This is my very first post!!!! I’m pretty technically challenged, so apologies if this isn’t great. My fella has an awful lot more to talk about but he’s more challenged than l am. I thought l’d try it though, then show him.

I do have a lot to say about MS and life in general.

I got diagnosed with MS in 2011 and once l’d found out (thru MS Society) that it wasn’t terminal l thought it was something easy to deal with and medicate! Boy!!! Was l wrong!!!!

They call it an invisible disease. Me being me, thought the pain was the invisible thing. Nah uh!!! One of the worst is how it affects your bladder. For 13 years l had to wear Tena PANTS! They are amazingly unsexy but also terribly embarrassing. Imagine how YOU would feel in your late 40’s having to wear what is pretty much a nappy 🤔

I was incredibly lucky enough to have met the love of my life/soul mate nearly 4 years ago. He has been amazingly understanding about my bladder issues and helped me cope for us to have a great sex life. I’d always imagined at my time of life to no longer have the urge. But he has made me feel SO sexy.

Like l said, l don’t know how these things work, but if by some chance you read this and are interested in hearing more just let me know and l’ll tell you 😊