I owe a lot of updates on
the blog.
I hope to find the time
soon.
Tuesday's MRI came back
how I thought.
The neurosurgeon was
running behind and we waited for quite some time.
We got there at 10:30a and
did not leave until 2:15p.
The neurosurgeon ended up
speaking with the neuro-radiologist prior to speaking with us.
Dr. Grossi (neurosurgeon)
will review my MRI with his Boss. He will also be sharing the MRI
with another neuro-radiologist and colleagues at The Duke Brain
Tumor Center.
The radiologist he spoke
with on Tuesday he was is #2 and the one at the Brain Tumor Center is
#1 and no one else come close to them.
He strongly recommends
that a biopsy be done.
There is a change in the
MRI. We don't have the official written report.
The most likely options
are a developmental cyst or a low-grade neoplasm.
The MRI is showing it more
consistent with the low-grade neoplasm, a glioma.
More specifically a Level
2 Glioma.
The Biopsy comes with
risks.
There is a 20-30% chance
they will not be able to identify it.
There is a 1% chance of a
bleed and 3-5% chance of seizure with the procedure.
We have a few more
questions for the Doctor and then will schedule the biopsy.
Depending on what the
biopsy shows will determine the next step.
If it is a Glioma I will
be sent to The Duke Brain Tumor Center to have it removed.
We thoroughly appreciate
all prayers anyone is willing to say for Our Family.
1 comment:
Oh my! I will keep you and your family in my prayers!!
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