This Is MS Multiple Sclerosis Community: Knowledge & Support

I suppose no one here is getting SSDI, as they probably can't afford an internet connection, computer, etc. It's no wonder I have never heard any replies to my inquiries to SSDI

When my parents pass, I too will lose everything, not to mention control of my body over time.

The main thing is, our beloved country wants me to eat out of trashcans and live in a homeless shelter.
GOD BLESS AMERICA

it's hard enough to be poor and able-bodied. how limited are you physically right now? do you think you'll be stuck for good not being able to work?

i'm usually relatively poor but also relatively able-bodied except during the first half of 2006, so i can imagine how aggravating it would be to be thinking the 637 is it, for the forseeable future. i really hope you can get sorted out so that you don't have to live off government payments!

I can't work. My stomach spasms can stay under wraps, but only if I'm not doing ANYTHING.

Can't pee unless I poop or squat, can't catheterize because of the parasthesia in my urethra that constantly burns.

I keep thinking I'm finding hope in supplements, and as some do really help, they won't fix me.

Every job I've had in the past 4 years, I have lost because of MS problems.

Ironically enough, I only found out two Febs ago what the hell was going on.

Our government sucks. And for those who tell me to move to another country...... think about the homeless people in our arrogant nation who are too disabled to work.

628 dollars will not even cover my rent, let alone copays on medicine, food, bills.

FUK~!!!!!!!!!!!!!

jim if i may ask, what exactly are you taking each day for supplements? in what quantities?

I'm about ready to give up on all of them.

I won't be able to afford clothes in about 10 years, let alone supplements.

On with another flare up, bring it on MS!!!!!!!!!

This link may provide you a place to start for info on money issues.

http://tinyurl.com/2gkgs5

gwa