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This may seem like an odd post but I want to THANK everyone on this page for sharing their experiences good and bad with MS!! Before I found this site I truly felt alone in what I was experiencing with my everyday life with this invader that has demolished my life. I have cried reading several post...

Good day all, Just want to say this site has really helped answer questions others couldn't also just having a platform to share with people who understand. I'm sure I'll have more comments and questions on the future but thanks to everyone for all the help thus far 🙂

Hey guys! We go through soooo much having MS and many people can’t relate and it is so frustrating. However, we are still here my loves. WE HAVE LIFE!!

Great evening everyone how’s you all day going ??❤️❤️

Does anyone suffer from wearing the wrong pee pad? Nothing seems to work. Please, let me know.

I just received my diagnosis last Friday and even though the news itself is unfortunate I feel so grateful for how the discussion was handled. I was called to the hospital’s immuno-neurology unit and two neurologists and the MS nurse gave me and my partner 1.5 hours — as much time as we needed to ex...

Hi everyone, I’ve had RRMS for over 20 years. I was diagnosed during a time when Australian TV was flooded with commercials of young women with MS in wheelchairs. So, when I was diagnosed naturally I assumed this was what my future held. Thankfully, I had a tribe of supporters who would not allow ...