Update on mold situation we had....chronic changes found in lungs

[Guest guest]

On April 2, Charlie Hart saw a pediatric pulmonologist for the first

time. (Finally, we were able to get him into one locally.)

His PA and Lateral X-rays showed the same thing as last time and

back in July (when we were living in the " mold house " ). It looks

like pneumonia to an untrained eye like my PCP or ME! However, in

the absence of clinical symptoms, she called it " chronic changes " . I

quizzed her a little and then came home and did my own research. It

is aka " Lung Disease " . Has anyone ever had any experience

with " chronic changes " or ever heard these terms before?

It is not looking good from what I am reading. Among high risk

children, it is the leading cause of death. Assuming MDS makes him

in the high risk category, I am extremely worried and biting my

nails.

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P.S. We are still on the path for finding an alternate attorney

(current one has a conflict of interest with their insurance

company), but it is looking good as of yesterday. Hopefully, i will

know something soon. BUT ALL THE MONEY IN THE WORLD WON'T SAVE MY

CHARLIE HART. WHAT DO I DO?