Re: Welcoming Kim -- Hello ALL!

[Guest guest]

Hi Kim, Welcome aboard!! ) I don't believe I've ever heard that term before (tumefactive MS). I'll have to remember I want to look it up tomorrow after my company leaves. The trick will be remembering! LOL I'm Challis and I don't have a dx yet. I did see a new Neuro not long ago and I liked him better that the first! At least this one seemed to listen and he didn't tell me all my symptoms come from breastfeeding. ROFL My Mother has MS and brought me to this list a little over two years ago now. She's Sharon (Wobbletowalk). ) If I think about it, I can probably trace symptoms back about ten years or just over? Very definite symptoms for the last 7 years or so, and they've just kept going. I live in Arizona, in a part of the state where snow is still melting on the

ground from the fall yesterday. It snowed all day long, but what was on the ground began disappearing quickly enough. Sure is pretty when it falls. ) My husband, , and I have four children. is getting very close to his 20th birthday, though I'm not sure he's allowed to. LOL is, Jenna is 6½ and Maya is 3. That is a very long hospital stay. It must feel great to be back home! ) What took you to the hospital in the first place? Challis Kim Latour wrote: My name is Kim and I have just been discharged from hospital where I was for just over a month. I have been diagnosed with a rare form of MS called tumefactive MS. This dx was achieved following a brain biopsy. I am eager to talk with others who are also living with MS, particularly those with this form of MS. __________________________________________________