I was misdiagnosed with belpalsy Until I had a MRI . And that was for a whole year With the misdiagnosis.

Im in northern CA looking to make some friends people to talk to im finally feeling up to trying this app and just seeing whos out there and whats going on

So I have mild dropfoot right now and I’m curious to know if anybody has used this product? It’s called Niivira and it’s a brace for drop foot that I saw on Facebook. If anyone has this, can you advise if it’s worth purchasing and if it helps. Thank you.🙏

I was diagnosed with spms. All I know is I get aggravated so easy and loud noises really bother me now. Is this normal? I feel like I'm losing my mind. They say they want to start me on teriflumonide has anyone ever been on or heard of this? They haven't started me on it yet , we are waiting on all ...

does a yone else take this supplement? no one told me to, I just read it was essential for nerve regeneration & as MS effects nerves I just thought may as well take it. Also read it's water soluble so any excess is peed out so you can't overdo it? Does anyone have any thoughts on this 🙂

I was diagnosed in August 2025, so this is all still new to me. I’m doing the best I can, listening to my body and trying not to feel overwhelmed. Most days I’m okay. Today hit me kind of hard. I got to work today and saw a fellow coworker (who also has MS) that I haven’t seen in months. I won’t go...