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In the hospital

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In Michigan we are praying for you and your family!

It is so sad that medical treatment can be available to our children, but

because of a price tag, they STILL have to suffer with the pain!

Widdis

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Allie,

I'm so sorry to hear this. Sending prayers your way. Please keep us posted.

Krissy (emmie systemic Jra/uveitis )(Landen pauci)

Sent from my iPhone

On Mar 11, 2010, at 9:05 AM, Allie Pleiter <alliepleiter@...> wrote:

I'm emailing from the hospital, where my son has been admitted because his

latest bloodwork was so alarming. His SED rate is through the roof, his blood

sugar is rising, and his iron is so low they're considering a transfusion. His

rheumy (whom we love) is bringing in a whole team of specialists because the

methotrexate either isn't working or we don't have enough time to wait for it to

kick in. Time for new meds and stronger treatments. We're hoping this might

convince the insurance company to allow whatever meds the rheum recommends and

not to dink around with the less expensive stuff because we can't wait. We're

getting great treatment, and I do feel like this may a shocking yet useful

episode so we can get on with treatments. it's just so hard to see him getting

stuck with needles dozens of times a day knowing there's only more to come....

Allie P

Mom to CJ, 13, systemic JIA

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