▲ 4 r/SSDI
Losing insurance soon
I am a 55f diagnosed with MS since 2002. I stopped working at the end of January at a basically sedentary job with lots of typing and talking on the phone. I have a pretty aggressive tremor in my dominant hand and in my face as well as spasmodic torticollis. I can’t stand for more than 15-20 mins at a time and sitting is pretty painful as well. I lose my health care at the end of June and I’m not sure how to continue seeing all of my doctors without insurance. What does everyone else do? I applied for SSDI in March. I know I’ll need to continue my care in order to show that I’m disabled. Thanks in advance for any and all help!
u/Conscious-Life6090 — 1 day ago