Yes, my life is definitely better on SSDI.
For your information, if you're on the lower end of SSDI you may qualify for other benefits as well. I have no Medicare co-pay because my state pays for it. And I qualify for food stamps because so much of my income goes to medical expenses that aren't covered by Medicare.
I also go to school tuition free. This is a state program, so if you are stable enough in the future, it's worth looking into. But, only SSDI people qualify.
SSDI takes SO much stress off me financially. I wouldn't have been able to afford any medical care without it.
The only thing that stinks is the judgement by others. I've had former friends turn against me and use my disability status against me. Maybe it would be easier if I lost my legs or something so people could actually see my disability. The fact that I'm not "mental" 24/7 works against me. I can look normal when I go out in public, so people think I'm using the system. What they don't know is how hard it is to get on SSDI to begin with, coupled with almost 20 years of medical records documenting my disorder. Sometimes I feel like I need to prove myself to the world. But then I realize it's none of their business. Word to the wise, only tell those who need to know about your status.
I've rambled on enough. Just remember that you worked for this. Don't watch the news; those in power who want to cut our benefits and consider us moochers will drive you nuts. (I was in full panic mode the days leading up to the presidential election due to republican threats to cut/eliminate social security and Medicare).
And don't consider SSDI your final destination. Heck, the government says I'm not going to get better, but I'm not going to stop trying to get back on my feet. I may never be able to work a 40 hour 9-5 sort of week, but there are so many options out there. Good luck!
