Hi Everyone,

Was browsing the internet looking for information on painful injections (after a painful Betaseron injection) and came across this Board. Looked good, so I joined, and here I am!

I'm currently unemployed, a victim of the banking crisis, looking for my next position. My kids (2 girls, 7 and 9) call me a "clumser" when I stumble, lose my balance, or bang my head on something (clumser, as in one who is clumsy).; When I saw the "Stumble Inn", I knew I was home!

I was diagnosed with PPMS 18 months ago, but suspect I've had MS for about 40 of my 47 years. I'm looking forward to posting more, meeting all of you, and learning from everyone's experiences.