My Mother...My mom was diagnosed with MS two years ago and I still know very little about it. Apart from being on Copaxone (which I only know because of its presence in the fridge), and the original tingly sensation she suffered in her extremities, she doesn't talk about it and I don't really understand. I assume that because 2 years have gone by with very little apparent change, she has the form that isn't as degenerative or can have one outbreak (wrong term?) and then never flare up again. I assume, but I don't know.
I mean, I'm 23 years old, so yes, I have gone online and looked things up and found all the medical bs which makes very little real sense to me. But I don't know what it means in terms of my mom. In terms of my someday children growing up without her. In terms of me growing up without her. In terms of time and changes and future plans.
And she doesn't want to talk about it.