After spending 36
hours in the ICU, Nick has been moved to a regular room at the hospital, which
is a good indication of the positive progress he is making toward recovery from
his Pulmonary Emboli. He was on complete bed rest the entire time he was in the
ICU and was being monitored around the clock. He is relieved to be out of there
although it was of great comfort to know that he was being watched so closely.
We continue to be
pleased with the level of care he is receiving at the hospital in Guatemala
City. He is still receiving injections of Lovenox every 12 hours and is likely
going to be on Coumadin for the rest of his life. Twenty-six years old is very
young to have blood clotting issues and a Pulmonary Embolism.
We know that there
is a genetic predisposition to clotting disorders on my side of the family as
my mother has a history of blood clots, my brother, Scott had a PE when he was
49 years old and my other brother, Ken has had multiple blood clots. Our plan
is to work with a Geneticist to determine what the gene or mutation is that
causes the clots. If Emily and/or Christopher test positive for it, we can then
get them on preventative care.
Yesterday
afternoon Nicholas had an Echocardiogram and they found that the right side of his heart
is quite enlarged. This is very common when having a Pulmonary Embolism as the
heart becomes strained. His doctor feels that with time, his heart will return
to its normal size.
Nicholas was in
good spirits when I spoke with him an hour ago. He walked around a little bit
(to the restroom and then over to the window) and became winded after that tiny
amount of movement but this is to be expected. He will gradually be able to
increase the distance he is able to walk as the clots dissolve and his blood
oxygen level improves. His heart rate is still high (also to be expected) but
his blood pressure is very good.
He will likely
remain in the hospital until Saturday. He needs to be at a therapeutic level on
the Coumadin before they will release him. He is not sure if he will stay in
Guatemala City or go back to Antigua to recover for 10 days before flying back
to Los Angeles. He will need to have his blood tested daily to determine his
INR (International Normalized Ratio), which is a universal number that
indicates how quickly the blood clots based on his PT (Prothrombin Time). Once
his INR remains at a consistent level (which takes months), he will be
able to stretch out the amount of time between blood tests, eventually needing
to go only once a month. I still go every other week (1 ½ years after my
Pulmonary Embolism) because my INR tends to fluctuate quite a bit but it has
simply become part of my routine and I think nothing of it. I am just thankful
to be on Coumadin and have peace of mind that the likelihood of forming more
blood clots is extremely low.
Thank you for all
of your notes of encouragement and for your prayers! We are so very grateful
for all of you and thankful for God’s blessing on Nick’s life.
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