Multiple Sclerosis (MS) Support Group
This community is a place where members can discuss current events and weigh in on what's going on in the world.
This community is a place where members can discuss current events and weigh in on what's going on in the world.
I was diagnosed with RRMS 15 years ago and the one thing I still hold now at 34 is my virginity and extra lonelyness because none of my friends wanted to deal with my sudden strange/ scarey illness that no-one belived I said I had cause they saw I still had both legs and all that; so I must just be being lazy again and trying to be a spoiled rich girl and not use my right leg right!
I never have been rich or from a weathy family, my family is much more like the Ingels family on Little House on the Praire. I just thought it was nice that the new "fancy" Dr. a Neurologist (Which I hadn't heard of before in all my grade-school years) got me onto (The SSI and DSSI that I began collecting off of my fatha for a while) so I'd be able to see him and have other "fancy" things like MRIs to check an obviously no-existant illness I claimed to now have and then also some "medication" that I also claimed made me feel horrible the day after I took it...
Now I very much know that any SSI bearley keeps a person from having the kind of life they dreamed of, but if you can find a place that accepts disability/ Section 8 payments and you could still do most things for yourself, like getting to the bathroom and going to a phone to order a cab to drive you places like the Dr.s office and to get foods, you can live a reasonable life and just have the thoughts of having mizerable plans of doing what we alll will do at some point in our lives.
time job if possible. You need professional advice from social worker for your options. I wish the very best to you.