Finally: After almost three years and multiple... - LUPUS UK

LUPUS UK

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Finally

I814u24u profile image
3 Replies

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.

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I814u24u profile image
I814u24u
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Barnclown profile image
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 profile image
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 profile image
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 🌻🌻🌻

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