I was a member on the original boards and never came over when they migrated to the new system so it has been a while.
I was diagnosed in 2001 after spending almost 5 years trying to figure out why I was having trouble with my vision fading out when I was outdoors.
I have been in denial for many years as I have been lucky enough to have minimal attacks of numbness and weakness.
I have always been on one or another treatment, I have never quit because I am afraid what would happen if I did.
Over the last few years I have had increasing problems walking and can forget jogging or running.
So now I am reuniting with the MS community to keep up on treatments and therapies, and well to maybe have a shoulder to cry on when needed, my wife has always been supportive and understanding as she can, but you dont know unless you have it.
My personal shoulder to cry on passed away last year after fighting really aggressively progressive MS, she never lost her positive attitude until the day she passed and I miss her.
Thanks for your attention if you made it this far!
I was diagnosed in 2001 after spending almost 5 years trying to figure out why I was having trouble with my vision fading out when I was outdoors.
I have been in denial for many years as I have been lucky enough to have minimal attacks of numbness and weakness.
I have always been on one or another treatment, I have never quit because I am afraid what would happen if I did.
Over the last few years I have had increasing problems walking and can forget jogging or running.
So now I am reuniting with the MS community to keep up on treatments and therapies, and well to maybe have a shoulder to cry on when needed, my wife has always been supportive and understanding as she can, but you dont know unless you have it.
My personal shoulder to cry on passed away last year after fighting really aggressively progressive MS, she never lost her positive attitude until the day she passed and I miss her.
Thanks for your attention if you made it this far!
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