[dwarden]

Hi,

I'm Dave - dx June of 2008 with Multiple Sclerosis after having Optic Neuritis and almost going blind in right eye. I have foot drop and limited response and range of motion in my right extremities. Just got married on 10/31/09.

Been on Copaxone since March of 2009. Ive been to 2 different local Neuro's, NIH (National Institute of Health), and going to the Mellon Center at the Cleveland Clinic on 2/4/2010.

I'm in the "insurance process" of 3 denials and then an outside review board before I can get a WalkAide to improve my quality of life. If it gets denied the 4th time - I have to pay $5,000+ for it. I guess the insurance company would rather see me break my neck, hip or something else before they pay...

I've created an iPhone and iPod touch app to assist with my injection rotation tracking as well as all the other meds I take. I can't write so well if at all anymore. I am becoming left handed! My goal was to help others in a similar situation.

I have met many people who are far worse off than I (for now), so I can say I am thankful for knowing I am not alone going thru this.
I wish everyone the best success in their treatments.

Thanks for creating a great community!

Regards,
Dave