MS

[cbrodie13]

I know that Richard has MS. I hate that...I hate that anyone has it. I have primary progressive MS myself. I am doing the MS walk this year, as I have the past 5 years. I use my powerchair and zip around. I know they aren't the greatest organization, but they have helped me and others at times when needed (loaned me a chair when someone fucked mine up!). If you want to check out my little page please do. https://www.nationalmssociety.org//PAE/ ... 0050417ELM

Maybe someday there won't be this stinking disease. My 10 year old says he's goin to be a medical scientist and find a cure...hope we don't have to wait that long!

[bcddjjsc690]

cbrodie13, Best of luck to you and may you continue to find the strength needed to battle your illness .
https://www.nationalmssociety.org//PAE/ ... 0050417ELM - cbrodie13 link'
Here's a click on link to help those lazier than myself to
access your information, hope it helps in some small way.

[Visitor]

bcddjjsc690,
Thanks! I am not the brightest when it comes to computers...you wouldn't know I work with them-LOL!

[Appaloosa]

bcddjjsc690,
thanks for the link ...I am very lazy...I was chatting to someone about obsessive/compulsive behaviour....an I am too lazy to be obsessive........I am compulsive though

cbrodie
I do hope things become better......it is talking that makes people aware....wich leads to helping....an action..

[Jennifer]

cbrodie13,
i am glad that the ms society has helped you...so much money goes to salaries and not research...which is why we don't support them....but glad they did right by you!
Best to you girl!!!

[cbrodie13]

Jennifer,
I would love to see an organization to do research solely on progressive MS. I think the medical community closes their eyes to it.

[bcddjjsc690]

cbrodie13, No thanks is neccesary, Just wanted to lend a hand,,if you only knew how long it took me to figure out,

I just persevered ,and got lots of help from fellow members... {trust me LOTS OF HELP }

Appaloosa,