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Junior Member
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Join Date: May 2013
Location: California Coast
Posts: 67
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Junior Member
Join Date: May 2013
Location: California Coast
Posts: 67
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Does anyone else massage their bladder?
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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