Hello,

My husband was diagnosed in August with ALS and I'm here for support from a caregiver's perspective.

Let's see, what are useful things I can say . . . Well, he's 35 and I'm 30. I have generalized anxiety and I'm hoping I might be able to find some support for that here as well. (what an amazing community you have set up here, I'm excited to get more involved) We have a third partner who is contributing to everyone's health, well being, and needs. I don't know what we'd do without him.

I'm entirely new to all of this - the SSI, the SSDI, the paperwork, the disability, the slew of details. Any input is welcomed! Thanks for being here for me to find!