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Hey everyone! New here 😊 I’m in the USA and recently had to stop working about 7 weeks ago. My neurologist is suggesting signing up for disability. Anyone have any insight!? I’m nervous and have been told it’s a long process! TIA 🫶🏼

Hey everyone! New here 😊 I’m in the USA and recently had to stop working about 7 weeks ago. My neurologist is suggesting signing up for disability. Anyone have any insight!? I’m nervous and have been told it’s a long process! TIA 🫶🏼

For those of you who have needed to stop working and get on disability, what's been your experience? Personally, I haven't been able to work since May of this year and don't foresee myself going back to work anytime soon (I'm a massage therapist). I've been on state disability since the beginning of...

I'm too the point where I cant stay on my feet long at work. I'm having mobility issues and I'm constantly tired and fatigued. I need guidance and advice on how I can acquire disability perhaps, and what options I have.

Hello my fellow MSers I have RRMS and one of the permanent issues I have are bladder and bowel control. I've returned to work after a relapse (triggered by work-related stress) and have asked if I could have the ability to reserve a desk near the bathroom (we book desks) as part of my OH workplace...

Has anyone ever used short term disability insurance benefits to get through a relapse or allow time to get symptoms and management of symptoms under control?

Does anyone have experience with trying to apply for the disability tax credit? I’ve tried to get my family doctor to fill in the paper work and twice now she refused. This last time she suggested that I was lying. It was upsetting and at this point I feel like giving up on the whole thing. Has an...

I’m now the proud owner of a number of mobility aids, but I’m sure that getting out and using them would have been easier without the associated stigma and ableism in the world. I have a vent about all this in my latest blog post, link below. Anyone felt this too? https://janeharrison.substack.com/...

Hey, so my partner and I are trying to move because where we live right now there are no services for people with autism or MS. Does anyone know where might be better? Even a community MS nurse would be amazing, there are none in our current borough.

Sooooo, I got denied disability benefits for the second time. Can anyone give me some advice? Of course, I'm going to fight this. I just think it's crazy that SSA is making these decisions based off paperwork and not talking to the person or evaluating them medically first. I literally have confirma...