Multiple Sclerosis - I am not sure what kind I have I just know I am continuing to get new lesions.
Hello @A MyMSTeam Member, it is a hard subject to discuss, but lots of us here have been in your situation. I retired on medical grounds in 2018. I am in the UK so not the right person to offer suggestions to you, but I am sure others here will offer suggestions. Stay strong π€
I believe I have worked enough for the SSDI. I worked retail two full time jobs most of my life. The affect started about four years ago I could feel thing wrong but nothing to explain them. I have DDD in lumbar spine. I had to have surgery due to my spine pinching the sciatica nerve. After surgery I went back to early and the pain was unbearable. Due to this I had nerve blockers put in. I left retail and am now scheduling for health care for a call center. It is so fast paced and consistent changes and even though this was something that was supposed to be easy it is very challenging and overstimulating. It makes be feel so dumb I know answers but forget and brain stall. I started health care 1 year 9 months ago. I found out I had MS due to being stroke activated a year ago. Since then I have had a pretty substantial decline in health and comprehending some of these documents and process is very confusing. My only support is always tired and stressed itβs so hard to discuss this stuff and I am drowning in medical debt.
Yes, many MyMSTeam members have been in exactly this situation β and it can feel overwhelming at first. The good news is there are clear steps to get started.
There are two main programs to know about:
- SSDI β for people who have worked enough over their lifetime and can no longer work due to disability
- SSI β monthly Show Full Answer