Finally

[I814u24u]

After almost three years and multiple doctors I finally have a diagnoses of RRMS. Now they want do genetic testing for what I don't know, it's expensive and I'm not going to pay for it. I get my first round of solumedrol Monday. Wish me luck. It's got allot of side effects. I'm very apprehensive but the doc asked me it will be ok there's drugs to help most of the side effects.

[Barnclown]

Wishing you EVERY best wish! Do you know whether your lupus diagnosis still stand along side the Remitting Relapsing MS? Take care....hope you’ll keep us posted

🍀😘🍀😘 Coco

[I814u24u in reply to Barnclown]

Not lupus just the RRMS also semi blocked artery deep in brain not doing the biopsy thing yet that's another time still taking the aspirin though

[Ladyuponthelake]

I'm so pleased you have an answer!!! Sometimes knowing what we're fighting helps to fight. Fighting the unknown is like waving in the dark.

Good Luck with the meds I truly hope it helps daily life 🌻🌻🌻