Looking for Others Who Can Relate to My Misdiagnosis and Transgender Identity

I have only been seeing my rheumatologist 1.5yrs. She's been "suspecting" MS but thinking we could just rule it out. But cognitive/neurological stuff has gotten worse not better so now waiting on insurance to approve neurology for the MRIs and scans.

Hercules, same to you. I am brand new to this app so bare with me lol I'd say my biggest struggle is not knowing for sure if I hv lupus, MS or both. The cognitive stuff is what I despise the most. Days where my brain isn't working or just won't connect. I'd rather have more pain than a bad brain day. I hate never knowing if I'm going to hv a good day or not. How long did it take you to get a definitive diagnosis?

Hey y'all! I'm so very excited to have supporters and to finally find a few people who can mother fucking relate, guys. I live in a homeless shelter, working odd jobs soon to pay for rent while my disability case on as a claim, calls back. I reapplied for it two months ago. Please inbox me if you wanna rant or relate about shit . I don't know, just be there for each other. Bullshit lol. My gabapentin was actually stolen, along with my backpack.. from under my fucking bed. I've been mf smoking like a clowd train to deal with the palm. I've been searching for 30%+; bud for this. It's not strong enough and it's from Oklahoma. Idk wtf to do guys. Just got my gabas and remember, I hadn't taken them for two weeks, and I take over 1200 and I'm screwed right now. Well yeah that's my life but just about what's going on in my life.

Goldengirl1205 I live in Louisiana to and I was diagnosed with ms about 2 years ago and I also have no one to talk to you can send me a message anytime