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MichelleygGwine to beFrozen Tree.In the garden

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New Lupus Foundation Message Boards!!

I’ve said it before I’m all about social networking.  When I got the email announcement from the LFA group from Facebook talking about the new message boards I thought, “yay!!!”.  If it hadn’t been for a Lupus message board on yahoo, I wouldn’t have met some wonderful people that I am so grateful to [...]

the results are in…

Well, I got the results back from my MRI and there are no lesions!!!! That means no MS. I talked to my neuro’s nurse who had me up the dose on my Lyrica, and they are setting up a referral for me to get a punch biopsy done to check for small fiber neuropathy.

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