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Hi, All! (BMT/XHIM)

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I've been reading most of the posts that come to me by email, but

otherwise just lurking....finding it hard to keep up with this group,

another email support group and all the Caringbridge kids I follow!!!

But I did want to drop by and say hello and extend my help to anyone

who is considering BMT for their child and/or is dealing with X-linked

Hyper IgM (XHIM).

Welcome to all the newcomers...hope this group provides much support

to you!

Thinking of my fellow PID friends,

~ Tatem

Mom of Kaitlyn,13 (healthy donor for brothers' double BMT)

,10 (XHIM, 1 yr. post BMT @ Duke)

, 6 (XHIM, 1 yr. post BMT @ Duke)

www.caringbridge.org/va/tatem

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