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I have been deliquent myself in not being more forward and welcoming.

So...to all the relative 'newbies' here--whether or not you are dx'd with

MS,

or are newly diagnosed with MS or dx'd years ago, welcome to a group that

is by far, without doubt, a wonderful and warm gathering of folks. We share,

encourage and chat about many things, not all MS related. There is a sister

group as well--http://health.groups.yahoo.com/group/MSersHEALTH/

for more specific MS questions and health issues, not to say that MSers Life

isn't about that too.

My name is Kate, I'm 48 from NY, married for 21 yrs and mom to 5 kids. I was

diagnosed in Dec. of 05 with RRMS. I had been on Copaxone, but am currently

on Tysabri. Like many of us, I've run the gamut of various symptoms--

bladder, cognitive, visual--my primary complaints are left leg weakness,

fatigue,

depression and trigeminal neuralgia. Our founder and leader of this terrific

group

is Sharon who works so hard to keep this a smooth, cohesive and unified

bunch.

We each contribute a part with our various gifts and abilities--which makes

being

here always rich and interesting; fun and special. We hope you will join in

to enrich

us here as well, and will be able to learn something here from us; have a

laugh, or

a cry, or whatever you need at any particular moment. Thank you for coming

here.

blessings and hugs, kate

We can only be said to be alive in those moments

when our hearts are conscious of our treasures.

~Thornton Wilder

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