To Sue and Rachael and others with MCTD

[Guest guest]

Sue and ,

My official dx is MCTD with suspect Lupus. I know what you are going

through too. To me, it seems like limbo - always waiting for the

next show to drop. I would love to hear from you both how you handle

it. It seems some doctors don't take it too seriously because it's

not full blown Lupus yet. However, other than major organ

involvement, I have all the symptoms of Lupus PLUS sjogrens,

raynauds,scleroderma, etc.

I think it will be great for us (and others with MCTD) to share our

experiences as they are slightly different than regular Lupies. I

look forward to hearing from you.

Jerri