Welcome, SweetP..

Agreed, welcome SweetP!

Keri, get out there and rock it girl! You'll find a solution

"No right to complain"?..Really, Keri? I'd be complaining loud & proud about now..Sounds like you have outstanding doctors to help ~ things WILL get better, I believe it and pray for it for you!

Aw Keri . I'm so sorry. Copaxone, interferon, and just recently Tysabri have failed me. I'm not relapsing but having severe headaches and other problems from the infusions. My neuro is giving me a little time to decide whether to go off of Ty. I just decided (with dh's help) to stop the infusions. I'm gonna try LDN next. I've only been diagnosed since May of 2007 and it has been a nightmare of a rollercoaster ride. I have to use a wheelchair at airports. It's actually pretty great ! You get to jump to the head of the line and board the plane first! Hey, we have to take the small advantages we get and use them! . I really hope the IVSM does the trick for you. I'm really thinking that 2009 HAS to be better for us all.

You have had a tough year, and I wish nothing but the best for you in 2009!

Its hard to keep your spirits up when you crash so hard and feel so bad, but it sounds as if you are able for the most part to keep a positive look on things. When I get the "Woe as me's" as I call them, I think of one thing: It always comes down to just two options: Keep going, or give up. Most people opt to keep going, no matter how hard it is.

Keep going. Its amazing what we can do.

You're amazing.