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#1 | |||
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Junior Member
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I was diagnosed almost two months ago. The neuro asked me if I ever lost control of my bladder. I said no, but I experience a sense of urgency that does not match the out put. He told me to start massaging my bladder when I used the bathroom.
At first I wasn't sure I had found the right spot but after a few weeks I stopped getting up at least once a night feeling like my bladder was about to burst and only dribbling out and ounce or two. After almost two months I can now feel my bladder because it actually fills. I do not go as often and the sense of urgency is greatly reduced. I was wondering if anyone else has used this technique. Is it a long term solution?
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"Nothing has changed, but everything is different" -Hubby's statement after I received diagnosis. -DX RRMS 12/2013 |
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#2 | |||
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In Remembrance
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My old female Neuro told me the same thing. To push on your bladder,
to help empty your bladder. It works for me and cuts down on UTIs.
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~Love, Sally . "The best way out is always through". Robert Frost ~If The World Didn't Suck, We Would All Fall Off~ |
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#3 | |||
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Magnate
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Hello ker0pi,
I have been massaging the bladder, lower abdomen long before I was diagnosed with MS. I started dealing with chronic Urinary Tract Infections (UTIs) at the age of 4. The only reason given, Retention. I had an Urologist tell me a very long time ago to massage my bladder, abdomen to help empty my bladder.
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Dx RRMS 1984 |
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"Thanks for this!" says: | ANNagain (02-05-2014), Erika (01-30-2014), Grammie 2 3 (02-01-2014), ker0pi (01-30-2014), SallyC (01-30-2014) |
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#4 | |||
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Wisest Elder Ever
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How is it done?
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These forums are for mutual support and information sharing only. The forums are 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. |
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#5 | |||
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Junior Member
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My neuro told me to Google where the bladder was in the body and he showed me by pressing gently on my hand and going in a small circle. So I push gently on my abdomen where the bladder is located and rub in small circles, like massaging a small knot in a muscle.
Now that I can feel my bladder, like a hard lump, I concentrate on massaging gently there and as I go I feel it get smaller and smaller until I can't feel it.
__________________
"Nothing has changed, but everything is different" -Hubby's statement after I received diagnosis. -DX RRMS 12/2013 |
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#6 | |||
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Member
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Yes I do that - I have for a long time - except I use a fairly hard pressure and often squeeze the abdominal area tightly too. Otherwise I will be sitting there all night.
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Lyn . Multiple Sclerosis Dx 2001 Craniotomy to clip brain aneurysm 2004. ITP 1993. |
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#7 | |||
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Grand Magnate
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I push down at an angle and it works I had an UTI from hell l called it, but nothing since, don't think I can blame MS. Drink lots of water to make urine output a light color. Doesn't seem to increase out put noticeable increase in output, but produces a light color urine. Don't be afraid of hydrating. It can be a good thing. For me.
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Kicker PPMS, DXed 2002 Queen of Maryland Wise Elder no matter what my count is. |
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#8 | |||
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Junior Member
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Quote:
I don't get UTI's never had one and I drink 3-4 quarts of water per day. My neuro was trying to help me avoid a medication for bladder control. Massaging helps me not have to go every hour. ![]()
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"Nothing has changed, but everything is different" -Hubby's statement after I received diagnosis. -DX RRMS 12/2013 |
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#9 | |||
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Grand Magnate
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i believe in medical parlance it's called credeing (credAing). i may not have spelled it right but you could try googling it.
i would be fairly gentle. the bladder is a muscle. best not to be too hard, especially if it's full.
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Judy trying to be New Skinny Butt ______________________ You are a child of the universe, no less than the trees and the stars; you have a right to be here. And whether or not it is clear to you, no doubt the universe is unfolding as it should. -------------------------------------- "DESIDERATA" by Max Ehrmann |
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#10 | |||
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Grand Magnate
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I've tried a variety of bladder control meds. Made my mouth really dry and didn't notice big improvement. For me wasn't worth it but I don't work or anything and it wasn't a big problem. Not a big fan of any medications unless I feel there's a real need, so cut this one out. Shoot, I'd eat worms if it really helped MS. 8-}
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Kicker PPMS, DXed 2002 Queen of Maryland Wise Elder no matter what my count is. |
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