-09-2008 09:22 PM
Urinary incontinence Koala77 Multiple Sclerosis 19 02-06-2008 06:16 PM


All times are GMT -5. The time now is 07:00 AM.


Powered by vBulletin • Copyright ©2000 - 2025, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise (Lite) - vBulletin Mods & Addons Copyright © 2025 DragonByte Technologies Ltd.
 

NeuroTalk Forums

Helping support those with neurological and related conditions.

 

The material on this site is for informational purposes only,
and is not a substitute for medical advice, diagnosis or treatment
provided by a qualified health care provider.


Always consult your doctor before trying anything you read here.