Tag Archives: bladder retention

Some”ONE” with MS

They say when you meet someone with MS; you’ve met someONE with MS. Each person that lives with the disease has different symptoms and reacts differently to treatments/therapies. That’s important to know. A lot of people who I meet tell me about their Aunt who had MS, so they expect me to look like her (maybe she was confined to a wheelchair most of her adult life). When I don’t, it’s confusing to them. Or, I get, “But you don’t look sick”, because I’m walking OK right now, and most of my current symptoms are invisible (but chronic).

I’ve written about the struggles I’ve had with my bladder in a previous blog post titled I Really Need To Pee . It was a good overview of how MS affects my ability to pee (or not pee) when I need to. Continue reading

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I Really Need to Pee!

Let’s talk bladders. It’s a big topic on my mind right now because in the last few weeks I’ve been feeling the effects of bladder dysfunction — an MS symptom that’s plagued me since my early 30s.

I’ll admit that this isn’t something I love to discuss, but it’s an important issue because so many people with MS deal with it. The National MS Society says at least 80 percent of people with multiple sclerosis have bladder dysfunction. It’s invisible and uncomfortable. And unless you experience it, it’s difficult to comprehend the physical and emotional toll it takes on you.

Before I get into my personal story, here’s a quick explanation of bladder dysfunction — if you don’t mind some nitty gritty details. When people with a normal, healthy bladder feel like they have to pee, they can hold it until they know that they really gotta go. Then they can hurry to the toilet and Continue reading

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