@KevinKincaid 

Last reply

KevinKincaid

New person around.

Hello. Just to be friendly. I was diagnosed in 2009 and have gone from walking,to a cane, to a walker to a wheelchair. I have chronic spasams ( which equals to pain) I have learned the hard way that you have to be an advocate for yourself, or doctors will steamroll over you. After two different hospitals and four different MS doctors I was fed up, but now I have a great MS doctor and a good general practitioner. It just took me ten years to get things right . I am 44and live in Central Kentucky. I now have Primary Progress Relapsing MS. I've been through the wringer! as I am sure a bunch of people have too. That's it for now.
@Stumbler

Hi @kevinkincaid and welcome. We all go through that voyage of discovery to advocacy. It's such a bonus to have resources such as this Forum, to share advice and experience. I wish there had been such a resource when I started my MS journey. I'm sure I could have navigated a lot better than I did............

@merfield

Likewise @kevinkincaid. I’m in a wh/ch too with ppMS and getting spasms, mainly in the mornings. It’s a bugger but we just have to get on with it and go with the flow. It could be worse - we could be like this AND be refugees!!